Publications (9 results)
Please use discretion when following external links; Assaypro cannot guarantee the validity and security of all citation links provided.Complement system abnormalities in patients with atypical hemolytic uremic syndrome and catastrophic antiphospholipid syndrome
- http://vestnikramn.spr-journal.ru/jour/article/view/769
- KA Demyanova, NL Kozlovskaya… - Annals of the …, 2017 - vestnikramn.spr-journal.ru
- Background: The role of the alternative complement pathway (AP) abnormalities in the pathogenesis of aHUS is well studied. Clinical and morphological manifestations of atypical HUS …
Human Tamm-Horsfall protein, a renal specific protein, serves as a cofactor in complement 3b degradation
Сравнительный анализ изменений в системе комплемента при катастрофическом антифосфолипидном синдроме и атипичном гемолитико-уремическом …
Роль изменений комплемента в развитии поражения почек у больных с микроангиопатическими синдромами
* Kumar A et al. (2019) Utility of plasma exchange in early recurrent C3 glomerulopathy. Ind. J. Transplant. 13(2):122-126
* Nada R et al. (2018) Renal and Pulmonary Dense Deposit Disease Presenting as Pulmonary-Renal Syndrome. Kidney Int. Rep. 3(3):755-761
* Rhodes DC (2017) Human Tamm-Horsfall protein, a renal specific protein, serves as a cofactor in complement 3b degradation. PLoS One. 12(7):e0181857.
* Molins B et al. (2016) Complement factor H binding of monomeric C-reactive protein downregulates proinflammatory activity and is impaired with at risk polymorphic CFH variants. Sci Rep. 6:22889.