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Molecular Biology of the Cell, ISSN 1059-1524, 04/2011, Volume 22, Issue 8, pp. 1191 - 1206
.... Cyclin-dependent kinase 1 (Cdk1) is the primary upstream kinase that directs mitotic progression by phosphorylation of a large number of substrate proteins... 
ANAPHASE-PROMOTING COMPLEX | XENOPUS EGG EXTRACTS | PROTEIN PHOSPHATASES | CYCLE-DEPENDENT PHOSPHORYLATION | UBIQUITIN LIGASE | M-PHASE | CHROMOSOME ALIGNMENT | CELL-CYCLE | TUMOR-CELLS | SPINDLE-ASSEMBLY CHECKPOINT | CELL BIOLOGY | Cyclin-Dependent Kinases - metabolism | Gene Expression - drug effects | Xenopus Proteins - genetics | Mitosis | Protein-Tyrosine Kinases - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | G2 Phase - drug effects | CDC2 Protein Kinase - metabolism | Cell Cycle Proteins - antagonists & inhibitors | Protein-Tyrosine Kinases - genetics | Cyclin B - genetics | cdc25 Phosphatases - antagonists & inhibitors | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Cycle Proteins - genetics | Prometaphase - drug effects | Female | Cyclin-Dependent Kinases - antagonists & inhibitors | Phosphorylation - drug effects | cdc25 Phosphatases - metabolism | Cyclin-Dependent Kinases - genetics | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | CDC2 Protein Kinase - genetics | Protein Phosphatase 2 - antagonists & inhibitors | CDC2 Protein Kinase - antagonists & inhibitors | Xenopus laevis | Cell Cycle Proteins - metabolism | Protein Phosphatase 2 - genetics | Protein-Serine-Threonine Kinases - genetics | Nuclear Proteins - metabolism | Phosphoprotein Phosphatases - antagonists & inhibitors | cdc25 Phosphatases - genetics | Xenopus Proteins - antagonists & inhibitors | Membrane Proteins | Animals | Phosphoprotein Phosphatases - genetics | Nuclear Proteins - antagonists & inhibitors | Protein Phosphatase 2 - metabolism | Cyclin B - metabolism | Feedback, Physiological - drug effects | Xenopus Proteins - metabolism | Protein Kinase Inhibitors - pharmacology | S Phase - drug effects | HeLa Cells | Protein-Tyrosine Kinases - antagonists & inhibitors
Journal Article
Cell (Cambridge), ISSN 0092-8674, 2007, Volume 129, Issue 7, pp. 1415 - 1426
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 08/2018, Volume 18, Issue 2, pp. 1433 - 1438
Cardiac fibrosis is a deleterious effect of many cardiovascular diseases. Previous studies have shown that curcumin has exhibited protective effects on... 
Cardiac fibroblasts | Curcumin | P38 mitogen-activated protein kinase/extracellular signal-regulated kinases signaling pathway | FIBROSIS | MEDICINE, RESEARCH & EXPERIMENTAL | ONCOLOGY | cardiac fibroblasts | DISEASE | extracellular signal-regulated kinases signaling pathway | EXTRACELLULAR-MATRIX | p38 mitogen-activated protein kinase | curcumin | Transforming Growth Factor beta1 - antagonists & inhibitors | Humans | Mitogen-Activated Protein Kinase 3 - antagonists & inhibitors | Actins - metabolism | Collagen Type III - metabolism | Smad3 Protein - metabolism | Actins - genetics | CDC2 Protein Kinase - metabolism | Smad3 Protein - genetics | Collagen Type I - genetics | Cyclin B - genetics | G2 Phase Cell Cycle Checkpoints - drug effects | Mitogen-Activated Protein Kinase 1 - genetics | Myocardium - metabolism | Smad2 Protein - genetics | p38 Mitogen-Activated Protein Kinases - metabolism | Transforming Growth Factor beta1 - pharmacology | Fibroblasts - metabolism | Cell Line | CDC2 Protein Kinase - genetics | Collagen Type I - metabolism | Mitogen-Activated Protein Kinase 3 - genetics | Signal Transduction | Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors | Curcumin - pharmacology | Gene Expression Regulation | Smad2 Protein - metabolism | p38 Mitogen-Activated Protein Kinases - genetics | Collagen Type III - genetics | Myocardium - cytology | G2 Phase Cell Cycle Checkpoints - genetics | Mitogen-Activated Protein Kinase 3 - metabolism | Cell Differentiation - drug effects | Fibroblasts - drug effects | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Cyclin B - metabolism | Cell Proliferation - drug effects | Fibroblasts - cytology | Mitogen-Activated Protein Kinase 1 - metabolism
Journal Article
Immunologic research, ISSN 1559-0755, 2011, Volume 51, Issue 1, pp. 45 - 60
... and transcription factors and inhibiting apoptosis. This induction by C5b-9 is dependent upon the activation of the phosphatidylinositol 3-kinase/Akt/FOXO1 and ERK1 pathways in a Gi protein-dependent manner... 
