(Q33222942)

24 July 2017

title

Canine COL4A3 and COL4A4: sequencing, mapping and genomic organization (English)

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24 July 2017

Anje C Wiersma

1

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24 July 2017

Lee V Millon

2

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24 July 2017

Matthew S Hestand

3

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24 July 2017

Bernard A Van Oost

4

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24 July 2017

Danika L Bannasch

5

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24 July 2017

publication date

1 August 2005

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24 July 2017

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24 July 2017

volume

16

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24 July 2017

issue

4

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24 July 2017

page(s)

241-251

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Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome

24 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Identification of a new mutation in the alpha4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Three novel COL4A4 mutations resulting in stop codons and their clinical effects in autosomal recessive Alport syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Novel COL4A4 splice defect and in‐frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Bull terrier hereditary nephritis: a model for autosomal dominant Alport syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Correlation of histopathological features and renal impairment in autosomal dominant Alport syndrome in Bull terriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Radiation hybrid mapping of the canine type I and type IV collagen gene subfamilies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Two genes, COL4A3 and COL4A4 coding for the human alpha3(IV) and alpha4(IV) collagen chains are arranged head-to-head on chromosome 2q36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Gene organization and homology modeling of two iron superoxide dismutases of the early branching protist Perkinsus marinus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

An integrated cytogenetic, radiation-hybrid, and comparative map of dog chromosome 5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Coordinate gene expression of the alpha3, alpha4, and alpha5 chains of collagen type IV. Evidence from a canine model of X-linked nephritis with a COL4A5 gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170500136822

10.1080/10425170500136822

21 January 2018

Identifiers

DOI

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24 July 2017

1 reference