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A J L Clark

Showing results (11-20 of 25) with videos related to

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European Journal of Endocrinology|October 9, 2009
Identification and characterisation of a novel GHR defect disrupting the polypyrimidine tract and resulting in GH insensitivityA David, F Miraki-Moud, N J Shaw, et al.
European Journal of Endocrinology|September 29, 2011
Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory proteinV Jain, L A Metherell, A David, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing's disease?F M Swords, S Aylwin, L Perry, et al.
Journal of Endocrinological Investigation|December 13, 2003
Rapid desensitisation of the GH secretagogue (ghrelin) receptor to hexarelin in vitroR D Orkin, D I New, D Norman, et al.
European Journal of Endocrinology|October 13, 2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiencyL A Metherell, M O Savage, M Dattani, et al.
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.
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|December 31, 2009
d3-GHR genotype does not explain heterogeneity in GH responsiveness in hypopituitary adultsV J Moyes, D M Walker, S Owusu-Antwi, 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 (11-20 of 25) with videos related to

Sort By:
Pageof 3
European Journal of Endocrinology|October 9, 2009
Identification and characterisation of a novel GHR defect disrupting the polypyrimidine tract and resulting in GH insensitivityA David, F Miraki-Moud, N J Shaw, et al.
European Journal of Endocrinology|September 29, 2011
Neonatal presentation of familial glucocorticoid deficiency resulting from a novel splice mutation in the melanocortin 2 receptor accessory proteinV Jain, L A Metherell, A David, et al.
The Journal of Clinical Endocrinology and Metabolism|February 12, 2005
The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing's disease?F M Swords, S Aylwin, L Perry, et al.
Journal of Endocrinological Investigation|December 13, 2003
Rapid desensitisation of the GH secretagogue (ghrelin) receptor to hexarelin in vitroR D Orkin, D I New, D Norman, et al.
European Journal of Endocrinology|October 13, 2004
TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiencyL A Metherell, M O Savage, M Dattani, et al.
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.
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|December 31, 2009
d3-GHR genotype does not explain heterogeneity in GH responsiveness in hypopituitary adultsV J Moyes, D M Walker, S Owusu-Antwi, 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