The DOI matches its Crossref record; 713 of the 713 references it cites were found in a registry or an index.
MicroRNAs in Development and Disease
Abstract
MicroRNAs (miRNAs) are a class of posttranscriptional regulators that have recently introduced an additional level of intricacy to our understanding of gene regulation. There are currently over 10,000 miRNAs that have been identified in a range of species including metazoa, mycetozoa, viridiplantae, and viruses, of which 940, to date, are found in humans. It is estimated that more than 60% of human protein-coding genes harbor miRNA target sites in their 3′ untranslated region and, thus, are potentially regulated by these molecules in health and disease. This review will first briefly describe the discovery, structure, and mode of function of miRNAs in mammalian cells, before elaborating on their roles and significance during development and pathogenesis in the various mammalian organs, while attempting to reconcile their functions with our existing knowledge of their targets. Finally, we will summarize some of the advances made in utilizing miRNAs in therapeutics.
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Items 601–713 of 713
A Dual Role for Src Homology 2 Domain–Containing Inositol-5-Phosphatase (Ship) in Immunity
Helgason, C. D., Kalberer, C. P., Damen, J. E., Chappel, S. M., Pineault, N., Krystal, G., & Humphries, R. K. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.5.781 · Cited by 150
Song, B., Wang, Y., Kudo, K., Gavin, E. J., Xi, Y., & Ju, J. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-08-1422 · Cited by 150
Li, Q., Song, X., Zou, J., Wang, G., Kremneva, E., Li, X.-Q., Zhu, N., Sun, T., Lappalainen, P., Yuan, W., et al. (2010) · Journal of Cell Science · doi:10.1242/jcs.067165 · Cited by 148
Cardiomyopathy in transgenic mice with cardiac-specific overexpression of serum response factor
Zhang, X., Azhar, G., Chai, J., Sheridan, P. L., Nagano, K., Brown, T., Yang, J., Khrapko, K., Borras, A. M., Lawitts, J. A., et al. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.280.4.h1782 · Cited by 147
Methamphetamine Inhibits Antigen Processing, Presentation, and Phagocytosis
Tallóczy, Z., Martínez, J., Joset, D., Ray, Y., Gácser, A., Toussi, S., Mizushima, N., Nosanchuk, J., Goldstein, H., Loike, J., et al. (2008) · PLoS Pathogens · doi:10.1371/journal.ppat.0040028 · Cited by 147
MicroRNA-127 modulates fetal lung development
Bhaskaran, M., Wang, Y., Zhang, H., Weng, T., Baviskar, P. S., Guo, Y., Gou, D., & Liu, L. (2009) · Physiological Genomics · doi:10.1152/physiolgenomics.90268.2008 · Cited by 147
MicroRNA-15b regulates cell cycle progression by targeting cyclins in glioma cells
Xia, H., Qi, Y., Ng, S. S., Chen, X., Chen, S., Fang, M., Li, D., Zhao, Y. F., Ge, R., Guo, L., et al. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2008.12.169 · Cited by 146
Quantitative differential expression analysis reveals miR-7 as major islet microRNA
Bravo-Egaña, V., Rosero, S., Molano, R. D., Pileggi, A., Ricordi, C., Domínguez‐Bendala, J., & Pastori, R. L. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.12.052 · Cited by 142
Regulation of pri-microRNA BIC transcription and processing in Burkitt lymphoma
Kluiver, J. L., van den Berg, A., de Jong, D., Blokzijl, T., Harms, G., Bouwman, E., Jacobs, S. C., Poppema, S., & Kroesen, B. J. (2006) · Oncogene · doi:10.1038/sj.onc.1210147 · Cited by 141
MicroTar: predicting microRNA targets from RNA duplexes
Thadani, R., & Tammi, M. T. (2006) · BMC Bioinformatics · doi:10.1186/1471-2105-7-s5-s20 · Cited by 141
MicroRNA-183 family members regulate sensorineural fates in the inner ear
Li, H., Kloosterman, W., & Fekete, D. M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4948-09.2010 · Cited by 140
Rupp, H. (1981) · Basic Research in Cardiology · doi:10.1007/bf01908164 · Cited by 139
Epstein–Barr virus growth/latency III program alters cellular microRNA expression
Cameron, J. E., Fewell, C., Yin, Q., McBride, J., Wang, X., Lin, Z. N., & Flemington, E. K. (2008) · Virology · doi:10.1016/j.virol.2008.09.018 · Cited by 139
Bellovin, D. I., Simpson, K. J., Danilov, T. A., Maynard, E., Rimm, D. L., Oettgen, P., & Mercurio, A. M. (2006) · Oncogene · doi:10.1038/sj.onc.1209682 · Cited by 139
A Risk Variant in an miR-125b Binding Site in BMPR1B Is Associated with Breast Cancer Pathogenesis
Sætrom, P., Biesinger, J., Li, S. M., Smith, D., Thomas, L. F., Majzoub, K., Rivas, G. E., Alluin, J., Rossi, J. J., Krontiris, T. G., et al. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1201 · Cited by 138 · cited 1×
“(BMPR1B) (522) that are associated with breast cancer, confirms its role in the underlying pathogenesis.”
