The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
A Novel Protein That Interacts with the Death Domain of Fas/APO1 Contains a Sequence Motif Related to the Death Domain
Open accessAbstract
Signaling for cell death by Fas/APO1 occurs via a distinct region in its intracellular domain. This region contains a conserved sequence motif, the death domain motif, that is also found in the intracellular domains of the p55 tumor necrosis factor receptor and the low affinity nerve growth factor receptor, as well as in the regulatory domain of the ankyrins. A novel protein that specifically binds to the death domain of Fas/APO1 but not to Fas/APO1 molecules with a loss of function point mutation occurring in lprcg mice was cloned by a two-hybrid screen of a HeLa cells' cDNA library. The cloned protein itself contains a death domain motif, and this region binds to the death domain of Fas/APO1, while the region upstream to the death domain prompts self-association of the protein. Induced expression of the protein results in ligand-independent triggering of cytotoxicity, suggesting that it is involved in cell death induction by Fas/APO1.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In the case of FAS and TRAILRs, the cognate ligands—namely, FAS ligand (FASLG; also known as CD95L or APO-1L) and TNF superfamily member 10 (TNFSF10; best known as TRAIL), respectively—stabilize preformed receptor homotrimers to induce a conformational change at their intracellular tails that enables the death domain (DD)-dependent association of the adapter Fas associated via death domain (FADD)”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [277]
Citations
Cites
A novel genetic system to detect protein–protein interactions
Fields, S., & Song, O.-K. (1989) · Nature · doi:10.1038/340245a0 · Cited by 6,152
Tight control of gene expression in mammalian cells by tetracycline-responsive promoters.
Gossen, M., & Bujard, H. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5547 · Cited by 4,943
An endotoxin-induced serum factor that causes necrosis of tumors
Carswell, E. A., Old, L. J., Kassel, R. L., Green, S., Fiore, N., & Williamson, B. (1975) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.72.9.3666 · Cited by 4,532
Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis
Watanabe‐Fukunaga, R., Brannan, C., Copeland, N., Jenkins, N., & Nagata, S. (1992) · Nature · doi:10.1038/356314a0 · Cited by 3,153
Monoclonal Antibody-Mediated Tumor Regression by Induction of Apoptosis
Trauth, B. C., Klas, C., Peters, A. M. J., Matzku, S., Mӧller, P., Falk, W., Debatin, K., & Krammer, P. H. (1989) · Science · doi:10.1126/science.2787530 · Cited by 1,716
Database of homology‐derived protein structures and the structural meaning of sequence alignment
Sander, C., & Schneider, R. (1991) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.340090107 · Cited by 1,646
Yonehara, S., Ishii, A., & Yonehara, M. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.5.1747 · Cited by 1,398
A novel domain within the 55 kd TNF receptor signals cell death
Tartaglia, L. A., Ayres, T. M., Wong, G. H., & Goeddel, D. V. (1993) · Cell · doi:10.1016/0092-8674(93)90464-2 · Cited by 1,290
Expression and structure of the human NGF receptor
Johnson, D., Lanahan, A. A., Buck, C. R., Sehgal, A., Morgan, C. J., Mercer, E., Bothwell, M. A., & Chao, M. V. (1986) · Cell · doi:10.1016/0092-8674(86)90619-7 · Cited by 963
Frangioni, J. V., & Neel, B. G. (1993) · Analytical Biochemistry · doi:10.1006/abio.1993.1170 · Cited by 883
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 992
NMR structure and mutagenesis of the Fas (APO-1/CD95) death domain
Huang, B., Eberstadt, M., Olejniczak, E. T., Meadows, R. P., & Fesik, S. W. (1996) · Nature · doi:10.1038/384638a0 · Cited by 385
THE CENTRAL EFFECTORS OF CELL DEATH IN THE IMMUNE SYSTEM
Rathmell, J. C., & Thompson, C. B. (1999) · Annual Review of Immunology · doi:10.1146/annurev.immunol.17.1.781 · Cited by 383
Fas death receptor signalling: roles of Bid and XIAP
Kaufmann, T., Strasser, A., & Jost, P. J. (2011) · Cell Death and Differentiation · doi:10.1038/cdd.2011.121 · Cited by 388
Sneller, M. C., Wang, J., Dale, J. K., Strober, W., Middelton, L. A., Choi, Y., Fleisher, T. A., Lim, M. S., Jaffe, E. S., Puck, J. M., et al. (1997) · Blood · doi:10.1182/blood.v89.4.1341 · Cited by 367
Cytokine storm in acute pancreatitis.
