Výsledky vyhledávání - "Paula Aliberti"

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

Autor: M A Rivarola, Natalia Perez Garrido, N. Saraco, Alicia Belgorosky, María Sonia Baquedano, Esperanza Berensztein, Paula Aliberti, Javier Goñi

Publikováno v: Molecular and Cellular Endocrinology. 441:46-54

We hypothesized that DNA methylation is involved in human adrenal functional zonation. mRNAsexpression and methylation pattern of RARB, NR4A1 and HSD3B2 genes in human adrenal tissues (HAT)and in pediatric virilizing adrenocortical tumors (VAT) were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02ffd10e158f1f81dcbeeea8d2348f53
https://doi.org/10.1016/j.mce.2016.09.024

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Gonadotrophin-mediated miRNA expression in testis at onset of puberty in rhesus monkey: predictions on regulation of thyroid hormone activity and DLK1-DIO3 locus

Autor: Tony M. Plant, Uma R. Chandran, William H. Walker, Alicia Belgorosky, Paula Aliberti, Rahil Sethi

Publikováno v: Molecular human reproduction. 25(3)

Molecular mechanisms responsible for the initiation of primate spermatogenesis remain poorly characterized. Previously, 48 h stimulation of the testes of three juvenile rhesus monkeys with pulsatile LH and FSH resulted in down-regulation of a cohort

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73c1aac9865d3ca9f3f4c1340d0486ef
https://pubmed.ncbi.nlm.nih.gov/30590698

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

Autor: Marco A. Rivarola, Esperanza Berensztein, Pablo Ramírez, Alberto J. Solari, Alicia Belgorosky, María Sonia Baquedano, Paula Aliberti, Marcela Bailez, Gabriela Guercio, Natalia Perez Garrido, Roxana Marino, Roberta Beatriz Sciurano, Diana Monica Warman, Mariana Costanzo

Publikováno v: Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 11(5-6)

Androgen insensitivity syndrome (AIS) is a hereditary condition in patients with a 46,XY karyotype in which loss-of-function mutations of the androgen receptor (AR) gene are responsible for defects in virilization. The aim of this study was to invest

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf53aafa28b253e95a7354eb5b0e0a85
https://pubmed.ncbi.nlm.nih.gov/29895016

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The testicular transcriptome associated with spermatogonia differentiation initiated by gonadotrophin stimulation in the juvenile rhesus monkey (Macaca mulatta)

Autor: William H. Walker, Uma R. Chandran, Rahil Sethi, Alyxzandria Smith, Mark P. Hedger, Alicia Belgorosky, Tony M. Plant, Gary R. Marshall, Suresh Ramaswamy, Paula Aliberti, Seyedmehdi Nourashrafeddin

Publikováno v: CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

STUDY QUESTION What is the genetic landscape within the testis of the juvenile rhesus monkey (Macaca mulatta) that underlies the decision of undifferentiated spermatogonia to commit to a pathway of differentiation when puberty is induced prematurely

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07cbd5b434b80aec09ce8553405358f0
https://academic.oup.com/humrep/article/32/10/2088/4098165

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