Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Eduardo H, Charreau"'
Autor:
María C. Díaz Flaqué, Natalia M. Galigniana, Wendy Béguelin, Rocío Vicario, Cecilia J. Proietti, Rosalía Cordo Russo, Martín A. Rivas, Mercedes Tkach, Pablo Guzmán, Juan C. Roa, Esteban Maronna, Viviana Pineda, Sergio Muñoz, María Florencia Mercogliano, Eduardo H. Charreau, Patricio Yankilevich, Roxana Schillaci, Patricia V. Elizalde
Publikováno v:
Breast Cancer Research, Vol 25, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/291557641cce44d291680059236d5d3c
Autor:
María C Díaz Flaqué, Natalia M Galigniana, Wendy Béguelin, Rocío Vicario, Cecilia J Proietti, Rosalía Cordo Russo, Martín A Rivas, Mercedes Tkach, Pablo Guzmán, Juan C Roa, Esteban Maronna, Viviana Pineda, Sergio Muñoz, María Florencia Mercogliano, Eduardo H Charreau, Patricio Yankilevich, Roxana Schillaci, Patricia V Elizalde
Publikováno v:
Breast Cancer Research, Vol 15, Iss 6, Pp 1-24 (2013)
Abstract Introduction The role of the progesterone receptor (PR) in breast cancer remains a major clinical challenge. Although PR induces mammary tumor growth, its presence in breast tumors is a marker of good prognosis. We investigated coordinated P
Externí odkaz:
https://doaj.org/article/97467e939197489fb4e4a743f410f448
Autor:
Carolina Minutolo, Alejandro D Nadra, Cecilia Fernández, Melisa Taboas, Noemí Buzzalino, Bárbara Casali, Susana Belli, Eduardo H Charreau, Liliana Alba, Liliana Dain
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e15899 (2011)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most frequent inborn error of metabolism, and accounts for 90-95% of CAH cases. The affected enzyme, P450C21, is encoded by the CYP21A2 gene, located together with a 98% nuc
Externí odkaz:
https://doaj.org/article/0b3ff7a736854c4088db0fd43b6b4937
Autor:
Roxana Schillaci, Zoya Kikhtyak, Rosalia I. Cordo Russo, Luke A. Selth, Violeta A. Chiauzzi, Patricia Elizalde, Wayne D. Tilley, Theresa E. Hickey, Esmaeil Ebrahimie, María F. Chervo, Cecilia J. Proietti, Santiago Madera, Eduardo H. Charreau
Publikováno v:
Oncology Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b86042416d7d5ac05ab5c7939f7774b
https://doi.org/10.1530/oncolabs.1.p014
https://doi.org/10.1530/oncolabs.1.p014
Autor:
Patricia V. Elizalde, Eduardo H. Charreau, Santiago Madera, Rosalia Ines Cordo Russo, María F. Chervo
Publikováno v:
Hormonescancer. 10(2-3)
Membrane overexpression of ErbB-2 (MErbB-2), a member of the ErbB family of receptor tyrosine kinases, occurs in 15– 20% of breast cancers (BC) and constitutes a therapeutic target in this BC subtype (ErbB-2-positive). Although MErbB-2- targeted th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26bf6a0b9393ab44f090a2292eb7525c
https://pubmed.ncbi.nlm.nih.gov/30656558
https://pubmed.ncbi.nlm.nih.gov/30656558
Autor:
Aleksandar Rajkovic, S. Christin-Maitre, Anu Bashamboo, Liliana Dain, Caroline Schluth-Bolard, McLean Whi, ossetti R, Caroline Eozenou, Svetlana A. Yatsenko, Inas Mazen, Etienne Patin, Selma F. Witchel, Ralf Jauch, Rajpert-De Meyts E, Joelle Bignon-Topalovic, Kristian Almstrup, Ken McElreavey, Marie-Charlotte Dumargne, Louis-Sylvestre C, Sandra Chantot-Bastaraud, de Malleray Pichard C, Jean-Pierre Siffroi, Célia Ravel, Violeta A. Chiauzzi, Capucine Hyon, John C. Achermann, Hassan Rouba, Stuart A. MacGowan, Reyes-ugica M, Andrew J. Duncan, Eduardo H. Charreau, Leila Fusee, Marie-France Portnoi, Sandra Rojo, Luca Persani, Raja Brauner, Validire P, Yogesh Srivastava
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Human Molecular Genetics
