A Global Map of p53 Transcription-Factor Binding Sites in the Human Genome

WAF1, a potential mediator of p53 tumor suppression

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Genome sequencing in microfabricated high-density picolitre reactors

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Surfing the p53 network

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Finishing the euchromatic sequence of the human genome

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Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells

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Capturing Chromosome Conformation

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A model for p53-induced apoptosis

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The ENCODE (ENCyclopedia Of DNA Elements) Project

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Definition of a consensus binding site for p53

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Genome-Wide Location and Function of DNA Binding Proteins

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The State-of-the-Art of Chromatin Immunoprecipitation

Collas, P. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-414-2_1 · Cited by 43

Integrative bioinformatics analysis of transcriptional regulatory programs in breast cancer cells

Niida, A., Smith, A. D., Imoto, S., Tsutsumi, S., Aburatani, H., Zhang, M. Q., & Akiyama, T. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-404 · Cited by 40

Reply to Enrichment of regulatory motifs upstream of predicted DAF-16 targets

Oh, S. W., Mukhopadhyay, A., Dixit, B. L., Raha, T., Tissenbaum, H. A., & Green, M. R. (2006) · Nature Genetics · doi:10.1038/ng0406-398 · Cited by 41

Quantitative Proteomics Profiling of Murine Mammary Gland Cells Unravels Impact of Annexin-1 on DNA Damage Response, Cell Adhesion, and Migration

Swa, H. L. F., Blackstock, W. P., Lim, L. H. K., & Gunaratne, J. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.011205 · Cited by 40

Stra6, a retinoic acid-responsive gene, participates in p53-induced apoptosis after DNA damage

Carrera, S., Cuadrado‐Castano, S., Samuel, J., Jones, G. D. D., Villar, E., Lee, S. W., & Macip, S. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2013.14 · Cited by 40

Unraveling Regulatory Programs for NF-kappaB, p53 and MicroRNAs in Head and Neck Squamous Cell Carcinoma

Yan, B., Li, H., Yang, X., Shao, J., Jang, M., Guan, D., Zou, S., Waes, C. V., Chen, Z., & Zhan, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073656 · Cited by 39

The Cytidine Deaminase APOBEC3 Family Is Subject to Transcriptional Regulation by p53

Menéndez, D., Nguyen, T., Snipe, J. R., & Resnick, M. A. (2017) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-17-0019 · Cited by 43

ATM Dependent DUSP6 Modulation of p53 Involved in Synergistic Targeting of MAPK and p53 Pathways with Trametinib and MDM2 Inhibitors in Cutaneous Melanoma

Wu, C., Koay, T. S., Esfandiari, A., Ho, Y.-H., Lovat, P. E., & Lunec, J. (2018) · Cancers · doi:10.3390/cancers11010003 · Cited by 40

Role of the p53‑TRPM1/miR‑211‑MMP9 axis in UVB‑induced human melanocyte migration and its potential in repigmentation

Su, M., Fang, M., Jiang, S., Shi, Y., Luo, L., He, X., Wan, J., Xu, S., & Lei, T. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4478 · Cited by 40

Cell Type–Specific Whole-Genome Landscape of ΔFOSB Binding in the Nucleus Accumbens After Chronic Cocaine Exposure

Yeh, S.-Y., Estill, M. S., Lardner, C. K., Browne, C. J., Minier-Toribio, A. M., Futamura, R., Beach, K., McManus, C. A., Xu, S., Zhang, S., et al. (2022) · Biological Psychiatry · doi:10.1016/j.biopsych.2022.12.021 · Cited by 35

Exploiting the p53 Pathway for the Diagnosis and Therapy of Human CancerPreprint

Lane, D. P. (2005) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2005.70.049 · Cited by 40

Predicting functionality of protein–DNA interactions by integrating diverse evidence

Ucar, D., Beyer, A., Parthasarathy, S., & Workman, C. T. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp213 · Cited by 37

Genome-wide analysis of p53 transcriptional programs in B cells upon exposure to genotoxic stress in vivo

