نتائج البحث

المساهمون: University of Helsinki, Clinicum, Nefrologian yksikkö, Diabetes and Obesity Research Program, Research Programs Unit, Department of Medicine, Per Henrik Groop / Principal Investigator, HUS Abdominal Center

المصدر: Kidney international. 91(5)

مصطلحات موضوعية: 0301 basic medicine, Male, type 1 diabetes, Glucose Transport Proteins, Facilitative, PROGRESSION, urologic and male genital diseases, DISEASE, Diabetic nephropathy, chemistry.chemical_compound, 0302 clinical medicine, Risk Factors, Diabetic Nephropathies, METABOLIC SYNDROME, RISK, Kidney, ASSOCIATION, Middle Aged, medicine.anatomical_structure, Nephrology, Disease Progression, Female, medicine.symptom, Glomerular Filtration Rate, Adult, serum uric acid, RENAL-FUNCTION, medicine.medical_specialty, Renal function, 030209 endocrinology & metabolism, Polymorphism, Single Nucleotide, URATE, Excretion, 03 medical and health sciences, Internal medicine, Mendelian randomization, medicine, Albuminuria, Humans, Type 1 diabetes, business.industry, diabetic nephropathy, TRANSPORTER, INSTRUMENTS, ta3121, Mendelian Randomization Analysis, 3126 Surgery, anesthesiology, intensive care, radiology, medicine.disease, Uric Acid, 030104 developmental biology, Endocrinology, Cross-Sectional Studies, Diabetes Mellitus, Type 1, chemistry, Uric acid, Metabolic syndrome, business, Biomarkers, Follow-Up Studies

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f794d2248a80e37c8cdbca4f066661a7Test
https://pubmed.ncbi.nlm.nih.gov/28407875Test

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An intergenic region on chromosome 13q33.3 is associated with the susceptibility to kidney disease in type 1 and 2 diabetes

المؤلفون: Stephen S. Rich, Adam M. Smiles, Jan Skupien, G. David Poznik, Andrzej S. Krolewski, James H. Warram, Josyf C. Mychaleckyj, Marcus G. Pezzolesi

المصدر: Kidney International. 80:105-111

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic association, type 1 diabetes, Locus (genetics), Single-nucleotide polymorphism, Type 2 diabetes, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Article, White People, Nephropathy, Diabetic nephropathy, 03 medical and health sciences, 0302 clinical medicine, Intergenic region, Asian People, Diabetes mellitus, Internal medicine, medicine, Humans, Diabetic Nephropathies, Genetic Predisposition to Disease, 030304 developmental biology, Genetics, 0303 health sciences, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 11, diabetic nephropathy, Middle Aged, medicine.disease, Diabetes Mellitus, Type 1, Endocrinology, Diabetes Mellitus, Type 2, Nephrology, Case-Control Studies, DNA, Intergenic, Female, type 2 diabetes, Genome-Wide Association Study, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::811631c499db469dfa2a31a002367ee9Test
https://doi.org/10.1038/ki.2011.64Test

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Regression of microalbuminuria in type 1 diabetes is associated with lower levels of urinary tubular injury biomarkers, kidney injury molecule-1, and N-acetyl-β-D-glucosaminidase

المؤلفون: Joseph V. Bonventre, Amanda C. Johnson, Monika A. Niewczas, Fitz B. Collings, James H. Warram, Andrzej S. Krolewski, Linda H. Ficociello, Vishal S. Vaidya

المصدر: Kidney International. 79:464-470

مصطلحات موضوعية: Male, Remission, Spontaneous, 030204 cardiovascular system & hematology, urologic and male genital diseases, Diabetic nephropathy, 0302 clinical medicine, Diabetic Nephropathies, Hepatitis A Virus Cellular Receptor 1, Chemokine CCL2, 0303 health sciences, Membrane Glycoproteins, Proteinuria, Middle Aged, 3. Good health, Nephrology, Disease Progression, Receptors, Virus, Female, Inflammation Mediators, medicine.symptom, Adult, medicine.medical_specialty, Urinary system, Urology, Article, 03 medical and health sciences, Internal medicine, Diabetes mellitus, Acetylglucosaminidase, medicine, Albuminuria, Humans, 030304 developmental biology, Type 1 diabetes, Interleukin-6, urogenital system, business.industry, diabetic nephropathy, Interleukin-8, medicine.disease, Chemokine CXCL10, Cross-Sectional Studies, Diabetes Mellitus, Type 1, Endocrinology, Case-Control Studies, renal proximal tubule cell, tubular epithelium, Microalbuminuria, business, Biomarkers, chronic kidney disease, Follow-Up Studies, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288fa8af1f22f3e27ad5c6669e0265abTest
https://doi.org/10.1038/ki.2010.404Test

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The renin–aldosterone axis in kidney transplant recipients and its association with allograft function and structure

المؤلفون: Naim, Issa, Fernando, Ortiz, Scott A, Reule, Aleksandra, Kukla, Bertram L, Kasiske, Michael, Mauer, Scott, Jackson, Arthur J, Matas, Hassan N, Ibrahim, Behzad, Najafian

المصدر: Kidney international

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Time Factors, Biopsy, Renal function, Peptidyl-Dipeptidase A, Kidney, urologic and male genital diseases, Plasma renin activity, Article, Losartan, Renin-Angiotensin System, chemistry.chemical_compound, Risk Factors, Internal medicine, Renin, medicine, Albuminuria, Humans, Aldosterone, Creatinine, Polymorphism, Genetic, business.industry, Kidney metabolism, Middle Aged, Allografts, Fibrosis, Kidney Transplantation, female genital diseases and pregnancy complications, Treatment Outcome, Endocrinology, medicine.anatomical_structure, chemistry, Nephrology, Kidney Failure, Chronic, Female, medicine.symptom, business, Angiotensin II Type 1 Receptor Blockers, Biomarkers, Glomerular Filtration Rate, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fd7bffad548f9c24b93dea2b5a8efc6Test
https://doi.org/10.1038/ki.2013.278Test

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The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis

المصدر: Kidney international. 91(5)

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, DNA Mutational Analysis, 030232 urology & nephrology, distal renal tubular acidosis, Disease, Bioinformatics, Genetic analysis, 0302 clinical medicine, Distal renal tubular acidosis, Anion Exchange Protein 1, Erythrocyte, Child, medicine.diagnostic_test, Medicine (all), High-Throughput Nucleotide Sequencing, Acidosis, Renal Tubular, Middle Aged, Phenotype, Nephrology, Child, Preschool, Sensorineural hearing loss, Female, Adult, chronic kidney disease, deafness, mutations, nephrocalcinosis, medicine.medical_specialty, Vacuolar Proton-Translocating ATPases, Adolescent, Genotype, Hearing Loss, Sensorineural, Biology, NO, 03 medical and health sciences, Young Adult, Rare Diseases, medicine, Humans, Genetic Testing, Renal Insufficiency, Chronic, Gene, Genetic Association Studies, Genetic testing, Retrospective Studies, Infant, medicine.disease, Large cohort, 030104 developmental biology, Mutation, Kidney disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cd17abc8122173fc50183250391435eTest
https://pubmed.ncbi.nlm.nih.gov/28233610Test

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