(Q24563403)

English

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

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scholarly article

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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 (English)

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author name string

K Zheng

1

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P S Thorner

2

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P Marrano

3

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R Baumal

4

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R R McInnes

5

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language of work or name

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publication date

26 April 1994

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Proceedings of the National Academy of Sciences of the United States of America

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91

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9

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3989-93

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Samoyed hereditary glomerulopathy (SHG). Evolution of splitting of glomerular capillary basement membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Human collagen genes encoding basement membrane alpha 1 (IV) and alpha 2 (IV) chains map to the distal long arm of chromosome 13

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Complete primary structure of the triple-helical region and the carboxyl-terminal domain of a new type IV collagen chain, alpha 5(IV)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Glomerular basement membrane. Identification of a fourth chain, alpha 4, of type IV collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Characterization of the 3' half of the human type IV collagen alpha 5 gene that is affected in the Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Complete amino acid sequence of the human alpha 5 (IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an Alport syndrome patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

24 March 2017

Ribonucleic acid isolated by cesium chloride centrifugation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

7 April 2017

Molecular genetics of Alport syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Alport's syndrome: experience at Hôpital Necker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

The role of the main noncollagenous domain (NC1) in type IV collagen self-assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Localization of the human procollagen alpha 1(IV) gene to chromosome 13q34 by in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Mode of inheritance of Samoyed hereditary glomerulopathy: an animal model for hereditary nephritis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Samoyed hereditary glomerulopathy. Immunohistochemical staining of basement membranes of kidney for laminin, collagen type IV, fibronectin, and Goodpasture antigen, and correlation with electron microscopy of glomerular capillary basement membranes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Mapping of Alport syndrome to the long arm of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Alport familial nephritis. Absence of 28 kilodalton non-collagenous monomers of type IV collagen in glomerular basement membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Goodpasture syndrome: molecular architecture and function of basement membrane antigen.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Renal disease in carrier female dogs with X-linked hereditary nephritis. Implications for female patients with this disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Relationship of familial nephritis and Goodpasture antigens to novel collagen chains and

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

27 September 2017

Genetic heterogeneity of Alport syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

30 May 2018

Structural heterogeneity of the noncollagenous domain of basement membrane collagen.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

30 May 2018

Localization of the gene for X-linked Alport's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

30 May 2018

The alpha 4(IV) chain of basement membrane collagen. Isolation of cDNAs encoding bovine alpha 4(IV) and comparison with other type IV collagens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=43708

30 May 2018

Localization of the Goodpasture epitope to a novel chain of basement membrane collagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the Goodpasture antigen as the alpha 3(IV) chain of collagen IV

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities in the NC1 domain of collagen type IV in GBM in canine hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nephritis: immunoblotting studies of the glomerular basement membrane

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The specificity of split renal membranes in hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for separate networks of classical and novel basement membrane collagen. Characterization of alpha 3(IV)-alport antigen heterodimer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structural organization of type IV collagen. Identification of three NC1 populations in the glomerular basement membrane

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical spectrum of hereditary nephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8171024

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.91.9.3989

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1994PNAS...91.3989Z

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PMC publication ID

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PubMed publication ID

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ResearchGate publication ID

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