The IRF family of transcription factors: Inception, impact and implications in oncogenesis

Jak-STAT Pathways and Transcriptional Activation in Response to IFNs and Other Extracellular Signaling Proteins

Darnell, J. E., Kerr, L. M., & Stark, G. R. (1994) · Science · doi:10.1126/science.8197455 · Cited by 6,080

Papillomaviruses and cancer: from basic studies to clinical application

Hausen, H. Z. (2002) · Nature reviews. Cancer · doi:10.1038/nrc798 · Cited by 4,031

IRF-7 is the master regulator of type-I interferon-dependent immune responses

Honda, K., Yanai, H., Negishi, H., Asagiri, M., Sato, M., Mizutani, T., Shimada, N., Ohba, Y., Takaoka, A., Yoshida, N., et al. (2005) · Nature · doi:10.1038/nature03464 · Cited by 2,229

IRFs: master regulators of signalling by Toll-like receptors and cytosolic pattern-recognition receptors

Honda, K., & Taniguchi, T. (2006) · Nature reviews. Immunology · doi:10.1038/nri1900 · Cited by 1,716

IRF Family of Transcription Factors as Regulators of Host Defense

Taniguchi, T., Ogasawara, K., Takaoka, A., & Tanaka, N. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.623 · Cited by 1,658

Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma

Guichard, C., Amaddeo, G., Imbeaud, S., Ladeiro, Y., Pelletier, L., Benmaad, I., Caldéraro, J., Bioulac‐Sage, P., Letexier, M., Degos, F., et al. (2012) · Nature Genetics · doi:10.1038/ng.2256 · Cited by 1,522

Nucleotide sequence of the Kaposi sarcoma-associated herpesvirus (HHV8)

Russo, J. J., Bohenzky, R. A., Chien, M.-C., Chen, J., Yan, M., Maddalena, D., Parry, J. P., Peruzzi, D., Edelman, I. S., Chang, Y., et al. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.25.14862 · Cited by 1,457

Inflammation meets cancer, with NF-κB as the matchmaker

Ben‐Neriah, Y., & Karin, M. (2011) · Nature Immunology · doi:10.1038/ni.2060 · Cited by 1,408

Distinct and Essential Roles of Transcription Factors IRF-3 and IRF-7 in Response to Viruses for IFN-α/β Gene Induction

Sato, M., Suemori, H., Hata, N., Asagiri, M., Ogasawara, K., Nakao, K., Nakaya, T., Katsuki, M., Noguchi, S., Tanaka, N., et al. (2000) · Immunity · doi:10.1016/s1074-7613(00)00053-4 · Cited by 1,342

The IRF Family Transcription Factors in Immunity and Oncogenesis

Tamura, T., Yanai, H., Savitsky, D., & Taniguchi, T. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090400 · Cited by 1,259

The Spatial Transcriptomic Atlas of Human Limbus and Vital Niche Microenvironment Regulating the Fate of Limbal Epithelial Stem Cells

Li, S., Sun, H., Fang, F., Zhang, S., Chen, J., Shao, C., Fu, Y., & Chen, L. (2025) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.66.3.52 · Cited by 3

MicroRNAs and the immune system

Frasca, F., Scordio, M., & Scagnolari, C. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89774-7.00007-8 · Cited by 4

Human inborn errors of immunity associated with IRF4

Thouenon, R., & Kracker, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1236889 · Cited by 3

The Link of Interferon Regulatory Factors 4 and 7 on the Patient’s Survival in Lung Adenocarcinoma

Kara, A., Aydin, A., Morva, A., Ceker, D., Küçüker, S., & Karadağ, A. (2018) · International Conference on Cancer Care Informatics (CCI) · doi:10.1109/cancercare.2018.8618159 · Cited by 3

Valproic acid enhances the anti-tumor effect of pegylated interferon-α towards pancreatic cancer cell lines.

