(Q33620180)

English

Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

P Weisman-Shomer

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

E Cohen

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

M Fry

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 April 2000

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

28

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1535-1541

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Screening for fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Molecular basis of genetic instability of triplet repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Solution structures of the individual single strands of the fragile X DNA triplets (GCC)n.(GGC)n

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

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=102797

28 July 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

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=102797

28 July 2018

Fragile X gene instability: anchoring AGGs and linked microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

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=102797

28 July 2018

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=102797

28 July 2018

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=102797

28 July 2018

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=102797

28 July 2018

Factor D is a selective single-stranded oligodeoxythymidine binding protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Molecular cloning and analysis of the fragile X region in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Instability of a 550-base pair DNA segment and abnormal methylation 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=102797

28 July 2018

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Molecular heterogeneity of the fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Absence of expression of the FMR-1 gene 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=102797

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

DNA methylation represses FMR-1 transcription 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=102797

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

28 July 2018

NGG-triplet repeats form similar intrastrand structures: implications for the triplet expansion diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

Striking founder effect for the fragile X syndrome in Finland.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

Population genetics of fragile X: a multiple allele model with variable risk of CGG repeat expansion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

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=102797

30 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation†

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102797

30 October 2018

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/10710419

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/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of founder chromosomes in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The trinucleotide repeat sequence d(CGG)15 forms a heat-stable hairpin containing Gsyn. Ganti base pairs

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precursor arrays for triplet repeat expansion at the fragile X locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

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/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trinucleotide repeats affect DNA replication in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)n tracts

1 reference

https://pubmed.ncbi.nlm.nih.gov/10710419

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1093/NAR/28.7.1535

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Europe PubMed Central

PubMed publication ID

28 July 2017

release_ai3l2zrxqfbgjpobif4fiolkxm

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https://api.fatcat.wiki/v0/release/ai3l2zrxqfbgjpobif4fiolkxm

24 November 2022

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Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

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Europe PubMed Central

PubMed publication ID

28 July 2017

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