IgA nephropathy: pathogenesis of the most common form of glomerulonephritis
SN Emancipator, ME Lamm - Pathology Reviews• 1990, 1990 - Springer
IgA nephropathy (IgAN) is being recognized increasingly as a common form of
glomerulonephritis with progressive potential (17, 29, 42). Our initial goal here is briefly to …
glomerulonephritis with progressive potential (17, 29, 42). Our initial goal here is briefly to …
Glomerulosclerosis and renal cysts in mice transgenic for the early region of SV40
K MacKay, LJ Striker, CA Pinkert, RL Brinster… - Kidney international, 1987 - Elsevier
Glomerulosclerosis and renal cysts in mice transgenic for the early region of SV40.
Considerable evidence indicates that genetic determinants play a major role in the …
Considerable evidence indicates that genetic determinants play a major role in the …
Association of thin glomerular basement membrane with other glomerulopathies
FG Cosio, ME Falkenhain, DD Sedmak - Kidney international, 1994 - Elsevier
Association of thin glomerular basement membrane with other glomerulopathies. In the
present study we assessed the prevalence of thin glomerular basement membrane (TGBM) …
present study we assessed the prevalence of thin glomerular basement membrane (TGBM) …
Recurrent glomerulonephritis following renal transplantation
Glomerulonephritis (GN*) is the most important cause of end-stage renal disease (ESRD)
leading to renal transplantation. In the United Kingdom and Ireland, 27% of renal transplant …
leading to renal transplantation. In the United Kingdom and Ireland, 27% of renal transplant …
Current understanding of complement proteins as therapeutic targets for the treatment of immunoglobulin a nephropathy
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerulonephritis
worldwide and a frequent cause of kidney failure. Currently, the diagnosis necessitates a …
worldwide and a frequent cause of kidney failure. Currently, the diagnosis necessitates a …
Familial risk, age at onset, and cause of end-stage renal disease in white Americans.
BJ Spray, NG Atassi, AB Tuttle… - Journal of the American …, 1995 - journals.lww.com
A strong familial clustering of ESRD has been reported among African Americans,
suggesting that factors predisposing to renal failure, whether genetic, environmental, or …
suggesting that factors predisposing to renal failure, whether genetic, environmental, or …
IgA nephropathy susceptibility loci and disease progression
M Shi, Y Ouyang, M Yang, M Yang… - Clinical Journal of the …, 2018 - journals.lww.com
Results A four-SNP model, rs11150612 (ITGAM-ITGAX), rs7634389 (ST6GAL1), rs2412971
(HORMAD2), and rs2856717 (HLA-DQ/DR), was selected as the best predictive model. The …
(HORMAD2), and rs2856717 (HLA-DQ/DR), was selected as the best predictive model. The …
Familial hemolytic-uremic syndrome and homozygous factor H deficiency
V Pichette, S Quérin, W Schürch, G Brun… - American journal of …, 1994 - Elsevier
Inherited hemolytic-uremic syndrome (HUS) is unusual. We report the occurrence of HUS in
two siblings; one died at an early age while the other (the proband) has presented with three …
two siblings; one died at an early age while the other (the proband) has presented with three …
Genome-wide scan in a novel IgA nephropathy model identifies a susceptibility locus on murine chromosome 10, in a region syntenic to human IGAN1 on …
H Suzuki, Y Suzuki, T Yamanaka, S Hirose… - Journal of the …, 2005 - journals.lww.com
Genetic factors are considered to be involved in the initiation and progression of IgA
nephropathy (IgAN) on the basis of racial differences in the prevalence and familial …
nephropathy (IgAN) on the basis of racial differences in the prevalence and familial …