Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Edith Brisson"'
Autor:
Albert Pastink, Claudine Junien, Geneviève Gourdon, Edith Brisson, Jeroen Essers, Roland Kanaar, Hein te Riele, Cédric Savouret
Publikováno v:
EMBO Journal, 22(9), 2264-2273. Wiley-Blackwell
Type 1 myotonic dystrophy is caused by the expansion of an unstable CTG repeat in the DMPK gene. We have investigated the molecular mechanisms underlying the CTG repeat instability by crossing transgenic mice carrying >300 unstable CTG repeats in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7931003791aba245690abd9a4d1de7f
https://doi.org/10.1093/emboj/cdg202
https://doi.org/10.1093/emboj/cdg202
Autor:
Claudine Junien, Nacira Tabti, Chantal Duros, Cédric Savouret, Nicolas Sergeant, Antoine Ghestem, Hervé Seznec, Gillian Butler-Browne, Onnik Agbulut, Geneviève Gourdon, Edith Brisson, Jean-Claude Willer, Lucie Ourth, André Delacourte, Coralie Fouquet
Publikováno v:
Scopus-Elsevier
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2001, 10, pp.2717-2726
Human Molecular Genetics, 2001, 10, pp.2717-2726
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2001, 10, pp.2717-2726
Human Molecular Genetics, 2001, 10, pp.2717-2726
The autosomal dominant mutation causing myotonic dystrophy (DM1) is a CTG repeat expansion in the 3'-UTR of the DM protein kinase (DMPK) gene. This multisystemic disorder includes myotonia, progressive weakness and wasting of skeletal muscle and extr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ddeb510f331ea33cbb6528d319763f6
https://doi.org/10.1093/hmg/10.23.2717
https://doi.org/10.1093/hmg/10.23.2717
DM1 CTG expansions affect insulin receptor isoforms expression in various tissues of transgenic mice
Autor:
Mário Gomes-Pereira, Geneviève Gourdon, Céline Guiraud-Dogan, Edith Brisson, Aline Huguet, Guillaume Bassez, Claudine Junien
Publikováno v:
Biochimica et Biophysica Acta-Molecular Basis of Disease
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2007, 1772 (11-12), pp.1183. ⟨10.1016/j.bbadis.2007.08.004⟩
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2007, 1772 (11-12), pp.1183. ⟨10.1016/j.bbadis.2007.08.004⟩
Myotonic dystrophy (DM1) is a dominant autosomal multisystemic disorder caused by the expansion of an unstable CTG trinucleotide repeat in the 3′ untranslated region of the DMPK gene. Nuclear accumulation of the enlarged CUG-containing DMPK transcr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343ea7ed11d2575f6a901c7656c0a45a
https://pubmed.ncbi.nlm.nih.gov/17950578
https://pubmed.ncbi.nlm.nih.gov/17950578
Autor:
Marie-Paule Kieny, Luc Montagnier, David Klatzmann, Jean Claude Gluckman, Patrick Salmon, I Yves Riviere, René Olivier, I Edith Brisson
Publikováno v:
The Journal of Experimental Medicine
Using mAbs and genomic probe to the CD4 molecule, the HIV receptor, we demonstrated that HIV replication induces the disappearance of its functional receptor from the cell surface by two distinct mechanisms. First, after being expressed onto the cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::699f317c0b8ceaeefbef36023630f442
https://doi.org/10.1084/jem.168.6.1953
https://doi.org/10.1084/jem.168.6.1953