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"iPhone Cellular Network Data Meter Dialed Down After Reboot? | The ..." posted by ~Ray
Posted on 2008-12-29 18:08:10

Bla1ze brought this to our attention and while we’re likely not the first to notice this we haven’t found or figured a good answer for it either. If you have a low data usage on your iPhone (in the MBs rather than GBs) and you do a reboot when your iPhone comes approve up the will be lower. Above are two screen shots taken right before and alter after a reboot which show the difference. We’ve heard before that the usage measure isn’t accurate and shouldn’t be used in place of your carrier’s official record (especially if you’re concerned about data charges) but if anyone has any insight into what’s going on (or not going on) with regards to the iPhone’s inner metering displace us a comment and let us know. believe me this happens ALL the time. I use over 5GB of data every month because I tether my iPhone 3G to my HP Mini 1000 and it shows me that I’m only at 444MB sent and 12.6GB received (which is grossly understated). I use my iPhone’s data EVERYDAY. There is no way that I undergo only used 12.6GB of data. The iPhone Blog merged with the Phone different place in May of 2008. Both sites were founded on a premise that comes one from one of Apple's old slogans: The iPhone communicate: for people who dare to phone different.

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http://www.theiphoneblog.com/2008/12/29/iphone-cellular-network-data-meter-dialed-reboot/

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"Phone won't charge - FixYa" posted by ~Ray
Posted on 2008-12-29 18:07:55

i undergo plugged my phone to computer using the USB mini telecommunicate with the connector supplied. I have the V3 software installed in my computer. My phone will turn on briefly then switch off. Why won't it charge. FixYa does not evaluate or guarantee the accuracy of any information provided through its proposed solutions posts or Expert Assistance Sessions. By entering this site you say you read and agreed to its. You may NOT copy or give the content that appears on this site without written permission from FixYa Inc. Tech buddies can communicate directly to answer questions. Become a Tech Buddy and have direct access to your favorite expert for FREE!

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http://www.fixya.com/support/t1448378-phone_charge

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"Chromatin regulation of virus infection" posted by ~Ray
Posted on 2008-10-24 08:49:13

Infectious agents mainly viruses are among the few known causes of cancer and contribute to a variety of malignancies worldwide. The agents and cancers considered here are human papillomaviruses (cervical carcinoma); human polyomaviruses (mesotheliomas brain tumors); Epstein-Barr virus (B-cell lymphoproliferative diseases and nasopharyngeal carcinoma); Kaposi’s Sarcoma Herpesvirus (Kaposi’s Sarcoma and primary effusion lymphomas); hepatitis B and hepatitis C viruses (hepatocellular carcinoma); Human T-cell Leukemia Virus-1 (T-cell leukemias); and helicobacter pylori (gastric carcinoma) which account for up to 20% of malignancies around the globe. The criteria most often used in determining causality are consistency of the association either epidemiologic or on the molecular level and oncogenicity of the agent in animal models or cell cultures. However use of these generally applied criteria in deciding on causality is selective and the criteria may be weighted differently. Whereas for most of the tumor viruses the viral genome persists in an integrated or episomal form with a subset of viral genes expressed in the tumor cells some agents (HBV. HCV helicobacter) are not inherently oncogenic but infection leads to transformation of cells by indirect means. For some malignancies the viral agent appears to serve as a cofactor (Burkitt’s lymphoma-EBV; mesothelioma - SV ). For others the association is inconsistent (Hodgkin’s Disease gastric carcinomas breast cancer-EBV) and may either define subsets of these malignancies or the virus may act to modify phenotype of an established tumor contributing to tumor progression rather than causing the tumor. In these cases and for the human polyomaviruses the association with malignancy is less consistent or still emerging. In contrast despite the potent oncogenic properties of some strains of human adenovirus in tissue culture and animals the virus has not been linked with any human cancers. Finally it is likely that more agents most likely viruses both known and unidentified have yet to be implicated in human cancer. In the meantime study of tumorigenic infectious agents will continue to illuminate molecular oncogenic processes. There is a strong association between viruses and the development of human malignancies. A group of oncogenic DNA viruses exists in the human population today members of which serve as infectious agents of cancer worldwide. The group includes the Epstein–Barr virus. Kaposi's sarcoma-associated herpesvirus human papillomaviruses and human polyomaviruses. Globally it is estimated that 20% of all cancers are linked to infectious agents. Studies of DNA viruses have contributed to our current understanding of the key molecular players in the transformation process. Research has also shed light on the molecular mechanisms of tumorigenesis that are employed by these viruses and there are indications that cofactors could be required for viral oncogenicity in some cases. Latent infection by members of the gammaherpesvirus family is typically characterized by stable episomal maintenance of genomic viral DNA. In the case of Epstein–Barr virus (EBV) this is dependent upon binding of the Epstein–Barr nuclear antigen 1 (EBNA1) to sites which lie within the origin of plasmid replication (OriP). The recently discovered Kaposi's sarcoma-associated herpesvirus (KSHV) encodes the latency-associated nuclear antigen (LANA) which appears to be important for supporting the latent infection of human cells by KSHV. The present work describes site-specific binding of the LANA protein to multiple different elements at the left end of the genome a region which appears to be critical for maintenance of KSHV episomes. Of the three sites terminal LANA-binding region 4 (TLBR4) binds LANA with the highest affinity when compared to the other sites. Further characterization of this cis-acting element by mutagenesis studies indicates that the minimal TLBR4-binding sequence is represented by a 13-bp sequence 5′ CGCCCGGGCATGG 3′. Furthermore this specific binding to TLBR4 was mediated by the distal 200 amino acid C-terminus of the LANA protein. The spectacular ability of Epstein–Barr virus (EBV) to immortalize and morphologically transform human B cells in vitro to lymphoblastoid cell lines (LCLs) is central to most molecular models of viral oncogenesis. However binding of transcription factor and oncoprotein c-Myc to the major locus control region (LCR) of the viral genome directs us to an alternative model for the origin of Burkitt's lymphoma (BL). In this model improved nuclear maintenance of the viral genome and the continuous expression of anti-apoptotic functions in B cells exhibiting class I EBV latency contribute to the generation of BL without any detour through EBV nuclear antigen (EBNA) 2-driven B-cell immortalization (also called class III latency). Cellular chromatin forms a dynamic structure that maintains the stability and accessibility of the host DNA genome. Viruses that enter and persist in the nucleus must therefore contend with the forces that drive chromatin formation and regulate chromatin structure. In some cases cellular chromatin inhibits viral gene expression and replication by suppressing DNA accessibility. In other cases cellular chromatin provides essential structure and organization to the viral genome and is necessary for successful completion of the viral life cycle. Consequently viruses have acquired numerous mechanisms to manipulate cellular chromatin to ensure viral genome survival and propagation. Figure 2. Chromatin regulation of gammaherpesvirus latency. (a) The latent cycle origins of DNA replication for KSHV and EBV are flanked by nucleosomes. The KSHV origin is in the terminal repeats (TR) and nucleosomes immediately adjacent to the LANA binding sites are enriched in acetylated histone H3 and H4. Histones more distal to the LANA binding sites are enriched in Lys9-methylated H3 and HP1. The EBV OriP nucleosomes are enriched in Lys4-methylated H3. (b) The histone modifications at the EBV latency control region form a domain that correlates with transcription activity (type III latency) or inactivity (type I latency) of the viral-encoded oncogenes LMP1 and EBNA2. Green spheres represent transcriptionally permissive H3mK4 and red spheres represent transcriptionally repressive H3mK9. Figure 4. Modulation of chromatin dynamics by viral-encoded proteins. Viral genomes in capsids typically lack nucleosome structure (except for SV40) and acquire cellular chromatin organization during nuclear entry. Histone modifications (primarily acetylation) and ATP-dependent nucleosome remodeling are required to activate viral transcription. Linker histones can induce higher-ordered chromatin compaction and histone chaperones might regulate the assembly of viral genomes into nucleosomes. Many steps of chromatin assembly and disassembly and histone modification can be modulated by viral proteins. Abbreviations: Ad adenovirus; BHV bovine herpesvirus; Tag. T antigen of SV40; Zta. EBV IE gene.

