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Biochimica Et Biophysica Acta
|
April 12, 1997
Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency
X Q Song, T Fukao, G A Mitchell, et al.
The Journal of Biological Chemistry
|
February 25, 1993
3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency
G A Mitchell, M F Robert, P W Hruz, et al.
American Journal of Human Genetics
|
September 1, 1996
Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient
S Kassovska-Bratinova, T Fukao, X Q Song, et al.
Genomics
|
August 31, 2000
Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations
T Fukao, G A Mitchell, X Q Song, et al.
American Journal of Human Genetics
|
May 23, 2000
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype
C Bétard, A Rasquin-Weber, C Brewer, et al.
Neurology
|
July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defects
F-G Debray, Y Boulanger, A Khiat, et al.
Pediatric Research
|
March 3, 2001
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients
L Bouchard, M F Robert, D Vinarov, et al.
Diabetologia
|
July 27, 2006
Beta cell compensation for insulin resistance in Zucker fatty rats: increased lipolysis and fatty acid signalling
C J Nolan, J L Leahy, V Delghingaro-Augusto, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
December 20, 2012
Diversity of ARSACS mutations in French-Canadians
I Thiffault, M J Dicaire, M Tetreault, et al.
Clinical Genetics
|
March 4, 2017
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation
L Peña-Quintana, G Scherer, M L Curbelo-Estévez, et al.
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of 11
Search research articles
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Showing results (101-110 of 110) with videos related to
Sort By:
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You have reached the last page of results.
This site can display upto 110 results.
Biochimica Et Biophysica Acta
|
April 12, 1997
Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency
X Q Song, T Fukao, G A Mitchell, et al.
The Journal of Biological Chemistry
|
February 25, 1993
3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL). Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency
G A Mitchell, M F Robert, P W Hruz, et al.
American Journal of Human Genetics
|
September 1, 1996
Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient
S Kassovska-Bratinova, T Fukao, X Q Song, et al.
Genomics
|
August 31, 2000
Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations
T Fukao, G A Mitchell, X Q Song, et al.
American Journal of Human Genetics
|
May 23, 2000
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype
C Bétard, A Rasquin-Weber, C Brewer, et al.
Neurology
|
July 2, 2008
Reduced brain choline in homocystinuria due to remethylation defects
F-G Debray, Y Boulanger, A Khiat, et al.
Pediatric Research
|
March 3, 2001
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients
L Bouchard, M F Robert, D Vinarov, et al.
Diabetologia
|
July 27, 2006
Beta cell compensation for insulin resistance in Zucker fatty rats: increased lipolysis and fatty acid signalling
C J Nolan, J L Leahy, V Delghingaro-Augusto, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
December 20, 2012
Diversity of ARSACS mutations in French-Canadians
I Thiffault, M J Dicaire, M Tetreault, et al.
Clinical Genetics
|
March 4, 2017
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation
L Peña-Quintana, G Scherer, M L Curbelo-Estévez, et al.
Page
of 11