Human Genome Epidemiology Literature Finder
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Records 1 - 18 (of 18 Records) |
| Query Trace: Disease and NCF2[original query] |
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| Genetic polymorphisms and susceptibility to lung disease. Journal of negative results in biomedicine 2006 5 (): 5. Lee Pauline L, West Carol, Crain Karen, Wang L |
| The association between single-nucleotide polymorphisms of NCF2 and systemic lupus erythematosus in Chinese mainland population. Clinical rheumatology 2011 Apr 30 (4): 521-7. Yu Bo, Chen Yuewen, Wu Qi, Li Ping, Shao Yong, Zhang Jie, Zhong Qili, Peng Xi, Yang Hong, Hu Xiaoping, Chen Bancheng, Guan Ming, Wan Jun, Zhang W |
| NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2. Gut 2012 Jul 61 (7): 1028-35. Muise Aleixo M, Xu Wei, Guo Cong-Hui, Walters Thomas D, Wolters Victorien M, Fattouh Ramzi, Lam Grace Y, Hu Pingzhao, Murchie Ryan, Sherlock Mary, Gana Juan Cristóbal, , Russell Richard K, Glogauer Michael, Duerr Richard H, Cho Judy H, Lees Charlie W, Satsangi Jack, Wilson David C, Paterson Andrew D, Griffiths Anne M, Silverberg Mark S, Brumell John |
| Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidase. Proceedings of the National Academy of Sciences of the United States of America 2012 Jan 109 (2): E59-67. Jacob Chaim O, Eisenstein Miriam, Dinauer Mary C, Ming Wenyu, Liu Qiang, John Sutha, Quismorio Francesco P, Reiff Andreas, Myones Barry L, Kaufman Kenneth M, McCurdy Deborah, Harley John B, Silverman Earl, Kimberly Robert P, Vyse Timothy J, Gaffney Patrick M, Moser Kathy L, Klein-Gitelman Marisa, Wagner-Weiner Linda, Langefeld Carl D, Armstrong Don L, Zidovetzki Rapha |
| Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. PLoS genetics 2011 Oct 7 (10): e1002341. Cunninghame Graham Deborah S, Morris David L, Bhangale Tushar R, Criswell Lindsey A, Syvänen Ann-Christine, Rönnblom Lars, Behrens Timothy W, Graham Robert R, Vyse Timothy |
| Encore: Genetic Association Interaction Network centrality pipeline and application to SLE exome data. Genetic epidemiology 2013 Sep 37 (6): 614-21. Davis Nicholas A, Lareau Caleb A, White Bill C, Pandey Ahwan, Wiley Graham, Montgomery Courtney G, Gaffney Patrick M, McKinney B |
| A novel mutation in NCF2 associated with autoimmune disease and a solitary late-onset infection. Clinical immunology (Orlando, Fla.) 2015 Aug . Chou Janet, Hsu Joyce T, Bainter Wayne, Al-Attiyah Raja'a, Al-Herz Waleed, Geha Raif |
Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
Arthritis & rheumatology (Hoboken, N.J.) 2015 Nov . Alarcón-Riquelme Marta E, Ziegler Julie T, Molineros Julio, Howard Timothy D, Moreno-Estrada Andrés, Sánchez-Rodríguez Elena, Ainsworth Hannah C, Ortiz-Tello Patricia, Comeau Mary E, Rasmussen Astrid, Kelly Jennifer A, Adler Adam, Acevedo-Vázquez Eduardo, Cucho Jorge Mariano, la Torre Ignacio García-De, Cardiel Mario H, Miranda Pedro, Catoggio Luis, Maradiaga-Ceceña Marco, Gaffney Patrick, Vyse Timothy, Criswell Lindsey A, Tsao Betty P, Sivils Kathy L, Bae Sang-Cheol, James Judith A, Kimberly Robert, Kaufman Ken, Harley John B, Esquivel-Valerio Jorge, Moctezuma José F, García Mercedes A, Berbotto Guillermo, Babini Alejandra, Scherbarth Hugo, Toloza Sergio, Baca Vicente, Nath Swapan K, Salinas Carlos Aguilar, Orozco Lorena, Tusié-Luna Teresa, Zidovetzki Raphael, Pons-Estel Bernardo A, Langefeld Carl D, Jacob Chaim |
| Candidate gene analysis in the São Paulo Epidemiologic Sleep Study (EPISONO) shows an association of variant in PDE4D and sleepiness. Sleep medicine 2018 Jan 47 106-112. Pak Victoria M, Mazzotti Diego R, Keenan Brendan T, Hirotsu Camila, Gehrman Philip, Bittencourt Lia, Pack Allan I, Tufik Serg |
