Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Berta Marcó de la Cruz"'
Autor:
Alejandro López-Tobón, Carlo Emanuele Villa, Cristina Cheroni, Sebastiano Trattaro, Nicolò Caporale, Paola Conforti, Raffaele Iennaco, Maria Lachgar, Marco Tullio Rigoli, Berta Marcó de la Cruz, Pietro Lo Riso, Erika Tenderini, Flavia Troglio, Marco De Simone, Isabel Liste-Noya, Giuseppe Macino, Massimiliano Pagani, Elena Cattaneo, Giuseppe Testa
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 847-861 (2019)
Summary: The regulation of the proliferation and polarity of neural progenitors is crucial for the development of the brain cortex. Animal studies have implicated glycogen synthase kinase 3 (GSK3) as a pivotal regulator of both proliferation and pola
Externí odkaz:
https://doaj.org/article/59aa1d8855cf47e49b953ab485034343
Autor:
Yicheng Ding, Aisling O'Brien, Berta Marcó de la Cruz, Meimei Yang, Yin Lu, Xiaohong Qian, Guangming Yang, Veronica McInerney, Janusz Krawczyk, Sally A. Lynch, Linda Howard, Nicholas M. Allen, Timothy O'Brien, Louise Gallagher, Sanbing Shen
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102254- (2021)
NRXN1 deletions are commonly found in autism spectrum disorder (ASD) and other neurodevelopmental/neuropsychiatric disorders. Derivation of induced pluripotent stem cells (iPSCs) from different diseases involving different deletion regions are essent
Externí odkaz:
https://doaj.org/article/f9e86826ed454b82bf011cf698ad984b
Autor:
Yicheng Ding, Aisling O'Brien, Berta Marcó de la Cruz, Meimei Yang, Jacqueline Fitzgerald, Guangming Yang, Weidong Li, Veronica McInerney, Janusz Krawczyk, Sally A. Lynch, Linda Howard, Nicholas M. Allen, Timothy O'Brien, Louise Gallagher, Sanbing Shen
Publikováno v:
Stem Cell Research, Vol 52, Iss , Pp 102222- (2021)
NRXN1 encodes thousands of splicing variants categorized into long NRXN1α, short NRXN1β and extremely short NRXN1γ, which exert differential roles in neuronal excitation/inhibition. NRXN1α deletions are common in autism spectrum disorder (ASD) an
Externí odkaz:
https://doaj.org/article/e838199a5f194dc29c0e8c4705086fbb
Autor:
Yicheng Ding, Berta Marcó de la Cruz, Veronica McInerney, Yin Lu, Guangming Yang, Xiaohong Qian, Weidong Li, Janusz Krawczyk, Linda Howard, Timothy O'Brien, Louise Gallagher, Sanbing Shen
Publikováno v:
Stem Cell Research, Vol 49, Iss , Pp 102101- (2020)
The induced pluripotent stem cell (iPSC) technology has offered an unprecedented opportunity for disease modelling and drug discovery. Here we used non-integrating Sendai viral method and derived iPSCs from three young healthy Caucasian donors. All i
Externí odkaz:
https://doaj.org/article/45c95f48048348b58d7bf66f31e15452
Autor:
Berta Marcó de la Cruz, Yicheng Ding, Veronica McInerney, Janusz Krawczyk, Yin Lu, Guangming Yang, Xiaohong Qian, Weidong Li, Linda Howard, Nicholas M. Allen, Timothy O'Brien, Louise Gallagher, Sanbing Shen
Publikováno v:
Stem Cell Research, Vol 44, Iss , Pp - (2020)
Hundreds of rare risk factors have been identified for ASD, however, the underlying causes for ~70% of sporadic cases are unknown. Sporadic ASD models are thus essential for validating phenotypic commonality and drug suitability to the majority of pa
Externí odkaz:
https://doaj.org/article/4e7ba36deedd4a7aa63705ba1ab4d6c7
Autor:
Yicheng Ding, Berta Marcó de la Cruz, Yawen Xia, Min Liu, Yin Lu, Veronica McInerney, Janusz Krawczyk, Sally A. Lynch, Linda Howard, Timothy O'Brien, Louise Gallagher, Sanbing Shen
