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AIDS and Behavior
|
December 24, 2013
Sampling methodologies for epidemiologic surveillance of men who have sex with men and transgender women in Latin America: an empiric comparison of convenience sampling, time space sampling, and respondent driven sampling
J L Clark, K A Konda, A Silva-Santisteban, et al.
Nature Genetics
|
January 18, 2005
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Louise A Metherell, J Paul Chapple, Sadani Cooray, et al.
Diabetes
|
May 27, 2003
Fetal programming of perivenous glucose uptake reveals a regulatory mechanism governing hepatic glucose output during refeeding
Helena C Murphy, Gemma Regan, Irina G Bogdarina, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 8, 2014
Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD)
Rathi Prasad, Li F Chan, Claire R Hughes, et al.
AIDS and Behavior
|
April 17, 2019
Social Network Organization, Structure, and Patterns of Influence Within a Community of Transgender Women in Lima, Peru: Implications for Biomedical HIV Prevention
J L Clark, A G Perez-Brumer, S L Reisner, 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 phenotypes
A David, C Camacho-Hübner, A Bhangoo, et al.
Clinical Endocrinology
|
June 9, 2007
GH responsiveness in a large multinational cohort of SGA children with short stature (NESTEGG) is related to the exon 3 GHR polymorphism
M Tauber, W Ester, F Auriol, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 2009
MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family
Li F Chan, Tom R Webb, Teng-Teng Chung, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 6, 2004
Growth hormone (GH) insensitivity syndrome due to a GH receptor truncated after Box1, resulting in isolated failure of STAT 5 signal transduction
A Milward, L Metherell, M Maamra, et al.
The Journal of Endocrinology
|
April 24, 2016
Loss of Mrap2 is associated with Sim1 deficiency and increased circulating cholesterol
T V Novoselova, R Larder, D Rimmington, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 204) with videos related to
Sort By:
Page
of 21
AIDS and Behavior
|
December 24, 2013
Sampling methodologies for epidemiologic surveillance of men who have sex with men and transgender women in Latin America: an empiric comparison of convenience sampling, time space sampling, and respondent driven sampling
J L Clark, K A Konda, A Silva-Santisteban, et al.
Nature Genetics
|
January 18, 2005
Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2
Louise A Metherell, J Paul Chapple, Sadani Cooray, et al.
Diabetes
|
May 27, 2003
Fetal programming of perivenous glucose uptake reveals a regulatory mechanism governing hepatic glucose output during refeeding
Helena C Murphy, Gemma Regan, Irina G Bogdarina, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 8, 2014
Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD)
Rathi Prasad, Li F Chan, Claire R Hughes, et al.
AIDS and Behavior
|
April 17, 2019
Social Network Organization, Structure, and Patterns of Influence Within a Community of Transgender Women in Lima, Peru: Implications for Biomedical HIV Prevention
J L Clark, A G Perez-Brumer, S L Reisner, 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 phenotypes
A David, C Camacho-Hübner, A Bhangoo, et al.
Clinical Endocrinology
|
June 9, 2007
GH responsiveness in a large multinational cohort of SGA children with short stature (NESTEGG) is related to the exon 3 GHR polymorphism
M Tauber, W Ester, F Auriol, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 31, 2009
MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family
Li F Chan, Tom R Webb, Teng-Teng Chung, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 6, 2004
Growth hormone (GH) insensitivity syndrome due to a GH receptor truncated after Box1, resulting in isolated failure of STAT 5 signal transduction
A Milward, L Metherell, M Maamra, et al.
The Journal of Endocrinology
|
April 24, 2016
Loss of Mrap2 is associated with Sim1 deficiency and increased circulating cholesterol
T V Novoselova, R Larder, D Rimmington, et al.
Page
of 21