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C Van Dop

Showing results (41-50 of 50) with videos related to

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Biochemical and Biophysical Research Communications|April 29, 1986
Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genesP A Donohoue, N Jospe, C J Migeon, et al.
Tissue Antigens|September 1, 1995
The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III regionP A Donohoue, L Guethlein, M M Collins, et al.
Biochemical and Biophysical Research Communications|November 30, 1992
Prevalence of three mutations in the Gs alpha gene among 24 families with pseudohypoparathyroidism type IaC K Lin, M J Hakakha, J M Nakamoto, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1985
Amino acid sequence of the alpha subunit of transducin deduced from the cDNA sequenceD C Medynski, K Sullivan, D Smith, et al.
Biochemical and Molecular Medicine|June 1, 1996
Concurrent hormone resistance (pseudohypoparathyroidism type Ia) and hormone independence (testotoxicosis) caused by a unique mutation in the G alpha s geneJ M Nakamoto, D Zimmerman, E A Jones, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
The Journal of Clinical Investigation|July 1, 1988
Increase of the 40,000-mol wt pertussis toxin substrate (G protein) in the failing human heartA M Feldman, A E Cates, W B Veazey, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophyM A Levine, T G Ahn, S F Klupt, et al.
Circulation|April 1, 1990
Diminished beta-adrenergic receptor responsiveness and cardiac dilation in hearts of myopathic Syrian hamsters (BIO 53.58) are associated with a functional abnormality of the G stimulatory proteinA M Feldman, R G Tena, P D Kessler, et al.
The Journal of Clinical Investigation|February 1, 1993
An arginine to histidine mutation in codon 311 of the C-erbA beta gene results in a mutant thyroid hormone receptor that does not mediate a dominant negative phenotypeM E Geffner, F Su, N S Ross, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Biochemical and Biophysical Research Communications|April 29, 1986
Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genesP A Donohoue, N Jospe, C J Migeon, et al.
Tissue Antigens|September 1, 1995
The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III regionP A Donohoue, L Guethlein, M M Collins, et al.
Biochemical and Biophysical Research Communications|November 30, 1992
Prevalence of three mutations in the Gs alpha gene among 24 families with pseudohypoparathyroidism type IaC K Lin, M J Hakakha, J M Nakamoto, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1985
Amino acid sequence of the alpha subunit of transducin deduced from the cDNA sequenceD C Medynski, K Sullivan, D Smith, et al.
Biochemical and Molecular Medicine|June 1, 1996
Concurrent hormone resistance (pseudohypoparathyroidism type Ia) and hormone independence (testotoxicosis) caused by a unique mutation in the G alpha s geneJ M Nakamoto, D Zimmerman, E A Jones, et al.
Human Molecular Genetics|February 1, 1995
Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious pubertyS Kosugi, C Van Dop, M E Geffner, et al.
The Journal of Clinical Investigation|July 1, 1988
Increase of the 40,000-mol wt pertussis toxin substrate (G protein) in the failing human heartA M Feldman, A E Cates, W B Veazey, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1988
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophyM A Levine, T G Ahn, S F Klupt, et al.
Circulation|April 1, 1990
Diminished beta-adrenergic receptor responsiveness and cardiac dilation in hearts of myopathic Syrian hamsters (BIO 53.58) are associated with a functional abnormality of the G stimulatory proteinA M Feldman, R G Tena, P D Kessler, et al.
The Journal of Clinical Investigation|February 1, 1993
An arginine to histidine mutation in codon 311 of the C-erbA beta gene results in a mutant thyroid hormone receptor that does not mediate a dominant negative phenotypeM E Geffner, F Su, N S Ross, et al.
Pageof 5