Makhija, R., & Kingsnorth, A. N. (2002) · Journal of Hepato-Biliary-Pancreatic Surgery · doi:10.1007/s005340200049 · Cited by 365
Sprick, M. R., Rieser, E., Stahl, H. F., Große-Wilde, A., Weigand, M. A., & Walczak, H. (2002) · The EMBO Journal · doi:10.1093/emboj/cdf441 · Cited by 364
Apoptotic cell death in disease—Current understanding of the NCCD 2023
Vitale, I., Pietrocola, F., Guilbaud, E., Aaronson, S. A., Abrams, J., Adam, D., Agostini, M., Agostinis, P., Alnemri, E. S., Altucci, L., et al. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01153-w · Cited by 352
Pidd, a new death-domain–containing protein, is induced by p53 and promotes apoptosis
Lin, Y., Ma, W., & Benchimol, S. (2000) · Nature Genetics · doi:10.1038/79102 · Cited by 359
Chinnaiyan, A. M., & Dixit, V. M. (1996) · Current Biology · doi:10.1016/s0960-9822(02)00541-9 · Cited by 349
FLICE Induced Apoptosis in a Cell-free System
Muzio, M., Salvesen, G. S., & Dixit, V. M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.5.2952 · Cited by 343
The concept of intrinsic versus extrinsic apoptosis
Lossi, L. (2022) · Biochemical Journal · doi:10.1042/bcj20210854 · Cited by 372
Hu, S., Vincenz, C., Buller, M., & Dixit, V. M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.15.9621 · Cited by 342
A death-domain-containing receptor that mediates apoptosis
Kitson, J., Raven, T., Jiang, Y., Goeddel, D. V., Giles, K. M., Pun, K., Grinham, C. J., Brown, R., & Farrow, S. N. (1996) · Nature · doi:10.1038/384372a0 · Cited by 335
Ishida, T., Tojo, T., Aoki, T., Kobayashi, N., Ohishi, T., Watanabe, T., Yamamoto, T., & Inoue, J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9437 · Cited by 337
Yaar, M., Zhai, S., Pilch, P. F., Doyle, S. M., Eisenhauer, P. B., Fine, R. E., & Gilchrest, B. A. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119772 · Cited by 331
Grønbæk, K., Straten, P. T., Ralfkiaer, E. M., Ahrenkiel, V., Andersen, M. K., Hansen, N. E., Zeuthen, J., HOU-JENSEN, K., & Guldberg, P. (1998) · Blood · doi:10.1182/blood.v92.9.3018 · Cited by 336
Lewis, J., Devin, A., Miller, A., Lin, Y., Rodriguez, Y., Neckers, L., & Liu, Z.-G. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.14.10519 · Cited by 331
FLAME-1, a Novel FADD-like Anti-apoptotic Molecule That Regulates Fas/TNFR1-induced Apoptosis
Srinivasula, S. M., Ahmad, M., Ottilie, S., Bullrich, F., Banks, S., Wang, Y., Fernandes‐Alnemri, T., Croce, C. M., Litwack, G., Tomaselli, K. J., et al. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.18542 · Cited by 335
Apoptosis in Neural Development and Disease
Nijhawan, D., Honarpour, N., & Wang, X. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.73 · Cited by 326
Apoptosis: definition, mechanisms, and relevance to disease
Saikumar, P., Dong, Z., Mikhailov, V. M., Denton, M. L., Weinberg, J. M., & Venkatachalam, M. A. (1999) · The American Journal of Medicine · doi:10.1016/s0002-9343(99)00259-4 · Cited by 332
Cell death induced by the Fas/Fas ligand pathway and its role in pathology
Waring, P., & Müllbacher, A. (1999) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.1999.00837.x · Cited by 317
Programmed Cell Death Tunes Tumor Immunity
Liu, J., Hong, M., Li, Y., Chen, D., Wu, Y., & Hu, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.847345 · Cited by 330
CASH, a Novel Caspase Homologue with Death Effector Domains
Goltsev, Y. V., Kovalenko, A., Arnold, E., Varfolomeev, E. E., Brodianskii, V. M., & Wallach, D. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.32.19641 · Cited by 318
Self-citationCaspase-independent Cell Killing by Fas-associated Protein with Death Domain
Kawahara, A., Ohsawa, Y., Matsumura, H., Uchiyama, Y., & Nagata, S. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.5.1353 · Cited by 318
