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Southern Medical Journal
|
March 27, 1999
Basal cell carcinoma with lung metastasis diagnosed by fine-needle aspiration biopsy
M S Patel, J T Thigpen, R B Vance, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 30, 2000
Adaptive changes in insulin secretion by islets from neonatal rats raised on a high-carbohydrate formula
M Srinivasan, R Aalinkeel, F Song, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 15, 1992
Characterization of the transcriptional regulatory region of the human dihydrolipoamide dehydrogenase gene
G L Johanning, J I Morris, K T Madhusudhan, et al.
Pediatric Research
|
July 1, 1988
A deficiency of both subunits of pyruvate dehydrogenase which is not expressed in fibroblasts
D S Kerr, S A Berry, M M Lusk, et al.
Molecular and Cellular Endocrinology
|
April 1, 1991
Regulation of human growth hormone receptor gene expression by human growth hormone in a human hepatoma cell line
P E Mullis, T Lund, M S Patel, et al.
Pediatric Research
|
October 1, 1973
Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome)
A B Gruskin, M S Patel, M Linshaw, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1989
Characterization of cDNAs encoding human pyruvate dehydrogenase alpha subunit
L Ho, I D Wexler, T C Liu, et al.
Genome
|
August 1, 1994
Identification of a sequence motif upstream of the Drosophila dopa decarboxylase gene that enhances heterologous gene expression
R B Hodgetts, M S Patel, J Piorecky, et al.
Clinical Endocrinology
|
April 1, 1991
Growth characteristics and response to growth hormone therapy in patients with hypochondroplasia: genetic linkage of the insulin-like growth factor I gene at chromosome 12q23 to the disease in a subgroup of these patients
P E Mullis, M S Patel, P M Brickell, et al.
Human Mutation
|
January 1, 1996
Three new mutations of the pyruvate dehydrogenase alpha subunit: a point mutation (M181V), 3 bp deletion (-R282), and 16 bp insertion/frameshift (K358SVS-->TVDQS)
A Tripatara, D S Kerr, M M Lusk, et al.
Page
of 23
Search research articles
Search
Showing results (161-170 of 224) with videos related to
Sort By:
Page
of 23
Southern Medical Journal
|
March 27, 1999
Basal cell carcinoma with lung metastasis diagnosed by fine-needle aspiration biopsy
M S Patel, J T Thigpen, R B Vance, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 30, 2000
Adaptive changes in insulin secretion by islets from neonatal rats raised on a high-carbohydrate formula
M Srinivasan, R Aalinkeel, F Song, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 15, 1992
Characterization of the transcriptional regulatory region of the human dihydrolipoamide dehydrogenase gene
G L Johanning, J I Morris, K T Madhusudhan, et al.
Pediatric Research
|
July 1, 1988
A deficiency of both subunits of pyruvate dehydrogenase which is not expressed in fibroblasts
D S Kerr, S A Berry, M M Lusk, et al.
Molecular and Cellular Endocrinology
|
April 1, 1991
Regulation of human growth hormone receptor gene expression by human growth hormone in a human hepatoma cell line
P E Mullis, T Lund, M S Patel, et al.
Pediatric Research
|
October 1, 1973
Renal function studies and kidney pyruvate carboxylase in subacute necrotizing encephalomyelopathy (Leigh's syndrome)
A B Gruskin, M S Patel, M Linshaw, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1989
Characterization of cDNAs encoding human pyruvate dehydrogenase alpha subunit
L Ho, I D Wexler, T C Liu, et al.
Genome
|
August 1, 1994
Identification of a sequence motif upstream of the Drosophila dopa decarboxylase gene that enhances heterologous gene expression
R B Hodgetts, M S Patel, J Piorecky, et al.
Clinical Endocrinology
|
April 1, 1991
Growth characteristics and response to growth hormone therapy in patients with hypochondroplasia: genetic linkage of the insulin-like growth factor I gene at chromosome 12q23 to the disease in a subgroup of these patients
P E Mullis, M S Patel, P M Brickell, et al.
Human Mutation
|
January 1, 1996
Three new mutations of the pyruvate dehydrogenase alpha subunit: a point mutation (M181V), 3 bp deletion (-R282), and 16 bp insertion/frameshift (K358SVS-->TVDQS)
A Tripatara, D S Kerr, M M Lusk, et al.
Page
of 23