(Q22253241)

DNA-binding transcription repressor activity, RNA polymerase II-specific

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Heidrun L Deissler

1 reference

ORCID Public Data File 2021

H Müller-Hartmann

1

H

Müller-Hartmann

1 reference

7 February 2023

H Deissler

2

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F Naumann

3

F

Naumann

1 reference

7 February 2023

B Schmitz

4

B

Schmitz

1 reference

7 February 2023

J Schröer

5

J

Schröer

1 reference

7 February 2023

W Doerfler

6

W

Doerfler

1 reference

Journal of Biological Chemistry

7 February 2023

language of work or name

English

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publication date

3 March 2000

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published in

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volume

275

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issue

9

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page(s)

6447-52

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cites work

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The expanding world of trinucleotide repeats

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

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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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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

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Molecular genetics of the fragile-X syndrome: a novel type of unstable mutation

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Normal phenotype in two brothers with a full FMR1 mutation.

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In vitro reactivation of the FMR1 gene involved in fragile X syndrome

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The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

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

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Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications

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

21 January 2018

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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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Nuclear targeting sequences--a consensus?

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Comparative mutagenesis of nuclear localization signals reveals the importance of neutral and acidic amino acids

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

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A rapid method for determining the molecular weight of a protein bound to nucleic acid in a mobility shift assay

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Complete sequence of the 43-kb human ribosomal DNA repeat: analysis of the intergenic spacer

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Location of Ribosomal DNA in the Human Chromosome Complement

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Trinucleotide repeat expansion and human disease

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Small slipped register genetic instabilities in Escherichia coli in triplet repeat sequences associated with hereditary neurological diseases

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The impact of 5'-CG-3' methylation on the activity of different eukaryotic promoters: a comparative study

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STUDIES ON THE MECHANISM OF POLIOVIRUS-INDUCED CELL DAMAGE. I. THE RELATION BETWEEN POLIOVIRUS,-INDUCED METABOLIC AND MORPHOLOGICAL ALTERATIONS IN CULTURED CELLS

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