IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. (Q44253360)

1 December 2017

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. (English)

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Battini G

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Gharavi AG

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Yan Y

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Scolari F

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Schena FP

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Frasca GM

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Cooper K

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Amoroso A

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Viola BF

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Canova C

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Farhi A

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Subramanian V

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Nelson-Williams C

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Woodford S

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Julian BA

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Lifton RP

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language of work or name

English

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publication date

1 November 2000

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26

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354-357

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3

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https://scigraph.springernature.com/pub.10.1038/81677

1 December 2017

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Distribution of primary renal diseases leading to end-stage renal failure in the United States, Europe, and Australia/New Zealand: results from an international comparative study

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7 January 2021

Immunoglobulin and complement deposition in glomeruli of 756 subjects who had committed suicide or met with a violent death

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7 January 2021

IgA nephropathy, the most common glomerulonephritis worldwide. A neglected disease in the United States?

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7 January 2021

A retrospective analysis of the natural history of primary IgA nephropathy worldwide

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7 January 2021

Immunogenetic aspects of primary IgA nephropathy

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Low incidence of IgA nephropathy in blacks

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7 January 2021

Mesangial proliferative glomerulonephritis in southwestern American Indians

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7 January 2021

Familial IgA nephropathy. Evidence of an inherited mechanism of disease

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7 January 2021

Familial clustering of IgA nephropathy: further evidence in an Italian population

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7 January 2021

Familial occurrence of primary glomerulonephritis: evidence for a role of genetic factors

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7 January 2021

IgA nephropathy: pros and cons for a familial disease

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7 January 2021

HLA-DQ gene polymorphism in primary IgA nephropathy in three European populations

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7 January 2021

Leucocyte beta 1,3 galactosyltransferase activity in IgA nephropathy

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7 January 2021

Reduced binding of immunoglobulin A (IgA) from patients with primary IgA nephropathy to the myeloid IgA Fc-receptor, CD89.

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7 January 2021

Uteroglobin is essential in preventing immunoglobulin A nephropathy in mice

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7 January 2021

Distribution of the admixture test for the detection of linkage under heterogeneity.

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7 January 2021

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

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7 January 2021

Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

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7 January 2021

Human uteroglobin gene: structure, subchromosomal localization, and polymorphism

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7 January 2021

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

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7 January 2021

Identifiers

DOI

10.1038/81677

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1 December 2017

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