Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: CCR1[original query] |
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CCR5Delta32 polymorphism effects on CCR5 expression, patterns of immunopathology and disease course in multiple sclerosis. Journal of neuroimmunology 2005 Dec 169 (1-2): 137-43. Kantarci Orhun H, Morales Yazmín, Ziemer Patricia A, Hebrink David D, Mahad Don J, Atkinson Elizabeth J, Achenbach Sara J, De Andrade Mariza, Mack Matthias, Ransohoff Richard M, Lassmann Hans, Bruck Wolfgang, Weinshenker Brian G, Lucchinetti Claudia |
Genotypes and haplotypes of CCR2 and CCR3 genes in Japanese cedar pollinosis. International archives of allergy and immunology 2007 142 (4): 329-34. Nakamura Hiroyuki, Higashikawa Fumiko, Nobukuni Yoshitaka, Miyagawa Kiyoshi, Endo Tomohiko, Imai Toru, Hatta Kotaro, Ozasa Kotaro, Motohashi Yutaka, Matsuzaki Ichiyo, Sasahara Shinichiro, Ogino Keiki, Akimaru Kunihiro, Eboshida Aki |
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 |
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 |
Single-nucleotide polymorphisms in genes encoding for CC chemokines were not associated with the risk of non-Hodgkin lymphoma. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2013 Jul 22 (7): 1332-5. Chen Qiong, Zheng Tongzhang, Lan Qing, Lerro Catherine, Zhao Nan, Qin Qin, Hu Xiaobin, Huang Huang, Liang Jiaxin, Holford Theodore, Leaderer Brian, Boyle Peter, Chanock Stephen J, Rothman Nathaniel, Zhang Yaw |
Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease. Proceedings of the National Academy of Sciences of the United States of America 2013 May 110 (20): 8134-9. Kirino Yohei, Zhou Qing, Ishigatsubo Yoshiaki, Mizuki Nobuhisa, Tugal-Tutkun Ilknur, Seyahi Emire, Özyazgan Yilmaz, Ugurlu Serdal, Erer Burak, Abaci Neslihan, Ustek Duran, Meguro Akira, Ueda Atsuhisa, Takeno Mitsuhiro, Inoko Hidetoshi, Ombrello Michael J, Satorius Colleen L, Maskeri Baishali, Mullikin James C, Sun Hong-Wei, Gutierrez-Cruz Gustavo, Kim Yoonhee, Wilson Alexander F, Kastner Daniel L, Gül Ahmet, Remmers Elaine |
Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
Nature genetics 2013 Jan . Kirino Y, Bertsias G, Ishigatsubo Y, Mizuki N, Tugal-Tutkun I, Seyahi E, Ozyazgan Y, Sacli FS, Erer B, Inoko H, Emrence Z, Cakar A, Abaci N, Ustek D, Satorius C, Ueda A, Takeno M, Kim Y, Wood GM, Ombrello MJ, Meguro A, Gül A, Remmers EF, Kastner DL |
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 |
A novel predictive approach for GVHD after allogeneic SCT based on clinical variables and cytokine gene polymorphisms. Blood advances 2018 7 2 (14): 1719-1737. Martínez-Laperche Carolina, Buces Elena, Aguilera-Morillo M Carmen, Picornell Antoni, González-Rivera Milagros, Lillo Rosa, Santos Nazly, Martín-Antonio Beatriz, Guillem Vicent, Nieto José B, González Marcos, de la Cámara Rafael, Brunet Salut, Jiménez-Velasco Antonio, Espigado Ildefonso, Vallejo Carlos, Sampol Antonia, Bellón José María, Serrano David, Kwon Mi, Gayoso Jorge, Balsalobre Pascual, Urbano-Izpizua Álvaro, Solano Carlos, Gallardo David, Díez-Martín José Luis, Romo Juan, Buño Ismael, |
GWAS-identified CCR1 and IL10 loci contribute to M1 macrophage-predominant inflammation in Behçet's disease. Arthritis research & therapy 2018 Jun 20 (1): 124. Nakano Hiroto, Kirino Yohei, Takeno Mitsuhiro, Higashitani Kana, Nagai Hideto, Yoshimi Ryusuke, Yamaguchi Yukie, Kato Ikuma, Aoki Ichiro, Nakajima Hidea |
Genetic variants in chemokine CC subfamily genes influence hepatitis C virus viral clearance. Journal of human genetics 2018 Jul 63 (7): 831-839. Yao Yinan, Yue Ming, Zang Feng, Liu Mei, Fan Haozhi, Zhuo Lingyun, Wu Jingjing, Xia Xueshan, Feng Yue, Huang Peng, Yu Rongb |
