Homo sapiens Fas associated via death domain (FADD), RefSeqGene (LRG_2 - Nucleotide

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Deciphering DED assembly mechanisms in FADD-procaspase-8-cFLIP complexes regulating apoptosis. [Nat Commun. 2024]
Deciphering DED assembly mechanisms in FADD-procaspase-8-cFLIP complexes regulating apoptosis.
Yang CY, Lien CI, Tseng YC, Tu YF, Kulczyk AW, Lu YC, Wang YT, Su TW, Hsu LC, Lo YC, et al. Nat Commun. 2024 May 6; 15(1):3791. Epub 2024 May 6.
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing. [J Allergy Clin Immunol. 2024]
Abnormal biomarkers predict complex FAS or FADD defects missed by exome sequencing.
Rensing-Ehl A, Lorenz MR, Führer M, Willenbacher W, Willenbacher E, Sopper S, Abinun M, Maccari ME, König C, Haegele P, et al. J Allergy Clin Immunol. 2024 Jan; 153(1):297-308.e12. Epub 2023 Nov 17.
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome. [J Allergy Clin Immunol. 2024]
Combined germline and somatic human FADD mutations cause autoimmune lymphoproliferative syndrome.
Pellé O, Moreno S, Lorenz MR, Riller Q, Fuehrer M, Stolzenberg MC, Maccari ME, Lenoir C, Cheminant M, Hinze T, et al. J Allergy Clin Immunol. 2024 Jan; 153(1):203-215. Epub 2023 Oct 2.

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Nucleotide