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Biochemistry
|
August 2, 1994
In vitro reconstitution of the 24-meric E2 inner core of bovine mitochondrial branched-chain alpha-keto acid dehydrogenase complex: requirement for chaperonins GroEL and GroES
R M Wynn, J R Davie, W Zhi, et al.
The Journal of Biological Chemistry
|
May 28, 1998
Impaired assembly of E1 decarboxylase of the branched-chain alpha-ketoacid dehydrogenase complex in type IA maple syrup urine disease
R M Wynn, J R Davie, J L Chuang, et al.
Methods in Enzymology
|
September 16, 2000
Expression of E1 component of human branched-chain alpha-keto acid dehydrogenase complex in Escherichia coli by cotransformation with chaperonins GroEL and GroES
R M Wynn, J R Davie, J L Song, et al.
Photosynthesis Research
|
January 21, 2014
Isolation of cytochrome bc 1 complexes from the photosynthetic bacteria Rhodopseudomonas viridis and Rhodospirillum rubrum
R M Wynn, D F Gaul, W K Choi, et al.
Structure (London, England : 1993)
|
April 4, 2000
Crystal structure of human branched-chain alpha-ketoacid dehydrogenase and the molecular basis of multienzyme complex deficiency in maple syrup urine disease
A AEvarsson, J L Chuang, R M Wynn, et al.
The Journal of Nutrition
|
June 1, 1995
Molecular basis of maple syrup urine disease and stable correction by retroviral gene transfer
D T Chuang, J R Davie, R M Wynn, et al.
Molecular Biology & Medicine
|
February 1, 1991
Maple syrup urine disease: domain structure, mutations and exon skipping in the dihydrolipoyl transacylase (E2) component of the branched-chain alpha-keto acid dehydrogenase complex
D T Chuang, C W Fisher, K S Lau, et al.
The Journal of Clinical Investigation
|
March 1, 1995
Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients
J L Chuang, J R Davie, J M Chinsky, et al.
Biochemical and Biophysical Research Communications
|
January 31, 1991
A 17-bp insertion and a Phe215----Cys missense mutation in the dihydrolipoyl transacylase (E2) mRNA from a thiamine-responsive maple syrup urine disease patient WG-34
C W Fisher, K S Lau, C R Fisher, et al.
The Journal of Biological Chemistry
|
August 25, 1995
Expression and characterization of branched-chain alpha-ketoacid dehydrogenase kinase from the rat. Is it a histidine-protein kinase?
J R Davie, R M Wynn, M Meng, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Biochemistry
|
August 2, 1994
In vitro reconstitution of the 24-meric E2 inner core of bovine mitochondrial branched-chain alpha-keto acid dehydrogenase complex: requirement for chaperonins GroEL and GroES
R M Wynn, J R Davie, W Zhi, et al.
The Journal of Biological Chemistry
|
May 28, 1998
Impaired assembly of E1 decarboxylase of the branched-chain alpha-ketoacid dehydrogenase complex in type IA maple syrup urine disease
R M Wynn, J R Davie, J L Chuang, et al.
Methods in Enzymology
|
September 16, 2000
Expression of E1 component of human branched-chain alpha-keto acid dehydrogenase complex in Escherichia coli by cotransformation with chaperonins GroEL and GroES
R M Wynn, J R Davie, J L Song, et al.
Photosynthesis Research
|
January 21, 2014
Isolation of cytochrome bc 1 complexes from the photosynthetic bacteria Rhodopseudomonas viridis and Rhodospirillum rubrum
R M Wynn, D F Gaul, W K Choi, et al.
Structure (London, England : 1993)
|
April 4, 2000
Crystal structure of human branched-chain alpha-ketoacid dehydrogenase and the molecular basis of multienzyme complex deficiency in maple syrup urine disease
A AEvarsson, J L Chuang, R M Wynn, et al.
The Journal of Nutrition
|
June 1, 1995
Molecular basis of maple syrup urine disease and stable correction by retroviral gene transfer
D T Chuang, J R Davie, R M Wynn, et al.
Molecular Biology & Medicine
|
February 1, 1991
Maple syrup urine disease: domain structure, mutations and exon skipping in the dihydrolipoyl transacylase (E2) component of the branched-chain alpha-keto acid dehydrogenase complex
D T Chuang, C W Fisher, K S Lau, et al.
The Journal of Clinical Investigation
|
March 1, 1995
Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients
J L Chuang, J R Davie, J M Chinsky, et al.
Biochemical and Biophysical Research Communications
|
January 31, 1991
A 17-bp insertion and a Phe215----Cys missense mutation in the dihydrolipoyl transacylase (E2) mRNA from a thiamine-responsive maple syrup urine disease patient WG-34
C W Fisher, K S Lau, C R Fisher, et al.
The Journal of Biological Chemistry
|
August 25, 1995
Expression and characterization of branched-chain alpha-ketoacid dehydrogenase kinase from the rat. Is it a histidine-protein kinase?
J R Davie, R M Wynn, M Meng, et al.
Page
of 7