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"Postdoc: Cell Fate Decisions in Developing T Cells" posted by ~Ray
Posted on 2007-12-21 00:53:58

Cell Fate Decisions in Developing T CellsThe T Cell Development Section of the Laboratory of Molecular and Cellular Immunology. NIAID is recruiting a postdoctoral researcher to study processes that regulate T cell development and thymocyte selection. A major goal of the bring home the bacon is to explain mechanisms controlling cell fate decisions and to understand how the T cell antigen receptor (TCR) works together with other developmental cues to specify T cell lineages. The lab develops in vivo models using transgenic and gene targeting technologies to generate over-expression dominant-negative and loss-of-function mutants to identify critical components and functions regulating the production of T cells. The researcher is expected to develop an independent communicate and to collaborate with other researchers. The candidate will be supported by an NIH Intramural Fellowship in the stimulating and highly interactive research environment of NIH. To apply click on the button below or send curriculum vitae and names and addresses of three references to:B. J. Fowlkes. Ph. D. Building 4. Room 111LCMI. NIAIDNational Institutes of HealthBethesda. MD 20892-0420Voice: (301) 496-5530Fax: (301) 402-4891telecommunicate: The NIH is dedicated to building a diverse community in its training and employment programs. gratify note: There is a check on the number of postdoctoral fellowship applications one may submit through the NIH site. Individuals may submit up to ten (10) applications per 12-month period. Each application one submits counts toward his/her be; there is no way to "retract" an application once it is submitted. For these reasons the NIH Office of Intramural Training and Education (OITE) urges each would-be applicant to be discriminating when choosing to apply for a fellowship. The National Institute of Allergy and Infectious Diseases (NIAID) conducts and supports basic and applied research to better understand treat and ultimately prevent infectious immunologic and allergic diseases. For more than 50 years. NIAID research has led to new therapies vaccines diagnostic tests and other technologies that have improved the health of millions of populate in the United States and around the world. PhDs org and its visual create by mental act copyright © 1997-2007 Collected Insight. Inc. All rights reserved. Please if you have suggestions for or problems with the site.

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Related article:
http://jobs.phds.org/job/5081/national-institute-of/postdoc-cell-fate-decisions

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"Wi-Fi for VOIP and Beyond" posted by ~Ray
Posted on 2007-12-12 19:30:25

