Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: DNASE2[original query] |
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Homozygosity for DNASE2 single nucleotide polymorphisms in the 5'-regulatory region is associated with rheumatoid arthritis. Annals of the rheumatic diseases 2009 Sep 68 (9): 1498-503. Rossol M, Pierer M, Arnold S, Keysser G, Burkhardt H, Baerwald C, Wagner |
Negative association of the chemokine receptor CCR5 d32 polymorphism with systemic inflammatory response, extra-articular symptoms and joint erosion in rheumatoid arthritis. Arthritis research & therapy 2009 Jun 11 (3): 3. Rossol M, Pierer M, Arnold S, Keyszer G, Burkhardt H, Baerwald C, Wagner U |
Distribution and haplotype analysis of all the non-synonymous and autoimmunity-related single nucleotide polymorphisms in the human deoxyribonuclease II gene using worldwide populations. Legal medicine (Tokyo, Japan) 2012 Nov . Kimura-Kataoka K, Yasuda T, Fujihara J, Toga T, Ono RI, Otsuka Y, Ueki M, Iida R, Kato H, Takeshita H |
Seven nonsynonymous SNPs in the gene encoding human deoxyribonuclease II may serve as a functional SNP potentially implicated in autoimmune dysfunction. Electrophoresis 2013 Dec 34 (24): 3361-9. Kimura-Kataoka Kaori, Ueki Misuzu, Takeshita Haruo, Fujihara Junko, Iida Reiko, Kato Hideaki, Yasuda Toshihi |
Functional Single Nucleotide Polymorphisms (SNPs) in the Genes Encoding the Human Deoxyribonuclease (DNase) Family Potentially Relevant to Autoimmunity. Immunological investigations 2016 Jul 45 (5): 406-19. Fujihara Junko, Ueki Misuzu, Kimura-Kataoka Kaori, Iida Reiko, Takeshita Haruo, Yasuda Toshihi |
Molecular and biochemical study of glutaric aciduria type 1 in 49 Russian families: nine novel mutations in the GCDH gene. Metabolic brain disease 2020 4 35 (6): 1009-1016. Kurkina Marina V, Mihaylova Svetlana V, Baydakova Galina V, Saifullina Elena V, Korostelev Sergey A, Pyankov Denis V, Kanivets Ilya V, Yunin Maksim A, Pechatnikova Natalya L, Zakharova Ekaterina |
Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing. European journal of medical genetics 2020 3 63 (5): 103920. Batlle-Masó Laura, Mensa-Vilaró Anna, Solís-Moruno Manuel, Marquès-Bonet Tomàs, Arostegui Juan I, Casals Ferr |
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