Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mariana RAMOS-BROSSIER"'
Autor:
Mariana Ramos-Brossier, David Romeo-Guitart, Fabien Lanté, Valérie Boitez, François Mailliet, Soham Saha, Manon Rivagorda, Eleni Siopi, Ivan Nemazanyy, Christine Leroy, Stéphanie Moriceau, Sarah Beck-Cormier, Patrice Codogno, Alain Buisson, Laurent Beck, Gérard Friedlander, Franck Oury
Publikováno v:
Cell Death and Disease, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract In recent years, primary familial brain calcification (PFBC), a rare neurological disease characterized by a wide spectrum of cognitive disorders, has been associated to mutations in the sodium (Na)-Phosphate (Pi) co-transporter SLC20A2. How
Externí odkaz:
https://doaj.org/article/72e96d92ec03461d8acc5a19f2ed7abf
Autor:
Mariana RAMOS-BROSSIER, David ROMEO-GUITART, Fabien LANTE, Valerie Boitez, François MAILLIET, Sohame SAHA, Manon RIVAGORDA, Eleni SIOPI, Ivan Namazanyy, Leroy Christine, Stéphanie Moriceau, Sarah BECK-CORMIER, Patrice Codogno, Alain BUISSON, Laurent BECK, Gerard Friedlander, Franck Oury
In recent years, primary familial brain calcification (PFBC), a rare neurological disease characterized by a wide spectrum of cognitive disorders, has been associated to mutations in the sodium (Na)-Phosphate (Pi) co-transporter SLC20A2. However, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::159ed62f10b94f4f626fe9278e49c520
https://doi.org/10.21203/rs.3.rs-2727315/v1
https://doi.org/10.21203/rs.3.rs-2727315/v1
Publikováno v:
Hormone Molecular Biology and Clinical Investigation. 28:69-83
Reciprocal relationships between organs are essential to maintain whole body homeostasis. An exciting interplay between two apparently unrelated organs, the bone and the brain, has emerged recently. Indeed, it is now well established that the brain i
Autor:
Stylianos Kosmidis, Mariana Ramos-Brossier, Frédéric Saudou, Paula Mera, Arnaud Obri, Franck Oury, Lori Khrimian, Xiao-Bing Gao, Eric R. Kandel, Theodoros Karnavas, Gerard Karsenty, Stéphanie Moriceau, Anne-Sophie Nicot, Audrey Rousseaud
Publikováno v:
The Journal of Experimental Medicine
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
This study by Khrimian et al. demonstrates that the bone-derived hormone osteocalcin is necessary and sufficient to correct age-related cognitive decline in the mouse. It also provides genetic, molecular, and neurophysiological evidence that Gpr158 i
Autor:
Mary R. Shanley, Nadir Boudarene, Patrice Codogno, Mariana Ramos-Brossier, Audrey Rousseaud, Anna Chiara Nascimbeni, Mélissa Glatigny, Carmine Settembre, Nicolas Kuperwasser, Franck Oury, Gérard Friedlander, Stéphanie Moriceau, Etienne Morel, Allyson K. Friedman, Alain Buisson, Fabien Lanté, Manon Rivagorda
Publikováno v:
Current Biology-CB
Current Biology-CB, Elsevier, 2019, 29, pp.435-448.e8. ⟨10.1016/j.cub.2018.12.021⟩
Current Biology-CB, Elsevier, 2019, 29, pp.435-448.e8. ⟨10.1016/j.cub.2018.12.021⟩
Age-related declines in cognitive fitness are associated with a reduction in autophagy, an intracellular lysosomal catabolic process that regulates protein homeostasis and organelle turnover. However, the functional significance of autophagy in regul
Publikováno v:
SpringerPlus
Synapse and dendrite deficits induced by mutations in the X-linked intellectual disability gene Il1rapl1 Caterina Montani, Mariana Ramos-Brossier, Pierre Billuart, Carlo Sala Mutations and deletions of Interleukin-1 receptor accessory protein like 1
Autor:
Mariana Ramos-Brossier, Chiara Verpelli, Benedetta Terragni, Luisa Ponzoni, Yoann Saillour, Laura Gritti, Pierre Billuart, Carlo Sala, Caterina Montani, Mariaelvina Sala, Massimo Mantegazza, Daniela Braida, Andrzej W. Cwetsch
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 37(28)
Mutations and deletions of the interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene, located on the X chromosome, are associated with intellectual disability (ID) and autism spectrum disorder (ASD). IL1RAPL1 protein is located at the posts
Autor:
R. Frank Kooy, Olivier Dorseuil, Eric Bieth, Delphine Héron, Sarah Moreno, Carlo Sala, Laura Gritti, Jozef Gecz, Anna Hackett, Caterina Montani, Christelle Martin, Anne Faudet, Aurélie Toussaint, Karine Poirier, Jamel Chelly, Bart Loeys, Yann Humeau, Pierre Billuart, Mariana Ramos-Brossier, Nicolas Lebrun, Christine Seminatore-Nole
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2014, pp.523
Human Molecular Genetics, 2014, pp.523
Human molecular genetics
Human Molecular Genetics, Oxford University Press (OUP), 2014, pp.523
Human Molecular Genetics, 2014, pp.523
Human molecular genetics
Mutations in interleukin-1 receptor accessory protein like 1 (IL1RAPL1) gene have been associated with non-syndromic intellectual disability and autism spectrum disorder. This protein interacts with synaptic partners like PSD-95 and PTPδ, regulating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7c1109e2f7a37dc1d525565e4a6715d
https://www.hal.inserm.fr/inserm-01102927
https://www.hal.inserm.fr/inserm-01102927
Autor:
Jonathan Davila, Mavis R. Swerdel, Mariana Ramos-Brossier, Martha Lapid-Volosin, Ronald P. Hart, Israel Pichardo-Casas, Alejandro Athie, Wilma J. Friedman, Luis Vaca, Loyal A. Goff
In recent years, microRNAs or miRNAs have been proposed to target neuronal mRNAs localized near the synapse, exerting a pivotal role in modulating local protein synthesis, and presumably affecting adaptive mechanisms such as synaptic plasticity. In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25cc48d57c78606f645d1fe172d966c8
https://europepmc.org/articles/PMC4431575/
https://europepmc.org/articles/PMC4431575/
Autor:
Ramos-Brossier, Mariana, Romeo-Guitart, David, Lanté, Fabien, Boitez, Valérie, Mailliet, François, Saha, Soham, Rivagorda, Manon, Siopi, Eleni, Nemazanyy, Ivan, Leroy, Christine, Moriceau, Stéphanie, Beck-Cormier, Sarah, Codogno, Patrice, Buisson, Alain, Beck, Laurent, Friedlander, Gérard, Oury, Franck
Publikováno v:
Cell Death & Disease; Jan2024, Vol. 15 Issue 1, p1-18, 18p