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Human Molecular Genetics
|
July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Vera B Kaiser, Victoria Svinti, James G Prendergast, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3
Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Nature
|
June 26, 2020
Pervasive lesion segregation shapes cancer genome evolution
Sarah J Aitken, Craig J Anderson, Frances Connor, et al.
Cell
|
September 18, 2012
Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma
Christine Guo Lian, Yufei Xu, Craig Ceol, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood
Elena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 31, 2020
Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations
Carlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Montenegro, et al.
The Lancet. Diabetes & Endocrinology
|
March 5, 2026
Risk of recurrence after successful surgery for Cushing's disease and association with USP8 genotype and tumour size: an international, retrospective, longitudinal cohort study
Qilin Zhang, Yixin Cai, Yuyu Liu, et al.
Nature Reviews. Endocrinology
|
September 5, 2023
Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement
Stephan Petersenn, Maria Fleseriu, Felipe F Casanueva, et al.
The Lancet. Diabetes & Endocrinology
|
June 29, 2023
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study
Ana P M Canton, Flávia R Tinano, Leonardo Guasti, et al.
Nature Reviews. Endocrinology
|
October 17, 2023
Author Correction: Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement
Stephan Petersenn, Maria Fleseriu, Felipe F Casanueva, et al.
Page
of 49
Search research articles
Search
Showing results (471-480 of 482) with videos related to
Sort By:
Page
of 49
Human Molecular Genetics
|
July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populations
Vera B Kaiser, Victoria Svinti, James G Prendergast, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3
Delanie B Macedo, Ana Paula Abreu, Ana Claudia S Reis, et al.
Nature
|
June 26, 2020
Pervasive lesion segregation shapes cancer genome evolution
Sarah J Aitken, Craig J Anderson, Frances Connor, et al.
Cell
|
September 18, 2012
Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma
Christine Guo Lian, Yufei Xu, Craig Ceol, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 25, 2010
TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood
Elena Gianetti, Cintia Tusset, Sekoni D Noel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 31, 2020
Genotype-Phenotype Correlations in Central Precocious Puberty Caused by MKRN3 Mutations
Carlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Montenegro, et al.
The Lancet. Diabetes & Endocrinology
|
March 5, 2026
Risk of recurrence after successful surgery for Cushing's disease and association with USP8 genotype and tumour size: an international, retrospective, longitudinal cohort study
Qilin Zhang, Yixin Cai, Yuyu Liu, et al.
Nature Reviews. Endocrinology
|
September 5, 2023
Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement
Stephan Petersenn, Maria Fleseriu, Felipe F Casanueva, et al.
The Lancet. Diabetes & Endocrinology
|
June 29, 2023
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study
Ana P M Canton, Flávia R Tinano, Leonardo Guasti, et al.
Nature Reviews. Endocrinology
|
October 17, 2023
Author Correction: Diagnosis and management of prolactin-secreting pituitary adenomas: a Pituitary Society international Consensus Statement
Stephan Petersenn, Maria Fleseriu, Felipe F Casanueva, et al.
Page
of 49