Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Huijie Feng"'
Autor:
Joanna Mattis, Ala Somarowthu, Kevin M Goff, Evan Jiang, Jina Yom, Nathaniel Sotuyo, Laura M Mcgarry, Huijie Feng, Keisuke Kaneko, Ethan M Goldberg
Publikováno v:
eLife, Vol 11 (2022)
Dravet syndrome (DS) is a neurodevelopmental disorder due to pathogenic variants in SCN1A encoding the Nav1.1 sodium channel subunit, characterized by treatment-resistant epilepsy, temperature-sensitive seizures, developmental delay/intellectual disa
Externí odkaz:
https://doaj.org/article/31cb96e7bcb84203b9d4601d65b25be7
Autor:
Huijie Feng, Casandra L Larrivee, Elena Y Demireva, Huirong Xie, Jeff R Leipprandt, Richard R Neubig
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0258912 (2021)
Externí odkaz:
https://doaj.org/article/8bb112cae0a64c7bbd912c70b5d1735f
Publikováno v:
Neurobiology of Disease, Vol 116, Iss , Pp 131-141 (2018)
Mutations in the GNAO1 gene cause a complex constellation of neurological disorders including epilepsy, developmental delay, and movement disorders. GNAO1 encodes Gαo, the α subunit of Go, a member of the Gi/o family of heterotrimeric G protein sig
Externí odkaz:
https://doaj.org/article/313152d83c4f4bb5a7fc7941e59abcf5
Autor:
Huijie Feng, Casandra L Larrivee, Elena Y Demireva, Huirong Xie, Jeff R Leipprandt, Richard R Neubig
Publikováno v:
PLoS ONE, Vol 14, Iss 1, p e0211066 (2019)
BackgroundInfants and children with dominant de novo mutations in GNAO1 exhibit movement disorders, epilepsy, or both. Children with loss-of-function (LOF) mutations exhibit Epileptiform Encephalopathy 17 (EIEE17). Gain-of-function (GOF) mutations or
Externí odkaz:
https://doaj.org/article/d258bc089b254efd8bb9bf326492a2e1
Publikováno v:
Journal of Applied Remote Sensing. 16
Autor:
Yu Zhang, Fei Zhu, Jian Teng, Baoxiao Zheng, Zhengjia Lou, Huijie Feng, Liangyi Xue, Yunxia Qian
Publikováno v:
Fishshellfish immunology. 129
Salinity is an important environmental factor that affects the yield and quality of large yellow croaker (Larimichthys crocea) during aquaculture. Here, whole-genome bisulfite sequencing (WGBS), RNA-seq, bisulfite sequencing PCR (BSP), quantitative r
Autor:
Dai Zhang, HuiJie Feng, WenBo Li, Hao Rong, Qian Feng, XuRan Zhang, Weihong Ren, Yan Tong, ZhenQiang Zhang, Wei Wang, ShiChun Tu
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports
Scientific Reports
Myeloid-derived suppressor cells (MDSCs) are a group of heterogeneous cells derived from immature myeloid cells (IMCs). MDSCs are known to play important roles in tumor immune evasion. While we know that there are a large number of circulating and tu
Autor:
Huijie, Feng, Yukun, Yuan, Michael R, Williams, Alex J, Roy, Jeffery R, Leipprandt, Richard R, Neubig
Publikováno v:
Journal of neurophysiology. 127(3)
Autor:
Joanna Mattis, Ala Somarowthu, Kevin M Goff, Evan Jiang, Jina Yom, Nathaniel Sotuyo, Laura M Mcgarry, Huijie Feng, Keisuke Kaneko, Ethan M Goldberg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::515995690b0a7540d215636b5d868336
https://doi.org/10.7554/elife.69293.sa2
https://doi.org/10.7554/elife.69293.sa2
Autor:
Richard R. Neubig, Huijie Feng, Michael Williams, Jeffery Leipprandt, Yukun Yuan, Alex J. Roy
GNAO1 encodes Gαo, a heterotrimeric G protein alpha subunit in the Gi/o family. In this report, we used a Gnao1 mouse model “G203R” previously described as a “gain-of-function” Gnao1 mutant with movement abnormalities and enhanced seizure su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::933570e7704391294ddec536bdb072c1
https://doi.org/10.1101/2021.09.23.461583
https://doi.org/10.1101/2021.09.23.461583