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1. Full Text Bidirectional regulation of neutrophil migration by mitogen-activated protein kinases
by Liu, Xiaowen and Ma, Bo and Malik, Asrar B and Tang, Haiyang and Yang, Tao and Sun, Bo and Wang, Gang and Minshall, Richard D and Li, Yan and Zhao, Yong and Ye, Richard D and Xu, Jingsong
Nature Immunology, ISSN 1529-2908, 05/2012, Volume 13, Issue 5, pp. 457 - 464
To kill invading bacteria, neutrophils must interpret spatial cues, migrate and reach target sites. Although the initiation of chemotactic migration has been... 
SIGNALING PATHWAYS | POLARITY | SPECIFICITY | CHEMOTAXIS | PHOSPHORYLATION | CELL-MIGRATION | DESENSITIZATION | FORMYL PEPTIDE RECEPTOR | ALPHA | IMMUNOLOGY | BETA | Chemotaxis, Leukocyte | Neutrophils - enzymology | Humans | Neutrophils - drug effects | Neutrophils - immunology | Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors | Imidazoles - pharmacology | Extracellular Signal-Regulated MAP Kinases - metabolism | G-Protein-Coupled Receptor Kinase 2 - metabolism | Mice, Knockout | N-Formylmethionine Leucyl-Phenylalanine - metabolism | Animals | Signal Transduction - drug effects | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | HEK293 Cells | Receptors, Formyl Peptide - metabolism | HL-60 Cells | Signal Transduction - physiology | Flavonoids - pharmacology | Mice | Pyridines - pharmacology | p38 Mitogen-Activated Protein Kinases - metabolism | Physiological aspects | Immune response | Research | Properties | Neutrophils | Mitogen-activated protein kinases | Index Medicus
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2. Full Text Mitogen Activated Protein Kinases
by Jose Lozano and Jose M. Lizcano and Ana Cuenda
2017, ISBN 9782889453399
Mitogen-activated protein kinase (MAPK) pathways are evolutionarily conserved in all eukaryotes and allow cells to respond to changes in the physical and... 
kinase | cell differentiation | p38 | MSK | scaffold | inflammation | JNK | cancer | MAPK | ERK
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3. Full Text Pyrrolopyridine inhibitors of mitogen-activated protein kinase-activated protein kinase 2 (MK-2)
by Anderson, David R and Meyers, Marvin J and Vernier, William F and Mahoney, Matthew W and Kurumbail, Ravi G and Caspers, Nicole and Poda, Gennadiy I and Schindler, John F and Reitz, David B and Mourey, Robert J
Journal of Medicinal Chemistry, ISSN 0022-2623, 05/2007, Volume 50, Issue 11, pp. 2647 - 2654
A new class of potent kinase inhibitors selective for mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP-K2 or MK-2) for the treatment of... 
RHEUMATOID-ARTHRITIS | CHEMISTRY, MEDICINAL | BIOSYNTHESIS | P38 MAP KINASE | Acute Disease | Pyridines - chemistry | Humans | Pyridines - chemical synthesis | Intracellular Signaling Peptides and Proteins | Models, Molecular | Rats | Anti-Inflammatory Agents, Non-Steroidal - chemistry | Crystallography, X-Ray | Structure-Activity Relationship | Anti-Inflammatory Agents, Non-Steroidal - pharmacology | Pyrroles - pharmacology | Animals | Pyrroles - chemical synthesis | Inflammation - drug therapy | U937 Cells | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Pyrroles - chemistry | Protein-Serine-Threonine Kinases - chemistry | Pyridines - pharmacology | Anti-Inflammatory Agents, Non-Steroidal - chemical synthesis | Tumor Necrosis Factor-alpha - biosynthesis | Tumor Necrosis Factor-alpha - antagonists & inhibitors | Index Medicus
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4. Full Text Multiple sodium channel isoforms and mitogen-activated protein kinases are present in painful human neuromas
by Black, Joel A and Nikolajsen, Lone and Kroner, Karsten and Jensen, Troels S and Waxman, Stephen G
Annals of Neurology, ISSN 0364-5134, 12/2008, Volume 64, Issue 6, pp. 644 - 653
Objective: Although axons within neuromas have been shown to produce inappropriate spontaneous ectopic discharges, the molecular basis for pain in patients... 
