Human Genome Epidemiology Literature Finder
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Records 1 - 29 (of 29 Records) |
| Query Trace: Disease and CCR3[original query] |
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| Association of genetic variants of the chemokine receptor CCR5 and its ligands, RANTES and MCP-2, with outcome of HCV infection. Hepatology (Baltimore, Md.) 2003 Dec 38 (6): 1468-76. Hellier Simon, Frodsham Angela J, Hennig Branwen J W, Klenerman Paul, Knapp Suzanne, Ramaley Patricia, Satsangi Jack, Wright Mark, Zhang Lyna, Thomas Howard C, Thursz Mark, Hill Adrian V |
| Frequency of polymorphisms of genes coding for HIV-1 co-receptors CCR5 and CCR2 in a Brazilian population. The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases 2003 Aug 7 (4): 236-40. Munerato Patrícia, Azevedo Maria Lúcia, Sucupira Maria Cecília Araripe, Pardini Regina, Pinto Gedson Humberto Novaes, Catroxo Márcia, Souza Inara Espinelli, Diaz Ricardo Sobh |
| Association of interleukin 10 haplotype with low bone mineral density in Korean postmenopausal women. Journal of biochemistry and molecular biology 2004 Nov 37 (6): 691-9. Park Byung Lae, Han In Kwon, Lee Ho Sa, Kim Lyoung Hyo, Kim Sa Jin, Shin Joon-Shik, Kim Shin-Yoon, Shin Hyoung D |
| Polymorphisms in chemokine receptor genes and susceptibility to Kawasaki disease. Clinical and experimental immunology 2007 Oct 150 (1): 83-90. Breunis W B, Biezeveld M H, Geissler J, Kuipers I M, Lam J, Ottenkamp J, Hutchinson A, Welch R, Chanock S J, Kuijpers T |
| Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease. Journal of medical genetics 2009 Jan 46 (1): 60-3. Romanos J, Barisani D, Trynka G, Zhernakova A, Bardella M T, Wijmenga |
| Association of four-locus gene interaction with aspirin-intolerant asthma in Korean asthmatics. Journal of clinical immunology 2008 Jul 28 (4): 336-42. Kim Seung-Hyun, Jeong Hyun-Hwan, Cho Bo-Young, Kim Myoungki, Lee Hyun-Young, Lee Jungseob, Wee Kyubum, Park Hae-S |
Newly identified genetic risk variants for celiac disease related to the immune response.
Nature genetics 2008 Apr 40 (4): 395-402. Hunt Karen A, Zhernakova Alexandra, Turner Graham, Heap Graham A R, Franke Lude, Bruinenberg Marcel, Romanos Jihane, Dinesen Lotte C, Ryan Anthony W, Panesar Davinder, Gwilliam Rhian, Takeuchi Fumihiko, McLaren William M, Holmes Geoffrey K T, Howdle Peter D, Walters Julian R F, Sanders David S, Playford Raymond J, Trynka Gosia, Mulder Chris J J, Mearin M Luisa, Verbeek Wieke H M, Trimble Valerie, Stevens Fiona M, O'Morain Colm, Kennedy Nicholas P, Kelleher Dermot, Pennington Daniel J, Strachan David P, McArdle Wendy L, Mein Charles A, Wapenaar Martin C, Deloukas Panos, McGinnis Ralph, McManus Ross, Wijmenga Cisca, van Heel David |
| Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort. Genes and immunity 2010 Jan 11 (1): 79-86. Amundsen S S, Rundberg J, Adamovic S, Gudjónsdóttir A H, Ascher H, Ek J, Nilsson S, Lie B A, Naluai A T, Sollid L |
| Association of IL18RAP and CCR3 with coeliac disease in the Spanish population. Journal of medical genetics 2009 Jun . Dema B, Martínez A, Fernández-Arquero M, Maluenda C, Polanco I, G de la Concha E, Urcelay E, Núñez C |
