Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Aurelie Carabalona"'
Autor:
Déborah Cardoso, Solenn Guilbert, Philippe Guigue, Aurélie Carabalona, Karim Harhouri, Cécile Peccate, Johana Tournois, Zoheir Guesmia, Lino Ferreira, Catherine Bartoli, Nicolas Levy, Laurence Colleaux, Xavier Nissan, Antoine Muchir
Publikováno v:
Cell Death and Disease, Vol 15, Iss 10, Pp 1-14 (2024)
Abstract Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare genetic disorder associated with features of accelerated aging. HGPS is an autosomal dominant disease caused by a de novo mutation of LMNA gene, encoding A-type lamins, resulti
Externí odkaz:
https://doaj.org/article/dc9bc6f3476e46378df90ad4de499f20
Autor:
Aurelie Carabalona, Henna Kallo, Liliia Andriichuk, Maryanne Gonzalez, Ellinoora Elomaa, Florence Molinari, Christiana Fragkou, Pekka Lappalainen, Marja Wessels, Juha Saarikangas, Claudio Rivera
Publikováno v:
SSRN Electronic Journal.
The cerebral cortex is responsible for higher cognitive functions. Its correct development depends on coordinated asymmetric division cycles by polarized radial glial progenitor cells. Mitotic defects in neuronal stem cells are linked to the aetiolog
Publikováno v:
Nature neuroscience
Brain neural stem cells (radial glial progenitors, RGPs) undergo a mysterious form of cell cycle-entrained interkinetic nuclear migration (INM) that is driven apically by cytoplasmic dynein and basally by the kinesin KIF1A, which has recently been im
Autor:
Ville Jokinen, Marcus N Leiwe, Aurelie Carabalona, Claudio Rivera, Mikhail Yuryev, Liliia Andriichuk
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8 (1), ⟨10.1038/s41598-018-34410-x⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports, Nature Publishing Group, 2018, 8 (1), ⟨10.1038/s41598-018-34410-x⟩
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Prior to sensory experience spontaneous activity appears to play a fundamental role in the correct formation of prominent functional features of different cortical regions. The use of anaesthesia during pregnancy such as ketamine is largely considere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6467966f4b687ec36eb01fbcf09775a0
https://hal.archives-ouvertes.fr/hal-01961924/document
https://hal.archives-ouvertes.fr/hal-01961924/document
Autor:
Carlos Cardoso, Jenny C. Taylor, David Antony Keays, Alistair T. Pagnamenta, Valerio Conti, Antonio Falace, Françoise Watrin, Francesca Novara, Emilie Pallesi-Pocachard, Agathe A. Deparis, Renzo Guerrini, Aurelie Carabalona, Alfonso Represa, Emmanuelle Buhler, Elena Parrini, Orsetta Zuffardi, Richard J. Leventer, Stefano Lise, Usha Kini, Fabienne Schaller
Publikováno v:
Journal of Visualized Experiments.
Birth defects that involve the cerebral cortex - also known as malformations of cortical development (MCD) - are important causes of intellectual disability and account for 20-40% of drug-resistant epilepsy in childhood. High-resolution brain imaging
Publikováno v:
Cytoskeleton (Hoboken, N.J.). 73(10)
Over the past two decades, substantial progress has been made in visualizing and understanding neuronal cell migration and morphogenesis during brain development. Distinct mechanisms have evolved to support migration of the various cell types that co
Autor:
David D. Doobin, Alexandre D. Baffet, Richard B. Vallee, Tiago J. Dantas, Aurelie Carabalona, Daniel J. Hu
Development of the cerebral cortex is a very dynamic process, involving a series of complex morphogenetic events. Following division of progenitor cells in the ventricular zone, neurons undergo a series of morphological changes and migrate outward to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94b8eb9d8a3eb13674134d63aaab8c8e
https://doi.org/10.1016/bs.mcb.2015.06.013
https://doi.org/10.1016/bs.mcb.2015.06.013
Autor:
Philippe Hubert, Alfonso Represa, Karen Arnaud, Aurelie Carabalona, Carlos Cardoso, Mehdi Oualha, Jean Pierre Siffroi, Emilie Pallesi-Pocachard, Cyril Goizet, Christophe Pellegrino, Isabelle Coupry, Sabrina Khantane, Shirley Beguin, Emmanuelle Buhler, Antoinette Gelot
Publikováno v:
Human Molecular Genetics. 21:1004-1017
Periventricular nodular heterotopia (PH) is a human brain malformation caused by defective neuronal migration that results in ectopic neuronal nodules lining the lateral ventricles beneath a normal appearing cortex. Most affected patients have seizur
Autor:
Alistair T. Pagnamenta, George McGillivray, Jill Clayton-Smith, Stephen P. Robertson, Emilie Pallesi-Pocachard, William B. Dobyns, Samuel F. Berkovic, Francesca Novara, Valerio Conti, Davide Mei, Aurelie Carabalona, Jenny C. Taylor, Stefano Lise, Usha Kini, Carlos Cardoso, David A. Keays, Ingrid E. Scheffer, Orsetta Zuffardi, Richard J. Leventer, Emmanuelle Buhler, Françoise Watrin, François Michel, Alfonso Represa, Renzo Guerrini, Elena Parrini, Pasquale Striano
Publikováno v:
Brain : a journal of neurology. 136(Pt 11)
Periventricular nodular heterotopia is caused by defective neuronal migration that results in heterotopic neuronal nodules lining the lateral ventricles. Mutations in filamin A (FLNA) or ADP-ribosylation factor guanine nucleotide-exchange factor 2 (A
Autor:
Diane Frankel, Valérie Delecourt, Elva-María Novoa-del-Toro, Jérôme D. Robin, Coraline Airault, Catherine Bartoli, Aurélie Carabalona, Sophie Perrin, Kilian Mazaleyrat, Annachiara De Sandre-Giovannoli, Frederique Magdinier, Anaïs Baudot, Nicolas Lévy, Elise Kaspi, Patrice Roll
Publikováno v:
iScience, Vol 25, Iss 2, Pp 103757- (2022)
Summary: Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disorder, in which an abnormal and toxic protein called progerin, accumulates in cell nuclei, leading to major cellular defects. Among them, chromatin remodeling drives gene expre
Externí odkaz:
https://doaj.org/article/1068381b12894a3784d9ad1250954c43