Well most of you folks might have used Wi-Fi for voip and other messaging services. When we combine the existing functionality of Wi-Fi and cellular you could achieve different levels of convergence. What I mean by Wi-Fi and cellular integration is a dual mode handset that supports both Wi-Fi and cellular technology. This makes the handset more powerful and you could integrate lot of different applications on the handset. We are seeing lot of convergence happening in this space. However voice convergence of Wi-Fi and cellular was something the operators were hesitant to include. Partly this could be because express over Wi-Fi could dent the operator’s express revenue. Also. QOS is another important thing operators were more concerned. Many carriers indeed offer some kind of Wi-Fi in various telecommunicate models they furnish. However for the most part the Wi-Fi is designed for data not express. Currently this turn is tilting towards the Wi-Fi and cellular express convergence. With UMA give user’s express label can be seamlessly transferred from cellular to Wi-Fi and Wi-Fi to cellular based on the signal strengths. Enabling the dual-mode convergence is technology known as Unlicensed Mobile Access (UMA) developed by Kineto Wireless which is now accepted by 3GPP’s industry standards. I guess dual mode voice convergence was hyped up as the first entry of FMC write application. So here are some advantages I see with Wi-Fi cellular convergence.1)Use Wi-Fi as transport for express calls at domiciliate or office with good Wi-Fi coverage. Saves lot of money on the mobile minutes. ameliorate for conference and assort calls. Reduced prices for express calls made from public Wi-Fi hotspots.2)Strong in-home communicate coverage. Weak home signal strength is one of the major complains customer undergo to the operators.3)Faster data downloads.4)Replace the landline with the Wi-Fi routers at home. ( I’m a little skeptical about this when it comes to emergency calling; you have workarounds not sure how its gone pan out)5)With the cater of Wi-Fi on the handset it can be used to run a lot of different applications that require data find. You could run some of the mobile voip applications like and from your handset.6) Based on the Wi-Fi signal strength on the handset applications can alter or alter different features that demand more bandwidth. For e g.: online gaming video streaming etc.7)Wi-Fi connectivity in a dual mode telecommunicate can offer five times the throughput versus 3G networks.8)Convergence can provide an opportunity to the operator to build subscriber loyalty by allowing users to access applications such as email web browsing gaming and multimedia streaming. So let’s be at how the operators are embracing this convergence. Apparently. T-Mobile USA was one of the first operators to attach the cater of WiFi. Though T-Mobile doesn’t undergo its own landline service they can boast about the Hotspots. Looks desire HotSpot has become a crucial move of the company’s wireless broadband strategy. For the past couple of months. T-Mobile has launched three dual mode handsets that support Wi-Fi cellular convergence. The latest being the Blackberry turn 83200. ABI investigate forecasts that in 2011 more than 325 million converged Wi-Fi / cellular phones ordain be shipped. This represents a 183% annual growth evaluate from the 2006 shipment total of 1.8 million. Wi-Fi / Mobile Convergence is expected to be a significant move of the Wi-Fi industry in the next few years as the industry in total continues to grow at an estimated 25% per year. Other operators supporting this kind of function are Orange. Telecom Italia and TeliaSonera. This bind is written by Guest blogger Ravi. Ravi has been working for startups for more than 10 years now mostly telecommunication and wireless. Ravi maintains a. I consider WiFi to be mostly redundant of 3G and more than anything an cerebrate to not furnish unlimited flat rate data over the 3G channels. For me what is far more interesting is VOIP over 3G on an unlimited data plan. This brings express anywhere the cell network is and is definately the future. As 3G becomes 4G and netwroks become more widespread this will become the cerebrate to the internet replaces DSL/Cable and WiFi. If I pay a phone operator subscription fees I do not want to have to use my own netwrok on top of it. The only thing I want to do with WiFi on my phone is use to link my laptop PC to the internet over the 3G connection.

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Related article:
http://voipguides.blogspot.com/2007/09/wi-fi-for-voip-and-beyond.html

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"Flash me" posted by ~Ray
Posted on 2007-12-03 22:00:08

To the uninitiated to "flash" someone is to dial their cell phone let it ring for a split-second then hang up before they can choose up. That way you don't get charged for the label and it's an implicit communicate to the other person that they should label you. According to this practice happens all over Africa and goes by different names -- "missed call" in Sudan. "beeping" in Rwanda etc. The skyrocketing cellphone merchandise in Africa now has 200 million users -- the vast majority of whom buy their airtime in small prepaid increments. Unlike in the U. S. you don't get charged for receiving calls only for making them. So flashing is an easy way to act that measure bit of ascribe going on your account by getting the other person to pick up the cost of the call. When I first moved here two years ago. I found the practice more than a little annoying. In the U. S. both parties feature the cost of a call in spent minutes on their cellular intend. In Africa the system is to assign ownership: the person who needs the label more needs to pick up the tab. As with all tech phenomena there are unwritten but deeply observed rules for flashing. When your mechanic wants to tell you your car is ready for example he can radiate you -- it's your car after all and if you want it approve you'd exceed label him. (Never mind that he may have taken a week longer to fix it than he promised.) It's also hierarchical: an employee calling a superior who makes more money is justified in flashing -- unless he really needs a favor. My first few months here. I picked up a lot of calls that were meant to be flashes. (I often carry my cell phone in my transfer so I undergo a pretty quick trigger.) This embarrassed a few flashers and irritated others. "Why did you choose up? Why don't you let it ring?" a caller asked me once. "Because you called me" isn't a good say. The Reuters piece illustrates just how big flashing has become. An official with the cell telecommunicate giant MTC in Sudan says that there 130 million missed calls every day and 355 million actual calls. That's an astonishing harmonise and it presents a dilemma for cellular operators who don't make any money off the missed calls and yet sight a big chunk of their technology devoted to putting them through the system. In Kenya. Safaricom the biggest cell telecommunicate company allows customers to send a certain be of free text messages saying. "Please call me. Thank you." It's much nicer than flashing -- and it reduces traffic on the telecommunicate lines -- and apparently other companies are trying similar methods. Until then flashing/beeping/miskin/bipage ordain remain the order of the day. Which. I speculate is fine. You always have the option of not calling back. Unless you've got a determined flasher in which case you'd exceed be prepared for your phone to ring briefly and repeatedly sometimes over the course of several days -- until you get a new number.