Rasper, D., Vaillancourt, J. P., Hadano, S., Houtzager, V. M., Seiden, I. M., Keen, S., Tawa, P., Xanthoudakis, S., Nasir, J., Martindale, D. W., et al. (1998) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400370 · Cited by 322
CLARP, a death effector domain-containing protein interacts with caspase-8 and regulates apoptosis
Inohara, N., Koseki, T., Hu, Y., Chen, S., & Núñez, G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.20.10717 · Cited by 316
Nitric Oxide Inhibits Fas-induced Apoptosis
Mannick, J. B., Miao, X. Q., & Stamler, J. S. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.39.24125 · Cited by 309
CD40-CD40 Ligand: A Multifunctional Receptor-Ligand Pair
van Kooten, C., & Banchereau, J. (1996) · Advances in immunology · doi:10.1016/s0065-2776(08)60865-2 · Cited by 311
Contenders in FasL/TNF death signaling
Cleveland, J. L., & Ihle, J. N. (1995) · Cell · doi:10.1016/0092-8674(95)90068-3 · Cited by 309
Yes and PI3K Bind CD95 to Signal Invasion of Glioblastoma
Kleber, S., Sancho-Martinez, I., Wiestler, B., Beisel, A., Gieffers, C., Hill, O., Thiemann, M., Mueller, W., Sykora, J., Kuhn, A., et al. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.02.003 · Cited by 309
Early events in neurotrophin signalling via Trk and p75 receptors
Greene, L. A., & Kaplan, D. R. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80062-x · Cited by 309
The death domain: a module shared by proteins with diverse cellular functions
Feinstein, E. (1995) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(00)89070-2 · Cited by 307
NMR structure of the death domain of the p75 neurotrophin receptor
Liepinsh, E., Ilag, L. L., Otting, G., & Ibáñez, C. F. (1997) · The EMBO Journal · doi:10.1093/emboj/16.16.4999 · Cited by 300
Takeuchi, M., Rothe, M., & Goeddel, D. V. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.33.19935 · Cited by 301
Caspases Induce Cytochrome c Release from Mitochondria by Activating Cytosolic Factors
Bossy‐Wetzel, E., & Green, D. R. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.25.17484 · Cited by 299
Huang, D. C. S., Hahne, M., Schroeter, M., Frei, K., Fontana, A., Villunger, A., Newton, K., Tschopp, J. F., & Strasser, A. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.26.14871 · Cited by 300
Liou, A. K. F., Clark, R. S. B., Henshall, D. C., Yin, X., & Chen, J. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00005-4 · Cited by 295
Identification and functional characterization of DR6, a novel death domain‐containing TNF receptor
Pan, G., Bauer, J. H., Haridas, V., Wang, S., Ding, L., Yu, G., Vincenz, C., Aggarwal, B. B., Ni, J., & Dixit, V. M. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00791-1 · Cited by 292
Delmas, D., Rébé, C., Lacour, S., Filomenko, R., Athias, A., Gambert, P., Cherkaoui‐Malki, M., Jannin, B., Dubrez, L., Latruffe, N., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304896200 · Cited by 291
Cifone, M. G., Roncaioli, P., Maria, R. D., Camarda, G., Santoni, A., Ruberti, G., & Testi, R. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00274.x · Cited by 288
Juo, P., Kuo, C. J., Reynolds, S. E., Konz, R. F., Raingeaud, J., Davis, R. J., Biemann, H.-P., & Blenis, J. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.1.24 · Cited by 287
Regulation of death receptor-mediated apoptosis pathways
Schmitz, I., Kirchhoff, S., & Krammer, P. H. (2000) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(00)00048-0 · Cited by 287
Activation of NF-κB by FADD, Casper, and Caspase-8
Hu, W.-H., Johnson, H. L., & Shu, H. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.15.10838 · Cited by 288
Modulation of the NF-κB pathway by virally encoded Death Effector Domains-containing proteins