BackgroundVerras, M., Brown, J. D., Li, X., Nusse, R., & Sun, Z. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-2370 · Cited by 137
Mir-144 selectively regulates embryonic alpha-hemoglobin synthesis during primitive erythropoiesis.
Fu, Y.-F., Du, T., Dong, M., Zhu, K.-Y., Jing, C.-B., Zhang, Y., Wang, L., Fan, H.-B., Chen, Y., Jin, Y., et al. (2009) · Blood · doi:10.1182/blood-2008-08-174854 · Cited by 137
Watanabe, N., Kurabayashi, M., Shimomura, Y., Kawai‐Kowase, K., Hoshino, Y.-I., Manabe, I., Watanabe, M., Aikawa, M., Kuro‐o, M., Suzuki, T., et al. (1999) · Circulation Research · doi:10.1161/01.res.85.2.182 · Cited by 136
Gfi1 regulates miR-21 and miR-196b to control myelopoiesis
Velu, C. S., Baktula, A. M., & Grimes, H. L. (2009) · Blood · doi:10.1182/blood-2008-11-190215 · Cited by 136
Agrawal, R., Tran, U., & Wessely, O. (2009) · Development · doi:10.1242/dev.037432 · Cited by 134
Pardal, R., Molofsky, A. V., He, S., & Morrison, S. J. (2005) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2005.70.057 · Cited by 134
Overexpression of stathmin in breast carcinomas points out to highly proliferative tumours
Curmi, P. A., Noguès, C., Lachkar, S., Calmels, N., Gonthier, M., Sobel, A., Lidereau, R., & Bièche, I. (2000) · British Journal of Cancer · doi:10.1054/bjoc.1999.0891 · Cited by 133
Taniguchi, K., Kohno, R.-I., Ayada, T., Kato, R., Ichiyama, K., Morisada, T., Oike, Y., Yonemitsu, Y., Maehara, Y., & Yoshimura, A. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01600-06 · Cited by 132
Notch-1 regulates transcription of the epidermal growth factor receptor through p53
Purow, B. W., Sundaresan, T. K., Burdick, M. J., Kefas, B. A., Comeau, L., Hawkinson, M. P., Su, Q., Kotliarov, Y., Lee, J., Zhang, W., et al. (2008) · Carcinogenesis · doi:10.1093/carcin/bgn079 · Cited by 132
Niu, Z., Yu, W., Zhang, S. X., Barron, M., Belaguli, N. S., Schneider, M. D., Parmacek, M. S., Nordheim, A., & Schwartz, R. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501372200 · Cited by 128
Slitrk1-deficient mice display elevated anxiety-like behavior and noradrenergic abnormalities
Katayama, K., Yamada, K., Ornthanalai, V. G., Inoue, T., Ota, M., Murphy, N. P., & Aruga, J. (2010) · Molecular Psychiatry · doi:10.1038/mp.2008.97 · Cited by 127
MicroRNA-206 is overexpressed in the diaphragm but not the hindlimb muscle of mdx mouse
McCarthy, J. J., Esser, K. A., & Andrade, F. H. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00077.2007 · Cited by 127
Epidermal growth factor receptor‐regulated miR‐125a‐5p – a metastatic inhibitor of lung cancer
Wang, G., Mao, W., Zheng, S. S., & Ye, J. (2009) · FEBS Journal · doi:10.1111/j.1742-4658.2009.07238.x · Cited by 126
Xie, Y., Xu, K., Dai, B.-T., Guo, Z., Jiang, T., Chen, H., & Qiu, Y. (2005) · Oncogene · doi:10.1038/sj.onc.1209058 · Cited by 126
Pandey, P., Brors, B., Srivastava, P. K., Bott, A., Boehn, S. N. E., Groene, H.-J., & Gretz, N. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-624 · Cited by 126
Puri, N., Khramtsov, A., Ahmed, S., Nallasura, V., Hetzel, J. T., Jagadeeswaran, R., Karczmar, G. S., & Salgia, R. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-4416 · Cited by 126
