Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Angélique Terray"'
Autor:
Amélie Rodrigues, Amélie Slembrouck-Brec, Céline Nanteau, Angélique Terray, Yelyzaveta Tymoshenko, Yvrick Zagar, Sacha Reichman, Zhouhuan Xi, José-Alain Sahel, Stéphane Fouquet, Gael Orieux, Emeline F. Nandrot, Leah C. Byrne, Isabelle Audo, Jérôme E. Roger, Olivier Goureau
Publikováno v:
npj Regenerative Medicine, Vol 7, Iss 1, Pp 1-22 (2022)
Abstract Mutations in the ubiquitously expressed pre-mRNA processing factor (PRPF) 31 gene, one of the most common causes of dominant form of Retinitis Pigmentosa (RP), lead to a retina-specific phenotype. It is uncertain which retinal cell types are
Externí odkaz:
https://doaj.org/article/9c275654ee034394a4e7eff764d4f7bb
Autor:
Angélique Terray, Victoire Fort, Amélie Slembrouck, Céline Nanteau, José-Alain Sahel, Sacha Reichman, Isabelle Audo, Olivier Goureau
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 26-29 (2017)
A human iPS cell line was generated from fibroblasts of a phenotypically unaffected patient from a family with PRPF31-associated retinitis pigmentosa (RP). The transgene-free iPS cells were generated with the human OSKM transcription factors using th
Externí odkaz:
https://doaj.org/article/f0758e53ad46412d8f94f47cac7aea39
Autor:
Angélique Terray, Amélie Slembrouck, Céline Nanteau, Christel Chondroyer, Christina Zeitz, José-Alain Sahel, Isabelle Audo, Sacha Reichman, Olivier Goureau
Publikováno v:
Stem Cell Research, Vol 24, Iss C, Pp 1-4 (2017)
A human iPSC line was generated from fibroblasts of a patient affected with autosomal dominant Retinitis Pigmentosa (RP) carrying the mutation p.Gly56Arg in the NR2E3 gene. The transgene-free iPSCs were generated with the human OSKM transcription fac
Externí odkaz:
https://doaj.org/article/8e9844f9a19d4290b8c0fb1f14eddb62
Autor:
Amélie Rodrigues, Amélie Slembrouck-Brec, Céline Nanteau, Angélique Terray, Yelyzaveta Tymoshenko, Yvrick Zagar, Sacha Reichman, Zhouhuan Xi, José-Alain Sahel, Stéphane Fouquet, Gael Orieux, Emeline F. Nandrot, Leah C. Byrne, Isabelle Audo, Jérôme E. Roger, Olivier Goureau
Publikováno v:
NPJ Regenerative medicine
NPJ Regenerative medicine, 2022, 7, pp.39. ⟨10.1038/s41536-022-00235-6⟩
NPJ Regenerative medicine, 2022, 7, pp.39. ⟨10.1038/s41536-022-00235-6⟩
Mutations in the ubiquitously expressedpre-mRNA processing factor(PRPF)31gene, one of the most common causes of dominant form of Retinitis Pigmentosa (RP), lead to a retina-specific phenotype. It is uncertain which retinal cell types are affected and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39d0163641b58e202e3e801bc9dc3954
https://pubmed.ncbi.nlm.nih.gov/35974011
https://pubmed.ncbi.nlm.nih.gov/35974011
Autor:
Hynek Wichterle, Virginie Rouiller-Fabre, Nour Nicolas, Gist F. Croft, Vincent Mouilleau, Vanessa Ribes, Léa Lesueur, Célia Vaslin, Mathieu Daynac, Stéphane Nedelec, Angélique Terray, Margot Jarrige, Simona Gribaudo, Mackenzie W. Mathis, Cécile Martinat, Rémi Robert
Publikováno v:
Development (Cambridge, England)
Development (Cambridge, England), 2021, 148 (6), ⟨10.1242/dev.194514⟩
Development
Development (Cambridge, England), 2021, 148 (6), ⟨10.1242/dev.194514⟩
Development
Rostro-caudal patterning of vertebrates depends on the temporally progressive activation of HOX genes within axial stem cells that fuel axial embryo elongation. Whether the pace of sequential activation of HOX genes, the 'HOX clock', is controlled by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03e0481a9887cbd9be52c24e87935e7c
