Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nuwan Hettige"'
Autor:
Malvin Jefri, Scott Bell, Huashan Peng, Nuwan Hettige, Gilles Maussion, Vincent Soubannier, Hanrong Wu, Heika Silveira, Jean‐Francois Theroux, Luc Moquin, Xin Zhang, Zahia Aouabed, Jeyashree Krishnan, Liam A. O'Leary, Lilit Antonyan, Ying Zhang, Vincent McCarty, Naguib Mechawar, Alain Gratton, Andreas Schuppert, Thomas M. Durcan, Edward A. Fon, Carl Ernst
Publikováno v:
Stem Cells Translational Medicine, Vol 9, Iss 6, Pp 697-712 (2020)
Abstract Making high‐quality dopamine (DA)‐producing cells for basic biological or small molecule screening studies is critical for the development of novel therapeutics for disorders of the ventral midbrain. Currently, many ventral midbrain assa
Externí odkaz:
https://doaj.org/article/3c072113bbe542c08f988aada0c191f2
Autor:
Ali Bani-Fatemi, Samia Tasmim, Ariel Graff, Philip Gerretsen, Oluwagbenga O. Dada, James L. Kennedy, Nuwan Hettige, Clement Zai, Danilo de Jesus, Andrea de Bartolomeis, Vincenzo De Luca
Publikováno v:
Comprehensive Psychiatry, Vol 89, Iss , Pp 28-32 (2019)
Background: Treatment resistance is a common issue among schizophrenia patients undergoing antipsychotic treatment. According to the American Psychiatric Association (APA) guidelines, treatment-resistant status is defined as little or no symptom redu
Externí odkaz:
https://doaj.org/article/9a59933960b446b68b92c558d038e239
Autor:
Scott Bell, Nuwan Hettige, Heika Silveira, Huashan Peng, Hanrong Wu, Malvin Jefri, Lilit Antonyan, Ying Zhang, Xin Zhang, Carl Ernst
Publikováno v:
Bio-Protocol, Vol 9, Iss 5 (2019)
Induced Pluripotent Stem Cells (iPSCs) are pluripotent stem cells that can be generated from somatic cells, and provide a way to model the development of neural tissues in vitro. One particularly interesting application of iPSCs is the development of
Externí odkaz:
https://doaj.org/article/0c95ec7edd8f429cbabbca7081c9c317
Autor:
Malvin Jefri, Xin Zhang, Patrick S Stumpf, Li Zhang, Huashan Peng, Nuwan Hettige, Jean-Francois Theroux, Zahia Aouabed, Khadija Wilson, Shriya Deshmukh, Lilit Antonyan, Anjie Ni, Shaima Alsuwaidi, Ying Zhang, Nada Jabado, Benjamin A Garcia, Andreas Schuppert, Hans T Bjornsson, Carl Ernst
Publikováno v:
Hum Mol Genet
Kabuki syndrome is frequently caused by loss-of-function mutations in one allele of histone 3 lysine 4 (H3K4) methyltransferase KMT2D and is associated with problems in neurological, immunological and skeletal system development. We generated heteroz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeab4ef4fa96903759154ace52cb290a
https://europepmc.org/articles/PMC9616574/
https://europepmc.org/articles/PMC9616574/
