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1. Full Text The cotton XLIM protein (GhXLIM6) is required for fiber development via maintaining dynamic F‐actin cytoskeleton and modulating cellulose biosynthesis
by Li, Yang and Wang, Na‐Na and Wang, Yao and Liu, Dong and Gao, Ya and Li, Lan and Li, Xue‐Bao
The Plant Journal, ISSN 0960-7412, 12/2018, Volume 96, Issue 6, pp. 1269 - 1282
LIM domain proteins are cysteine‐rich proteins, and are often considered as actin bundlers and transcription factors in plants. However, the roles of XLIM... 
F‐actin binding | XLIM | transcriptional regulation | protein | fiber elongation | cotton | Gossypium hirsutum | secondary cell wall formation | F-actin binding | XLIM protein | cotton (Gossypium hirsutum) | SUCROSE SYNTHASE | INITIATION | AMMONIA-LYASE GENE | BINDING-PROTEIN | LIM DOMAIN | FAMILY | PLANT SCIENCES | CELL-WALL | ELONGATION | TRANSCRIPTION FACTOR | EXPRESSION | Cysteine | Actin | Genetically modified crops | Analysis | Cellulose | Physiological aspects | Polymerization | Genetic engineering | DNA binding proteins | Protein binding | Binding | Transcription factors | Cell walls | Cellulose fibers | Transgenic | Biosynthesis | Cotton | Gene expression | Cotton fibers | Fibers | Proteins | LIM domain proteins | Cytoskeleton | Elongation
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2. Full Text MiR‐21 regulates epithelial‐mesenchymal transition phenotype and hypoxia‐inducible factor‐1α expression in third‐sphere forming breast cancer stem cell‐like cells
by Han, Mingli and Wang, Yimeng and Liu, Manran and Bi, Xiaokai and Bao, Junjie and Zeng, Ni and Zhu, Zhikun and Mo, Zhiqiang and Wu, Chengyi and Chen, Xin
Cancer Science, ISSN 1347-9032, 06/2012, Volume 103, Issue 6, pp. 1058 - 1064
Cancer stem cells ( CSC s) are predicted to be critical drivers of tumor progression due to their “stemness”, but the molecular mechanism of CSC s in... 
Actins - biosynthesis | MicroRNAs - antagonists & inhibitors | Vimentin - biosynthesis | Neoplasm Invasiveness | Retinal Dehydrogenase - biosynthesis | Humans | Spheroids, Cellular - metabolism | Gene Expression Regulation, Neoplastic | MicroRNAs - metabolism | Hyaluronan Receptors - biosynthesis | Cadherins - biosynthesis | Breast Neoplasms - metabolism | Neoplastic Stem Cells - metabolism | Oligonucleotides - pharmacology | Breast Neoplasms - pathology | Epithelial-Mesenchymal Transition | Cell Line, Tumor | Neoplastic Stem Cells - pathology | Female | Cadherins - antagonists & inhibitors | Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis | Isoenzymes - biosynthesis | CD24 Antigen - biosynthesis | Cell Movement | Index Medicus
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3. Full Text Increasing Plasma Membrane Phosphatidylinositol(4,5)Bisphosphate Biosynthesis Increases Phosphoinositide Metabolism in Nicotiana tabacum
by Yang Ju Im and Imara Y. Perera and Irena Brglez and Amanda J. Davis and Jill Stevenson-Paulik and Brian Q. Phillippy and Eva Johannes and Nina S. Allen and Wendy F. Boss
The Plant Cell, ISSN 1040-4651, 5/2007, Volume 19, Issue 5, pp. 1603 - 1616
A genetic approach was used to increase phosphatidylinositol(4,5)bisphosphate [PtdIns(4,5)P₂] biosynthesis and test the hypothesis that PtdInsP kinase (PIPK)... 
