Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ane Cristina Ayo‐Martin"'
Autor:
Francesco Di Matteo, Fabrizia Pipicelli, Christina Kyrousi, Isabella Tovecci, Eduardo Penna, Marianna Crispino, Angela Chambery, Rosita Russo, Ane Cristina Ayo‐Martin, Martina Giordano, Anke Hoffmann, Emilio Ciusani, Laura Canafoglia, Magdalena Götz, Rossella Di Giaimo, Silvia Cappello
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 6, Pp 1-21 (2020)
Abstract Progressive myoclonus epilepsy (PME) of Unverricht–Lundborg type (EPM1) is an autosomal recessive neurodegenerative disorder with the highest incidence of PME worldwide. Mutations in the gene encoding cystatin B (CSTB) are the primary gene
Externí odkaz:
https://doaj.org/article/d7924a20df5e4060b7e35a5b2deeec27
Publikováno v:
Frontiers in Molecular Biosciences, Vol 7 (2020)
Cortical development is a very complex process in which any temporal or spatial alterations can give rise to a wide range of cortical malformations. Among those malformations, periventricular heterotopia (PH) is characterized by clusters of neurons t
Externí odkaz:
https://doaj.org/article/58df76782da24486b88ee31ad59ccbd3
Autor:
Javier Díaz-Alonso, Juan Paraíso-Luna, Samuel Simón-Sánchez, Ane Cristina Ayo-Martin, Silvia Cappello, José Sánchez-Prieto, Daniel García-Rincón, Ricardo Martín, José Aguareles, Carlos Costas-Insua, Isabel Liste, Adán de Salas-Quiroga, Ismael Galve-Roperh, Elena García-Taboada, Manuel Guzmán
Publikováno v:
Repisalud
Instituto de Salud Carlos III (ISCIII)
Instituto de Salud Carlos III (ISCIII)
The endocannabinoid (eCB) system, via the cannabinoid CB1 receptor, regulates neurodevelopment by controlling neural progenitor proliferation and neurogenesis. CB1 receptor signalling in vivo drives corticofugal deep layer projection neuron developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c15d2a5d13dc3bab0063eddac413a64
https://doi.org/10.1242/dev.192161
https://doi.org/10.1242/dev.192161
Autor:
Christina Kyrousi, Francesco Di Matteo, Rossella Di Giaimo, Laura Canafoglia, Marianna Crispino, Fabrizia Pipicelli, Isabella Tovecci, Rosita Russo, Martina Giordano, Ane Cristina Ayo-Martin, Anke Hoffmann, Eduardo Penna, Angela Chambery, Emilio Ciusani, Magdalena Götz, Silvia Cappello
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 12, Iss 6, Pp n/a-n/a (2020)
EMBO Molecular Medicine, Vol 12, Iss 6, Pp n/a-n/a (2020)
Progressive myoclonus epilepsy (PME) of Unverricht–Lundborg type (EPM1) is an autosomal recessive neurodegenerative disorder with the highest incidence of PME worldwide. Mutations in the gene encoding cystatin B (CSTB) are the primary genetic cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a145c09b3277e23392b863ac0acc084
http://hdl.handle.net/11591/430276
http://hdl.handle.net/11591/430276
Autor:
Mariana Schroeder, Johannes Klaus, Stephen P. Robertson, Silvia Cappello, Malgorzata Santel, Micha Drukker, Christina Kyrousi, Rossella Di Giaimo, Barbara Treutlein, J. Gray Camp, Adam C. O’Neill, Chiara Tocco, Ane Cristina Ayo-Martin, Ejona Rusha, Stephan Riesenberg, Sabina Kanton, Magdalena Götz
Publikováno v:
Nature Medicine, 25
Nature Medicine
Nature Medicine
Malformations of the human cortex represent a major cause of disability1. Mouse models with mutations in known causal genes only partially recapitulate the phenotypes and are therefore not unlimitedly suited for understanding the molecular and cellul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e13544b3b6e8d5f033c45744e8bf4cf
https://doi.org/10.1038/s41591-019-0371-0
https://doi.org/10.1038/s41591-019-0371-0
Autor:
Johannes, Klaus, Sabina, Kanton, Christina, Kyrousi, Ane Cristina, Ayo-Martin, Rossella, Di Giaimo, Stephan, Riesenberg, Adam C, O'Neill, J Gray, Camp, Chiara, Tocco, Malgorzata, Santel, Ejona, Rusha, Micha, Drukker, Mariana, Schroeder, Magdalena, Götz, Stephen P, Robertson, Barbara, Treutlein, Silvia, Cappello
Publikováno v:
Nature medicine. 25(4)
Malformations of the human cortex represent a major cause of disability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::442277be195580f8fbf83395a8634291
https://pubmed.ncbi.nlm.nih.gov/30858616
https://pubmed.ncbi.nlm.nih.gov/30858616