Results 161 to 170 of about 14,262 (208)

Altered olfactory responses in Fmr1 KO mice. [PDF]

Sci Rep
Tuma J, Rana AN, Philip T, Park JB, Lee HY.   +4 more
europepmc   +1 more source

Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice

, 2008
Lujian Liao, Sung Kyu Park, Tao Xu, Peter W. Vanderklish, John R. Yates   +4 more
openalex   +1 more source

Frequency of FMR1 premutation in individuals with ataxia and/or tremorand/or parkinsonism

, 2008
A.H.O. Reis, Andressa Coelho Ferreira, Karina Braga Gomes, Marcos José Burle de Aguiar, Carmen Fonseca, F.E. Cardoso, Victor Cavalcanti Pardini, Maria Raquel Santos Carvalho   +7 more
openalex   +1 more source

Spontaneous distal middle cerebral artery aneurysm in a young male with full mutation of the fragile X syndrome with a high-functioning phenotype: illustrative case. [PDF]

J Neurosurg Case Lessons
Papadopoulos E, Abrimian A, Zarzour H, Hagerman RJ, Schmidt RF.   +4 more
europepmc   +1 more source

GABAergic Progenitor Cell Graft Rescues Cognitive Deficits in Fragile X Syndrome Mice. [PDF]

Adv Sci (Weinh)
Wang C, Liu JY, Su LD, Wang XT, Bian YP, Wang ZX, Ye LY, Lu XJ, Zhou L, Chen W, Yang W, Liu J, Wang L, Shen Y.   +13 more
europepmc   +1 more source

Nanopore Long-Read Sequencing as a First-Tier Diagnostic Test to Detect Repeat Expansions in Neurological Disorders. [PDF]

Int J Mol Sci
de Boer EN, Scheper AJ, Hendriksen D, Charbon B, van der Vries G, Ten Berge AM, Grootscholten PM, Lemmink HH, Jongbloed JDH, Bosscher L, Knoers NVAM, Swertz MA, Sikkema-Raddatz B, Dijkstra DJ, Johansson LF, van Diemen CC.   +15 more
europepmc   +1 more source

Clinical application of polar body-based preimplantation genetic testing for maternal mutations in women with a limited number of oocytes. [PDF]

Orphanet J Rare Dis
Chen J, Wu X, Xu Q, Ding T, Chen G, Chen H, Zou Y, Huang J, Zhang Z, Tian L, Zhao Y, Duan R, Li Z, Wu Q, Liu Y.   +14 more
europepmc   +1 more source

Non-ionotropic signaling through the NMDA receptor GluN2B carboxy-terminal domain drives dendritic spine plasticity and reverses fragile X phenotypes. [PDF]

Cell Rep
Barnes SA, Thomazeau A, Finnie PSB, Heinrich MJ, Heynen AJ, Komiyama NH, Grant SGN, Menniti FS, Osterweil EK, Bear MF.   +9 more
europepmc   +1 more source

FMR1 KH0-KH1 Domains Coordinate m6A Binding and Phase Separation in Fragile X Syndrome

Zhou X, Guo C, Wang R, Li Y, Zhang T, Qiu Z, Gao S, Liu J, Gao Y.   +8 more
europepmc   +1 more source

Neurobiological basis of autism spectrum disorder: mini review. [PDF]

Front Psychol
Holanda MVF, Paiva EDS, de Souza LN, Paiva KM, Oliveira RF, Tavares ÉAF, Morais PLAG, de Andrade AM, Knackfuss MI, do Nascimento EGC, Cavalcanti JRLP.   +10 more
europepmc   +1 more source