Maria S. Baquedano

B, Argentina

Last Updated: 09/26/2026

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Found 10 publications

Exploring the Association between Prenatal Growth and Differences in Sexual Development in Newborns.

Exploring the Association between Prenatal Growth and Differences in Sexual Development in Newborns.

Journal: Hormone research in paediatrics
Published: January 29, 2025

ERRγ1 and Aromatase Expression in Human Placental Tissues from Term Deliveries of Large for Gestational Age Newborns.

ERRγ1 and Aromatase Expression in Human Placental Tissues from Term Deliveries of Large for Gestational Age Newborns.

Journal: Hormone research in paediatrics
Published: July 04, 2023

Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone.

Mutation of HSD3B2 Gene and Fate of Dehydroepiandrosterone.

Journal: Vitamins and hormones
Published: July 22, 2018

Androgen Insensitivity Syndrome at Prepuberty: Marked Loss of Spermatogonial Cells at Early Childhood and Presence of Gonocytes up to Puberty.

Androgen Insensitivity Syndrome at Prepuberty: Marked Loss of Spermatogonial Cells at Early Childhood and Presence of Gonocytes up to Puberty.

Journal: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation
Published: November 09, 2017

Human Adrenal Cortex: Epigenetics and Postnatal Functional Zonation.

Human Adrenal Cortex: Epigenetics and Postnatal Functional Zonation.

Journal: Hormone research in paediatrics
Published: October 16, 2017

DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortex.

DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortex.

Journal: Molecular and cellular endocrinology
Published: June 16, 2016

A novel missense mutation in the HSD3B2 gene, underlying nonsalt-wasting congenital adrenal hyperplasia. new insight into the structure-function relationships of 3β-hydroxysteroid dehidrogenase type II.

A novel missense mutation in the HSD3B2 gene, underlying nonsalt-wasting congenital adrenal hyperplasia. new insight into the structure-function relationships of 3β-hydroxysteroid dehidrogenase type II.

Journal: The Journal of clinical endocrinology and metabolism
Published: October 17, 2014

Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia

Novel heterozygous mutation in the steroidogenic acute regulatory protein gene in a 46,XY patient with congenital lipoid adrenal hyperplasia

Journal: Medicina
Published: August 09, 2013

Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia.

Unique dominant negative mutation in the N-terminal mitochondrial targeting sequence of StAR, causing a variant form of congenital lipoid adrenal hyperplasia.

Journal: The Journal of clinical endocrinology and metabolism
Published: November 24, 2012

Preserved fertility in a patient with a 46,XY disorder of sex development due to a new heterozygous mutation in the NR5A1/SF-1 gene: evidence of 46,XY and 46,XX gonadal dysgenesis phenotype variability in multiple members of an affected kindred.

Preserved fertility in a patient with a 46,XY disorder of sex development due to a new heterozygous mutation in the NR5A1/SF-1 gene: evidence of 46,XY and 46,XX gonadal dysgenesis phenotype variability in multiple members of an affected kindred.

Journal: Hormone research in paediatrics
Published: December 16, 2011
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Last Updated: 09/26/2026