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Cancer Cell, ISSN 1535-6108, 02/2014, Volume 25, Issue 2, pp. 166 - 180
Journal Article
Cell Metabolism, ISSN 1550-4131, 09/2013, Volume 18, Issue 3, pp. 416 - 430
Journal Article
by Kang, SH and Lee, HA and Kim, M and Lee, E and Sohn, UD and Kim, I
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, ISSN 0193-1849, 06/2017, Volume 312, Issue 6, pp. E495 - E507
Cushing's syndrome is caused by overproduction of the adrenocorticotropic hormone (ACTH), which stimulates the adrenal grand to make cortisol. Skeletal muscle... 
glucocorticoid receptor | PHYSIOLOGY | PROTEIN | ANTAGONIST | skeletal muscle atrophy | COMPONENTS | Cushing's syndrome | AUTOPHAGY | FOXO TRANSCRIPTION FACTORS | HYPERTROPHY | GLUCOCORTICOID-RECEPTOR | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | forkhead box O3 | CROSSTALK | UP-REGULATION | Receptors, Glucocorticoid - antagonists & inhibitors | Cushing Syndrome - physiopathology | SKP Cullin F-Box Protein Ligases - genetics | Ubiquitin-Protein Ligases - antagonists & inhibitors | Male | Muscle, Skeletal - metabolism | Receptors, Glucocorticoid - metabolism | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | Cushing Syndrome - metabolism | Promoter Regions, Genetic - drug effects | Receptors, Glucocorticoid - agonists | Forkhead Box Protein O3 - genetics | Chromatin Immunoprecipitation | Cushing Syndrome - pathology | RNA Interference | Muscle, Skeletal - drug effects | Muscle Proteins - metabolism | Forkhead Box Protein O3 - antagonists & inhibitors | Muscle Proteins - antagonists & inhibitors | Muscular Atrophy - etiology | Disease Models, Animal | Cell Line | Tripartite Motif Proteins - antagonists & inhibitors | Ubiquitin-Protein Ligases - metabolism | Tripartite Motif Proteins - agonists | Tripartite Motif Proteins - genetics | SKP Cullin F-Box Protein Ligases - metabolism | SKP Cullin F-Box Protein Ligases - antagonists & inhibitors | Rats, Sprague-Dawley | Forkhead Box Protein O3 - metabolism | Hormone Antagonists - pharmacology | Forkhead Box Protein O3 - agonists | Gene Expression Regulation - drug effects | Muscle Proteins - genetics | Response Elements - drug effects | Muscle Proteins - agonists | Animals | Active Transport, Cell Nucleus - drug effects | Muscle Fibers, Skeletal - pathology | Glucocorticoids - pharmacology | Genes, Reporter - drug effects | Tripartite Motif Proteins - metabolism | Muscle, Skeletal - pathology | Ubiquitin-Protein Ligases - genetics | Muscles | Physiological aspects | Atrophy, Muscular | Cushing syndrome | Index Medicus
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 04/2007, Volume 356, Issue 15, pp. 1517 - 1526
The expression of interleukin-1–receptor antagonist is reduced in pancreatic islets in type 2 diabetes, and high glucose concentrations induce interleukin-1β... 
INSULIN | MEDICINE, GENERAL & INTERNAL | HUMAN PANCREATIC-ISLETS | OBESITY | GLUCOSE | BETA-CELL APOPTOSIS | DISEASE | MUSCLE | EXPRESSION | RECEPTOR ANTAGONIST | NIDDM | Recombinant Proteins - therapeutic use | Insulin-Secreting Cells - secretion | Glucose Transporter Type 4 - metabolism | Glycated Hemoglobin A - metabolism | Humans | Middle Aged | Male | Diabetes Mellitus, Type 2 - metabolism | RNA, Messenger - metabolism | Heat-Shock Proteins - genetics | Insulin Resistance - physiology | Interleukin-6 - blood | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Female | Interleukin 1 Receptor Antagonist Protein - pharmacology | Body Mass Index | Glucose Tolerance Test | Double-Blind Method | Glucose Transporter Type 4 - genetics | Heat-Shock Proteins - metabolism | C-Reactive Protein - secretion | Recombinant Proteins - pharmacology | Transcription Factors - genetics | Gene Expression Regulation - drug effects | Transcription Factors - metabolism | Interleukin 1 Receptor Antagonist Protein - therapeutic use | Insulin-Secreting Cells - drug effects | Interleukin 1 Receptor Antagonist Protein - adverse effects | Blood Glucose - metabolism | Diabetes Mellitus, Type 2 - drug therapy | Receptors, Interleukin-1 - antagonists & inhibitors | Type 2 diabetes | Interleukin-1 | Research | Drug therapy | Pancreas | Diabetes | Apoptosis | Index Medicus | Abridged Index Medicus | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Journal Article
Biochemical Journal, ISSN 0264-6021, 12/2007, Volume 408, Issue 3, pp. 297 - 315
The specificities of 65 compounds reported to be relatively specific inhibitors of protein kinases have been profiled against a panel of 70-80 protein kinases.... 
