Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Amélie Slembrouck‐Brec"'
Autor:
Andréa Amprou, Tasnim Ben Yacoub, Camille Letellier, Vincenzo Degaetano, Cécile Méjécase, Leila Azizzadeh Pormehr, Christel Condroyer, Amélie Slembrouck-Brec, Juliette Wohlschlegel, Olivier Goureau, Christina Zeitz, Isabelle Audo
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103558- (2024)
A Human induced pluripotent stem cell (iPSC) line was generated from dermal fibroblasts of a patient affected with an autosomal recessive retinal dystrophy carrying the homozygous c.910-7G>A variant in UBAP1L. Three isogenic control iPSC lines derive
Externí odkaz:
https://doaj.org/article/cfe1bf2bef494c38813b8b13c8c4cb1d
Autor:
Tual Monfort, Salvatore Azzollini, Jérémy Brogard, Marilou Clémençon, Amélie Slembrouck-Brec, Valerie Forster, Serge Picaud, Olivier Goureau, Sacha Reichman, Olivier Thouvenin, Kate Grieve
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-17 (2023)
Abstract Dynamic full-field optical coherence tomography (D-FFOCT) has recently emerged as a label-free imaging tool, capable of resolving cell types and organelles within 3D live samples, whilst monitoring their activity at tens of milliseconds reso
Externí odkaz:
https://doaj.org/article/d7c6030c66464d5a921793a68612340c
Autor:
Tasnim Ben yacoub, Camille Letellier, Juliette Wohlschlegel, Christel Condroyer, Amélie Slembrouck-Brec, Olivier Goureau, Christina Zeitz, Isabelle Audo
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103166- (2023)
The ITM2B-related retinal dystrophy (ITM2B-RD) was identified within patients carrying the autosomal dominant variant [c.782A > C, p.(Glu261Ala)] in ITM2B from whom induced pluripotent stem cell (IPSC) lines were previously generated. Here, we report
Externí odkaz:
https://doaj.org/article/bc69cd3fd8fe48078ae624987b44ed21
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:
Oriane Rabesandratana, Antoine Chaffiol, Antoine Mialot, Amélie Slembrouck-Brec, Corentin Joffrois, Céline Nanteau, Amélie Rodrigues, Giuliana Gagliardi, Sacha Reichman, José-Alain Sahel, Alain Chédotal, Jens Duebel, Olivier Goureau, Gael Orieux
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Optic neuropathies are a major cause of visual impairment due to retinal ganglion cell (RGC) degeneration. Human induced-pluripotent stem cells (iPSCs) represent a powerful tool for studying both human RGC development and RGC-related pathological mec
Externí odkaz:
https://doaj.org/article/1110a7efc5424ef18f2b689f99244a88
Autor:
Giuliana Gagliardi, Karim Ben M'Barek, Antoine Chaffiol, Amélie Slembrouck-Brec, Jean-Baptiste Conart, Céline Nanteau, Oriane Rabesandratana, José-Alain Sahel, Jens Duebel, Gael Orieux, Sacha Reichman, Olivier Goureau
Publikováno v:
Stem Cell Reports, Vol 11, Iss 3, Pp 665-680 (2018)
Summary: Photoreceptor degenerative diseases are a major cause of blindness for which cell replacement is one of the most encouraging strategies. For stem cell-based therapy using human induced pluripotent stem cells (hiPSCs), it is crucial to obtain
Externí odkaz:
https://doaj.org/article/832558c026a64479877cad4a7e382e28
Autor:
Juliette Wohlschlegel, Camille Letellier, Bingqian Liu, Cécile Méjécase, Amélie Slembrouck-Brec, Christel Condroyer, Christelle Michiels, José-Alain Sahel, Sacha Reichman, Christina Zeitz, Olivier Goureau, Isabelle Audo
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Human induced pluripotent stem cell (iPSC) lines were generated from fibroblasts of a patient affected with an autosomal dominant retinal dystrophy carrying the mutation c.782A>C, p.Glu261Ala in ITM2B and from an unaffected brother. Three different i
Externí odkaz:
https://doaj.org/article/773cc77a70734b14a4f8c98a98c55f03
Autor:
Amélie Slembrouck-Brec, Amélie Rodrigues, Oriane Rabesandratana, Giuliana Gagliardi, Céline Nanteau, Stéphane Fouquet, Gilles Thuret, Sacha Reichman, Gael Orieux, Olivier Goureau
Publikováno v:
Stem Cells International, Vol 2019 (2019)
The reprogramming of human somatic cells to induced pluripotent stem cells (iPSCs) has broad applications in regenerative medicine. The generation of self-organized retinal structures from these iPSCs offers the opportunity to study retinal developme
Externí odkaz:
https://doaj.org/article/028b997cd5304c089fbd690b8b3935b1
Autor:
Tual Monfort, Salvatore Azzollini, Jeremy Brogard, Marilou Clémençon, Amélie Slembrouck Brec, Valérie Forster, Serge Picaud, Olivier Goureau, Sacha Reichman, Olivier Thouvenin, Kate Grieve
Dynamic full-field optical coherence tomography (D-FFOCT) has recently emerged as a label-free imaging tool, capable of resolving cell types and organelles within 3D live samples, whilst monitoring their activity at tens of milliseconds resolution. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94e2056a0a770045f0d967826f7afe60
https://doi.org/10.21203/rs.3.rs-2624414/v1
https://doi.org/10.21203/rs.3.rs-2624414/v1
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