(Q37483297)

English

Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)n is mediated by homolog-conserved domains in three members of the hnRNP family

scientific article published on 09 August 2004

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)n is mediated by homolog-conserved domains in three members of the hnRNP family (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Samer Khateb

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Pnina Weisman-Shomer

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Inbal Hershco

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Lawrence A Loeb

4

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Michael Fry

5

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

9 August 2004

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

32

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

14

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

4145-4154

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Mutations in the G-quadruplex silencer element and their relationship to c-MYC overexpression, NM23 repression, and therapeutic rescue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Did quadruplex DNA play a role in the evolution of the eukaryotic linear chromosome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Direct evidence for a G-quadruplex in a promoter region and its targeting with a small molecule to repress c-MYC transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

G-quadruplex DNA structures--variations on a theme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Functional and dysfunctional roles of quadruplex DNA in cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

CArG binding factor A (CBF-A) is involved in transcriptional regulation of the rat Ha-ras promoter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Characterization of CArG-binding protein A initially identified by differential display

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

The Saccharomyces cerevisiae Sgs1 helicase efficiently unwinds G-G paired DNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

DNA tetraplex formation in the control region of c-myc

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Solution structure of a DNA quadruplex containing the fragile X syndrome triplet repeat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

Formation of parallel four-stranded complexes by guanine-rich motifs in DNA and its implications for meiosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

A protein binding to CArG box motifs and to single-stranded DNA functions as a transcriptional repressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

MyoD binds to the guanine tetrad nucleic acid structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

23 August 2017

The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)n

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

6 September 2017

Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

6 September 2017

The fragile X syndrome single strand d(CGG)n nucleotide repeats readily fold back to form unimolecular hairpin structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

6 September 2017

Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)n

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

14 September 2017

Transcription of the FMR1 gene in individuals with fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

28 September 2017

Changes in CArG-binding protein A expression levels following injection(s) of the D1-dopamine agonist SKF-82958 in the intact and 6-hydroxydopamine-lesioned rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

26 June 2018

Purification and characterization of a protein binding to the SP6 kappa promoter. A potential role for CArG-box binding factor-A in kappa transcription.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

26 June 2018

Purification and characterization of qTBP42, a new single-stranded and quadruplex telomeric DNA-binding protein from rat hepatocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

26 June 2018

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

2 September 2018

Translational suppression by trinucleotide repeat expansion at FMR1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514371

2 September 2018

Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human insulin gene-linked polymorphic region adopts a G-quartet structure in chromatin assembled in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of fragile X syndrome with delayed replication of the FMR1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Posttranscriptional regulation of insulin-like growth factor II mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure-function correlations of the insulin-linked polymorphic region

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomeric and Tetraplex DNA Binding Properties ofqTBP42:A Homologue of the CArG Box Binding Protein CBF-A

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Bloom's syndrome helicase unwinds G4 DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/15302914

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/GKH745

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

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