Human Molecular Genetics, 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Human molecular genetics, vol 27, iss 7
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Human Molecular Genetics
Human Molecular Genetics, 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
Human molecular genetics, vol 27, iss 7
Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (7), pp.1228-1240. ⟨10.1093/hmg/ddy037⟩
SOX8 is an HMG-box transcription factor closely related to SRY and SOX9. Deletion of the gene encoding Sox8 in mice causes reproductive dysfunction but the role of SOX8 in humans is unknown. Here, we show that SOX8 is expressed in the somatic cells o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c3735ed6276ab345f922c6d19eef946
https://academic.oup.com/hmg/article/27/7/1228/4823478
https://academic.oup.com/hmg/article/27/7/1228/4823478
Autor:
Violeta A. Chiauzzi, Andrea Solari, Liliana Dain, Lucía D. Espeche, Noemí Buzzalino, Mehrnoosh Arrar, Susana Belli, Carlos David Bruque, Marisol Delea, Eduardo H. Charreau, Cecilia Fernández, Ianina C. Ferder
Publikováno v:
Genes; Volume 8; Issue 8; Pages: 194
Genes
Genes, Vol 8, Iss 8, p 194 (2017)
Genes
Genes, Vol 8, Iss 8, p 194 (2017)
The premutation state of FMR1 (Fragile X Mental Retardation 1) has been associated with primary ovarian insufficiency (POI), and is the most common known genetic cause for 46,XX patients. Nevertheless, very few studies have analyzed its frequency in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f325b13fc4fbe6b86c3a2990971dfc
Autor:
Patricia V. Elizalde, Mercedes Tkach, Cecilia J. Proietti, Leandro Venturutti, R I Cordo Russo, Natalia M. Galigniana, Eduardo H. Charreau, Neil A. O'Brien, Pablo Guzmán, Juan Carlos Roa, M C Díaz Flaqué, Wendy Béguelin, Roxana Schillaci
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Membrane overexpression of ErbB-2/HER2 receptor tyrosine kinase (membrane ErbB-2 (MErbB-2)) has a critical role in breast cancer (BC). We and others have also shown the role of nuclear ErbB-2 (NErbB-2) in BC, whose presence we identified as a poor pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3b423c7bd4429f0b770fd024be64ae1
https://doi.org/10.1038/onc.2014.272
https://doi.org/10.1038/onc.2014.272
Autor:
Eduardo H. Charreau, Cecilia J. Proietti, Patricia V. Elizalde, Mercedes Tkach, Martín A. Rivas, Roxana Schillaci, Wendy Béguelin, María Celeste Díaz Flaqué, Florencia Cayrol
Publikováno v:
Steroids. 76:381-392
Interactions between progesterone receptor (PR) and signal transducer and activator of transcription 3 (Stat3)-mediated signaling pathways have already been described. In the present study, we explored the capacity of Stat3 to functionally interact w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa233eef8d1008ec102fa03727edef4
https://doi.org/10.1016/j.steroids.2010.12.008
https://doi.org/10.1016/j.steroids.2010.12.008
Autor:
Cecilia J. Proietti, Martín A. Rivas, Patricia V. Elizalde, Wendy Béguelin, Mercedes Tkach, Eduardo H. Charreau, Cinthia Rosemblit, Roxana Schillaci
Publikováno v:
Breast Cancer Research and Treatment. 122:111-124
Tumor necrosis factor alpha (TNFalpha) is a pleiotropic cytokine which, acting locally, induces tumor growth. Accumulating evidence, including our findings, showed that TNFalpha is mitogenic in breast cancer cells in vitro and in vivo. In the present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09870ae77408463299fd6def84bac31a
https://doi.org/10.1007/s10549-009-0546-3
https://doi.org/10.1007/s10549-009-0546-3