Sugimoto, K., Shimada, M., Utsunomiya, T., Morine, Y., Imura, S., Ikemoto, T., & Iwahashi, S. (2014) · PubMed · Cited by 3

Highly preserved consensus gene modules in human papilloma virus 16 positive cervical cancer and head and neck cancers

Zhang, X., Cha, I., & Kim, K. (2017) · Oncotarget · doi:10.18632/oncotarget.23116 · Cited by 3

Identification and characterization of interferon regulatory factor 1 from Lateolabrax japonicus involved in antiviral immune response against grouper nervous necrosis virus infection

Ma, Z., Xu, C., Yang, R., Jing Hua, H. U., Zhou, S., & Yang, Q.-B. (2019) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2019.12.066 · Cited by 3

SARS‐CoV‐2 Genome and S2 Spike Protein: IRF‐Driven Interferon Regulation and Host Cell Responses

Singh, E., Nishi, N., Tripathi, M., & Prakash, K. S. (2025) · Reviews in Medical Virology · doi:10.1002/rmv.70094 · Cited by 2

Multi-omics analysis reveals comprehensive aberrant protein and phosphorylation characteristics in breast cancer and paired metastatic lymph nodes

Zhai, L., Liu, C., Zhao, L., Zheng, L.-W., Chu, C., Hong, H., Cai, Y., Chen, L., Liu, Y.-M., Wang, Y., et al. (2026) · Protein & Cell · doi:10.1093/procel/pwag002 · Cited by 2

The role of IRF1 in positive feedback of type I IFN transcription to combat Siniperca chuatsi rhabdovirus (SCRV) infection in teleost fish

Li, L., Wang, K. L., Li, N., Peng, X. Y., Liu, L. H., Chen, S. N., & Nie, P. (2026) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2026.105567 · Cited by 2

IRF4 Suppresses Osteogenic Differentiation of Periodontal Ligament Stem Cells by Activating IL‐18 Signaling Pathway in Periodontitis

Hu, Z., Luo, Y., Lin, W., & Wu, X. (2024) · Advanced Biology · doi:10.1002/adbi.202400099 · Cited by 2

The primate‐specific presence of interferon regulatory factor‐5 pseudogene 1

Marquis, A., Hubing, V., Ziemann, C., Moriyama, E. N., & Zhang, L. (2024) · Journal of Medical Virology · doi:10.1002/jmv.29879 · Cited by 2

Structure and expression identification of Cherry Valley duck IRF8

Zhang, T., Zhai, X., Wang, X., Wang, J., Xing, B., Miao, R., Li, T., Hong, T., & Wei, L. (2021) · Poultry Science · doi:10.1016/j.psj.2021.101598 · Cited by 2

MicroRNAs Involved in Small-cell Lung Cancer as Possible Agents for Treatment and Identification of New Targets

Weidle, U. H., & Nopora, A. (2021) · Cancer Genomics & Proteomics · doi:10.21873/cgp.20283 · Cited by 2

A framework for associating structural variants with cell-specific transcription factors and histone modifications in defect phenotypes

Becker, T., Bayarsaihan, D., & Shin, D. (2022) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm55620.2022.9995130 · Cited by 3

Interferon Regulatory Factor

Shah, M., & Choi, S. (2017) · Springer eBooks · doi:10.1007/978-3-319-67199-4_101496 · Cited by 2

Systematic analysis of transcription factor combinatorial binding uncovers TEAD1 as an antagonist of tissue-specific transcription factors in human organogenesisPreprint

Garcia-Mora, A., Mallen, J., Zarrineh, P., Hanley, N. A., Gerrard, D. T., & Bobola, N. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.05.561094 · Cited by 1

PBRM1-dependent PBAF targeting is required for EMT and metastasis in breast cancer

Dhiman, A., Ayers, M. G., McCuiston, J. L., Shinde, A. B., Akhand, S. S., Jiao, G., Jauregui-Lozano, J. P. P., Hadisurya, M., Porter, E. G. P., Tao, W. A., et al. (2026) · Science Advances · doi:10.1126/sciadv.aed8038 · Cited by 1

Interferon regulatory factors: the next prospective targets for tissue ischemia–reperfusion injury?