SPINAL SENSORY NEURONS | NEUROPATHIC PAIN | ECTOPIC IMPULSE GENERATION | PERIPHERAL-NERVES | PRIMARY AFFERENT NEURONS | DRG NEURONS | CLOSED-STATE INACTIVATION | P38 MAPK | UP-REGULATION | NEUROSCIENCES | CORD-INJURY | CLINICAL NEUROLOGY | Pain - surgery | Humans | Middle Aged | Mitogen-Activated Protein Kinases - biosynthesis | Male | Protein Isoforms - analysis | Sodium Channels - physiology | Neuroma - surgery | Pain - metabolism | Sodium Channels - biosynthesis | Neuroma - enzymology | Protein Isoforms - metabolism | Mitogen-Activated Protein Kinases - analysis | Pain - enzymology | Protein Isoforms - biosynthesis | Up-Regulation - physiology | Sodium Channels - metabolism | Adult | Female | Mitogen-Activated Protein Kinases - metabolism | Neuroma - metabolism | Index Medicus
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5. Full Text Mechanical impact induces cartilage degradation via mitogen activated protein kinases
by Ding, L and Heying, E and Nicholson, N and Stroud, N.J and Homandberg, G.A and Buckwalter, J.A and Guo, D and Martin, J.A
Osteoarthritis and Cartilage, ISSN 1063-4584, 2010, Volume 18, Issue 11, pp. 1509 - 1517
Summary Objective To determine the activation of Mitogen activated protein (MAP) kinases in and around cartilage subjected to mechanical damage and to... 
Rheumatology | Impact | Post-traumatic osteoarthritis | Inhibitors | Cartilage damage | MAP kinases | INDIVIDUAL CELLS | APOPTOTIC CELL-DEATH | INJURY | KAPPA-B | COMPRESSION | RHEUMATOLOGY | P38 MAP KINASE | IN-VITRO | ARTICULAR-CARTILAGE | OSTEOARTHRITIS | CHONDROCYTE APOPTOSIS | ORTHOPEDICS | Stress, Mechanical | Immunoblotting | Proteoglycans - analysis | Extracellular Signal-Regulated MAP Kinases - metabolism | Cartilage, Articular - enzymology | Chondrocytes - enzymology | Animals | Cell Death - physiology | Chondrocytes - physiology | Cartilage, Articular - metabolism | Cattle | Polymerase Chain Reaction | Cartilage, Articular - injuries | p38 Mitogen-Activated Protein Kinases - metabolism | Cell Death - drug effects | Cell Survival - physiology | Disease Models, Animal | Mitogen-Activated Protein Kinases - metabolism | Mitogens | Protein kinases | Index Medicus | Post-traumatic Osteoarthritis
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6. Full Text Irisin stimulates browning of white adipocytes through mitogen-activated protein kinase p38 MAP kinase and ERK MAP kinase signaling
by Zhang, Yuan and Li, Rui and Meng, Yan and Li, Shiwu and Donelan, William and Zhao, Yan and Qi, Lei and Zhang, Mingxiang and Wang, Xingli and Cui, Taixing and Yang, Li-Jun and Tang, Dongqi
Diabetes, ISSN 0012-1797, 02/2014, Volume 63, Issue 2, pp. 514 - 525
The number and activity of brown adipocytes are linked to the ability of mammals to resist body fat accumulation. In some conditions, certain white adipose... 
