S Zhang|I N Day|S Ye - JoVE Visualize

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Genetics and Molecular Research : GMR|July 1, 2015

Effect of high-concentrate diet on amino acid transporter expression and milk quality in Holstein dairy cowsZ L Xie, P S Ye, Y S Zhang, et al.

Human Molecular Genetics|July 13, 2001

Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult malesT R Gaunt, J A Cooper, G J Miller, et al.

Nucleic Acids Research|July 11, 1995

Electrophoresis for genotyping: temporal thermal gradient gel electrophoresis for profiling of oligonucleotide dissociationI N Day, S D O'Dell, I D Cash, et al.

Annals of Human Genetics|April 17, 1998

Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindredsL Haddad, L B Day, J Attwood, et al.

Lancet (London, England)|July 21, 2001

Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective studyS E Humphries, P J Talmud, E Hawe, et al.

Human Mutation|September 30, 1999

Comparison of three methods for single nucleotide polymorphism typing for DNA bank studies: sequence-specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE)J W Holloway, B Beghé, S Turner, et al.

Journal of Medical Genetics|July 1, 1995

Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor geneR Whittall, V Gudnason, G P Weavind, et al.

Journal of Lipid Research|June 5, 1999

Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindredL Haddad, I N Day, S Hunt, et al.

Clinical Genetics|July 11, 1998

Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemiaE R De Oliveira e Silva, L Haddad, P O Kwiterovich, et al.

Journal of Medical Genetics|February 1, 1997

Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394I N Day, L Haddad, S D O'Dell, et al.

Pageof 518

Showing results (41-50 of 5,176) with videos related to

Sort By:

Pageof 518

Genetics and Molecular Research : GMR|July 1, 2015

Effect of high-concentrate diet on amino acid transporter expression and milk quality in Holstein dairy cowsZ L Xie, P S Ye, Y S Zhang, et al.

Human Molecular Genetics|July 13, 2001

Positive associations between single nucleotide polymorphisms in the IGF2 gene region and body mass index in adult malesT R Gaunt, J A Cooper, G J Miller, et al.

Nucleic Acids Research|July 11, 1995

Electrophoresis for genotyping: temporal thermal gradient gel electrophoresis for profiling of oligonucleotide dissociationI N Day, S D O'Dell, I D Cash, et al.

Annals of Human Genetics|April 17, 1998

Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindredsL Haddad, L B Day, J Attwood, et al.

Lancet (London, England)|July 21, 2001

Apolipoprotein E4 and coronary heart disease in middle-aged men who smoke: a prospective studyS E Humphries, P J Talmud, E Hawe, et al.

Human Mutation|September 30, 1999

Comparison of three methods for single nucleotide polymorphism typing for DNA bank studies: sequence-specific oligonucleotide probe hybridisation, TaqMan liquid phase hybridisation, and microplate array diagonal gel electrophoresis (MADGE)J W Holloway, B Beghé, S Turner, et al.

Journal of Medical Genetics|July 1, 1995

Utilities for high throughput use of the single strand conformational polymorphism method: screening of 791 patients with familial hypercholesterolaemia for mutations in exon 3 of the low density lipoprotein receptor geneR Whittall, V Gudnason, G P Weavind, et al.

Journal of Lipid Research|June 5, 1999

Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindredL Haddad, I N Day, S Hunt, et al.

Clinical Genetics|July 11, 1998

Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemiaE R De Oliveira e Silva, L Haddad, P O Kwiterovich, et al.

Journal of Medical Genetics|February 1, 1997

Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394I N Day, L Haddad, S D O'Dell, et al.

Pageof 518