Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations

التفاصيل البيبلوغرافية
العنوان: Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations
المؤلفون: Brendan J. Keating, Rudaynah Al Ali, Cyril Cyrus, Hatem O. Qutub, Shahanas Chathoth, Brian Kim-Mozeleski, Chittibabu Vatte, Amein Al Ali, Yun Li, Abdullah M. Al-Rubaish, Samir H Al-Mueilo, Khaled R. Alkharsah, Fahad Al-Muhanna, Matthew B. Lanktree
المصدر: BMC Nephrology
BMC Nephrology, Vol 19, Iss 1, Pp 1-6 (2018)
بيانات النشر: BioMed Central, 2018.
سنة النشر: 2018
مصطلحات موضوعية: 0301 basic medicine, Male, 030232 urology & nephrology, Genome-wide association study, SLC7A9, Logistic regression, urologic and male genital diseases, lcsh:RC870-923, MYH9, Genetic biomarkers, 0302 clinical medicine, Risk Factors, Chronic kidney disease, Genotype, Cholecalciferol, Molecular Motor Proteins, Microfilament Proteins, CST3, Middle Aged, Nephrology, Cohort, Female, Research Article, Glomerular Filtration Rate, Adult, medicine.medical_specialty, Saudi Arabia, Renal function, SNP, Polymorphism, Single Nucleotide, 03 medical and health sciences, Internal medicine, medicine, Vitamin D and neurology, Humans, Cystatin C, Renal Insufficiency, Chronic, Alleles, Aged, Myosin Heavy Chains, business.industry, SHROOM3, medicine.disease, lcsh:Diseases of the genitourinary system. Urology, Minor allele frequency, Fibroblast Growth Factors, Fibroblast Growth Factor-23, 030104 developmental biology, Case-Control Studies, Amino Acid Transport Systems, Basic, business, Kidney disease
الوصف: Background Genome wide association studies of patients with European descent have identified common variants associated with risk of reduced estimated glomerular filtration rate (eGFR). A panel of eight variants were selected to evaluate their association and prevalence in a Saudi Arabian patient cohort with chronic kidney disease (CKD). Methods Eight genetic variants in four genes (SHROOM3, MYH9, SLC7A9, and CST3) were genotyped in 160 CKD patients and 189 ethnicity-matched healthy controls. Genetic variants were tested for association with the development of CKD (eGFR
اللغة: English
تدمد: 1471-2369
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb643827947207bcc5650c23a797150dTest
http://europepmc.org/articles/PMC5905143Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....fb643827947207bcc5650c23a797150d
قاعدة البيانات: OpenAIRE