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 301–400 of 992
DEDD, a novel death effector domain‐containing protein, targeted to the nucleolus
Stegh, A. H., Schickling, O., Ehret, A., Scaffidi, C., Peterhänsel, C., Hofmann, T. G., Grummt, I., Krammer, P. H., & Peter, M. E. (1998) · The EMBO Journal · doi:10.1093/emboj/17.20.5974 · Cited by 120
p53-dependent impairment of T-cell proliferation in FADD dominant-negative transgenic mice
Zörnig, M., Hueber, A., & Evan, G. I. (1998) · Current Biology · doi:10.1016/s0960-9822(98)70182-4 · Cited by 120
Control of neuronal branching by the death receptor CD95 (Fas/Apo-1)
Zuliani, C., Kleber, S., Klussmann, S., Wenger, T., Kenzelmann, M., Schreglmann, N., Martinez, A., del Rio, J. A., Soriano, E., Vodrazka, P., et al. (2006) · Cell Death & Differentiation · doi:10.1038/sj.cdd.4401720 · Cited by 117
Apoptosis: An Overview of the Process and Its Relevance in Disease
Webb, S. J., Harrison, D. J., & Wyllie, A. H. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)61052-2 · Cited by 120
Huisman, C., Ferreira, C. G., Bröker, L. E., Rodríguez, J. A., Smit, E. F., Postmus, P. E., Kruyt, F. A. E., & Giaccone, G. (2002) · PubMed · Cited by 118
Zhang, J., & Winoto, A. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.6.2756 · Cited by 119
Grimm, S., Stanger, B. Z., & Leder, P. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.20.10923 · Cited by 117
Molecular evidence for the nuclear localization of FADD
Gómez-Angelats, M., & Cidlowski, J. A. (2003) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401237 · Cited by 115
DR3 Regulates Negative Selection during Thymocyte Development
Wang, E. C. Y., Thern, A. M., Denzel, A., Kitson, J., Farrow, S. N., & Owen, M. J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.10.3451-3461.2001 · Cited by 115
Seol, D., Li, J., Seol, M. H., Park, S., Talanian, R. V., & Billiar, T. R. (2001) · PubMed · Cited by 115
HIV induces lymphocyte apoptosis by a p53‐initiated, mitochondrial‐mediated mechanism
Genini, D., Sheeter, D. A., Rought, S. E., Zaunders, J. J., Susín, S. A., Kroemer, G., Richman, D. D., Carson, D. A., Corbeil, J., & Leoni, L. M. (2000) · The FASEB Journal · doi:10.1096/fj.00-0336fje · Cited by 114
Hofmann, K., & Tschopp, J. (1995) · FEBS Letters · doi:10.1016/0014-5793(95)00931-x · Cited by 113
Bcl-xL Acts Downstream of Caspase-8 Activation by the CD95 Death-inducing Signaling Complex
Medema, J. P., Scaffidi, C., Krammer, P. H., & Peter, M. E. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.6.3388 · Cited by 114
Tumor Necrosis Factor (TNF) Receptor 1 Signaling Downstream of TNF Receptor-associated Factor 2
Natoli, G., Costanzo, A., Moretti, F., Fulco, M., Balsano, C., & Levrero, M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.42.26079 · Cited by 114
Endoplasmic Reticulum Stress Signaling and Neuronal Cell Death
Merighi, A., & Lossi, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315186 · Cited by 123
T cell-specific FADD-deficient mice: FADD is required for early T cell development
Kabra, N. H., Kang, C., Hsing, L. C., Zhang, J., & Winoto, A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111158698 · Cited by 111
Kissil, J. L., Cohen, O., Raveh, T. B., & Kimchi, A. (1999) · The EMBO Journal · doi:10.1093/emboj/18.2.353 · Cited by 110
Augmentation of naive, Th1 and Th2 effector CD4 Responses by IL-6, IL-1 and TNF
Joseph, S. B., Miner, K. T., & Croft, M. (1998) · European Journal of Immunology · doi:10.1002/(sici)1521-4141(199801)28:01 · Cited by 100
Gnesutta, N., & Minden, A. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.21.7838-7848.2003 · Cited by 107
Bélanger, C., Gravel, A., Tomoiu, A., Me, J., Gosselin, J., Mj, T., & Flamand, L. (2001) · PubMed · Cited by 108
Fas-associated Factor 1, FAF1, Is a Member of Fas Death-inducing Signaling Complex
Ryu, S.-W., Lee, S.-J., Park, M.-Y., Jun, J.-I., Jung, Y., & Kim, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302200200 · Cited by 107
Stephens, L. A., Thomas, H. E., Li, M., DARWICHE, M. G. R., Volodin, L., & Kay, T. W. H. (1999) · Endocrinology · doi:10.1210/endo.140.7.6873 · Cited by 107
E1B 19K Inhibits Fas-mediated Apoptosis through FADD-dependent Sequestration of FLICE
Perez, D., & White, E. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.5.1255 · Cited by 107
Cock, J. G. R. B.-D., Tepper, A. D., de Vries, E., BLITTERSWIJK, W. J. V., & Borst, J. G. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.13.7560 · Cited by 104
Klingenbeck, L., Eckart, R. A., Berens, C., & Lührmann, A. (2012) · Cellular Microbiology · doi:10.1111/cmi.12066 · Cited by 102
Cai, Z., Bettaı̈eb, A., Mahdani, N. E., Legrès, L., Stancou, R., Masliah, J., & Chouaı̈b, S. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.11.6918 · Cited by 103
Perkins, C. L., Kim, C. N., Fang, G., & Bhalla, K. N. (1998) · PubMed · Cited by 103
Hawkins, C. J., Uren, A. G., Häcker, G. A., Medcalf, R. L., & Vaux, D. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.24.13786 · Cited by 102
How apoptosis got the immune system in shape
Feig, C., & Peter, M. E. (2007) · European Journal of Immunology · doi:10.1002/eji.200737462 · Cited by 108
The death effector domain protein family
Barnhart, B. C., Lee, J. C., Alappat, E. C., & Peter, M. E. (2003) · Oncogene · doi:10.1038/sj.onc.1207103 · Cited by 104
Wang, H. Q., Quan, T., He, T., Franke, T. F., Voorhees, J. J., & Fisher, G. J. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m300574200 · Cited by 101
Kamada, S., Kusano, H., Fujita, H., Ohtsu, M., Koya, R. C., Kuzumaki, N., & Tsujimoto, Y. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.15.8532 · Cited by 101
Autoimmunity and Apoptosis: The Crohn's Connection
Beutler, B. (2001) · Immunity · doi:10.1016/s1074-7613(01)00176-5 · Cited by 118
The complex interplay between autophagy, apoptosis, and necrotic signals promotes T‐cell homeostasis
Walsh, C. M., & Edinger, A. L. (2010) · Immunological Reviews · doi:10.1111/j.1600-065x.2010.00919.x · Cited by 99
Natoli, G., Costanzo, A., Guido, F., Moretti, F., Bernardo, A., BURGIO, V. L., Agresti, C., & Levrero, M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.47.31262 · Cited by 99
Kulms, D., Düßmann, H., Pöppelmann, B., Ständer, S., Schwarz, A., & Schwarz, T. (2002) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401002 · Cited by 100
Meldrum, D. R., & DONNAHOO, K. K. (1999) · Journal of Surgical Research · doi:10.1006/jsre.1999.5660 · Cited by 99
Berglund, H., Olerenshaw, D., Sankar, A., Federwisch, M., McDonald, N. Q., & Driscoll, P. C. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.4011 · Cited by 99
Zhu, N., Ware, C. F., & Lai, M. M. C. (2001) · Virology · doi:10.1006/viro.2001.0896 · Cited by 99
STAT1 Is Inactivated by a Caspase
King, P., & Goodbourn, S. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.15.8699 · Cited by 97
Nagata, S. (1998) · Journal of Human Genetics · doi:10.1007/s100380050029 · Cited by 97
TNF-Related Ligands and Their Receptors
Orlinick, J. R., & Chao, M. V. (1998) · Cellular Signalling · doi:10.1016/s0898-6568(98)00018-7 · Cited by 94
A1 Functions at the Mitochondria to Delay Endothelial Apoptosis in Response to Tumor Necrosis Factor
Duriez, P. J., Wong, F., Dorovini‐Zis, K., Shahidi, R., & Karsan, A. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m908925199 · Cited by 95
Gómez-Angelats, M., & Cidlowski, J. A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104919200 · Cited by 94
Howard, P. L., Chia, M. C., Rizzo, S. D., Liu, F., & Pawson, T. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1934711100 · Cited by 92
Fas-mediated apoptosis in mouse hepatocytes involves the processing and activation of caspases
Jones, R. A., Johnson, V., Buck, N. R., Dobrota, M., Hinton, R. H., Chow, S. C., & Kass, G. E. N. (1998) · Hepatology · doi:10.1002/hep.510270624 · Cited by 91
Rupinder, S. K., Aulakh, G. K., & Singh, M. (2007) · Vascular Pharmacology · doi:10.1016/j.vph.2007.01.006 · Cited by 93
The Death Effector Domain of PEA-15 Is Involved in Its Regulation of Integrin Activation
Ramos, J. W., Kojima, T. K., Hughes, P. E., Fenczik, C. A., & Ginsberg, M. H. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.51.33897 · Cited by 91
Viard, I., Veyrenc, S., French, L. E., Brambilla, C., & Brambilla, E. M. (2003) · The Journal of Pathology · doi:10.1002/path.1428 · Cited by 90
Contribution of Fas to diabetes development
Savinov, A. Y., Tcherepanov, A., Green, E. A., Flavell, R. A., & Chervonsky, A. V. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0237359100 · Cited by 90
Mechanism of apoptosis induced by copper in PC12 cells
Kawakami, M., Inagawa, R., Hosokawa, T., Saito, T., & Kurasaki, M. (2008) · Food and Chemical Toxicology · doi:10.1016/j.fct.2008.02.014 · Cited by 90
An introduction to death receptors in apoptosis
Kumar, R., Herbert, P. E., & Warrens, A. Ν. (2005) · International Journal of Surgery · doi:10.1016/j.ijsu.2005.05.002 · Cited by 92
TRAF1 is a TNF inducible regulator of NF‐κB activation
Carpentier, I., & Beyaert, R. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)01356-3 · Cited by 90
Fernández, M., Segura, M. F., Solé, C., Colino, A., Comella, J. X., & Ceña, V. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04767.x · Cited by 90
Himeji, D., Horiuchi, T., Tsukamoto, H., Hayashi, K., Watanabe, T., & Harada, M. (2002) · Blood · doi:10.1182/blood.v99.11.4070 · Cited by 89
Belshawl, P. J., Spencer, D. M., Crabtree, G. R., & Schreiber, S. L. (1996) · Chemistry & Biology · doi:10.1016/s1074-5521(96)90249-5 · Cited by 89
Murphy, K. M., Streips, U. N., & Lock, R. B. (1999) · Oncogene · doi:10.1038/sj.onc.1203001 · Cited by 89
DDX24 Negatively Regulates Cytosolic RNA-Mediated Innate Immune Signaling
Ma, Z., Moore, R. H., Xu, X., & Barber, G. N. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003721 · Cited by 89
FADD at the Crossroads between Cancer and Inflammation
Mouasni, S., & Tourneur, L. (2018) · Trends in Immunology · doi:10.1016/j.it.2018.10.005 · Cited by 89
Pyrin N-Terminal Homology Domain- and Caspase Recruitment Domain-Dependent Oligomerization of ASC
Masumoto, J., Taniguchi, S., & Sagara, J. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.4190 · Cited by 88
Kinase Inhibitors in Cancer Therapy
Sedlacek, H. H. (2000) · Drugs · doi:10.2165/00003495-200059030-00004 · Cited by 89
Chang, H. Y., Yang, X., & Baltimore, D. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1252 · Cited by 88
Chlichlia, K., Peter, M. E., Rocha, M., Scaffidi, C., Bucur, M., Krammer, P. H., Schirrmacher, V., & Umansky, V. (1998) · Blood · doi:10.1182/blood.v91.11.4311 · Cited by 88
Crystal Structure of a Viral FLIP
Li, F.-Y., Jeffrey, P. D., Yu, J. W., & Shi, Y. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m511074200 · Cited by 86
Kim, S., Song, S., Kim, S., Chun, K., Lim, S.-Y., Na, H., Kim, J., Surh, Y., Bang, Y., & Song, Y. S. (2004) · Journal of Cancer Research and Clinical Oncology · doi:10.1007/s00432-004-0567-6 · Cited by 88
FADD-deficient T Cells Exhibit a Disaccord in Regulation of the Cell Cycle Machinery
Zhang, J., Kabra, N. H., Cado, D., Kang, C., & Winoto, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103838200 · Cited by 86
Identification of a nuclear protein that promotes NF-κB activation
Chen, D., Li, Z., Yang, Q., Zhang, J., Zhai, Z., & Shu, H. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2003.09.074 · Cited by 85
Inoue, N., Matsuda, F., Goto, Y., & MANABE, N. (2011) · Journal of Reproduction and Development · doi:10.1262/jrd.10-198e · Cited by 85
Uno, K., Inukai, T., Kayagaki, N., Goi, K., Sato, H., Nemoto, A., Takahashi, K., Kagami, K., Yamaguchi, N., Yagita∥, H., et al. (2003) · Blood · doi:10.1182/blood-2002-06-1770 · Cited by 85
Darnay, B. G., & Aggarwal, B. B. (1999) · Annals of the Rheumatic Diseases · doi:10.1136/ard.58.2008.i2 · Cited by 84
A glycoprotein from Laminaria japonica induces apoptosis in HT-29 colon cancer cells
Go, H., Hwang, H., & Nam, T. (2010) · Toxicology in Vitro · doi:10.1016/j.tiv.2010.06.018 · Cited by 84
FADD/MORT1, a signal transducer that can promote cell death or cell growth
Strasser, A., & Newton, K. (1999) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(99)00003-5 · Cited by 84
Cell death‐independent activities of the death receptors CD 95, TRAILR 1, and TRAILR 2
Siegmund, D., Lang, I., & Wajant, H. (2016) · FEBS Journal · doi:10.1111/febs.13968 · Cited by 83
Molecular and clinical aspects of apoptosis
Uren, A. G., & Vaux, D. L. (1996) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(96)00098-8 · Cited by 83
Activation-induced Aggregation and Processing of the Human Fas Antigen
Kamitani, T., Nguyen, H. P., & Yeh, E. T. H. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.35.22307 · Cited by 81
Hyer, M. L., Voelkel‐Johnson, C., Rubinchik, S., Dong, J.-Y., & Norris, J. S. (2000) · Molecular Therapy · doi:10.1006/mthe.2000.0139 · Cited by 83
Wu, G. S., Kim, K., & El‐Deiry, W. S. (2002) · Advances in experimental medicine and biology · doi:10.1007/0-306-46817-4_13 · Cited by 84
Kim, S. G., Jong, H.-S., Kim, T.-Y., Lee, S. E., Kim, N. K., Hong, S. H., & Bang, Y. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-04-0201 · Cited by 82
Peter, M. E., Scaffidi, C., Medema, J. P., Kischkel, F. C., & Krammer, P. H. (1999) · Results and problems in cell differentiation · doi:10.1007/978-3-540-69184-6_3 · Cited by 82
Majkut, J., Sgobba, M., Holohan, C., Crawford, N., Logan, A. E., Kerr, E., Higgins, C. A., Redmond, K. L., Riley, J. S., Stasik, I., et al. (2014) · Nature Communications · doi:10.1038/ncomms4350 · Cited by 81
Programmed necrosis and autophagy in immune function
Lu, J. V., & Walsh, C. M. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01147.x · Cited by 82
Nonapoptotic functions of Fas/ CD 95 in the immune response
Guégan, J., & Legembre, P. (2017) · FEBS Journal · doi:10.1111/febs.14292 · Cited by 85
Imtiyaz, H. Z., Rosenberg, S., Zhang, Y., Rahman, Z. S. M., Hou, Y.-J., Manser, T. L., & Zhang, J. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.11.6852 · Cited by 79
Acheampong, E. A., Parveen, Z., Muthoga, L. W., Kalayeh, M., Mukhtār, M., & Pomerantz, R. J. (2005) · Journal of Virology · doi:10.1128/jvi.79.7.4257-4269.2005 · Cited by 81
Proteasome inhibitors induce mitochondria‐independent apoptosis in human glioma cells
Kitagawa, H., Tani, E., Ikemoto, H., Ozaki, I., Nakano, A., & Ōmura, S. (1999) · FEBS Letters · doi:10.1016/s0014-5793(98)01709-8 · Cited by 81
Recent advances in tumor necrosis factor and CD40 signaling
Tewari, M., & Dixit, V. M. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)90008-8 · Cited by 81
Varadhachary, A. S., Peter, M. E., Perdow, S. N., Krammer, P. H., & Salgame, P. R. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.9.4772 · Cited by 81
The role of apoptosis in the pathogenesis and treatment of diseases
Solary, É., Dubrez, L., & Eymin, B. (1996) · European Respiratory Journal · doi:10.1183/09031936.96.09061293 · Cited by 81
Signalling by proteolysis: death receptors induce apoptosis
Muzio, M. (1998) · International Journal of Clinical & Laboratory Research · doi:10.1007/s005990050035 · Cited by 80
Sayers, T. J., Brooks, A. D., Lee, J., Fenton, R. G., Komschlies, K. L., Wigginton, J. M., Winkler-Pickett, R. T., & Wiltrout, R. H. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.8.3957 · Cited by 79
Dürkop, H., Foss, H., Demel, G., Klotzbach, H., Hahn, C., & Stein, H. (1999) · Blood · doi:10.1182/blood.v93.2.617 · Cited by 80
CD95L/FasL and TRAIL in Tumour Surveillance and Cancer Therapy
Wajant, H. (2006) · Cancer treatment and research · doi:10.1007/0-387-26283-0_7 · Cited by 80
Structural Determinants of Neurotrophin Action
McDonald, N. Q., & Chao, M. V. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.34.19669 · Cited by 82
Segura, M. F., Solé, C., Pascual, M., Moubarak, R. S., Pérez‐García, M. J., Gozzelino, R., Iglesias‐Guimarais, V., Badiola, N., Bayascas, J. R., Llecha, N., et al. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3462-07.2007 · Cited by 79
Activation of Fas inhibits heat‐induced activation of HSF1 and up‐regulation of hsp70
Schett, G. A., Steiner, C.-W., Gröger, M., Winkler, S., Graninger, W. B., Smolen, J. S., Xu, Q., & Steiner, G. E. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.8.833 · Cited by 79
Transgenic models of lymphoid neoplasia and development of a pan-hematopoietic vector
Adams, J. M., Harris, A. W., Strasser, A., Ogilvy, S., & Cory, S. (1999) · Oncogene · doi:10.1038/sj.onc.1202997 · Cited by 80
Yoram Vodovotz, B., Kim, P., Bagci, E. Z., Ermentrout, B., Chow, C. C., Bahar, İ., & Billiar, T. R. (2004) · Current Molecular Medicine · doi:10.2174/1566524043359944 · Cited by 78
Role of the CNS microvascular pericyte in the blood-brain barrier
Balabanov, R. D., & Dore‐Duffy, P. (1998) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19980915)53:6 · Cited by 309
Apoptosis and autoimmune disease
O’Reilly, L. A., & Strasser, A. (1999) · Inflammation Research · doi:10.1007/s000110050369 · Cited by 78
CD95/Fas, Non-Apoptotic Signaling Pathways, and Kinases
Gallo, M. L., Poissonnier, A., Blanco, P., & Legembre, P. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01216 · Cited by 80
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