(Q34430581)

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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

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scholarly article

1 reference

Europe PubMed Central

2 August 2017

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 (English)

1 reference

Europe PubMed Central

2 August 2017

Heidrun L Deissler

1 reference

ORCID Public Data File 2021

author name string

Deissler H

1

1 reference

Europe PubMed Central

2 August 2017

Wilm M

2

1 reference

Europe PubMed Central

2 August 2017

Genç B

3

1 reference

Europe PubMed Central

2 August 2017

Schmitz B

4

1 reference

Europe PubMed Central

2 August 2017

Ternes T

5

1 reference

Europe PubMed Central

2 August 2017

Naumann F

6

1 reference

Europe PubMed Central

2 August 2017

Mann M

7

1 reference

Europe PubMed Central

2 August 2017

Doerfler W

8

1 reference

Europe PubMed Central

2 August 2017

language of work or name

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publication date

1 July 1997

1 reference

Europe PubMed Central

2 August 2017

Journal of Biological Chemistry

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Europe PubMed Central

2 August 2017

272

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Europe PubMed Central

2 August 2017

27

1 reference

Europe PubMed Central

2 August 2017

16761-16768

1 reference

Europe PubMed Central

2 August 2017

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Acid-facilitated supramolecular assembly of G-quadruplexes in d(CGG)4.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Trinucleotide repeats that expand in human disease form hairpin structures in vitro

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Compact structures of d(CNG)n oligonucleotides in solution and their possible relevance to fragile X and related human genetic diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

The trinucleotide repeat sequence d(GTC)15 adopts a hairpin conformation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

CTG triplet repeat in mouse growth inhibitory factor/metallothionein III gene promoter represses the transcriptional activity of the heterologous promoters.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

CTG triplet repeats from human hereditary diseases are dominant genetic expansion products in Escherichia coli.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Single-stranded DNA binding proteins isolated from mouse brain recognize specific trinucleotide repeat sequences in vitro

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Novel proteins with binding specificity for DNA CTG repeats and RNA CUG repeats: implications for myotonic dystrophy

1 reference

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21 January 2018

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

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Electrospray and Taylor-Cone theory, Dole's beam of macromolecules at last?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Analytical properties of the nanoelectrospray ion source

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Error-tolerant identification of peptides in sequence databases by peptide sequence tags

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

dbEST--database for "expressed sequence tags"

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Proposal for a common nomenclature for sequence ions in mass spectra of peptides

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Activation of DNA-binding activity in an apparently cytoplasmic precursor of the NF-kappa B transcription factor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Normal phenotype in two brothers with a full FMR1 mutation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.27.16761

21 January 2018

Identifiers

10.1074/JBC.272.27.16761

1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

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