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1دورية أكاديمية
المؤلفون: Swan EJ; Centre for Public Health, Queen's University of Belfast., Maxwell AP; Centre for Public Health, Queen's University of Belfast.; Regional Nephrology Unit, Belfast City Hospital, Belfast, UK., McKnight AJ; Centre for Public Health, Queen's University of Belfast.
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2015 Aug; Vol. 32 (8), pp. 1110-5. Date of Electronic Publication: 2015 May 10.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: DNA, Mitochondrial/*metabolism , Diabetes Mellitus, Type 1/*complications , Diabetic Nephropathies/*genetics , Kidney Failure, Chronic/*genetics , Mitochondria/*genetics, Case-Control Studies ; DNA Methylation ; Diabetic Nephropathies/etiology ; Epigenesis, Genetic ; Genes, Mitochondrial ; Humans ; Kidney Failure, Chronic/etiology ; Mitochondria/metabolism ; Renal Insufficiency, Chronic/etiology ; Renal Insufficiency, Chronic/genetics
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2دورية أكاديمية
المؤلفون: Swan EJ; Centre for Public Health, Queen's University of Belfast, Belfast, UK., Salem RM; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA., Sandholm N; Folkhälsan Institute of Genetics, Folkhälsan Research Centre, Helsinki, Finland.; Department of Medicine, Division of Nephrology, Helsinki University Central Hospital, Helsinki, Finland., Tarnow L; Nordsjaellands Hospital, Hilleroed, Denmark and Health, Aarhus University, Aarhus, Denmark.; Steno Diabetes Centre, Gentofte, Denmark., Rossing P; Steno Diabetes Centre, Gentofte, Denmark., Lajer M; Steno Diabetes Centre, Gentofte, Denmark., Groop PH; Folkhälsan Institute of Genetics, Folkhälsan Research Centre, Helsinki, Finland.; Department of Medicine, Division of Nephrology, Helsinki University Central Hospital, Helsinki, Finland.; Baker IDI Heart and Diabetes Institute, Melbourne, Australia., Maxwell AP; Centre for Public Health, Queen's University of Belfast, Belfast, UK.; Regional Nephrology Unit, Belfast City Hospital, Belfast, UK., McKnight AJ; Centre for Public Health, Queen's University of Belfast, Belfast, UK.
مؤلفون مشاركون: GENIE Consortium
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2015 Aug; Vol. 32 (8), pp. 1104-9. Date of Electronic Publication: 2015 Apr 13.
نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: Diabetes Mellitus, Type 1/*complications , Diabetic Nephropathies/*genetics , Kidney Failure, Chronic/*genetics , Mitochondria/*genetics, Adult ; Aged ; Case-Control Studies ; Diabetic Nephropathies/etiology ; Female ; Genetic Predisposition to Disease ; Genome, Mitochondrial ; Humans ; Kidney Failure, Chronic/etiology ; Male ; Middle Aged ; Mitochondria/metabolism ; Polymorphism, Single Nucleotide ; Renal Insufficiency, Chronic/etiology ; Renal Insufficiency, Chronic/genetics
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3دورية أكاديمية
المؤلفون: Currie D; Nephrology, Queen's University of Belfast, Belfast, UK. nephres@qub.ac.uk, McKnight AJ, Patterson CC, Sadlier DM, Maxwell AP
مؤلفون مشاركون: UK Warren 3/GoKinD Study Group
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2010 Oct; Vol. 27 (10), pp. 1188-94.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: Diabetes Mellitus, Type 1/*genetics , Diabetic Nephropathies/*genetics , Peptidyl-Dipeptidase A/*genetics , Polymorphism, Single Nucleotide/*genetics , Receptor, Angiotensin, Type 1/*genetics, Adult ; Angiotensin-Converting Enzyme 2 ; Case-Control Studies ; Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 1/epidemiology ; Diabetic Nephropathies/epidemiology ; Diabetic Nephropathies/etiology ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Humans ; Male ; Phenotype ; United Kingdom
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4دورية أكاديمية
المؤلفون: McKnight AJ; Nephrology Research Group, Queen's University of Belfast, Belfast, UK. a.j.mcknight@qub.ac.uk, Pettigrew KA, Patterson CC, Kilner J, Sadlier DM, Maxwell AP
مؤلفون مشاركون: Warren 3/UK GoKinD Study Group
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2010 Jun; Vol. 27 (6), pp. 624-30.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: Bone Morphogenetic Proteins/*genetics , Diabetes Mellitus, Type 1/*genetics , Diabetic Nephropathies/*genetics , Kidney Failure, Chronic/*genetics, Adult ; Bone Morphogenetic Protein 2/genetics ; Bone Morphogenetic Protein 4/genetics ; Bone Morphogenetic Protein 7/genetics ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide
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5دورية أكاديمية
المؤلفون: Martin RJ; Nephrology, Queen's University of Belfast, Belfast, UK. rosalind.martin@qub.ac.uk, Savage DA, Carson DJ, McKnight AJ, Maxwell AP, Patterson CC
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2010 Feb; Vol. 27 (2), pp. 143-9.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: Diabetes Mellitus, Type 1/*genetics , Macrophage Migration-Inhibitory Factors/*genetics , Polymorphism, Single Nucleotide/*genetics, Adolescent ; Case-Control Studies ; Family ; Female ; Gene Frequency ; Genetic Predisposition to Disease ; Genotype ; Haplotypes ; Humans ; Introns ; Linkage Disequilibrium ; Male ; Sequence Analysis, DNA ; United Kingdom
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6Editorial & Opinion
المؤلفون: Pettigrew KA, McKnight AJ, Martin RJ, Patterson CC, Kilner J, Sadlier D, Maxwell AP, Savage DA
مؤلفون مشاركون: Warren 3/UK GoKinD Study Group
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2008 Sep; Vol. 25 (9), pp. 1127-9.
نوع المنشور: Letter
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
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7دورية أكاديمية
المؤلفون: Currie D; Nephrology Research Group, Queen's University of Belfast, Belfast, Northern Ireland, UK., Maxwell AP, Sadlier D, McKnight AJ
مؤلفون مشاركون: Warren 3/UK GoKinD Study Group
المصدر: Diabetic medicine : a journal of the British Diabetic Association [Diabet Med] 2008 Aug; Vol. 25 (8), pp. 1001-5.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
بيانات الدورية: Publisher: Blackwell Science Country of Publication: England NLM ID: 8500858 Publication Model: Print Cited Medium: Internet ISSN: 1464-5491 (Electronic) Linking ISSN: 07423071 NLM ISO Abbreviation: Diabet Med Subsets: MEDLINE
مواضيع طبية MeSH: Calmodulin-Binding Proteins/*genetics , Diabetes Mellitus, Type 1/*genetics , Diabetic Nephropathies/*genetics , Gene Frequency/*genetics , Polymorphism, Genetic/*genetics, Adolescent ; Case-Control Studies ; Chi-Square Distribution ; Child ; Diabetic Nephropathies/epidemiology ; Genetic Predisposition to Disease/genetics ; Genetic Testing ; Genotype ; Humans ; United Kingdom/epidemiology ; Young Adult