Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Thiéry de Serres-Bérard"'
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103587- (2024)
Lymphoblastoid cell lines serve as a readily and continuous resource for generating induced pluripotent stem cells (iPSCs), enabling the modeling of various genetic disorders in vitro. When investigating congenital and infantile diseases, age-matched
Externí odkaz:
https://doaj.org/article/d21c686475c94d479dd53c821a0c5a0c
Publikováno v:
Stem Cell Research, Vol 77, Iss , Pp 103430- (2024)
Congenital myotonic dystrophy (CDM) is a genetic disease caused by an abnormally long CTG repeat expansion in the DMPK gene, which generally increases in size following intergenerational transmission. CDM is the rarest and most severe form of myotoni
Externí odkaz:
https://doaj.org/article/9574c314e79f4d7d96d89a99d3cbafcb
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103234- (2023)
Congenital myotonic dystrophy (CDM) is an autosomal dominant multisystemic disorder attributed to a large expansion of CTG trinucleotide repeats within the myotonic dystrophy protein kinase (DMPK) gene. In this study, we successfully reprogrammed der
Externí odkaz:
https://doaj.org/article/fee75a1a77474c828411d3e7eafd5548
Publikováno v:
Neurobiology of Disease, Vol 160, Iss , Pp 105532- (2021)
Myotonic dystrophy type 1 (DM1) is a multisystemic and heterogeneous disorder caused by the expansion of CTG repeats in the 3’ UTR of the myotonic dystrophy protein kinase (DMPK) gene. There is a congenital form (CDM1) of the disease characterized
Externí odkaz:
https://doaj.org/article/8759f92d2eac44d2beeb669ed7d4ec37
Autor:
Mathias Lemarchand, Kiefer Thouin, Thiéry De Serres‐Bérard, Sabrina Bellenfant, Sébastien Cadau, François Berthod
Publikováno v:
Biotechnology and Bioengineering. 120:1657-1666
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5f9b6e2cd54f00dee5054c397c360f4
https://doi.org/10.1002/bit.28359
https://doi.org/10.1002/bit.28359
Autor:
Siham Ait Benichou, Dominic Jauvin, Thiéry De Serres-Bérard, Frank Bennett, Frank Rigo, Genevieve Gourdon, Mohamed Boutjdir, Mohamed Chahine, Jack Puymirat
Publikováno v:
Human gene therapy. 33(15-16)
Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder that affects many organs. It is caused by the expansion of a cytosine-thymine-guanine triplet repeat in the 3' untranslated region of the human dystrophia myotonica protein kinase (h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf31b497bcda63c76dfb02d3a6a49a87
https://pubmed.ncbi.nlm.nih.gov/35794764
https://pubmed.ncbi.nlm.nih.gov/35794764
Publikováno v:
ACS Applied Polymer Materials. 2:5790-5797
Chronic wounds associated with diabetes remain a worldwide clinical challenge. Substance P (SP), which is an 11-amino acid neuropeptide secreted in the skin mainly by sensory neurons, has been repo...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::550183f2ec98267d5c38bb2c7f86d1c2
https://doi.org/10.1021/acsapm.0c01034
https://doi.org/10.1021/acsapm.0c01034
Autor:
Siham Ait Benichou, Dominic Jauvin, Thiéry De Serres-Bérard, Marion Pierre, Karen K. Ling, C. Frank Bennett, Frank Rigo, Genevieve Gourdon, Mohamed Chahine, Jack Puymirat
Publikováno v:
Gene therapy. 29(12)
Myotonic dystrophy, or dystrophia myotonica type 1 (DM1), is a multi-systemic disorder and is the most common adult form of muscular dystrophy. It affects not only muscles but also many organs, including the brain. Cerebral impairments include cognit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a8470e53a6cd878f0189e8ae4ce11d
https://pubmed.ncbi.nlm.nih.gov/35075265
https://pubmed.ncbi.nlm.nih.gov/35075265
Autor:
Thiéry De Serres-Bérard, Siham Ait Benichou, Dominic Jauvin, Mohamed Boutjdir, Jack Puymirat, Mohamed Chahine
Publikováno v:
International Journal of Molecular Sciences. 23:13359
Myotonic dystrophy type 1 (DM1) is a dominant genetic disease in which the expansion of long CTG trinucleotides in the 3′ UTR of the myotonic dystrophy protein kinase (DMPK) gene results in toxic RNA gain-of-function and gene mis-splicing affecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c44dbe33ce1b22fef9f1ae8cc37fabba
https://doi.org/10.3390/ijms232113359
https://doi.org/10.3390/ijms232113359
Autor:
Quentin Muller, Marie-Josée Beaudet, Valérie Chaumet, Thiéry de Serres-Bérard, Sabrina Bellenfant, Vincent FLACHER, François Berthod
Publikováno v:
Revue Française d'Histotechnologie
Revue Française d'Histotechnologie, Association française d'histotechnologie, A paraître
HAL
Revue Française d'Histotechnologie, Association française d'histotechnologie, A paraître
HAL
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0a61df279b7c9e6dd87ef85a5d497f53
https://hal.archives-ouvertes.fr/hal-03035596v2/document
https://hal.archives-ouvertes.fr/hal-03035596v2/document
