M R Hayden|M M Nelson - JoVE Visualize

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Journal of Lipid Research|November 1, 1994

Mutagenesis in four candidate heparin binding regions (residues 279-282, 291-304, 390-393, and 439-448) and identification of residues affecting heparin binding of human lipoprotein lipaseY Ma, H E Henderson, M S Liu, et al.

The Pharmacogenomics Journal|August 5, 2009

Application of principal component analysis to pharmacogenomic studies in CanadaH Visscher, C J D Ross, M-P Dubé, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 10, 1998

Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1J Nasir, K Duan, K Nichol, et al.

Journal of Lipid Research|September 1, 1993

Structure-function relationships of lipoprotein lipase: mutation analysis and mutagenesis of the loop regionH E Henderson, Y Ma, M S Liu, et al.

American Journal of Human Genetics|March 1, 1989

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.

Journal of Neuroscience Research|December 18, 2001

NMDA receptor function in mouse models of Huntington diseaseC Cepeda, M A Ariano, C R Calvert, et al.

American Journal of Human Genetics|January 1, 1988

A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease geneM R Hayden, J Hewitt, J J Wasmuth, et al.

Atherosclerosis|September 1, 1987

Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hyperlipidaemic individualsP J Talmud, N Barni, A M Kessling, et al.

Clinical Genetics|April 22, 2004

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisM B Delatycki, K J Allen, P Gow, et al.

Genomics|July 1, 1993

Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectivelyC Collins, C Duff, A M Duncan, et al.

Pageof 34

Showing results (221-230 of 333) with videos related to

Sort By:

Pageof 34

Journal of Lipid Research|November 1, 1994

Mutagenesis in four candidate heparin binding regions (residues 279-282, 291-304, 390-393, and 439-448) and identification of residues affecting heparin binding of human lipoprotein lipaseY Ma, H E Henderson, M S Liu, et al.

The Pharmacogenomics Journal|August 5, 2009

Application of principal component analysis to pharmacogenomic studies in CanadaH Visscher, C J D Ross, M-P Dubé, et al.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 10, 1998

Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1J Nasir, K Duan, K Nichol, et al.

Journal of Lipid Research|September 1, 1993

Structure-function relationships of lipoprotein lipase: mutation analysis and mutagenesis of the loop regionH E Henderson, Y Ma, M S Liu, et al.

American Journal of Human Genetics|March 1, 1989

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.

Journal of Neuroscience Research|December 18, 2001

NMDA receptor function in mouse models of Huntington diseaseC Cepeda, M A Ariano, C R Calvert, et al.

American Journal of Human Genetics|January 1, 1988

A polymorphic DNA marker that represents a conserved expressed sequence in the region of the Huntington disease geneM R Hayden, J Hewitt, J J Wasmuth, et al.

Atherosclerosis|September 1, 1987

Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hyperlipidaemic individualsP J Talmud, N Barni, A M Kessling, et al.

Clinical Genetics|April 22, 2004

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosisM B Delatycki, K J Allen, P Gow, et al.

Genomics|July 1, 1993

Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectivelyC Collins, C Duff, A M Duncan, et al.

Pageof 34