COMMON VARIABLE IMMUNODEFICIENCY AND EARLY-ONSET AUTOIMMUNE MANIFESTATIONS ASSOCIATED WITH COUPLED MUTATIONS IN NFKB2 AND STAT5A GENES

Maccari Maria-Elena; Floris Matteo; Corrente Stefania; Angius Andrea; Sartirana Claudia; Di Cesare Silvia; Rosenberg Jacob M.; Utz Paul J.; Bulfone Alessandro; Angelini Federica; Fierabracci Alessandra; Cambiaso Paola; Aiuti Alessandro; Cappa Marco; Cancrini Caterina; Bacchetta Rosa

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COMMON VARIABLE IMMUNODEFICIENCY AND EARLY-ONSET AUTOIMMUNE MANIFESTATIONS ASSOCIATED WITH COUPLED MUTATIONS IN NFKB2 AND STAT5A GENES

机译：NFKB2和STAT5A基因突变共同引起的常见可变免疫缺陷和早期自动免疫表现

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《Journal of Clinical Immunology》 |2015年第3期|共1页
作者
Maccari Maria-Elena; Floris Matteo; Corrente Stefania; Angius Andrea; Sartirana Claudia; Di Cesare Silvia; Rosenberg Jacob M.; Utz Paul J.; Bulfone Alessandro; Angelini Federica; Fierabracci Alessandra; Cambiaso Paola; Aiuti Alessandro; Cappa Marco; Cancrini Caterina; Bacchetta Rosa;
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正文语种 eng
中图分类医学免疫学;
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1. COMMON VARIABLE IMMUNODEFICIENCY AND EARLY-ONSET AUTOIMMUNE MANIFESTATIONS ASSOCIATED WITH COUPLED MUTATIONS IN NFKB2 AND STAT5A GENES [J] . Maccari Maria-Elena, Floris Matteo, Corrente Stefania, Journal of Clinical Immunology . 2015,第3期

机译：NFKB2和STAT5A基因突变共同引起的常见可变免疫缺陷和早期自动免疫表现
2. Psoriasiform dermatitis associated with common variable immunodeficiency 10 due to an Arg853*mutation in the NFKB2 gene [J] . Nagai Makoto, Imai Yasutomo, Yamanishi Kiyofumi The Journal of dermatology . 2019,第1期

机译：由于NFKB2基因中的ARG853 *突变，具有常见可变免疫缺陷10与常见可变免疫缺陷相关的牛皮癣皮炎
3. Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2 [J] . Slade Charlotte A., McLean Catriona, Scerri Thomas, Journal of Clinical Immunology . 2019,第3期

机译：患有常见可变免疫缺陷的患者患者患者患者患有新型突变在NFKB2中的致命肠道病变
4. Prurigo nodularis as the first manifestation of a common variable immunodeficiency [C] . Danieli M. G., Gambini S., Moretti R., European Society Immunodeficiencies., Meeting. . 2013

机译：Prurigo nodularis作为常见可变免疫缺陷的第一个表现
5. Modifier genes in the phenotypic manifestation of primary disease-causing mutations. [D] . Shankar, Suma Prabhu. 2005

机译：在原发性疾病突变的表型表现中的修饰基因。
6. Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency [O] . Karin Chen, Emily M. Coonrod, Attila Kumánovics, 2013

机译：NFKB2中的种系突变涉及非典型的NF-κB途径在共同可变免疫缺陷的发病机理中。
7. Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency [O] . Chen Karin, Coonrod Emily M., Kumánovics Attila, 2013

机译：NFKB2中的种系突变牵涉非典型的NF-κB途径在共同可变免疫缺陷的发病机理中。

COMMON VARIABLE IMMUNODEFICIENCY AND EARLY-ONSET AUTOIMMUNE MANIFESTATIONS ASSOCIATED WITH COUPLED MUTATIONS IN NFKB2 AND STAT5A GENES

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