نتایج جستجو برای: t 786c polymorphism

تعداد نتایج: 796707  

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
Bárbara Tazón-Vega Mireia Vilardell Laureano Pérez-Oller Elisabet Ars Patricia Ruiz Olivier Devuyst Xose Lens Patricia Fernández-Llama José Ballarín Roser Torra

BACKGROUND Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder with a wide spectrum of renal involvement. Differences in the age at onset of end-stage renal disease (ESRD) are partially explained by the genetic heterogeneity of the disease but intrafamilial variability remains to be explained. Modifier genes may play a role in disease severity. METHODS A total of 355 P...

Journal: : 2021

Досліджено порушення ліпідних параметрів крові у хворих на ревматоїдний артрит (РА) поєднанні з артеріальною гіпертензією (АГ), абдомінальним ожирінням (АО) та цукровим діабетом типу 2 (ЦД 2) залежно від поліморфізму гена T-786C ендотеліальної оксиду азоту синтази (eNOS). Матеріал і методи. Етап скринінгу пройшли 60 із АГ, АО ЦД 20 практично здорових осіб. Поліморфізм eNOS (rs2070744) визначали...

Journal: :iranian journal of allergy, asthma and immunology 0
hui xu department of clinical laboratory, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china yan-xiang pan department of clinical laboratory, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china junfeng zhang department of clinical laboratory, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china yujie liu department of clinical laboratory, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china jian-hua mao department of nephrology, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china wei li department of clinical laboratory, children’s hospital of zhejiang university, school of medicine, hangzhou, pr china

henoch–schönlein purpura (hsp), a common allergic hemorrhagic disease, occurs frequently in children affecting kidney, joint and skin. while interleukin-8 (il-8) plays an important role in inflammation, the association between il-8 gene +781 c/t polymorphism and hsp remains unclear. interleukin-8, an important chemokine related to the initiation and amplification of acute inflammatory responses...

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