I N Day|D I Wilson - JoVE Visualize

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The Cochrane Database of Systematic Reviews|July 20, 2007

Botulinum toxin injections for adults with overactive bladder syndromeJ Duthie, D I Wilson, G P Herbison, et al.

Letters in Applied Microbiology|April 19, 2017

Effects of culture conditions on the size, morphology and wet density of spores of Bacillus cereus 569 and Bacillus megaterium QM B1551K Xu Zhou, F Wisnivesky, D I Wilson, 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.

Stroke|September 8, 2001

Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhageB Zhang, S Dhillon, I Geary, 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.

Annals of Human Genetics|October 1, 1991

The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14Y H Edwards, M F Fox, S Povey, et al.

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Showing results (51-60 of 117) with videos related to

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Pageof 12

The Cochrane Database of Systematic Reviews|July 20, 2007

Botulinum toxin injections for adults with overactive bladder syndromeJ Duthie, D I Wilson, G P Herbison, et al.

Letters in Applied Microbiology|April 19, 2017

Effects of culture conditions on the size, morphology and wet density of spores of Bacillus cereus 569 and Bacillus megaterium QM B1551K Xu Zhou, F Wisnivesky, D I Wilson, 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.

Stroke|September 8, 2001

Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhageB Zhang, S Dhillon, I Geary, 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.

Annals of Human Genetics|October 1, 1991

The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14Y H Edwards, M F Fox, S Povey, et al.

Pageof 12