Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study
暂无分享,去创建一个
I. König | A. Franke | D. Ellinghaus | H. Lehnert | Theresa Dankowski | S. Möller | C. Sina | K. Fellermann | Xinhua Yu | Torsten Schröder | F. Bär | S. Ibrahim | S. Schreiber | T. Dankowski
[1] S. Arora,et al. Inflammatory Bowel Disease: Epidemiology , 2016 .
[2] I. Sousa,et al. Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control , 2016, Inflammatory bowel diseases.
[3] I. Johnston,et al. Evolutionary Inference across Eukaryotes Identifies Specific Pressures Favoring Mitochondrial Gene Retention. , 2016, Cell systems.
[4] J. Bábíčková,et al. Sex Differences in Experimentally Induced Colitis in Mice: a Role for Estrogens , 2015, Inflammation.
[5] K. Gyires,et al. Gut inflammation: current update on pathophysiology, molecular mechanism and pharmacological treatment modalities. , 2014, Current pharmaceutical design.
[6] H. Lehnert,et al. Mitochondrial gene polymorphisms that protect mice from colitis. , 2013, Gastroenterology.
[7] D. Wallace,et al. Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. , 2013, Cold Spring Harbor perspectives in biology.
[8] W. Hauswirth,et al. NADH-dehydrogenase type-2 suppresses irreversible visual loss and neurodegeneration in the EAE animal model of MS. , 2013, Molecular therapy : the journal of the American Society of Gene Therapy.
[9] M. Guo,et al. Mitochondrial ATP 6 and 8 polymorphisms in irritable bowel syndrome with diarrhea. , 2013, World journal of gastroenterology.
[10] J. Smeitink,et al. Cellular and animal models for mitochondrial complex I deficiency: A focus on the NDUFS4 subunit , 2013, IUBMB life.
[11] T. Yagi,et al. Mitochondrial complex I activity and NAD+/NADH balance regulate breast cancer progression. , 2013, The Journal of clinical investigation.
[12] T. Santa-Coloma,et al. The Mitochondrial Complex I Activity Is Reduced in Cells with Impaired Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Function , 2012, PloS one.
[13] A. Ramachandran,et al. Mitochondrial electron transport chain complex dysfunction in the colonic mucosa in ulcerative colitis , 2012, Inflammatory bowel diseases.
[14] F. Bedford. Sephardic signature in haplogroup T mitochondrial DNA , 2011, European Journal of Human Genetics.
[15] Takeo Suzuki,et al. Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases. , 2011, Annual review of genetics.
[16] G. Porro,et al. Mucosal healing predicts late outcomes after the first course of corticosteroids for newly diagnosed ulcerative colitis. , 2011, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[17] Philippe Seksik,et al. Epidemiology and natural history of inflammatory bowel diseases. , 2011, Gastroenterology.
[18] Günther Specht,et al. HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups , 2011, Human mutation.
[19] Neil J. Daily,et al. Novel Interactions of CAPS (Ca2+-dependent Activator Protein for Secretion) with the Three Neuronal SNARE Proteins Required for Vesicle Fusion* , 2010, The Journal of Biological Chemistry.
[20] Trygve E Bakken,et al. Association between mitochondrial DNA variations and Alzheimer's disease in the ADNI cohort , 2010, Neurobiology of Aging.
[21] Cindy E J Dieteren,et al. Mammalian mitochondrial complex I: biogenesis, regulation, and reactive oxygen species generation. , 2010, Antioxidants & redox signaling.
[22] F. Dal-Pizzol,et al. Mitochondrial respiratory chain in the colonic mucosal of patients with ulcerative colitis , 2010, Molecular and Cellular Biochemistry.
[23] Christian Gieger,et al. Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL) , 2010, Nature Genetics.
[24] P. Rosenstiel,et al. Towards a molecular risk map--recent advances on the etiology of inflammatory bowel disease. , 2009, Seminars in immunology.
[25] P. Mitchell,et al. Mitochondrial DNA Variants of Respiratory Complex I that Uniquely Characterize Haplogroup T2 Are Associated with Increased Risk of Age-Related Macular Degeneration , 2009, PloS one.
[26] Manfred Kayser,et al. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation , 2009, Human mutation.
[27] W. Hwu,et al. Mutation of mitochondrial DNA G13513A presenting with Leigh syndrome, Wolff-Parkinson-White syndrome and cardiomyopathy. , 2008, Pediatrics and neonatology.
[28] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[29] R. Gearry,et al. High incidence of Crohn's disease in Canterbury, New Zealand: Results of an epidemiologic study , 2006, Inflammatory bowel diseases.
[30] Thomas Meitinger,et al. SNP-Based Analysis of Genetic Substructure in the German Population , 2006, Human Heredity.
[31] Marty C. Brandon,et al. Mitochondrial mutations in cancer , 2006, Oncogene.
[32] R. Saxena,et al. Comprehensive association testing of common mitochondrial DNA variation in metabolic disease. , 2006, American journal of human genetics.
[33] Á. Carracedo,et al. Dissection of mitochondrial superhaplogroup H using coding region SNPs , 2006, Electrophoresis.
[34] Michael Krawczak,et al. PopGen: Population-Based Recruitment of Patients and Controls for the Analysis of Complex Genotype-Phenotype Relationships , 2006, Public Health Genomics.
[35] C. Gieger,et al. KORA-gen - Resource for Population Genetics, Controls and a Broad Spectrum of Disease Phenotypes , 2005 .
[36] N. Howell,et al. An evolutionary perspective on pathogenic mtDNA mutations: haplogroup associations of clinical disorders. , 2004, Mitochondrion.
[37] É. Lerebours,et al. Opposite evolution in incidence of Crohn’s disease and ulcerative colitis in Northern France (1988–1999) , 2004, Gut.
[38] J. Haines,et al. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. , 2003, American journal of human genetics.
[39] T. Martin,et al. Role of CAPS in Dense‐Core Vesicle Exocytosis , 2002, Annals of the New York Academy of Sciences.
[40] J. Saillard,et al. Mitochondrial DNA variant 11719G is a marker for the mtDNA haplogroup cluster HV. , 2000, Human biology.
[41] A. Harding,et al. Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. , 1995, Journal of medical genetics.
[42] S. Dimauro,et al. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome. , 1989, The New England journal of medicine.
[43] D. Wallace,et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. , 1988, Science.
[44] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .
[45] E. Szigethy,et al. Inflammatory bowel disease. , 2011, Pediatric clinics of North America.
[46] J. Lennard-jones,et al. Classification of inflammatory bowel disease. , 1989, Scandinavian journal of gastroenterology. Supplement.