Xie, J., An, X., Gao, Y., Du, K., Chen, H., Zhang, J. J., Chen, T., & Hou, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1782849 · Cited by 1

Functional analysis of IRF1/2 homolog in immune regulation of the sea urchin Strongylocentrotus intermedius

Liu, F., Xu, D., Ding, X., Ren, G., Thiyagarajan, V., Chu, X., Liu, T., Huang, B., & Wang, X. Y. (2026) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2026.105668 · Cited by 1

Switching of transcriptional control from interferon regulatory factor 2 to interferon regulatory factor 1 drives innate immune cell activation

Cadena, C., Reja, R., Bolech, E., Webster, J. D., Kameswaran, V., Simone, M. D., Chen, C., Jiang, J., Hötzel, K., Bjornson, C. R. R., et al. (2026) · Cell · doi:10.1016/j.cell.2026.08.049 · Cited by 1

Innate Immune Receptor Signaling and IRF Family of Transcription Factors: Good Deeds and Misdeeds in Oncogenesis

Ikushima, H., Yanai, H., & Taniguchi, T. (2015) · Springer eBooks · doi:10.1007/978-4-431-55327-4_7 · Cited by 1

Macrophage Defects

Rosenzweig, S. D., & Holland, S. M. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405546-9.00032-7 · Cited by 1

Investigating the association of rs920778T > C polymorphism in HOTAIR gene in breast cancer patients in the northwestern of Iran

Shavali, M., Pouladi, N., Abdolahi, S., Farajzadeh, D., & Moniri, S. (2020) · Meta Gene · doi:10.1016/j.mgene.2020.100756 · Cited by 1

Gut Microbiome and Cancer

Theodoropoulos, G. E. (2021) · The microbiomes of humans, animals, plants, and the environment · doi:10.1007/978-3-030-59642-2_4 · Cited by 1

Mesenchymal stem cells (MSCs) from the mouse bone marrow show differential expression of interferon regulatory factors IRF-1 and IRF-2

Chaudhary, J. K., Ahamad, N., & Rath, P. C. (2024) · Molecular Biology Reports · doi:10.1007/s11033-023-09025-9 · Cited by 1

Hunnivirus structural protein VP2 inhibits beta interferon production by targeting the IRF3 essential modulator

Zhu, X., Dong, Q., Zhang, K., Zou, Y., Zhang, G., Du, Y., Mo, X., Wu, A., Ouyang, K., Chen, Y., et al. (2024) · Veterinary Microbiology · doi:10.1016/j.vetmic.2024.110148 · Cited by 1

Elevated IRF9 raised cell apoptosis and tissue damages through suppressing SIRT1 in hyperlipidemia acute pancreatitis with liver injury

Pan, J.-G., Qin, R.-X., Ma, X., Han, Z., Lu, Z., Sun, Y. T., & Yu, W. (2024) · Egyptian Liver Journal · doi:10.1186/s43066-024-00352-5 · Cited by 1

Unlocking the Puzzle of Mammalian Transfection: The Role of the RNA-sensing-Mediated Interferon Response in the Cellular Defense Against Foreign DNA Intrusion

Li, X., Zhou, Y., Wei, J., Sun, W., Fan, L., & Yan, J. (2025) · International Journal of Biological Sciences · doi:10.7150/ijbs.107510 · Cited by 2

Identification of IRF8 as an immune infiltration‐related biomarker in hepatocellular carcinoma by bioinformatics analysis

Zhang, R., Guo, Y., Liu, Z., Kong, L., Li, C., He, L., Zhang, C., Chen, Z., Bian, H., & Ding, W. (2022) · MedComm · doi:10.1002/mco2.149 · Cited by 1

PARP inhibition in Ewing sarcoma: impact of germline DNA damage repair defects and activation of immunoregulatory pathwaysPreprint

