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[1]
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Cell cycle involvement in cancer therapy; WEE1 kinase, a potential target as therapeutic strategy
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis,
2022
DOI:10.1016/j.mrfmmm.2022.111776
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[2]
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The human ion channel TRPM2 modulates cell survival in neuroblastoma through E2F1 and FOXM1
Scientific Reports,
2022
DOI:10.1038/s41598-022-10385-8
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[3]
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Cell cycle involvement in cancer therapy; WEE1 kinase, a potential target as therapeutic strategy
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis,
2022
DOI:10.1016/j.mrfmmm.2022.111776
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[4]
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New Insights into CDK Regulators: Novel Opportunities for Cancer Therapy
Trends in Cell Biology,
2021
DOI:10.1016/j.tcb.2021.01.010
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[5]
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New Insights into CDK Regulators: Novel Opportunities for Cancer Therapy
Trends in Cell Biology,
2021
DOI:10.1016/j.tcb.2021.01.010
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[6]
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Protein – Protein Interaction Regulators
2020
DOI:10.1039/9781788016544-00109
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[7]
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Protein – Protein Interaction Regulators
2020
DOI:10.1039/9781788016544-00109
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[8]
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Cks1 regulates human hepatocellular carcinoma cell progression through osteopontin expression
Biochemical and Biophysical Research Communications,
2018
DOI:10.1016/j.bbrc.2018.11.070
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[9]
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Hormonal and Growth Regulation of Epithelial and Stromal Cells From the Normal and Malignant Endometrium by Pigment Epithelium-Derived Factor
Endocrinology,
2017
DOI:10.1210/en.2017-00028
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[10]
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The Cks1/Cks2 axis fine-tunes Mll1 expression and is crucial for MLL-rearranged leukemia cell viability
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research,
2017
DOI:10.1016/j.bbamcr.2017.09.009
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[11]
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High-expressed CKS2 is associated with hepatocellular carcinoma cell proliferation through down-regulating PTEN
Pathology - Research and Practice,
2017
DOI:10.1016/j.prp.2017.12.006
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[12]
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Increased expression of Cks1 protein is associated with lymph node metastasis and poor prognosis in nasopharyngeal carcinoma
Diagnostic Pathology,
2017
DOI:10.1186/s13000-016-0589-9
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[13]
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3-O-(Z)-coumaroyloleanolic acid overcomes Cks1b -induced chemoresistance in lung cancer by inhibiting Hsp90 and MEK pathways
Biochemical Pharmacology,
2017
DOI:10.1016/j.bcp.2017.03.007
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[14]
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CKS1BP7, a Pseudogene of CKS1B, is Co-Amplified with IGF1R in Breast Cancers
Pathology & Oncology Research,
2017
DOI:10.1007/s12253-017-0224-4
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[15]
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Long noncoding RNA MALAT1 affects the efficacy of radiotherapy for esophageal squamous cell carcinoma by regulating Cks1 expression
Journal of Oral Pathology & Medicine,
2017
DOI:10.1111/jop.12538
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[16]
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Gene signature associated with benign neurofibroma transformation to malignant peripheral nerve sheath tumors
PLOS ONE,
2017
DOI:10.1371/journal.pone.0178316
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[17]
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The cyclin dependent kinase subunit Cks1 is required for infection-associated development of the rice blast fungus M
agnaporthe oryzae
Environmental Microbiology,
2017
DOI:10.1111/1462-2920.13796
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[18]
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TORC1 coordinates the conversion of Sic1 from a target to an inhibitor of cyclin-CDK-Cks1
Cell Discovery,
2017
DOI:10.1038/celldisc.2017.12
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[19]
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TORC1 coordinates the conversion of Sic1 from a target to an inhibitor of cyclin-CDK-Cks1
Cell Discovery,
2017
DOI:10.1038/celldisc.2017.12
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[20]
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Long noncoding RNA MALAT1 affects the efficacy of radiotherapy for esophageal squamous cell carcinoma by regulating Cks1 expression
Journal of Oral Pathology & Medicine,
2017
DOI:10.1111/jop.12538
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[21]
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The cyclin dependent kinase subunit Cks1 is required for infection‐associated development of the rice blast fungus Magnaporthe oryzae
Environmental Microbiology,
2017
DOI:10.1111/1462-2920.13796
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[22]
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Regulation of Transient Site-specific Copy Gain by MicroRNA
Journal of Biological Chemistry,
2016
DOI:10.1074/jbc.M115.711648
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[23]
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TGF-β activates APC through Cdh1 binding for Cks1 and Skp2 proteasomal destruction stabilizing p27kip1 for normal endometrial growth
Cell Cycle,
2016
DOI:10.1080/15384101.2016.1150393
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[24]
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Hypoxia drives transient site-specific copy gain and drug-resistant gene expression
Genes & Development,
2015
DOI:10.1101/gad.259796.115
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[25]
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Cks1 proteasomal turnover is a predominant mode of regulation in breast cancer cells: Role of key tyrosines and lysines
International Journal of Oncology,
2015
DOI:10.3892/ijo.2014.2728
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[26]
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Cks1 proteasomal degradation is induced by inhibiting Hsp90-mediated chaperoning in cancer cells
Cancer Chemotherapy and Pharmacology,
2015
DOI:10.1007/s00280-014-2666-7
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[27]
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Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)
International Journal of Molecular Medicine,
2015
DOI:10.3892/ijmm.2015.2285
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[28]
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The basal transcription machinery as a target for cancer therapy
Cancer Cell International,
2014
DOI:10.1186/1475-2867-14-18
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