Drug discovery | Kinase profiling | Protein kinase | Anti-cancer drugs | Inhibitor specificity | RHO-ASSOCIATED KINASE | TUMOR PROGRESSION | FAMILY-MEMBERS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL-PROLIFERATION | protein kinase | P38 MAP KINASE | CYCLIN-DEPENDENT KINASES | RECEPTOR TYROSINE KINASES | drug discovery | kinase profiling | SB 203580 | anti-cancer drugs | ISOFORMS IN-VITRO | P90 RSK | inhibitor specificity | Amino Acid Sequence | Cell Line | Phosphorylation | Recombinant Proteins - antagonists & inhibitors | Animals | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Humans | Drug Design | Protein Kinase Inhibitors - pharmacology | Enzyme Activation | Mitogen-Activated Protein Kinases - metabolism | Spodoptera | Index Medicus | Yes1, Yamaguchi sarcoma viral oncogene homologue 1 | CSK, C-terminal Src kinase | Lck, lymphocyte cell-specific protein-tyrosine kinase | EGF, epidermal growth factor | FGF-R, fibroblast-growth-factor receptor | PAK, p21-activated protein kinase | PDK, 3-phosphoinositide-dependent protein kinase | PI3K, phosphatidylinositol (phosphoinositide) 3-kinase | NEK, NIMA (never in mitosis in Aspergillus nidulans)-related kinase | RSK, p90 ribosomal S6 kinase | HEK-293 cells, human embryonic kidney-293 cells | VEGF, vascular endothelial growth factor (vasoendothelial growth factor) | EF2K, elongation-factor-2 kinase | CK, casein kinase | PTEN, phosphatase and tensin homologue deleted on chromosome 10 | ERK, extracellular-signal-regulated kinase | ATM, ataxia telangiectasia mutated | SRPK, serine-arginine protein kinase | IL-1, interleukin 1 | MNK, MAPK-integrating protein kinase | ROCK, Rho-dependent protein kinase | CaMKK, CaMK kinase | GST, glutathione transferase | MKK1, MAPK kinase-1 (also called MEK1, MAPK or ERK kinase 1) | GAK, cyclin G-associated kinase | FMK, fluoromethylketone | MST, mammalian homologue Ste20-like kinase | PKA, cAMP-dependent protein kinase | FKBP, FK506-binding protein | PPAR, peroxisome-proliferator-activated receptor | IKK, inhibitory κB kinase | PH, pleckstrin homology | MBP, myelin basic protein | AICAR, aminoimidazole-4-carboxamide-1-β-D-ribofuranoside | MAPKAP-K, MAPK-activated protein kinase | Sf21, Spodoptera frugiperda (fall armyworm) 21 | MARK, microtubule-affinity-regulating kinase | PIM, provirus integration site for Moloney murine leukaemia virus | LPS, lipopolysaccharide | MSK, mitogen- and stress-activated protein kinase | MAPK, mitogen-activated protein kinase | MELK, maternal embryonic leucine-zipper kinase | His6, hexahistidine | CAK, cyclin-dependent kinase-activating kinase | Eph-A2, Ephrin A2 receptor | PLK, polo-like kinase | ATF2, activating transcription factor 2 | PKD, protein kinase D | Src, sarcoma kinase | AMPK, AMP-activated protein kinase | MMS, methyl methanesulfonate | CHK, checkpoint kinase | JNK, c-Jun N-terminal kinase | TORC1, mTOR (mammalian target of rapamycin)–raptor (regulatory associated protein of mTOR) complex | BRSK, brain-specific kinase | RIP2, receptor-interacting protein 2 | IGF-1, insulin-like growth factor-1 | S6K1, S6 kinase 1 | DYRK, dual-specificity tyrosine-phosphorylated and -regulated kinase | HIPK, homeodomain-interacting protein kinase | ZMP, aminoimidazole-4-carboxamide-1-β-D-ribofuranoside monophosphate | PRAK, p38-regulated activated kinase | PKC, protein kinase C | Src-I1, Src inhibitor 1 | TANK, TRAF (tumour-necrosis-factor-receptor-associated factor)-family-member-associated nuclear factor κB activator | NFAT, nuclear factor for activated T-cells | PHK, phosphorylase kinase | GSK3, glycogen synthase kinase 3 | PKB, protein kinase B (also called Akt) | CaMK, calmodulin-dependent kinase | CDK, cyclin-dependent protein kinase | NDRG, N-myc downstream-regulated gene | SmMLCK, smooth-muscle myosin light-chain kinase | TBK1, TANK-binding kinase 1 | PRK, protein kinase C-related kinase | SGK, serum- and glucocorticoid-induced kinase
Journal Article
Journal Article
Molecular Endocrinology, ISSN 0888-8809, 05/2012, Volume 26, Issue 5, pp. 716 - 735
Recently, we have identified serum response factor (SRF) as a mediator of clinically relevant androgen receptor (AR) action in prostate cancer (PCa). Genes... 
