IgA nephropathy type 1 is a probably autosomal dominant disorder associated with genetic alterations at chromosome position 6q22-q23. The exact gene is not yet discovered.
|
|
|
||
|
|
|
||
|
|
|
||
|
|
|
||
|
|
|
||
|
|
|
||
| 1. |
Brettle R et al. (1978) Mesangial IgA glomerulonephritis and HLA antigens.
|
| 2. |
Pei Y et al. (1997) Association of angiotensinogen gene T235 variant with progression of immunoglobin A nephropathy in Caucasian patients.
|
| 3. |
Julian BA et al. (1985) Familial IgA nephropathy. Evidence of an inherited mechanism of disease.
|
| 4. |
Jennette JC et al. (1985) Low incidence of IgA nephropathy in blacks.
|
| 5. |
None (1969) IgA glomerular deposits in renal disease.
|
| 6. |
Sabatier JC et al. (1979) Mesangial IgA glomerulonephritis in HLA-identical brothers.
|
| 7. |
McCoy RC et al. (1974) IgA nephropathy.
|
| 8. |
Croker BP et al. (1983) IgA nephropathy. Correlation of clinical and histologic features.
|
| 10. |
Berthoux FC et al. (1978) HLA-Bw35 and mesangial IgA glomerulonephritis.
|
| 11. |
Coppo R et al. (1986) Dietary gluten and primary IgA nephropathy.
|
| 12. |
Tolkoff-Rubin NE et al. (1978) IGA nephropathy in HLA-identical siblings.
|
| 13. |
Katz A et al. (1980) Family study in IgA nephritis: the possible role of HLA antigens.
|
| 14. |
Tomana M et al. (1997) Galactose-deficient IgA1 in sera of IgA nephropathy patients is present in complexes with IgG.
|
| 15. |
Shimokawa T et al. (2000) Identification and characterization of the promoter for the gene encoding the human myeloid IgA Fc receptor (FcalphaR, CD89).
|
| 16. |
Tsuge T et al. (2001) Polymorphism in promoter region of Fcalpha receptor gene in patients with IgA nephropathy.
|
| 17. |
Obara W et al. (2003) Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients.
|
| 18. |
Paterson AD et al. (2007) Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
|
| 19. |
Gharavi AG et al. (2011) Genome-wide association study identifies susceptibility loci for IgA nephropathy.
|
| 20. |
Wyatt RJ et al. (2013) IgA nephropathy.
|
| 21. |
Takei T et al. (2002) Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy.
|
| 22. |
Yoshida H et al. (1995) Role of the deletion of polymorphism of the angiotensin converting enzyme gene in the progression and therapeutic responsiveness of IgA nephropathy.
|
| 23. |
Song J et al. (2003) Peroxisome proliferator-activated receptor gamma C161T polymorphisms and survival of Japanese patients with immunoglobulin A nephropathy.
|
| 24. |
Scolari F et al. (1999) Familial clustering of IgA nephropathy: further evidence in an Italian population.
|
| 25. |
Zheng F et al. (1999) Uteroglobin is essential in preventing immunoglobulin A nephropathy in mice.
|
| 26. |
Hsu SI et al. (2000) Evidence for genetic factors in the development and progression of IgA nephropathy.
|
| 27. |
Gharavi AG et al. (2000) IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.
|
| 28. |
Hiki Y et al. (2001) Mass spectrometry proves under-O-glycosylation of glomerular IgA1 in IgA nephropathy.
|
| 29. |
Allen AC et al. (2001) Mesangial IgA1 in IgA nephropathy exhibits aberrant O-glycosylation: observations in three patients.
|
| 30. |
Asamoah A et al. (1987) A major gene model for the familial aggregation of plasma IgA concentration.
|
| 31. |
Donadio JV et al. (2002) IgA nephropathy.
|
| 32. |
Yoon HJ et al. (2003) Association of the CD14 gene -159C polymorphism with progression of IgA nephropathy.
|
| 33. |
Song J et al. (2003) Gender specific association of aldosterone synthase gene polymorphism with renal survival in patients with IgA nephropathy.
|
| 34. |
Wang J et al. (2004) Dysregulated LIGHT expression on T cells mediates intestinal inflammation and contributes to IgA nephropathy.
|
| 35. |
Bisceglia L et al. (2006) Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci.
|
| 36. |
Suzuki H et al. (2008) IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1.
|
| 37. |
None (1989) Familial cases of Berger's disease and anaphylactoid purpura: more frequent than previously thought.
|
| 38. |
None (1987) The commonest glomerulonephritis in the world: IgA nephropathy.
|
| 39. |
Julian BA et al. (1988) IgA nephropathy, the most common glomerulonephritis worldwide. A neglected disease in the United States?
|
| 40. |
OMIM.ORG article Omim 161950
|