Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: NLRP2[original query] |
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NLRP2, an inhibitor of the NF-kappaB pathway, is transcriptionally activated by NF-kappaB and exhibits a nonfunctional allelic variant. Journal of immunology (Baltimore, Md. : 1950) 2007 Dec 179 (12): 8519-24. Fontalba Ana, Gutierrez Olga, Fernandez-Luna Jose |
Common variants in NLRP2 and NLRP3 genes are strong prognostic factors for the outcome of HLA-identical sibling allogeneic stem cell transplantation. Blood 2008 Nov 112 (10): 4337-42. Granell Miquel, Urbano-Ispizua Alvaro, Pons Aina, Aróstegui Juan Ignacio, Gel Bernat, Navarro Alfons, Jansa Sonia, Artells Rosa, Gaya Anna, Talarn Carme, Fernández-Avilés Francesc, Martínez Carmen, Rovira Montserrat, Carreras Enric, Rozman Ciril, Juan Manel, Yagüe Jordi, Montserrat Emili, Monzó Maria |
A genetic association study of NLRP2 and NLRP7 genes in idiopathic recurrent miscarriage. Human reproduction (Oxford, England) 2013 Jan . Huang JY, Su M, Lin SH, Kuo PL |
Association of polymorphisms in SPARC and NLRP2 genes with rheumatoid arthritis in a Chinese Han population. Modern rheumatology / the Japan Rheumatism Association 2015 Jan 25 (1): 67-71. Yang Xing-lin, Hu Zhong-dan, Wu Qian, Liu Xi, Liu Qi-ji, Zhang Yuan-chao, Yang Qing-r |
No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility. Human reproduction (Oxford, England) 2015 Jan 30 (1): 232-8. Aghajanova L, Mahadevan S, Altmäe S, Stavreus-Evers A, Regan L, Sebire N, Dixon P, Fisher R A, Van den Veyver I |
Impact of CTLA4 genotype and other immune response gene polymorphisms on outcomes after single umbilical cord blood transplantation. Blood 2016 Nov . Cunha Renato, Zago Marco A, Querol Sergio, Volt Fernanda, Ruggeri Annalisa, Sanz Guillermo, Pouthier Fabienne, Kogler Gesine, Vicario José L, Bergamaschi Paola, Saccardi Riccardo, Lamas Carmen H, Díaz-de-Heredia Cristina, Michel Gerard, Bittencourt Henrique, Tavella Marli, Panepucci Rodrigo A, Fernandes Francisco, Pavan Julia, Gluckman Eliane, Rocha Vanders |
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. Epigenetics 2018 9 13 (9): 897-909. Fontana L, Bedeschi M F, Maitz S, Cereda A, Faré C, Motta S, Seresini A, D'Ursi P, Orro A, Pecile V, Calvello M, Selicorni A, Lalatta F, Milani D, Sirchia S M, Miozzo M, Tabano |
Expanding the genetic and phenotypic spectrum of the subcortical maternal complex genes in recurrent preimplantation embryonic arrest. Clinical genetics 2020 10 99 (2): 286-291. Zheng Wei, Hu Huiling, Dai Jing, Zhang Shuoping, Gu Yifan, Dai Can, Guo Jing, Xu Xinxin, Li Yuan, Zhang Shunji, Hu Liang, Gong Fei, Lu Guangxiu, Lin |
Six-gene signature for predicting survival in patients with head and neck squamous cell carcinoma. Aging 2020 Jan 12 (1): 767-783. Wang Juncheng, Chen Xun, Tian Yuxi, Zhu Gangcai, Qin Yuexiang, Chen Xuan, Pi Leiming, Wei Ming, Liu Guancheng, Li Zhexuan, Chen Changhan, Lv Yunxia, Cai Gengmi |
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny. Clinical epigenetics 2022 3 14 (1): 43. Tannorella Pierpaola, Calzari Luciano, Daolio Cecilia, Mainini Ester, Vimercati Alessandro, Gentilini Davide, Soli Fiorenza, Pedrolli Annalisa, Bonati Maria Teresa, Larizza Lidia, Russo Silv |
Identification of Survival-Specific Genes in Clear Cell Renal Cell Carcinoma Using a Customized Next-Generation Sequencing Gene Panel. Journal of personalized medicine 2022 Jan 12 (1): . Hwang Jia, Kim Heeeun, Han Jinseon, Lee Jieun, Hong Sunghoo, Kim Saewoong, Yoon Sungjoo Kim, Choi Keonwoo, Yang Jihoon, Park Unsang, Kim Kwangjoong, Yim Kwangil, Kim Yuil, Choi Yeongj |
Whole exon capture sequencing for identifying mutations associated with pulmonary benign metastasising leiomyoma. BMJ case reports 2023 3 16 (3): . Hu Zhijun, Liu Kaijiang, Liu Qing, Zhu Ho |
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- Page last updated:Apr 22, 2024
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