X inactivation of the FMR1 fragile X mental retardation gene - Test2 - elhamkhani - TriplyDB

X inactivation of the FMR1 fragile X mental retardation gene

X inactivation of the FMR1 fragile X mental retardation gene

http://www.wikidata.org/entity/Q33682895

about

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 pubert Expression of genes from the human active and inactive X chromosomes.Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others.Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.Epigenetics: a way to understand the origin and biology of testicular germ cell tumors.Characterization of loss-of-inactive X in Klinefelter syndrome and female-derived cancer cells.An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.Screening for fragile X syndrome: information needs for health planners.Genetic and maternal predictors of cognitive and behavioral trajectories in females with fragile X syndrome.

P2860

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P2860

X inactivation of the FMR1 fragile X mental retardation gene

http://www.wikidata.org/entity/Q33682895

description

1995 nî lūn-bûn

@nan

1995 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1995 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

1995年の論文

@ja

1995年論文

@yue

1995年論文

@zh-hant

1995年論文

@zh-hk

1995年論文

@zh-mo

1995年論文

@zh-tw

1995年论文

@wuu

name

X inactivation of the FMR1 fragile X mental retardation gene

@ast

X inactivation of the FMR1 fragile X mental retardation gene

@en

type

label

X inactivation of the FMR1 fragile X mental retardation gene

@ast

X inactivation of the FMR1 fragile X mental retardation gene

@en

prefLabel

X inactivation of the FMR1 fragile X mental retardation gene

@ast

X inactivation of the FMR1 fragile X mental retardation gene

@en

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P1433

Journal of Medical Genetics

P1476

X inactivation of the FMR1 fragile X mental retardation gene

@en

P2093

C U Kirchgessner

http://www.w3.org/2001/XMLSchema#string

H F Willard

http://www.w3.org/2001/XMLSchema#string

S T Warren

http://www.w3.org/2001/XMLSchema#string

P2860

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome.

Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.

Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl

The cell surface antigen locus, MIC2X, escapes X-inactivation

X-linked Hunter syndrome: the heterozygous phenotype in cell culture.

Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes

P304

925-929

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P31

scholarly article

P356

10.1136/JMG.32.12.925

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P407

P433

12

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P478

32

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P577

1995-12-01T00:00:00Z

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14379277

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8825916

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P932

1051769

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