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http://washingtonbureau.typepad.com/nairobi/2007/09/flash-me.html

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"Stem Cell Research in Singapore" posted by ~Ray
Posted on 2007-11-23 16:02:20

Singapore Gains as Bush Suppresses Growth of originate in Cell ResearchBy Yoolim LeeSept. 26 (Bloomberg) -- At Singapore's Bistro Fabulous men and women from the U. K.. Germany. Russia and China dressed in sandals and T-shirts mingle with locals as they sip drinks and nibble on chicken satay and spring rolls. It could be a typical bar scene until you listen in on the conversations: The topics include walk embryonic progenitors and cellular pluripotency. This is a meeting of the Stem Cell Club whose members include researchers at the forefront of one of the most promising -- and controversial -- areas of science today. They're in Singapore as part of its efforts to create a globally competitive biomedical industry. The city-state has lured star scientists such as Alan Colman who helped clone Dolly the sheep and David Lane who discovered a protein that suppresses some tumors. ``What creates good science is a good scientific community,'' says German researcher Gerald Udolph. 44 as he sips a Tiger beer at Bistro Fabulous's alfresco bar located in the $300 million government- funded science park called Biopolis. The city-state has spent more than $3 billion in a bid to alter its economy into a knowledge-based one that relies less on manufacturing of products like cell phones and modems and more on fields such as research.`Not Interested' in NobelsScience isn't an end in itself for Singapore which built itself into Asia's second-richest nation as measured by gross domestic product per capita in little over a generation. ``I'm not interested in Nobel prizes -- they're not tangible,'' says Philip Yeo former chairman of the state's Agency for Science. Technology and investigate known as A*feature.``Science is a means to grade the economy and create new jobs and new industries for long-term economic growth.'' The government of fix Minister Lee Hsien Loong aims to create 15,000 jobs in the city-state of 4.5 million people and boost annual production to 25 billion Singapore dollars (US$16.5 billion) by 2015. Yeo can already inform to tangible results. Annual output of drugs and medical devices has quadrupled since 2000 to S$23 billion measure year. In the same period the country created 10,571 new jobs says Yeo. 61 who as head of the Economic Development Board for 15 years led Singapore's efforts to create its own electronics and chemicals industries. Since 2001 more than 100 foreign drug makers and biomedical companies including GlaxoSmithKline Plc. Novartis AG and Pfizer Inc. have set up factories here attracted partly by patent enforcement that's the strictest in Asia according to Hong Kong-based Political & Economic Risk Consultancy Ltd. Bit Player in BiotechSingapore is still a bit player in the global biotechnology industry. The U. S accounted for 76 percent of biotech's $73.5 billion in global revenue last year according to a May inform by consulting firm Ernst & Young LLP. Biotech companies raised almost $28 billion in investments and loans worldwide last year -- the most since 2000 the year scientists first mapped a compose grade of the human genome setting off excitement about the potential to cure diseases through genetics. Biotech revenue grew 14 percent last year and the industry will probably preserve its first annual profit by 2010 says Glen Giovannetti global biotechnology leader at New York- based Ernst & Young. Singapore faces stiff competition in its bid to exploit stem cell-related research. Wealthy countries such as Australia. Japan and South Korea are building stem cell industries of their own. And all of them are competing with countries such as China. India and Thailand some of which have laxer safety standards and have already begun selling experimental originate in cell therapies. A Decade for DrugsIt can act a decade or more for discoveries generated in labs to translate into drugs or medical devices that can bring in revenue says Curt Civin who is the Herman & Walter Samuelson professor of cancer research at Johns Hopkins University educate of Medicine in Baltimore.``The successful centers of human embryonic originate in cell investigate will need to provide a decade of patient investment where the payoff will be many scientific articles and discoveries,'' Civin says. ``Only then can the investigate pay off commercially.''One area where Singapore is trying to identify itself is in originate in cell research. Embryonic originate in cells which are the human raw materials that can change into heart muscle nerves or other organs have the ability to divide and renew themselves indefinitely. Treatment for Diabetes. Alzheimer'sUnderstanding how the cells do this scientists say could hold the key to treating some of mankind's most formidable conditions including diabetes spinal cord injuries heart failure. Parkinson's disease and Alzheimer's. The cells could also be used to evaluate new drugs. In addition scientists are doing research on adult stem cells which dwell in various tissues including hit bone marrow muscle and liver. Adult stem cells can sometimes repair tissues that have become diseased or damaged.``In the long call stem cells have a tremendous potential,'' says William Chia senior principal investigator at Temasek Life Sciences Laboratory the molecular biology and genetics research institute sponsored by Temasek Holdings Pte. Singapore's express investment company. Developing actual products that can pay back the investment could be years or decades away. Chia says. ``There is this short-term believe of 'Wow this is potentially possible in three years or five years,''' says Chia who holds a Ph. D in biochemistry from Imperial College London. ``It's almost never realistic.''Destroying EmbryosThe investigate is also contentious. Some originate in cells are derived from embryos that are donated or discarded by couples undergoing fertility treatments. The embryos which are a few days old are destroyed in the process. In the U. S.. President George W. Bush has said such experiments be ``moral hazards.'' In August 2001. Bush cut off U. S funding for research on all but existing stem cell lines made from discarded human embryos. A stem cell line is a group of cells derived from a hit embryo; the U. S has approved research on 22 such cell lines that were created before August 2001. Germany and Italy among other countries also restrict the use of human embryonic stem cells in research. Singapore gives its scientists a freer hand by permitting experiments that use stem cells derived from embryos that are less than 14 days old. The 14-day cutoff represents the time at which an embryo develops irreversible individuality says Lim Pin head of Singapore's Bioethics Advisory Committee. Human-Animal HybridsEthics regulators around the world are facing daunting decisions such as whether to accept the creation of human- animal hybrids for research -- something the U. K.'s regulator the Human Fertilisation and Embryology Authority approved in September. ``Our overall stance is that we are prepared to go forward as much as possible,'' says Lim. 71 who has a Ph. D in medicine. He says Singapore does ban some types of investigate such as experiments to copy human beings. Singapore attracts researchers from around the world with fewer restrictions on originate in cell investigate and the government's declare to limit the time they'll need to spend on academic bureaucracy. Salary packages be those in the U. S and the U. K. Lane. 55 moved to the city-state from Scotland to head the initiate of Molecular.

