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Lon R Cardon

Showing results (71-80 of 102) with videos related to

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Human Molecular Genetics|May 23, 2002
Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factorsDavid A van Heel, Irina A Udalova, Arjuna P De Silva, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2011
HLA-DQA1*02:01 is a major risk factor for lapatinib-induced hepatotoxicity in women with advanced breast cancerColin F Spraggs, Laura R Budde, Linda P Briley, et al.
Nature Genetics|June 30, 2015
The support of human genetic evidence for approved drug indicationsMatthew R Nelson, Hannah Tipney, Jeffery L Painter, et al.
American Journal of Human Genetics|March 5, 2005
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphismsMarcos M Miretti, Emily C Walsh, Xiayi Ke, et al.
Pharmacogenetics and Genomics|December 17, 2016
Characterization of ADME gene variation in 21 populations by exome sequencingDaniel H Hovelson, Zhengyu Xue, Matthew Zawistowski, et al.
Nature Communications|April 14, 2021
Identifying therapeutic drug targets using bidirectional effect genesKarol Estrada, Steven Froelich, Arthur Wuster, et al.
American Journal of Human Genetics|August 17, 2004
The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitisAndrew E Timms, Alison M Crane, Anne-Marie Sims, et al.
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.
Pageof 11

Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|May 23, 2002
Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factorsDavid A van Heel, Irina A Udalova, Arjuna P De Silva, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 20, 2011
HLA-DQA1*02:01 is a major risk factor for lapatinib-induced hepatotoxicity in women with advanced breast cancerColin F Spraggs, Laura R Budde, Linda P Briley, et al.
Nature Genetics|June 30, 2015
The support of human genetic evidence for approved drug indicationsMatthew R Nelson, Hannah Tipney, Jeffery L Painter, et al.
American Journal of Human Genetics|March 5, 2005
A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphismsMarcos M Miretti, Emily C Walsh, Xiayi Ke, et al.
Pharmacogenetics and Genomics|December 17, 2016
Characterization of ADME gene variation in 21 populations by exome sequencingDaniel H Hovelson, Zhengyu Xue, Matthew Zawistowski, et al.
Nature Communications|April 14, 2021
Identifying therapeutic drug targets using bidirectional effect genesKarol Estrada, Steven Froelich, Arthur Wuster, et al.
American Journal of Human Genetics|August 17, 2004
The interleukin 1 gene cluster contains a major susceptibility locus for ankylosing spondylitisAndrew E Timms, Alison M Crane, Anne-Marie Sims, et al.
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.
Pageof 11