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John R Gilbert

Showing results (41-50 of 98) with videos related to

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Neurogenetics|September 30, 2004
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer diseaseKristin K Nicodemus, Judith E Stenger, Donald E Schmechel, et al.
Human Genetics|September 23, 2009
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West AfricansDigna Rosa Velez, Christian Wejse, Martin E Stryjewski, et al.
Plos One|December 19, 2013
KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriersDeborah G Murdock, Yuki Bradford, Nathalie Schnetz-Boutaud, et al.
Nature Genetics|December 18, 2001
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21Rachel V Baxter, Kamel Ben Othmane, Julie M Rochelle, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 3, 2008
Refinement of 2q and 7p loci in a large multiplex NTD familyDemetra S Stamm, Deborah G Siegel, Lorraine Mehltretter, et al.
Neuroscience Letters|November 16, 2004
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genesRaquel Rabionet, James M Jaworski, Allison E Ashley-Koch, et al.
American Journal of Human Genetics|March 5, 2002
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorderYujun Shao, Kimberly L Raiford, Chantelle M Wolpert, et al.
Molecular and Cellular Neurosciences|September 8, 2007
A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer diseasePu-Ting Xu, Yi-Ju Li, Xue-Jun Qin, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 21, 2005
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2Kristen L Deak, Margaret E Dickerson, Elwood Linney, et al.
American Journal of Medical Genetics|February 13, 2002
No association between the WNT2 gene and autistic disorderPinky A McCoy, Yujun Shao, Chantelle M Wolpert, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Neurogenetics|September 30, 2004
Comprehensive association analysis of APOE regulatory region polymorphisms in Alzheimer diseaseKristin K Nicodemus, Judith E Stenger, Donald E Schmechel, et al.
Human Genetics|September 23, 2009
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West AfricansDigna Rosa Velez, Christian Wejse, Martin E Stryjewski, et al.
Plos One|December 19, 2013
KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriersDeborah G Murdock, Yuki Bradford, Nathalie Schnetz-Boutaud, et al.
Nature Genetics|December 18, 2001
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21Rachel V Baxter, Kamel Ben Othmane, Julie M Rochelle, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 3, 2008
Refinement of 2q and 7p loci in a large multiplex NTD familyDemetra S Stamm, Deborah G Siegel, Lorraine Mehltretter, et al.
Neuroscience Letters|November 16, 2004
Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genesRaquel Rabionet, James M Jaworski, Allison E Ashley-Koch, et al.
American Journal of Human Genetics|March 5, 2002
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorderYujun Shao, Kimberly L Raiford, Chantelle M Wolpert, et al.
Molecular and Cellular Neurosciences|September 8, 2007
A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer diseasePu-Ting Xu, Yi-Ju Li, Xue-Jun Qin, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|October 21, 2005
Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2Kristen L Deak, Margaret E Dickerson, Elwood Linney, et al.
American Journal of Medical Genetics|February 13, 2002
No association between the WNT2 gene and autistic disorderPinky A McCoy, Yujun Shao, Chantelle M Wolpert, et al.
Pageof 10