Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis (Q36732263)

16 August 2017

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title

Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis (English)

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16 August 2017

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Cosgrove D

1

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16 August 2017

Kalluri R

2

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16 August 2017

Miner JH

3

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16 August 2017

Segal Y

4

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16 August 2017

Borza DB

5

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16 August 2017

language of work or name

English

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publication date

7 February 2007

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16 August 2017

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16 August 2017

71

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16 August 2017

7

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16 August 2017

615-618

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https://scigraph.springernature.com/pub.10.1038/sj.ki.5002115

16 August 2017

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cites work

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

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Role of distinct type IV collagen networks in glomerular development and function

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Alport syndromes: phenotypic heterogeneity of progressive hereditary nephritis

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https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

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

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Mouse model of X-linked Alport syndrome.

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https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Molecular genetic and immunohistochemical study of autosomal recessive Alport's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Glomerular basement membrane. Identification of a novel disulfide-cross-linked network of alpha3, alpha4, and alpha5 chains of type IV collagen and its implications for the pathogenesis of Alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Integrin alpha1beta1 and transforming growth factor-beta1 play distinct roles in alport glomerular pathogenesis and serve as dual targets for metabolic therapy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Laminin-1 reexpression in Alport mouse glomerular basement membranes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Role for transforming growth factor-beta1 in alport renal disease progression.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Role for macrophage metalloelastase in glomerular basement membrane damage associated with alport syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Stage-specific action of matrix metalloproteinases influences progressive hereditary kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.KI.5002115

7 January 2021

Identifiers

DOI

10.1038/SJ.KI.5002115

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Dimensions Publication ID

16 August 2017

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