Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Charlotte Baudouin"'
Autor:
Estelle Renaux, Charlotte Baudouin, Olivier Schakman, Ondine Gay, Manon Martin, Damien Marchese, Younès Achouri, René Rezsohazy, Françoise Gofflot, Frédéric Clotman
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Motor activity is organized by neuronal networks composed of motor neurons and a wide variety of pre-motor interneuron populations located in the brainstem and spinal cord. Differential expression and single-cell RNA sequencing studies recently unvei
Externí odkaz:
https://doaj.org/article/4df343ff15cd4de595e1c6ea2dfabe69
Publikováno v:
genesis. 59
Autor:
Pranav, Garg, Sabrina, Semmler, Charlotte, Baudouin, Christine, Vande Velde, Steven S, Plotkin
Publikováno v:
Journal of Molecular Biology. 434:167697
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease primarily impacting motor neurons. Mutations in superoxide dismutase 1 (SOD1) are the second most common cause of familial ALS. Several of these mutations lead to misfolding or
Publikováno v:
genesis. 59
In the spinal cord, ventral interneurons regulate the activity of motor neurons, thereby controlling motor activities including locomotion. Interneurons arise during embryonic development from distinct progenitor domains orderly distributed along the
Autor:
Alexandra T. Star, Heidi M. McBride, Thomas M. Durcan, Elizabeth M. Meiering, Myriam Gagné, Janice Robertson, Christine Vande Velde, Jean-François Trempe, Sabrina Semmler, Neil R. Cashman, Pranav Garg, Elise Caron, Andrew N. Bayne, Nathalie Grandvaux, Steven S. Plotkin, Laurie Destroismaisons, Yousra Khalfallah, Sarah Pickles, Charlotte Baudouin, Mathilde Chaineau, Arsalan S. Haqqani, Emeline Hamon-Keromen
Publikováno v:
J Biol Chem
Amyotrophic lateral sclerosis (ALS) is a fatal disease, characterized by the selective loss of motor neurons leading to paralysis. Mutations in the gene encoding superoxide dismutase 1 (SOD1) are the second most common cause of familial ALS, and cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e140f4f50d7b9cd9106484395b1381a
https://nrc-publications.canada.ca/eng/view/object/?id=a04144de-e1cd-4b3e-a9fd-85a9f8650044
https://nrc-publications.canada.ca/eng/view/object/?id=a04144de-e1cd-4b3e-a9fd-85a9f8650044
Autor:
Olivier Schakman, Xiuqian Mu, Frédéric Clotman, Audrey Harris, Elena Kondratskaya, Stéphanie Debrulle, María Hidalgo-Figueroa, Nicolas Dauguet, Jean-Luc Boulland, Alexander Gow, Mathilde Toch, Fadel Tissir, Joel C. Glover, Charlotte Baudouin
Publikováno v:
Scientific Reports Volume 10, Issue 1, 1 December 2020, Article number 996
RODIN. Repositorio de Objetos de Docencia e Investigación de la Universidad de Cádiz
instname
Scientific Reports
Scientific reports, Vol. 10, no. 1, p. 996 [1-17] (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-17 (2020)
RODIN. Repositorio de Objetos de Docencia e Investigación de la Universidad de Cádiz
instname
Scientific Reports
Scientific reports, Vol. 10, no. 1, p. 996 [1-17] (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-17 (2020)
In the developing spinal cord, Onecut transcription factors control the diversification of motor neurons into distinct neuronal subsets by ensuring the maintenance of Isl1 expression during differentiation. However, other genes downstream of the Onec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32e1509c47d908247f47d46d4b5874f
http://hdl.handle.net/10498/22972
http://hdl.handle.net/10498/22972
Autor:
Steven S. Plotkin, Neil R. Cashman, Elise Caron, Laurie Destroismaisons, Alexandra T. Star, Mathilde Chaineau, Andrew N. Bayne, Charlotte Baudouin, Christine Vande Velde, Thomas M. Durcan, Yousra Khalfallah, Elizabeth M. Meiering, Heidi M. McBride, Myriam Gagné, Pranav Garg, Janice Robertson, Sabrina Semmler, Sarah Pickles, Arsalan S. Haqqani, Nathalie Grandvaux, Jean-François Trempe, Emeline Hamon-Keromen
Amyotrophic lateral sclerosis (ALS) is a fatal disease, characterized by the selective loss of motor neurons leading to paralysis. Mutations in the gene encoding superoxide dismutase1(SOD1) are the second most common cause of familial ALS, and consid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::231767bf007cffe9a8e0311f65929bfb
Publikováno v:
Biophysical Journal. 120:297a