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Showing results (71-80 of 126) with videos related to

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Annals of Human Genetics|May 22, 2012
Molecular and population analysis of natural selection on the human haptoglobin duplicationSantiago Rodriguez, Dylan M Williams, Philip A I Guthrie, et al.
Human Molecular Genetics|January 30, 2004
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traitsSantiago Rodríguez, Tom R Gaunt, Sandra D O'Dell, et al.
Pharmacogenetics and Genomics|May 15, 2007
Haplotype of growth hormone and angiotensin I-converting enzyme genes, serum angiotensin I-converting enzyme and ventricular growth: pathway inference in pharmacogeneticsShuwen Huang, Xiao-He Chen, John R Payne, et al.
Disease Markers|December 20, 2014
Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective studyPhilip A I Guthrie, Mohammad R Abdollahi, Tom Gaunt, et al.
Disease Markers|December 7, 2007
Homogeneous assay of rs4343, an ACE I/D proxy, and an analysis in the British Women's Heart and Health Study (BWHHS)Mohammad Reza Abdollahi, Shuwen Huang, Santiago Rodriguez, et al.
Biochemical Society Transactions|March 26, 2003
A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohortB Zhang, S Ye, A A Sayer, et al.
The Journal of Rheumatology|June 3, 2009
A study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort studyElaine M Dennison, Holly E Syddall, Karen A Jameson, et al.
Pharmacogenetics and Genomics|November 8, 2005
CYP2A6, MAOA, DBH, DRD4, and 5HT2A genotypes, smoking behaviour and cotinine levels in 1518 UK adolescentsShuwen Huang, Derek G Cook, Lesley J Hinks, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
Plos One|June 4, 2009
Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohortSantiago Rodriguez, Amanda J Hall, Raquel Granell, et al.
Pageof 13

Showing results (71-80 of 126) with videos related to

Sort By:
Pageof 13
Annals of Human Genetics|May 22, 2012
Molecular and population analysis of natural selection on the human haptoglobin duplicationSantiago Rodriguez, Dylan M Williams, Philip A I Guthrie, et al.
Human Molecular Genetics|January 30, 2004
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traitsSantiago Rodríguez, Tom R Gaunt, Sandra D O'Dell, et al.
Pharmacogenetics and Genomics|May 15, 2007
Haplotype of growth hormone and angiotensin I-converting enzyme genes, serum angiotensin I-converting enzyme and ventricular growth: pathway inference in pharmacogeneticsShuwen Huang, Xiao-He Chen, John R Payne, et al.
Disease Markers|December 20, 2014
Haptoglobin duplicon, hemoglobin, and vitamin C: analyses in the british women's heart and health study and Caerphilly prospective studyPhilip A I Guthrie, Mohammad R Abdollahi, Tom Gaunt, et al.
Disease Markers|December 7, 2007
Homogeneous assay of rs4343, an ACE I/D proxy, and an analysis in the British Women's Heart and Health Study (BWHHS)Mohammad Reza Abdollahi, Shuwen Huang, Santiago Rodriguez, et al.
Biochemical Society Transactions|March 26, 2003
A study of mitochondrial DNA mutations in peripheral lymphocytes in an aging cohortB Zhang, S Ye, A A Sayer, et al.
The Journal of Rheumatology|June 3, 2009
A study of relationships between single nucleotide polymorphisms from the growth hormone-insulin-like growth factor axis and bone mass: the Hertfordshire cohort studyElaine M Dennison, Holly E Syddall, Karen A Jameson, et al.
Pharmacogenetics and Genomics|November 8, 2005
CYP2A6, MAOA, DBH, DRD4, and 5HT2A genotypes, smoking behaviour and cotinine levels in 1518 UK adolescentsShuwen Huang, Derek G Cook, Lesley J Hinks, et al.
Mitochondrion|August 19, 2017
Cardiometabolic phenotypes and mitochondrial DNA copy number in two cohorts of UK womenAnna L Guyatt, Kimberley Burrows, Philip A I Guthrie, et al.
Plos One|June 4, 2009
Carrier status for the common R501X and 2282del4 filaggrin mutations is not associated with hearing phenotypes in 5,377 children from the ALSPAC cohortSantiago Rodriguez, Amanda J Hall, Raquel Granell, et al.
Pageof 13