OBESITY | GENE | ENDOCRINOLOGY & METABOLISM | MUSCLE | RECEPTOR | PROLIFERATION | DIFFERENTIATION | EXPRESSION | FAT-CELL | EXERCISE | ADIPOSE-TISSUE | MAP Kinase Signaling System - physiology | Nitriles - pharmacology | Adipose Tissue, White - metabolism | Caenorhabditis elegans Proteins - metabolism | Adipocytes - cytology | Male | Adipocytes - drug effects | Extracellular Signal-Regulated MAP Kinases - metabolism | Recombinant Proteins | Extracellular Signal-Regulated MAP Kinases - genetics | Pichia - metabolism | Membrane Transport Proteins - genetics | Dietary Fats | Membrane Transport Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Butadienes - pharmacology | Fibronectins - pharmacology | Fibronectins - administration & dosage | Mice, Inbred C57BL | Rats | p38 Mitogen-Activated Protein Kinases - genetics | Imidazoles - pharmacology | 3T3-L1 Cells | Rats, Sprague-Dawley | Animals | Adipocytes - metabolism | Pichia - genetics | Protein Binding | Adipose Tissue, Brown - drug effects | Adipose Tissue, Brown - metabolism | Fibronectins - genetics | Mice | Pyridines - pharmacology | Mutation | Mitochondrial Uncoupling Proteins | Caenorhabditis elegans Proteins - genetics | Adipose Tissue, White - drug effects | Physiological research | Cellular signal transduction | Research | Identification and classification | Membrane proteins | Proteins | Homeostasis | Diabetes | Kinases | Genes | Cells | Index Medicus | Abridged Index Medicus
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7. Full Text Increased phosphorylated p38 mitogen-activated protein kinase in COPD Lungs
by Gaffey, K and Reynolds, S and Plumb, J and Kaur, M and Singh, D
EUROPEAN RESPIRATORY JOURNAL, ISSN 0903-1936, 07/2013, Volume 42, Issue 1, pp. 28 - 41
The p38 mitogen-activated protein kinase (MAPK) pathway is upregulated in chronic obstructive pulmonary disease (COPD). To date, dual labelling to identify... 
OBSTRUCTIVE PULMONARY-DISEASE | SEVERE ASTHMA | HUMAN NEUTROPHILS | BRONCHIAL EPITHELIAL-CELLS | RESPIRATORY SYSTEM | MAP KINASE | IN-VIVO | ALVEOLAR MACROPHAGES | AIRWAY NEUTROPHILS | SELECTIVE ACTIVATION | EXPRESSION | Immunohistochemistry | CD8-Positive T-Lymphocytes - cytology | Phosphorylation | Cytokines - metabolism | Neutrophils - enzymology | Cells, Cultured - cytology | Humans | Middle Aged | Male | Inflammation | Pulmonary Disease, Chronic Obstructive - physiopathology | Macrophages - enzymology | Pulmonary Disease, Chronic Obstructive - enzymology | Gene Expression Regulation, Enzymologic | Epithelial Cells - enzymology | Female | Aged | p38 Mitogen-Activated Protein Kinases - metabolism | Neutrophils - metabolism | Smoking | Index Medicus
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8. Full Text Heat shock factor 1 is a substrate for p38 mitogen-activated protein kinases
by Naidu, Sharadha Dayalan and Sutherland, Calum and Zhang, Ying and Risco, Ana and de la Vega, Laureano and Caunt, Christopher J and Hastie, C. James and Lamont, Douglas J and Torrente, Laura and Chowdhry, Sudhir and Benjamin, Ivor J and Keyse, Stephen M and Cuenda, Ana and Dinkova-Kostovaa, Albena T
Molecular and Cellular Biology, ISSN 0270-7306, 2016, Volume 36, Issue 18, pp. 2403 - 2417
Heat shock factor 1 (HSF1) monitors the structural integrity of the proteome. Phosphorylation at S326 is a hallmark for HSF1 activation, but the identity of... 
ISOTHIOCYANATES | RESPONSES | CELLS | TRANSCRIPTIONAL ACTIVITY | DNA-BINDING | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HSF1 | CYTOPROTECTION | COILED-COIL | STRESS | CELL BIOLOGY | Cell Line | Phosphorylation | Transcription Factors - chemistry | Humans | Protein Multimerization | Mouse Embryonic Stem Cells - cytology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Serine - metabolism | Mouse Embryonic Stem Cells - metabolism | HSP70 Heat-Shock Proteins - metabolism | Heat Shock Transcription Factors | Protein Transport | Animals | HSP90 Heat-Shock Proteins - antagonists & inhibitors | Transcription, Genetic | Mice | p38 Mitogen-Activated Protein Kinases - metabolism | HeLa Cells | Isothiocyanates - pharmacology | Index Medicus
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9. Full Text The regulation of ATF3 gene expression by mitogen-activated protein kinases
by Lu, Dan and Chen, Jingchun and Hai, Tsonwin
Biochemical Journal, ISSN 0264-6021, 01/2007, Volume 401, Issue 2, pp. 559 - 567
ATF3 (activating transcription factor 3) gene encodes a member of the ATF/CREB (cAMP-response-element-binding protein) family of transcription factors. Its... 
