Zobrazeno 1 - 10
of 38
pro vyhledávání: '"FRAGILE X MENTAL RETARDATION SYNDROME"'
Autor:
Zhengping Hou, Qiuying Ding, Yuqi Li, Zhibo Zhao, Fang Yan, Yanping Li, Xingxing Wang, Jingyuan Xu, Weiting Chen, Guicheng Wu, Xiongzhong Ruan, Lei Zhao
Publikováno v:
EBioMedicine, Vol 82, Iss , Pp 104181- (2022)
Summary: Background: Intestinal barrier dysfunction is crucial in alcohol-associated liver disease (ALD). The decreased beta-Klotho (KLB) expression caused by gene variation is associated with hyperpermeability in patients with irritable bowel syndro
Externí odkaz:
https://doaj.org/article/109eb99c96194e22a8263886ae9a1bd6
Publikováno v:
Психологическая наука и образование, Vol 21, Iss 3, Pp 34-46 (2016)
The article aims to present experimental protocol for investigation of visual cognitive function in children and adolescents with autism spectrum disorders. Description of experimental design is introduced by theoretical review of visual attention, p
Externí odkaz:
https://doaj.org/article/a6fe4f9fd28c4572a88f557aa9089ba7
Publikováno v:
The Journal of Biological Chemistry
Wilms’ tumor 1-associating protein (WTAP) is a core component of the N6-methyladenosine (m6A)-methyltransferase complex, along with VIRMA, CBLL1, ZC3H13 (KIAA0853), RBM15/15B, and METTL3/14, which generate m6A, a key RNA modification that affects v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a75a0e73b4f04a13642d9f9cd4d5690a
http://europepmc.org/articles/PMC8605363
http://europepmc.org/articles/PMC8605363
Akademický článek
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Publikováno v:
Психологическая наука и образование, Vol 21, Iss 3, Pp 34-46 (2016)
The article aims to present experimental protocol for investigation of visual cognitive function in children and adolescents with autism spectrum disorders. Description of experimental design is introduced by theoretical review of visual attention, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c6c8e34b60de5f1dcff549db5fa5407
https://doi.org/10.17759/pse.2016210305
https://doi.org/10.17759/pse.2016210305
Publikováno v:
eLife, Vol 5 (2016)
The distribution of proteins within sub-synaptic compartments is an essential aspect of their neurological function. Current methodologies, such as electron microscopy (EM) and super-resolution imaging techniques, can provide the precise localization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a93f9f93d231d40dbf66ccc3cba20ecf
https://elifesciences.org/articles/20560
https://elifesciences.org/articles/20560
Publikováno v:
Biology Open, Vol 2, Iss 1, Pp 68-81 (2012)
Biology Open
Biology Open
Summary FMRP is an evolutionarily conserved protein that is highly expressed in neurons and its deficiency causes fragile X mental retardation syndrome. FMRP controls the translation of target mRNAs in part by promoting their dynamic transport in neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb517030c97fd09ebf760af8ab0ee7e
http://bio.biologists.org/content/2/1/68
http://bio.biologists.org/content/2/1/68
Autor:
Ashley M. Galvan, Roberto Galvez
Publikováno v:
Brain Research. 1471:155-161
The Fragile X syndrome (FXS) is the leading form of inherited mental retardation. To date, the most prominent neuronal phenotype associated with the syndrome is an abundance of long thin spines exhibiting an immature morphology. However, in addition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4be6e9a9fd6890cb8b769fe23f9eef0
https://doi.org/10.1016/j.brainres.2012.06.056
https://doi.org/10.1016/j.brainres.2012.06.056
Publikováno v:
Structure. 15:1090-1098
SummaryFragile X syndrome is the most common form of inherited mental retardation in humans, with an estimated prevalence of about 1 in 4000 males. Although several observations indicate that the absence of functional Fragile X Mental Retardation Pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3aca94d3042a09e632ef3f678d65627e
https://doi.org/10.1016/j.str.2007.06.022
https://doi.org/10.1016/j.str.2007.06.022
Autor:
Saldarriaga Gil, Wilmar, Forero Forero, Jose Vicente, González Teshima, Laura Yuriko, Hagerman, Randi
Publikováno v:
Acta Neurológica Colombiana, Volume: 31, Issue: 3, Pages: 335-341, Published: JUL 2015
El síndrome de temblor y ataxia asociado al síndrome del cromosoma X frágil (FXTAS) es un desorden neurodegenerativo progresivo (1), de inicio tardío, que ocurre entre los portadores de la premutación del gen FMR1 (Fragile X Mental Retardation 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::90d65da95aabace4eae86b1ec3cfe53e
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0120-87482015000300015&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0120-87482015000300015&lng=en&tlng=en
