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R M WYNN

Showing results (31-40 of 45) with videos related to

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Biochimica Et Biophysica Acta|August 17, 1989
The Rhodospirillum rubrum cytochrome bc1 complex: peptide composition, prosthetic group content and quinone bindingA Kriauciunas, L Yu, C A Yu, et al.
The Journal of Biological Chemistry|July 13, 2001
Biochemical basis of type IB (E1beta ) mutations in maple syrup urine disease. A prevalent allele in patients from the Druze kindred in IsraelR M Wynn, J L Chuang, C Sansaricq, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2001
Structure of rat BCKD kinase: nucleotide-induced domain communication in a mitochondrial protein kinaseM Machius, J L Chuang, R M Wynn, et al.
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 GroESR 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 diseaseR M Wynn, J R Davie, J L Chuang, et al.
Photosynthesis Research|January 21, 2014
Isolation of cytochrome bc 1 complexes from the photosynthetic bacteria Rhodopseudomonas viridis and Rhodospirillum rubrumR 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 diseaseA 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 transferD 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 complexD 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 patientsJ L Chuang, J R Davie, J M Chinsky, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Biochimica Et Biophysica Acta|August 17, 1989
The Rhodospirillum rubrum cytochrome bc1 complex: peptide composition, prosthetic group content and quinone bindingA Kriauciunas, L Yu, C A Yu, et al.
The Journal of Biological Chemistry|July 13, 2001
Biochemical basis of type IB (E1beta ) mutations in maple syrup urine disease. A prevalent allele in patients from the Druze kindred in IsraelR M Wynn, J L Chuang, C Sansaricq, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2001
Structure of rat BCKD kinase: nucleotide-induced domain communication in a mitochondrial protein kinaseM Machius, J L Chuang, R M Wynn, et al.
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 GroESR 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 diseaseR M Wynn, J R Davie, J L Chuang, et al.
Photosynthesis Research|January 21, 2014
Isolation of cytochrome bc 1 complexes from the photosynthetic bacteria Rhodopseudomonas viridis and Rhodospirillum rubrumR 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 diseaseA 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 transferD 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 complexD 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 patientsJ L Chuang, J R Davie, J M Chinsky, et al.
Pageof 5