Chaudhary, P. M., Jasmin, A., Eby, M. T., & Hood, L. (1999) · Oncogene · doi:10.1038/sj.onc.1202976 · Cited by 287
An early history of T cell-mediated cytotoxicity
Golstein, P., & Griffiths, G. M. (2018) · Nature reviews. Immunology · doi:10.1038/s41577-018-0009-3 · Cited by 303
Regulated Commitment of TNF Receptor Signaling
Pimentel‐Muiños, F. X., & Seed, B. (1999) · Immunity · doi:10.1016/s1074-7613(00)80152-1 · Cited by 282
Transducing signals of life and death
Yuan, J. (1997) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(97)80069-5 · Cited by 281
REVIEW ARTICLE: THE ROLE OF TUMOR NECROSIS FACTOR IN RENAL ISCHEMIA-REPERFUSION INJURY
DONNAHOO, K. K., Shames, B. D., Harken, A. H., & Meldrum, D. R. (1999) · The Journal of Urology · doi:10.1097/00005392-199907000-00068 · Cited by 278
Cohen, O., Inbal, B., Kissil, J., Raveh, T., Berissi, H., Spivak-Kroizaman, T., Feinstein, E., & Kimchi, A. (1999) · Journal of Cell Biology · doi:10.1083/jcb.146.1.141 · Cited by 298
Human Daxx regulates Fas‐induced apoptosis from nuclear PML oncogenic domains (PODs)
Torii, S., Egan, D. A., Evans, R. M., & Reed, J. C. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.6037 · Cited by 272
Concepts of tissue injury and cell death in inflammation: a historical perspective
Wallach, D., Kang, T., & Kovalenko, A. (2013) · Nature reviews. Immunology · doi:10.1038/nri3561 · Cited by 266
Self-citationBodmer, J.-L., Burns, K., Schneider, P., Hofmann, K., Steiner, V., Thome, M., Bornand, T., Hahne, M., Schröter, M., Becker, K., et al. (1997) · Immunity · doi:10.1016/s1074-7613(00)80244-7 · Cited by 262
Mitogen-activated protein kinase-mediated Fas apoptotic signaling pathway
Goillot, E., Raingeaud, J., Ranger, A. M., Tepper, R. I., Davis, R. J., Harlow, E., & Sánchez, I. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.7.3302 · Cited by 260
A mathematical model of caspase function in apoptosis
Fussenegger, M., Bailey, J. E., & Varner, J. D. (2000) · Nature Biotechnology · doi:10.1038/77589 · Cited by 259
The NF-κB/Rel and IκB gene families: mediators of immune response and inflammation
Wulczyn, F. G., Krappmann, D., & Scheidereit, C. (1996) · Journal of Molecular Medicine · doi:10.1007/s001090050078 · Cited by 252
Marsters, S. A., Sheridan, J. P., Donahue, C. J., Pitti, R. M., Gray, C. L., Goddard, A. D., Bauer, K. D., & Ashkenazi, A. (1996) · Current Biology · doi:10.1016/s0960-9822(02)70791-4 · Cited by 252
Kulms, D., Zeise, E., Pöppelmann, B., & Schwarz, T. (2002) · Oncogene · doi:10.1038/sj.onc.1205743 · Cited by 253
The role of receptor internalization in CD95 signaling
Lee, K., Feig, C., Tchikov, V., Schickel, R., Hallas, C., Schütze, S., Peter, M. E., & Chan, A. C. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601016 · Cited by 245
Inohara, N., del Peso, L., Koseki, T., Chen, S., & Núñez, G. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.20.12296 · Cited by 245
Lack of a Role for Jun Kinase and AP-1 in Fas-Induced Apoptosis
Lenczowski, J. M., Domínguez, L., Eder, A. M., King, L. B., Zacharchuk, C., & Ashwell, J. D. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.1.170 · Cited by 245
Kataoka, T., Schröter, M., Hahne, M., Schneider, P., Irmler, M., Thome, M., Froelich, C. J., & Tschopp, J. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.8.3936 · Cited by 243
RIP3, a Novel Apoptosis-inducing Kinase
Sun, X., Lee, J., Navas, T. A., Baldwin, D. T., Stewart, T. A., & Dixit, V. M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.24.16871 · Cited by 240
Activation of the NF-κB pathway by Caspase 8 and its homologs
Chaudhary, P. M., Eby, M. T., Jasmin, A., Kumar, A., Liu, L., & Hood, L. (2000) · Oncogene · doi:10.1038/sj.onc.1203812 · Cited by 241
