(Q34732755)

4 August 2017

title

Characterisation of the potential function of SVA retrotransposons to modulate gene expression patterns (English)

1 reference

4 August 2017

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John P Quinn

4

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Gerome Breen

object named as

Gerome Breen

series ordinal

3

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author name string

Abigail L Savage

series ordinal

1

1 reference

4 August 2017

Vivien J Bubb

series ordinal

2

1 reference

4 August 2017

publication date

21 May 2013

1 reference

4 August 2017

published in

BMC Evolutionary Biology

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4 August 2017

volume

13

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4 August 2017

page(s)

101

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The minimal active human SVA retrotransposon requires only the 5'-hexamer and Alu-like domains

4 August 2017

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Retrotransposition of marked SVA elements by human L1s in cultured cells

7 July 2018

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The SLC6A4 VNTR genotype determines transcription factor binding and epigenetic variation of this gene in response to cocaine in vitro.

7 July 2018

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Long-range regulatory synergy is required to allow control of the TAC1 locus by MEK/ERK signalling in sensory neurones

7 July 2018

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7 July 2018

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SVA retrotransposons: Evolution and genetic instability

7 July 2018

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A mobile threat to genome stability: The impact of non-LTR retrotransposons upon the human genome

7 July 2018

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Polymorphic SVA retrotransposons at four loci and their association with classical HLA class I alleles in Japanese, Caucasians and African Americans.

7 July 2018

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Combinatorial interaction between two human serotonin transporter gene variable number tandem repeats and their regulation by CTCF.

7 July 2018

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A regulatory domain spanning the repeat sequence RE1 from herpes simplex virus type 1 has cell specific differential functions in trigeminal neurons and fibroblasts.

7 July 2018

1 reference

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Genomic views of distant-acting enhancers

7 July 2018

1 reference

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Loss of epigenetic silencing in tumors preferentially affects primate-specific retroelements

7 July 2018

1 reference

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5'-Transducing SVA retrotransposon groups spread efficiently throughout the human genome

7 July 2018

1 reference

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Exon-trapping mediated by the human retrotransposon SVA.

7 July 2018

1 reference

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Mobile elements create structural variation: analysis of a complete human genome.

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Molecular genetics of monoamine transporters: relevance to brain disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Differential regulation of the serotonin transporter gene by lithium is mediated by transcription factors, CCCTC binding protein and Y-box binding protein 1, through the polymorphic intron 2 variable number tandem repeat

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

A dopamine transporter gene functional variant associated with cocaine abuse in a Brazilian sample.

7 July 2018

1 reference

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Molecular mechanisms for maintenance of G-rich short tandem repeats capable of adopting G4 DNA structures

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Prevalence of quadruplexes in the human genome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Serotonin transporter gene promoter (5-HTTLPR) and intron 2 (VNTR) polymorphisms in Croatian suicide victims

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

A systematic review of association studies investigating genes coding for serotonin receptors and the serotonin transporter: I. Affective disorders.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Molecular mechanisms of autosomal recessive hypercholesterolemia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Proteomics-based identification of RS/DJ-1 as a novel circulating tumor antigen in breast cancer.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Molecular cloning of human and mouse DJ-1 genes and identification of Sp1-dependent activation of the human DJ-1 promoter

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene dupli

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

A novel human nonviral retroposon derived from an endogenous retrovirus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Mobile DNA in Old World monkeys: a glimpse through the rhesus macaque genome.

7 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

SVA elements: a hominid-specific retroposon family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

Transcriptional regulation of human-specific SVAF₁ retrotransposons by cis-regulatory MAST2 sequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

Modulation of orbitofrontal response to amphetamine by a functional variant of DAT1 and in vitro confirmation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

MAOA-uVNTR polymorphism may modify the protective effect of ALDH2 gene against alcohol dependence in antisocial personality disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

Smoking status moderates the association of the dopamine D4 receptor (DRD4) gene VNTR polymorphism with selective processing of smoking-related cues

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2148-13-101

Single-molecule study of G-quadruplex disruption using dynamic force spectroscopy.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Molecular analysis of the polymorphisms of thymidylate synthase on cell-free circulating DNA in blood of patients with advanced colorectal carcinoma

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Novel family of human transposable elements formed due to fusion of the first exon of gene MAST2 with retrotransposon SVA.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Founder SVA retrotransposal insertion in Fukuyama-type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Serotonin transporter promoter polymorphism and monoamine oxidase type A VNTR allelic variants together influence alcohol binge drinking risk in young women

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Multiple marker analysis at the promoter region of the DRD4 gene and ADHD: evidence of linkage and association with the SNP -616.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3667099

Insertion of an SVA element, a nonautonomous retrotransposon, in PMS2 intron 7 as a novel cause of Lynch syndrome

26 October 2018

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12 December 2020

Engineering in Genomics [variable number tandem repeats as agents of functional regulation in the genome]

1 reference

12 December 2020

Effect of DNA secondary structure on human telomerase activity

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12 December 2020

DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism

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12 December 2020

Deletion of entire HLA-A gene accompanied by an insertion of a retrotransposon

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12 December 2020

Identifiers

DOI

10.1186/1471-2148-13-101

1 reference

Dimensions Publication ID

4 August 2017

0 references

1 reference

4 August 2017

1 reference