Allergology | Signal transduction | Immunology | Medicine & Public Health | Cell cycle | Internal Medicine | Membrane attack complex | C5b-9 terminal complement complex | Transcriptional regulation | Medicine/Public Health, general | Apoptosis | ACTIVATED PROTEIN-KINASE | SYSTEMIC LUPUS-ERYTHEMATOSUS | GUILLAIN-BARRE-SYNDROME | ULCERATIVE-COLITIS | GLOMERULAR EPITHELIAL-CELLS | C5B-9 COMPLEX | IMMUNOLOGY | S-PROTEIN | MANNAN-BINDING LECTIN | ACUTE MYOCARDIAL-INFARCTION | SMOOTH-MUSCLE-CELLS | Forkhead Transcription Factors - immunology | CDC2 Protein Kinase | Complement Membrane Attack Complex - metabolism | Cyclin-Dependent Kinase 4 - genetics | Humans | Caspase 8 - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Complement Membrane Attack Complex - immunology | MAP Kinase Signaling System - immunology | Phosphatidylinositol 3-Kinases - immunology | Cell Cycle Proteins - immunology | Cyclin B - immunology | Forkhead Transcription Factors - metabolism | Muscle Proteins - metabolism | bcl-Associated Death Protein - metabolism | Cell Membrane - metabolism | Phosphorylation - immunology | Cyclin-Dependent Kinases | Proto-Oncogene Proteins c-akt - metabolism | BH3 Interacting Domain Death Agonist Protein - metabolism | Cyclin-Dependent Kinase 2 - metabolism | Mitogen-Activated Protein Kinase 3 - immunology | Muscle Proteins - immunology | G1 Phase - immunology | S Phase - immunology | Nerve Tissue Proteins - immunology | Cell Cycle Proteins - metabolism | bcl-Associated Death Protein - immunology | Cyclin-Dependent Kinase 4 - metabolism | Nerve Tissue Proteins - metabolism | Caspase 8 - immunology | Animals | Apoptosis - immunology | Proto-Oncogene Proteins c-akt - immunology | Mitogen-Activated Protein Kinase 3 - metabolism | BH3 Interacting Domain Death Agonist Protein - immunology | Cyclin B - metabolism | Cell Membrane - immunology | Forkhead Box Protein O1 | Cyclin-Dependent Kinase 2 - immunology | Medical colleges | Membranes | Immune system | apoptosis | membrane attack complex | cell cycle | signal transduction | transcriptional regulation
Journal Article
The Journal of cell biology, ISSN 0021-9525, 2012, Volume 198, Issue 6, pp. 981 - 990
Journal Article
BMC cancer, ISSN 1471-2407, 2014, Volume 14, Issue 1, p. 32
.... Recent studies have identified several cell cycle kinases as MYC synthetic-lethal genes... 