| The -17 T/C chemokine receptor 3 genetic polymorphism is associated asthma but not atopy: transmission and association studies. The Egyptian journal of immunology / Egyptian Association of Immunologists 2009 16 (1): 83-93. Al-Abdulhadi S A, Al-Rabia M |
| Revisiting genome wide association studies (GWAS) in coeliac disease: replication study in Spanish population and expression analysis of candidate genes. Journal of medical genetics 2011 Jul 48 (7): 493-6. Plaza-Izurieta Leticia, Castellanos-Rubio Ainara, Irastorza Iñaki, Fernández-Jimenez Nora, Gutierrez Galder, , Bilbao Jose Ram |
| Role of exonic variation in chemokine receptor genes on AIDS: CCRL2 F167Y association with pneumocystis pneumonia. PLoS genetics 2011 Oct 7 (10): e1002328. An Ping, Li Rongling, Wang Ji Ming, Yoshimura Teizo, Takahashi Munehisa, Samudralal Ram, O'Brien Stephen J, Phair John, Goedert James J, Kirk Gregory D, Troyer Jennifer L, Sezgin Efe, Buchbinder Susan P, Donfield Sharyne, Nelson George W, Winkler Cheryl |
| Improving the estimation of celiac disease sibling risk by non-HLA genes. PloS one 2011 6 (11): e26920. Izzo Valentina, Pinelli Michele, Tinto Nadia, Esposito Maria Valeria, Cola Arturo, Sperandeo Maria Pia, Tucci Francesca, Cocozza Sergio, Greco Luigi, Sacchetti Luc |
| Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behçet's disease susceptibility. Human genetics 2012 Jul . Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P |
| The genetics of Behçet's disease in a Chinese population. Frontiers of medicine 2012 Nov . Hou S, Kijlstra A, Yang P |
| Eotaxin/CCL11 in idiopathic retroperitoneal fibrosis. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2012 Oct 27 (10): 3875-84. Mangieri Domenica, Corradi Domenico, Martorana Davide, Malerba Giovanni, Palmisano Alessandra, Libri Irene, Bartoli Veronica, Carnevali Maria L, Goldoni Matteo, Govoni Paolo, Alinovi Rossella, Buzio Carlo, Vaglio Augus |
| Clinical course of patients with aspirin-exacerbated respiratory disease: can we predict the prognosis? Pharmacogenomics 2014 Mar 15 (4): 449-57. Kim Joo-Hee, Choi Gil-Soon, Kim Jeong-Eun, Jin Hyun-Jung, Ye Young-Min, Kim Seung-Hyun, Park Hae-S |
| Systematic review and meta-analysis of the association between IL18RAP rs917997 and CCR3 rs6441961 polymorphisms with celiac disease risks. Expert review of gastroenterology & hepatology 2015 Oct 9 (10): 1327-38. Yang Guang, Zhang Baohuan, Huang Weihuang, Zhang Na, Dong Fang, Jing Lipeng, Wang Man, Liu Yang, Guo Congcong, Pan Hongwei, Wei Xiangcai, Jing Chunx |
| A polymorphism in CCR1/CCR3 is associated with narcolepsy.
Brain, behavior, and immunity 2015 Oct 49 148-55. Toyoda Hiromi, Miyagawa Taku, Koike Asako, Kanbayashi Takashi, Imanishi Aya, Sagawa Yohei, Kotorii Nozomu, Kotorii Tatayu, Hashizume Yuji, Ogi Kimihiro, Hiejima Hiroshi, Kamei Yuichi, Hida Akiko, Miyamoto Masayuki, Imai Makoto, Fujimura Yota, Tamura Yoshiyuki, Ikegami Azusa, Wada Yamato, Moriya Shunpei, Furuya Hirokazu, Takeuchi Masaki, Kirino Yohei, Meguro Akira, Remmers Elaine F, Kawamura Yoshiya, Otowa Takeshi, Miyashita Akinori, Kashiwase Koichi, Khor Seik-Soon, Yamasaki Maria, Kuwano Ryozo, Sasaki Tsukasa, Ishigooka Jun, Kuroda Kenji, Kume Kazuhiko, Chiba Shigeru, Yamada Naoto, Okawa Masako, Hirata Koichi, Mizuki Nobuhisa, Uchimura Naohisa, Shimizu Tetsuo, Inoue Yuichi, Honda Yutaka, Mishima Kazuo, Honda Makoto, Tokunaga Katsus |
