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G J Cote

Showing results (41-50 of 57) with videos related to

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Molecular and Cellular Biochemistry|July 1, 1987
Hepatoma-associated nonhistone chromosomal proteins are present in active chromatinB G Wen, A L Burkhard, G J Cote, et al.
Nucleic Acids Research|July 11, 1991
Validation of an in vitro RNA processing system for CT/CGRP precursor mRNAG J Cote, I N Nguyen, C J Lips, et al.
Cancer Letters|March 1, 1985
Oncogene expression in rat hepatomas and during hepatocarcinogenesisG J Cote, B A Lastra, J R Cook, et al.
Endocrinology and Metabolism Clinics of North America|March 1, 1996
Application of genetic screening information to the management of medullary thyroid carcinoma and multiple endocrine neoplasia type 2N Wohllk, G J Cote, D B Evans, et al.
American Journal of Human Genetics|September 1, 1996
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, N Wohllk, E Huang, et al.
Molecular and Cellular Probes|February 20, 1999
A codon 891 exon 15 RET proto-oncogene mutation in familial medullary thyroid carcinoma: a detection strategyG T Dang, G J Cote, P N Schultz, et al.
Pain|February 13, 2001
Arthritic calcitonin/alpha calcitonin gene-related peptide knockout mice have reduced nociceptive hypersensitivityL Zhang, A O Hoff, S J Wimalawansa, et al.
Neoplasia (New York, N.Y.)|August 10, 2000
Calcium-induced activation of a mutant G-protein-coupled receptor causes in vitro transformation of NIH/3T3 cellsA O Hoff, G J Cote, H A Fritsche, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinomaN Wohllk, G J Cote, M M Bugalho, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Molecular and Cellular Biochemistry|July 1, 1987
Hepatoma-associated nonhistone chromosomal proteins are present in active chromatinB G Wen, A L Burkhard, G J Cote, et al.
Nucleic Acids Research|July 11, 1991
Validation of an in vitro RNA processing system for CT/CGRP precursor mRNAG J Cote, I N Nguyen, C J Lips, et al.
Cancer Letters|March 1, 1985
Oncogene expression in rat hepatomas and during hepatocarcinogenesisG J Cote, B A Lastra, J R Cook, et al.
Endocrinology and Metabolism Clinics of North America|March 1, 1996
Application of genetic screening information to the management of medullary thyroid carcinoma and multiple endocrine neoplasia type 2N Wohllk, G J Cote, D B Evans, et al.
American Journal of Human Genetics|September 1, 1996
Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, N Wohllk, E Huang, et al.
Molecular and Cellular Probes|February 20, 1999
A codon 891 exon 15 RET proto-oncogene mutation in familial medullary thyroid carcinoma: a detection strategyG T Dang, G J Cote, P N Schultz, et al.
Pain|February 13, 2001
Arthritic calcitonin/alpha calcitonin gene-related peptide knockout mice have reduced nociceptive hypersensitivityL Zhang, A O Hoff, S J Wimalawansa, et al.
Neoplasia (New York, N.Y.)|August 10, 2000
Calcium-induced activation of a mutant G-protein-coupled receptor causes in vitro transformation of NIH/3T3 cellsA O Hoff, G J Cote, H A Fritsche, et al.
Science (New York, N.Y.)|April 21, 1995
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancyP M Thomas, G J Cote, N Wohllk, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1996
Relevance of RET proto-oncogene mutations in sporadic medullary thyroid carcinomaN Wohllk, G J Cote, M M Bugalho, et al.
Pageof 6