Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Nathalie Douet-Guilbert"'
Autor:
Sahar El Fekih, Nadia Gueganic, Corinne Tous, Habib Ben Ali, Mounir Ajina, Nathalie Douet-Guilbert, Hortense Drapier, Damien Beauvillard, Frédéric Morel, Aurore Perrin
Publikováno v:
Asian Journal of Andrology, Vol 24, Iss 5, Pp 445-450 (2022)
We question whether, in men with an abnormal rate of sperm DNA fragmentation, the magnetic-activated cell sorting (MACS) could select spermatozoa with lower rates of DNA fragmentation as well as spermatozoa with unbalanced chromosome content. Cryopre
Externí odkaz:
https://doaj.org/article/1d0b81288adf409c9c8c4e0e77dfb8ba
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1658 (2022)
Myelodysplastic syndromes (MDS) are considered to be diseases associated with splicing defects. A large number of genes involved in the pre-messenger RNA splicing process are mutated in MDS. Deletion of 5q and 7q are of diagnostic value, and those ch
Externí odkaz:
https://doaj.org/article/957dcdb71d614d0f90c5d881fb25e4ec
Autor:
Cristina Bagacean, Adrian Tempescul, David Ternant, Anne Banet, Nathalie Douet-Guilbert, Anne Bordron, Boutahar Bendaoud, Hussam Saad, Mihnea Zdrenghea, Christian Berthou, Gilles Paintaud, Yves Renaudineau
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 7, Iss 1, Pp 1-5 (2019)
Abstract Chronic lymphocytic leukemia (CLL) is the most common type of leukemia and the anti-CD20 monoclonal antibody, rituximab, represents the therapeutic gold standard for more than 2 decades in this pathology, when used in combination with chemot
Externí odkaz:
https://doaj.org/article/874ce61e568a46c38d593ea120b275c2
Publikováno v:
Cancers, Vol 14, Iss 3, p 643 (2022)
RNA-Binding Proteins (RBP) are very diverse and cover a large number of functions in the cells. This review focuses on RBM22, a gene encoding an RBP and belonging to the RNA-Binding Motif (RBM) family of genes. RBM22 presents a Zinc Finger like and a
Externí odkaz:
https://doaj.org/article/66544c41f3fb4043940e1dc657f67501
Autor:
Yan Jiang, Su-Jun Gao, Benoit Soubise, Nathalie Douet-Guilbert, Zi-Ling Liu, Marie-Bérengère Troadec
Publikováno v:
Cancers, Vol 13, Iss 21, p 5392 (2021)
Myelodysplastic syndromes (MDSs) are heterogeneous for their morphology, clinical characteristics, survival of patients, and evolution to acute myeloid leukemia. Different prognostic scoring systems including the International Prognostic Scoring Syst
Externí odkaz:
https://doaj.org/article/ec8b25c4a03740d0ac190ec97f3a4263
Autor:
Cristina Bagacean, Christelle Le Dantec, Christian Berthou, Adrian Tempescul, Hussam Saad, Anne Bordron, Mihnea Zdrenghea, Victor Cristea, Nathalie Douet-Guilbert, Yves Renaudineau
Publikováno v:
Clinical Epigenetics, Vol 9, Iss 1, Pp 1-11 (2017)
Abstract Background Both defective DNA methylation and active DNA demethylation processes are emerging as important risk factors in chronic lymphocytic leukemia (CLL). However, associations between 5-cytosine epigenetic markers and the most frequent
Externí odkaz:
https://doaj.org/article/80743a1142cb47a49f5352e4ead74bf2
Autor:
Yan Jiang, Jean-Richard Eveillard, Marie-Anne Couturier, Benoit Soubise, Jian-Min Chen, Sujun Gao, Audrey Basinko, Frédéric Morel, Nathalie Douet-Guilbert, Marie-Bérengère Troadec
Publikováno v:
Cancers, Vol 13, Iss 3, p 481 (2021)
This study explores the hypothesis that genetic differences related to an ethnic factor may underlie differences in phenotypic expression of myelodysplastic syndrome (MDS). First, to identify clear ethnic differences, we systematically compared the e
Externí odkaz:
https://doaj.org/article/4bcb066614b945f38f6abde08a9b9dc0
Autor:
Tiffany Bergot, Eric Lippert, Nathalie Douet-Guilbert, Séverine Commet, Laurent Corcos, Delphine G. Bernard
Publikováno v:
Cancers, Vol 12, Iss 3, p 652 (2020)
Deregulation of pre-mRNA splicing is observed in many cancers and hematological malignancies. Genes encoding splicing factors are frequently mutated in myelodysplastic syndromes, in which SF3B1 mutations are the most frequent. SF3B1 is an essential c
Externí odkaz:
https://doaj.org/article/f76262f9b9cd468391e763109cbcd13a
Autor:
Sahar El Fekih, Nadia Gueganic, Corinne Tous, Nathalie Douet-Guilbert, Sophie Blesson, Frédéric Morel, Aurore Perrin
Publikováno v:
Cytogenetic and Genome Research. 162:34-39
Small supernumerary marker chromosomes (sSMCs) are defined as structurally abnormal chromosomes that are difficult to identify by conventional cytogenetic techniques. sSMCs are 3.75 times more common in infertile men than in the general population. T
Autor:
Anne-Gaëlle Rio, Zi-Ling Liu, Virginie Gandemer, Aurélien A. Sérandour, Benoit Soubise, Marie-Dominique Galibert, Hana Raslova, Jason S. Carroll, Laurent Corcos, Jocelyne Demengeot, Nathalie Douet-Guilbert, Lydie Debaize, Jérémie Rouger-Gaudichon, Marie-Bérengère Troadec, Gilles Salbert, Yan Jiang, David Gilot, Hélène Jakobczyk, Stéphane Avner
Publikováno v:
Leukemia
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2021, ⟨10.1038/s41375-021-01409-9⟩
Leukemia, 2022, 36 (2), pp.549-554. ⟨10.1038/s41375-021-01409-9⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2021, ⟨10.1038/s41375-021-01409-9⟩
Leukemia, 2022, 36 (2), pp.549-554. ⟨10.1038/s41375-021-01409-9⟩
Funder: Société Française de Biochimie et Biologie Moléculaire ; French Research Ministry
Funder: Cancéropole Grand Ouest ; Région Bretagne ; Société Française d’Hématologie
Funder: Ligue Régionale contre le cancer
ETV6-RU
Funder: Cancéropole Grand Ouest ; Région Bretagne ; Société Française d’Hématologie
Funder: Ligue Régionale contre le cancer
ETV6-RU