| Prediction of susceptible biomarkers for end stage renal disease among North Indians. Nephrology (Carlton, Vic.) 2015 Sep . Prakash Swayam, Sarangi Aditya Narayan, Tripathi Gaurav, Sharma Raj Kumar, Agrawal Suraks |
| HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes. PloS one 2017 11 12 (11): e0188402. Parkkola Anna, Laine Antti-Pekka, Karhunen Markku, Härkönen Taina, Ryhänen Samppa J, Ilonen Jorma, Knip Mikael, |
| Epigenome-wide association study of DNA methylation in narcolepsy: an integrated genetic and epigenetic approach. Sleep 2018 2 41 (4): . Shimada Mihoko, Miyagawa Taku, Toyoda Hiromi, Tokunaga Katsushi, Honda Mako |
| Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis. Proceedings of the National Academy of Sciences of the United States of America 2020 6 117 (25): 14405-14411. Manthiram Kalpana, Preite Silvia, Dedeoglu Fatma, Demir Selcan, Ozen Seza, Edwards Kathryn M, Lapidus Sivia, Katz Alexander E, , Feder Henry M, Lawton Maranda, Licameli Greg R, Wright Peter F, Le Julie, Barron Karyl S, Ombrello Amanda K, Barham Beverly, Romeo Tina, Jones Anne, Srinivasalu Hemalatha, Mudd Pamela A, DeBiasi Roberta L, Gül Ahmet, Marshall Gary S, Jones Olcay Y, Chandrasekharappa Settara C, Stepanovskiy Yuriy, Ferguson Polly J, Schwartzberg Pamela L, Remmers Elaine F, Kastner Daniel |
| A comprehensive overview on the genetics of Behçet's disease. International reviews of immunology 2020 Dec 1-64. Mahmoudi Mahdi, Aslani Saeed, Meguro Akira, Akhtari Maryam, Fatahi Yousef, Mizuki Nobuhisa, Shahram Farh |
| Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.
Arthritis & rheumatology (Hoboken, N.J.) 2021 Jan . Ortiz Fernández Lourdes, Coit Patrick, Yilmaz Vuslat, Yentür Sibel P, Alibaz-Oner Fatma, Aksu Kenan, Erken Eren, Düzgün Nursen, Keser Gokhan, Cefle Ayse, Yazici Ayten, Ergen Andac, Alpsoy Erkan, Salvarani Carlo, Casali Bruno, Kisacik Bünyamin, Kötter Ina, Henes Jörg, Çinar Muhammet, Schaefer Arne, Nohutcu Rahime M, Zhernakova Alexandra, Wijmenga Cisca, Takeuchi Fujio, Harihara Shinji, Kaburaki Toshikatsu, Messedi Meriam, Song Yeong-Wook, Kasifoglu Timuçin, Carmona F David, Guthridge Joel M, James Judith A, Martin Javier, González Escribano María Francisca, Saruhan-Direskeneli Güher, Direskeneli Haner, Sawalha Amr |
| The rs13075270 and rs13092160 polymorphisms of CCR1 and CCR3 genes on oral aphthous-like lesions in PFAPA syndrome. Cellular and molecular biology (Noisy-le-Grand, France) 2022 Jan 67 (4): 328-333. Li Weiwei, Li Na, Yang Guohai, Li Yanh |
| COVID-19 in pediatrics: Genetic susceptibility.
Frontiers in genetics 2022 9 13 928466. Glessner Joseph T, Chang Xiao, Mentch Frank, Qu Huiqi, Abrams Debra J, Thomas Alexandria, Sleiman Patrick M A, Hakonarson Hak |
| Main Polymorphisms in Aspirin-Exacerbated Respiratory Disease. Gene 2023 4 147326. Fathollahpour Aida, Abdi Abyaneh Fahimeh, Darabi Behzad, Ebrahimi Mohsen, Kooti Wesam, Nasiri Kalmarzi Raso |
| Association of LPP and ZMIZ1 Gene Polymorphism with Celiac Disease in Subjects from Punjab, Pakistan. Genes 2024 7 15 (7): . Sumaira Zulfiqar, Amna Fiaz, Waqas Ahmed Khan, Misbah Hussain, Ansar Ali, Nadeem Ahmed, Basharat Ali, Muhammad Adnan Maso |
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