Search research articles
Contact Us
Filters
Showing results (11-20 of 38) with videos related to
Page
of 4
Sort By:
Virology
|
March 3, 1997
Isolation and characterization of vesicular stomatitis virus PoIR revertants: polymerase readthrough of the leader-N gene junction is linked to an ATP-dependent function
J L Chuang, R L Jackson, J Perrault
The Journal of Biological Chemistry
|
April 15, 1993
Characterization of the promoter-regulatory region and structural organization of E1 alpha gene (BCKDHA) of human branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, R P Cox, D T Chuang
American Journal of Human Genetics
|
June 1, 1996
Maple syrup urine disease: the E1beta gene of human branched-chain alpha-ketoacid dehydrogenase complex has 11 rather than 10 exons, and the 3' UTR in one of the two E1beta mRNAs arises from intronic sequences
J L Chuang, R P Cox, D T Chuang
Biochimica Et Biophysica Acta
|
October 11, 1991
The midgut chymotrypsins of shrimps (Penaeus monodon, Penaeus japonicus and Penaeus penicillatus)
I H Tsai, P J Lu, J L Chuang
The Journal of Clinical Investigation
|
August 1, 1997
E2 transacylase-deficient (type II) maple syrup urine disease. Aberrant splicing of E2 mRNA caused by internal intronic deletions and association with thiamine-responsive phenotype
J L Chuang, R P Cox, D T Chuang
FEBS Letters
|
March 26, 1990
Molecular cloning of the mature E1b-beta subunit of human branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, R P Cox, D T Chuang
The Journal of Biological Chemistry
|
November 9, 2000
Roles of active site and novel K+ ion-binding site residues in human mitochondrial branched-chain alpha-ketoacid decarboxylase/dehydrogenase
R M Wynn, R Ho, J L Chuang, et al.
American Journal of Human Genetics
|
August 1, 1994
Molecular basis of maple syrup urine disease: novel mutations at the E1 alpha locus that impair E1(alpha 2 beta 2) assembly or decrease steady-state E1 alpha mRNA levels of branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, C R Fisher, R P Cox, et al.
Methods in Enzymology
|
September 16, 2000
Production of recombinant mammalian holo-E2 and E3 and reconstitution of functional branched-chain alpha-keto acid dehydrogenase complex with recombinant E1
J L Chuang, J R Davie, R M Wynn, et al.
The Journal of Biological Chemistry
|
April 3, 1999
GroEL/GroES-dependent reconstitution of alpha2 beta2 tetramers of humanmitochondrial branched chain alpha-ketoacid decarboxylase. Obligatory interaction of chaperonins with an alpha beta dimeric intermediate
J L Chuang, R M Wynn, J L Song, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Virology
|
March 3, 1997
Isolation and characterization of vesicular stomatitis virus PoIR revertants: polymerase readthrough of the leader-N gene junction is linked to an ATP-dependent function
J L Chuang, R L Jackson, J Perrault
The Journal of Biological Chemistry
|
April 15, 1993
Characterization of the promoter-regulatory region and structural organization of E1 alpha gene (BCKDHA) of human branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, R P Cox, D T Chuang
American Journal of Human Genetics
|
June 1, 1996
Maple syrup urine disease: the E1beta gene of human branched-chain alpha-ketoacid dehydrogenase complex has 11 rather than 10 exons, and the 3' UTR in one of the two E1beta mRNAs arises from intronic sequences
J L Chuang, R P Cox, D T Chuang
Biochimica Et Biophysica Acta
|
October 11, 1991
The midgut chymotrypsins of shrimps (Penaeus monodon, Penaeus japonicus and Penaeus penicillatus)
I H Tsai, P J Lu, J L Chuang
The Journal of Clinical Investigation
|
August 1, 1997
E2 transacylase-deficient (type II) maple syrup urine disease. Aberrant splicing of E2 mRNA caused by internal intronic deletions and association with thiamine-responsive phenotype
J L Chuang, R P Cox, D T Chuang
FEBS Letters
|
March 26, 1990
Molecular cloning of the mature E1b-beta subunit of human branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, R P Cox, D T Chuang
The Journal of Biological Chemistry
|
November 9, 2000
Roles of active site and novel K+ ion-binding site residues in human mitochondrial branched-chain alpha-ketoacid decarboxylase/dehydrogenase
R M Wynn, R Ho, J L Chuang, et al.
American Journal of Human Genetics
|
August 1, 1994
Molecular basis of maple syrup urine disease: novel mutations at the E1 alpha locus that impair E1(alpha 2 beta 2) assembly or decrease steady-state E1 alpha mRNA levels of branched-chain alpha-keto acid dehydrogenase complex
J L Chuang, C R Fisher, R P Cox, et al.
Methods in Enzymology
|
September 16, 2000
Production of recombinant mammalian holo-E2 and E3 and reconstitution of functional branched-chain alpha-keto acid dehydrogenase complex with recombinant E1
J L Chuang, J R Davie, R M Wynn, et al.
The Journal of Biological Chemistry
|
April 3, 1999
GroEL/GroES-dependent reconstitution of alpha2 beta2 tetramers of humanmitochondrial branched chain alpha-ketoacid decarboxylase. Obligatory interaction of chaperonins with an alpha beta dimeric intermediate
J L Chuang, R M Wynn, J L Song, et al.
Page
of 4