Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Justine Viet"'
Autor:
Matthieu Duot, Roselyne Viel, Justine Viet, Catherine Le Goff-Gaillard, Luc Paillard, Salil A. Lachke, Carole Gautier-Courteille, David Reboutier
Publikováno v:
Cells, Vol 12, Iss 20, p 2478 (2023)
Cataract, the opacification of the lens, is the leading cause of blindness worldwide. Although effective, cataract surgery is costly and can lead to complications. Toward identifying alternate treatments, it is imperative to develop organoid models r
Externí odkaz:
https://doaj.org/article/2abddc787b54408cb07a4682dc079426
Autor:
Archana D Siddam, Carole Gautier-Courteille, Linette Perez-Campos, Deepti Anand, Atul Kakrana, Christine A Dang, Vincent Legagneux, Agnès Méreau, Justine Viet, Jeffrey M Gross, Luc Paillard, Salil A Lachke
Publikováno v:
PLoS Genetics, Vol 14, Iss 3, p e1007278 (2018)
Opacification of the ocular lens, termed cataract, is a common cause of blindness. To become transparent, lens fiber cells undergo degradation of their organelles, including their nuclei, presenting a fundamental question: does signaling/transcriptio
Externí odkaz:
https://doaj.org/article/305a114dda59435fa444dfce3fd60c4b
Autor:
Masataka Kikuchi, Justine Viet, Kenichi Nagata, Masahiro Sato, Géraldine David, Yann Audic, Michael A. Silverman, Mitsuko Yamamoto, Hiroyasu Akatsu, Yoshio Hashizume, Kyoko Chiba, Shuko Takeda, Shoshin Akamine, Tesshin Miyamoto, Ryota Uozumi, Shiho Gotoh, Kohji Mori, Manabu Ikeda, Luc Paillard, Takashi Morihara
In an era when numerous disease-associated genes have been identified, determining the molecular mechanisms of complex diseases is still difficult. The CELF1 region was identified by genome-wide association studies as an Alzheimer’s disease (AD) ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a040415b930b0098b53dfc1e0e8ff3e
https://doi.org/10.1101/2022.02.28.22271320
https://doi.org/10.1101/2022.02.28.22271320
Autor:
Francisco G. Hernandez, Luc Paillard, Archana D. Siddam, Bailey A. T. Weatherbee, Salil A. Lachke, Carole Gautier-Courteille, Sandeep Aryal, Justine Viet
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2020, 139 (12), pp.1541-1554. ⟨10.1007/s00439-020-02195-7⟩
Human Genetics, 2020, 139 (12), pp.1541-1554. ⟨10.1007/s00439-020-02195-7⟩
Hum Genet
Human Genetics, Springer Verlag, 2020, 139 (12), pp.1541-1554. ⟨10.1007/s00439-020-02195-7⟩
Human Genetics, 2020, 139 (12), pp.1541-1554. ⟨10.1007/s00439-020-02195-7⟩
Hum Genet
International audience; The homeodomain transcription factors (TFs) Pax6 (OMIM 607108) and Prox1 (OMIM 601546) critically regulate gene expression in lens development. While PAX6 mutations in humans can cause cataract, aniridia, microphthalmia, and a
Autor:
Justine Viet, Carole Gautier-Courteille, Serge Hardy, David Reboutier, Luc Paillard, Salil A. Lachke
Publikováno v:
Developmental Dynamics
Developmental Dynamics, Wiley, 2020, 249 (5), pp.610-621. ⟨10.1002/dvdy.147⟩
Dev Dyn
Developmental Dynamics, 2020, 249 (5), pp.610-621. ⟨10.1002/dvdy.147⟩
Developmental Dynamics, Wiley, 2020, 249 (5), pp.610-621. ⟨10.1002/dvdy.147⟩
Dev Dyn
Developmental Dynamics, 2020, 249 (5), pp.610-621. ⟨10.1002/dvdy.147⟩
