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Quoted phrase not found in phrase index: "IgA nephropathy, susceptibility to, 3"
Page 1
IgA nephropathy and kidney transplantation according to the Oxford classification.
Vasconcelos AS, Mazzali M, de Sousa MV. Vasconcelos AS, et al. J Bras Nefrol. 2023 Jul-Sep;45(3):350-356. doi: 10.1590/2175-8239-JBN-2022-0051en. J Bras Nefrol. 2023. PMID: 36626310 Free PMC article.
INTRODUCTION: IgA nephropathy (IgAN) is the most common glomerular disease globally, and its susceptibility and the risk for the development of end-stage kidney disease are related to genetic and environmental factors. ...
INTRODUCTION: IgA nephropathy (IgAN) is the most common glomerular disease globally, and its susceptibility and …
GWAS-Based Discoveries in IgA Nephropathy, Membranous Nephropathy, and Steroid-Sensitive Nephrotic Syndrome.
Sanchez-Rodriguez E, Southard CT, Kiryluk K. Sanchez-Rodriguez E, et al. Clin J Am Soc Nephrol. 2021 Mar 8;16(3):458-466. doi: 10.2215/CJN.14031119. Epub 2020 Jul 17. Clin J Am Soc Nephrol. 2021. PMID: 32680915 Free PMC article. Review.
The GWAS approach has been successfully applied to primary glomerular disorders, providing numerous novel insights into the genetic architecture of IgA nephropathy, membranous nephropathy, and steroid-sensitive nephrotic syndrome. IgA nephropathy
The GWAS approach has been successfully applied to primary glomerular disorders, providing numerous novel insights into the genetic architec …
Interaction between GALNT12 and C1GALT1 Associates with Galactose-Deficient IgA1 and IgA Nephropathy.
Wang YN, Zhou XJ, Chen P, Yu GZ, Zhang X, Hou P, Liu LJ, Shi SF, Lv JC, Zhang H. Wang YN, et al. J Am Soc Nephrol. 2021 Mar;32(3):545-552. doi: 10.1681/ASN.2020060823. Epub 2021 Feb 16. J Am Soc Nephrol. 2021. PMID: 33593824 Free PMC article.
METHODS: To identify novel loci associated with galactose-deficient IgA1, we performed a quantitative genome-wide association study for serum galactose-deficient IgA1 levels, on the basis of two different genome-wide association study panels conducted in 1127 patients with IgA
METHODS: To identify novel loci associated with galactose-deficient IgA1, we performed a quantitative genome-wide association study for seru …
Pathogenesis of IgA nephropathy.
Wada J, Sugiyama H, Makino H. Wada J, et al. Semin Nephrol. 2003 Nov;23(6):556-63. doi: 10.1053/s0270-9295(03)00134-7. Semin Nephrol. 2003. PMID: 14631563 Review.
Immunoglobulin A (IgA) nephropathy is an immune-complex-mediated glomerulonephritis characterized by the presence of immunoglobulin A deposits in mesangial and paramesangial regions. ...The gene polymorphism studies for human leukocyte antigen (HLA), renin-an …
Immunoglobulin A (IgA) nephropathy is an immune-complex-mediated glomerulonephritis characterized by the presence of im …
Pathogenesis of immunoglobulin A nephropathy.
Novak J, Renfrow MB, Gharavi AG, Julian BA. Novak J, et al. Curr Opin Nephrol Hypertens. 2013 May;22(3):287-94. doi: 10.1097/MNH.0b013e32835fef54. Curr Opin Nephrol Hypertens. 2013. PMID: 23511518 Review.
Since 1968, when IgA nephropathy was described as an IgA-IgG immune-complex disease, the knowledge base expanded to allow definition of IgA nephropathy as an autoimmune disease with a multihit pathogenetic process. ...SUMMARY: Rece …
Since 1968, when IgA nephropathy was described as an IgA-IgG immune-complex disease, the knowledge base expanded …
Current Understanding of the Role of Complement in IgA Nephropathy.
