FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome [PDF]
, 2017 Indhu‐Shree Rajan‐Babu +7 more
openalex +1 more source
Overlapping Pathways: Autism Spectrum Disorder in Fragile X Carrier States and the Need for Greater Awareness. [PDF]
CureusFernandez MV +4 more
europepmc +1 more source
FMR1 gene expansion and scans without evidence of dopaminergic deficits in parkinsonism patients
, 2010 Deborah J. Hall +4 more
openalex +2 more sources
Triple CGG expansions on the FMR1 gene and response to ovarian stimulation [PDF]
, 2008 David H. Barad +3 more
openalex +1 more source
The relationship between the number of CGG repeats and serum level of anti-müllerian hormone in women without FMR1 premutation [PDF]
, 2013 S.K. Kim +3 more
openalex +1 more source
Behavioral benefits of GSK-3β inhibition and state-dependent microtubule signatures in the <i>Fmr1</i>-KO mouse. [PDF]
Front NeurosciKealy J +7 more
europepmc +1 more source
The Role of AGG Interruptions in the Transcription of FMR1 Premutation Alleles
, 2011 Carolyn M. Yrigollen +5 more
openalex +2 more sources
The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer [PDF]
, 2008 Marie-Cécile Didiot +5 more
openalex +1 more source
Comparing loss of individual fragile X proteins suggests strong links to cellular senescence and aging. [PDF]
Cell Mol Life SciMenge S +9 more
europepmc +1 more source
Combined Treatment with Minocycline and an mGluR5 Antagonist Alters Resting EEG Spectral Power, but Not Sound-Evoked Responses, in a Mouse Model of Fragile X Syndrome. [PDF]
ASN NeuroKassir MH +4 more
europepmc +1 more source