Inositols | Calcium | Memory interference | Cell lines | Actins | Lipids | Cell membranes | Plants | Plant cells | Phosphatidylinositols | MOLECULAR CHARACTERIZATION | F-ACTIN | ARABIDOPSIS-THALIANA | BIOCHEMISTRY & MOLECULAR BIOLOGY | MONOPHOSPHATE KINASE | PHOSPHOLIPASE D-ALPHA | PLANT SCIENCES | CELL BIOLOGY | PLECKSTRIN HOMOLOGY DOMAIN | ENDOPLASMIC-RETICULUM | CALCIUM MOBILIZATION | INOSITOL POLYPHOSPHATE 5-PHOSPHATASE | PHOSPHATE KINASES | Green Fluorescent Proteins - metabolism | Calcium - metabolism | Tobacco - metabolism | Humans | Lipid Metabolism | Tritium | Recombinant Fusion Proteins - metabolism | Subcellular Fractions - metabolism | Protein Transport | Tobacco - cytology | Cell Membrane - enzymology | Cell Respiration | Tobacco - genetics | Plants, Genetically Modified | Basal Metabolism | Cell Membrane - metabolism | Plant Proteins - metabolism | Phosphatidylinositol 4,5-Diphosphate - biosynthesis | Inositol 1,4,5-Trisphosphate - metabolism | Tobacco - enzymology | Cell metabolism | Phosphatidylinositol | Biosynthesis | Genetic aspects | Research | Tobacco (Plant) | Index Medicus
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4. Full Text Characterization of Fetal and Postnatal Enteric Neuronal Cell Lines With Improvement in Intestinal Neural Function
by Anitha, Mallappa and Joseph, Irene and Ding, Xiaokun and Torre, Enrique R and Sawchuk, Michael A and Mwangi, Simon and Hochman, Shawn and Sitaraman, Shanthi V and Anania, Frank and Srinivasan, Shanthi
Gastroenterology, ISSN 0016-5085, 2008, Volume 134, Issue 5, pp. 1424 - 1435
Background & Aims: The isolation and culture of primary enteric neurons is a difficult process and yields a small number of neurons. We developed fetal and... 
Gastroenterology and Hepatology | SURVIVAL | NERVOUS-SYSTEM | SEROTONIN TRANSPORTER | SMOOTH-MUSCLE | GDNF | PATHWAY | NEUROTROPHIC FACTOR | TRANSGENIC MOUSE | RECEPTORS | GASTROENTEROLOGY & HEPATOLOGY | MICE LACKING | Immunohistochemistry | Neuroglia - transplantation | ELAV-Like Protein 4 | Proto-Oncogene Proteins c-ret - biosynthesis | Serotonin - genetics | Membrane Glycoproteins - biosynthesis | Colon - innervation | Synaptophysin - genetics | S100 Proteins - genetics | Muscle, Smooth - physiology | Neurons - metabolism | S100 Proteins - biosynthesis | Serotonin - biosynthesis | Peripherins | Muscle, Smooth - innervation | S100 Calcium Binding Protein beta Subunit | Enteric Nervous System - metabolism | Glial Cell Line-Derived Neurotrophic Factor - biosynthesis | Glial Cell Line-Derived Neurotrophic Factor - genetics | Mice, Transgenic | Xenopus Proteins | Reverse Transcriptase Polymerase Chain Reaction | Ubiquitin Thiolesterase - genetics | Blotting, Western | Nerve Growth Factors - genetics | Synaptophysin - biosynthesis | Mice | ELAV Proteins - genetics | Nestin | Colon - embryology | Gastrointestinal Motility - physiology | Neurons - cytology | Actins - genetics | RNA - genetics | tau Proteins - biosynthesis | Neuroglia - cytology | tau Proteins - genetics | Gene Expression Regulation, Developmental | Intermediate Filament Proteins - genetics | Nerve Tissue Proteins - biosynthesis | Female | Isometric Contraction - physiology | Cell Line | Actins - biosynthesis | ELAV Proteins - biosynthesis | Mice, Inbred C57BL | Enteric Nervous System - embryology | Intermediate Filament Proteins - biosynthesis | Nerve Growth Factors - biosynthesis | Nerve Tissue Proteins - genetics | Colon - surgery | Membrane Glycoproteins - genetics | Pregnancy | Animals | Neuroglia - metabolism | Ubiquitin Thiolesterase - biosynthesis | Proto-Oncogene Proteins c-ret - genetics | Polymerase chain reaction | Physiological aspects | Biological response modifiers | Neurons | Index Medicus | Abridged Index Medicus | differentiation | Enteric neurons | proliferation | nNOS | Immorto | Piebald
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5. Full Text Intratracheal instillation of high dose adenoviral vectors is sufficient to induce lung injury and fibrosis in mice
by Zhou, Qiyuan and Chen, Tianji and Bozkanat, Melike and Ibe, Joyce C.hristina F and Christman, John W and Raj, J Usha and Zhou, Guofei
PloS one, ISSN 1932-6203, 2014, Volume 9, Issue 12, pp. e116142 - e116142
Rationale: Replication deficient adenoviruses (Ad) vectors are common tools in gene therapy. Since Ad vectors are known to activate innate and adaptive... 
