Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Disease and C6[original query] |
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| Cardiovascular disease genetics: a long and winding road. Current opinion in lipidology 2003 1 14 (1): 47-54. Ordovas Jose |
| Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration. Journal of vascular surgery 2005 Aug 42 (2): 309-14. Zamboni Paolo, Tognazzo Silvia, Izzo Marcello, Pancaldi Francesca, Scapoli Gian L, Liboni Alberto, Gemmati Dona |
| Prognostic role of factor XIII gene variants in nonhealing venous leg ulcers. Journal of vascular surgery 2006 Oct 44 (4): 815-9. Tognazzo Silvia, Gemmati Donato, Palazzo Annunziata, Catozzi Linda, Carandina Sergio, Legnaro Andrea, Tacconi Giovanna, Scapoli Gian L, Zamboni Pao |
| The cytosolic ß-glucosidase GBA3 does not influence type 1 Gaucher disease manifestation. Blood cells, molecules & diseases 2011 Jan 46 (1): 19-26. Dekker Nick, Voorn-Brouwer Tineke, Verhoek Marri, Wennekes Tom, Narayan Ravi S, Speijer Dave, Hollak Carla E M, Overkleeft Hermen S, Boot Rolf G, Aerts Johannes M F |
| Association analysis of C6 genetic variations and aspirin hypersensitivity in Korean asthmatic patients. Human immunology 2011 Oct 72 (10): 973-8. Pasaje Charisse Flerida A, Bae Joon Seol, Park Byung-Lae, Cheong Hyun Sub, Jang An-Soo, Uh Soo-Taek, Kim Mi-Kyeong, Koh In Song, Kim Jeong-Hyun, Park Tae-Joon, Lee Jin-Sol, Kim Yongha, Park Choon-Sik, Shin Hyoung D |
| Coding polymorphisms in the genes of the alternative complement pathway and abdominal aortic aneurysm. International journal of immunogenetics 2011 Jun 38 (3): 243-8. Bradley D T, Badger S A, Bown M J, Sayers R D, Hughes A |
| Complete deficiency of the sixth complement component (C6Q0), susceptibility to Neisseria meningitidis infections and analysis of the frequencies of C6Q0 gene defects in South Africans. Clinical and experimental immunology 2012 Mar 167 (3): 3. Orren A, Owen EP, Henderson HE, van der Merwe L, Leisegang F, Stassen C, Potter PC |
| Catechol-O-methyltransferase Val158Met polymorphism influences anxiety, depression, and disability, but not pressure pain sensitivity, in women with fibromyalgia syndrome. The journal of pain : official journal of the American Pain Society 2012 Sep . Fernández-de-Las-Peñas C, Ambite-Quesada S, Gil-Crujera A, Cigarán-Méndez M, Peñacoba-Puente C |
| Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery disease. Circulation. Cardiovascular genetics 2014 Dec 7 (6): 887-94. Xu Chengqi, Yang Qin, Xiong Hongbo, Wang Longfei, Cai Jianping, Wang Fan, Li Sisi, Chen Jing, Wang Chuchu, Wang Dan, Xiong Xin, Wang Pengyun, Zhao Yuanyuan, Wang Xiaojing, Huang Yufeng, Chen Shanshan, Yin Dan, Li Xiuchun, Liu Ying, Liu Jinqiu, Wang Jingjing, Li Hui, Ke Tie, Ren Xiang, Wu Yanxia, Wu Gang, Wan Jing, Zhang Rongfeng, Wu Tangchun, Wang Junhan, Xia Yunlong, Yang Yanzong, Cheng Xiang, Liao Yuhua, Chen Qiuyun, Zhou Yanhong, He Qing, Tu Xin, Wang Qing |
| TRPC6 single nucleotide polymorphisms and progression of idiopathic membranous nephropathy. PloS one 2014 9 (7): e102065. Hofstra Julia M, Coenen Marieke J H, Schijvenaars Mascha M V A P, Berden Jo H M, van der Vlag Johan, Hoefsloot Lies H, Knoers Nine V A M, Wetzels Jack F M, Nijenhuis T |
Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population.