International audience; BACKGROUND:Ocular lens clouding is termed as cataract, which depending on the onset, is classified as congenital or age-related. Developing new cataract treatments requires new models. Thus far, Xenopus embryos have not been e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9fe3ccb9264ce6e5bcc9987bdcd3b6a
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02440933
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02440933
Autor:
Archana D. Siddam, Justine Viet, Bailey A. T. Weatherbee, Carole Gautier-Courteille, Aryal Sandeep, Luc Paillard, Salil A. Lachke
Publikováno v:
The FASEB Journal. 33
Autor:
Agnès Méreau, Gaelle Angrand, Luc Paillard, Stéphanie Mottier, Serge Hardy, Hubert Lerivray, Justine Viet, Maud Noiret, Carole Gautier-Courteille, Yann Audic
Publikováno v:
Developmental Biology
Developmental Biology, Elsevier, 2016, 409 (2), pp.489-501. ⟨10.1016/j.ydbio.2015.11.002⟩
Developmental Biology, 2016, 409 (2), pp.489-501. ⟨10.1016/j.ydbio.2015.11.002⟩
Developmental Biology, Elsevier, 2016, 409 (2), pp.489-501. ⟨10.1016/j.ydbio.2015.11.002⟩
Developmental Biology, 2016, 409 (2), pp.489-501. ⟨10.1016/j.ydbio.2015.11.002⟩
International audience; In humans, genetic diseases affecting skin integrity (genodermatoses) are generally caused by mutations in a small number of genes that encode structural components of the dermal-epidermal junctions. In this article, we first
Autor:
Agnès Méreau, Atul Kakrana, Linette Perez-Campos, Deepti Anand, Justine Viet, Carole Gautier-Courteille, Vincent Legagneux, Christine Dang, Jeffrey M. Gross, Archana D. Siddam, Salil A. Lachke, Luc Paillard
Publikováno v:
PLoS Genetics, Vol 14, Iss 3, p e1007278 (2018)
PLoS Genetics
PLoS Genetics, 2018, 14 (3), pp.e1007278. ⟨10.1371/journal.pgen.1007278⟩
PLoS Genetics, Public Library of Science, 2018, 14 (3), pp.e1007278. ⟨10.1371/journal.pgen.1007278⟩
PLoS Genetics
PLoS Genetics, 2018, 14 (3), pp.e1007278. ⟨10.1371/journal.pgen.1007278⟩
PLoS Genetics, Public Library of Science, 2018, 14 (3), pp.e1007278. ⟨10.1371/journal.pgen.1007278⟩
Opacification of the ocular lens, termed cataract, is a common cause of blindness. To become transparent, lens fiber cells undergo degradation of their organelles, including their nuclei, presenting a fundamental question: does signaling/transcriptio
Autor:
Luc Paillard, Justine Viet, Kenichi Nagata, Takashi Morihara, Manabu Ikeda, Masahiro Sato, Hiroyasu Akatsu
Publikováno v:
Alzheimer's & Dementia. 15:P978-P978
Autor:
Agnès Méreau, Hubert Lerivray, Vincent Legagneux, Stéphane Deschamps, Marion Bervas, Luc Paillard, Serge Hardy, Maud Noiret, Yann Audic, Gaelle Angrand, Carole Gautier-Courteille, Justine Viet
Publikováno v:
Developmental Biology
Developmental Biology, Elsevier, 2017, 426 (2), pp.449-459. ⟨10.1016/j.ydbio.2016.08.021⟩
Developmental Biology, 2017, 426 (2), pp.449-459. ⟨10.1016/j.ydbio.2016.08.021⟩
Developmental Biology, Elsevier, 2017, 426 (2), pp.449-459. ⟨10.1016/j.ydbio.2016.08.021⟩
Developmental Biology, 2017, 426 (2), pp.449-459. ⟨10.1016/j.ydbio.2016.08.021⟩
Regulation of alternative splicing is an important process for cell differentiation and development. Down-regulation of Ptbp1, a regulatory RNA-binding protein, leads to developmental skin defects in Xenopus laevis. To identify Ptbp1-dependent splici