PATHOGENESIS | MATRIX | ACTIVATION | HIPPEL-LINDAU-PROTEIN | MULTIDISCIPLINARY SCIENCES | IN-VIVO | DISEASE | ANIMAL-MODELS | MEDIATED GENE-TRANSFER | IDIOPATHIC PULMONARY-FIBROSIS | EXPRESSION | Male | Interleukin-13 - biosynthesis | Lung Injury - virology | Proliferating Cell Nuclear Antigen - biosynthesis | Pulmonary Fibrosis - virology | Interleukin-16 - biosynthesis | Bronchoalveolar Lavage Fluid - cytology | Interleukin-1beta - biosynthesis | Adenoviridae - immunology | Integrins - biosynthesis | Matrix Metalloproteinase 2 - biosynthesis | Transforming Growth Factor beta1 - biosynthesis | Disease Models, Animal | Matrix Metalloproteinase 9 - biosynthesis | Actins - biosynthesis | Mice, Inbred C57BL | Inflammation - virology | Pulmonary Fibrosis - immunology | Inflammation - immunology | Bleomycin - administration & dosage | Collagen Type I - biosynthesis | Animals | Interleukin-1alpha - biosynthesis | Mice | Bronchoalveolar Lavage Fluid - chemistry | Wnt Proteins - biosynthesis | Lung Injury - immunology | RNA | Collagen | Adenoviruses | Fibrosis | Bone morphogenetic proteins | Transforming growth factors | Gene therapy | Health aspects | Integrins | Pediatrics | Collagen (type I) | Disease | Pathogenesis | Lung | Immunity | Proteins | Bleomycin | Proliferating cell nuclear antigen | Physiology | Chronic obstructive pulmonary disease | Drug dosages | Deoxyribonucleic acid--DNA | Cytokines | Bronchus | Interleukin 13 | Tumor necrosis factor-α | Gene expression | Interleukin 16 | DNA viruses | Vectors (Biology) | Pulmonary fibrosis | Interleukin 10 | Wnt protein | Laboratories | Staining | Critical care | Inflammatory response | Viruses | mRNA | Infections | Kinases | Tissues | Bronchoalveolar lavage | Rodents | Alveoli | Trachea | Injuries | Expression vectors | Lung diseases | Inflammation | Adaptive immunity | Gelatinase B | Gelatinase A | Signaling | Lungs | Molecular biology | Immunofluorescence | Index Medicus | Deoxyribonucleic acid | DNA
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6. Full Text Tumor cells induce the cancer associated fibroblast phenotype via caveolin-1 degradation: Implications for breast cancer and DCIS therapy with autophagy inhibitors
by Martinez-Outschoorn, Ubaldo E and Pavlides, Stephanos and Whitaker-Menezes, Diana and Daumer, Kristin M and Milliman, Janet N and Chiavarina, Barbara and Migneco, Gemma and Witkiewicz, Agnieszka K and Martinez-Cantarin, Maria P and Flomenberg, Neal and Howell, Anthony and Pestell, Richard G and Lisanti, Michael P and Sotgia, Federica
Cell Cycle, ISSN 1538-4101, 06/2010, Volume 9, Issue 12, pp. 2423 - 2433
Loss of stromal caveolin 1 (Cav-1) is a novel biomarker for cancer-associated fibroblasts that predicts poor clinical outcome in breast cancer and DCIS... 
