Similar articles for PMID: 32350755

Year	Number of Results
1981	1
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2000	2
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2005	5
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2008	1
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2011	6
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2013	6
2014	5
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2018	9
2019	1
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2024	0

1

Novel Compound Heterozygote Variations in FADD Identified to Cause FAS-Associated Protein with Death Domain Deficiency.

Kohn LA, Long JD, Trope EC, Kuo CY. Kohn LA, et al. J Clin Immunol. 2020 May;40(4):658-661. doi: 10.1007/s10875-020-00779-6. Epub 2020 Apr 29. J Clin Immunol. 2020. PMID: 32350755 Free PMC article. No abstract available.

2

Whole-exome-sequencing-based discovery of human FADD deficiency.

Bolze A, Byun M, McDonald D, Morgan NV, Abhyankar A, Premkumar L, Puel A, Bacon CM, Rieux-Laucat F, Pang K, Britland A, Abel L, Cant A, Maher ER, Riedl SJ, Hambleton S, Casanova JL. Bolze A, et al. Am J Hum Genet. 2010 Dec 10;87(6):873-81. doi: 10.1016/j.ajhg.2010.10.028. Epub 2010 Nov 25. Am J Hum Genet. 2010. PMID: 21109225 Free PMC article.

3

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency.

Chun HJ, Zheng L, Ahmad M, Wang J, Speirs CK, Siegel RM, Dale JK, Puck J, Davis J, Hall CG, Skoda-Smith S, Atkinson TP, Straus SE, Lenardo MJ. Chun HJ, et al. Nature. 2002 Sep 26;419(6905):395-9. doi: 10.1038/nature01063. Nature. 2002. PMID: 12353035

4

Rapid B cell apoptosis induced by antigen receptor ligation does not require Fas (CD95/APO-1), the adaptor protein FADD/MORT1 or CrmA-sensitive caspases but is defective in both MRL-+/+ and MRL-lpr/lpr mice.

Yoshida T, Higuchi T, Hagiyama H, Strasser A, Nishioka K, Tsubata T. Yoshida T, et al. Int Immunol. 2000 Apr;12(4):517-26. doi: 10.1093/intimm/12.4.517. Int Immunol. 2000. PMID: 10744653

5

RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease.

Mao H, Yang W, Latour S, Yang J, Winter S, Zheng J, Ni K, Lv M, Liu C, Huang H, Chan KW, Pui-Wah Lee P, Tu W, Fischer A, Lau YL. Mao H, et al. J Allergy Clin Immunol. 2018 Aug;142(2):595-604.e16. doi: 10.1016/j.jaci.2017.10.026. Epub 2017 Nov 15. J Allergy Clin Immunol. 2018. PMID: 29155103 Free article.

6

The Fas-FADD death domain complex structure reveals the basis of DISC assembly and disease mutations.

Wang L, Yang JK, Kabaleeswaran V, Rice AJ, Cruz AC, Park AY, Yin Q, Damko E, Jang SB, Raunser S, Robinson CV, Siegel RM, Walz T, Wu H. Wang L, et al. Nat Struct Mol Biol. 2010 Nov;17(11):1324-9. doi: 10.1038/nsmb.1920. Epub 2010 Oct 10. Nat Struct Mol Biol. 2010. PMID: 20935634 Free PMC article.

7

Autoimmune Lymphoproliferative Syndrome Presenting with Invasive Streptococcus pneumoniae Infection.

Oksenhendler E, Spaan AN, Neven B, Stolzenberg MC, Fusaro M, Casanova JL, Rieux-Laucat F, Boisson B, Magérus A. Oksenhendler E, et al. J Clin Immunol. 2020 Apr;40(3):543-546. doi: 10.1007/s10875-020-00765-y. Epub 2020 Mar 6. J Clin Immunol. 2020. PMID: 32144537 No abstract available.

8

FADD is essential for glucose uptake and survival of thymocytes.

Zhang XY, Yang BY, Wang JY, Mo X, Zhang J, Hua ZC. Zhang XY, et al. Biochem Biophys Res Commun. 2014 Aug 22;451(2):202-7. doi: 10.1016/j.bbrc.2014.07.092. Epub 2014 Jul 28. Biochem Biophys Res Commun. 2014. PMID: 25078620

9

Compound Heterozygous Mutations of IL12RB1 in a Patient with Selective Defects in Th17 Differentiation.

Liu M, Lu B, Zeng P, Huang B, Xu Y, Liang H, Yang D, Yang S, Luo HB, Lew AM, Masters SL, Geng L, Zeng H, Zhang Y. Liu M, et al. J Clin Immunol. 2020 May;40(4):647-652. doi: 10.1007/s10875-020-00771-0. Epub 2020 Mar 27. J Clin Immunol. 2020. PMID: 32221732 No abstract available.

10

Dominant Negative FADD/MORT1 Inhibits the Development of Intestinal Intraepithelial Lymphocytes With a Marked Defect on CD8αα+TCRγδ+ T Cells.

Zhang X, Huo L, Song L, Hu Z, Wang X, Han Y, Wang Y, Xu P, Zhang J, Hua ZC. Zhang X, et al. Front Immunol. 2018 Sep 10;9:2038. doi: 10.3389/fimmu.2018.02038. eCollection 2018. Front Immunol. 2018. PMID: 30250469 Free PMC article.

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