يعرض 1 - 10 نتائج من 28 نتيجة بحث عن '"Felekkis, Kyriacos N."', وقت الاستعلام: 1.75s تنقيح النتائج
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    دورية أكاديمية
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    المساهمون: Maxwell, Patrick [0000-0002-0338-2679], Apollo - University of Cambridge Repository, Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

    المصدر: PLoS ONE
    PLoS ONE, Vol 12, Iss 3, p e0174274 (2017)

    مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Pathology, Heredity, 030232 urology & nephrology, lcsh:Medicine, Pathology and Laboratory Medicine, immunoprecipitation, Mathematical and Statistical Techniques, 0302 clinical medicine, Framingham Heart Study, single nucleotide polymorphism, Risk Factors, Chronic Kidney Disease, middle aged, Medicine and Health Sciences, Medicine, genetics, membrane protein, Renal Insufficiency, lcsh:Science, education.field_of_study, Multidisciplinary, Proteinuria, adult, chronic kidney failure, Middle Aged, Genetic Mapping, female, risk factor, Nephrology, HEK293 cell line, Physical Sciences, Cohort, Slit diaphragm, Female, medicine.symptom, immunoblotting, Statistics (Mathematics), Research Article, Adult, Genotyping, medicine.medical_specialty, Immunoblotting, Population, Immunoglobulins, Variant Genotypes, complication, Research and Analysis Methods, Polymorphism, Single Nucleotide, albuminuria, Nephropathy, 03 medical and health sciences, Signs and Symptoms, male, Diagnostic Medicine, Internal medicine, Genetics, Albuminuria, Humans, Immunoprecipitation, Genetic Predisposition to Disease, human, Statistical Methods, Allele, Molecular Biology Techniques, education, Molecular Biology, Hematuria, business.industry, lcsh:R, Biology and Life Sciences, Membrane Proteins, Human Genetics, medicine.disease, kidney failure, hematuria, HEK293 Cells, 030104 developmental biology, Genetics of Disease, physiology, Kidney Failure, Chronic, lcsh:Q, Microalbuminuria, KIRREL2 protein, human, business, immunoglobulin, genetic predisposition, Mathematics, Meta-Analysis

    وصف الملف: application/pdf

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    المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

    المصدر: PLoS ONE
    PLoS ONE, Vol 7, Iss 2, p e31021 (2012)

    مصطلحات موضوعية: molecular cloning, podocyte, Anatomy and Physiology, genetic association, genotype, kidney disease, Glomerulonephritis, Membranous, Severity of Illness Index, Western blotting, single nucleotide polymorphism, Immune Physiology, Nucleic Acids, Molecular Cell Biology, genetic algorithm, genetic polymorphism, genetics, complement, Regulation of gene expression, microRNA 1207 5p, Multidisciplinary, medicine.diagnostic_test, microRNA, predictive value, disease course, article, allele, Transfection, gene expression regulation, bioinformatics, chronic kidney failure, luciferase, reporter gene, gene therapy, HBEGF gene, unclassified drug, CFHR5 gene, Disease Progression, Medicine, Intercellular Signaling Peptides and Proteins, disease severity, down regulation, hospitalization, Research Article, Heparin-binding EGF-like Growth Factor, marker gene, Science, heparin binding epidermal growth factor, DNA sequence, Single-nucleotide polymorphism, Biology, glomerulopathy, heparin-binding EGF-like growth factor, Nephropathy, Molecular Genetics, Western blot, medicine, Genetics, follow up, Humans, controlled study, signal peptide, human, Allele, gene, gene identification, Binding Sites, Polymorphism, Genetic, binding site, human cell, DNA fragment, MIRN1207 microRNA, human, Human Genetics, Complement System Proteins, Genetic Therapy, medicine.disease, 3' untranslated region, Molecular biology, MicroRNAs, FHR5 protein, human, Gene Expression Regulation, RNA, Kidney Failure, Chronic, CFHR5 nephropathy, genetic transfection, membranous glomerulonephritis, Population Genetics

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