Showing results (281-290 of 289) with videos related to
Sort By:
Pageof 29
You have reached the last page of results.This site can display upto 289 results.
The Journal of Infectious Diseases|March 24, 2009
A common CD4 gene variant is associated with an increased risk of HIV-1 infection in Kenyan female commercial sex workersJulius O Oyugi, Françoise C M Vouriot, Judie Alimonti, et al.Journal of Bacteriology|May 19, 2006
The genome of the obligately intracellular bacterium Ehrlichia canis reveals themes of complex membrane structure and immune evasion strategiesK Mavromatis, C Kuyler Doyle, A Lykidis, et al.Plos One|August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletionsDalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.Nature|February 8, 2013
APOBEC3B is an enzymatic source of mutation in breast cancerMichael B Burns, Lela Lackey, Michael A Carpenter, et al.Science (New York, N.Y.)|July 7, 2001
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolutionP Dehal, P Predki, A S Olsen, et al.Orphanet Journal of Rare Diseases|July 9, 2013
SURF1 deficiency: a multi-centre natural history studyYehani Wedatilake, Ruth M Brown, Robert McFarland, et al.Antimicrobial Agents and Chemotherapy|March 21, 2007
Bis-acridines as lead antiparasitic agents: structure-activity analysis of a discrete compound library in vitroConor R Caffrey, Dietmar Steverding, Ryan K Swenerton, et al.JAMA Neurology|October 9, 2013
COX10 mutations resulting in complex multisystem mitochondrial disease that remains stable into adulthoodRobert D S Pitceathly, Jan-Willem Taanman, Shamima Rahman, et al.Brain : a Journal of Neurology|November 21, 2013
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2A Reghan Foley, Manoj P Menezes, Amelie Pandraud, et al.Pageof 29