Tonelli, C., Morelli, M. J., Bianchi, S., Rotta, L., Capra, T., Sabò, A., Campaner, S., & Amati, B. B. (2015) · Oncotarget · doi:10.18632/oncotarget.5232 · Cited by 38

Acetylation of p53 stimulates miRNA processing and determines cell survival following genotoxic stress

Chang, J. J., Davis‐Dusenbery, B. N., Kashima, R., Jiang, X., Marathe, N., Sessa, R., Louie, J., Gu, W. J., Lagna, G., & Hata, A. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.242 · Cited by 38

Sensing the Environment Through Sestrins: Implications for Cellular Metabolism

Parmigiani, A., & Budanov, A. V. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.05.003 · Cited by 40

Autonomous feedback loop of RUNX1-p53-CBFB in acute myeloid leukemia cells

Morita, K., Noura, M., Tokushige, C., Maeda, S., Kiyose, H., Kashiwazaki, G., Taniguchi, J., Bando, T., Yoshida, K., Ozaki, T., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-16799-z · Cited by 40

p53 Isoforms as Cancer Biomarkers and Therapeutic Targets

Zhao, L., & Sanyal, S. (2022) · Cancers · doi:10.3390/cancers14133145 · Cited by 42

Immunohistochemistry in diagnostic surgical pathology: contributions of protein life-cycle, use of evidence-based methods and data normalization on interpretation of immunohistochemical stains.

Idikio, H. (2009) · PubMed Central · Cited by 38

Functions of MDMX in the Modulation of the p53‐Response

Lenos, K., & Jochemsen, A. G. (2011) · BioMed Research International · doi:10.1155/2011/876173 · Cited by 40

Skin as a living coloring book: how epithelial cells create patterns of pigmentation

Weiner, L., Fu, W.-Y., Chirico, W. J., & Brissette, J. L. (2014) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12301 · Cited by 37

PATZ1 Is a DNA Damage-Responsive Transcription Factor That Inhibits p53 Function

Keskin, N., Deniz, E., Eryilmaz, J., Ün, M., Batur, T., Erşahin, T., Çetin-Atalay, R., Sakaguchi, S., Ellmeier, W., & Erman, B. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.01475-14 · Cited by 39

Evolution of the Vertebrate Gene Regulatory Network Controlled by the Transcriptional Repressor REST

Johnson, R., Samuel, J., Ng, C. K. L., Jauch, R., Stanton, L. W., & Wood, I. C. (2009) · Molecular Biology and Evolution · doi:10.1093/molbev/msp058 · Cited by 37

WDR74 modulates melanoma tumorigenesis and metastasis through the RPL5–MDM2–p53 pathway

Li, Y., Zhou, Y., Li, B., Chen, F., Shen, W., Lu, Y., Zhong, C., Zhang, C., Xie, H., Katanaev, V. L., et al. (2020) · Oncogene · doi:10.1038/s41388-020-1179-6 · Cited by 37

TIFAB Regulates USP15-Mediated p53 Signaling during Stressed and Malignant Hematopoiesis

Niederkorn, M., Hueneman, K. M., Choi, K., Varney, M., Romano, L. M., Pujato, M., Greis, K., Inoue, J., Meetei, R. A., & Starczynowski, D. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.093 · Cited by 36

Estradiol-mediated inhibition of DNMT1 decreases p53 expression to induce M2-macrophage polarization in lung cancer progression

Chen, Y.-C., Young, M.-J., Chang, H.-P., Liu, C.-Y., Lee, C.-C., Tseng, Y., Wang, Y., Chang, W., & Hung, J. (2022) · Oncogenesis · doi:10.1038/s41389-022-00397-4 · Cited by 35

DNA topology influences p53 sequence-specific DNA binding through structural transitions within the target sites

Jagelská, E. B., Brázda, V., Pečínka, P., Paleček, E., & Fojta, M. (2008) · Biochemical Journal · doi:10.1042/bj20071648 · Cited by 37

