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T Conrad Gilliam

Showing results (11-20 of 43) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 10, 2004
Screen for expanded FMR1 alleles in patients with essential tremorDolores Garcia Arocena, Elan D Louis, Flora Tassone, et al.
Behavior Genetics|March 26, 2008
Rapid selection response for contextual fear conditioning in a cross between C57BL/6J and A/J: behavioral, QTL and gene expression analysisChristine A Ponder, Chetan P Huded, Michaelanne B Munoz, et al.
Biological Psychiatry|July 27, 2005
Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operationsGerard E Bruder, John G Keilp, Haiyan Xu, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2017
Strategic Integration of Multiple Bioinformatics Resources for System Level Analysis of Biological NetworksMark D'Souza, Dinanath Sulakhe, Sheng Wang, et al.
American Journal of Human Genetics|October 7, 2004
Evidence for sex-specific risk alleles in autism spectrum disorderJennifer L Stone, Barry Merriman, Rita M Cantor, et al.
Briefings in Bioinformatics|June 23, 2018
Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sourcesDinanath Sulakhe, Mark D'Souza, Sheng Wang, et al.
Human Molecular Genetics|September 11, 2003
Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factorsAlfredo Morabia, Eftihia Cayanis, Michael C Costanza, et al.
Nucleic Acids Research|June 21, 2014
Lynx web services for annotations and systems analysis of multi-gene disordersDinanath Sulakhe, Andrew Taylor, Sandhya Balasubramanian, et al.
The Journal of Investigative Dermatology|March 5, 2002
EB simplex superficialis resulting from a mutation in the type VII collagen geneAmalia Martinez-Mir, Jianjun Liu, Derek Gordon, et al.
Schizophrenia Research|November 23, 2006
DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory abilityHaiyan Xu, Christoph B Kellendonk, Eleanor H Simpson, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Movement Disorders : Official Journal of the Movement Disorder Society|August 10, 2004
Screen for expanded FMR1 alleles in patients with essential tremorDolores Garcia Arocena, Elan D Louis, Flora Tassone, et al.
Behavior Genetics|March 26, 2008
Rapid selection response for contextual fear conditioning in a cross between C57BL/6J and A/J: behavioral, QTL and gene expression analysisChristine A Ponder, Chetan P Huded, Michaelanne B Munoz, et al.
Biological Psychiatry|July 27, 2005
Catechol-O-methyltransferase (COMT) genotypes and working memory: associations with differing cognitive operationsGerard E Bruder, John G Keilp, Haiyan Xu, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 30, 2017
Strategic Integration of Multiple Bioinformatics Resources for System Level Analysis of Biological NetworksMark D'Souza, Dinanath Sulakhe, Sheng Wang, et al.
American Journal of Human Genetics|October 7, 2004
Evidence for sex-specific risk alleles in autism spectrum disorderJennifer L Stone, Barry Merriman, Rita M Cantor, et al.
Briefings in Bioinformatics|June 23, 2018
Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sourcesDinanath Sulakhe, Mark D'Souza, Sheng Wang, et al.
Human Molecular Genetics|September 11, 2003
Association of extreme blood lipid profile phenotypic variation with 11 reverse cholesterol transport genes and 10 non-genetic cardiovascular disease risk factorsAlfredo Morabia, Eftihia Cayanis, Michael C Costanza, et al.
Nucleic Acids Research|June 21, 2014
Lynx web services for annotations and systems analysis of multi-gene disordersDinanath Sulakhe, Andrew Taylor, Sandhya Balasubramanian, et al.
The Journal of Investigative Dermatology|March 5, 2002
EB simplex superficialis resulting from a mutation in the type VII collagen geneAmalia Martinez-Mir, Jianjun Liu, Derek Gordon, et al.
Schizophrenia Research|November 23, 2006
DRD2 C957T polymorphism interacts with the COMT Val158Met polymorphism in human working memory abilityHaiyan Xu, Christoph B Kellendonk, Eleanor H Simpson, et al.
Pageof 5