| Clinical and Genomic Correlates of Neutrophil Reactive Oxygen Species Production in Pediatric Patients With Crohn's Disease. Gastroenterology 2018 2 154 (8): 2097-2110. Denson Lee A, Jurickova Ingrid, Karns Rebekah, Shaw Kelly A, Cutler David J, Okou David T, Dodd Anne, Quinn Kathryn, Mondal Kajari, Aronow Bruce J, Haberman Yael, Linn Aaron, Price Adam, Bezold Ramona, Lake Kathleen, Jackson Kimberly, Walters Thomas D, Griffiths Anne, Baldassano Robert N, Noe Joshua D, Hyams Jeffrey S, Crandall Wallace V, Kirschner Barbara S, Heyman Melvin B, Snapper Scott, Guthery Stephen L, Dubinsky Marla C, Leleiko Neal S, Otley Anthony R, Xavier Ramnik J, Stevens Christine, Daly Mark J, Zwick Michael E, Kugathasan Sub |
| Genetic Association and Altered Gene Expression of CYBB in Multiple Sclerosis Patients. Biomedicines 2018 12 6 (4): . Cardamone Giulia, Paraboschi Elvezia Maria, Soldà Giulia, Duga Stefano, Saarela Janna, Asselta Rosan |
| Clinical and genetic characteristics of Chinese pediatric patients with chronic granulomatous disease. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2019 2 30 (3): 378-386. Gao Li-Wei, Yin Qing-Qin, Tong Yue-Juan, Gui Jin-Gang, Liu Xiu-Yun, Feng Xue-Li, Yin Ju, Liu Jun, Guo Yan, Yao Yao, Xu Bao-Ping, He Jian-Xin, Shen Kun-Ling, Lau Yu-Lung, Jiang Zai-Fa |
| A Novel Genetic Variation in NCF2, the Core Component of NADPH Oxidase, Contributes to the Susceptibility of Tuberculosis in Western Chinese Han Population. DNA and cell biology 2019 12 39 (1): 57-62. Jiao Lin, Song Jiajia, Ding Liu, Liu Tangyuheng, Wu Tao, Zhang Jingwei, Bai Hao, Chen Hao, Zhao Zhenzhen, Ying Bin |
| Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort. The journal of allergy and clinical immunology. In practice 2020 8 8 (10): 3525-3534.e1. Baris Hatice Ezgi, Ogulur Ismail, Akcam Bengu, Kiykim Ayca, Karagoz Dilek, Saraymen Berkay, Akgun Gamze, Eltan Sevgi Bilgic, Aydemir Sezin, Akidagi Zeynep, Bentli Esma, Nain Ercan, Kasap Nurhan, Baser Dilek, Altintas Derya Ufuk, Camcioglu Yildiz, Yesil Gözde, Ozen Ahmet, Koker Mustafa Yavuz, Karakoc-Aydiner Elif, Baris Sa |
| Potentially functional variants of ERAP1, PSMF1 and NCF2 in the MHC-I-related pathway predict non-small cell lung cancer survival. Cancer immunology, immunotherapy : CII 2021 3 70 (10): 2819-2833. Yang Sen, Tang Dongfang, Zhao Yu Chen, Liu Hongliang, Luo Sheng, Stinchcombe Thomas E, Glass Carolyn, Su Li, Shen Sipeng, Christiani David C, Wang Qiming, Wei Qing |
| Neutrophil cytosolic factor 2 (NCF2) gene polymorphism is associated with juvenile-onset systemic lupus erythematosus, but probably not with other autoimmune rheumatic diseases in children. Molecular genetics & genomic medicine 2021 12 10 (1): e1859. Bakutenko Ivan Y, Haurylchyk Irena D, Nikitchenko Natalia V, Sechko Elena V, Kozyro Inna A, Tchitchko Alexei M, Batyan Galina M, Sukalo Alexander V, Ryabokon Nadezhda |
| MYO5B and the Polygenic Landscape of Very Early-Onset Inflammatory Bowel Disease in an Ethnically Diverse Population. Inflammatory bowel diseases 2024 8 . Ashleigh Watson, R Alan Harris, Amy C Engevik, Numan Oezguen, Maribeth R Nicholson, Sarah Dooley, Rachel Stubler, Lisa Forbes Satter, Lina B Karam, Richard Kellermay |
| Clinical and molecular significance of flow cytometric analysis for reactive oxygen species production and residual p67 expression in p67-deficient chronic granulomatous disease. Scandinavian journal of immunology 2024 4 e13372. Hanae Miyazawa, Masahiro Muraoka, Yusuke Matsuda, Tomoko Toma, Tomohiro Morio, Tomonari Shigemura, Kohei Haraguchi, Tadashi Matsubayashi, Toshinao Kawai, Yuya Shirai, Taizo Wa |
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