Retrovirology

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Disease-associated XMRV sequences are consistent with laboratory contamination

Stéphane Hué, Eleanor R Gray, Astrid Gall, Aris Katzourakis, Choon P Tan, Charlotte J Houldcroft, Stuart McLaren, Deenan Pillay, Andrew Futreal, Jeremy A Garson, Oliver G Pybus, Paul Kellam* and Greg J Towers*

Retrovirology 2010, 7:111 doi:10.1186/1742-4690-7-111

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Conference highlights of the 15th international conference on human retrovirology: HTLV and related retroviruses, 4-8 june 2011, Leuven, Gembloux, Belgium

Fabiola Martin, Charles RM Bangham, Vincenzo Ciminale, Michael D Lairmore, Edward L Murphy, William M Switzer, Renaud Mahieux Retrovirology 2011, 8:86 (28 October 2011)

This report summarizes presentations made at the June 2011, 15th International Conference on Human Retrovirology: HTLV and Related Viruses.

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Equal versus equivalent access to the scientific literature

Kuan-Teh Jeang Retrovirology 2011, 8:83 (21 October 2011)

The concepts of equal versus equivalent access to the scientific literature are discussed.

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Xenotropic murine leukemia virus-related virus is not associated with chronic fatigue syndrome in patients from different areas of the us in the 1990s

Mir A Ali, Janet K Dale, Christine A Kozak, Raphaela Goldbach-Mansky, Frederick W Miller, Stephen E Straus, Jeffrey I Cohen Virology Journal 2011, 8:450 (24 September 2011)

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Contamination of clinical specimens with MLV-encoding nucleic acids: implications for XMRV and other candidate human retroviruses

Robert A Smith Retrovirology 2010, 7:112 (20 December 2010)

Efforts to assess the prevalence of xenotropic murine leukemia virus-related virus (XMRV) in patients with prostate cancer and chronic fatigue syndrome have relied heavily on PCR-based testing of clinical samples and have yielded widely divergent findings. This week in Retrovirology, reports from four independent research groups illustrate the extreme care needed to exclude DNA or RNA contamination in PCR analyses of XMRV. In addition, phylogenetic evidence suggesting that previously-published XMRV sequences originated from a commonly-used prostate carcinoma cell line (22Rv1) is presented. These findings raise important questions regarding the provenance of XMRV and its potential connection to human disease.