FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles.
about
Modeling diseases of noncoding unstable repeat expansions using mutant pluripotent stem cells.Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related DisordersMass spectrometry as a tool for studying autism spectrum disorder.Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubertPost-weaning selenium and folate supplementation affects gene and protein expression and global DNA methylation in mice fed high-fat dietsNovel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women.Abnormal methylation status of FBXW10 and SMPD3, and associations with clinical characteristics in clear cell renal cell carcinoma.Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis.A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysis.Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.Autism spectrum disorder: an omics perspective.A Set of Assays for the Comprehensive Analysis of FMR1 Alleles in the Fragile X-Related Disorders.Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study.Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia.Clinical and molecular correlates in fragile X premutation females.DNA methylation changes at SNCA intron 1 in patients with dementia with Lewy bodies.Elevated mRNA Expression and Low Methylation of SNCA in Japanese Alzheimer's Disease Subjects.Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X.A pilot proteomic study of protein markers in autism spectrum disorder.
P2860
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P2860
FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@ast
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@en
type
label
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@ast
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@en
prefLabel
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@ast
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@en
P2093
P2860
P1476
FMR1 intron 1 methylation pred ...... iers of expanded FMR1 alleles.
@en
P2093
Danuta Z Loesch
David E Godler
David Francis
David J Amor
Freya Gehling
Howard R Slater
Michele Ono
Quang M Bui
Randi Hagerman
P2860
P304
P356
10.1016/J.JMOLDX.2011.05.006
P577
2011-06-30T00:00:00Z