https://hal.science/hal-03550019
https://hal.science/hal-03550019
Autor:
Hynek Wichterle, Mackenzie W. Mathis, Vincent Mouilleau, Gist F. Croft, Vanessa Ribes, Stéphane Nedelec, Simona Gribaudo, Nour Nicolas, Virginie Rouiller-Fabre, Mathieu Daynac, Angélique Terray, Margot Jarrige, Célia Vaslin, Léa Lesueur, Rémi Robert, Cécile Martinat
SUMMARYRostro-caudal patterning of vertebrates depends on the temporally progressive activation ofHOXgenes within axial stem cells that fuel axial embryo elongation. WhetherHOXgenes sequential activation, the “HOXclock”, is paced by intrinsic chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23c8e588185764a2382f6fd931e7880b
https://doi.org/10.1101/2020.06.27.175646
https://doi.org/10.1101/2020.06.27.175646
Autor:
José-Alain Sahel, Olivier Goureau, Amélie Slembrouck, Céline Nanteau, Angélique Terray, Isabelle Audo, Sacha Reichman, Victoire Fort
Publikováno v:
Stem Cell Research, Vol 25, Iss C, Pp 26-29 (2017)
A human iPS cell line was generated from fibroblasts of a phenotypically unaffected patient from a family with PRPF31-associated retinitis pigmentosa (RP). The transgene-free iPS cells were generated with the human OSKM transcription factors using th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ff874feff594504a1428b15c33650a
https://doi.org/10.1016/j.scr.2017.10.007
https://doi.org/10.1016/j.scr.2017.10.007
Autor:
José-Alain Sahel, Laure Chatrousse, Karim Ben M'Barek, Christelle Monville, Sophie Domingues, Ying Yang, Yolande Masson, Alexandra Plancheron, Mohamed Jarraya, Olivier Goureau, Walter Habeler, Marc Peschanski, Florian Regent, Angélique Terray
Publikováno v:
Science Translational Medicine. 9
Replacing defective retinal pigment epithelial (RPE) cells with those derived from human embryonic stem cells (hESCs) or human-induced pluripotent stem cells (hiPSCs) is a potential strategy for treating retinal degenerative diseases. Early clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e17cbaf35b719e341f7d11512f26d0
https://doi.org/10.1126/scitranslmed.aai7471
https://doi.org/10.1126/scitranslmed.aai7471
Autor:
Zeitz, Said El Shamieh, Cécile Méjécase, Matteo Bertelli, Angélique Terray, Christelle Michiels, Christel Condroyer, Stéphane Fouquet, Maxime Sadoun, Emmanuelle Clérin, Binqian Liu, Thierry Léveillard, Olivier Goureau, José-Alain Sahel, Isabelle Audo, Christina
Publikováno v:
Genes; Volume 8; Issue 10; Pages: 277
We identified herein additional patients with rod-cone dystrophy (RCD) displaying mutations in KIZ, encoding the ciliary centrosomal protein kizuna and performed functional characterization of the respective protein in human fibroblasts and of its mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::f06342f8f1ee22e71098026f7ed8147f
Autor:
Said El Shamieh, Cécile Méjécase, Matteo Bertelli, Angélique Terray, Christelle Michiels, Christel Condroyer, Stéphane Fouquet, Maxime Sadoun, Emmanuelle Clérin, Binqian Liu, Thierry Léveillard, Olivier Goureau, José-Alain Sahel, Isabelle Audo, Christina Zeitz
Publikováno v:
Genes
Genes, Vol 8, Iss 10, p 277 (2017)
Genes, Vol 8, Iss 10, p 277 (2017)
We identified herein additional patients with rod-cone dystrophy (RCD) displaying mutations in KIZ, encoding the ciliary centrosomal protein kizuna and performed functional characterization of the respective protein in human fibroblasts and of its mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9642593d6b0f2e7bd747faf4b497ed4b
http://europepmc.org/articles/PMC5664127
http://europepmc.org/articles/PMC5664127