Death Receptor-Ligand Systems in Cancer, Cell Death, and InflammationPreprint
Walczak, H. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008698 · Cited by 250
Michaelson, J. S., Bader, D., Kuo, F. C., Kozak, C. A., & Leder, P. (1999) · Genes & Development · doi:10.1101/gad.13.15.1918 · Cited by 241
Apoptosis: A review of pro‐apoptotic and anti‐apoptotic pathways and dysregulation in disease
O'Brien, M., & Kirby, R. (2008) · Journal of Veterinary Emergency and Critical Care · doi:10.1111/j.1476-4431.2008.00363.x · Cited by 253
Necrotic Death Pathway in FAS Receptor Signaling
Matsumura, H., Shimizu, Y., Ohsawa, Y., Kawahara, A., Uchiyama, Y., & Nagata, S. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.6.1247 · Cited by 242
A Role for FADD in T Cell Activation and Development
Walsh, C. M., Wen, B. G., Chinnaiyan, A. M., O’Rourke, K. M., Dixit, V. M., & Hedrick, S. Μ. (1998) · Immunity · doi:10.1016/s1074-7613(00)80549-x · Cited by 239
NMR structure and mutagenesis of the FADD (Mort1) death-effector domain
Eberstadt, M., Huang, B., Chen, Z., Meadows, R. P., Ng, S., Zheng, L., Lenardo, M. J., & Fesik, S. W. (1998) · Nature · doi:10.1038/31972 · Cited by 239
Karsan, A., Yee, E., & Harlan, J. M. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.44.27201 · Cited by 238
MANABE, N., Goto, Y., MATSUDA‐MINEHATA, F., Inoue, N., Maeda, A., Sakamaki, K., & Miyano, T. (2004) · Journal of Reproduction and Development · doi:10.1262/jrd.50.493 · Cited by 238
Imai, Y., Kimura, T., Murakami, A., Yajima, N., Sakamaki, K., & Yonehara, S. (1999) · Nature · doi:10.1038/19709 · Cited by 237
Role of Fas-mediated cell death in the regulation of immune responses
Parijs, L. V., & Abbas, A. K. (1996) · Current Opinion in Immunology · doi:10.1016/s0952-7915(96)80125-7 · Cited by 234
The NOD: a signaling module that regulates apoptosis and host defense against pathogens
Inohara, N., & Núñez, G. (2001) · Oncogene · doi:10.1038/sj.onc.1204787 · Cited by 237
Brojatsch, J., Naughton, J., Rolls, M. M., Zingler, K., & Young, J. A. T. (1996) · Cell · doi:10.1016/s0092-8674(00)81992-3 · Cited by 233
Aggarwal, B. B. (2000) · Annals of the Rheumatic Diseases · doi:10.1136/ard.59.suppl_1.i6 · Cited by 234
Faris, M., Kokot, N., Latinis, K. M., Kasibhatla, S., Green, D. R., Koretzky, G. A., & Nel, A. E. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.1.134 · Cited by 231
Cell death induction by receptors of the TNF family: towards a molecular understanding
Wallach, D., Boldin, M., Varfolomeev, E. E., Beyaert, R., Vandenabeele, P., & Fiers, W. C. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00553-x · Cited by 233
Self-citationFADD Is Required for DR4- and DR5-mediated Apoptosis
Kuang, A. A., Diehl, G. E., Zhang, J., & Winoto, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.c000284200 · Cited by 231
Clemens, M. J., Bushell, M., Jeffrey, I. W., Pain, V. M., & Morley, S. (2000) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400695 · Cited by 228
Cell death induction by TNF: a matter of self control
Wallach, D. (1997) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(97)01015-3 · Cited by 226
Self-citationReactive oxygen intermediates in TNF signaling
Garg, A. K., & Aggarwal, B. B. (2002) · Molecular Immunology · doi:10.1016/s0161-5890(02)00207-9 · Cited by 227
Perlman, H., Pagliari, L. J., Georganas, C., Mano, T., Walsh, K., & Pope, R. M. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.190.11.1679 · Cited by 222
Toso, a Cell Surface, Specific Regulator of Fas-Induced Apoptosis in T Cells
Hitoshi, Y., Lorens, J. B., Kitada, S., Fisher, J. M., LaBarge, M. A., Ring, H. Z., Francke, U., Reed, J. C., Kinoshita, S. M., & Nolan, G. P. (1998) · Immunity · doi:10.1016/s1074-7613(00)80551-8 · Cited by 221
Vorburger, S. A., & Hunt, K. K. (2002) · The Oncologist · doi:10.1634/theoncologist.7-1-46 · Cited by 220
Hueber, A., Bernard, A., Hérincs, Z., Couzinet, A., & He, H. (2002) · EMBO Reports · doi:10.1093/embo-reports/kvf022 · Cited by 217
The death effector domain protein family: regulators of cellular homeostasis
Tibbetts, M. D., Zheng, L., & Lenardo, M. J. (2003) · Nature Immunology · doi:10.1038/ni0503-404 · Cited by 218
Li, Y., Kang, J., & Horwitz, M. S. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.3.1601 · Cited by 216
Harper, N. W., Hughes, M. A., MacFarlane, M., & Cohen, G. M. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303399200 · Cited by 209
Mandal, D., Mazumder, A. G., Das, P. K., Kundu, M., & Basu, J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m506928200 · Cited by 210
Majdan, M., Lachance, C., Gloster, A. T., Aloyz, R. S., Zeindler, C., Bamji, S. X., Bhakar, A. L., Belliveau, D. J., Fawcett, J., Miller, F. D., et al. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-18-06988.1997 · Cited by 208
Sphingomyelin breakdown and cell fate
Testi, R. (1996) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(96)10056-6 · Cited by 206
Dai, C., & Krantz, S. B. (1999) · Blood · doi:10.1182/blood.v93.10.3309.410k04_3309_3316 · Cited by 205
Denecker, G., Vercammen, D., Steemans, M., Berghe, T. V., Brouckaert, G., Loo, G., Zhivotovsky, B., Fiers, W., Grooten, J., Declercq, W., et al. (2001) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4400883 · Cited by 205
FADD: a regulator of life and death.
Tourneur, L., & Chiocchia, G. (2010) · Trends in immunology · doi:10.1016/j.it.2010.05.005 · Cited by 210
Reactive oxygen species are downstream products of TRAF-mediated signal transduction
Chandel, N. S., Schumacker, P. T., & Arch, R. H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103074200 · Cited by 203
Kawamata, S., Hori, T., Imura, A., Takaori‐Kondo, A., & Uchiyama, T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.10.5808 · Cited by 200
Graubert, T. A., DiPersio, J. F., Russell, J. H., & Ley, T. J. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119606 · Cited by 201
Identification of a Drosophila melanogaster ICE/CED‐3‐related protease, drICE
Fraser, A. G., & Evan, G. I. (1997) · The EMBO Journal · doi:10.1093/emboj/16.10.2805 · Cited by 201
Live and let die: regulatory mechanisms in Fas-mediated apoptosis
Curtin, J. F., & Cotter, T. G. (2003) · Cellular Signalling · doi:10.1016/s0898-6568(03)00093-7 · Cited by 200
Metadata
- Authors
- Boldin, M. P., Varfolomeev, E. E., Pancer, Z., Mett, I. L., Camonis, J. H., & Wallach, D.
- Affiliations
- Weizmann Institute of Science (IL)
- Inserm (FR)
- Corresponding author
- Wallach, David
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1995-04
- Volume
- 270
- Issue
- 14
- Pages
- 7795-7798
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1968328677
- Cited by
- 993
- References
- 27
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 10 · 2023: 5 · 2022: 8 · 2021: 3 · 2020: 4 · 2019: 15 · 2018: 17 · 2017: 11 · 2016: 8 · 2015: 6 · 2014: 10 · 2013: 15 · 2012: 10
- FWCI
- 34.99
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Keywords
- death domain, death receptor signaling, apoptosis, protein-protein interaction, p75 neurotrophin receptor, lpr mice, two-hybrid screen, protein self-association
- MeSH terms
- Amino Acid Sequence, Animals, Antigens, Surface, Carrier Proteins, Cloning, Molecular, HeLa Cells, Humans, Molecular Sequence Data, Proteins, Apoptosis, Sequence Homology, Amino Acid, DNA, Complementary, fas Receptor, Adaptor Proteins, Signal Transducing, Mice, Fas-Associated Death Domain Protein
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review