(Q40275731)

English

Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements

scientific article published on 24 May 2006

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scholarly article

1 reference

Europe PubMed Central

19 September 2017

Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements (English)

1 reference

Europe PubMed Central

19 September 2017

retrotransposon

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retinal degeneration

1 reference

based on heuristic

inferred from title

3

object named as

Jeremy Nathans

1 reference

Europe PubMed Central

19 September 2017

2

object named as

Amir Rattner

1 reference

Europe PubMed Central

19 September 2017

author name string

Jichao Chen

1

1 reference

Europe PubMed Central

19 September 2017

publication date

24 May 2006

1 reference

Europe PubMed Central

19 September 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

19 September 2017

15

1 reference

Europe PubMed Central

19 September 2017

2146-2156

1 reference

Europe PubMed Central

19 September 2017

13

1 reference

Europe PubMed Central

19 September 2017

Initial sequencing and analysis of the human genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Biology of mammalian L1 retrotransposons

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Molecular archeology of L1 insertions in the human genome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Initial sequencing and comparative analysis of the mouse genome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

The rod photoreceptor-specific nuclear receptor Nr2e3 represses transcription of multiple cone-specific genes.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Physiological function of S-cone system is not enhanced in rd7 mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Enhanced S cone syndrome: evidence for an abnormally large number of S cones.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Identification of a photoreceptor cell-specific nuclear receptor

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

An actively retrotransposing, novel subfamily of mouse L1 elements

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: a mechanism for non-LTR retrotransposition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Transduction of 3'-flanking sequences is common in L1 retrotransposition

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

When the message goes awry: disease-producing mutations that influence mRNA content and performance.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

A photoreceptor-specific cadherin is essential for the structural integrity of the outer segment and for photoreceptor survival

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Inefficient processing impairs release of RNA from the site of transcription

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Listening to silence and understanding nonsense: exonic mutations that affect splicing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

ESEfinder: A web resource to identify exonic splicing enhancers

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Interspersed repeats and other mementos of transposable elements in mammalian genomes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Retroelement distributions in the human genome: variations associated with age and proximity to genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Pre-mRNA processing and the CTD of RNA polymerase II: the tail that wags the dog?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

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

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

RNA truncation by premature polyadenylation attenuates human mobile element activity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

LINE-1 retrotransposons: modulators of quantity and quality of mammalian gene expression?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Lambda replacement vectors carrying polylinker sequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Genomic analysis of mouse retinal development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

The UCSC Table Browser data retrieval tool

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL138

21 January 2018

Identifiers

10.1093/HMG/DDL138

1 reference

Europe PubMed Central

19 September 2017

1 reference

Europe PubMed Central

19 September 2017

ResearchGate publication ID

0 references

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