Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Maria Elisa Salvalai"'
Autor:
Fiorenza Stagni, Maria Elisa Salvalai, Andrea Giacomini, Marco Emili, Beatrice Uguagliati, Er Xia, Mariagrazia Grilli, Renata Bartesaghi, Sandra Guidi
Publikováno v:
Neurobiology of Disease, Vol 129, Iss , Pp 44-55 (2019)
Down syndrome (DS), a genetic condition due to triplication of chromosome 21, is characterized by reduced proliferation of neural progenitor cells (NPCs) starting from early life stages. This defect is worsened by a reduction of neuronogenesis (accom
Externí odkaz:
https://doaj.org/article/bf9371e6fdda4661982a2e2384de7173
Autor:
Marco Emili, Fiorenza Stagni, Maria Elisa Salvalai, Beatrice Uguagliati, Andrea Giacomini, Christelle Albac, Marie-Claude Potier, Mariagrazia Grilli, Renata Bartesaghi, Sandra Guidi
Publikováno v:
Neurobiology of Disease, Vol 140, Iss , Pp 104874- (2020)
Down syndrome (DS), a neurodevelopmental disorder caused by triplication of chromosome 21, is characterized by intellectual disability. In DS, defective neurogenesis causes an overall reduction in the number of neurons populating the brain and defect
Externí odkaz:
https://doaj.org/article/43c80c89c48c44658892f3bcac563905
Autor:
Beatrice Uguagliati, Marie-Claude Potier, Maria Elisa Salvalai, Christelle Albac, Andrea Giacomini, Renata Bartesaghi, Mariagrazia Grilli, Marco Emili, Fiorenza Stagni, Sandra Guidi
Publikováno v:
Neurobiology of Disease, Vol 140, Iss, Pp 104874-(2020)
Down syndrome (DS), a neurodevelopmental disorder caused by triplication of chromosome 21, is characterized by intellectual disability. In DS, defective neurogenesis causes an overall reduction in the number of neurons populating the brain and defect
Autor:
Sandra Guidi, Er Xia, Renata Bartesaghi, Marco Emili, Andrea Giacomini, Fiorenza Stagni, Beatrice Uguagliati, Maria Elisa Salvalai, Mariagrazia Grilli
Publikováno v:
Neurobiology of Disease, Vol 129, Iss, Pp 44-55 (2019)
Down syndrome (DS), a genetic condition due to triplication of chromosome 21, is characterized by reduced proliferation of neural progenitor cells (NPCs) starting from early life stages. This defect is worsened by areduction of neuronogenesis (accomp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce2f45b6ffdd0d51f5687653d2a9a42d
http://hdl.handle.net/11585/689168
http://hdl.handle.net/11585/689168
Autor:
Fiorenza Stagni, Veronica Vidal-Sanchez, Renata Bartesaghi, Sandra Guidi, Maria Elisa Salvalai, Mariagrazia Grilli, Marco Emili, Andrea Giacomini, Carmen Martínez-Cué
Publikováno v:
Brain Research Bulletin Volume 140, June 2018, Pages 378-391
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Individuals with Down syndrome (DS), a genetic condition due to triplication of Chromosome 21, are characterized by intellectual disability that worsens with age. Since impairment of neurogenesis and dendritic maturation are very likely key determina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcdcd5cf9e7dff5ed54046902dae8323
http://hdl.handle.net/11585/646592
http://hdl.handle.net/11585/646592
Autor:
Maria Elisa Salvalai, Marie-Claude Potier, Mariagrazia Grilli, Christelle Albac, Renata Bartesaghi, Fiorenza Stagni
Publikováno v:
European Neuropsychopharmacology. 29:S445-S446
Autor:
B. Uguagliati, Marco Emili, Renata Bartesaghi, Fiorenza Stagni, Andrea Giacomini, Sandra Guidi, Maria Elisa Salvalai, Mariagrazia Grilli
Publikováno v:
European Neuropsychopharmacology. 29:S442-S443
Autor:
Marco Emili, Maria Elisa Salvalai, Roberto Rimondini, Renata Bartesaghi, Fiorenza Stagni, Andrea Giacomini, Valeria Bortolotto, Beatrice Uguagliati, Mariagrazia Grilli, Sandra Guidi
Intellectual disability is the unavoidable hallmark of Down syndrome (DS), with a heavy impact on public health. Reduced neurogenesis and impaired neuron maturation are considered major determinants of altered brain function in DS. Since the DS brain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25ba7029b56e3b62c6f83b1c32dcd420
http://hdl.handle.net/11585/612122
http://hdl.handle.net/11585/612122