Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: CR2[original query] |
---|
Polymeric immunoglobulin receptor polymorphisms and risk of nasopharyngeal cancer. BMC genetics 2003 Jan 4 (): 3. Hirunsatit Rungnapa, Kongruttanachok Narisorn, Shotelersuk Kanjana, Supiyaphun Pakpoom, Voravud Narin, Sakuntabhai Anavaj, Mutirangura Apiw |
Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosus. Proceedings of the National Academy of Sciences of the United States of America 2007 Mar 104 (10): 3961-6. Wu Hui, Boackle Susan A, Hanvivadhanakul Punchong, Ulgiati Daniela, Grossman Jennifer M, Lee Youngho, Shen Nan, Abraham Lawrence J, Mercer Timothy R, Park Elly, Hebert Lee A, Rovin Brad H, Birmingham Dan J, Chang Deh-Ming, Chen Chung Jen, McCurdy Deborah, Badsha Humeira M, Thong Bernard Y H, Chng Hiok H, Arnett Frank C, Wallace Daniel J, Yu C Yung, Hahn Bevra H, Cantor Rita M, Tsao Betty |
Analysis of variation in NF-kappaB genes and expression levels of NF-kappaB-regulated molecules. BMC proceedings 2007 1 Suppl 1 S126. Liu-Mares Wen, Sun Zhifu, Bamlet William R, Atkinson Elizabeth J, Fridley Brooke L, Slager Susan L, de Andrade Mariza, Goode Ellen |
Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus. Rheumatology (Oxford, England) 2008 Feb 47 (2): 158-64. Miyagawa H, Yamai M, Sakaguchi D, Kiyohara C, Tsukamoto H, Kimoto Y, Nakamura T, Lee J-H, Tsai C-Y, Chiang B-L, Shimoda T, Harada M, Tahira T, Hayashi K, Horiuchi |
Complement receptor 2 polymorphisms associated with systemic lupus erythematosus modulate alternative splicing. Genes and immunity 2009 Jul 10 (5): 457-69. Douglas K B, Windels D C, Zhao J, Gadeliya A V, Wu H, Kaufman K M, Harley J B, Merrill J, Kimberly R P, Alarcón G S, Brown E E, Edberg J C, Ramsey-Goldman R, Petri M, Reveille J D, Vilá L M, Gaffney P M, James J A, Moser K L, Alarcón-Riquelme M E, Vyse T J, Gilkeson G S, Jacob C O, Ziegler J T, Langefeld C D, Ulgiati D, Tsao B P, Boackle S |
Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation. Human mutation 2010 1 31 (3): 284-94. Kobayashi Tomoko, Aoki Yoko, Niihori Tetsuya, Cavé Hélène, Verloes Alain, Okamoto Nobuhiko, Kawame Hiroshi, Fujiwara Ikuma, Takada Fumio, Ohata Takako, Sakazume Satoru, Ando Tatsuya, Nakagawa Noriko, Lapunzina Pablo, Meneses Antonio G, Gillessen-Kaesbach Gabriele, Wieczorek Dagmar, Kurosawa Kenji, Mizuno Seiji, Ohashi Hirofumi, David Albert, Philip Nicole, Guliyeva Afag, Narumi Yoko, Kure Shigeo, Tsuchiya Shigeru, Matsubara Yoic |
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 |
The prognostic impact of FLT3-ITD and NPM1 mutations in patients with relapsed acute myeloid leukemia and intermediate-risk cytogenetics. Blood cancer journal 2013 3 e116. How J, Sykes J, Minden M D, Gupta V, Yee K W L, Schimmer A D, Schuh A C, Kamel-Reid S, Brandwein J |
Functional polymorphism in the 5'-UTR of CR2 is associated with susceptibility to nasopharyngeal carcinoma. Oncology reports 2013 Jul 30 (1): 11-6. Fan Qin, He Jun-Fang, Wang Qi-Rui, Cai Hong-Bing, Sun Xue-Gang, Zhou Xin-Xi, Qin Hai-De, Shugart Yin Yao, Jia Wei-H |
Maternal coding variants in complement receptor 1 and spontaneous idiopathic preterm birth. Human genetics 2013 Aug 132 (8): 935-42. McElroy Jude J, Gutman Courtney E, Shaffer Christian M, Busch Tamara D, Puttonen Hilkka, Teramo Kari, Murray Jeffrey C, Hallman Mikko, Muglia Louis |
Univariate and multiple linear regression analyses for 23 single nucleotide polymorphisms in 14 genes predisposing to chronic glomerular diseases and IgA nephropathy in Han Chinese. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 2014 Sep 25 (5): 992-7. Wang Hui, Sui Weiguo, Xue Wen, Wu Junyong, Chen Jiejing, Dai Yo |
Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA. Annals of the rheumatic diseases 2014 Sep . Zhao Jian, Giles Brendan M, Taylor Rhonda L, Yette Gabriel A, Lough Kara M, Ng Han Leng, Abraham Lawrence J, Wu Hui, Kelly Jennifer A, Glenn Stuart B, Adler Adam J, Williams Adrienne H, Comeau Mary E, Ziegler Julie T, Marion Miranda, Alarcón-Riquelme Marta E, , Alarcón Graciela S, Anaya Juan-Manuel, Bae Sang-Cheol, Kim Dam, Lee Hye-Soon, Criswell Lindsey A, Freedman Barry I, Gilkeson Gary S, Guthridge Joel M, Jacob Chaim O, James Judith A, Kamen Diane L, Merrill Joan T, Sivils Kathy Moser, Niewold Timothy B, Petri Michelle A, Ramsey-Goldman Rosalind, Reveille John D, Scofield R Hal, Stevens Anne M, Vilá Luis M, Vyse Timothy J, Kaufman Kenneth M, Harley John B, Langefeld Carl D, Gaffney Patrick M, Brown Elizabeth E, Edberg Jeffrey C, Kimberly Robert P, Ulgiati Daniela, Tsao Betty P, Boackle Susan |
Association of complement receptor 2 polymorphisms with innate resistance to HIV-1 infection. Genes and immunity 2015 Mar 16 (2): 134-41. Herrero R, Real L M, Rivero-Juárez A, Pineda J A, Camacho Á, Macías J, Laplana M, Konieczny P, Márquez F J, Souto J C, Soria J M, Saulle I, Lo Caputo S, Biasin M, Rivero A, Fibla J, Caruz |
Association of Complement Receptor 2 Gene Polymorphisms with Susceptibility to Osteonecrosis of the Femoral Head in Systemic Lupus Erythematosus. BioMed research international 2016 2016 9208035. Kim Tae-Ho, Bae Sang-Cheol, Lee Sang-Han, Kim Shin-Yoon, Baek Seung-Ho |
5'UTR +24T>C CR2 is not associated with nasopharyngeal carcinoma development in the North Region of Portugal. Oral diseases 2016 Jan . Sousa Hugo, Bastos Maria José, Ribeiro Joana, Oliveira Sara, Breda Eduardo, Catarino Raquel, Medeiros R |
Sparking Fire Under the Skin? Answers From the Association of Complement Genes With Pemphigus Foliaceus. Frontiers in immunology 2018 9 695. Bumiller-Bini Valéria, Cipolla Gabriel Adelman, de Almeida Rodrigo Coutinho, Petzl-Erler Maria Luiza, Augusto Danillo Gardenal, Boldt Angelica Beate Wint |
Extramedullary relapses after allogeneic stem cell transplantation for acute myeloid leukemia: clinical characteristics, incidence, risk factors and outcomes. Bone marrow transplantation 2018 1 53 (7): 838-843. Alhashim Noura, Aljurf Mahmoud, Hassanein Mona, Chaudhri Naeem, Hashmi Shahrukh, El-Gohary Ghada, Alsharif Fahad, Alsermani Maamoun, Alhumaid Muhned, Beihany Amal Al, Shaheen Marwan, Hanbali Amr, Alfraih Feras, Mohamed Said, Alzahrani Hazzaa, Elhassan Tusneem, Eldali Abdelmoneim, Rasheed Walid, Ahmed Syed, Almohareb Fahad, El Fakih Ri |
Association of Epstein-Barr virus serological reactivation with transitioning to systemic lupus erythematosus in at-risk individuals. Annals of the rheumatic diseases 2019 Jun . Jog Neelakshi R, Young Kendra A, Munroe Melissa E, Harmon Michael T, Guthridge Joel M, Kelly Jennifer A, Kamen Diane L, Gilkeson Gary S, Weisman Michael H, Karp David R, Gaffney Patrick M, Harley John B, Wallace Daniel J, Norris Jill M, James Judith |
Association of complement C3d receptor 2 genotypes with the acquisition of HIV infection in a trial of recombinant glycoprotein 120 vaccine. AIDS (London, England) 2019 Oct . Meza Giovanna, Expósito Almudena, Royo José L, Ruiz-García Celia, Sánchez-Arcas Beatriz, Marquez Francisco J, Gómez-Vidal María A, Omar Mohamed, Sinangil Faruk, Higgins Keith, Forthal Donald, Real Luis M, Caruz Anton |
Gene testing for osteonecrosis of the femoral head in systemic lupus erythematosus using targeted next-generation sequencing: A pilot study. World journal of clinical cases 2020 7 8 (12): 2530-2541. Sun Hong-Sheng, Yang Qing-Rui, Bai Yan-Yan, Hu Nai-Wen, Liu Dong-Xia, Qin Cheng-Yo |