Cyclin-dependent kinase | Breast cancer | Synthetic lethality | MYC | SYNTHETIC LETHAL | C-MYC | TUMOR-CELLS | PROLIFERATION | INHIBITION | GENE | ONCOLOGY | PATHWAY | ESTROGEN | THERAPEUTIC TARGETS | EXPRESSION | Cyclin-Dependent Kinase 6 - antagonists & inhibitors | Phosphorylation | Cyclin-Dependent Kinase 4 - genetics | Humans | Molecular Targeted Therapy | CDC2 Protein Kinase - metabolism | Dose-Response Relationship, Drug | Breast Neoplasms - enzymology | Transfection | Bcl-2-Like Protein 11 | RNA Interference | Female | Antineoplastic Agents - pharmacology | Membrane Proteins - metabolism | Cell Death - drug effects | Cyclin-Dependent Kinase 4 - antagonists & inhibitors | Proto-Oncogene Proteins - metabolism | Cyclin-Dependent Kinase 2 - metabolism | CDC2 Protein Kinase - genetics | CDC2 Protein Kinase - antagonists & inhibitors | Cyclin-Dependent Kinase 6 - genetics | Tumor Suppressor Protein p53 - metabolism | Cyclin-Dependent Kinase 2 - genetics | Cyclin-Dependent Kinase 6 - metabolism | Cyclin-Dependent Kinase 4 - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Apoptosis Regulatory Proteins - metabolism | Breast Neoplasms - genetics | Signal Transduction - drug effects | Breast Neoplasms - pathology | Cell Cycle Checkpoints - drug effects | Cell Line, Tumor | Cyclin-Dependent Kinase 2 - antagonists & inhibitors | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Proto-Oncogene Proteins c-myc - genetics
Journal Article
Biology of Reproduction, ISSN 0006-3363, 02/2008, Volume 78, Issue 2, pp. 218 - 233
Maturation of immature bovine oocytes requires cytoplasmic polyadenylation and synthesis of a number of proteins involved in meiotic progression and metaphase-II arrest... 
Gamete biology | Aurora kinases | Bovine | CPEB | Meiosis | Oocyte development | Kinases | Oocyte | MESSENGER-RNA TRANSLATION | meiosis | PARTHENOGENETIC ACTIVATION | MAP KINASE | oocyte development | CHROMOSOME CONDENSATION | gamete biology | REPRODUCTIVE BIOLOGY | kinases | oocyte | IN-VITRO MATURATION | CPEB PHOSPHORYLATION | II TRANSITION | MOUSE OOCYTES | GENE-EXPRESSION | bovine | XENOPUS-OOCYTES | Protein-Serine-Threonine Kinases - analysis | Nitriles - pharmacology | mRNA Cleavage and Polyadenylation Factors - metabolism | Cytoplasm - metabolism | RNA, Messenger - metabolism | Cyclin B1 | Embryo, Mammalian - metabolism | Aurora Kinase A | CDC2 Protein Kinase - metabolism | Proto-Oncogene Proteins c-mos - genetics | Aurora Kinase B | Aurora Kinase C | Meiosis - drug effects | Cyclin B - genetics | Cattle | Female | Proto-Oncogene Proteins c-mos - metabolism | mRNA Cleavage and Polyadenylation Factors - genetics | Protein-Serine-Threonine Kinases - metabolism | Cytoplasm - chemistry | mRNA Cleavage and Polyadenylation Factors - analysis | Butadienes - pharmacology | CDC2 Protein Kinase - genetics | Oocytes - growth & development | Fertilization | Oocytes - metabolism | Purines - pharmacology | Metformin - pharmacology | Oocytes - chemistry | Protein-Serine-Threonine Kinases - genetics | Aurora Kinases | Piperazines - pharmacology | Proto-Oncogene Proteins c-mos - analysis | Cyclin B - analysis | Animals | Polyadenylation | CDC2 Protein Kinase - analysis | Cyclin B - metabolism | Protein Kinase Inhibitors - pharmacology | CDC2 Protein Kinase | Piperazines | Embryo, Mammalian | Protein-Serine-Threonine Kinases | Proto-Oncogene Proteins c-mos | Butadienes | Cellular Biology | Oocytes | Life Sciences | Purines | Protein Kinase Inhibitors | Cyclin B | Nitriles | Metformin | RNA, Messenger | mRNA Cleavage and Polyadenylation Factors | Cytoplasm | Reproductive Biology
Journal Article
Genes & development, ISSN 0890-9369, 2010, Volume 24, Issue 20, pp. 2303 - 2316
Drosophila contains one (dCDK12) and humans contain two (hCDK12 and hCDK13) proteins that are the closest evolutionary relatives of yeast Ctk1, the catalytic subunit of the major elongation-phase C-terminal repeat domain (CTD... 
