Human molecular genetics - JoVE Visualize

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Human Molecular Genetics|April 30, 2002

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsyJosé M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.

Human Molecular Genetics|April 30, 2002

Pallister-Hall syndrome phenotype in mice mutant for Gli3Jens Böse, Lars Grotewold, Ulrich Rüther

Human Molecular Genetics|April 30, 2002

Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtinAndreas Wyttenbach, Olivier Sauvageot, Jenny Carmichael, et al.

Human Molecular Genetics|February 1, 1995

Structure and function of ASP, the human homolog of the mouse agouti geneB D Wilson, M M Ollmann, L Kang, et al.

Human Molecular Genetics|February 1, 1995

Slow N-acetylation genotype is a susceptibility factor in occupational and smoking related bladder cancerA Risch, D M Wallace, S Bathers, et al.

Human Molecular Genetics|February 1, 1995

Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)H J Han, M Maruyama, S Baba, et al.

Human Molecular Genetics|February 1, 1995

The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotesP J Rocques, J Clark, S Ball, et al.

Human Molecular Genetics|February 1, 1995

The DXS423E gene in Xp11.21 escapes X chromosome inactivationC J Brown, A P Miller, L Carrel, et al.

Human Molecular Genetics|February 1, 1995

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.

Human Molecular Genetics|February 1, 1995

A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimerG R Mortier, D J Wilkin, W R Wilcox, et al.

Pageof 1,196

Showing results (681-690 of 11,953) with videos related to

Sort By:

Pageof 1,196

Human Molecular Genetics|April 30, 2002

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsyJosé M Morante-Redolat, Ana Gorostidi-Pagola, Salomé Piquer-Sirerol, et al.

Human Molecular Genetics|April 30, 2002

Pallister-Hall syndrome phenotype in mice mutant for Gli3Jens Böse, Lars Grotewold, Ulrich Rüther

Human Molecular Genetics|April 30, 2002

Heat shock protein 27 prevents cellular polyglutamine toxicity and suppresses the increase of reactive oxygen species caused by huntingtinAndreas Wyttenbach, Olivier Sauvageot, Jenny Carmichael, et al.

Human Molecular Genetics|February 1, 1995

Structure and function of ASP, the human homolog of the mouse agouti geneB D Wilson, M M Ollmann, L Kang, et al.

Human Molecular Genetics|February 1, 1995

Slow N-acetylation genotype is a susceptibility factor in occupational and smoking related bladder cancerA Risch, D M Wallace, S Bathers, et al.

Human Molecular Genetics|February 1, 1995

Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)H J Han, M Maruyama, S Baba, et al.

Human Molecular Genetics|February 1, 1995

The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotesP J Rocques, J Clark, S Ball, et al.

Human Molecular Genetics|February 1, 1995

The DXS423E gene in Xp11.21 escapes X chromosome inactivationC J Brown, A P Miller, L Carrel, et al.

Human Molecular Genetics|February 1, 1995

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19pB von Brederlow, A F Hahn, W J Koopman, et al.

Human Molecular Genetics|February 1, 1995

A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimerG R Mortier, D J Wilkin, W R Wilcox, et al.

Pageof 1,196