Mitogen activated protein kinase (MAPK) | Activating transcription factor 3 (ATF3) | p38 | Stress response | Stress kinase | MAPK kinase (MKK) | APOPTOSIS | activating transcription factor 3 (ATF3) | stress kinase | PHOSPHORYLATION | MAP KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION FACTOR-3 | mitogen activated protein kinase (MAPK) | JUN NH2-TERMINAL KINASE | INDUCTION | stress response | VASCULAR ENDOTHELIAL-CELLS | C-JUN | STRESS | INHIBITOR | JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors | Humans | Gene Expression Regulation | Activating Transcription Factor 3 - biosynthesis | Cercopithecus aethiops | JNK Mitogen-Activated Protein Kinases - metabolism | Imidazoles - pharmacology | MAP Kinase Kinase 7 - metabolism | Transcription Factors - metabolism | Animals | Mitogen-Activated Protein Kinases - physiology | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Enzyme Induction - drug effects | Anisomycin - pharmacology | Flavonoids - pharmacology | Pyridines - pharmacology | p38 Mitogen-Activated Protein Kinases - metabolism | Enzyme Activation | HeLa Cells | COS Cells | Activating Transcription Factor 3 - genetics | Index Medicus | IL-1β, interleukin 1β | JNK, c-Jun N-terminal kinase | DTT, dithiothreitol | shRNA, small-hairpin RNA | ERK, extracellular-signal-regulated kinase | SAPK, stress-activated protein kinase | DMEM, Dulbecco's modified Eagle's medium | ERK kinase 1 | CREB, CRE-binding protein | RT, reverse transcriptase | gadd153, growth-arrest and DNA-damage-inducible protein 153 | TNFα, tumour necrosis factor α | enhancer-binding protein | EBP-homologous protein 10 | GAPDH, glyceraldehyde-3-phosphate dehydrogenase | CRE, cAMP-response element | GST, glutathione S-transferase | HEK-293 cells, human embryonic kidney 293 cells | tetO, tet operator | NF-κB, nuclear factor κB | EBP, CCAAT | DN, dominant negative | FBS, fetal bovine serum | β-Gal, β-galactosidase | MKK, MAPK kinase | HA, haemagglutinin | CA, constitutively active | IP–kinase, immunoprecipitation coupled with kinase | MEK1, MAPK | ATF, activating transcription factor | Chop10, C | TGF-β, transforming growth factor-β | MEF, mouse embryonic fibroblast | MAPK, mitogen-activated protein kinase
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10. Full Text Mitogen-activated protein kinase signal transduction in solid tumors
by Lei, Yuan-Yuan and Wang, Wei-Jia and Mei, Jin-Hong and Wang, Chun-Liang
Asian Pacific Journal of Cancer Prevention, ISSN 1513-7368, 2014, Volume 15, Issue 20, pp. 8539 - 8548
Mitogen-activated protein kinase (MAPK) is an important signaling pathway in living beings in response to extracellular stimuli. There are 5 main subgroups... 
Mechanisms of action | Treatment | MAPK | Tumor development | treatment | PTEN LOSS | P38 MAPK | tumor development | mechanisms of action | BREAST-CANCER | LIVER-CANCER | TARGETED THERAPIES | IN-VITRO | MELANOMA | ONCOLOGY | GASTRIC-CANCER | PATHWAY | PROSTATE-CANCER
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11. Full Text Inflammation and Mechanical Stretch Promote Aortic Stiffening in Hypertension Through Activation of p38 Mitogen-Activated Protein Kinase
by Wu, Jing and Thabet, Salim R and Kirabo, Annet and Trott, Daniel W and Saleh, Mohamed A and Xiao, Liang and Madhur, Meena S and Chen, Wei and Harrison, David G
Circulation Research, ISSN 0009-7330, 02/2014, Volume 114, Issue 4, pp. 616 - 625
RATIONALE:Aortic stiffening commonly occurs in hypertension and further elevates systolic pressure. Hypertension is also associated with vascular inflammation... 