Transcription | C-terminal repeat domain | CTD kinase | RNA polymerase II | P-TEFb | RNA-POLYMERASE-II | RECRUITMENT | COMPLEX | transcription | TERMINAL REPEAT DOMAIN | PHOSPHORYLATION | PROTEIN-KINASE | CYCLIN-DEPENDENT KINASE | DEVELOPMENTAL BIOLOGY | PHOSPHOCTD | CELL BIOLOGY | IN-VIVO | GENETICS & HEREDITY | LARGEST SUBUNIT | Protein Kinases - metabolism | Phosphorylation | Protein Kinases - genetics | Cyclin T - metabolism | Cyclin-Dependent Kinases - metabolism | Saccharomyces cerevisiae - genetics | Humans | RNA Polymerase II - metabolism | Drosophila Proteins - metabolism | Drosophila melanogaster - genetics | Genetic Complementation Test | Recombinant Fusion Proteins - metabolism | CDC2 Protein Kinase - metabolism | Drosophila melanogaster - metabolism | Saccharomyces cerevisiae - metabolism | RNA Interference | Cyclin-Dependent Kinases - genetics | Cell Line | CDC2 Protein Kinase - genetics | Cyclin-Dependent Kinase 9 - genetics | Cyclin T - genetics | Drosophila melanogaster - cytology | Chromosome Mapping | Saccharomyces cerevisiae Proteins - genetics | Blotting, Western | Animals | Saccharomyces cerevisiae Proteins - metabolism | Recombinant Fusion Proteins - genetics | RNA Polymerase II - genetics | Cyclin-Dependent Kinase 9 - metabolism | Drosophila Proteins - genetics | HeLa Cells | Mutation | Microscopy, Fluorescence | Saccharomyces cerevisiae - growth & development | Usage | Transcription factors | Drosophila | Physiological aspects | Genetic aspects | Chemical properties | Research | Structure | Brewer's yeast | Phosphotransferases | Fluorescence microscopy | RNA polymerases | Research Paper
Journal Article
Leukemia, ISSN 1476-5551, 2014, Volume 29, Issue 4, pp. 807 - 818
AZD1775 targets the cell cycle checkpoint kinase Wee1 and potentiates genotoxic agent cytotoxicity through p53-dependent or -independent mechanisms... 
CYCLIN-DEPENDENT KINASES | GENOMIC INSTABILITY | HISTONE DEACETYLASE INHIBITOR | DNA-DAMAGING AGENTS | ONCOLOGY | MITOTIC CATASTROPHE | THERAPEUTIC TARGET | TUMOR-CELLS | HOMOLOGOUS RECOMBINATION | HEMATOLOGY | PRECLINICAL EVALUATION | CANCER-THERAPY | Protein Kinases - metabolism | CDC2 Protein Kinase | Phosphorylation | Protein Kinases - genetics | Cyclin-Dependent Kinases - metabolism | Apoptosis - drug effects | Protein-Tyrosine Kinases - metabolism | Humans | Tumor Suppressor Protein p53 - genetics | Cell Cycle Proteins - antagonists & inhibitors | fms-Like Tyrosine Kinase 3 - genetics | Protein-Tyrosine Kinases - genetics | Cell Cycle Proteins - genetics | Leukemia, Myeloid, Acute - drug therapy | Cyclin-Dependent Kinases - antagonists & inhibitors | DNA Fragmentation - drug effects | Cyclin-Dependent Kinases - genetics | Drug Therapy, Combination | Nuclear Proteins - genetics | Hydroxamic Acids - pharmacology | Signal Transduction | Leukemia, Myeloid, Acute - pathology | Cell Cycle Proteins - metabolism | Tumor Suppressor Protein p53 - metabolism | Nuclear Proteins - metabolism | Gene Expression Regulation, Leukemic | fms-Like Tyrosine Kinase 3 - metabolism | Drug Synergism | Leukemia, Myeloid, Acute - mortality | Xenograft Model Antitumor Assays | Animals | Cell Cycle Checkpoints - drug effects | Nuclear Proteins - antagonists & inhibitors | Survival Analysis | Myeloid Cells - metabolism | Checkpoint Kinase 1 | Histone Deacetylase Inhibitors - pharmacology | Mice | Protein Kinase Inhibitors - pharmacology | Myeloid Cells - pathology | Primary Cell Culture | Leukemia, Myeloid, Acute - genetics | Protein-Tyrosine Kinases - antagonists & inhibitors | Cdc2 protein | Histone deacetylase | Toxicity | Leukemia | p53 Protein | DNA damage | Xenotransplantation | Genotoxicity | Cytotoxicity | Kinases | Next-generation sequencing | CD38 antigen | Cell cycle | Xenografts | CD123 antigen | Damage | Deoxyribonucleic acid--DNA | Genotoxic chemicals | CD34 antigen | Myeloid leukemia | CHK1 protein | Abnormalities | Hemopoiesis | Mutants | Inhibitors | Mutation | Acute myeloid leukemia | Apoptosis | checkpoint | AML | HDAC inhibitor | Cdk1 | Chk1 | Wee1 inhibitor | cdc2
Journal Article
Molecules (Basel, Switzerland), ISSN 1420-3049, 2017, Volume 22, Issue 12, p. 2045
.... The WEE kinase family consists of three proteins: WEE1, PKMYT1, and the less important WEE1B... 