Proteins | Binding | Landes | Calcium | Biology | Bioscience | Cell | Cycle | Organogenesis | Cancer | Caveolin-1 | Lysosomal degradation | Chloroquine | Myofibroblast | Tumor stroma | TGFbeta signaling | Cancer associated fibroblasts | Autophagy | ACTIVATION | autophagy | TGF-BETA | lysosomal degradation | myofibroblast | SYSTEMIC-SCLEROSIS | cancer associated fibroblasts | CELL BIOLOGY | chloroquine | caveolin-1 | GROWTH | GENE-EXPRESSION | STROMAL FIBROBLASTS | VIMENTIN EXPRESSION | tumor stroma | TENASCIN | MMP-9 | PROGRESSION | Prognosis | Extracellular Matrix Proteins - biosynthesis | Coculture Techniques | Humans | Carcinoma, Intraductal, Noninfiltrating - metabolism | Transforming Growth Factor beta - biosynthesis | Autophagy - drug effects | Actins - genetics | Breast Neoplasms - metabolism | Chloroquine - pharmacology | Smad2 Protein - biosynthesis | Vimentin - genetics | Female | Microfilament Proteins - genetics | Fibroblasts - metabolism | Actins - biosynthesis | Calcium-Binding Proteins - biosynthesis | Vimentin - biosynthesis | Extracellular Matrix Proteins - genetics | Caveolin 1 - genetics | Caveolin 1 - metabolism | Microfilament Proteins - biosynthesis | Phenotype | Cell Line, Tumor | Biomarkers, Tumor - genetics | Transforming Growth Factor beta - metabolism | Biomarkers, Tumor - biosynthesis | Calcium-Binding Proteins - genetics | Index Medicus
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7. Full Text The swinholide biosynthesis gene cluster from a terrestrial cyanobacterium, Nostoc sp. strain UHCC 0450
by Humisto, Anu and Jokela, Jouni and Liu, Liwei and Wahlsten, Matti and Wang, Hao and Permi, Perttu and Machado, João Paulo and Antunes, Agostinho and Fewer, David P and Sivonen, Kaarina
Applied and Environmental Microbiology, ISSN 0099-2240, 02/2018, Volume 84, Issue 3
Swinholides are 42-carbon ring polyketides with a 2-fold axis of symmetry. They are potent cytotoxins that disrupt the actin cytoskeleton. Swinholides were... 
Swinholide | Polyketides | "Candidatus Entotheonella" | Anabaena | Cyanobacteria | Trans-AT PKS | Scytophycin | Nostoc | Horizontal gene transfer | scytophycin | NATURAL-PRODUCT DISCOVERY | MICROBIOLOGY | CYTOTOXIC DIMERIC MACROLIDES | polyketides | POLYKETIDE SYNTHASES | horizontal gene transfer | NONRIBOSOMAL PEPTIDE | swinholide | EVOLUTION | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | cyanobacteria | DIVERSITY | trans-AT PKS | SPONGE THEONELLA-SWINHOEI | CONGENERS | MARINE CYANOBACTERIA | INSIGHTS | Physiological aspects | Biosynthesis | Analysis | Fungicides | Nucleotide sequence | Gene clusters | Genes | Terrestrial environments | Group theory | Cytotoxicity | Genomes | Phylogeny | Polyketide synthase | Cytotoxins | Actin | Phylogenetics | Clusters | Bacteria | Cytoskeleton | Catalysis
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8. Full Text Imaging Peptidoglycan Biosynthesis in Bacillus subtilis with Fluorescent Antibiotics
by Kittichoat Tiyanont and Thierry Doan and Michael B. Lazarus and Xiao Fang and David Z. Rudner and Suzanne Walker
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2006, Volume 103, Issue 29, pp. 11033 - 11038
The peptidoglycan (PG) layers surrounding bacterial cells play an important role in determining cell shape. The machinery controlling when and where new PG is... 
