Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Wesley Schwind"'
Autor:
Summer R. Fair, Wesley Schwind, Dominic Julian, Alecia Biel, Swetha Ramadesikan, Jesse Westfall, Katherine E. Miller, Meisam Naeimi Kararoudi, Scott E. Hickey, Theresa Mihalic Mosher, Kim L. McBride, Reid Neinast, James Fitch, Dean Lee, Peter White, Richard K. Wilson, Tracy A. Bedrosian, Daniel C. Koboldt, Mark E. Hester
Variants in the AUTS2 gene are associated with a broad spectrum of neurological conditions characterized by intellectual disability, microcephaly, and congenital brain malformations. Here, we use a human cerebral organoid (CO) model to investigate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0275a6d7c80b5dd9695c6a4201539129
https://doi.org/10.1101/2022.02.23.22271091
https://doi.org/10.1101/2022.02.23.22271091
Autor:
Summer R Fair, Wesley Schwind, Dominic L Julian, Alecia Biel, Gongbo Guo, Ryan Rutherford, Swetha Ramadesikan, Jesse Westfall, Katherine E Miller, Meisam Naeimi Kararoudi, Scott E Hickey, Theresa Mihalic Mosher, Kim L McBride, Reid Neinast, James Fitch, Dean A Lee, Peter White, Richard K Wilson, Tracy A Bedrosian, Daniel C Koboldt, Mark E Hester
Publikováno v:
Brain : a journal of neurology. 146(1)
Variants in the AUTS2 gene are associated with a broad spectrum of neurological conditions characterized by intellectual disability, microcephaly, and congenital brain malformations. Here, we use a human cerebral organoid model to investigate the pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::120caeea67440949a4e0d83af1184f4b
https://pubmed.ncbi.nlm.nih.gov/35802027
https://pubmed.ncbi.nlm.nih.gov/35802027
Autor:
Elaine R. Mardis, Daniel C. Koboldt, James Fitch, Katherine E. Miller, Christopher R. Pierson, Sean McGrath, Mai-Lan Ho, Tracy A. Bedrosian, Vincent Magrini, Summer R. Fair, Adam P. Ostendorf, Saranga Wijeratne, Jeffrey R. Leonard, Jocelyn M Bush, Kristen M. Leraas, Mark E. Hester, Wesley Schwind, Richard K. Wilson, Erin Crist, Ammar Shaikhouni, Anthony R. Miller
Publikováno v:
Brain
Phosphatase and tensin homologue (PTEN) regulates cell growth and survival through inhibition of the mammalian target of rapamycin (MTOR) signalling pathway. Germline genetic variation of PTEN is associated with autism, macrocephaly and PTEN hamartom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05d0aade759fdba741ebaa7b9e0b8965
https://europepmc.org/articles/PMC8634064/
https://europepmc.org/articles/PMC8634064/