Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Esperanza Berensztein"'
Autor:
Maria Sol Touzon, Natalia Perez Garrido, Roxana Marino, Pablo Ramirez, Mariana Costanzo, Gabriela Guercio, Esperanza Berensztein, Marco A. Rivarola, Alicia Belgorosky
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 24-33 (2019)
Objective:The aim of this study was the molecular characterization of the AR gene as the cause of 46,XY disorder in our population.Methods:We studied 41, non related, 46,XY disorder of sexual differentiation index cases, having characteristics consis
Externí odkaz:
https://doaj.org/article/c6602376e5884b39b76c135a2b3fd8fe
Autor:
Gabriela Guercio, Nora Saraco, Mariana Costanzo, Roxana Marino, Pablo Ramirez, Esperanza Berensztein, Marco A. Rivarola, Alicia Belgorosky
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Several reports in humans as well as transgenic mouse models have shown that estrogens play an important role in male reproduction and fertility. Estrogen receptor alpha (ERα) and beta (ERβ) are expressed in different male tissues including the bra
Externí odkaz:
https://doaj.org/article/e33a22b8ae8d48318e95a41a69c43a3f
Autor:
Lucila Gallino, Vanesa Hauk, Laura Fernández, Elizabeth Soczewski, Soledad Gori, Esteban Grasso, Guillermina Calo, Nora Saraco, Esperanza Berensztein, James A. Waschek, Claudia Pérez Leirós, Rosanna Ramhorst
Publikováno v:
Frontiers in Immunology, Vol 10 (2020)
Uterine receptivity and embryo implantation are two main processes that need a finely regulated balance between pro-inflammatory and tolerogenic mediators to allow a successful pregnancy. The neuroimmune peptide vasoactive intestinal peptide (VIP) is
Externí odkaz:
https://doaj.org/article/3724df3d88e04688bd3a950ed0823b54
Autor:
María Celeste Mattone, María Victoria Lobo de la Vega, Emiro J. Redondo, Pablo D’Alessandro, Natalia Perez Garrido, María Laura Galluzzo, Mariana Costanzo, Verónica Zaidman, Juan Manuel Lazzati, Esperanza Berensztein, Pablo Ramirez, Roxana Marino, Alicia Belgorosky, Marta Ciaccio, Marcela Bailez, Gabriela Guercio
Publikováno v:
Sexual Development. :1-7
Background: Persistent müllerian duct syndrome (PMDS) is characterized by the persistence of müllerian duct derivatives in otherwise normally virilized 46,XY males. Biallelic mutations of the anti-müllerian hormone (AMH) and AMH receptor type 2 (A
Autor:
Adriana María Belén Abiuso, María Luisa Varela, Trinidad Raices, Griselda Irusta, Juan Manuel Lazzati, Marcos Besio Moreno, Alina Cavallotti, Alicia Belgorosky, Omar Pedro Pignataro, Esperanza Berensztein, Carolina Mondillo
Publikováno v:
Journal of Endocrinology. 255:103-116
Recent reports indicate an increase in Leydig cell tumor (LCT) incidence. Radical orchiectomy is the standard therapy in children and adults, although it entails physical and psychosocial side effects. Testis-sparing surgery can be a consideration fo
Autor:
Mariana Costanzo, María Sol Touzon, Roxana Marino, Gabriela Guercio, Pablo Ramirez, María Celeste Mattone, Natalia Pérez Garrido, María Marcela Bailez, Elisa Vaiani, Marta Ciaccio, María Laura Galluzzo Mutti, Alicia Belgorosky, Esperanza Berensztein
Publikováno v:
European journal of endocrinology. 187(3)
Background Differences/disorders of sex development (DSD) are congenital conditions in which the development of chromosomal, gonadal, or anatomical sex is atypical. Objective The aim of this study is to report the histological characteristics and imm
Autor:
Masomeh Askari, Svetlana A. Yatsenko, Robin Lovell-Badge, Tiphanie Merel-Chali, Balázs Gellén, Nitzan Gonen, Leila Fusee, Rana Mainpal, Mariana Costanzo, Inas Mazen, Anu Bashamboo, Anahita Mohseni Meybodi, Esperanza Berensztein, Joelle Bignon-Topalovic, Caroline Eozenou, Natalia Perez Garrido, Alicia Belgorosky, Andrea J. Berman, Roberta Migale, Ken McElreavey, Rita Bertalan, Alaa K. Kamel, Mona K. Mekkawy, Maria Sol Touzon, Priti Singh, Pablo Ramirez, Gabriela Guercio, Aleksandar Rajkovic, Mehdi Totonchi, Selma F. Witchel, Roxana Marino, John C. Schimenti, Anne Jørgensen
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2020, 117 (24), pp.13680-13688. ⟨10.1073/pnas.1921676117⟩
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117 (24), pp.13680-13688. ⟨10.1073/pnas.1921676117⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2020, 117 (24), pp.13680-13688. ⟨10.1073/pnas.1921676117⟩
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117 (24), pp.13680-13688. ⟨10.1073/pnas.1921676117⟩
International audience; Sex determination in mammals is governed by antagonistic interactions of two genetic pathways, imbalance in which may lead to disorders/differences of sex development (DSD) in human. Among 46,XX individuals with testicular DSD
Autor:
Caroline, Eozenou, Nitzan, Gonen, Maria Sol, Touzon, Anne, Jorgensen, Svetlana A, Yatsenko, Leila, Fusee, Alaa K, Kamel, Balazs, Gellen, Gabriela, Guercio, Priti, Singh, Selma, Witchel, Andrea J, Berman, Rana, Mainpal, Mehdi, Totonchi, Anahita, Mohseni Meybodi, Masomeh, Askari, Tiphanie, Merel-Chali, Joelle, Bignon-Topalovic, Roberta, Migale, Mariana, Costanzo, Roxana, Marino, Pablo, Ramirez, Natalia, Perez Garrido, Esperanza, Berensztein, Mona K, Mekkawy, John C, Schimenti, Rita, Bertalan, Inas, Mazen, Ken, McElreavey, Alicia, Belgorosky, Robin, Lovell-Badge, Aleksandar, Rajkovic, Anu, Bashamboo
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Significance Sex development involves a precise spatiotemporal expression and interactions of numerous genetic factors, including the WT1 (Wilms tumor 1) gene. Complete and partial loss-of-function WT1 variants are associated with 46,XY disorders/dif
Autor:
Yen-Shan Chen, Esperanza Berensztein, María Sonia Baquedano, Michael A. Weiss, Pablo Ramírez, Alicia Belgorosky, Maria Sol Touzon, Maria del carmen Malosetti, Elisa Vaiani, Marcela Bailez, Mariana Costanzo, Joseph D Racca, Laura Galuzzo, Roxana Marino
Publikováno v:
Journal of the Endocrine Society
Context: SRY, an architectural transcription factor containing a SOX-related high-mobility group (HMG) box, initiates testis formation in the mammalian bipotential gonadal ridge. Inherited human SRY mutations can be associated with differences in sex
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