Identification of variant Alport phenotypes using an Alport-specific antibody probe. (Q50556128)

15 March 2018

title

Identification of variant Alport phenotypes using an Alport-specific antibody probe. (English)

1 reference

15 March 2018

author name string

Kashtan CE

1

1 reference

15 March 2018

Atkin CL

2

1 reference

15 March 2018

Gregory MC

3

1 reference

15 March 2018

Michael AF

4

1 reference

15 March 2018

language of work or name

English

0 references

publication date

1 October 1989

1 reference

15 March 2018

published in

Kidney International

1 reference

15 March 2018

volume

36

1 reference

15 March 2018

issue

4

1 reference

15 March 2018

page(s)

669-674

1 reference

15 March 2018

https://scigraph.springernature.com/pub.10.1038/ki.1989.244

exact match

0 references

cites work

Genetic heterogeneity of Alport syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Apparently changing patterns of inheritance in Alport's hereditary nephritis: genetic heterogeneity versus altered diagnostic criteria.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Early pathologic features of hereditary nephritis: a clinicopathologic correlation

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

The glomerular basal lamina in hereditary nephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Diagnosis of hereditary nephritis by failure of glomeruli to bind anti-glomerular basement membrane antibodies

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Absence of Goodpasture's Antigen in Male Patients With Familial Nephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

The Goodpasture antigen in Alport's syndrome: studies with a monoclonal antibody

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Use of a monoclonal antibody in differential diagnosis of children with haematuria and hereditary nephritis

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Population genetics of Alport's syndrome. Hypothesis of abnormal segregation and the necessary existence of mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Healthy female carriers of a gene for the Alport syndrome: Importance for genetic counseling

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Alport's syndrome or hereditary nephritis?

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Chromosomal assignments of the genes coding for human types II, III, and IV collagen: a dispersed gene family

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

The single copy gene coding for human alpha 1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13.

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

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://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Partial structure of the human alpha 2(IV) collagen chain and chromosomal localization of the gene (COL4A2)

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Hereditary macrothrombocytopathia, nephritis and deafness

1 reference

https://api.crossref.org/works/10.1038%2FKI.1989.244

7 January 2021

Identifiers

DOI

10.1038/KI.1989.244

1 reference

15 March 2018

PubMed ID

2478752

1 reference

15 March 2018