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M S Patel

Showing results (181-190 of 224) with videos related to

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FEBS Letters|November 21, 1988
Nucleotide sequence of a cDNA for the dihydrolipoamide acetyltransferase component of human pyruvate dehydrogenase complexT J Thekkumkara, L Ho, I D Wexler, et al.
The International Journal of Biochemistry & Cell Biology|July 20, 2001
Human dihydrolipoamide dehydrogenase gene transcription is mediated by cAMP-response element-like site and TACGAC direct repeatH S Yang, J I Morris, Q Wang, et al.
The Journal of Biological Chemistry|March 3, 1995
Identification of the tryptophan residue in the thiamin pyrophosphate binding site of mammalian pyruvate dehydrogenaseM S Ali, B C Shenoy, D Eswaran, et al.
Biochimica Et Biophysica Acta|October 25, 1995
Arginine-239 in the beta subunit is at or near the active site of bovine pyruvate dehydrogenaseD Eswaran, M S Ali, B C Shenoy, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 15, 2013
Evidence of ancillary trigeminal innervation of levator palpebrae in the general populationA M Lehman, C C Dong, A M Harries, et al.
Journal of Postgraduate Medicine|April 1, 1980
Hand Schüller Christian diseaseA M Vaze, M G Koppikar, M S Patel, et al.
Journal of Postgraduate Medicine|July 1, 1980
Mesenteric fibromatosisM G Koppikar, A M Vaze, M S Patel, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Pageof 23

Showing results (181-190 of 224) with videos related to

Sort By:
Pageof 23
FEBS Letters|November 21, 1988
Nucleotide sequence of a cDNA for the dihydrolipoamide acetyltransferase component of human pyruvate dehydrogenase complexT J Thekkumkara, L Ho, I D Wexler, et al.
The International Journal of Biochemistry & Cell Biology|July 20, 2001
Human dihydrolipoamide dehydrogenase gene transcription is mediated by cAMP-response element-like site and TACGAC direct repeatH S Yang, J I Morris, Q Wang, et al.
The Journal of Biological Chemistry|March 3, 1995
Identification of the tryptophan residue in the thiamin pyrophosphate binding site of mammalian pyruvate dehydrogenaseM S Ali, B C Shenoy, D Eswaran, et al.
Biochimica Et Biophysica Acta|October 25, 1995
Arginine-239 in the beta subunit is at or near the active site of bovine pyruvate dehydrogenaseD Eswaran, M S Ali, B C Shenoy, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testingY S Hong, D S Kerr, T C Liu, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 15, 2013
Evidence of ancillary trigeminal innervation of levator palpebrae in the general populationA M Lehman, C C Dong, A M Harries, et al.
Journal of Postgraduate Medicine|April 1, 1980
Hand Schüller Christian diseaseA M Vaze, M G Koppikar, M S Patel, et al.
Journal of Postgraduate Medicine|July 1, 1980
Mesenteric fibromatosisM G Koppikar, A M Vaze, M S Patel, et al.
Pediatric Research|August 1, 1992
A mutation in the E1 alpha subunit of pyruvate dehydrogenase associated with variable expression of pyruvate dehydrogenase complex deficiencyI D Wexler, S G Hemalatha, T C Liu, et al.
Human Molecular Genetics|December 1, 1996
Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiencyY S Hong, D S Kerr, W J Craigen, et al.
Pageof 23