Allele-specific transcript isoforms in human (Q45140161)

10 December 2017

title

Allele-specific transcript isoforms in human (English)

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10 December 2017

2

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Janet Kelso

4

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Fabiana Bettoni

series ordinal

3

object named as

Fabiana Bettoni

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10 December 2017

Victoria Nembaware

1

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10 December 2017

Cathal Seoighe

series ordinal

5

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10 December 2017

language of work or name

English

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publication date

1 November 2004

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10 December 2017

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10 December 2017

volume

577

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issue

1-2

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10 December 2017

page(s)

233-238

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A genomic view of alternative splicing

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cites work

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Frequent alternative splicing of human genes

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

How prevalent is functional alternative splicing in the human genome?

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

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

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Increase of functional diversity by alternative splicing

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Alternative splicing: multiple control mechanisms and involvement in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Genomic variants in exons and introns: identifying the splicing spoilers

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

ASAP: the Alternative Splicing Annotation Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

The UCSC Genome Browser Database

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Genome-wide detection of tissue-specific alternative splicing in the human transcriptome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Species-specific alternative splice mimicry at the growth hormone receptor locus revealed by the lineage of retroelements during primate evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Association of a human G-protein beta3 subunit variant with hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Identification and ethnic distribution of major haplotypes in the gene GNB3 encoding the G-protein beta3 subunit

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Alternative splicing in the human, mouse and rat genomes is associated with an increased frequency of exon creation and/or loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

The evolving roles of alternative splicing

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

Conservation of human alternative splice events in mouse

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome

21 January 2018

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https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2004.10.018

10.1016/J.FEBSLET.2004.10.018

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Identifiers

DOI

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10 December 2017

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