PKMYT1 | WEE1 | G2/M transition | CANCER-CELLS | CELL-CYCLE REGULATION | PROTEIN-KINASE | TYROSINE KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MATURATION-PROMOTING FACTOR | MITOTIC CATASTROPHE | M transition | TUMOR-CELLS | G CHECKPOINT | PHOSPHORYLATES CDC2 | CHEMISTRY, MULTIDISCIPLINARY | DNA-DAMAGING AGENTS | Neoplasms - metabolism | Multigene Family | Protein-Tyrosine Kinases - metabolism | Humans | Antineoplastic Agents - therapeutic use | Structure-Activity Relationship | Molecular Targeted Therapy | Cell Cycle Proteins - antagonists & inhibitors | Cell Cycle Proteins - chemistry | Protein-Tyrosine Kinases - genetics | G2 Phase Cell Cycle Checkpoints - drug effects | Neoplasms - genetics | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Protein-Tyrosine Kinases - chemistry | Cell Cycle Proteins - genetics | Antineoplastic Agents - pharmacology | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Membrane Proteins - genetics | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Nuclear Proteins - metabolism | Enzyme Activation - drug effects | Nuclear Proteins - chemistry | Neoplasms - drug therapy | Animals | Membrane Proteins - antagonists & inhibitors | Membrane Proteins - chemistry | Protein Kinase Inhibitors - therapeutic use | Nuclear Proteins - antagonists & inhibitors | Protein Kinase Inhibitors - pharmacology | Protein-Serine-Threonine Kinases - chemistry | Protein-Tyrosine Kinases - antagonists & inhibitors | Proteins | Phosphorylation | Mitosis | Cyclin B | Cell cycle | Inhibition | Kinases | DNA repair | Deoxyribonucleic acid--DNA | Cancer
Journal Article
Cell Reports, ISSN 2211-1247, 12/2015, Volume 13, Issue 11, pp. 2425 - 2439
... networks commonly altered in GBM and GSCs (e.g., oncogenic drivers). In vitro and in vivo validation of GSC-specific targets revealed several strong hits, including the wee1-like kinase, PKMYT1/Myt1... 
WEE1 | CRISPR-Cas9 | Glioblastoma | cancer therapeutics | functional genomics | PKMYT1 | gene editing | Myt1 | Cancer therapeutics | Gene editing | Functional genomics | ACTIVATION | PROTEIN | GENE-EXPRESSION | GOLGI | PHOSPHORYLATES CDC2 | HUMAN MYT1 | INHIBITORY KINASE | BRAIN | RNAI SCREEN | REQUIREMENT | CELL BIOLOGY | Neoplastic Stem Cells - cytology | Phosphorylation | Mitosis | Protein-Tyrosine Kinases - metabolism | Humans | Microscopy, Video | Time-Lapse Imaging | Tumor Suppressor Protein p53 - genetics | CDC2 Protein Kinase - metabolism | Cell Cycle Proteins - antagonists & inhibitors | Protein-Tyrosine Kinases - genetics | Neoplastic Stem Cells - metabolism | RNA Interference | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Cell Cycle Proteins - genetics | Glioblastoma - metabolism | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Proto-Oncogene Proteins c-akt - metabolism | Protein-Serine-Threonine Kinases - metabolism | Pyrazoles - pharmacology | Cell Survival - drug effects | ErbB Receptors - metabolism | Gene Library | CDC2 Protein Kinase - antagonists & inhibitors | Membrane Proteins - genetics | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Pyrimidinones | Tumor Suppressor Protein p53 - metabolism | Nuclear Proteins - metabolism | Pyrimidines - pharmacology | CRISPR-Cas Systems - genetics | Membrane Proteins - antagonists & inhibitors | Glioblastoma - pathology | Nuclear Proteins - antagonists & inhibitors | Cyclin B - metabolism | Genome, Human | Protein-Tyrosine Kinases - antagonists & inhibitors
Journal Article