Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: CD1A[original query] |
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Multifocal motor neuropathy is not associated with genetic variation in PTPN22, BANK1, Blk, FCGR2B, CD1A/E, and TAG-1 genes. Journal of the peripheral nervous system : JPNS 2011 Sep 16 (3): 175-9. Vlam Lotte, Cats Elisabeth A, Seelen Meinie, van Vught Paul W J, van den Berg Leonard H, van der Pol W-Lu |
B-RAF mutant alleles associated with Langerhans cell histiocytosis, a granulomatous pediatric disease. PloS one 2012 7 (4): e33891. Satoh Takeshi, Smith Alexander, Sarde Aurelien, Lu Hui-chun, Mian Syed, Mian Sophie, Trouillet Celine, Mufti Ghulam, Emile Jean-Francois, Fraternali Franca, Donadieu Jean, Geissmann Freder |
CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. PloS one 2012 7 (1): e29872. Barbier Mathieu, Sabbagh Audrey, Kasper Edwige, Asheuer Muriel, Ahouansou Ornella, Pribill Ingrid, Forss-Petter Sonja, Vidaud Michel, Berger Johannes, Aubourg Patri |
The effect of TNF-alpha, Fc?R and CD1 polymorphisms on Guillain-Barré syndrome risk: evidences from a meta-analysis. Journal of neuroimmunology 2012 Feb 243 (1-2): 18-24. Wu Li-Ya, Zhou You, Qin Chao, Hu Bang- |
A polymorphism in human CD1A is associated with susceptibility to tuberculosis. Genes and immunity 0 15 (3): 195-8. Seshadri C, Thuong N T T, Yen N T B, Bang N D, Chau T T H, Thwaites G E, Dunstan S J, Hawn T |
Polymorphism in Exon 2 of CD1 Genes in Southwest of Iran. Iranian journal of public health 2013 42 (7): 775-82. Golmoghaddam Hossein, Arandi Nargess, Ghaderi Abbas, Doroudchi Mehrnoo |
[Clinical and pathologic characteristics of Erdheim-Chester disease]. Zhonghua bing li xue za zhi Chinese journal of pathology 2014 Dec 43 (12): 809-13. Lu Tao, Cao Xinxin, Luo Yufeng, Cai Huacong, Zhang Wei, Zhong Dingro |
Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2015 Jan . Lopez de Lapuente Aitzkoa, Pinto-Medel María Jesús, Astobiza Ianire, Alloza Iraide, Comabella Manuel, Malhotra Sunny, Montalban Xavier, Zettl Uwe K, Rodríguez-Antigüedad Alfredo, Fernández Oscar, Vandenbroeck Ko |
BRAFV600E and MAP2K1 mutations in Langerhans cell histiocytosis occur predominantly in children. Hematological oncology 2016 Sep . Zeng Kaixuan, Ohshima Koichi, Liu Yixiong, Zhang Weichen, Wang Lu, Fan Linni, Li Mingyang, Li Xia, Wang Zhe, Guo Shuangping, Yan Qingguo, Guo Yi |
Polymorphisms in exon 2 of CD1 genes are associated with susceptibility to Guillain-Barré syndrome. Journal of the neurological sciences 2016 Oct 369 39-42. Liu Hongbo, Xing Yanmeng, Guo Yake, Liu Peidong, Zhang Hui, Xue Bing, Shou Jifei, Qian Juanfeng, Peng Jing, Wang Rui, Gao YiWei, Fang Shuy |
[Erdheim-Chester disease (ECD), an inflammatory myeloid neoplasia]. Presse medicale (Paris, France : 1983) 2016 May . Haroche Julien, Papo Matthias, Cohen-Aubart Fleur, Charlotte Frédéric, Maksud Philippe, Grenier Philippe A, Cluzel Philippe, Mathian Alexis, Emile Jean-François, Amoura Zah |
CD1A, D and E gene polymorphisms in a North African population from Morocco. Human immunology 2016 May . Aureli Anna, Oumhani Khadija, Del Beato Tiziana, El Aouad Rajae, Piancatelli Danie |
Recurrent NRAS mutations in pulmonary Langerhans cell histiocytosis. The European respiratory journal 2016 Apr . Mourah Samia, How-Kit Alexandre, Meignin Véronique, Gossot Dominique, Lorillon Gwenaël, Bugnet Emmanuelle, Mauger Florence, Lebbe Celeste, Chevret Sylvie, Tost Jörg, Tazi Abdellat |
Association of IL-12Bpro polymorphism with tumor-infiltrating dendritic cells in colorectal cancer. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 0 22 (4): 888-893. Aleksandrova Elina, Vlaykova Tatyana, Ananiev Julian, Gulubova Ma |
Association of CD1 and Fc?R gene polymorphisms with Guillain-Barré syndrome susceptibility: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2018 Sep . Zhang Liang, Liu Lijun, Li Hong, Guo Lei, Yu Qing, Teng Jij |
A case of interdigitating dendritic cell sarcoma studied by whole-exome sequencing. Genes & genomics 2018 8 40 (12): 1279-1285. Hong Ki Hwan, Song Soyoung, Shin Wonseok, Kang Keunsoo, Cho Chun-Sung, Hong Yong Tae, Han Kyudong, Moon Jeong Hw |
Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations. American journal of ophthalmology case reports 2018 2 9 10-13. Meyer Peter, Graeff Elisabeth, Kohler Corina, Munier Francis, Bruder Elisabe |
Ethnic differences in CD1E, but not CD1A, gene polymorphisms between Sub-Saharan Africans, West Asians and Europeans. Human immunology 2019 Mar 80 (3): 204-207. Mombo Landry Erik, Ramasawmy Rajendranath, Zertal-Zidani Samia, Charron Dominique, Tamouza Ry |
CD1A and CD1E gene polymorphisms are not associated with susceptibility to Guillain-Barré syndrome in the Bangladeshi population. Journal of neuroimmunology 2018 Jan 314 8-12. Rahman Mohammad I, Jahan Iffat, Khalid Mir M, Jahan Israt, Ahammad Rijwan U, Nahar Shamsun, Islam Zhahir |
[Rosai-Dorfman disease: a clinicopathologic analysis and whole exome sequencing in 23 cases]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2019 9 40 (8): 656-661. Fu W J, Du J, Lu J, Wang L Z, Yang J M, He M X, Hu X |
Guillain-Barre syndrome outbreak in Peru: Association with polymorphisms in IL-17, ICAM1, and CD1. Molecular genetics & genomic medicine 2019 Aug e960. Jaramillo-Valverde Luis, Levano Kelly S, Villanueva Isolina, Hidalgo Meylin, Cornejo Marco, Mazzetti Pilar, Cornejo-Olivas Mario, Sanchez Cesar, Poterico Julio A, Valdivia-Silva Julio, Guio Heinn |
Genome-wide association study identifies CD1A associated with rate of increase in plasma neurofilament light in non-demented elders.