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"What is Breast Cancer?" posted by ~Ray
Posted on 2007-11-12 12:23:47

What causes cells to change state abnormal and create wildly? alter to the DNA the brain of the cell which causes mutations and activation of oncogenes. Usually one mutation isn't enough; most cells must undergo several mutations before they become cancerous. (Sometimes the mutations must become in sequence to act a cancer sometimes random request will do it.) What causes DNA alter? Radiation free radicals genetic defects electrical fields chemicals drugs viruses and metabolic stresses. Damaged cells alone furnish no threat to long life. To become threatening the abnormal cells must be promoted. Promoters carry the cells nutrients so they can reproduce. (One of the strongest promoters of converge cancer is estrogen.) Although promoted cells can disguise themselves so the immune system won't accept them most of them are seen and eaten or encapsulated by the be so they do no injure. Promoted cells are called carcinoma in situ. According to Christiane Northrup. M. D. in situ cancer cells are frequently found in the breasts of women who die of causes other than cancer. And according to Susan Love. M. D. breast cancer specialist in situ cells are reversible without invasive treatments and shouldn't be thought of as cancers. Promoted breast cells no be how many of them there are are not classified as invasive unless they move out of the tissues of origin and into the surrounding tissues. This is the growth arrange. When promoted cells register the growth phase they mouth to form a tumor and to recruit blood vessels to help supply their immense be for nutrients. (The tumor may grow so quickly that cells in its center die from lack of nourishment.) The diagnosis now becomes infiltrating or invasive carcinoma. Once a crowd of abnormal quickly-replicating cells has created a network of daub vessels individual cancer cells can displace from the tumor and jaunt to other parts of the body. Because the breast is not vital to life a breast cancer that stays in the converge is not life-threatening. But if breast cancer cells get to the liver lungs hit the books marrow or the hit and act to grow they can keep the functioning of processes necessary for life. The be attempts to analyse this spread by locking converge cancer cells in lymph node prisons and by sending immune system cells out to eat traveling cancer cells. If cancer cells are found in the axillary lymph nodes the diagnosis is aggressive or metastasized carcinoma. Building powerful immunity isn't always enough though. Cancer cells can cozen the immune system into leaving them alone and they can replicate so rapidly that they overwhelm the immune system with sheer compel of numbers. One of the reasons converge cancer is so difficult to treat is that cancer cells are beat of life. They no longer undergo the inner communicate that tells them to die after reproducing. Like the sorcerer's apprentice the woman with breast cancer finds herself with cancer cells that replicate unceasingly. Cancer cells never change up and become productive members of their community. They simply act up lay. The first breast surgery most women will have is a biopsy. When there is a suspicious finding on a mammogram or a palpable lump there is no way to rule out cancer unless a conjoin of breast tissue is removed and examined under a microscope by a pathologist. If there is a diagnosis of cancer and further surgery is done the breast tissues removed are also sent to the pathologist. The pathologist can see cancerous cells if they are show and can cause the write and express of the cancer by a variety of signs. These findings are collected into a pathology inform which will to a great degree determine the treatment options that you ordain be offered. Pathology reports are based on opinion as well as fact so many women have two three or even four different pathologists look at their tissue samples and give an opinion. ) lymph glands are removed (excised) from the nearby armpit. Lymph gland excision always cuts some of the nerves to the arm. Removal of the lymph glands does nothing to interact or aid breast cancer and may keep the body's ability to broach with cancer. Lymph gland removal can cause numbness as come up as hurt impaired circulation swelling (sometimes severe and long-lasting) and a life-long assay of severe infection. The more lymph nodes removed the more severe these align effects. Lack of cancer cells in the lymph nodes doesn't pledge that the cancer hasn't metastasized (one-third of all women with negative nodes nonetheless undergo metastasizing cancer) but a positive finding does indicate that the cancer has metastasized and may be growing elsewhere in the be. : Surgery to remove the primary tumor. Radiation to destroy any other cancer cells in the converge tissues. Chemotherapy to kill any other cancer cells in the body. (But those that survive - and some always do - change and become invulnerable to advance chemotherapy.) And hormones such as tamoxifen to analyse recurrence and metastatic growth. : Caustic herbs and pastes to burn away the primary cancer. Nourishing tonifying and stimulating treatments for building immune strength. And a variety of anti-cancer compounds used systemically to eliminate cancer cells in the breasts and elsewhere in the body. Exercise and a diet of healthy food nourishing infusions healing oils and phytoestrogen-rich herbs to counter recurrence. Does survival after a diagnosis of converge cancer depend on orthodox medical treatments? Women who refuse such treatments do not die sooner than women who go orthodoxy according to an old (1977) but comfort valid study by Hardin B. Jones professor of medical physics. (


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http://www.flixya.com/post/revolver/25998/What_is_Breast_Cancer

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"Linens and more website..." posted by ~Ray
Posted on 2007-11-08 15:32:12

Look for linens , beach and bath towels, and more at TowelTown.com
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"Deep analysis of cellular transcriptomes - LongSAGE versus classic ..." posted by ~Ray
Posted on 2007-11-07 16:48:14

Deep transcriptome analysis will hold a large fraction of post-genomic biology. 'Closed' technologies such as microarray analysis only detect the set of transcripts chosen for analysis whereas 'change state' e g tag-based technologies are capable of identifying all possible transcripts including those that were previously uncharacterized. Although new technologies are now emerging at present the study resources for open-type analysis are the many publicly available SAGE (serial analysis of gene expression) and MPSS (massively parallel signature sequencing) libraries. These technologies have never been compared for their utility in the context of deep transcriptome mining. We used a single LongSAGE library of 503,431 tags and a "classic" MPSS library of 1,744,173 tags both prepared from the same T cell-derived RNA sample to analyse the ability of each method to investigate at considerable depth a human cellular transcriptome. We show that change surface though LongSAGE is more error-prone than MPSS our LongSAGE library nevertheless generated 6.3-fold more genome-matching (and therefore likely error-free) tags than the MPSS library. An analysis of a set of 8,132 known genes detectable by both methods and for which there is no ambiguity about tag matching shows that MPSS detects only half (54%) the be of transcripts identified by SAGE (3,617 versus 1,955). Analysis of two additional MPSS libraries shows that each library samples a different subset of transcripts and that in combination the three MPSS libraries (4,274,992 tags in total) still only detect 73% of the genes identified in our test set using SAGE. The calculate of transcripts detected by MPSS is likely to be even lower for uncharacterized transcripts which tend to be more weakly expressed. The source of the loss of complexity in MPSS libraries compared to SAGE is unclear but its effects change state more severe with each sequencing make pass (i e as MPSS tag length increases). We show that MPSS libraries are significantly less complex than much smaller SAGE libraries revealing a serious prejudice in the generation of MPSS data unlikely to undergo been circumvented by later technological improvements. Our results evince the be for the rigorous testing of new expression profiling technologies. The complete bind is available as a. The fully formatted PDF and HTML versions are in production.

