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Clinical Endocrinology
|
July 5, 2007
The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues
Carolina M Pepe, Nora I Saraco, Maria Sonia Baquedano, et al.
Oncogene
|
April 14, 2009
Artemin is oncogenic for human mammary carcinoma cells
J Kang, J K Perry, V Pandey, et al.
Molecular and Cellular Biology
|
October 5, 2016
Endoplasmic Reticulum Stress Enhances Mitochondrial Metabolic Activity in Mammalian Adrenals and Gonads
Manoj Prasad, Anna N Walker, Jasmeet Kaur, et al.
Frontiers in Endocrinology
|
April 20, 2018
GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD Genes
Idoia Martinez de LaPiscina, Carmen de Mingo, Stefan Riedl, et al.
International Journal of Molecular Sciences
|
March 28, 2024
A Novel Mutation in the <i>INSR</i> Gene Causes Severe Insulin Resistance and Rabson-Mendenhall Syndrome in a Paraguayan Patient
Maria Natalia Rojas Velazquez, Fabiola Blanco, Ana Ayala-Lugo, et al.
International Journal of Molecular Sciences
|
September 2, 2020
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
Efstathios Katharopoulos, Natascia Di Iorgi, Paula Fernandez-Alvarez, et al.
American Journal of Human Genetics
|
March 29, 2005
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis
Ningwu Huang, Amit V Pandey, Vishal Agrawal, et al.
European Journal of Endocrinology
|
August 3, 2024
Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant
Cécile Brachet, Alexander Laemmle, Martine Cools, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 16, 2020
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype
Shaheena Parween, Mónica Fernández-Cancio, Sara Benito-Sanz, et al.
The Journal of Clinical Investigation
|
December 20, 2022
Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation
Cécily Lucas, Kay-Sara Sauter, Michael Steigert, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 157) with videos related to
Sort By:
Page
of 16
Clinical Endocrinology
|
July 5, 2007
The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues
Carolina M Pepe, Nora I Saraco, Maria Sonia Baquedano, et al.
Oncogene
|
April 14, 2009
Artemin is oncogenic for human mammary carcinoma cells
J Kang, J K Perry, V Pandey, et al.
Molecular and Cellular Biology
|
October 5, 2016
Endoplasmic Reticulum Stress Enhances Mitochondrial Metabolic Activity in Mammalian Adrenals and Gonads
Manoj Prasad, Anna N Walker, Jasmeet Kaur, et al.
Frontiers in Endocrinology
|
April 20, 2018
GATA4 Variants in Individuals With a 46,XY Disorder of Sex Development (DSD) May or May Not Be Associated With Cardiac Defects Depending on Second Hits in Other DSD Genes
Idoia Martinez de LaPiscina, Carmen de Mingo, Stefan Riedl, et al.
International Journal of Molecular Sciences
|
March 28, 2024
A Novel Mutation in the <i>INSR</i> Gene Causes Severe Insulin Resistance and Rabson-Mendenhall Syndrome in a Paraguayan Patient
Maria Natalia Rojas Velazquez, Fabiola Blanco, Ana Ayala-Lugo, et al.
International Journal of Molecular Sciences
|
September 2, 2020
Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia
Efstathios Katharopoulos, Natascia Di Iorgi, Paula Fernandez-Alvarez, et al.
American Journal of Human Genetics
|
March 29, 2005
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis
Ningwu Huang, Amit V Pandey, Vishal Agrawal, et al.
European Journal of Endocrinology
|
August 3, 2024
Insight into the role of TXNRD2 in steroidogenesis through a novel homozygous TXNRD2 splice variant
Cécile Brachet, Alexander Laemmle, Martine Cools, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 16, 2020
Molecular Basis of CYP19A1 Deficiency in a 46,XX Patient With R550W Mutation in POR: Expanding the PORD Phenotype
Shaheena Parween, Mónica Fernández-Cancio, Sara Benito-Sanz, et al.
The Journal of Clinical Investigation
|
December 20, 2022
Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation
Cécily Lucas, Kay-Sara Sauter, Michael Steigert, et al.
Page
of 16