Loss of p73 promotes dissemination of Myc-induced B cell lymphomas in mice

Nemajerová, A., Petrenko, O., Trümper, L. H. P., Palacios, G. F., & Moll, U. M. (2010) · Journal of Clinical Investigation · doi:10.1172/jci40331 · Cited by 37

The cytoskeleton adaptor protein ankyrin-1 is upregulated by p53 following DNA damage and alters cell migration

Hall, A. E., Lu, W.-T., Godfrey, J. D., Antonov, A. V., Paicu, C., Moxon, S., Dalmay, T., Wilczynska, A., Muller, P. A. J., & Bushell, M. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.91 · Cited by 37

High-throughput biochemical analysis of in vivo location data reveals novel distinct classes of POU5F1(Oct4)/DNA complexesPreprint

Tantin, D. R., Gemberling, M. P., Callister, C., & Fairbrother, W. G. (2008) · Genome Research · doi:10.1101/gr.072942.107 · Cited by 36

Gene and microRNA expression in p53‐deficient day 8.5 mouse embryos

Hosako, H., Martin, G. S., Barrier, M., Chen, Y. A., Ivanov, I. V., & Mirkes, P. E. (2009) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.20565 · Cited by 36

Genome-wide transcription factor binding site/promoter databases for the analysis of gene sets and co-occurrence of transcription factor binding motifs

Veerla, S., Ringnér, M., & Höglund, M. (2010) · BMC Genomics · doi:10.1186/1471-2164-11-145 · Cited by 36

p53-dependent stimulation of redox-related genes in the lymphoid organs of -irradiated mice identification of Haeme-oxygenase 1 as a direct p53 target gene

Meiller, A., Alvarez, S., Drané, P., Lallemand, C., Blanchard, B., Tovey, M. G., & May, E. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm824 · Cited by 41

Temporal Proteomic Analysis of BK Polyomavirus Infection Reveals Virus-Induced G 2 Arrest and Highly Effective Evasion of Innate Immune Sensing

Caller, L., Davies, C. T. R., Antrobus, R., Lehner, P. J., Weekes, M. P., & Crump, C. M. (2019) · Journal of Virology · doi:10.1128/jvi.00595-19 · Cited by 35

Novel roles of ER stress in repressing neural activity and seizures through Mdm2- and p53-dependent protein translation

Liu, D.-C., Eagleman, D. E., & Tsai, N. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1008364 · Cited by 36

Molecular background of α‐fetoprotein in liver cancer cells as revealed by global RNA expression analysis

Saito, S., Ojima, H., Ichikawa, H., Hirohashi, S., & Kondo, T. (2008) · Cancer Science · doi:10.1111/j.1349-7006.2008.00973.x · Cited by 36

Identification and analysis of large intergenic non-coding RNAs regulated by p53 family members through a genome-wide analysis of p53-binding sites

Idogawa, M., Ohashi, T., Sasaki, Y., Maruyama, R., Kashima, L., Suzuki, H., & Tokino, T. (2014) · Human Molecular Genetics · doi:10.1093/hmg/ddt673 · Cited by 37

Proposed megakaryocytic regulon of p53: the genes engaged to control cell cycle and apoptosis during megakaryocytic differentiation

Apostolidis, P. A., Lindsey, S. C., Miller, W. M., & Papoutsakis, E. T. (2012) · Physiological Genomics · doi:10.1152/physiolgenomics.00028.2012 · Cited by 36

A Novel Naphthalimide Compound Restores p53 Function in Non-small Cell Lung Cancer by Reorganizing the Bak·Bcl-xl Complex and Triggering Transcriptional Regulation

Zhang, G., An, Y.-F., Lü, X., Zhong, H., Zhu, Y., Wu, Y., Ma, F.-E., Yang, J., Liu, Y., Zhou, Z., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.669978 · Cited by 36

Feedback modulation of neural network synchrony and seizure susceptibility by Mdm2-p53-Nedd4-2 signaling

