Gene structure and expression of the 5'-(CGG)(n)-3'-binding protein (CGGBP1). (Q34282647)

1 August 2017

Gene structure and expression of the 5'-(CGG)(n)-3'-binding protein (CGGBP1). (English)

1 reference

1 August 2017

4

Walter Doerfler

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1 August 2017

Frauke Naumann

1

1 reference

PubMed ID

14667814

1 August 2017

Ralph Remus

series ordinal

2

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PubMed ID

14667814

1 August 2017

Birgit Schmitz

series ordinal

3

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1 August 2017

1 January 2004

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1 August 2017

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1 August 2017

83

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1 August 2017

106-118

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1 August 2017

1

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Dynamic mutations: a new class of mutations causing human disease

1 August 2017

1 reference

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7 January 2021

Trinucleotide repeat expansion and neuropsychiatric disease

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7 January 2021

Fourteen and counting: unraveling trinucleotide repeat diseases

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7 January 2021

Expansion explosion: new clues to the pathogenesis of repeat expansion neurodegenerative diseases

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Dominantly inherited, non-coding microsatellite expansion disorders

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7 January 2021

Understanding the molecular basis of fragile X syndrome

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7 January 2021

A decade of molecular studies of fragile X syndrome

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Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes.

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7 January 2021

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

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7 January 2021

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

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7 January 2021

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

1 reference

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7 January 2021

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

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7 January 2021

The fragile X premutation: into the phenotypic fold

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7 January 2021

Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.

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7 January 2021

Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA

1 reference

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7 January 2021

Enzymatic amplification of synthetic oligodeoxyribonucleotides: implications for triplet repeat expansions in the human genome

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7 January 2021

DNA secondary structure: a common and causative factor for expansion in human disease

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7 January 2021

Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG)n in the human FMR1 gene

1 reference

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7 January 2021

Rapid protein sequencing by tandem mass spectrometry and cDNA cloning of p20-CGGBP. A novel protein that binds to the unstable triplet repeat 5'-d(CGG)n-3' in the human FMR1 gene

1 reference

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7 January 2021

The human 20-kDa 5'-(CGG)(n)-3'-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter

1 reference

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7 January 2021

dbEST--database for "expressed sequence tags"

1 reference

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7 January 2021

Initial sequencing and analysis of the human genome

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7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

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7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

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7 January 2021

Point mutations in AAUAAA and the poly (A) addition site: effects on the accuracy and efficiency of cleavage and polyadenylation in vitro

1 reference

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7 January 2021

Highly specific localization of promoter regions in large genomic sequences by PromoterInspector: a novel context analysis approach

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7 January 2021

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

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7 January 2021

New 5'-(CGG)n-3' repeats in the human genome

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7 January 2021

Microsatellites in different eukaryotic genomes: survey and analysis

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7 January 2021

Differential distribution of simple sequence repeats in eukaryotic genome sequences.

1 reference

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7 January 2021

Characterization of the full fragile X syndrome mutation in fetal gametes.

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7 January 2021

Interpreting cDNA sequences: some insights from studies on translation

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7 January 2021

Eukaryotic mRNAs encoding abundant and scarce proteins are statistically dissimilar in many structural features

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7 January 2021

Control of eukaryotic protein synthesis by upstream open reading frames in the 5'-untranslated region of an mRNA

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7 January 2021

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.

1 reference

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7 January 2021

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

1 reference

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7 January 2021

DNA methylation and gene activity

1 reference

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7 January 2021

Initial sequencing and comparative analysis of the mouse genome

1 reference

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7 January 2021

High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones

1 reference

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7 January 2021

10.1016/S0888-7543(03)00212-X

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

14667814