Soukup, G. A., Fritzsch, B., Pierce, M. L., Weston, M. D., Jahan, I., McManus, M. T., & Harfe, B. D. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.01.037 · Cited by 125
The Promoter of the pri-miR-375 Gene Directs Expression Selectively to the Endocrine Pancreas
Avnit-Sagi, T., Kantorovich, L., Kredo‐Russo, S., Hornstein, E., & WALKER, M. D. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005033 · Cited by 125
The involvement of the transcription factor Yin Yang 1 in cancer development and progression
Castellano, G., Torrisi, E., Ligresti, G., Malaponte, G., Militello, L., RUSSO, A. E., McCubrey, J. A., Canevari, S., & Libra, M. (2009) · Cell Cycle · doi:10.4161/cc.8.9.8314 · Cited by 124
Lee, C.-C., Putnam, A. J., Miranti, C. K., Gustafson, M. F., Wang, L.-M., Woude, G. F. V., & Gao, C.-F. (2004) · Oncogene · doi:10.1038/sj.onc.1207646 · Cited by 124
Bae, S.-N., Arand, G., Azzam, H. S., Pavasant, P., Torri, J. A., Frandsen, T. L., & Thompson, E. W. (1993) · Breast Cancer Research and Treatment · doi:10.1007/bf01833264 · Cited by 123
TRAP230/ARC240 and TRAP240/ARC250 Mediator subunits are functionally conserved through evolution
Samuelsen, C. O., Baraznenok, V., Khorosjutina, O., Spåhr, H., Kieselbach, T., Holmberg, S., & Gustafsson, C. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1030497100 · Cited by 123
Ferracini, R., Olivero, M., Renzo, M. F. D., Martano, M., Giovanni, C. D., Nanni, P., Basso, G., Scotlandi, K., Lollini, P., & Comoglio, P. M. (1996) · PubMed · Cited by 122
SHH Pathway and Cerebellar Development
Vaillant, C., & Monard, D. (2009) · The Cerebellum · doi:10.1007/s12311-009-0094-8 · Cited by 121
Mechanism of growth inhibition by MicroRNA 145: The role of the IGF‐I receptor signaling pathway
Rocca, G. L., Badin, M., Shi, B., Xu, S., DeAngelis, T., Sepp‐Lorenzino, L., & Baserga, R. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21796 · Cited by 121
Homeobox D10 Induces Phenotypic Reversion of Breast Tumor Cells in a Three-Dimensional Culture Model
Carrió, M., Arderiu, G., Myers, C. A., & Boudreau, N. J. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-1717 · Cited by 121
Comprehensive whole genome array CGH profiling of mantle cell lymphoma model genomes
de Leeuw, R. J., Davies, J. J., Rosenwald, A., Bebb, G. D., Gascoyne, R. D., Dyer, M. J. S., Staudt, L. M., Martinez-Climent, J. A., & Lam, W. L. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh195 · Cited by 121
Spred-1 negatively regulates allergen-induced airway eosinophilia and hyperresponsiveness
Inoue, H., Kato, R., Fukuyama, S., Nonami, A., Taniguchi, K., Matsumoto, K., Nakano, T., Tsuda, M., Matsumura, M., Kubo, M., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20040616 · Cited by 121
Sonoki, T., Iwanaga, E., Mitsuya, H., & Asou, N. (2005) · Leukemia · doi:10.1038/sj.leu.2403938 · Cited by 119
The E2F3-Oncomir-1 Axis Is Activated in Wilms' Tumor
Kort, E. J., Farber, L. J., Tretiakova, M., Petillo, D., Furge, K. A., Yang, X. J., Cornelius, A. S., & Teh, B. T. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-0592 · Cited by 117
Aberrant expression of HOX genes in human invasive breast carcinoma
Makiyama, K., Hamada, J.-I., Takada, M., Murakawa, K., Takahashi, Y., Tada, M., Tamoto, E., Shindo, G., Matsunaga, A., Teramoto, K., et al. (2005) · Oncology Reports · doi:10.3892/or.13.4.673 · Cited by 115
