Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jingqun Yang"'
Publikováno v:
Genetics
LKB1 is known as a master kinase for 14 kinases related to the adenosine monophosphate (AMP)-activated protein kinase (AMPK). Two of them (SIK3 and AMPKa) have previously been implicated in sleep regulation. We generated loss-of-function (LOF) mutant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e563b1c343a43fec57f862bd0dba90fc
https://europepmc.org/articles/PMC9252283/
https://europepmc.org/articles/PMC9252283/
LKB1 is known as a master kinase for 14 kinases related to the adenosine monophosphate (AMP)-activated protein kinase (AMPK). Two of them (SIK3 and AMPKα) have previously been implicated in sleep regulation. We generated loss-of-function (LOF) mutan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eb38c5a8c7ede192ff5524a8175d440
https://doi.org/10.1101/2021.12.13.472078
https://doi.org/10.1101/2021.12.13.472078
Autor:
Jianjun Yu, Yang Li, Yuxiang Liu, Yufeng Cui, Chaoyi Li, Tao Wang, Chengang Li, Enxing Zhou, Ziyi Liu, Jingqun Yang, Yi Rao
Sleep need drives sleep and plays a key role in homeostatic regulation of sleep. So far sleep need can only be inferred by animal behaviors and indicated by electroencephalography (EEG). Here we report that threonine 221 (T221) of the salt inducible
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7e15d38b03016ea01ab6b5b9106922d
https://doi.org/10.1101/2021.11.06.467421
https://doi.org/10.1101/2021.11.06.467421
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(8)
Clinical examination and molecular genetic analysis were carried out for one case with special facial features with developmental retardation, hearing impairment and cleft lip and palate.The intelligence test, hearing test, and MRI test were performe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::750d50e01d93a48646bc03ff15afbfe1
https://pubmed.ncbi.nlm.nih.gov/34365617
https://pubmed.ncbi.nlm.nih.gov/34365617
Publikováno v:
Ear, Nose & Throat Journal. 97:E33-E38
Mutations in the GJB2, SLC26A4, GJB3, and MT-RNR1 genes are known to be a common cause of hearing loss. However, the frequency of hot-spot mutations and genotype-phenotype correlations in patients with sensorineural hearing loss (SNHL) has been less
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d55b9ad27961bb56e881deae7c354e5
https://doi.org/10.1177/014556131809700603
https://doi.org/10.1177/014556131809700603
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 32(3)
To screen for common mutations of deafness-related genes in order to determine the carrier rate, types of mutation, and their relevance to hearing loss.For 4 deafness-related genes GJB2, GJB3, 12S rRNA and SLC26A4, 20 common mutations were screened a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b16ab8f6e78409a05b8c5a54ef9b249a
https://pubmed.ncbi.nlm.nih.gov/26037344
https://pubmed.ncbi.nlm.nih.gov/26037344
Publikováno v:
ENT: Ear, Nose & Throat Journal; Jun2018, Vol. 97 Issue 6, pE33-E38, 6p, 5 Charts, 1 Graph
Autor:
Yang Li1,2,3,4, Chengang Li2,3,4, Yuxiang Liu1,2,3,4, Jianjun Yu1, Jingqun Yang2,3,4, Yunfeng Cui5, Wang, Tao V.1, Chaoyi Li2,3,4, Lifen Jiang2,3,4, Meilin Song2,3,4, Yi Rao1,2,3,4,5 yrao@pku.edu.cn
Publikováno v:
Genetics. Sep2023, Vol. 225 Issue 1, p1-13. 13p.