inflammation | C-REACTIVE PROTEIN | RHEUMATOID-ARTHRITIS | CARDIAC & CARDIOVASCULAR SYSTEMS | ENDOTHELIAL DYSFUNCTION | WAVE REFLECTION | VASCULAR DYSFUNCTION | HEART-FAILURE | ANGIOTENSIN-II | BLOOD-PRESSURE | II-INDUCED HYPERTENSION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | INCREASED ARTERIAL STIFFNESS | Vasculitis - metabolism | Vasculitis - physiopathology | Stress, Mechanical | Male | Adoptive Transfer | Aortic Diseases - metabolism | Inflammation - metabolism | T-Lymphocytes - metabolism | Hypertension - chemically induced | p38 Mitogen-Activated Protein Kinases - metabolism | T-Lymphocytes - pathology | CD4 Antigens - genetics | Disease Models, Animal | Fibroblasts - metabolism | Vasoconstrictor Agents - pharmacology | Elastin - metabolism | Angiotensin II - pharmacology | Cells, Cultured | Interleukin-17 - genetics | Homeodomain Proteins - genetics | Hypertension - physiopathology | Hypertension - metabolism | Mice, Knockout | Collagen - metabolism | Aortic Diseases - physiopathology | Animals | Vascular Stiffness - physiology | CD8 Antigens - genetics | Fibroblasts - cytology | Mice | Index Medicus
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12. Full Text Mitogen-Activated Protein Kinases and Retinal Ischemia
by Roth, Steven and Shaikh, Afzhal R and Hennelly, Meghann M and Li, Qing and Bindokas, Vytas and Graham, Christine E
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 12/2003, Volume 44, Issue 12, pp. 5383 - 5395
PURPOSE. Mitogen-activated protein kinases (MAPKs), consisting of three major enzymes- extracellular signal-regulated kinase (ERK), p38, and c-jun N-terminal... 
CALCIUM-BINDING PROTEINS | TRANSIENT FOREBRAIN ISCHEMIA | MAP KINASE | NEUROTROPHIC FACTOR | N-TERMINAL KINASE | FOCAL CEREBRAL-ISCHEMIA | RAT RETINA | REPERFUSION INJURY | OPHTHALMOLOGY | C-JUN | CELL-DEATH | Electroretinography | Immunohistochemistry | In Situ Nick-End Labeling | Phosphorylation | Cell Count | Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Ischemia - enzymology | Rats | Rats, Sprague-Dawley | Retinal Vessels - enzymology | Blotting, Western | Ischemia - prevention & control | Retina - physiology | Retinal Vessels - pathology | Animals | Mitogen-Activated Protein Kinases - antagonists & inhibitors | JNK Mitogen-Activated Protein Kinases | p38 Mitogen-Activated Protein Kinases | Ischemia - pathology | Mitogen-Activated Protein Kinase 3 | Apoptosis | Mitogen-Activated Protein Kinase 1 - metabolism | Mitogen-Activated Protein Kinases - metabolism | Index Medicus
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13. Full Text Mitogen-activated protein kinases, Erk and p38, phosphorylate and regulate Foxo1
by Asada, Sachie and Daitoku, Hiroaki and Matsuzaki, Hitomi and Saito, Tomoko and Sudo, Tatsuhiko and Mukai, Hidehito and Iwashita, Shintaro and Kako, Koichiro and Kishi, Tsutomu and Kasuya, Yoshitoshi and Fukamizu, Akiyoshi
Cellular Signalling, ISSN 0898-6568, 2007, Volume 19, Issue 3, pp. 519 - 527
The members of the transcription factor Foxo family regulate the expression of genes concerned with the stress response, cell cycle and gluconeogenesis. Foxo1... 
Ets-1 | p38 | Flk-1 | Transcription | Foxo1 | Erk | SURVIVAL | FORKHEAD TRANSCRIPTION FACTOR | transcription | ANGIOGENESIS | MAP KINASE | FKHR FOXO1 | CELL BIOLOGY | SIGNAL-TRANSDUCTION | IN-VITRO | ENDOTHELIAL-CELLS | EXPRESSION | Cell Line | NIH 3T3 Cells | Phosphorylation | Luciferases - metabolism | Humans | Enzyme Inhibitors - pharmacology | Imidazoles - pharmacology | Extracellular Signal-Regulated MAP Kinases - metabolism | Calcium-Calmodulin-Dependent Protein Kinases - antagonists & inhibitors | Forkhead Transcription Factors - genetics | Gene Expression Regulation, Enzymologic | Animals | Forkhead Transcription Factors - metabolism | Anisomycin - pharmacology | Flavonoids - pharmacology | Forkhead Box Protein O1 | Mice | Pyridines - pharmacology | p38 Mitogen-Activated Protein Kinases - metabolism | Epidermal Growth Factor - pharmacology | Protein Synthesis Inhibitors - pharmacology | Genes, Reporter | Proteins | Protein kinases | Index Medicus
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14. Full Text Improved immunohistochemical detection of phosphorylated mitogen-activated protein kinases in the injured rat optic nerve head
by Mammone, Teresa and Chidlow, Glyn and Casson, Robert J and Wood, John P. M
Histochemistry and Cell Biology, ISSN 0948-6143, 5/2019, Volume 151, Issue 5, pp. 435 - 456
The activity of mitogen-activated protein kinases (MAPKs) is largely controlled by addition or removal of phosphate groups, which are carried out by kinase or... 
