Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yam Stern"'
Autor:
Shani Stern, Shong Lau, Andreea Manole, Idan Rosh, Menachem Mendel Percia, Ran Ben Ezer, Maxim N. Shokhirev, Fan Qiu, Simon Schafer, Abed AlFatah Mansour, Kile P. Mangan, Tchelet Stern, Polina Ofer, Yam Stern, Ana Paula Diniz Mendes, Jose Djamus, Lynne Randolph Moore, Ritu Nayak, Sapir Havusha Laufer, Aidan Aicher, Amanda Rhee, Thomas L. Wong, Thao Nguyen, Sara B. Linker, Beate Winner, Beatriz C. Freitas, Eugenia Jones, Irit Sagi, Cedric Bardy, Alexis Brice, Juergen Winkler, Maria C. Marchetto, Fred H. Gage
Publikováno v:
npj Parkinson's Disease, Vol 8, Iss 1, Pp 1-16 (2022)
Abstract Several mutations that cause Parkinson’s disease (PD) have been identified over the past decade. These account for 15–25% of PD cases; the rest of the cases are considered sporadic. Currently, it is accepted that PD is not a single monol
Externí odkaz:
https://doaj.org/article/2fa050a5687248eaa0da9d23e96a5eb4
Autor:
Shani Stern, Shong Lau, Andreea Manole, Idan Rosh, Menahem Percia, Ran Ben Ezer, Maxim N. Shokhirev, Fan Qiu, Simon Schafer, Abed Mansour, Tchelet Stern, Pola Ofer, Yam Stern, Ana Mendes Diniz, Lynne Randolph Moore, Ritu Nayak, Aidan Aicher, Amanda Rhee, Thomas L. Wong, Thao Nguyen, Sara B. Linker, Beate Winner, Beatriz C. Freitas, Eugenia Jones, Cedric Bardy, Alexis Brice, Juergen Winkler, Maria C. Marchetto, Fred H. Gage
Several mutations that cause Parkinson’s disease (PD) have been identified over the past decade. These account for 15-25% of PD cases; the rest of the cases are considered sporadic. Currently, it is accepted that PD is not a single monolithic disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b45c602fcde062bde33415f1c163fa90
https://doi.org/10.1101/2021.12.31.474654
https://doi.org/10.1101/2021.12.31.474654
Autor:
Liron Mizrahi, Ayat Asleh, Boris Brant, Andrew P. Levy, Reem Jada, George K.E. Umanah, Tchelet Stern, Nina S. Levy, Shani Stern, Idan Rosh, Huda Adwan Shekhidem, Yam Stern, Polina Ofer
Publikováno v:
Molecular psychiatry. 26(12)
Mutations in the IQSEC2 gene are associated with drug-resistant, multifocal infantile and childhood epilepsy; autism; and severe intellectual disability (ID). We used induced pluripotent stem cell (iPSC) technology to obtain hippocampal neurons to in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::256016cd8f82b5db949b43615541c727
https://pubmed.ncbi.nlm.nih.gov/34535765
https://pubmed.ncbi.nlm.nih.gov/34535765
Autor:
Guy A. Rouleau, Tchelet Stern, Thao Nguyen, Yongsung Kim, Gabriela Goldberg, Ana P.D. Mendes, Anne G. Bang, Renata Santos, Arianna Mei, Anindita Sarkar, Dekel Galor, Lynne Randolph-Moore, Fred H. Gage, Yam Stern, Maria C. Marchetto, Shani Stern, Martin Alda
Publikováno v:
Biological Psychiatry
Biological Psychiatry, Elsevier, 2019, ⟨10.1016/j.biopsych.2019.09.018⟩
Biol Psychiatry
Biological Psychiatry, Elsevier, 2019, ⟨10.1016/j.biopsych.2019.09.018⟩
Biol Psychiatry
Background Approximately 1 in every 50 to 100 people is affected with bipolar disorder (BD), making this disease a major economic burden. The introduction of induced pluripotent stem cell methodology enabled better modeling of this disorder. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::155dd9689d0a07bfd3f9d1f7de76978f
https://pubmed.ncbi.nlm.nih.gov/32616198
https://pubmed.ncbi.nlm.nih.gov/32616198