Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome (Q28504496)

24 January 2017

title

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome (English)

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Collagen, type IV, alpha 4

24 January 2017

main subject

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GOA release 2020-03-11

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W. Lu

1

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24 January 2017

C. L. Phillips

2

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24 January 2017

P. D. Killen

3

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24 January 2017

T. Hlaing

4

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24 January 2017

W. R. Harrison

5

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24 January 2017

F. F. Elder

6

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24 January 2017

J. H. Miner

7

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24 January 2017

P. A. Overbeek

8

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24 January 2017

M. H. Meisler

9

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24 January 2017

language of work or name

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15 October 1999

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24 January 2017

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24 January 2017

volume

61

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24 January 2017

issue

2

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24 January 2017

page(s)

113–124

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Alpha 1(IV) and alpha 2(IV) collagen genes are regulated by a bidirectional promoter and a shared enhancer

24 January 2017

cites work

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The glomerular response to injury: progression or resolution?

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Immunohistochemical study of alpha 1-5 chains of type IV collagen in hereditary nephritis

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The retinoblastoma protein-binding region of simian virus 40 large T antigen alters cell cycle regulation in lenses of transgenic mice

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Isoform switching of type IV collagen is developmentally arrested in X-linked Alport syndrome leading to increased susceptibility of renal basement membranes to endoproteolysis

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Ultrastructural immunocytochemistry of collagenous and non-collagenous proteins in fast-frozen, freeze-substituted, and low-temperature-embedded renal tissue in Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The alpha chains of type IV collagen.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The type IV collagen gene family.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Alport syndrome--clinical phenotypes, incidence, and pathology.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Colocalization of the genes for the alpha 3(IV) and alpha 4(IV) chains of type IV collagen to chromosome 2 bands q35-q37

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Rescue of the albino phenotype by introduction of a functional tyrosinase gene into mice.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Coinjection strategy for visual identification of transgenic mice

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

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

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Mapping of Col3a1 and Col6a3 to proximal murine chromosome 1 identifies conserved linkage of structural protein genes between murine chromosome 1 and human chromosome 2q.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Comparative distribution of the alpha 1(IV), alpha 5(IV), and alpha 6(IV) collagen chains in normal human adult and fetal tissues and in kidneys from X-linked Alport syndrome patients

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Progression of glomerular diseases: is the podocyte the culprit?

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Alport's syndrome. A report of 58 cases and a review of the literature

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Expression of novel basement membrane components in the developing human kidney and eye.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Identification of a novel sequence element in the common promoter region of human collagen type IV genes, involved in the regulation of divergent transcription

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The genes COL4A5 and COL4A6, coding for basement membrane collagen chains alpha 5(IV) and alpha 6(IV), are located head-to-head in close proximity on human chromosome Xq22 and COL4A6 is transcribed from two alternative promoters

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

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

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

The cyclin kinase inhibitor p21CIP1/WAF1 limits glomerular epithelial cell proliferation in experimental glomerulonephritis

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Multiple common fragile sites are expressed in the genome of the laboratory rat.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Cloning of inv, a gene that controls left/right asymmetry and kidney development.

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Alport syndrome: from bedside to genome to bedside

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Renal biopsy collagen I mRNA predicts scarring in rabbit anti-GBM disease: comparison with conventional measures

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

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

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Autosomal recessive Alport syndrome: Immunohistochemical study of type IV collagen chain distribution

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Glomerular fibrin deposition and removal

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Fluorescence in situ hybridization mapping of 25 markers on distal human chromosome 2q surrounding the human Waardenburg syndrome, type I (WS1) locus (PAX3 gene)

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

A model of autosomal recessive Alport syndrome in English cocker spaniel dogs

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Distribution of the alpha 1 and alpha 2 chains of collagen IV and of collagens V and VI in Alport syndrome

1 reference

5 June 2022

https://opencitations.net/index/coci/api/v1/references/10.1006/GENO.1999.5943

Identifiers

DOI

10.1006/GENO.1999.5943

0 references

1 reference