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Nature|May 21, 2010
Thousands of chemical starting points for antimalarial lead identificationFrancisco-Javier Gamo, Laura M Sanz, Jaume Vidal, et al.Human Mutation|March 15, 2012
Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in EuropeJustin P Rubio, Simon Topp, Liling Warren, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|October 20, 2011
An 18-kDa translocator protein (TSPO) polymorphism explains differences in binding affinity of the PET radioligand PBR28David R Owen, Astrid J Yeo, Roger N Gunn, et al.American Journal of Human Genetics|October 30, 2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United StatesClyde Francks, Silvia Paracchini, Shelley D Smith, et al.Gut|June 12, 2012
The intermediate filament protein, vimentin, is a regulator of NOD2 activityCraig Stevens, Paul Henderson, Elaine R Nimmo, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 18, 2011
Pazopanib efficacy in renal cell carcinoma: evidence for predictive genetic markers in angiogenesis-related and exposure-related genesChun-Fang Xu, Nan X Bing, Howard A Ball, et al.Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.Gastroenterology|July 5, 2016
Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish FamiliesAdam P Levine, Nikolas Pontikos, Elena R Schiff, et al.Genome Research|June 23, 2019
Exome-wide assessment of the functional impact and pathogenicity of multinucleotide mutationsJoanna Kaplanis, Nadia Akawi, Giuseppe Gallone, et al.Plos One|July 27, 2011
The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traitsJosine L Min, Jennifer M Taylor, J Brent Richards, et al.Pageof 19