Maurer, L. M., Venier, R. E., Mukherjee, E., Julian, C. M., Daley, J. D., Bailey, N. G., Jacobs, M. F., Kumar‐Sinha, C., Raphel, H., Weiss, K. R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.09.18.304238 · Cited by 1

Epigenome priming dictates transcription response and white matter fate upon perinatal inflammationPreprint

Schang, A., Steenwinckel, J. V., Lipecki, J., Rich‐Griffin, C., Woolley-Allen, K., Dyer, N. P., Charpentier, T. L., Schäfer, P., Fleiss, B., Ott, S., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/411702 · Cited by 2

Systematic analysis of transcription factor combinatorial binding uncovers TEAD1 as an antagonist of tissue-specific transcription factors in human organogenesisPreprint

Garcia-Mora, A., Mallen, J., Zarrineh, P., Hanley, N. A., Gerrard, D. T., & Bobola, N. (2025) · eLife · doi:10.7554/elife.105338 · Cited by 2

A systems based framework to computationally predict putative transcription factors and signaling pathways regulating glycan biosynthesisPreprint

Groth, T., & Neelamegham, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.19.257956

Interferon Regulatory Factor

Shah, M., & Choi, S. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6438-9_101496-1

Additional file 1 of ExplaiNN: interpretable and transparent neural networks for genomics

Novakovsky, G., Fornés, O., Saraswat, M., Mostafavi, S., & Wasserman, W. W. (2023) · Figshare · doi:10.6084/m9.figshare.23590426

Additional file 3 of ExplaiNN: interpretable and transparent neural networks for genomics

Novakovsky, G., Fornés, O., Saraswat, M., Mostafavi, S., & Wasserman, W. W. (2023) · Figshare · doi:10.6084/m9.figshare.23590432

Additional file 4 of ExplaiNN: interpretable and transparent neural networks for genomics

Novakovsky, G., Fornés, O., Saraswat, M., Mostafavi, S., & Wasserman, W. W. (2023) · Figshare · doi:10.6084/m9.figshare.23590435

Promotor Analysis of Cattle Endometrium throughout Oestrous Cycle and Early Gestation Period

Musavi, S. A. A., Hakim, M. A., & Akbari, N. A. (2023) · Asian Journal of Research in Animal and Veterinary Sciences · doi:10.9734/ajravs/2023/v6i4266

Gene expression levels associated with impaired immune response and increased proliferation could serve as biomarkers for women following cervical cancer screening programmes

Øvestad, I. T., Dalen, I., Søreng, K., Akbari, S., Lapin, M., Janssen, E. A. M., Austdal, M., Munk, A. C., & Gudlaugsson, E. G. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1507193

Interferon regulatory factor -9 in Labeo rohita, an insight into its interacting domain residues and dynamic responses to PAMPs stimulation and pathogenic challenges

Ganguly, B., Mahapatra, S., Pani, S., Das, R., Saha, A., & Samanta, M. (2025) · Comparative Immunology Reports · doi:10.1016/j.cirep.2025.200209

Systematic analysis of transcription factor combinatorial binding uncovers TEAD1 as an antagonist of tissue-specific transcription factors in human organogenesisPreprint

Garcia-Mora, A., Mallen, J., Zarrineh, P., Hanley, N. A., Gerrard, D. T., & Bobola, N. (2025) · eLife · doi:10.7554/elife.105338.1

Meta-analysis of transcriptome profiles of B16 melanoma cells after in vivo treatment with dacarbazine

Lapkina, E. Z., Zinchenko, I. S., Bondar, E. I., & Ruksha, T. G. (2025) · Kazan medical journal · doi:10.17816/kmj678601

IRF2 degradation tunes the innate immune responsePreprint

Cadena, C., Reja, R., Bolech, E., Webster, J. D., Kameswaran, V., Simone, M. C. D., Chen, C., Jiang, J. W., Hötzel, K., Alegre, K. O., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.23.678148

Additional file 3 of Cyproheptadine, an epigenetic modifier, exhibits anti-tumor activity by reversing the epigenetic silencing of IRF6 in urothelial carcinoma