Maillard N, Wyatt RJ, Julian BA, Kiryluk K, Gharavi A, Fremeaux-Bacchi V, Novak J. Maillard N, et al. J Am Soc Nephrol. 2015 Jul;26(7):1503-12. doi: 10.1681/ASN.2014101000. Epub 2015 Feb 18. J Am Soc Nephrol. 2015. PMID: 25694468 Free PMC article. Review.
Complement activation has a role in the pathogenesis of IgA nephropathy, an autoimmune disease mediated by pathogenic immune complexes consisting of galactose-deficient IgA1 bound by antiglycan antibodies. ...Notably, complement factors and their fragments ma …
Complement activation has a role in the pathogenesis of IgA nephropathy, an autoimmune disease mediated by pathogenic i …
Mutations in the alternative complement pathway in multiple myeloma patients with carfilzomib-induced thrombotic microangiopathy.
Moscvin M, Liacos CI, Chen T, Theodorakakou F, Fotiou D, Hossain S, Rowell S, Leblebjian H, Regan E, Czarnecki P, Bagnoli F, Bolli N, Richardson P, Rennke HG, Dimopoulos MA, Kastritis E, Bianchi G. Moscvin M, et al. Blood Cancer J. 2023 Feb 27;13(1):31. doi: 10.1038/s41408-023-00802-0. Blood Cancer J. 2023. PMID: 36849497 Free PMC article.
We identified a frequency of deletions in the complement Factor H genes 3 and 1 (delCFHR3-CFHR1) and genes 1 and 4 (delCFHR1-CFHR4) in MM patients with carfilzomib-associated TMA that was higher as compared to the general population and matched controls. Our data suggest t …
We identified a frequency of deletions in the complement Factor H genes 3 and 1 (delCFHR3-CFHR1) and genes 1 and 4 (delCFHR1-CFHR4) i …
Monogenic and polygenic concepts in chronic kidney disease (CKD).
Jefferis J, Hudson R, Lacaze P, Bakshi A, Hawley C, Patel C, Mallett A. Jefferis J, et al. J Nephrol. 2024 Jan;37(1):7-21. doi: 10.1007/s40620-023-01804-8. Epub 2023 Nov 21. J Nephrol. 2024. PMID: 37989975 Free PMC article. Review.
Certain kidney diseases, such as membranous nephropathy and IgA nephropathy that have significant genetic components, may benefit most from polygenic risk scores for improved risk stratification. ...In this review, we provide an overview of the heritability o …
Certain kidney diseases, such as membranous nephropathy and IgA nephropathy that have significant genetic components, m …
Hematuria and risk for end-stage kidney disease.
Vivante A, Calderon-Margalit R, Skorecki K. Vivante A, et al. Curr Opin Nephrol Hypertens. 2013 May;22(3):325-30. doi: 10.1097/MNH.0b013e32835f7241. Curr Opin Nephrol Hypertens. 2013. PMID: 23449218 Review.
RECENT FINDINGS: It has been recently recognized that young persons with persistent isolated microscopic hematuria have an increased risk for end-stage kidney disease, mainly secondary to primary glomerular diseases. These predominantly include IgA nephropathy
RECENT FINDINGS: It has been recently recognized that young persons with persistent isolated microscopic hematuria have an increased risk fo …
The landscape and diagnostic potential of T and B cell repertoire in Immunoglobulin A Nephropathy.
Huang C, Li X, Wu J, Zhang W, Sun S, Lin L, Wang X, Li H, Wu X, Zhang P, Xu G, Wang H, Liu H, Liu Y, Chen D, Zhuo L, Li W, Yang H, Wang J, Wang L, Liu X. Huang C, et al. J Autoimmun. 2019 Feb;97:100-107. doi: 10.1016/j.jaut.2018.10.018. Epub 2018 Oct 29. J Autoimmun. 2019. PMID: 30385082 Free article.
Immunoglobulin A Nephropathy (IgAN) is the most common glomerulonephritis worldwide. ...We found that some features of TCRB and IGH in renal tissues were remarkably different from that in the blood, including decreased repertoire diversity, increased IgA and …
Immunoglobulin A Nephropathy (IgAN) is the most common glomerulonephritis worldwide. ...We found that some features of TCRB an …
46 results