THERAPY | REMAINS HORMONE DRIVEN | ENDOCRINOLOGY & METABOLISM | NUCLEOTIDE EXCHANGE FACTOR | SERUM RESPONSE FACTOR | RECEPTOR | KINASE INHIBITOR | CASTRATION | COREGULATOR EXPRESSION | PROGRESSION | SMALL-MOLECULE INHIBITOR | Humans | Male | Neoplasm Proteins - antagonists & inhibitors | rhoA GTP-Binding Protein - metabolism | Protein Transport - drug effects | Promoter Regions, Genetic - drug effects | Prostate - pathology | Cell Nucleus - metabolism | rho-Associated Kinases - metabolism | Prostate - drug effects | Neoplasm Proteins - genetics | Recombinant Proteins - antagonists & inhibitors | DNA-Binding Proteins - antagonists & inhibitors | rhoA GTP-Binding Protein - antagonists & inhibitors | Muscle Proteins - genetics | Receptors, Androgen - genetics | Androgens - pharmacology | Signal Transduction - drug effects | Mice, Nude | Mice | Prostatic Neoplasms - metabolism | Oncogene Proteins, Fusion - metabolism | LIM-Homeodomain Proteins - metabolism | Receptors, Androgen - metabolism | rhoA GTP-Binding Protein - genetics | Neoplasm Proteins - metabolism | Prostate - metabolism | rho-Associated Kinases - antagonists & inhibitors | DNA-Binding Proteins - metabolism | Muscle Proteins - metabolism | Androgens - adverse effects | Gene Expression Regulation, Neoplastic - drug effects | Recombinant Proteins - metabolism | Prostatic Neoplasms - pathology | Prostatic Neoplasms - surgery | Trans-Activators | Neoplasm Recurrence, Local | rho-Associated Kinases - genetics | Recombinant Proteins - agonists | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Transcription Factors - metabolism | LIM-Homeodomain Proteins - genetics | Animals | Neoplasm Proteins - agonists | Oncogene Proteins, Fusion - genetics | Oncogene Proteins, Fusion - antagonists & inhibitors | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | rhoA GTP-Binding Protein - agonists | Cell Nucleus - drug effects | Index Medicus | Original Research
Journal Article
The EMBO Journal, ISSN 0261-4189, 01/2012, Volume 31, Issue 2, pp. 301 - 316
Tissue‐specific transcriptional activators initiate differentiation towards specialized cell types by inducing chromatin modifications permissive for... 
myod | muscle differentiation | p38 | chromatin | gene expression | TRANSCRIPTION FACTORS | MYOD BINDING | DNA-BINDING | ACTIVATION | PHOSPHORYLATION | P300 | MYOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MECHANISMS | DISTINCT ROLES | CELL BIOLOGY | MUSCLE-SPECIFIC GENES | Phosphorylation | Transcription Factors - chemistry | Humans | Multiprotein Complexes | HeLa Cells - metabolism | MAP Kinase Signaling System | Chromosomal Proteins, Non-Histone - antagonists & inhibitors | Myoblasts - metabolism | RNA Interference | Muscle Proteins - antagonists & inhibitors | Chromosomal Proteins, Non-Histone - physiology | Muscle Proteins - physiology | Fibroblasts - metabolism | Cell Line | Transcription Factors - physiology | p38 Mitogen-Activated Protein Kinases - physiology | Gene Expression Regulation - genetics | Muscle Development - physiology | RNA, Small Interfering - pharmacology | Transcription Factors - antagonists & inhibitors | Transcription Factors - genetics | Chromosomal Proteins, Non-Histone - genetics | Muscle Proteins - genetics | Two-Hybrid System Techniques | Animals | Phosphothreonine - analysis | Mice | Muscle Proteins - chemistry | Nuclear Proteins - physiology | Protein Processing, Post-Translational | Chromatin - genetics | Chromosomal Proteins, Non-Histone - chemistry | DNA Helicases - physiology | MyoD Protein - physiology | Signal transduction | Chromatin | Cellular biology | Molecular biology | Gene expression | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2017, Volume 292, Issue 24, pp. 10180 - 10196
We have previously shown that dysbindin is a potent inducer of cardiomyocyte hypertrophy via activation of Rho-dependent serum-response factor (SRF) signaling.... 