DNMT1 and DNMT3B Modulate Distinct Polycomb-Mediated Histone Modifications in Colon Cancer
Jin, B., Yao, B., Li, J., Fields, C. R., Delmas, A. L., Liu, C., & Robertson, K. D. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0116 · Cited by 115
Cicek, M., Fukuyama, R., Welch, D. R., et al. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-3139 · Cited by 115
A novel mechanism of tumor suppression by destabilizing AU-rich growth factor mRNA
Stoecklin, G., Gross, B., Ming, X., & Moroni, C. (2003) · Oncogene · doi:10.1038/sj.onc.1206418 · Cited by 115
Associations among IRS1, IRS2, IGF1, and IGFBP3 Genetic Polymorphisms and Colorectal Cancer
Slattery, M. L., Samowitz, W. S., Curtin, K., Ma, K.-N., Hoffman, M. D., Caan, B. J., & Neuhausen, S. L. (2004) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.1206.13.7 · Cited by 112
Wang, M., Tan, L., Dijkstra, M. K., van Lom, K., Robertus, J., Harms, G., Blokzijl, T., Kooistra, K., Veer, M. B. V., Rosati, S., et al. (2008) · The Journal of Pathology · doi:10.1002/path.2333 · Cited by 112
Changing genetic information through RNA editing
Maas, S., & Rich, A. S. (2000) · BioEssays · Cited by 111
Transcriptional regulation of the murine promoter by cardiac factors Nkx2-5, GATA4 and Tbx5
Linhares, V. L., Almeida, N. A. S., MENEZES, D., Elliott, D. A., Lai, D., Beyer, E. C., CAMPOSDECARVALHO, A., & Costa, M. W. (2004) · Cardiovascular Research · doi:10.1016/j.cardiores.2004.09.021 · Cited by 110
Bernstein, J., Evan, A. P., & Gardner, K. (1987) · PubMed · Cited by 107
The C Terminus of Sprouty Is Important for Modulation of Cellular Migration and Proliferation
Yigzaw, Y., Cartin, L., Pierre, S. C., Scholich, K., & Patel, T. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m100123200 · Cited by 106
Araya, R., Eckardt, D., Maxeiner, S., Krüger, O., Theis, M., Willecke, K., & Sáez, J. C. (2004) · Journal of Cell Science · doi:10.1242/jcs.01553 · Cited by 105
Expression and Processing of a Small Nucleolar RNA from the Epstein-Barr Virus Genome
Hutzinger, R., Feederle, R., Mrazek, J., Schiefermeier-Mach, N., Balwierz, P. J., Zavolan, M., Polacek, N., Delecluse, H., & Hüttenhofer, A. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000547 · Cited by 104
Germline mutation of microRNA-125a is associated with breast cancer
Li, W., Duan, R., Kooy, R. F., Sherman, S. L., Zhou, W., & Jin, P. (2009) · Journal of Medical Genetics · doi:10.1136/jmg.2008.063123 · Cited by 102
Lu, L., Katsaros, D., Shaverdashvili, K., Qian, B., Wu, Y., de la Longrais, I. A. R., Preti, M., Menato, G., & Yu, H. (2009) · European Journal of Cancer · doi:10.1016/j.ejca.2009.05.003 · Cited by 100
Lee, C., Subramanian, S., Beck, A. H., Espinosa, Í., Senz, J., Zhu, S., Huntsman, D. D., van de Rijn, M., & Gilks, C. B. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007314 · Cited by 99
Class 1A PI3K regulates vessel integrity during development and tumorigenesis
Yuan, T. L., Choi, H. S., Matsui, A., Benes, C. H., Lifshits, E., Luo, J., Frangioni, J. V., & Cantley, L. C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804123105 · Cited by 99
Chen, X., Wang, K., Chen, J., Guo, J., Yin, Y., Cai, X. F., Guo, X., Wang, G., Yang, R. L., Zhu, L., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m807523200 · Cited by 99