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
NRXN1 copy number variation is a rare genetic factor commonly shared among autism spectrum disorder (ASD), schizophrenia, intellectual disability, epilepsy and developmental delay. Human induced pluripotent stem cells (iPSCs) are essential for diseas
Externí odkaz:
https://doaj.org/article/2d8cecdca7964838860545db65b61e29
Autor:
Nicholas M. Allen, Jacqueline Fitzgerald, Guangming Yang, Aisling O'Brien, Louise Gallagher, Janusz Krawczyk, Sally Ann Lynch, Yicheng Ding, Sanbing Shen, Weidong Li, Veronica McInerney, Linda Howard, Meimei Yang, Timothy O'Brien, Berta Marcó de la Cruz
Publikováno v:
Stem Cell Research, Vol 52, Iss, Pp 102222-(2021)
NRXN1 encodes thousands of splicing variants categorized into long NRXN1α, short NRXN1β and extremely short NRXN1γ, which exert differential roles in neuronal excitation/inhibition. NRXN1α deletions are common in autism spectrum disorder (ASD) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37242a9ced12b7bad6bbae846b71554
https://pubmed.ncbi.nlm.nih.gov/33578364
https://pubmed.ncbi.nlm.nih.gov/33578364
Autor:
Aisling O'Brien, Yin Lu, Xiaohong Qian, Linda Howard, Louise Gallagher, Sally Ann Lynch, Timothy O'Brien, Meimei Yang, Nicholas M. Allen, Berta Marcó de la Cruz, Guangming Yang, Janusz Krawczyk, Yicheng Ding, Sanbing Shen, Veronica McInerney
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102254-(2021)
NRXN1 deletions are commonly found in autism spectrum disorder (ASD) and other neurodevelopmental/neuropsychiatric disorders. Derivation of induced pluripotent stem cells (iPSCs) from different diseases involving different deletion regions are essent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c50b16a84f2c79687748facf9c58b74
https://doi.org/10.1016/j.scr.2021.102254
https://doi.org/10.1016/j.scr.2021.102254
Autor:
Louise Gallagher, Weidong Li, Timothy O'Brien, Yicheng Ding, Berta Marcó de la Cruz, Sanbing Shen, Veronica McInerney, Linda Howard, Xiaohong Qian, Janusz Krawczyk, Yin Lu, Guangming Yang
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102101-(2020)
The induced pluripotent stem cell (iPSC) technology has offered an unprecedented opportunity for disease modelling and drug discovery. Here we used non-integrating Sendai viral method and derived iPSCs from three young healthy Caucasian donors. All i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43749451dfcdb6d96311af8383a293e6
https://doi.org/10.1016/j.scr.2020.102101
https://doi.org/10.1016/j.scr.2020.102101
Autor:
Cristina Cheroni, Raffaele Iennaco, Sebastiano Trattaro, Giuseppe Macino, Massimiliano Pagani, Carlo Emanuele Villa, Elena Cattaneo, Nicolò Caporale, Flavia Troglio, Alejandro López-Tobón, Maria Lachgar, Pietro Lo Riso, Erika Tenderini, Marco Tullio Rigoli, Berta Marcó de la Cruz, Isabel Liste-Noya, Giuseppe Testa, Marco De Simone, Paola Conforti
Publikováno v:
Stem Cell Reports
Repisalud
Instituto de Salud Carlos III (ISCIII)
Stem Cell Reports, Vol 13, Iss 5, Pp 847-861 (2019)
Repisalud
Instituto de Salud Carlos III (ISCIII)
Stem Cell Reports, Vol 13, Iss 5, Pp 847-861 (2019)
Summary The regulation of the proliferation and polarity of neural progenitors is crucial for the development of the brain cortex. Animal studies have implicated glycogen synthase kinase 3 (GSK3) as a pivotal regulator of both proliferation and polar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff22ff8461ab220e52430e585d8d020b