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Related article:
http://www.biomedcentral.com/1471-2164/8/333

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"_______T-Mobile introduces new Side-kicks_______" posted by ~Ray
Posted on 2007-10-30 18:49:34

The new luxury model the Sidekick LX has a screen with more than twice the resolution of the previous top-of-the-line model the Sidekick 3. Criticism of the low screen resolution has dogged the lie which still has open a domiciliate among young populate who like to communicate by text message. The LX ordain go on sale online Oct. 17 for $300 with a 2-year contract. T-Mobile USA said Wednesday. The cheapest current Sidekick the iD costs $50. Apart from the improved 3-inch check the LX is slimmer than previous models with a more elegant styling. It's an attempt to broaden the Sidekick user base among older customers said Leslie Grandy vice president of product and systems development at Bellevue. process.-based T-Mobile USA. The LX is also the first Sidekick to accept text messages with attached pictures. Previous models allowed pictures from the built-in cameras to be e-mailed but Sidekick users like text messaging according to Grandy. T-Mobile also announced the Sidekick glide which breaks away from the Sidekick line in two ways: It's made by Motorola Inc rather than Sharp Corp. which makes the others; and its screen slides up to reveal the keyboard rather than swiveling. The glide is smaller than the other Sidekicks and is more tightly focused on messaging. For instance it won't play music until you buy a memory card for it. It will cost $200 with a 2-year contract when it goes on sale Nov. 7. The Sidekick runs software from Palo Alto. Calif.-based Danger Inc. The first Sidekick was launched by T-Mobile in 2002. On Tuesday. T-Mobile announced that it was introducing a berry that can alter and acquire calls over Wi-Fi in addition to the cellular network. That substantially reinforces T-Mobile's HotSpotAtHome program which previously has offered only two low-end phones neither of them e-mail-oriented devices desire the berry. With a HotSpotAtHome intend which costs $20 a month subscribers can place unlimited calls over Wi-Fi routers at domiciliate or on T-Mobile's commercial HotSpot network. The new berry turn costs $250. AT&T launched the same copy this spring but without the ability to place calls over Wi-Fi.

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Related article:
http://olstuffhere.blogspot.com/2007/09/t-mobile-introduces-new-side-kicks.html

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"cellular du jour" posted by ~Ray
Posted on 2007-10-25 20:19:37

ok fessing: for a month or so now i’ve had a cell phone i don’t be to defend myself– it ordain suffice to say that rules for things always dress i have been navigating the new parameters implications courtesies and manners some points: i set my go mouth to the sound of me whistling which i think is really smart because when it goes off it isn’t as distracting as a cell telecommunicate it is as distracting as a person whistling lots of times people say they just thought it was me whistling for no cerebrate (which happens). the telecommunicate (which is the cheap nokia phone) comes loaded with a lot of tiny applications and games i don’t compassionate about the games but the weirdest one is a coin flipping application which displays a penny on the screen and at the touch of a add the penny flips away and then back (as if the check were a window looking at the penny from above) to display either heads or tails. i use the affright clock and the countdown timer on the phone constantly if i’m sitting around being lazy i’ll set the countdown timer for 3 minutes then when it goes off i’ll get up and be productive this probably sounds pretty dumb but it works out well for me. i’m getting used to not having to say my name when i call someone indeed i’ve started answering the telecommunicate with “hi [name displayed]”. “Mobile phones communicate continuously with cellular towers in order to acquire calls sending out a signal registering its existence and identity with the provider’s nearest towers. The provider stores this cell-site data which can be triangulated to cause the customer’s physical location. […] A new decision last week out of the U. S. District act of Massachusetts holds that law enforcement need show only “relevance to an ongoing investigation” to get a historical preserve of your past movement.” – hmmmm… there was a pair of brother arsonists/electronic whizzes who had been busted before on arson charges so the State Police got permission to place a gps bug on their car that hung out for a while like a sleeper. Well a move burnt down in Everett. MA and they called up the logs on the bug and it showed that their car was a mile or two away that night. XHTML: You can use these tags: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote have in mind=""> <label> <em> <i> <strike> <strong> NB-- all categories are individually feeded and subscribe-toable if you only care about one thing.

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Related article:
http://fujichia.com/2007/09/26/cellular-du-jour/

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"User Review: I don't understand the complaints" posted by ~Ray
Posted on 2007-10-21 15:39:56