COACTIVATOR HTIF1 | SCHIZOPHRENIA-RELATED PROTEIN | NUCLEAR RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC-HYPERTROPHY | IN-VIVO | TRIPARTITE MOTIF | SERUM RESPONSE FACTOR | FAMILY PROTEINS | MUSCLE RING FINGER-1 | E3 UBIQUITIN LIGASE | Serum Response Factor - agonists | Serum Response Factor - genetics | Cardiomyopathy, Dilated - pathology | Rats, Wistar | Serum Response Factor - antagonists & inhibitors | Humans | Ubiquitin-Protein Ligases - antagonists & inhibitors | Recombinant Fusion Proteins - metabolism | Dystrophin-Associated Proteins - genetics | Dystrophin-Associated Proteins - metabolism | RNA Interference | Dystrophin-Associated Proteins - chemistry | Proteolysis | HEK293 Cells | Protein Stability | Peptide Fragments - genetics | Animals, Newborn | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Myocytes, Cardiac - cytology | Signal Transduction | Serum Response Factor - metabolism | Tripartite Motif Proteins - antagonists & inhibitors | Cardiomyopathy, Hypertrophic - metabolism | Carrier Proteins - antagonists & inhibitors | Cells, Cultured | Ubiquitin-Protein Ligases - metabolism | Rats | Recombinant Proteins - chemistry | Tripartite Motif Proteins - genetics | Transcription Factors - antagonists & inhibitors | Recombinant Fusion Proteins - chemistry | Transcription Factors - genetics | Cardiomyopathy, Dilated - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Myocytes, Cardiac - pathology | Peptide Fragments - chemistry | Animals | Carrier Proteins - metabolism | Myocytes, Cardiac - metabolism | Tripartite Motif Proteins - metabolism | Ubiquitin-Protein Ligases - genetics | Dysbindin | Apoptosis | Cardiomyopathy, Hypertrophic - pathology | Index Medicus | Molecular Bases of Disease | cardiac signaling | cardiomyocyte | TRIM24 | apoptosis | SRF-signaling | cardiac hypertrophy | cardiomyopathy | dysbindin | TRIM32 | X-linked inhibitor of apoptosis protein (XIAP)
Journal Article
Science, ISSN 0036-8075, 8/2000, Volume 289, Issue 5481, pp. 950 - 953
Wnts are secreted signaling proteins that regulate developmental processes. Here we show that Wnt signaling, likely mediated by Wnt-10b, is a molecular switch... 
3T3 L1 cells | NIH 3T3 cells | Genetic vectors | Cell lines | Retroviridae | Reports | Adipocytes | Lipogenesis | Cellular differentiation | Synapses | Myoblasts | BINDING-PROTEIN-ALPHA | 3T3-L1 ADIPOCYTES | FAT PADS | REGULATOR | TRANSCRIPTIONAL ACTIVATION | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | ADIPOCYTE DIFFERENTIATION | PPAR-GAMMA | BETA-CATENIN | FIBROBLASTS | Repressor Proteins | Adipocytes - cytology | Wnt Proteins | Mesoderm - cytology | CCAAT-Enhancer-Binding Proteins | DNA-Binding Proteins - metabolism | Retroviridae - genetics | TCF Transcription Factors | Cytoskeletal Proteins - metabolism | Cell Differentiation | Muscles - metabolism | Nuclear Proteins - genetics | Proto-Oncogene Proteins - metabolism | Gene Transfer Techniques | Retroviridae - physiology | DNA-Binding Proteins - antagonists & inhibitors | Signal Transduction | beta Catenin | Trans-Activators | Zebrafish Proteins | Nuclear Proteins - metabolism | Proto-Oncogene Proteins - genetics | Transcription Factors - antagonists & inhibitors | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Transcription Factor 7-Like 2 Protein | Proteins - genetics | Transcription Factors - metabolism | Cell Lineage | Animals | Proteins - metabolism | Mice, Nude | Adipocytes - metabolism | Nuclear Proteins - antagonists & inhibitors | Receptors, Cytoplasmic and Nuclear - antagonists & inhibitors | Axin Protein | Mice | Genetic Vectors | 3T3 Cells | Muscles - cytology | Receptors, Cytoplasmic and Nuclear - metabolism | Cell research | Fat cells | Research | Analysis | Wnt-10b protein | PPAR^g protein | adipogenesis | peroxisome proliferator-activated receptor ^g | CCAAT/enhancer binding protein ^a | C/EBP^a protein | Index Medicus
Journal Article