Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sophia, Palant"'
Autor:
Arryn T. Blaine, Yiming Miao, Jinling Yuan, Sophia Palant, Rebecca J. Liu, Zhong-Yin Zhang, Richard. M. van Rijn
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
The δ-opioid receptor (δOR) has been considered as a therapeutic target in multiple neurological and neuropsychiatric disorders particularly as δOR agonists are deemed safer alternatives relative to the more abuse-liable µ-opioid receptor drugs.
Externí odkaz:
https://doaj.org/article/ca344bb1a084418dbaf758bf8b8f1159
Publikováno v:
The FASEB Journal. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bfdd1560c645bf5ef4273a41e0fa29b
https://doi.org/10.1096/fasebj.2021.35.s1.02144
https://doi.org/10.1096/fasebj.2021.35.s1.02144
Autor:
William C. Skarnes, Jiaxiang Wu, Shirong Lai, Muriel Eaton, Huynhvi P Nguyen, Jingliang Zhang, Xiaoling Chen, Zhefu Que, Emma E Lietzke, Sophia Palant, Yang Yang, Tiange Xiao, Zhixiong Ma, Chloe Maricela Romero, Anthony C Park, Ji Hea Lee, Emily Rose Coleman, Yushuang Liu, Zhuo Huang, Wendy Ann Koss
Publikováno v:
Genes, Brain and Behavior. 20
Large-scale genetic studies revealed SCN2A as one of the most frequently mutated genes in patients with neurodevelopmental disorders. SCN2A encodes for the voltage-gated sodium channel isoform 1.2 (Nav 1.2) expressed in the neurons of the central ner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9cf550f0066124ff9a7214b8fd2a90ce
https://doi.org/10.1111/gbb.12725
https://doi.org/10.1111/gbb.12725
Autor:
Muriel, Eaton, Jingliang, Zhang, Zhixiong, Ma, Anthony C, Park, Emma, Lietzke, Chloé M, Romero, Yushuang, Liu, Emily R, Coleman, Xiaoling, Chen, Tiange, Xiao, Zhefu, Que, Shirong, Lai, Jiaxiang, Wu, Ji Hea, Lee, Sophia, Palant, Huynhvi P, Nguyen, Zhuo, Huang, William C, Skarnes, Wendy A, Koss, Yang, Yang
Publikováno v:
Genes, brain, and behaviorREFERENCES. 20(4)
Large-scale genetic studies revealed SCN2A as one of the most frequently mutated genes in patients with neurodevelopmental disorders. SCN2A encodes for the voltage-gated sodium channel isoform 1.2 (Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5295c04574008c26f1bebed3bba59c02
https://pubmed.ncbi.nlm.nih.gov/33369088
https://pubmed.ncbi.nlm.nih.gov/33369088