Molecular medicine reports 2016 Dec . Baek Seung-Hoon, Kim Kang-Il, Yoon Kyung-Sik, Kim Tae-Ho, Kim Shin-Yo |
| Genetic predisposition for chronic venous insufficiency in several genes for matrix metalloproteinases (MMP-2, MMP-9, MMP-12) and their inhibitor TIMP-2. Journal of the European Academy of Dermatology and Venereology : JEADV 2017 Jun . Slonková V, Slonková V, Vašk? A, Vašk? |
| Alzheimer Disease and Selected Risk Factors Disrupt a Co-regulation of Monoamine Oxidase-A/B in the Hippocampus, but Not in the Cortex. Frontiers in neuroscience 2018 12 419. Quartey Maa O, Nyarko Jennifer N K, Pennington Paul R, Heistad Ryan M, Klassen Paula C, Baker Glen B, Mousseau Darrell |
| Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Jul . Squitieri Ferdinando, Mazza Tommaso, Maffi Sabrina, De Luca Alessandro, AlSalmi Qasem, AlHarasi Salma, Collins Jennifer A, Kay Chris, Baine-Savanhu Fiona, Landwhermeyer Bernard G, Sabatini Umberto, Hayden Michael |
| Hb Athens-Georgia (beta 40(C6) Arg?>?Lys, HBB:c.122G?>?A) with a single ?-globin gene (Hb H disease) in a Thai family: molecular, hematological, and diagnostic aspects. Scandinavian journal of clinical and laboratory investigation 2020 Dec 1-7. Panyasai Sitthichai, Kunyanone Naowarat, Satthakarn Sura |
| Identification of a novel mutation in the C6 gene of a Han Chinese C6SD child with meningococcal disease. Experimental and therapeutic medicine 2021 4 21 (5): 510. Zhang Ai-Qian, Liu Yu-Xing, Jin Jie-Yuan, Wang Chen-Yu, Fan Liang-Liang, Xu Da-B |
| The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease. The Turkish journal of pediatrics 2021 63 (1): 118-125. Balamtekin Necati, Baysoy Gökhan, Tan Ça?man, K?z?lkan Nuray Uslu, Demir Hülya, Salt?k-Temizel ?nci Nur, Özen Hasan, Yüce Aysel, Tezcan ?lhan, Gürakan Fig |
| Moyamoya Disease Associated with a Deficiency of Complement Component 6. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2022 Jun 31 (8): 106601. Kato Masaru, Kudo Yuki, Hatase Masanao, Tsuchida Naohisa, Takeyama Shuhei, Sugiyama Taku, Fujimura Miki, Yabe Ichiro, Tsujimoto Hiroshi, Fukumori Yasuo, Inoue Norimitsu, Atsumi Tatsu |
| Rare variants in complement system genes associate with endothelial damage after pediatric allogeneic hematopoietic stem cell transplantation. Frontiers in immunology 2023 9 14 1249958. Lilli Leimi, Jessica R Koski, Outi Kilpivaara, Kim Vettenranta, A Inkeri Lokki, Seppo Me |
| Circulating Acylcarnitines Associated with Hypertrophic Cardiomyopathy Severity: an Exploratory Cross-Sectional Study in MYBPC3 Founder Variant Carriers. Journal of cardiovascular translational research 2023 6 . Mark Jansen, A F Schmidt, J J M Jans, I Christiaans, S N van der Crabben, Y M Hoedemaekers, D Dooijes, J D H Jongbloed, L G Boven, R H Lekanne Deprez, A A M Wilde, J van der Velden, R A de Boer, J P van Tintelen, F W Asselbergs, A F Ba |
| Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia. Research square 2024 4 . A Lokki, Michael Triebwasser, Emma Daly, Finnpec Cohort, Mrtja Kurki, Markus Perola, Kirsi Auro, Jane Salmon, Anuja Java, Mark Daly, John Atkinson, Hannele Laivuori, Seppo Me |
| Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia. Genes and immunity 2024 12 . A Inkeri Lokki, Michael Triebwasser, Emma Daly, , Mitja I Kurki, Markus Perola, Kirsi Auro, Jane E Salmon, Java Anuja, Mark Daly, John P Atkinson, Hannele Laivuori, Seppo Me |
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