Evidence for X-Chromosomal Schizophrenia Associated with microRNA Alterations
Feng, J., Sun, G., Jin, Y., Noltner, K., Li, W., Buzin, C. H., Longmate, J., Heston, L. L., Rossi, J. J., & Sommer, S. S. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006121 · Cited by 98
Faggad, A., Budczies, J., Tchernitsa, O. I., Darb‐Esfahani, S., Sehouli, J., Müller, B. M., Wirtz, R. M., Chekerov, R., Weichert, W., Sinn, B. V., et al. (2009) · The Journal of Pathology · doi:10.1002/path.2658 · Cited by 98
Modification of Cognitive Performance in Schizophrenia by Complexin 2 Gene Polymorphisms
Begemann, M., Grube, S., Papiol, S., Malzahn, D., Krampe, H., Ribbe, K., Friedrichs, H., Radyushkin, K., El-Kordi, A., Benseler, F., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.107 · Cited by 96
MicroRNAs and target site screening reveals a pre-microRNA-30e variant associated with schizophrenia
Xu, Y. J., Li, F., Zhang, B., Zhang, K., Zhang, F., Huang, X., Sun, N., Ren, Y., Sui, M., & Liu, P. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.02.1070 · Cited by 95
HIV-1 Tat interaction with Dicer: requirement for RNA
Bennasser, Y., & Jeang, K. (2006) · Retrovirology · doi:10.1186/1742-4690-3-95 · Cited by 95
Larsson, E., Fuchs, P. F., Heldin, J., Barkefors, I., Bondjers, C., Genové, G., Arrondel, C., Gerwins, P., Kurschat, C. E., Schermer, B., et al. (2009) · Genome Medicine · doi:10.1186/gm108 · Cited by 93
Gusella, J. F., & MacDonald, M. E. (1995) · Seminars in Cell Biology · doi:10.1016/1043-4682(95)90011-x · Cited by 93
Romania, P., Lulli, V., Pelosi, E., Biffoni, M., Peschle, C., & Marziali, G. (2008) · British Journal of Haematology · doi:10.1111/j.1365-2141.2008.07382.x · Cited by 91
Rane, S., He, M., Sayed, D. H., Yan, L., Vatner, D. E., & Abdellatif, M. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.02.008 · Cited by 91
Self-citationAbsence of DICER in Monocytes and Its Regulation by HIV-1
Coley, W., Duyne, R. V., Carpio, L., Guendel, I., Kehn‐Hall, K., Chevalier, S. A., Narayanan, A., Luu, T. V., Lee, N., Klase, Z. A., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.101709 · Cited by 91
Thomas‐Tikhonenko, A., Black, D. J., & Linial, M. L. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.48.30741 · Cited by 90
Activation of the Myc oncoprotein leads to increased turnover of thrombospondin-1 mRNA
Janz, A. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.11.2268 · Cited by 89
Epstein-Barr virus-mediated dysregulation of human microRNA expression
Godshalk, S. E., Bhaduri‐McIntosh, S., & Slack, F. J. (2008) · Cell Cycle · doi:10.4161/cc.7.22.7120 · Cited by 88
Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract
Pastorelli, L. M., Wells, S., Fray, M., Smith, A. P. L., Hough, T., Harfe, B. D., McManus, M. T., Smith, L. B., Woolf, A. S., Cheeseman, M. T., et al. (2009) · Mammalian Genome · doi:10.1007/s00335-008-9169-y · Cited by 86
MicroRNA-661, a c/EBPα Target, Inhibits Metastatic Tumor Antigen 1 and Regulates Its Functions
Reddy, S. D. N., Pakala, S. B., Ohshiro, K., Rayala, S. K., & Kumar, R. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-0898 · Cited by 85
An in vivo function for the transforming Myc protein: elicitation of the angiogenic phenotype.