Microbial sensitivity tests | Antibiotics | Bacillus subtilis | Imaging | Stem cells | Actins | Lipids | Bacteria | Biosynthesis | Polymers | Helix | Ramoplanin | Vancomycin | Bacterial cytoskeleton | Mbl | WALL | LYTIC TRANSGLYCOSYLASE | CAULOBACTER | MUREIN SACCULUS | GLYCOPEPTIDE | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | ramoplanin | CELL-SHAPE | bacterial cytoskeleton | MORPHOGENESIS | helix | PENICILLIN-BINDING PROTEINS | vancomycin | Peptidoglycan - biosynthesis | Fluorescent Dyes - chemistry | Vancomycin - chemistry | Depsipeptides - metabolism | Vancomycin - pharmacology | Actins - metabolism | Depsipeptides - pharmacology | Molecular Structure | Vancomycin - metabolism | Bacillus subtilis - metabolism | Depsipeptides - chemistry | Actins - genetics | Cytoskeleton | Research | Chemical synthesis | Bacterial proteins | Cells | Index Medicus | Biological Sciences
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9. Full Text Biosynthesis and actions of 5-oxoeicosatetraenoic acid (5-oxo-ETE) on feline granulocytes
by Cossette, Chantal and Gravel, Sylvie and Reddy, Chintam Nagendra and Gore, Vivek and Chourey, Shishir and Ye, Qiuji and Snyder, Nathaniel W and Mesaros, Clementina A and Blair, Ian A and Lavoie, Jean-Pierre and Reinero, Carol R and Rokach, Joshua and Powell, William S
Biochemical Pharmacology, ISSN 0006-2952, 08/2015, Volume 96, Issue 3, pp. 247 - 255
The 5-lipoxygenase product 5-oxo-6,8,11,14-eicosatetraenoic acid (5-oxo-ETE) is the most powerful human eosinophil chemoattractant among lipid mediators and... 
Eicosanoids | Inflammation | 5-Lipoxygenase | OXE receptor | Neutrophils | Eosinophils | 5-OXO-6,8,11,14-EICOSATETRAENOIC ACID | OXIDATIVE STRESS | RADICAL PRODUCTION | RECEPTOR | POTENT CHEMOATTRACTANT | HUMAN EOSINOPHILS | LIQUID-CHROMATOGRAPHY | 5-OXO-EICOSATETRAENOATE | PHARMACOLOGY & PHARMACY | LEUKOTRIENE | 5-OXO-EICOSANOIDS | Asthma - metabolism | Eosinophils - metabolism | Receptors, Eicosanoid - antagonists & inhibitors | Eosinophils - drug effects | Arachidonate 5-Lipoxygenase - genetics | Humans | Actins - metabolism | Male | Arachidonic Acids - biosynthesis | Actins - genetics | Cynodon - chemistry | Allergens - immunology | Asthma - immunology | Female | Bronchoalveolar Lavage Fluid - cytology | Eosinophils - pathology | Chemotaxis - immunology | Cynodon - immunology | Benzeneacetamides - pharmacology | Neutrophils - metabolism | Disease Models, Animal | Neutrophils - pathology | Cats | Gene Expression | Arachidonate 5-Lipoxygenase - metabolism | Benzothiazoles - pharmacology | Neutrophils - drug effects | Polymerization | Chemotaxis - drug effects | Arachidonic Acids - pharmacology | Asthma - chemically induced | Asthma - genetics | Leukotriene B4 - pharmacology | Animals | Receptors, Eicosanoid - metabolism | Prostaglandin D2 - pharmacology | Receptors, Eicosanoid - genetics | Primary Cell Culture | Index Medicus
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10. Full Text Pyrimidine biosynthesis links mitochondrial respiration to the p53 pathway
by Anastasia A. Khutornenko and Vladimir V. Roudko and Boris V. Chernyak and Andrey B. Vartapetian and Peter M. Chumakov and Alexandra G. Evstafieva and George R. Stark
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2010, Volume 107, Issue 29, pp. 12828 - 12833
While many functions of the p53 tumor suppressor affect mitochondrial processes, the role of altered mitochondrial physiology in a modulation of p53 response... 