Jewett, K. A., Christian, C. A., Bacos, J. T., Lee, K. Y., Zhu, J., & Tsai, N. (2016) · Molecular Brain · doi:10.1186/s13041-016-0214-6 · Cited by 36

p53 binding sites in normal and cancer cells are characterized by distinct chromatin context

Bao, F., LoVerso, P. R., Fisk, J. N., Zhurkin, V. B., & Cui, F. (2017) · Cell Cycle · doi:10.1080/15384101.2017.1361064 · Cited by 36

Nuclear Receptor Location Analyses in Mammalian Genomes: From Gene Regulation to Regulatory Networks

Deblois, G., & Giguère, V. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0546 · Cited by 36

Calling cards for DNA-binding proteinsPreprint

Wang, H., Johnston, M., & Mitra, R. D. (2007) · Genome Research · doi:10.1101/gr.6510207 · Cited by 35

Large-scale production of SAGE libraries from microdissected tissues, flow-sorted cells, and cell lines

Khattra, J., Delaney, A. D., Zhao, Y., Siddiqui, A., Asano, J., McDonald, H., Pandoh, P., Dhalla, N., Prabhu, A.-L., Ma, K., et al. (2007) · Genome Research · doi:10.1101/gr.5488207 · Cited by 40

p53: Its Mutations and Their Impact on Transcription

Vaughan, C. A., Pearsall, I., Yeudall, W. A., Deb, S. P., & Deb, S. (2014) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-94-017-9211-0_4 · Cited by 37

High-throughput sequencing identifies STAT3 as the DNA-associated factor for p53-NF-κB-complex-dependent gene expression in human heart failure

Choy, M., Movassagh, M., Siggens, L., Vujić, A., Goddard, M. J., Sanchez, A. M., Perkins, N. D., Figg, N. L., Bennett, M. R., Carroll, J. S., et al. (2010) · Genome Medicine · doi:10.1186/gm158 · Cited by 35

microRNA 21‐mediated suppression of sprouty1 by Pokemon affects liver cancer cell growth and proliferation

Jin, X., Sun, Q., Liu, F., Yang, H., Liu, M., Liu, H., Xu, W., & Jiang, Y. (2013) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24504 · Cited by 35

Two p53 tetramers bind one consensus DNA response element

Kearns, S., Lurz, R., Orlova, E. V., & Okorokov, A. L. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw215 · Cited by 37

Antagonists of growth hormone-releasing hormone receptor induce apoptosis specifically in retinoblastoma cells

Chu, W. K., Law, K. S., Chan, S. O., Yam, J. C. S., Chen, L. J., Zhang, H., Cheung, H. S., Block, N. L., Schally, A. V., & Pang, C. P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617427113 · Cited by 36

Gene-Specific and Genome-Wide ChIP Approaches to Study Plant Transcriptional Networks

Belostotsky, D. A. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-563-7_1 · Cited by 35

Recognition of Local DNA Structures by p53 Protein

Brázda, V., & Coufal, J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020375 · Cited by 41

A New p53 Target Gene, RKIP, Is Essential for DNA Damage-Induced Cellular Senescence and Suppression of ERK Activation

Lee, S.-J., Lee, S.-H., Yoon, M.-H., & Park, B.-J. (2013) · Neoplasia · doi:10.1593/neo.121862 · Cited by 36

The Novel Protein Complex with SMARCAD1/KIAA1122 Binds to the Vicinity of TSS

Okazaki, N., Ikeda, S., Ohara, R., Shimada, K., Yanagawa, T., Nagase, T., Ohara, O., & Koga, H. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.07.031 · Cited by 34

Regulation of the Interferon-Inducible p53 Target Gene TRIM22 (Staf50) in Human T Lymphocyte Activation

Obad, S., Olofsson, T., Mechti, N., Gullberg, U., & Drott, K. (2007) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2006.0180 · Cited by 35

Gene set-based module discovery in the breast cancer transcriptome

Niida, A., Smith, A. D., Imoto, S., Aburatani, H., Zhang, M. Q., & Akiyama, T. (2009) · BMC Bioinformatics · doi:10.1186/1471-2105-10-71 · Cited by 33

