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I N Day

Showing results (51-60 of 80) with videos related to

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Clinical Chemistry|November 1, 1995
High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresisM K Bolla, L Haddad, S E Humphries, et al.
Biochimica Et Biophysica Acta|October 3, 1993
Characterisation of an epitope specific to the neuron-specific isoform of human enolase recognised by a monoclonal antibody raised against a synthetic peptide corresponding to the C-terminus of beta/A4-proteinC R Harrington, G B Quinn, J Hurt, et al.
Clinical Chemistry|April 29, 1998
CpG-PCR combined with sample pooling and mutant enrichment for CpG mutation screening in population studiesS D O'Dell, D J Wilson, P N Durrington, 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.
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.
Atherosclerosis|August 23, 1996
Rapid testing for three mutations causing familial defective apolipoprotein B100 in 562 patients with familial hypercholesterolaemiaP J Talmud, O J Tamplin, K Heath, 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.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
Clinical Chemistry|November 1, 1995
High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresisM K Bolla, L Haddad, S E Humphries, et al.
Biochimica Et Biophysica Acta|October 3, 1993
Characterisation of an epitope specific to the neuron-specific isoform of human enolase recognised by a monoclonal antibody raised against a synthetic peptide corresponding to the C-terminus of beta/A4-proteinC R Harrington, G B Quinn, J Hurt, et al.
Clinical Chemistry|April 29, 1998
CpG-PCR combined with sample pooling and mutant enrichment for CpG mutation screening in population studiesS D O'Dell, D J Wilson, P N Durrington, 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.
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.
Atherosclerosis|August 23, 1996
Rapid testing for three mutations causing familial defective apolipoprotein B100 in 562 patients with familial hypercholesterolaemiaP J Talmud, O J Tamplin, K Heath, 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.
Pageof 8