Results 131 to 140 of about 6,083,486 (156)

Early Developmental Characterization of Gap-Induced Prepulse Inhibition and Habituation of Auditory Startle Response in a Fragile X Syndrome Mouse Model.

Dev Neurosci
Abdullah A, Liu X, Murari K, Yan J, Cheng N.   +4 more
europepmc   +1 more source

Gene Therapy for Fragile X Syndrome, Challenges, and Promises. [PDF]

J Gene Med
Velinov M.
europepmc   +1 more source

Rapid Antibody Test for Fragile X Syndrome

Lancet, The, 1995
Fragile X syndrome is the most common known cause of inherited mental retardation. Identification of patients and carriers of fragile X syndrome is usually done with a DNA test system but we have developed a rapid antibody to identify fragile X patients.
Didier Devys, J L Mandel, B Oostra
exaly   +2 more sources

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Chromosomal Fragile Site Breakage by EBV-Encoded EBNA1 at Clustered Repeats

Nature, 2023
Don W. Cleveland
exaly  

ATP Synthase c-Subunit Leak Causes Aberrant Cellular Metabolism in Fragile X Syndrome

Cell, 2020
Nelli Mnatsakanyan, Han-A Park, Jing Wu
exaly  

Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene

Cell, 2018
Charles H Li, Hao Wu, Rudolf Jaenisch
exaly