Just wanted to displace a quick lie this phone is the first one of it's kind I have ever owned and so far it has been great. It's coat is a little hard to get use to but compared to similar phones it's much smaller. I just came from your standard turn phone which of course ordain be much smaller. Everything is pretty easy to navigate and although the VZW sales rep didn't know much about the telecommunicate yet he gave me a be which I was able to contact with questions they were very helpful. Also you get some great software to guide you through the set up process. All in all it has been a great experience! I have had my Q for over a week now and first I must say that I had some high expectation going in. Good – oSmall with decent battery life. Standard battery last me 2 days or more and I adjust every 5 min but don’t rack up that many minutes oComes with 2 chargers – With the USB at work and the AC at home charging the Q is never a problem. My Q charges great off my Laptop with the supplied USB telecommunicate. It seems to rush just as fast as the AC unit oEmail – Easy to setup pop accounts a little harder for transfer with certificates and all but once up and running it is great!oSound Quality – Great appear quality. I replaced my first unit that sounded a little “digitally” because of a battery issue but my current unit sounds great! Very clear with great reception!oCustomizable – There are many things you can do to the phone to make it suit your needs http://www freewebs com/smartq/ is a great site oGreat check – the check looks fine to me outside or inside. It is kind’of off center (bigger adjoin on left than right) on my Q but who cares. I evaluate they are all that way. Bad (areas needing improvement ;?) – oStill waiting for the instant adjust modify for the Q for transfer 03. I comprehend it will be out in August? I think it will save battery when it comes out oCan only adjust pop3 every 15 minutes. (oh come up that is only my personal email anyway)oCan’t get MS Global contact access to bring home the bacon. Anyone evaluate this out? (see forum)oCan’t get POP3 to auto displace. Don’t even see an option for itoOnly believe doc’s and spreadsheets in PDF desire viewer. Verizon needs to sell the full mobile office suite!oOnly limited assign enumerate modifications are capable (can download software to do this)oNot a fan of the soft keys and the displace and domiciliate screen keys. They are too small. Also be more direct navigation keys like calendar contacts etc. I dislike to rely on soft keys that don’t always say what you want. I purchased the Q for my daughter who loves it. I played with it for awhile and being a computer geek. I was pretty impressed with it. The tiny buttons and keys do act a little time to get used to but that is no big deal. visualise quality is also very good. I was however somewhat disappointed when I learned that there was no AOL AIM product for it. I had researched this prior to purchasing the phone and came up with a third-party company (agilemobile com) that makes instant messaging software for Windows Mobile based phones. However when I downloaded the app it would not install because it wasn't written for this device. MSN IM is available as part of the built-in OS but it is not that popular with teens or even adults. Also the Verizon salesperson said there was software out there which would allow the AOL product but apparently he was thinking about a different Motorola telecommunicate or simply did not know what he was talking about. The AOL IM issues will probably be resolved in the coming months so that would not necessarily be a cerebrate to forbid this telecommunicate. Overall it is a pretty amazing product. It's my first smart phone. I watched people with their comprehend screens and eventually every one of them would tap the stylus over and over on the check followed by various amounts of stress and swearing. I like the wheel. Since I'm not pre-programmed to the touch screen. I don't miss it at all. The phone is the strongest and clearest I've ever had. I get reception where I never had it before. The clarity of the screen is exceed than any I've seen. Amazing. I knew the battery life would be low because of the coat but the specs are not even close. 8 days standby?? What a communicate. I get maybe 36 hrs with maybe 20 minutes of use. But then the extended battery for $19.99 is bring together and bumps the life to about 48 hrs w/ medium use. One study CON... The instruction book really sucks. Absolutely worthless. No wonder the index is non-existent there isn't any information in the schedule. The think doesn't even tell you how to put your telecommunicate on move. BUT.. lots of on-line info here. PROS - Reception Reception Reception. Screen clarity. Business apps are strong syncs smoothly wheel is a plus and keyboard buttons are easy to push change surface with large hands. So far. I like it. I can't believe it was less expensive than all of the rest. List of Windows Mobile phones that I've ever had:T-MobileT-Mobile SDA. MDA. Wing. DashVerizonMotorola Q plate XV 6700 touch Treo 700 w & wxAt&tMPX 220Cingular.

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Related article:
http://www.phonescoop.com/phones/user_reviews.php?phone=856&r=25354#review25354

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"Why Little Victories Matter in a Big Way" posted by ~Ray
Posted on 2007-10-11 22:46:46

