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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 8, 2018
MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonation
Tatiana V Novoselova, Mashal Hussain, Peter J King, et al.
Endocrine Development
|
December 4, 2009
Diagnosis and treatment of Cushing's disease in children
Martin O Savage, Renuka P Dias, Li F Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 25, 2022
C-type natriuretic peptide is a pivotal regulator of metabolic homeostasis
Cristina Perez-Ternero, Aisah A Aubdool, Raj Makwana, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 3, 2014
NNT pseudoexon activation as a novel mechanism for disease in two siblings with familial glucocorticoid deficiency
Tatiana V Novoselova, Shoshana R Rath, Karen Carpenter, et al.
Molecular and Cellular Endocrinology
|
January 3, 2013
Familial glucocorticoid deficiency: New genes and mechanisms
Eirini Meimaridou, Claire R Hughes, Julia Kowalczyk, et al.
Endocrine Connections
|
December 14, 2022
Identification of a novel specific small-molecule melanocortin-2-receptor antagonist
Rachel Forfar, Mashal Hussain, Puneet Khurana, et al.
JMIR Formative Research
|
October 15, 2025
Exploring the Use of Digital Technology to Support Health Behavior Change in Young People Under the Care of Complications of Excess Weight (CCEW) Clinics: Qualitative Patient-Centered Design Study
Brioney Gee, Bonnie Teague, Matt Farrar, et al.
Clinical Endocrinology
|
January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
Li F Chan, Louise A Metherell, Heiko Krude, 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.
Aging Clinical and Experimental Research
|
June 23, 2025
Metabolic dysfunction over a life course key to healthy ageing inequality
Katie Littlewood, Jasleen Gegic, Mike Hickman, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 50) with videos related to
Sort By:
Page
of 5
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 8, 2018
MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonation
Tatiana V Novoselova, Mashal Hussain, Peter J King, et al.
Endocrine Development
|
December 4, 2009
Diagnosis and treatment of Cushing's disease in children
Martin O Savage, Renuka P Dias, Li F Chan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 25, 2022
C-type natriuretic peptide is a pivotal regulator of metabolic homeostasis
Cristina Perez-Ternero, Aisah A Aubdool, Raj Makwana, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 3, 2014
NNT pseudoexon activation as a novel mechanism for disease in two siblings with familial glucocorticoid deficiency
Tatiana V Novoselova, Shoshana R Rath, Karen Carpenter, et al.
Molecular and Cellular Endocrinology
|
January 3, 2013
Familial glucocorticoid deficiency: New genes and mechanisms
Eirini Meimaridou, Claire R Hughes, Julia Kowalczyk, et al.
Endocrine Connections
|
December 14, 2022
Identification of a novel specific small-molecule melanocortin-2-receptor antagonist
Rachel Forfar, Mashal Hussain, Puneet Khurana, et al.
JMIR Formative Research
|
October 15, 2025
Exploring the Use of Digital Technology to Support Health Behavior Change in Young People Under the Care of Complications of Excess Weight (CCEW) Clinics: Qualitative Patient-Centered Design Study
Brioney Gee, Bonnie Teague, Matt Farrar, et al.
Clinical Endocrinology
|
January 28, 2009
Homozygous nonsense and frameshift mutations of the ACTH receptor in children with familial glucocorticoid deficiency (FGD) are not associated with long-term mineralocorticoid deficiency
Li F Chan, Louise A Metherell, Heiko Krude, 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.
Aging Clinical and Experimental Research
|
June 23, 2025
Metabolic dysfunction over a life course key to healthy ageing inequality
Katie Littlewood, Jasleen Gegic, Mike Hickman, et al.
Page
of 5