Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Radhia, M'Kacher"'
Autor:
Haifaou Younoussa, Macoura Gadji, Mamadou Soumboundou, Bruno Colicchio, Ahmed Said, Ndeye Aby Ndoye, Steffen Junker, Andreas Plesch, Leonhard Heidingsfelder, Ndeye Rama Diagne, Alain Dieterlen, Philippe Voisin, Patrice Carde, Eric Jeandidier, Radhia M’kacher
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 565 (2024)
Differences/Disorders of sex development (DSDs) are conditions in which the development of chromosomal, gonadal, and anatomical sexes is atypical. DSDs are relatively rare, but their incidence is becoming alarmingly common in sub-Saharan Africa (SSA)
Externí odkaz:
https://doaj.org/article/a08af83f695b448587cdf0649128c85d
Autor:
David Gentien, Elnaz Saberi-Ansari, Nicolas Servant, Ariane Jolly, Pierre de la Grange, Fariba Némati, Géraldine Liot, Simon Saule, Aurélie Teissandier, Deborah Bourc’his, Elodie Girard, Jennifer Wong, Julien Masliah-Planchon, Erkan Narmanli, Yuanlong Liu, Emma Torun, Rebecca Goulancourt, Manuel Rodrigues, Laure Villoing Gaudé, Cécile Reyes, Matéo Bazire, Thomas Chenegros, Emilie Henry, Audrey Rapinat, Mylene Bohec, Sylvain Baulande, Radhia M’kacher, Eric Jeandidier, André Nicolas, Giovanni Ciriello, Raphael Margueron, Didier Decaudin, Nathalie Cassoux, Sophie Piperno-Neumann, Marc-Henri Stern, Johan Harmen Gibcus, Job Dekker, Edith Heard, Sergio Roman-Roman, Joshua J. Waterfall
Publikováno v:
Cell Reports, Vol 42, Iss 9, Pp 113132- (2023)
Summary: Uveal melanoma (UM) is a rare cancer resulting from the transformation of melanocytes in the uveal tract. Integrative analysis has identified four molecular and clinical subsets of UM. To improve our molecular understanding of UM, we perform
Externí odkaz:
https://doaj.org/article/1572404d6b2643f898a51a4a704e001b
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100393- (2023)
Externí odkaz:
https://doaj.org/article/557dfd60c5ae41e3bdf45698d9287ec0
Autor:
Radhia M’Kacher, Bruno Colicchio, Steffen Junker, Elie El Maalouf, Leonhard Heidingsfelder, Andreas Plesch, Alain Dieterlen, Eric Jeandidier, Patrice Carde, Philippe Voisin
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5699 (2023)
In the event of a radiological or nuclear accident, or when physical dosimetry is not available, the scoring of radiation-induced chromosomal aberrations in lymphocytes constitutes an essential tool for the estimation of the absorbed dose of the expo
Externí odkaz:
https://doaj.org/article/b161973347de42a1ba6d74da351d203e
Autor:
Mamadou Soumboundou, Julien Dossou, Yossef Kalaga, Innocent Nkengurutse, Ibrahima Faye, Albert Guingani, Macoura Gadji, Koudbi J. Yameogo, Henri Zongo, Gora Mbaye, Ahmadou Dem, Mounibé Diarra, Rached Adjibade, Catherine Djebou, Steffen Junker, Noufissa Oudrhiri, William M. Hempel, Alain Dieterlen, Eric Jeandidier, Patrice Carde, Elie El Maalouf, Bruno Colicchio, Annelise Bennaceur-Griscelli, Michael Fenech, Philippe Voisin, Claire Rodriguez-Lafrasse, Radhia M’Kacher
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Exposure to genotoxic stress such as radiation is an important public health issue affecting a large population. The necessity of analyzing cytogenetic effects of such exposure is related to the need to estimate the associated risk. Cytog
Externí odkaz:
https://doaj.org/article/cd20f47c95294feaaaf0222946c326ec
Autor:
Radhia M’Kacher, Steffen Junker, Bruno Colicchio, Wala Najar, Justyna Mika, Alain Dieterlen, Joanna Polanska, Philippe Voisin, Eric Jeandidier, Patrice Carde
Publikováno v:
HemaSphere, Vol 6, Pp 14-14 (2022)
Externí odkaz:
https://doaj.org/article/faf72bc287994d5ba56a3855eaaa051b
Autor:
Radhia M’Kacher, Madeleine Jaillet, Bruno Colicchio, Eirini Vasarmidi, Arnaud Mailleux, Alain Dieterlen, Caroline Kannengiesser, Claire Borie, Noufissa Oudrhiri, Steffen Junker, Philippe Voisin, Eric Jeandidier, Patrice Carde, Michael Fenech, Annelise Bennaceur-Griscelli, Bruno Crestani, Raphael Borie
Publikováno v:
Biomedicines, Vol 10, Iss 2, p 310 (2022)
Idiopathic pulmonary fibrosis (IPF) is associated with several hallmarks of aging including telomere shortening, which can result from germline mutations in telomere related genes (TRGs). Here, we assessed the length and stability of telomeres as wel
Externí odkaz:
https://doaj.org/article/97fa3df9ab42486c86d5399f09ed72a6
Autor:
Akram Kaddour, Bruno Colicchio, Diane Buron, Elie El Maalouf, Eric Laplagne, Claire Borie, Michelle Ricoul, Aude Lenain, William M. Hempel, Luc Morat, Mustafa Al Jawhari, Corina Cuceu, Leonhard Heidingsfelder, Eric Jeandidier, Georges Deschênes, Alain Dieterlen, Michèle El May, Theodore Girinsky, Annelise Bennaceur-Griscelli, Patrice Carde, Laure Sabatier, Radhia M’kacher
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract The mechanisms behind the transmission of chromosomal aberrations (CA) remain unclear, despite a large body of work and major technological advances in chromosome identification. We reevaluated the transmission of CA to second- and third-div
Externí odkaz:
https://doaj.org/article/4d919127e5124bc98a5cd9b87f10782d
Autor:
Isabelle Guinobert, Claude Blondeau, Bruno Colicchio, Noufissa Oudrhiri, Alain Dieterlen, Eric Jeandidier, Georges Deschenes, Valérie Bardot, César Cotte, Isabelle Ripoche, Patrice Carde, Lucile Berthomier, Radhia M’Kacher
Publikováno v:
Biomedicines, Vol 8, Iss 2, p 31 (2020)
A link between telomere shortening and oxidative stress was found in aging people and patients with cancer or inflammatory diseases. Extracts of Astragalus spp. are known to stimulate telomerase activity, thereby compensating telomere shortening. We
Externí odkaz:
https://doaj.org/article/e4408510d29146f48499f413742428e2
Autor:
Noufissa Oudrhiri, Radhia M’kacher, Diana Chaker, Bruno Colicchio, Claire Borie, Eric Jeandidier, Alain Dieterlen, Frank Griscelli, Annelise Bennaceur-Griscelli, Ali G. Turhan
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1395
Coats plus (CP) syndrome is an inherited autosomal recessive condition that results from mutations in the conserved telomere maintenance component 1 gene (CTC1). The CTC1 protein functions as a part of the CST protein complex, a protein heterotrimer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff959dedddc41e2cac80ac5ad8c50dc7
https://pubmed.ncbi.nlm.nih.gov/36011306
https://pubmed.ncbi.nlm.nih.gov/36011306