Jou, Y.-C., Lin, G.-L., Lin, H.-Y., Huang, W.-H., Chuang, Y.-M., Lin, R.-I., Chen, P.-C., Wu, S.-F., Shen, C.-H., & Chan, M. W. Y. (2021) · Figshare · doi:10.6084/m9.figshare.14450709

Additional file 4 of IRF4 expression is low in Philadelphia negative myeloproliferative neoplasms and is associated with a worse prognosis

Cumbo, C., Tarantini, F., Anelli, L., Zagaria, A., Redavid, I., Minervini, C. F., Coccaro, N., Tota, G., Ricco, A., Parciante, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17598219

Additional file 1 of IRF4 expression is low in Philadelphia negative myeloproliferative neoplasms and is associated with a worse prognosis

Cumbo, C., Tarantini, F., Anelli, L., Zagaria, A., Redavid, I., Minervini, C. F., Coccaro, N., Tota, G., Ricco, A., Parciante, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17598201

Additional file 5 of IRF4 expression is low in Philadelphia negative myeloproliferative neoplasms and is associated with a worse prognosis

Cumbo, C., Tarantini, F., Anelli, L., Zagaria, A., Redavid, I., Minervini, C. F., Coccaro, N., Tota, G., Ricco, A., Parciante, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17598228

Additional file 2 of ExplaiNN: interpretable and transparent neural networks for genomics

Novakovsky, G., Fornés, O., Saraswat, M., Mostafavi, S., & Wasserman, W. W. (2023) · Figshare · doi:10.6084/m9.figshare.23590429

Additional file 1 of Cyproheptadine, an epigenetic modifier, exhibits anti-tumor activity by reversing the epigenetic silencing of IRF6 in urothelial carcinoma

Jou, Y.-C., Lin, G.-L., Lin, H.-Y., Huang, W.-H., Chuang, Y.-M., Lin, R.-I., Chen, P.-C., Wu, S.-F., Shen, C.-H., & Chan, M. W. Y. (2021) · Figshare · doi:10.6084/m9.figshare.14450703

Additional file 2 of IRF4 expression is low in Philadelphia negative myeloproliferative neoplasms and is associated with a worse prognosis

Cumbo, C., Tarantini, F., Anelli, L., Zagaria, A., Redavid, I., Minervini, C. F., Coccaro, N., Tota, G., Ricco, A., Parciante, E., et al. (2021) · Figshare · doi:10.6084/m9.figshare.17598204

T cell exhaustion associated genes IRF1 and PDGFRB modulate immune infiltration and affect prognosis in colon adenocarcinoma

Yi, H., Liu, H.-H., Ding, J.-T., Zhou, H.-N., Huang, H.-Y., Liu, J., Huang, Y.-F., Taicheng, Z., & Zong, Z. (2025) · Heliyon · doi:10.1016/j.heliyon.2025.e43767

Non-Coding RNAs as key regulators of interferon signaling in cancer immunotherapy: mechanistic insights and clinical prospects

Sayed, U., Abdulsahib, W. K., Jyothi, S. R., Nayak, P. P., Chauhan, A. S., Singla, S., Polatova, D. S., Sead, F. F., & Akhavan‐Sigari, R. (2026) · Clinical and Experimental Medicine · doi:10.1007/s10238-025-02027-w · Cited by 1

2’-5’ Oligoadenylate Synthetase-Like 1- (OASL1-) deficient mice promote antiviral protection against pseudorabies virus infection associated with enhanced production of type I interferon

Bao, T. H. T. N., Leya, M., Van, T. P., Ham, G., Oh, B., Oh, S.-I., Kim, W.-I., Park, S., & Kim, B. (2026) · Scientific Reports · doi:10.1038/s41598-026-43144-0 · Cited by 1

Role of SWI/SNF chromatin-remodeling complexes in tumorigenesis : insights in dedifferentiated melanoma and renal medullary carcinoma

