Results 161 to 170 of about 7,199,374 (204)

SPG601-associated modulation of resting-state EEG and improvement in executive function in a fragile X syndrome randomized controlled crossover study. [PDF]

Sci Rep
Pedapati EV, Vanderklish PW, Sarraf ST, Gargosky S, Nelson M, Richter S, Westerkamp G, Erickson CA.   +7 more
europepmc   +1 more source

Astrocytes in Genetic Epilepsies: Supporting Actor or Key Player? [PDF]

J Neurosci Res
Lange J, Zhao E, O'Connell E, Gillham O, McTague A.   +4 more
europepmc   +1 more source

Altered ECM deposition and cell adhesion signaling in a human cortical organoid model of fragile X syndrome. [PDF]

Mol Brain
Havusha-Laufer S, Krishnaswamy VR, Krugliak-Shechter N, Shenoy A, Karlinski Zur M, Kuznitsov-Yanovsky L, Solomonov I, Hanna JH, Sagi I, Ben Yosef D.   +9 more
europepmc   +1 more source

Beyond Surface Performance: Analyzing Grammatical Production and Judgment Abilities in Boys With Fragile X Syndrome. [PDF]

Am J Speech Lang Pathol
Edgar TC, Schabes C, Elmquist M, Sterling A.   +3 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Establishment of FXS-A9 Panel With a Single Human X Chromosome From Fragile X Syndrome-Associated Individual

Experimental Cell Research, 2021
Fragile X syndrome (FXS) is the most common inheritable form of intellectual disability. FMR1, the gene responsible for FXS, is located on human chromosome Xq27.3 and contains a stretch of CGG trinucleotide repeats in its 5' untranslated region.
Hiroyuki Kugoh, Yuji Nakayama
exaly   +3 more sources