(Q42048146)

15 October 2017

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

1 reference

15 October 2017

1 reference

quantitative trait locus

1 reference

1 reference

4

Jeffrey H Miner

1 reference

15 October 2017

Kaya L Andrews

1

1 reference

15 October 2017

Jacqueline L Mudd

series ordinal

2

1 reference

15 October 2017

Cong Li

series ordinal

3

1 reference

15 October 2017

language of work or name

English

0 references

publication date

1 February 2002

1 reference

The American Journal of Pathology

15 October 2017

1 reference

15 October 2017

160

1 reference

15 October 2017

2

1 reference

15 October 2017

721-730

1 reference

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

15 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Gelatinase B (MMP-9) is not essential in the normal kidney and does not influence progression of renal disease in a mouse model of Alport syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Renal basement membrane components

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Overview of QTL mapping software and introduction to map manager QT.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Genetic identification of two major modifier loci of polycystic kidney disease progression in pcy mice

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

The clinical spectrum of type IV collagen mutations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Genetic, clinical, and morphologic heterogeneity in Alport's syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

A Macintosh program for storage and analysis of experimental genetic mapping data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Type IV collagen: structure, gene organization, and role in human diseases. Molecular basis of Goodpasture and Alport syndromes and diffuse leiomyomatosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Alport syndrome: from bedside to genome to bedside

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Empirical threshold values for quantitative trait mapping

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Molecular genetics of basement membranes: the paradigm of Alport syndrome.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Origin of the glomerular basement membrane visualized after in vivo labeling of laminin in newborn rat kidneys

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Evidence for splicing new basement membrane into old during glomerular development in newborn rat kidneys

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850644

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

17 August 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Type IV collagen of the glomerular basement membrane. Evidence that the chain specificity of network assembly is encoded by the noncollagenous NC1 domains

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Alport syndrome in Réunion Island: phenotypic heterogeneity of the recessive-autosomal form

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Self-assembly of laminin isoforms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Diffuse Leiomyomatosis of the Esophagus: Disorder of Cell-Matrix Interaction?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Genetic modifiers of polycystic kidney disease in intersubspecific KAT2J mutants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2964892-4

Quantitative trait loci modulate renal cystic disease severity in the mouse bpk model

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11839593

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Abnormal glomerular basement membrane laminins in murine, canine, and human Alport syndrome: aberrant laminin alpha2 deposition is species independent

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11839593

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

New form of X-linked dominant hereditary nephritis in dogs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11839593

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)64892-4

1 reference

15 October 2017

1 reference

15 October 2017

PubMed publication ID

11839593

1 reference