(Q35800504)

10 August 2017

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title

Retrotransposon-derived elements in the mammalian genome: a potential source of disease (English)

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10 August 2017

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Druker R

1

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10 August 2017

Whitelaw E

series ordinal

2

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10 August 2017

language of work or name

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1 January 2004

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Journal of Inherited Metabolic Disease

10 August 2017

published in

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10 August 2017

volume

27

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10 August 2017

issue

3

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10 August 2017

page(s)

319-330

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Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron

10 August 2017

cites work

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12 December 2020

Rapid amplification of a retrotransposon subfamily is evolving the mouse genome

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12 December 2020

LINE-mediated retrotransposition of marked Alu sequences

1 reference

12 December 2020

Cytosine methylation and the ecology of intragenomic parasites

1 reference

12 December 2020

Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage

1 reference

12 December 2020

Characterization of a nondeleterious L1 insertion in an intron of the human factor VIII gene and further evidence of open reading frames in functional L1 elements

1 reference

12 December 2020

The intracisternal A-particle gene family: structure and functional aspects

1 reference

12 December 2020

Retrotransposons as epigenetic mediators of phenotypic variation in mammals

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12 December 2020

Neomorphic agouti mutations in obese yellow mice

1 reference

12 December 2020

An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness

1 reference

12 December 2020

HERV-K: the biologically most active human endogenous retrovirus family

1 reference

12 December 2020

Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes

1 reference

12 December 2020

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis

1 reference

12 December 2020

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

1 reference

12 December 2020

DNA sequence insertion and evolutionary variation in gene regulation

1 reference

12 December 2020

High polymorphism level of genomic sequences flanking insertion sites of human endogenous retroviral long terminal repeats

1 reference

12 December 2020

The bg allele mutation is due to a LINE1 element retrotransposition

1 reference

12 December 2020

Many human L1 elements are capable of retrotransposition

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12 December 2020

Biology of mammalian L1 retrotransposons

1 reference

12 December 2020

The Long Terminal Repeat of an Endogenous Intracisternal A-Particle Gene Functions as a Promoter When Introduced into Eucaryotic Cells by Transfection

1 reference

12 December 2020

Exon shuffling by L1 retrotransposition

1 reference

12 December 2020

X-chromosome inactivation: a repeat hypothesis

1 reference

12 December 2020

Alu repeats and human disease

1 reference

12 December 2020

Hot L1s account for the bulk of retrotransposition in the human population

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12 December 2020

The molecular basis for dominant yellow agouti coat color mutations

1 reference

12 December 2020

Alu sequences are processed 7SL RNA genes

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12 December 2020

Sequence organization of cloned intracisternal a particle genes

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12 December 2020

Influence of maternal phenotype on metabolic differentiation of agouti locus mutants in the mouse

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12 December 2020

High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes

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12 December 2020

Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon

1 reference

12 December 2020

Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse.

1 reference

12 December 2020

Interspersed repeats and other mementos of transposable elements in mammalian genomes

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12 December 2020

Sequences associated with intracisternal a particles are reiterated in the mouse genome

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12 December 2020

High frequency retrotransposition in cultured mammalian cells

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12 December 2020

The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element

1 reference

12 December 2020

Insertional polymorphisms of full-length endogenous retroviruses in humans

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12 December 2020

Phenotypic and molecular analysis of a transgenic insertional allele of the mouse Fused locus

1 reference

12 December 2020

Transgenerational inheritance of epigenetic states at the murine Axin(Fu) allele occurs after maternal and paternal transmission

1 reference

12 December 2020

Initial sequencing and comparative analysis of the mouse genome

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12 December 2020

A novel active L1 retrotransposon subfamily in the mouse

1 reference

12 December 2020

Multiple sclerosis-associated virus-related pol sequences found both in multiple sclerosis and healthy donors are more frequently expressed in multiple sclerosis patients

1 reference

12 December 2020

Demystified. Human endogenous retroviruses

1 reference

12 December 2020

Apolipoprotein(a) gene enhancer resides within a LINE element

1 reference

12 December 2020

LINE drive. retrotransposition and genome instability

1 reference

12 December 2020

Two dominant mutations in the mouse fused gene are the result of transposon insertions.

1 reference

12 December 2020

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

1 reference

12 December 2020

Transposable B2 SINE elements can provide mobile RNA polymerase II promoters

1 reference

12 December 2020

Differing populations of intracisternal A-particle genes in myeloma tumors and mouse subspecies

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12 December 2020

Molecular identification of a novel retrovirus repeatedly isolated from patients with multiple sclerosis. The Collaborative Research Group on Multiple Sclerosis

1 reference

12 December 2020

IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa

1 reference

12 December 2020

Inactivation of the mouse HPRT locus by a 203-bp retroposon insertion and a 55-kb gene-targeted deletion: establishment of new HPRT-deficient mouse embryonic stem cell lines

1 reference

12 December 2020

Epigenetic inheritance at the agouti locus in the mouse

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12 December 2020

The mouse Fused locus encodes Axin, an inhibitor of the Wnt signaling pathway that regulates embryonic axis formation

1 reference

12 December 2020

Transcription of IAP endogenous retroviruses is constrained by cytosine methylation

1 reference

12 December 2020

Molecular basis of the pleiotropic phenotype of mice carrying the hypervariable yellow (Ahvy) mutation at the agouti locus

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12 December 2020

Molecular characterization of the mouse agouti locus.

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12 December 2020

Many human genes are transcribed from the antisense promoter of L1 retrotransposon

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12 December 2020

The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome

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12 December 2020

The human growth hormone locus control region mediates long-distance transcriptional activation independent of nuclear matrix attachment regions

1 reference

12 December 2020

Intracisternal A-particle genes as movable elements in the mouse genome

1 reference

12 December 2020

Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion.

1 reference

12 December 2020

Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia

1 reference

12 December 2020

Creation of genomic methylation patterns

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12 December 2020

Full-length human L1 insertions retain the capacity for high frequency retrotransposition in cultured cells

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12 December 2020

Initial sequencing and analysis of the human genome

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12 December 2020

The recent evolution of mammalian repetitive DNA elements

1 reference

Crossref

https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031096.81518.66

7 January 2021

inferred from DOI database lookup

Human biology by proxy

1 reference

Crossref

https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031096.81518.66

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1023/B:BOLI.0000031096.81518.66

1 reference

Dimensions Publication ID

10 August 2017

1012147988

0 references

Fatcat ID

release_4lonizv42jhjhapp5cvaxrm5jm

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4lonizv42jhjhapp5cvaxrm5jm

24 November 2022

mapped directly with Wikidata item

1 reference