Up regulation | Pyrimidines | HCT116 cells | Epithelial cells | Cell lines | HeLa cells | Actins | Biosynthesis | Respiration | Apoptosis | p53 tumor suppressor | NQO1 and NQO2 | Dihydroorotate dehydrogenase | Mitochondrial electron transport chain | dihydroorotate dehydrogenase | mitochondrial electron transport chain | ACTIVATION | PROTEASOMAL DEGRADATION | MULTIDISCIPLINARY SCIENCES | DNA-DAMAGE | PROTHYMOSIN-ALPHA | apoptosis | HYPOXIA | ARREST | INHIBITION | TUMOR-SUPPRESSOR | S-PHASE | STRESS | Mitochondria - enzymology | Electron Transport Complex III - metabolism | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Humans | Pyrimidines - biosynthesis | Membrane Potential, Mitochondrial - drug effects | Oxidoreductases Acting on CH-CH Group Donors - antagonists & inhibitors | Oxidoreductases Acting on CH-CH Group Donors - deficiency | Protein Processing, Post-Translational - drug effects | Cell Respiration - drug effects | Methacrylates - pharmacology | Potassium Cyanide - pharmacology | Quinone Reductases - metabolism | Tumor Suppressor Protein p53 - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | Isoxazoles - pharmacology | Up-Regulation - drug effects | Electron Transport Complex III - antagonists & inhibitors | Signal Transduction - drug effects | Cell Line, Tumor | NAD(P)H Dehydrogenase (Quinone) - metabolism | Thiazoles - pharmacology | Proteasome Endopeptidase Complex - metabolism | Observations | Health aspects | Signal transduction | Tissue | Enzymes | DNA damage | Electron transfer | Organic chemicals | Tumors | Index Medicus | Phosphorylation | Carcinoma | Serine | Data processing | Nuclei | p53 protein | Electron transport chain | Mitochondria | Cytochrome bc1 | NAD(P)H dehydrogenase (quinone) | Hypoxia | Tumor suppressor genes | Intoxication | pyrimidines | Electron transport | p14ARF protein | Biological Sciences
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11. Full Text Propranolol induces regression of hemangioma cells via the down‐regulation of the PI3K/Akt/eNOS/VEGF pathway
by Pan, Wei‐Kang and Li, Peng and Guo, Zheng‐Tuan and Huang, Qiang and Gao, Ya
Pediatric Blood & Cancer, ISSN 1545-5009, 08/2015, Volume 62, Issue 8, pp. 1414 - 1420
BackgroundInfantile hemangioma (IH) is a benign vascular neoplasm resulting from the abnormal proliferation of endothelial cells and pericytes in infants.... 
eNOS | infantile hemangioma | VEGF | propranolol | Infantile hemangioma | Propranolol | ENOS | ANGIOGENESIS | NITRIC-OXIDE SYNTHASE | PANCREATIC-CANCER | ACTIN DYNAMICS | PROGENITOR-CELL | ONCOLOGY | SIGNALING PATHWAY | IN-VIVO | INFANTILE HEMANGIOMAS | PEDIATRICS | HEMATOLOGY | EXPRESSION | ENDOTHELIAL GROWTH-FACTOR | Norepinephrine - pharmacology | Vascular Endothelial Growth Factor A - biosynthesis | Phosphorylation | Humans | Nitric Oxide Synthase Type III - biosynthesis | Propranolol - therapeutic use | Infant | Vascular Endothelial Growth Factor A - antagonists & inhibitors | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Vascular Endothelial Growth Factor Receptor-2 - antagonists & inhibitors | Proliferating Cell Nuclear Antigen - biosynthesis | Neoplasm Invasiveness - pathology | Angiogenesis Inhibitors - therapeutic use | Nitric Oxide Synthase Type III - metabolism | Chromones - pharmacology | Hemangioma - drug therapy | Phosphatidylinositol 3-Kinases - biosynthesis | Proto-Oncogene Proteins c-akt - metabolism | Infant, Newborn | Adrenergic beta-Antagonists - therapeutic use | NG-Nitroarginine Methyl Ester - pharmacology | Nitric Oxide - biosynthesis | Cyclin A2 - biosynthesis | Cyclin-Dependent Kinase Inhibitor p21 - biosynthesis | Endothelial Cells - metabolism | Pericytes - metabolism | Cells, Cultured | Morpholines - pharmacology | Vascular Endothelial Growth Factor Receptor-2 - metabolism | Cinnamates - pharmacology | Nitric Oxide Synthase Type III - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - biosynthesis | Vascular Endothelial Growth Factor Receptor-1 - pharmacology | Cell Cycle Checkpoints - drug effects | Neovascularization, Pathologic - drug therapy | Cell Proliferation - drug effects | Cyclin D2 - biosynthesis | Proteins | Propranolol hydrochloride | Hemangioma | Vascular endothelial growth factor | Cell proliferation | Regression | AKT protein | Infants | Endothelial cells | 1-Phosphatidylinositol 3-kinase | Cyclin D2 | Vascular endothelial growth factor receptors | Antiangiogenics | Cell cycle | Cofilin | Pericytes | Norepinephrine | Inhibition | Pretreatment | Cancer | Index Medicus
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