Pre-transplant FLT3/ITD status predicts outcome in FLT3-mutated acute myeloid leukemia following allogeneic stem cell transplantation. Annals of hematology 2020 Apr . Helbig Grzegorz, Kocl?ga Anna, Wieczorkiewicz-Kabut Agata, Wo?niczka Krzysztof, Kopi?ska Anna, Boral Kinga, Grygoruk-Wi?niowska Iwona, Stachowicz Ma?gorzata, Karolczyk Agniesz |
A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders. Current Alzheimer research 2020 Nov . El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Na |
Allogeneic HCT for adults with B-cell precursor acute lymphoblastic leukemia harboring IKZF1 gene mutations. A study by the Acute Leukemia Working Party of the EBMT. Bone marrow transplantation 2020 11 56 (5): 1047-1055. Giebel Sebastian, Labopin Myriam, Socié Gerard, Beauvais David, Klein Stefan, Wagner-Drouet Eva Maria, Blaise Didier, Nguyen-Quoc Stephanie, Bourhis Jean Henri, Thiebaut Anne, Labussière-Wallet Hélène, Charbonnier Amandine, Berceanu Ana, Diez-Martin José Luis, Fegueux Nathalie, Esteve Jordi, Nagler Arnon, Mohty Moham |
Genetic variants of the EGFR ligand-binding domain and their association with structural alterations in Arab cancer patients. BMC research notes 2021 Apr 14 (1): 146. Marzouq Maryam, Nairouz Ali, Ben Khalaf Noureddine, Bourguiba-Hachemi Sonia, Quaddorah Raed, Ashoor Dana, Fathallah M Dahma |
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID). Scientific reports 2021 Apr 11 (1): 8308. Bisgin Atil, Sonmezler Ozge, Boga Ibrahim, Yilmaz Musta |
Additional impact of mutational genotype on prognostic determination in resistant and relapsed acute myeloid leukaemia. Leukemia research 2021 3 108 106553. Linch David C, Hills Robert K, Gilkes Amanda, Burnett Alan K, Russell Nigel, Gale Rosemary |
Phylogenomic Analysis of Human Papillomavirus Type 31 and Cervical Carcinogenesis: A Study of 2093 Viral Genomes. Viruses 2021 Sep 13 (10): . Pinheiro Maisa, Harari Ariana, Schiffman Mark, Clifford Gary M, Chen Zigui, Yeager Meredith, Cullen Michael, Boland Joseph F, Raine-Bennett Tina, Steinberg Mia, Bass Sara, Xiao Yanzi, Tenet Vanessa, Yu Kai, Zhu Bin, Burdett Laurie, Turan Sevilay, Lorey Thomas, Castle Philip E, Wentzensen Nicolas, Burk Robert D, Mirabello Li |
Comprehensive profiling of 1015 patients' exomes reveals genomic-clinical associations in colorectal cancer. Nature communications 2022 4 13 (1): 2342. Zhao Qi, Wang Feng, Chen Yan-Xing, Chen Shifu, Yao Yi-Chen, Zeng Zhao-Lei, Jiang Teng-Jia, Wang Ying-Nan, Wu Chen-Yi, Jing Ying, Huang You-Sheng, Zhang Jing, Wang Zi-Xian, He Ming-Ming, Pu Heng-Ying, Mai Zong-Jiong, Wu Qi-Nian, Long Renwen, Zhang Xiaoni, Huang Tanxiao, Xu Mingyan, Qiu Miao-Zheng, Luo Hui-Yan, Li Yu-Hong, Zhang Dong-Shen, Jia Wei-Hua, Chen Gong, Ding Pei-Rong, Li Li-Ren, Lu Zheng-Hai, Pan Zhi-Zhong, Xu Rui-H |
Measurable residual disease, FLT3-ITD mutation, and disease status have independent prognostic influence on outcome of allogeneic stem cell transplantation in NPM1-mutated acute myeloid leukemia. Cancer medicine 2022 Feb 11 (4): 1068-1080. Al Hamed Rama, Labopin Myriam, Daguindau Etienne, Niittyvuopio Riitta, Huynh Anne, Socié Gerard, Srour Micha, Henri Bourhis Jean, Kröger Nicolaus, Tholouli Eleni, Choi Goda, Poiré Xavier, Martin Hans, Rubio Marie-Thérèse, Jindra Pavel, Blaise Didier, Beelen Dietrich, Labussière-Wallet Hélène, Nagler Arnon, Bazarbachi Ali, Mohty Moham |
Complement receptor type 1 and 2 (CR1 and CR2) gene polymorphisms and plasma protein levels are associated with the Dengue disease severity. Scientific reports 2023 10 13 (1): 17377. Nguy Thi Diep, Ngo Truong Giang, Nguyen Thi Thuy Diu, Nguyen Minh Nam, Le Van Khanh, Ha Van Quang, Ngo Thu Hang, Can Van Mao, Ho Van Son, Nguyen Lan Hieu, Phan Tung Linh, Ella H Sklan, Nguyen Linh Toan, Hoang Van To |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: