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p53 is required for radiation-induced apoptosis in mouse thymocytes
Abstract
The p53 tumour suppressor gene is the most widely mutated gene in human tumorigenesis. p53 encodes a transcriptional activator whose targets may include genes that regulate genomic stability, the cellular response to DNA damage, and cell-cycle progression. Introduction of wild-type p53 into cell lines that have lost endogenous p53 function can cause growth arrest or induce a process of cell death known as apoptosis. During normal development, self-reactive thymocytes undergo negative selection by apoptosis, which can also be induced in immature thymocytes by other stimuli, including exposure to glucocorticoids and ionizing radiation. Although normal negative selection involves signalling through the T-cell receptor, the induction of apoptosis by other stimuli is poorly understood. We have investigated the requirement for p53 during apoptosis in mouse thymocytes. We report here that immature thymocytes lacking p53 die normally when exposed to compounds that may mimic T-cell receptor engagement and to glucocorticoids but are resistant to the lethal effects of ionizing radiation. These results demonstrate that p53 is required for radiation-induced cell death in the thymus but is not necessary for all forms of apoptosis.
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“The checkpoints also actively stimulate the repair processes [1–9] and, in higher eukaryotes, trigger the apoptotic response, if damage cannot be dealt with successfully [10–12].”
From Mind the gap: keeping UV lesions in check (2011) · cites this paper as [10]
In the citing paper
“In both the pigmentation induction and DNA repair activation processes, POMC/α-MSH functions as the crucial downstream target of the “guardian of genome” protein p53 (47).”
From Melanocyte-stimulating hormone directly enhances UV-Induced DNA repair in keratinocytes by a xeroderma pigmentosum group A-dependent mechanism (2010) · cites this paper as [47]
Citations
Cites
Antibodies, a laboratory manual
(1989) · Biomedicine & Pharmacotherapy · doi:10.1016/0753-3322(89)90130-3 · Cited by 12,318
p53 Mutations in Human Cancers
Hollstein, M., Sidransky, D., Vogelstein, B., & Harris, C. C. (1991) · Science · doi:10.1126/science.1905840 · Cited by 8,018
Antibodies: A laboratory manual
J.L. (1989) · Trends in Biochemical Sciences · doi:10.1016/0968-0004(89)90307-1 · Cited by 5,141
Lane, D. P. (1992) · Nature · doi:10.1038/358015a0 · Cited by 5,138
Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumours
Donehower, L. A., Harvey, M., Slagle, B. L., McArthur, M. J., Montgomery, C. A., Butel, J. S., & Bradley, A. (1992) · Nature · doi:10.1038/356215a0 · Cited by 4,649
Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation
Wyllie, A. H. (1980) · Nature · doi:10.1038/284555a0 · Cited by 4,499
The p53 tumour suppressor gene
Levine, A. J., Momand, J. A., & Finlay, C. A. (1991) · Nature · doi:10.1038/351453a0 · Cited by 3,785
Participation of p53 protein in the cellular response to DNA damage.
Kastan, M. B., Onyekwere, O. C., Sidransky, D., Vogelstein, B., & Craig, R. W. (1991) · PubMed · Cited by 3,761
Kastan, M. B., Zhan, Q., El-Deiry, W. S., Carrier, F., Jacks, T., Walsh, W. V., Plunkett, B. S., Vogelstein, B., & Fornace, A. J. (1992) · Cell · doi:10.1016/0092-8674(92)90593-2 · Cited by 3,047
Self-citationHandbook of Experimental Immunology.
Denman, A. (1968) · Annals of Internal Medicine · doi:10.7326/0003-4819-68-6-1376_1 · Cited by 2,414
Flagged first, then by citations
1 of the 44 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Kastan, M. B., Onyekwere, O., Sidransky, D., Vogelstein, B. & Craig, R. W. Cancer Res. 51, 6304–6311 (1991).
Cited by
Sorted by citations
Items 301–400 of 1,005
The Retinoblastoma Protein: A Master Regulator of Cell Cycle, Differentiation and Apoptosis
Herwig, S., & Strauss, M. (1997) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1997.t01-2-00581.x · Cited by 249
Malaquin, N., Martinez, A., & Rodier, F. (2016) · Experimental Gerontology · doi:10.1016/j.exger.2016.05.010 · Cited by 247
Waldmann, T. A., White, J., Carrasquillo, J. A., Reynolds, J., Paik, C. H., Gansow, O. A., Brechbiel, M., Jaffe, E., Fleisher, T., & Goldman, C. K. (1995) · Blood · doi:10.1182/blood.v86.11.4063.bloodjournal86114063 · Cited by 246
The WT1 gene product stabilizes p53 and inhibits p53-mediated apoptosis.Preprint
Maheswaran, S., Englert, C., Bennett, P., Heinrich, G., & Haber, D. A. (1995) · Genes & Development · doi:10.1101/gad.9.17.2143 · Cited by 248
A teratologic suppressor role for p53 in benzo(a)pyrene–treated transgenic p53-deficient mice
Nicol, C. J. B., Harrison, M. L., Laposa, R. R., Gimelshtein, I. L., & Wells, P. G. (1995) · Nature Genetics · doi:10.1038/ng0695-181 · Cited by 247
p53-dependent apoptosis suppresses radiation–induced teratogenesis
Norimura, T., Nomoto, S., Katsuki, M., Gondo, Y., & Kondo, S. (1996) · Nature Medicine · doi:10.1038/nm0596-577 · Cited by 245
Increased airway epithelial and T-cell apoptosis in COPD remains despite smoking cessation
Hodge, S. J., Hodge, G. L., Holmes, M., & Reynolds, P. N. (2005) · European Respiratory Journal · doi:10.1183/09031936.05.00077604 · Cited by 244
Apoptosis induced by inhibition of intercellular contact.
Bates, R. C., Buret, A. G., Helden, D. F. V., Horton, M. A., & Burns, G. F. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.2.403 · Cited by 244
Expression and Role of Bcl–Xl in Human Hepatocellular Carcinomas
Takehara, T., Liu, X., Fujimoto, J., Friedman, S. L., & Takahashi, H. (2001) · Hepatology · doi:10.1053/jhep.2001.25387 · Cited by 246
HCV NS5A interacts with p53 and inhibits p53-mediated apoptosis
Lan, K., Sheu, M., Hwang, S., Yen, S., Chen, S., Wu, J., Wang, Y.-J., Kato, N., Omata, M., Chang, F., et al. (2002) · Oncogene · doi:10.1038/sj.onc.1205589 · Cited by 252
Jain, M. V., Paczulla, A., Klonisch, T. C., Dimgba, F. N., Rao, S. B., Roberg, K. B., Schweizer, F., Lengerke, C., Davoodpour, P., Palicharla, V. R., et al. (2013) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12001 · Cited by 248
Apoptosis induction resulting from proteasome inhibition
Shinohara, K., Tomioka, M., Nakano, H., Toné, S., Itô, H., & Kawashima, S. (1996) · Biochemical Journal · doi:10.1042/bj3170385 · Cited by 241
Biomarkers for Response to Neoadjuvant Chemoradiation for Rectal Cancer
Kuremsky, J. G., Tepper, J. E., & McLeod, H. L. (2009) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2009.03.003 · Cited by 240
Mechanisms of glucocorticoid-mediated apoptosis in hematological malignancies.
Greenstein, S., Ghias, K. K., Krett, N. L., & Rosen, S. T. (2002) · PubMed · Cited by 239
van der Pluijm, I., Garinis, G. A., Brandt, R. M. C., Gorgels, T. G. M. F., Wijnhoven, S., Diderich, K. E. M., de Wit, J., Mitchell, J. R., van Oostrom, C., Beems, R. B., et al. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0050002 · Cited by 240
An inducible long noncoding RNA amplifies DNA damage signaling
Schmitt, A. M., Garcia, J. T., Hung, T., Flynn, R. A., Shen, Y., Qu, K., Payumo, A. Y., Peres-da-Silva, A., Brož, D. K., Baum, R., et al. (2016) · Nature Genetics · doi:10.1038/ng.3673 · Cited by 242
Chen, Y., Wang, W., Kong, A.-N. T., & Tan, T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.3.1769 · Cited by 238
Cell‐free reconstitution of Fas‐, UV radiation‐ and ceramide‐induced apoptosis.
Martin, S. J., Newmeyer, D. D., Mathias, S., Farschon, D. M., Wang, H., Reed, J. C., Kolesnick, R., & Green, D. R. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00203.x · Cited by 237
Pettitt, A. R., Sherrington, P. D., Stewart, G. S., Cawley, J. C., Taylor, A. M. R., & Stanković, T. (2001) · Blood · doi:10.1182/blood.v98.3.814 · Cited by 237
ZIP Kinase, a Novel Serine/Threonine Kinase Which Mediates Apoptosis
Kawai, T., Matsumoto, M., Takeda, K., Sanjo, H., & Akira, S. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.3.1642 · Cited by 240
The Bcl-2 family of proteins: regulators of cell death and survival
Núñez, G., & Clarke, M. F. (1994) · Trends in Cell Biology · doi:10.1016/0962-8924(94)90053-1 · Cited by 233
Midgley, C., Owens, B. M., Briscoe, C. V., Thomas, D. B., Lane, D. P., & Hall, P. A. (1995) · Journal of Cell Science · doi:10.1242/jcs.108.5.1843 · Cited by 233
Pan, H., & Griep, A. E. (1995) · Genes & Development · doi:10.1101/gad.9.17.2157 · Cited by 238
Wills, K. N., Maneval, D. C., Menzel, P., Harris, M. P., Sutjipto, S., Vaillancourt, M.-T., Huang, W.-M., Johnson, D. E., Anderson, S. C., Wen, S. F., et al. (1994) · Human Gene Therapy · doi:10.1089/hum.1994.5.9-1079 · Cited by 232
Chiou, S., Tseng, C. C., Rao, L., & White, E. (1994) · Journal of Virology · doi:10.1128/jvi.68.10.6553-6566.1994 · Cited by 230
Squier, M. K. T., Sehnert, A. J., & Cohen, J. (1995) · Journal of Leukocyte Biology · doi:10.1002/jlb.57.1.2 · Cited by 230
Cancer Metabolism: Current Understanding and Therapies
Counihan, J. L., Grossman, E. A., & Nomura, D. K. (2018) · Chemical Reviews · doi:10.1021/acs.chemrev.7b00775 · Cited by 236
Xia, H. H., & Talley, N. J. (2001) · The American Journal of Gastroenterology · doi:10.1016/s0002-9270(00)02240-1 · Cited by 229
DNA damage and p53-mediated cell cycle arrest: A reevaluation
Pellegata, N. S., Antoniono, R. J., Redpath, J. L., & Stanbridge, E. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15209 · Cited by 229
TP53 Mutations and Outcomes in Breast Cancer: Reading beyond the Headlines
Shahbandi, A., Nguyen, H. D., & Jackson, J. G. (2020) · Trends in cancer · doi:10.1016/j.trecan.2020.01.007 · Cited by 241
Harvey, M., Vogel, H. S., Morris, D. K., Bradley, A., Bernstein, A., & Donehower, L. A. (1995) · Nature Genetics · doi:10.1038/ng0395-305 · Cited by 232
Activation-induced apoptosis in lymphocytes
Green, D. R., & Scott, D. W. (1994) · Current Opinion in Immunology · doi:10.1016/0952-7915(94)90130-9 · Cited by 228
Apoptosis and cancer chemotherapy
Makin, G., & Hickman, J. A. (2000) · Cell and Tissue Research · doi:10.1007/s004419900160 · Cited by 227
Deconstructing networks of p53-mediated tumor suppression in vivo
Kaiser, A. M., & Attardi, L. D. (2017) · Cell Death and Differentiation · doi:10.1038/cdd.2017.171 · Cited by 232
Induction of Apoptosis by c-Fos Protein
Preston, G. A., Lyon, T., Yin, Y., Lang, J. E., Solomon, G. G., Annab, L. A., Srinivasan, D. G., Alcorta, D. A., & Barrett, J. C. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.1.211 · Cited by 228
Westphal, C. H., Rowan, S., Schmaltz, C., Elson, A., Fisher, D. E., & Leder, P. (1997) · Nature Genetics · doi:10.1038/ng0897-397 · Cited by 227
Lysosomal destabilization in p53-induced apoptosis
Yuan, X., Li, W., Dalen, H., Lotem, J., Kama, R., Sachs, L., & Brunk, U. T. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092135599 · Cited by 230
Btf, a Novel Death-Promoting Transcriptional Repressor That Interacts with Bcl-2-Related Proteins
Kasof, G. M., Goyal, L., & White, E. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.6.4390 · Cited by 225
Difilippantonio, M. J., Petersen, S., Chen, H. T., Johnson, R., Jasin, M., Kanaar, R., Ried, T., & Nussenzweig, A. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020851 · Cited by 231
Reciprocal repression between P53 and TCTP
Amson, R. B., Pece, S., Lespagnol, A., Vyas, R., Mazzarol, G., Tosoni, D., Colaluca, I. N., Viale, G., Rodrigues-Ferreira, S., Wynendaele, J., et al. (2011) · Nature Medicine · doi:10.1038/nm.2546 · Cited by 232
The bcl-2 Gene Product Prevents Programmed Cell Death of Ventricular Myocytes
Kirshenbaum, L. A., & de Moissac, D. (1997) · Circulation · doi:10.1161/01.cir.96.5.1580 · Cited by 223
Clinical implications of p53 mutations
Wallace-Brodeur, R. R., & Lowe, S. W. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050270 · Cited by 226
Self-citationTissue-specific induction of p53 targets in vivo.
Fei, P., Bernhard, E. J., & El‐Deiry, W. S. (2002) · PubMed · Cited by 223
Signal Transduction Pathways in Apoptosis
McConkey, D. J., & Orrenius, S. (1996) · Stem Cells · doi:10.1002/stem.140619 · Cited by 223
Predicting response to cancer chemotherapy: the role of p53
Weller, M. (1998) · Cell and Tissue Research · doi:10.1007/s004410051072 · Cited by 221
Mdm-2 and ubiquitin-independent p53 proteasomal degradation regulated by NQO1
Asher, G., Lotem, J., Sachs, L., Kahana, C., & Shaul, Y. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.202480499 · Cited by 223
Vorburger, S. A., & Hunt, K. K. (2002) · The Oncologist · doi:10.1634/theoncologist.7-1-46 · Cited by 220
Wang, H., Gao, X., Fukumoto, S., Tademoto, S., Sato, K., & Hirai, K. (1999) · Journal of Cellular Physiology · doi:10.1002/(sici)1097-4652(199911)181:2 · Cited by 45
Bouvard, V., Zaitchouk, T., Vacher, M., Duthu, A., Canivet, M., Choisy, C., Nieruchalski, M., & May, E. (2000) · Oncogene · doi:10.1038/sj.onc.1203366 · Cited by 221
Autoimmune disease. a problem of defective apoptosis
Mountz, J. D., Wu, J., Cheng, J., & Zhou, T. (1994) · Arthritis & Rheumatism · doi:10.1002/art.1780371002 · Cited by 219
Dial 9-1-1 for p53: Mechanisms of p53 Activation by Cellular Stress
Ljungman, M. E. (2000) · Neoplasia · doi:10.1038/sj.neo.7900073 · Cited by 222
Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma.
Diller, L., Sexsmith, E., Gottlieb, A., Li, F. P., & Malkin, D. M. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117834 · Cited by 218
Apoptosis and cancer drug targeting
Sellers, W. R., & Fisher, D. E. (1999) · Journal of Clinical Investigation · doi:10.1172/jci9053 · Cited by 216
Impact of p53 loss on reversal and recurrence of conditional Wnt-induced tumorigenesisPreprint
Gunther, E. J., Moody, S. E., Belka, G. K., Hahn, K. T., Innocent, N., Dugan, K. D., Cardiff, R. D., & Chodosh, L. A. (2003) · Genes & Development · doi:10.1101/gad.1051603 · Cited by 214
The effects of glucocorticoids on human eosinophils
Schleimer, R. P., & Bochner, B. S. (1994) · Journal of Allergy and Clinical Immunology · doi:10.1016/0091-6749(94)90333-6 · Cited by 218
Russell, K., Wiens, L. W., Demers, G. W., Galloway, D. A., Plon, S. E., & Groudine, M. T. (1995) · PubMed · Cited by 213
Interaction of p53 with the Human Rad51 Protein
Buchhop, S., Gibson, M. K., Wang, X. W., Wagner, P., Stürzbecher, H.-W., & Harris, C. C. (1997) · Nucleic Acids Research · doi:10.1093/nar/25.19.3868 · Cited by 212
Butt, A. J., Firth, S. M., King, M. A., & Baxter, R. C. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m908888199 · Cited by 211
Curing metastatic cancer: lessons from testicular germ-cell tumours
Masters, J. R., & Köberle, B. (2003) · Nature reviews. Cancer · doi:10.1038/nrc1120 · Cited by 210
Radiosensitization of p53 mutant cells by PD0166285, a novel G(2) checkpoint abrogator.
Wang, Y., Li, J., Booher, R. N., Kraker, A. J., Lawrence, T. S., Leopold, W. R., & Sun, Y. (2001) · PubMed · Cited by 210
Miyazaki, T., Hirokami, Y., Matsuhashi, N., Takatsuka, H., & Naito, M. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.2.413 · Cited by 210
c-myc and bcl-2 modulate p53 function by altering p53 subcellular trafficking during the cell cycle.
Ryan, J. J., Prochownik, E. V., Gottlieb, C. A., Apel, I. J., Merino, R., Núñez, G., & Clarke, M. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.13.5878 · Cited by 208
Abid‐Essefi, S., Baudrimont, I., Hassen, W., Ouanes, Z., Mobio, T. A., Anane, R., Creppy, E. E., & Bacha, H. (2003) · Toxicology · doi:10.1016/s0300-483x(03)00329-9 · Cited by 207
Targeted point mutations of p53 lead to dominant-negative inhibition of wild-type p53 function
de Vries, A., Flores, E. R., Miranda, B., Hsieh, H.-M., van Oostrom, C. T. M., Sage, J., & Jacks, T. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052713099 · Cited by 207
Self-citationLiu, V. F., & Weaver, D. T. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.12.7222 · Cited by 207
Hinds, P. W., & Weinberg, R. A. (1994) · Current Opinion in Genetics & Development · doi:10.1016/0959-437x(94)90102-3 · Cited by 210
Methylation-Acetylation Interplay Activates p53 in Response to DNA Damage
Ivanov, G. S., Ivanova, T., Kurash, J. K., Ivanov, A. V., Chuikov, S., Gizatullin, F., Herrera-Medina, E. M., Rauscher, F. J., Reinberg, D., & Barlev, N. A. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00460-07 · Cited by 210
Lutzker, S. G., & Levine, A. J. (1996) · Nature Medicine · doi:10.1038/nm0796-804 · Cited by 206
Razvi, E. S., & Welsh, R. M. (1995) · Advances in virus research · doi:10.1016/s0065-3527(08)60057-3 · Cited by 206
Michalak, E. M., Villunger, A., Adams, J. M., & Strasser, A. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.16 · Cited by 211
Lavoie, J. N., Nguyen, M.-H., Marcellus, R. C., Branton, P. E., & Shore, G. C. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.140.3.637 · Cited by 205
Halazonetis, T. D., & Kandil, A. N. (1993) · The EMBO Journal · doi:10.1002/j.1460-2075.1993.tb06199.x · Cited by 211
Sanjo, H., Kawai, T., & Akira, S. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.44.29066 · Cited by 204
Naik, P., Karrim, J., & Hanahan, D. (1996) · Genes & Development · doi:10.1101/gad.10.17.2105 · Cited by 205
Bcl-2 and Bcl-2-Related Proteins in Apoptosis Regulation
Boise, L., GOTTSCHALK, A. R., Quintáns, J., & Thompson, C. B. (1995) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-79437-7_8 · Cited by 203
Neat1 is a p53-inducible lincRNA essential for transformation suppressionPreprint
Mello, S. S., Sinow, C., Raj, N., Mazur, P. K., Bieging-Rolett, K. T., Brož, D. K., Conklin, J. F., Vogel, H. S., Wood, L. D., Sage, J., et al. (2017) · Genes & Development · doi:10.1101/gad.284661.116 · Cited by 209
Inoue, A., Seidel, M. G., Wu, W., Kamizono, S., Ferrando, A. A., Bronson, R. T., Iwasaki, H., Akashi, K., Morimoto, A., Hitzler, J. K., et al. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00155-1 · Cited by 202
An Essential Role for Nuclear Factor κB in Promoting Double Positive Thymocyte Apoptosis
Hettmann, T., DiDonato, J. A., Karin, M., & Leiden, J. M. (1999) · The Journal of Experimental Medicine · doi:10.1084/jem.189.1.145 · Cited by 202
UVA1 Radiation Triggers Two Different Final Apoptotic Pathways
Godar, D. E. (1999) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.1999.00474.x · Cited by 201
Sugimoto, A., Friesen, P. D., & Rothman, J. H. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06475.x · Cited by 201
p53 Signaling and Cell Cycle Checkpoints
Stewart, Z. A., & Pietenpol, J. A. (2001) · Chemical Research in Toxicology · doi:10.1021/tx000199t · Cited by 204
The role of p53 in tumour suppression: lessons from mouse models
Attardi, L. D., & Jacks, T. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050269 · Cited by 203
Self-citationExpression and Function of the Leucine Zipper Protein Par-4 in Apoptosis
Sells, S. F., Han, S., Muthukkumar, S., Maddiwar, N. G., Johnstone, R. W., Boghaert, E. R., Gillis, D., Liu, G., Nair, P., Monnig, S., et al. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.7.3823 · Cited by 200
Wang, S.-G. (2008) · Oncogene · doi:10.1038/onc.2008.298 · Cited by 201
Swarbrick, A., Woods, S. L., Shaw, A., Balakrishnan, A., Phua, Y. W., Nguyen, A., Chanthery, Y. H., Lim, L., Ashton, L. J., Judson, R. L., et al. (2010) · Nature Medicine · doi:10.1038/nm.2227 · Cited by 202
Bystander effect produced by radiolabeled tumor cells in vivo
Xue, L. Y., Butler, N. J., Makrigiorgos, G. M., Adelstein, S. J., & Kassis, A. I. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182209699 · Cited by 199
Accelerated Neutrophil Apoptosis in Mice Lacking A1-a, a Subtype of the bcl-2–related A1 Gene
Hamasaki, A., Sendo, F., Nakayama, K., Ishida, N., Negishi, I., Nakayama, K., & Hatakeyama, S. (1998) · The Journal of Experimental Medicine · doi:10.1084/jem.188.11.1985 · Cited by 199
Wen, S.-T., Jackson, P. K., & Etten, R. A. V. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00503.x · Cited by 199
High metastatic potential in mice inheriting a targeted p53 missense mutation
Liu, G., McDonnell, T. J., Luna, R. M. D. O., Kapoor, M., Mims, B. H., El‐Naggar, A. K., & Lozano, G. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.8.4174 · Cited by 201
Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathways
Barlow, C., Brown, K. D., Deng, C., Tagle, D. A., & Wynshaw-Boris, A. J. (1997) · Nature Genetics · doi:10.1038/ng1297-453 · Cited by 198
Apoptosis (Programmed Cell Death) in Arteries of the Neonatal Lamb
Cho, A., Courtman, D. W., & Langille, B. L. (1995) · Circulation Research · doi:10.1161/01.res.76.2.168 · Cited by 198
Intact p53-Dependent Responses in miR-34–Deficient Mice
Concepcion, C. P., Han, Y.-C., Mu, P., Bonetti, C., Yao, E., D'Andrea, A., Vidigal, J. A., Maughan, W. P., Ogrodowski, P., & Ventura, A. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002797 · Cited by 197
Kwon, H. J., Owa, T., Hassig, C. A., Shimada, J., & Schreiber, S. L. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3356 · Cited by 197
Xia, F., Wang, X., Wang, Y. H., Tsang, N. M., Yandell, D. W., Kelsey, K. T., & Liber, H. L. (1995) · PubMed · Cited by 197
Takenaka, I. M., Morin, F., Seizinger, B. R., & Kley, N. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.10.5405 · Cited by 198
Absence of p53 gene mutations in primary neuroblastomas.
Vogan, K. J., Bernstein, M. L., Leclerc, J., Brisson, L., Brossard, J., Brodeur, G. M., Pelletier, J., & Gros, P. (1993) · PubMed · Cited by 196
What to do at an end: DNA double-strand-break repair
Weaver, D. T. (1995) · Trends in Genetics · doi:10.1016/s0168-9525(00)89121-0 · Cited by 197
Nees, M., Homann, N., Discher, H., Andl, T., Enders, C., Herold‐Mende, C. C., Schuhmann, A., & Bosch, F. X. (1993) · PubMed · Cited by 195
Mechanisms of G2 Arrest in Response to Overexpression of p53
Taylor, W. R., DePrimo, S. E., Agarwal, A. M., Agarwal, M. L., Schönthal, A. H., Katula, K. S., & Stark, G. R. (1999) · Molecular Biology of the Cell · doi:10.1091/mbc.10.11.3607 · Cited by 195
Rusch, V. W., Klimstra, D. S., Venkatraman, E. S., Oliver, J., Martini, N., Gralla, R. J., Kris, M. G., & Dmitrovsky, E. (1995) · PubMed · Cited by 194
Metadata
- Authors
- Lowe, S. W., Schmitt, E. M., Smith, S. W., Osborne, B. A., & Jacks, T.
- Affiliations
- Massachusetts Institute of Technology (US)
- University of Massachusetts Amherst (US)
- Venue
- Nature
- Published
- 1993-04
- Volume
- 362
- Issue
- 6423
- Pages
- 847-849
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2078581194
- Cited by
- 2,864
- References
- 44
- Citations by year
- 2026: 8 · 2025: 15 · 2024: 28 · 2023: 18 · 2022: 9 · 2021: 24 · 2020: 19 · 2019: 23 · 2018: 31 · 2017: 28 · 2016: 34 · 2015: 24 · 2014: 30 · 2013: 37 · 2012: 40
- FWCI
- 123.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- p53, radiation-induced apoptosis, thymocytes, ionizing radiation, negative selection, T cell receptor signaling, glucocorticoids, T cell development, tumor suppressor, radioresistance (biology)
- MeSH terms
- Animals, Cells, Cultured, Dexamethasone, Gamma Rays, Mice, Inbred C57BL, Mutation, Thymus Gland, Genes, p53, Tumor Suppressor Protein p53, Apoptosis, Mice
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