Ngo, C., Gee, M. F. W., Akhtar, N., Yu, D., Volpert, O. V., Auerbach, R., & Thomas‐Tikhonenko, A. (2000) · PubMed · Cited by 81
DNMT cooperativity—the developing links between methylation, chromatin structure and cancer
El‐Osta, A. (2003) · BioEssays · doi:10.1002/bies.10345 · Cited by 80
(2002) · PubMed · Cited by 79
Suzuki, T., Sawaki, D., Aizawa, K., Munemasa, Y., Matsumura, T., Ishida, J., & Nagai, R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m806230200 · Cited by 77
Nakajima, N., Takahashi, T., Kitamura, R., Isodono, K., Asada, S., Ueyama, T., Matsubara, H., & Oh, H. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.09.153 · Cited by 76
Identification of Genes Regulated During Mechanical Load-induced Cardiac Hypertrophy
Johnatty, S. E., Dyck, J. R. B., Michael, L. H., Olson, E. N., & Abdellatif, M. (2000) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.2000.1122 · Cited by 74
Self-citationLand, P. W., & Monaghan, A. P. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.9.921 · Cited by 73
Hurst, D. R., Xie, Y., Vaidya, K. S., Mehta, A., Moore, B. P., Accavitti-Loper, M. A., Samant, R. S., Saxena, R. R., Silveira, A. C., & Welch, D. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709446200 · Cited by 72
Reduced Hepatic Tumor Incidence in Cyclin G1–Deficient Mice
Jensen, M. R., Factor, V. M., Fantozzi, A., Helin, K., Huh, C.-G., & Thorgeirsson, S. S. (2003) · Hepatology · doi:10.1053/jhep.2003.50137 · Cited by 70
Free energy of DNA duplex formation on short oligonucleotide microarrays
Zhang, L., Wu, C., Carta, R., et al. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl1064 · Cited by 68
Larribère, L., Hilmi, C., Khaled, M., Gaggioli, C., Bille, K., Auberger, P., Ortonne, J. P., Ballotti, R., & Bertolotto, C. (2005) · Genes & Development · doi:10.1101/gad.335905 · Cited by 67
Jeng, S., Rau, C., Liliang, P., Wu, C., Lu, T., Chen, Y.-C., Lin, C., & Hsieh, C. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2009.0960 · Cited by 62
Regulation of Vascular Smooth Muscle Cell Proliferation and Migration by Human Sprouty 2
Zhang, C., Chaturvedi, D., Jaggar, L., Magnuson, D. J., Lee, J. M., & Patel, T. B. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000155461.50450.5a · Cited by 62
Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene
Metcalf, D., Carpinelli, M. R., Hyland, C. D., Mifsud, S., DiRago, L., Nicola, N. A., Hilton, D. J., & Alexander, W. S. (2005) · Blood · doi:10.1182/blood-2004-12-4806 · Cited by 61
Zakowicz, H., Yang, H., Stark, C., Wlodawer, A., LaRonde-LeBlanc, N. A., & Colburn, N. H. (2005) · RNA · doi:10.1261/rna.7191905 · Cited by 60
The expression of microRNA‐203 during human skin morphogenesis
Wei, T., Orfanidis, K., Xu, N., Janson, P., Ståhle, M., Pivarcsi, A., & Sonkoly, E. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01118.x · Cited by 60
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Ghosh, R., Gu, G., Tillman, E., Yuan, J., Wang, Y., Fazli, L., Rennie, P. S., & Kasper, S. (2007) · The Prostate · doi:10.1002/pros.20601 · Cited by 58
