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PLoS ONE, ISSN 1932-6203, 07/2014, Volume 9, Issue 7, p. e102065
textabstractBackground: Activating mutations in the Transient Receptor Potential channel C6 (TRPC6) cause autosomal dominant focal segmental glomerular... 
GLOMERULONEPHRITIS | ACTIVATION | COMPLEMENT | PODOCYTE INJURY | MULTIDISCIPLINARY SCIENCES | IGA NEPHROPATHY | RECEPTOR | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | ASSOCIATION | EXPRESSION | GLOMERULAR-DISEASE | Genetic Predisposition to Disease | TRPC6 Cation Channel | Genetic Association Studies | Gene Frequency | Humans | Middle Aged | Glomerulonephritis, Membranous - genetics | Molecular Sequence Data | DNA Primers - genetics | Glomerulonephritis, Membranous - physiopathology | Sequence Analysis, DNA | TRPC Cation Channels - chemistry | Disease Progression | Base Sequence | Polymorphism, Single Nucleotide - genetics | Adult | Amino Acid Substitution - genetics | Protein Conformation | TRPC Cation Channels - genetics | Development and progression | Genetic aspects | Single nucleotide polymorphisms | Kidney diseases | Chromosomes | Analysis | Animal models | Nephrology | Pathogenesis | Genomes | Complement | Statistical methods | Single-nucleotide polymorphism | Sclerosis | Gene sequencing | Amino acid substitution | Transient receptor potential proteins | Rodents | Population | Genetics | Remission | Genotypes | Deoxyribonucleic acid--DNA | Immunoglobulins | Statistical analysis | Glycoproteins | Patients | Genetic variance | Nephropathy | Membranous nephropathy | Gene frequency | Biopsy | Alleles | Renal failure | Mutation | Proteinuria | Deoxyribonucleic acid | DNA
Journal Article
Kidney International, ISSN 0085-2538, 01/2010, Volume 77, Issue 1, pp. 17 - 22
Journal Article
Journal Article
Lancet, The, ISSN 0140-6736, 2014, Volume 383, Issue 9931, pp. 1844 - 1859
Summary At least 10% of adults and nearly all children who receive renal-replacement therapy have an inherited kidney disease. These patients rarely die when... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | PROTEIN | UMOD GENE | PHARMACOLOGICAL CHAPERONES | GENERATION | HYPOKALEMIC ALKALOSIS | MUTATIONS | NEPHROTIC SYNDROME | IDENTIFICATION | CELL | BARTTERS-SYNDROME | Care and treatment | Kidney diseases | Health aspects | Patient outcomes | Genetics | Nephrology | Mutation
Journal Article
by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2008, Volume 3, Issue 1, pp. 22 - 22
Journal Article
Frontiers in Pediatrics, ISSN 2296-2360, 2018, Volume 6
Journal Article