Genetic Polymorphism at CCL5 Is Associated With Protection in Chagas' Heart Disease: Antagonistic Participation of CCR1 and CCR5 Cells in Chronic Chagasic Cardiomyopathy. Frontiers in immunology 2018 4 9 615. Batista Angelica Martins, Alvarado-Arnez Lucia Elena, Alves Silvia Marinho, Melo Gloria, Pereira Isabela Resende, Ruivo Leonardo Alexandre de Souza, da Silva Andrea Alice, Gibaldi Daniel, da Silva Thayse do E S Protásio, de Lorena Virginia Maria Barros, de Melo Adriene Siqueira, de Araújo Soares Ana Karine, Barros Michelle da Silva, Costa Vláudia Maria Assis, Cardoso Cynthia C, Pacheco Antonio G, Carrazzone Cristina, Oliveira Wilson, Moraes Milton Ozório, Lannes-Vieira Jose |
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 |
Differences in clinical and genetic characteristics between early- and late-onset narcolepsy in a Han Chinese cohort. Neural regeneration research 2020 Oct 15 (10): 1887-1893. Ouyang Hui, Han Fang, Zhou Ze-Chen, Zhang J |
Hypertension delays viral clearance and exacerbates airway hyperinflammation in patients with COVID-19. Nature biotechnology 2020 12 39 (6): 705-716. Trump Saskia, Lukassen Soeren, Anker Markus S, Chua Robert Lorenz, Liebig Johannes, Thürmann Loreen, Corman Victor Max, Binder Marco, Loske Jennifer, Klasa Christina, Krieger Teresa, Hennig Bianca P, Messingschlager Marey, Pott Fabian, Kazmierski Julia, Twardziok Sven, Albrecht Jan Philipp, Eils Jürgen, Hadzibegovic Sara, Lena Alessia, Heidecker Bettina, Bürgel Thore, Steinfeldt Jakob, Goffinet Christine, Kurth Florian, Witzenrath Martin, Völker Maria Theresa, Müller Sarah Dorothea, Liebert Uwe Gerd, Ishaque Naveed, Kaderali Lars, Sander Leif-Erik, Drosten Christian, Laudi Sven, Eils Roland, Conrad Christian, Landmesser Ulf, Lehmann Iri |
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 |
A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study. Journal of molecular neuroscience : MN 2020 11 71 (6): 1284-1289. Padula Maria Carmela, Leccese Pietro, Lascaro Nancy, Padula Angela Anna, Carbone Teresa, Martelli Giuseppe, D'Angelo Salvato |
Rs7853346 Polymorphism in lncRNA-PTENP1 and rs1799864 Polymorphism in CCR2 are Associated with Radiotherapy-Induced Cognitive Impairment in Subjects with Glioma Via Regulating PTENP1/miR-19b/CCR2 Signaling Pathway. Biochemical genetics 2021 11 60 (4): 1159-1176. Yang Sen, Fu Zhan-Zhao, Zhang Yan-Qiu, Fu Bao-Hong, Dong Li-X |
Severe COVID-19 associated variants linked to chemokine receptor gene control in monocytes and macrophages. bioRxiv : the preprint server for biology 2021 Jan . Stikker Bernard, Stik Grégoire, Hendriks Rudi W, Stadhouders Ral |
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 |
Severe COVID-19-associated variants linked to chemokine receptor gene control in monocytes and macrophages. Genome biology 2022 4 23 (1): 96. Stikker Bernard S, Stik Grégoire, van Ouwerkerk Antoinette F, Trap Lianne, Spicuglia Salvatore, Hendriks Rudi W, Stadhouders Ral |
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 |
The Relationship of CCL5 and CCR1 Variants with Response Rate and Survival Taking into Account Thalidomide/Bortezomib Treatment in Patients with Multiple Myeloma. Journal of clinical medicine 2023 3 12 (6): . Popek-Marciniec Sylwia, Styk Wojciech, Wojcierowska-Litwin Magdalena, Szudy-Szczyrek Aneta, Dudek Paul, Swiderska-Kolacz Grazyna, Czerwik-Marcinkowska Joanna, Zmorzynski Szym |
High-expression of the innate-immune related gene UNC93B1 predicts inferior outcomes in acute myeloid leukemia. Frontiers in genetics 2023 2 14 1063227. Li Qiaoli, Pan Hong, Gao Zhen, Li Weiwang, Zhang Lele, Zhao Jingyu, Fang Liwei, Chu Yajing, Yuan Weiping, Shi J |
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- Page last updated:Apr 22, 2024
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