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Morita, S., Hara, A., Kojima, I., Horii, T., Kimura, M., Kitamura, T., Ochiya, T., Nakanishi, K., Matoba, R., Matsubara, K., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004212 · Cited by 55
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Kim, T. W., Yim, S., Choi, B. J., Jang, Y., Lee, J. J., Sohn, B. H., Yoo, H., Yeom, Y. I., & Park, K. C. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.11.174 · Cited by 54
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Mahdavi, V., LOMPRE, A., Chambers, A. P., & Nadal‐Ginard, B. (1984) · European Heart Journal · doi:10.1093/eurheartj/5.suppl_f.181 · Cited by 50
Zhang, H., Yang, J., Zheng, Y., Zhang, P., Chen, X., Wu, J., Xu, L., Luo, X., Ke, Z., Zhou, H., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006849 · Cited by 49
Neat, M. J., Foot, N. J., Jenner, M., Goff, L. K., Ashcroft, K. J., Burford, D. C., Dunham, A., Norton, A. J., Lister, T. A., & Fitzgibbon, J. (2001) · Genes Chromosomes and Cancer · doi:10.1002/gcc.1187 · Cited by 43
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Rees, H., Williamson, D., Papanastasiou, A., Jina, N., Nabarro, S., SHIPLEY, J. M., & Anderson, J. (2006) · Growth Factors · doi:10.1080/08977190600759923 · Cited by 38
Rane, S., Sayed, D. H., & Abdellatif, M. (2007) · Cell Cycle · doi:10.4161/cc.6.15.4551 · Cited by 35
Self-citationRowland, R. T., Meng, X., Cleveland, J. C., Meldrum, D. R., Harken, A. H., & Brown, J. M. (1997) · Journal of Surgical Research · doi:10.1006/jsre.1997.5142 · Cited by 33
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Boutaud, O. G., Dixon, D. A., Oates, J. A., & Sawaoka, H. (2003) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-9194-2_32 · Cited by 31
Linke, A., Goren, I., Bösl, M. R., Pfeilschifter, J. M., & Frank, S. (2009) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.344 · Cited by 30
Duan, W., Gao, L., Wu, X., Wang, L., Nana-Sinkam, S. P., Otterson, G. A., & Villalona-Calero, M. A. (2009) · International Journal of Cancer · doi:10.1002/ijc.25049 · Cited by 28
Shi, J., Zhang, L., Shen, A., Zhang, J., Wang, Y., Zhao, Y., Zou, L., Ke, Q., He, F., Wang, P., et al. (2009) · Journal of Neuro-Oncology · doi:10.1007/s11060-009-0045-8 · Cited by 28
Jegga, A. G., Chen, J., Gowrisankar, S., Deshmukh, M. A., Gudivada, R. C., Kong, S., Kaimal, V., & Aronow, B. J. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl1011 · Cited by 26
Zeng, J., Yan, J., Wang, T., Mosbrook-Davis, D., Dolan, K. T., Christensen, R. G., Stormo, G. D., Haussler, D. H., Lathrop, R. H., Brachmann, R. K., et al. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkm1117 · Cited by 25
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Metadata
- Authors
- Sayed, D., & Abdellatif, M.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2011-07
- Volume
- 91
- Issue
- 3
- Pages
- 827-887
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2171260596
- Cited by
- 1,078
- References
- 713
- FWCI
- 3.95
- Type
- journal article
- Language
- en
- Open access
- closed
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 ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