Current and emerging breast cancer biomarkers

Sana, M., & Malik, H. J. (2015) · Journal of Cancer Research and Therapeutics · doi:10.4103/0973-1482.163698 · Cited by 33

The tumor suppressor p53 guides GluA1 homeostasis through Nedd4‐2 during chronic elevation of neuronal activity

Jewett, K. A., Zhu, J., & Tsai, N. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13271 · Cited by 35

Stimulus-Specific Transcriptional Regulation Within the p53 Network

Donner, A. J., Hoover, J. M., Szostek, S. A., & Espinosa, J. M. (2007) · Cell Cycle · doi:10.4161/cc.6.21.4893 · Cited by 33

Structural Basis for p53 Lys120-Acetylation-Dependent DNA-Binding Mode

Vainer, R., Cohen, S., Shahar, A., Zarivach, R., & Arbely, E. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.06.009 · Cited by 33

Gene expression profiles reveal an upregulation of E2F and downregulation of interferon targets by HPV18 but no changes between keratinocytes with integrated or episomal viral genomes

Karstensen, B., Poppelreuther, S., von Bonin, M., Walter, M. J., Iftner, T., & Stubenrauch, F. (2006) · Virology · doi:10.1016/j.virol.2006.05.030 · Cited by 33

Genome-wide location analysis: insights on transcriptional regulation

Hawkins, R. D., & Ren, B. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl043 · Cited by 33

Engineering versatile nano-bacteria hybrids for efficient tumor therapy

Wang, W., Yu, W., Li, G., Huang, H., Song, X., Chen, Y., & Chen, Y. (2023) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2023.215178 · Cited by 33

A genetic variant of p53 restricts the mucous secretory phenotype by regulating SPDEF and Bcl-2 expression

Chand, H. S., Montano, G., Huang, X., Randell, S. H., Mebratu, Y. A., Petersen, H. V., & Tesfaigzi, Y. (2014) · Nature Communications · doi:10.1038/ncomms6567 · Cited by 33

Induction of Retinoid X Receptor Activity and Consequent Upregulation of p21WAF1/CIP1 by Indenoisoquinolines in MCF7 Cells

Park, E., Kondratyuk, T. P., Morrell, A. E., Kiselev, E., Conda‐Sheridan, M., Cushman, M., Ahn, S., Choi, Y., White, J. J., van Breemen, R. B., et al. (2011) · Cancer Prevention Research · doi:10.1158/1940-6207.capr-10-0004 · Cited by 32

Mutated p53 in HGSC—From a Common Mutation to a Target for Therapy

Saleh, A., & Perets, R. (2021) · Cancers · doi:10.3390/cancers13143465 · Cited by 33

TP53 Gene Therapy as a Potential Treatment for Patients with COVID-19

Harford, J. B., Kim, S. S., Pirollo, K. F., & Chang, E. H. (2022) · Viruses · doi:10.3390/v14040739 · Cited by 31

Discovery of novel tumor suppressor p53 response elements using information theory

Lyakhov, I. G., Krishnamachari, A., & Schneider, T. D. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn189 · Cited by 32

P53 Family Members Modulate the Expression of PRODH, but Not PRODH2, via Intronic p53 Response Elements

Raimondi, I., Ciribilli, Y., Monti, P., Bisio, A., Pollegioni, L., Fronza, G., Inga, A., & Campomenosi, P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069152 · Cited by 32

Sequence variations in DNA repair gene XPCis associated with lung cancer risk in a Chinese population: a case-control study

Bai, Y., Xu, L., Yang, X., Hu, Z., Yuan, J., Wang, F., Shao, M., Yuan, W., Qian, J., Ma, H., et al. (2007) · BMC Cancer · doi:10.1186/1471-2407-7-81 · Cited by 32

The HaloTag: Improving Soluble Expression and Applications in Protein Functional Analysis

Peterson, S. N. (2012) · Current Chemical Genomics · doi:10.2174/1875397301206010008 · Cited by 31

