Suppr超能文献

相似文献

1
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency.
J Allergy Clin Immunol. 2021 Aug;148(2):381-393. doi: 10.1016/j.jaci.2021.03.045. Epub 2021 Apr 17.
2
Mitochondria-localised ZNFX1 functions as a dsRNA sensor to initiate antiviral responses through MAVS.
Nat Cell Biol. 2019 Nov;21(11):1346-1356. doi: 10.1038/s41556-019-0416-0. Epub 2019 Nov 4.
3
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.
Proc Natl Acad Sci U S A. 2021 Apr 13;118(15). doi: 10.1073/pnas.2102804118.
4
Biallelic ZNFX1 variants are associated with a spectrum of immuno-hematological abnormalities.
Clin Genet. 2022 Feb;101(2):247-254. doi: 10.1111/cge.14081. Epub 2021 Nov 6.
5
The human disease-associated gene ZNFX1 controls inflammation through inhibition of the NLRP3 inflammasome.
EMBO J. 2024 Nov;43(22):5469-5493. doi: 10.1038/s44318-024-00236-9. Epub 2024 Sep 27.
6
Impaired control of multiple viral infections in a family with complete IRF9 deficiency.
J Allergy Clin Immunol. 2019 Jul;144(1):309-312.e10. doi: 10.1016/j.jaci.2019.02.019. Epub 2019 Feb 28.
7
A glimpse on metazoan ZNFX1 helicases, ancient players of antiviral innate immunity.
Fish Shellfish Immunol. 2022 Feb;121:456-466. doi: 10.1016/j.fsi.2022.01.019. Epub 2022 Jan 19.
8
IFIH1 loss of function predisposes to inflammatory and SARS-CoV-2-related infectious diseases.
Scand J Immunol. 2024 Aug;100(2):e13373. doi: 10.1111/sji.13373. Epub 2024 May 16.
9
Host genetic susceptibility to viral infections: the role of type I interferon induction.
Genes Immun. 2020 Dec;21(6-8):365-379. doi: 10.1038/s41435-020-00116-2. Epub 2020 Nov 20.
10
A Novel Complete Autosomal-Recessive STAT1 LOF Variant Causes Immunodeficiency with Hemophagocytic Lymphohistiocytosis-Like Hyperinflammation.
J Allergy Clin Immunol Pract. 2020 Oct;8(9):3102-3111. doi: 10.1016/j.jaip.2020.06.034. Epub 2020 Jun 27.

引用本文的文献

1
Consanguinity and rare monogenic systemic autoinflammatory disorders: implications for prevalence and genetic variability.
Pediatr Rheumatol Online J. 2025 Jul 30;23(1):83. doi: 10.1186/s12969-025-01133-z.
4
ATP functions as a pathogen-associated molecular pattern to activate the E3 ubiquitin ligase RNF213.
Nat Commun. 2025 May 13;16(1):4414. doi: 10.1038/s41467-025-59444-4.
5
ZNFX1: a multifunctional modulator of the innate immune response.
Front Immunol. 2025 Mar 18;16:1564628. doi: 10.3389/fimmu.2025.1564628. eCollection 2025.
6
Gene expression in soft-shell clam (Mya arenaria) transmissible cancer reveals survival mechanisms during host infection and seawater transfer.
PLoS Genet. 2025 Mar 31;21(3):e1011629. doi: 10.1371/journal.pgen.1011629. eCollection 2025 Mar.
8
Rare disease genomics and precision medicine.
Genomics Inform. 2024 Dec 3;22(1):28. doi: 10.1186/s44342-024-00032-1.
9
Lethal COVID-19 associates with RAAS-induced inflammation for multiple organ damage including mediastinal lymph nodes.
Proc Natl Acad Sci U S A. 2024 Dec 3;121(49):e2401968121. doi: 10.1073/pnas.2401968121. Epub 2024 Nov 27.
10
Rare genetic interstitial lung diseases: a pictorial essay.
Eur Respir Rev. 2024 Nov 13;33(174). doi: 10.1183/16000617.0101-2024. Print 2024 Oct.

本文引用的文献

1
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19.
Science. 2020 Oct 23;370(6515). doi: 10.1126/science.abd4570. Epub 2020 Sep 24.
2
SARS-CoV-2 viral load predicts COVID-19 mortality.
Lancet Respir Med. 2020 Sep;8(9):e70. doi: 10.1016/S2213-2600(20)30354-4. Epub 2020 Aug 6.
4
RNA-binding protein isoforms ZAP-S and ZAP-L have distinct antiviral and immune resolution functions.
Nat Immunol. 2019 Dec;20(12):1610-1620. doi: 10.1038/s41590-019-0527-6. Epub 2019 Nov 18.
5
Mitochondria-localised ZNFX1 functions as a dsRNA sensor to initiate antiviral responses through MAVS.
Nat Cell Biol. 2019 Nov;21(11):1346-1356. doi: 10.1038/s41556-019-0416-0. Epub 2019 Nov 4.
7
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function.
J Exp Med. 2019 Dec 2;216(12):2778-2799. doi: 10.1084/jem.20190147. Epub 2019 Oct 10.
9
Recurrent inflammatory disease caused by a heterozygous mutation in CD48.
J Allergy Clin Immunol. 2019 Nov;144(5):1441-1445.e17. doi: 10.1016/j.jaci.2019.07.038. Epub 2019 Aug 13.
10
Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines.
J Exp Med. 2019 Sep 2;216(9):2057-2070. doi: 10.1084/jem.20182295. Epub 2019 Jul 3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验