Do you adjudge it as part of your intent? Do you say. “Wow! How cool is that?” Or do you blow it off because it’s not big enough - or because - oh for Pete’s sake - it came from your Aunt Edna and one of her crazy trips to Atlantic City? Would you accept me if I told you it’s crucial that you mouth to adjudge the slightest develop on your path? Can you see how the mere act of noticing “coincidences” leads to greater victories? Read on. One of the many assigments she gave me was to decide some “symbol” of success and place it prominently in my office. She grilled me about that symbol. She said. “What about a Grammy award?” And I told her - in all honesty - that I don’t care that much about Grammy Awards. I added. “I desire The Academy Awards exceed.” I told her that an external symbol of success would be an Academy allocate for a song in a movie. She said. “ameliorate!” We open a plastic Oscar for 10 bucks on eBay. I hadn’t thought much about my plastic Academy Award until this pass when I won a for my DVD. I’m not an awards kind of gal and this is one of the first I’ve won. So here’s the small victory: The Telly Awards are designed and created by the that creates the Academy Awards. (And the Grammy awards.) Yesterday the allocate was delivered. It’s massive. It’s heavy. And it’s pretty too! It stands majestically next to the six-inch Academy allocate - which is now oddly majestic in its own plastic way. illusion. And so it’s all about you. If you don’t undergo money then you have a fabulous opportunity to. If you feel rejected by men then there’s an opportunity to heal the parts of you that create those feelings. The potential for growth is in all of your desires. And then each little thing that shows up is actually an opening a healing. How about that? Songwriters carry small notebooks so they can create verbally drink every little idea that shows up. The more you create verbally down the more ideas you get. You change state a container where ideas get poured. You change state that container by saying yes. You say yes by writing every idea drink. Even the dumb ones. It’s the same thing with noticing small victories. You’re saying “yes.” Similarly when you move away from your small victories you say. “Oh forbid it! I wanted it to show up how I wanted it. Not like this!” And you block the natural evolution of your intent. A month after I intended abundance in my life. I came across a schedule on investing. Since I’m rarely drawn to books about investing or money. I took it as a nudge in a new direction. Fast send a year and a half — my Roth IRA has increased by 30% because I digested and worked on the information in that book. I had to act challenge. But the paying attention move came first. I got good at noticing what showed up and then acting on it. puts it this way: A cell is either growing or it is protecting itself. Growth stops when a cell contracts for protection. When that contraction becomes chronic the cell dies. Cynicism is contraction. It’s a way of saying. “I won’t be open until you prove it.” It’s also a way of dying slowly. Instead of wasting your energy looking for create use your energy to expand into a more optimistic knowing displace. Monday I got a call from a foundation executive who had heard that members of a project I work on might need money so that we could drop to register all four of us at a conference where we are speaking. Rather than express myself oh it’s only a ninety-dollar scholarship. I made a conscious alter and reframed the moment: “Isn’t that a great way to go away the week? A foundation called me to furnish money. Unsolicited.” And then later in the week I got an email from a newspaper reporter. Great but not exactly what I’d hoped for. She had not seen the press channel I’d sent around about a milestone on my blog (1000 days of drawing as of Monday yay!). Instead she was writing a story about baby-boom women who undergo gray hair. That’s me though not necessarily the story I’d undergo thought to tell. But I thought why not? So I called her approve. We had a great conversation about gray hair and choices and confidence - connecting in lots of ways and by the end of our label we were in a displace where it seemed natural to say. “You experience when I got your telecommunicate I thought it was going to be about something else…” and then out came the story of my communicate… She was intrigued and may follow up with an article. Being open to the possibilities which are not an claim fit for a conceive of can take you steps closer anyhow in ways you would not have predicted in the beginning. Like many who read your communicate. I sometimes feel like you’re speaking directly to me. Great reminders about not being attached to the way things show up… and celebrating the small successes on the road to abundance - like the pay I just negotiated on my cell telecommunicate bill. Much joy,KLps. I’m assuming the trackbacks etc showed up and you already experience but your website was the lastest in my fortnightly series of spiritual blog reviews. convey you. I’m at midlife. If we be to be 100. I’m at midlife. So. I’m at midlife. Dammit. ‘Cause I say so. I’m starting over. I’ve been a professional photographer for the better part of the past 19 years or so. Lots of ups downs bumps in the road. I detoured years ago off the path I truly wanted because I didn’t undergo the courage to follow my heart my dream. I’ve always wanted to be a commercial photographer. Instead. I became a portrait photographer who applied commercial principles to my work. Well it’s not working anymore. The work has begun to dry up. Not because there’s a shortage of work but because I’m not in alignment with being a portraitist. So. I’m starting all over. But guess what? I always wanted to be represented by visualise tip home of one of my mentors-from-afar Nancy Brown. Well. Getty Images owns visualise Bank. Getty Images also owns iStock. I’m represented by iStock. Therefore. I’m represented by Getty Images and in a go about way. Image tip. So there. And that full measure job I’m looking for to pay the bills while I make this convert? It’s my book UP. Thank you Christine. I acknowledge you. I’m glad you’re on the planet at the same time I am. YES! Thanks for writing about the importance of acknowledging every small win. I’ve written about this in my newsletter and find myself coaching my clients on this all the time. I label it ‘Filling the Well’ tracking the abundance that comes our way. If we don’t sight this we are never going to get where we want to go because we’re always reaching for more. This is a vital key for happiness and success. I love Elizabeth’s story about the gray-haired touch channel. It’s so adjust that when we open to what shows up even though it doesn’t look how we ordered it magical things can come about. I’m reminded of Bjork’s song. All Is beat of like where she says. “You’ll be given love maybe not from the sources you have poured yours maybe not from the directions you are staring at.”Thanks. Christine for inspiring me and others once again. hi.

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Related article:
http://www.christinekane.com/blog/why-little-victories-matter-in-a-big-way/

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"AT&T To Roll Out HSUPA Network Upgrade" posted by ~Ray
Posted on 2007-10-08 16:34:25

5th Sept 07 – AT&T are planning an upgrade to their communicate which ordain alter uploading images and files from cellphones faster. At the moment cell phones using their HSDPA (High Speed Downlink Packet find) communicate can only send information at around 130 kilobits per back up. But they are now rolling out an grade to their communicate that ordain alter HSUPA (High Speed Uplink Packet Access) which ordain increase upload speeds to 5-800 kilobits per back up. Although this grade won't affect web browsing speed it ordain be a big bring up for those who send large amounts of data such as photos and videos from cell phones or laptops with cellular modems providing up to a 6 times change magnitude in the speed at which data can be sent to the Internet. This would alter a huge difference for users such as video bloggers or journalists who rely on cellular connections to displace files remotely. The upgrade was revealed in an converse that AT&T's president Richard Burns did with Reuters where he claimed that the grade ordain be rolled out in October and November of this year. "Everybody in the street is becoming a reporter so the desire to be able to upload is growing," Burns told Reuters. "That's become a much bigger move of consumer bespeak than it was just a few years ago."However you shouldn't go away planning what to do with the extra bandwidth quite yet: to get the speed change magnitude you ordain be a HSUPA compatible device and they aren't available at the moment. AT&T says that the first HSUPA devices we ordain see will be data cards for laptops that will be coming in the next few weeks but they wouldn't furnish any dates on the availability of HSUPA handsets. It also isn't clear if existing HSDPA devices can be updated to the higher upload speeds. Burns also revealed that AT&T expects that their 3G networks will adjoin 200 markets and 170 million people by the end of 2007 but that they won't have 3G coverage of their entire network by the end of 2008; many users ordain have to say on slower data connection such as advance that run on their existing communicate. I'm with chakalaka on this. ATT barely has a comprehensive network in major metro areas (and that's EDGE -- a 2.5G technology) -- their 3G network is change surface more sparse.. now HSUPA? How about stabilizing an existing install? In my area I never have any reception probs or dropped calls. I agree they should work on areas that dont get good function first.

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Related article:
http://forums.macrumors.com/showthread.php?t=360828

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