Vokshi, B. (2020) · theses.fr (ABES) · doi:10.70675/059b4951z271fz4649za800z1b92769ff8e2

Transcriptional regulations of inflammasome-related genes by Interferon Regulatory Factors

Cornut, M. (2020) · theses.fr (ABES) · doi:10.70675/fa5bf18bz82a6z4879za183z27963c062531

Human inherited IRF1 deficiency

Rosain, J. (2022) · theses.fr (ABES) · doi:10.70675/067993b6zab73z45fazb9aez6af7872f8ba2

Cortical mechanisms of comorbidity between pain sensitization and attention-deficit/hyperactivity disorder (ADHD) in a mouse model

Nehme, S. B. S. (2024) · theses.fr (ABES) · doi:10.70675/7ad70482z0961z4eebzbc86z84355cab1f1d

TroIRF6, a teleost interferon regulatory factor of Golden pompano (Trachinotus ovatus), enhances antimicrobial defense and immune potentiation

Zhang, P., He, Z., Chen, G., Wu, Y., Zheng, X., Wang, J., Cao, Z., Zhang, C., Sun, J., Tu, Z., et al. (2026) · Aquaculture · doi:10.1016/j.aquaculture.2026.744093

Functional characterization of IRF2 and IRF2a in Japanese eel (Anguilla japonica) identifies dual pathways suppressing interferon responses

Qin, H., Li, D., Zhao, G., Nie, P., Huang, W., & Huang, B. (2026) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2026.111393

Comparative analysis of the impact of interferon regulatory factors on basal and induced interferon and interferon stimulated gene expression in human and canine keratinocytes

Quinlan, S., May, S. P., Weeks, R. D., & Luff, J. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1810139

TLR9 contributes to tumor progression and cisplatin resistance in esophageal squamous cell carcinoma

Xiang, D., Zhu, M., Zhang, M., Wang, Y., Gai, Q., Lu, H., Zhang, P., Cui, Y., Jiang, J., Wang, Y., et al. (2026) · Genes & Diseases · doi:10.1016/j.gendis.2026.102361

Nanoadjuvant-based membrane poration boosts antitumor immunity via modulating mitochondrial metabolism to downregulate PD-L1 and upregulate STING

You, W., Gao, F., Wang, H.-L., Shen, A., Zhang, Z., Nie, X., Huang, W.-Q., Wang, L., & You, Y. (2026) · Bioactive Materials · doi:10.1016/j.bioactmat.2026.08.026

Sexual reproduction impacts vertebrate organ agingPreprint

Chen, J., Tsenter, A., Costa, E. K., Yu, D., Lin, X., Chen, K. L., Bot, V. A., Housh, M. J., Heraud, L.-P., Perry, S. V., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.08.757363

Interferon regulatory factor family of transcription factors and regulation of oncogenesis

Takaoka, A., Tamura, T., & Taniguchi, T. (2008) · Cancer Science · doi:10.1111/j.1349-7006.2007.00720.x · Cited by 152

Regulation of immunity and oncogenesis by the IRF transcription factor family

Savitsky, D., Tamura, T., Yanai, H., & Taniguchi, T. (2010) · Cancer Immunology, Immunotherapy · doi:10.1007/s00262-009-0804-6 · Cited by 298

The interferon regulatory factors and oncogenesis

Tanaka, N., & Taniguchi, T. (2000) · Seminars in Cancer Biology · doi:10.1006/scbi.2000.0310 · Cited by 85

The IRF Family Transcription Factors in Immunity and Oncogenesis

Tamura, T., Yanai, H., Savitsky, D., & Taniguchi, T. (2008) · Annual Review of Immunology · doi:10.1146/annurev.immunol.26.021607.090400 · Cited by 1,259

Genetic and Epigenetic Regulation of Interferon Regulatory Factor Expression: Implications in Human Malignancies

Fragale, A. (2013) · Journal of Genetic Syndromes & Gene Therapy · doi:10.4172/2157-7412.1000205 · Cited by 6