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Journal of Neuroscience Research
|
December 18, 2001
NMDA receptor function in mouse models of Huntington disease
C 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 gene
M 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 individuals
P 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 hemochromatosis
M 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, respectively
C Collins, C Duff, A M Duncan, et al.
Clinical Genetics
|
August 18, 1999
A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease: the Framingham Offspring Study
S E Gagné, M G Larson, S N Pimstone, et al.
The Journal of Clinical Investigation
|
February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease
H Funke, A von Eckardstein, P H Pritchard, et al.
The American Journal of Cardiology
|
February 15, 1994
Comparative efficacy and safety of pravastatin, nicotinic acid and the two combined in patients with hypercholesterolemia
J Davignon, G Roederer, M Montigny, et al.
American Journal of Medical Genetics
|
February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"
L L Estabrooks, W R Breg, M R Hayden, et al.
Annales De Genetique
|
January 1, 1992
Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada)
C Dionne, C Gagné, P Julien, et al.
Page
of 30
Search research articles
Search
Showing results (191-200 of 292) with videos related to
Sort By:
Page
of 30
Journal of Neuroscience Research
|
December 18, 2001
NMDA receptor function in mouse models of Huntington disease
C 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 gene
M 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 individuals
P 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 hemochromatosis
M 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, respectively
C Collins, C Duff, A M Duncan, et al.
Clinical Genetics
|
August 18, 1999
A common truncation variant of lipoprotein lipase (Ser447X) confers protection against coronary heart disease: the Framingham Offspring Study
S E Gagné, M G Larson, S N Pimstone, et al.
The Journal of Clinical Investigation
|
February 1, 1993
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease
H Funke, A von Eckardstein, P H Pritchard, et al.
The American Journal of Cardiology
|
February 15, 1994
Comparative efficacy and safety of pravastatin, nicotinic acid and the two combined in patients with hypercholesterolemia
J Davignon, G Roederer, M Montigny, et al.
American Journal of Medical Genetics
|
February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"
L L Estabrooks, W R Breg, M R Hayden, et al.
Annales De Genetique
|
January 1, 1992
Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada)
C Dionne, C Gagné, P Julien, et al.
Page
of 30