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L A Metherell

Showing results (21-30 of 26) with videos related to

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Hormone Research in Paediatrics|April 15, 2010
Acid-labile subunit deficiency and growth failure: description of two novel casesA David, S J Rose, F Miraki-Moud, et al.
American Journal of Human Genetics|July 27, 2001
Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivityL A Metherell, S A Akker, P B Munroe, et al.
The Journal of Endocrinology|February 8, 2006
A 36 residues insertion in the dimerization domain of the growth hormone receptor results in defective trafficking rather than impaired signalingM Maamra, A Milward, H Zarkesh Esfahani, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2008
The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the receptor to the cell surfaceT T Chung, T R Webb, L F Chan, et al.
Clinical Endocrinology|September 30, 2000
Tall stature in familial glucocorticoid deficiencyL L Elias, A Huebner, L A Metherell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 7, 2006
An intronic growth hormone receptor mutation causing activation of a pseudoexon is associated with a broad spectrum of growth hormone insensitivity phenotypesA David, C Camacho-Hübner, A Bhangoo, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Hormone Research in Paediatrics|April 15, 2010
Acid-labile subunit deficiency and growth failure: description of two novel casesA David, S J Rose, F Miraki-Moud, et al.
American Journal of Human Genetics|July 27, 2001
Pseudoexon activation as a novel mechanism for disease resulting in atypical growth-hormone insensitivityL A Metherell, S A Akker, P B Munroe, et al.
The Journal of Endocrinology|February 8, 2006
A 36 residues insertion in the dimerization domain of the growth hormone receptor results in defective trafficking rather than impaired signalingM Maamra, A Milward, H Zarkesh Esfahani, et al.
The Journal of Clinical Endocrinology and Metabolism|October 9, 2008
The majority of adrenocorticotropin receptor (melanocortin 2 receptor) mutations found in familial glucocorticoid deficiency type 1 lead to defective trafficking of the receptor to the cell surfaceT T Chung, T R Webb, L F Chan, et al.
Clinical Endocrinology|September 30, 2000
Tall stature in familial glucocorticoid deficiencyL L Elias, A Huebner, L A Metherell, et al.
The Journal of Clinical Endocrinology and Metabolism|December 7, 2006
An intronic growth hormone receptor mutation causing activation of a pseudoexon is associated with a broad spectrum of growth hormone insensitivity phenotypesA David, C Camacho-Hübner, A Bhangoo, et al.
Pageof 3