Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Iryna, Pirozhkova"'
Autor:
Jeremy Rich, Melanie Bennaroch, Laura Notel, Polina Patalakh, Julien Alberola, Fayez Issa, Paule Opolon, Olivia Bawa, Windy Rondof, Antonin Marchais, Philippe Dessen, Guillaume Meurice, Morgane Le-Gall, Melanie Polrot, Karine Ser-Le Roux, Kamel Mamchaoui, Nathalie Droin, Hana Raslova, Pascal Maire, Birgit Geoerger, Iryna Pirozhkova
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 8, Pp 1840-1885 (2024)
Abstract We have recently identified the uncharacterized ZNF555 protein as a component of a productive complex involved in the morbid function of the 4qA locus in facioscapulohumeral dystrophy. Subsequently named DiPRO1 (Death, Differentiation, and P
Externí odkaz:
https://doaj.org/article/3399c70743a941bc831dd23135024135
Autor:
Ana C. Glembotsky, Dominika Sliwa, Dominique Bluteau, Nathalie Balayn, Cecilia P. Marin Oyarzún, Anna Raimbault, Marie Bordas, Nathalie Droin, Iryna Pirozhkova, Valance Washington, Nora P. Goette, Rosana F. Marta, Rémi Favier, Hana Raslova, Paula G. Heller
Publikováno v:
Haematologica, Vol 104, Iss 6 (2019)
Germline RUNX1 mutations lead to thrombocytopenia and platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia (AML). Multiple aspects of platelet function are impaired in these patients, associated with al
Externí odkaz:
https://doaj.org/article/339e7f5175834da7a016b084f1a82957
Autor:
Jeremy Rich, Melanie Bennaroch, Laura Notel, Polina Patalakh, Julien Alberola, Paule Opolon, Olivia Bawa, Windy Rondof, Antonin Marchais, Philippe Dessen, Guillaume Meurice, Melanie Porlot, Karine Ser-Le Roux, Nathalie Droin, Hana Raslova, Birgit Geoerger, Iryna Pirozhkova
We have recently identified the uncharacterized ZNF555 protein as a component of a productive complex, which is involved in the morbid function of the 4qA locus in facioscapulohumeral dystrophy. As a result of our current findings, ZNF555 is hereinaf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::064fe5330f426b1f7e80c6670887cf96
https://doi.org/10.1101/2023.01.08.523169
https://doi.org/10.1101/2023.01.08.523169
Autor:
Iryna Pirozhkova, Ana Barat, Petr Dmitriev, Elena Kim, Thomas Robert, Justine Guégan, Chrystèle Bilhou-Nabera, Florence Busato, Jörg Tost, Gilles Carnac, Dalila Laoudj-Chenivesse, Marc Lipinski, Yegor Vassetzky
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53033 (2013)
Little is known about differences between induced pluripotent stem cells produced from tissues originating from the same germ layer. We have generated human myoblast-derived iPS cells by retroviral transduction of human primary myoblasts with the OCT
Externí odkaz:
https://doaj.org/article/814da61bcb1446f3a61f5c3027b5edbe
Autor:
Elena S Ioudinkova, Ana Barat, Andrey Pichugin, Elena Markova, Ilya Sklyar, Iryna Pirozhkova, Chloe Robin, Marc Lipinski, Vasily Ogryzko, Yegor S Vassetzky, Sergey V Razin
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e47157 (2012)
BACKGROUND:It becomes increasingly evident that nuclesomes are far from being identical to each other. This nucleosome diversity is due partially to the existence of histone variants encoded by separate genes. Among the known histone variants the les
Externí odkaz:
https://doaj.org/article/ab25aa0999524a24b0288e6fa52ba604
Autor:
Iryna Pirozhkova, Andrei Petrov, Petr Dmitriev, Dalila Laoudj, Marc Lipinski, Yegor Vassetzky
Publikováno v:
PLoS ONE, Vol 3, Iss 10, p e3389 (2008)
The number of D4Z4 repeats in the subtelomeric region of chromosome 4q is strongly reduced in patients with Facio-Scapulo-Humeral Dystrophy (FSHD). We performed chromosome conformation capture (3C) analysis to document the interactions taking place a
Externí odkaz:
https://doaj.org/article/224483de63ba460589e85dd9b5d6fc82
Autor:
Aurore Gelin, Thierry Ragot, Ingrid Breuskin, François Bidault, Thibault Dayris, Caroline Even, Philippe Gorphe, Iryna Pirozhkova, Valérie Rouffiac, Héla Hachicha, Philippe Busson
Publikováno v:
Cancer Research. 81:2656-2656
Introduction: Cancer cachexia is a multifactorial syndrome associated with a skeletal muscle atrophy that affects at least 55% of patients bearing Head and Neck Squamous Cell Carcinomas (HNSCCs). To our knowledge, molecular mechanisms of muscle alter
Autor:
Ana C, Glembotsky, Dominika, Sliwa, Dominique, Bluteau, Nathalie, Balayn, Cecilia P, Marin Oyarzún, Anna, Raimbault, Marie, Bordas, Nathalie, Droin, Iryna, Pirozhkova, Valance, Washington, Nora P, Goette, Rosana F, Marta, Rémi, Favier, Hana, Raslova, Paula G, Heller
Publikováno v:
Haematologica
Germline RUNX1 mutations lead to thrombocytopenia and platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia (AML). Multiple aspects of platelet function are impaired in these patients, associated with al
Publikováno v:
Aging Cell
The H3.3 histone variant has been a subject of increasing interest in the field of chromatin studies due to its two distinguishing features. First, its incorporation into chromatin is replication independent unlike the replication-coupled deposition
Autor:
Sergey V. Razin, A A Gavrilov, Olga V. Iarovaia, Yegor S. Vassetzky, Iryna Pirozhkova, Andrei Petrov, Marc Lipinski, Elvira R. Eivazova
Publikováno v:
Journal of Molecular Biology. 386:929-937
In interphase nuclei as in metaphase chromosomes, the genome is organized into topologically closed loop domains. Here, we have mapped the ends of the loop domain that contains the Ifng (interferon-gamma) gene in primary and cultured murine T-lymphoc