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J L Clark

Showing results (171-180 of 204) with videos related to

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Molecular Endocrinology (Baltimore, Md.)|October 3, 2013
Melanocortin 4 receptor becomes an ACTH receptor by coexpression of melanocortin receptor accessory protein 2Maria Josep Agulleiro, Raúl Cortés, Begoña Fernández-Durán, et al.
Human Genetics|October 18, 2002
Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneityEmmanuelle Génin, Angela Huebner, Christine Jaillard, et al.
Endocrine Reviews|April 29, 2011
Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivityAlessia David, Vivian Hwa, Louise A Metherell, et al.
The Journal of Clinical Investigation|July 1, 1988
Detection and characterization of human serum antibodies to polycyclic aromatic hydrocarbon diol-epoxide DNA adductsM J Newman, B A Light, A Weston, et al.
Molecular Endocrinology (Baltimore, Md.)|November 29, 2002
Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activityFrancesca M Swords, Asma Baig, Diana M Malchoff, et al.
International Journal of Cancer|October 3, 1999
Modulation of invasive properties of murine squamous carcinoma cells by heterologous expression of cathepsin B and cystatin CS Coulibaly, H Schwihla, M Abrahamson, 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|September 4, 2012
Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndromeRenuka P Dias, Irina Bogdarina, Jean-Baptiste Cazier, et al.
The Journal of Clinical Investigation|February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humansClaire R Hughes, Leonardo Guasti, Eirini Meimaridou, 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.
Pageof 21

Showing results (171-180 of 204) with videos related to

Sort By:
Pageof 21
Molecular Endocrinology (Baltimore, Md.)|October 3, 2013
Melanocortin 4 receptor becomes an ACTH receptor by coexpression of melanocortin receptor accessory protein 2Maria Josep Agulleiro, Raúl Cortés, Begoña Fernández-Durán, et al.
Human Genetics|October 18, 2002
Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneityEmmanuelle Génin, Angela Huebner, Christine Jaillard, et al.
Endocrine Reviews|April 29, 2011
Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivityAlessia David, Vivian Hwa, Louise A Metherell, et al.
The Journal of Clinical Investigation|July 1, 1988
Detection and characterization of human serum antibodies to polycyclic aromatic hydrocarbon diol-epoxide DNA adductsM J Newman, B A Light, A Weston, et al.
Molecular Endocrinology (Baltimore, Md.)|November 29, 2002
Impaired desensitization of a mutant adrenocorticotropin receptor associated with apparent constitutive activityFrancesca M Swords, Asma Baig, Diana M Malchoff, et al.
International Journal of Cancer|October 3, 1999
Modulation of invasive properties of murine squamous carcinoma cells by heterologous expression of cathepsin B and cystatin CS Coulibaly, H Schwihla, M Abrahamson, 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|September 4, 2012
Multiple segmental uniparental disomy associated with abnormal DNA methylation of imprinted Loci in silver-russell syndromeRenuka P Dias, Irina Bogdarina, Jean-Baptiste Cazier, et al.
The Journal of Clinical Investigation|February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humansClaire R Hughes, Leonardo Guasti, Eirini Meimaridou, 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.
Pageof 21