Aging 2019 Jul 11 . Wang Zuo-Teng, Chen Shi-Dong, Xu Wei, Chen Ke-Liang, Wang Hui-Fu, Tan Chen-Chen, Cui Mei, Dong Qiang, Tan Lan, Yu Jin-Tai, |
Association between genetic variants in CD1A and CD1D genes and pulmonary tuberculosis in an Iranian population. Biomedical reports 2019 Apr 10 (4): 259-265. Taheri Mohsen, Danesh Hiva, Bizhani Fatemeh, Bahari Gholamreza, Naderi Mohammad, Hashemi Mohamm |
CD1 gene polymorphism and susceptibility to celiac disease: Association of CD1E*02/02 in Moroccans. Human immunology 2020 May . Aureli Anna, Aboulaghras Sara, Oumhani Khadija, Del Beato Tiziana, Sebastiani Pierluigi, Colanardi Alessia, El Aouad Rajae, Ben El Barhdadi Imane, Piancatelli Danie |
Rosai-Dorfman Disease Displays a Unique Monocyte-Macrophage Phenotype Characterized by Expression of OCT2. The American journal of surgical pathology 2020 11 45 (1): 35-44. Ravindran Aishwarya, Goyal Gaurav, Go Ronald S, Rech Karen L, |
A study of pathological characteristics and BRAF V600E status in Langerhans cell histiocytosis of Vietnamese children. Journal of pathology and translational medicine 2021 Jan . Phan Thu Dang Anh, Phung Bao Gia, Duong Tu Thanh, Hoang Vu Anh, Ngo Dat Quoc, Trinh Nguyen Dinh The, Tran Tung Tha |
Clinicogenomic associations in childhood Langerhans cell histiocytosis: an international cohort study. Blood advances 2022 Sep . Kemps Paul G, Zondag Timo C E, Arnardóttir Helga B, Solleveld-Westerink Nienke, Borst Jelske, Steenwijk Eline C, van Egmond Demi, Swennenhuis Joost F, Stelloo Ellen, Trambusti Irene, Verdijk Robert M, van Noesel Carel J M, Cleven Arjen H G, Scheijde-Vermeulen Marijn A, Koudijs Marco J, Krsková Lenka, Hawkins Cynthia, Egeler R Maarten, Brok Jesper, von Bahr Greenwood Tatiana, Svojgr Karel, Beishuizen Auke, van Laar Jan A M, Pötschger Ulrike, Hutter Caroline, Sieni Elena, Minkov Milen, Abla Oussama, van Wezel Tom, van den Bos Cor, van Halteren Astrid G |
Integrated clinical genotype-phenotype characteristics of early T-cell precursor acute lymphoblastic leukemia. Cancer 2022 Oct . Ye Matthew T, Wang Yi, Zuo Zhuang, Calin Steliana, He Hua, Tang Zhenya, Jabbour Elias J, Borthakur Gautam, Zhang Yizhuo, Yang Yaling, You M Jam |
Tumor Necrosis Factor-?, CD1A and CD1E Genetic Polymorphisms in Guillain-Barré Syndrome: A Study from India. Annals of Indian Academy of Neurology 2023 5 26 (2): 167-173. Rajarshi Chakraborty, Rajesh Verma, Amita Jain, Ravindra K Garg, Virendra Atam, Hardeep S Malhotra, Praveen K Sharma, Shantanu Prakash, Neeraj Kumar, Shweta Pandey, Ravi Uniyal, Imran Riz |
The Role of CD1 Gene Polymorphism in the Genetic Susceptibility to Spondyloarthropathies in the Moroccan Population and the Possible Cross-Link with Celiac Disease. Vaccines 2023 2 11 (2): . Canossi Angelica, Oumhani Khadija, Del Beato Tiziana, Sebastiani Pierluigi, Colanardi Alessia, Aureli An |
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- Page last updated:Apr 22, 2024
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