首页> 外文OA文献 >Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 ( NLRP3 ) Gene

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Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 ( NLRP3 ) Gene

机译：Keratoendothelienis fugax噬菌体：一种新的核苷酸结合结构域，富含亮氨酸的重复系列，含吡林域的3（NLRP3）基因引起的新型乳蛋白相关的周期性综合征

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Joni A. Turunen; Juho Wedenoja; Pauliina Repo; Reetta-Stiina Järvinen; Johannes E. Jäntti; Sanna Mörtenhumer; Antti S. Riikonen; Anna-Elina Lehesjoki; Anna Majander; Tero T. Kivelä;
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1. Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 ( NLRP3 ) Gene [J] . Joni A. Turunen, Juho Wedenoja, Pauliina Repo, American Journal of Ophthalmology: The International Journal of Ophthalmology . 2018,第期

机译：Keratoendothelienis fugax噬细胞：一种新的核苷酸结合结构域，富含亮氨酸的重复系列，含吡林域的3（NLRP3）基因引起的新型乳蛋白相关的周期性综合征
2. Activation of Autophagy and Nucleotide-Binding Cross Mark Domain Leucine-Rich Repeat-Containing-Like Receptor Family, Pyrin Domain-Containing 3 Inflammasome during Leishmania infantum-Associated Glomerulonephritis [J] . Esch Kevin J., Schaut Robert G., Lamb Ian M., American Journal of Pathology: Official Publication of the American Association of Pathologists . 2015,第8期

机译：婴儿利什曼原虫相关性肾小球肾炎期间自噬和核苷酸结合十字标记域富含亮氨酸的重复序列样受体家族，含吡喃结构域的3炎性体的激活。
3. Activation of Autophagy and Nucleotide-Binding Domain Leucine-Rich Repeat-Containing-Like Receptor Family, Pyrin Domain-Containing 3 Inflammasome during Leishmania infantum-Associated Glomerulonephritis [J] . Kevin J. Esch, Robert G. Schaut, Ian M. Lamb, The American journal of pathology. . 2015,第8期

机译：婴儿利什曼原虫相关性肾小球肾炎期间自噬和核苷酸结合域富含亮氨酸的重复序列样受体家族，含吡喃结构域的3炎性体的激活。
4. Monocytes from patients with rheumatoid arthritis and type 2 diabetes mellitus display an increased production of interleukin (IL)-1β via the nucleotide-binding domain and leucine-rich repeat containing family pyrin 3(NLRP3)-inflammasome activation: a possible implication for therapeutic decision in these patients [O] . P Ruscitti, P Cipriani, P Di Benedetto, 2015

机译：类风湿性关节炎和2型糖尿病患者的单核细胞通过核苷酸结合结构域和富含亮氨酸的重复序列家族3（NLRP3）-炎症小体活化显示出白介素（IL）-1β的增加：可能是治疗决策的暗示在这些病人中
5. Keratoendotheliitis fugax hereditaria is caused by a mutation in the NLRP3 gene [O] . 2018

机译：Keratoendotheliitis fugax噬菌体是由NLRP3基因的突变引起的

Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 ( NLRP3 ) Gene

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