Biomedicine, general | Biochemistry, general | Immunohistochemistry | Phosphorylation | Phosphatase inhibitor | Biomedicine | Mitogen-activated protein kinase (MAPK) | Ocular hypertension | Retina | Developmental Biology | Cell Biology | PATHWAYS | PANEL | TISSUE | MODEL | MICROSCOPY | CELL BIOLOGY | HYPERGLYCEMIA | FORMALIN | P38 | GLAUCOMA | EXPRESSION | Isoenzymes - analysis | Ocular Hypertension - pathology | Rats | Optic Disk - injuries | Ocular Hypertension - metabolism | Rats, Sprague-Dawley | Animals | Mitogen-Activated Protein Kinases - analysis | Isoenzymes - metabolism | Optic Disk - metabolism | Female | Optic Disk - pathology | Disease Models, Animal | Mitogen-Activated Protein Kinases - metabolism | Hypertension | Phosphates | Phosphatases | Isoenzymes | Physiological aspects | Mitogens | Protein kinases | Optic nerve | Labelling | MAP kinase | Dephosphorylation | Phosphatase | Kinases
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15. Full Text p38 mitogen-activated protein kinase downregulates endothelial progenitor cells
by Seeger, Florian H and Haendeler, Judith and Walter, Dirk H and Rochwalsky, Ulrich and Reinhold, Johannes and Urbich, Carmen and Rössig, Lothar and Corbaz, Anne and Chvatchko, Yolande and Zeiher, Andreas M and Dimmeler, Stefanie
Circulation, ISSN 0009-7322, 03/2005, Volume 111, Issue 9, pp. 1184 - 1191
Background - Transplantation of endothelial progenitor cells (EPCs) improves neovascularization after ischemia, but patients with coronary artery disease (... 
Angiogenesis | Glucose | Tumor necrosis factor-α | Stem cells | Mitogen-activated protein kinases | stem cells | glucose | CORONARY-ARTERY DISEASE | CARDIAC & CARDIOVASCULAR SYSTEMS | angiogenesis | MAP KINASE | PROLIFERATION | TRANSPLANTATION | tumor necrosis factor-alpha | PATHWAY | mitogen-activated protein kinases | INCREASE | PERIPHERAL VASCULAR DISEASE | DYSFUNCTION | INHIBITORS | HEMATOLOGY | EXPRESSION | Cell Count | Cells, Cultured - cytology | Humans | Middle Aged | Ischemia - enzymology | Molecular Sequence Data | Coronary Disease - epidemiology | Male | Transplantation, Heterologous | Stem Cells - cytology | Stem Cell Transplantation | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Isoquinolines - pharmacology | Protein Processing, Post-Translational - drug effects | Stem Cells - enzymology | Adult | Female | Cell Differentiation | Phosphorylation - drug effects | Ischemia - pathology | Amino Acid Sequence | Cells, Cultured - drug effects | p38 Mitogen-Activated Protein Kinases - physiology | Comorbidity | Risk Factors | Glucose - pharmacology | Imidazoles - pharmacology | Sulfonamides - pharmacology | Cell Division - drug effects | Transcription Factors - metabolism | Tumor Necrosis Factor-alpha - pharmacology | Coronary Disease - pathology | Animals | Coronary Disease - enzymology | Signal Transduction - drug effects | Hindlimb - blood supply | Mice, Nude | Activating Transcription Factor 2 | p38 Mitogen-Activated Protein Kinases - antagonists & inhibitors | Cyclic AMP Response Element-Binding Protein - metabolism | Aged | Mice | Pyridines - pharmacology | Apoptosis | Index Medicus | Abridged Index Medicus
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