Changing the p53 master regulatory network: ELEMENTary, my dear Mr Watson

Menéndez, D., Inga, A., Jordan, J. J., & Resnick, M. A. (2007) · Oncogene · doi:10.1038/sj.onc.1210277 · Cited by 32

A functional analysis of the CREB signaling pathway using HaloCHIP-chip and high throughput reporter assays

Hartzell, D., Trinklein, N. D., Méndez, J., Murphy, N., Aldred, S. F., Wood, K. V., & Urh, M. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-497 · Cited by 31

p53-Induced DNA Bending: The Interplay between p53−DNA and p53−p53 Interactions

Pan, Y., & Nussinov, R. (2008) · The Journal of Physical Chemistry B · doi:10.1021/jp800680w · Cited by 31

Microbial regulatory and metabolic networks

Cho, B., Charusanti, P., Herrgård, M. J., & Palsson, B. Ø. (2007) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2007.07.002 · Cited by 31

The Notch-1 receptor in prostate tumorigenesis

O'Brien, R. M., & Marignol, L. H. (2017) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2017.04.003 · Cited by 31

5-Lipoxygenase is a direct p53 target gene in humans

Gilbert, B., Ahmad, K. A., Roos, J., Lehmann, C., Chiba, T., Ulrich-Rückert, S., Smeenk, L., van Heeringen, S. J., Maier, T. J., Groner, B., et al. (2015) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2015.06.004 · Cited by 31

Associating transcription factor-binding site motifs with target GO terms and target genes

Mikael Bodén, A., & Bailey, T. L. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn374 · Cited by 31

PET-Tool: a software suite for comprehensive processing and managing of Paired-End diTag (PET) sequence data

Chiu, K. P., Wong, C., Chen, Q., Ariyaratne, P. N., Ooi, H., Wei, C., Sung, W.-K. K., & Ruan, Y. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-390 · Cited by 31

p53 rapidly restructures 3D chromatin organization to trigger a transcriptional response

Serra, F., Nieto-Aliseda, A., Fanlo, L., Rovirosa, L., Cabrera-Pasadas, M., Lazarenkov, A., Urmeneta, B., Alcalde-Merino, A., Nola, E., Okorokov, A. L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46666-1 · Cited by 30

Ionizing radiation-induced gene expression changes in TP53 proficient and deficient glioblastoma cell lines

Godoy, P. R. D. V., Mello, S. S., Magalhães, D. A. R., Donaires, F. S., Nicolucci, P., Donadi, E. A., Passos, G. A. S., & Sakamoto‐Hojo, E. T. (2013) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2013.06.010 · Cited by 30

Insights into the Effect of the G245S Single Point Mutation on the Structure of p53 and the Binding of the Protein to DNA

Lepre, M. G., Omar, S. I., Grasso, G., Morbiducci, U., Deriu, M. A., & Tuszyński, J. A. (2017) · Molecules · doi:10.3390/molecules22081358 · Cited by 31

P53 represses pyrimidine catabolic gene dihydropyrimidine dehydrogenase (DPYD) expression in response to thymidylate synthase (TS) targeting

Gokare, P. R., Finnberg, N. K., Abbosh, P. H., Dai, J., Murphy, M. E., & El‐Deiry, W. S. (2017) · Scientific Reports · doi:10.1038/s41598-017-09859-x · Cited by 30

PPM1D suppresses p53-dependent transactivation and cell death by inhibiting the Integrated Stress Response

Andrysík, Z., Sullivan, K. D., Kieft, J. S., & Espinosa, J. M. (2022) · Nature Communications · doi:10.1038/s41467-022-35089-5 · Cited by 31

Brain metastasis in breast cancer: focus on genes and signaling pathways involved, blood–brain barrier and treatment strategies

Chhichholiya, Y., Ruthuparna, M., Velagaleti, H., & Munshi, A. (2023) · Clinical & Translational Oncology · doi:10.1007/s12094-022-03050-z · Cited by 33

p53: a molecular marker for the detection of cancer

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