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Journal of Biological Chemistry, ISSN 0021-9258, 01/2014, Volume 289, Issue 1, pp. 365 - 378
Neuronal nitric-oxide synthase (nNOS) has various splicing variants and different subcellular localizations. nNOS can be found also in the nucleus; however,... 
LOCALIZATION | SIGNALING PATHWAYS | PGC-1-ALPHA | BIOCHEMISTRY & MOLECULAR BIOLOGY | Nitric-oxide Synthase | Scaffold Proteins | MUSCULAR-DYSTROPHY | NEUROBLASTOMA-CELLS | Myogenesis | CU,ZN SUPEROXIDE-DISMUTASE | S-Nitrosylation | SKELETAL-MUSCLE | Mitochondria | ARGININE | PROTEINS | EXPRESSION | Humans | Mitochondrial Proteins - genetics | Muscle Fibers, Skeletal - metabolism | Cell Nucleus - metabolism | Mitochondria - genetics | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Muscle Proteins - metabolism | Membrane Proteins - metabolism | Active Transport, Cell Nucleus - genetics | Calcium-Binding Proteins - metabolism | Protein Structure, Tertiary | Gene Expression Regulation - genetics | Membrane Proteins - genetics | Muscular Diseases - metabolism | Alternative Splicing - genetics | Transcription Factors - biosynthesis | Mitochondria - metabolism | Mitochondrial Proteins - biosynthesis | Muscular Diseases - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Muscle Proteins - genetics | Animals | Cell Nucleus - genetics | Nitric Oxide Synthase Type I - metabolism | High Mobility Group Proteins - biosynthesis | Mice | Nitric Oxide Synthase Type I - genetics | HeLa Cells | Muscular Diseases - genetics | DNA-Binding Proteins - biosynthesis | Calcium-Binding Proteins - genetics | High Mobility Group Proteins - genetics | Signal Transduction
Journal Article
Circulation, ISSN 0009-7322, 10/2004, Volume 110, Issue 15, pp. 2226 - 2232
Background-Previous studies have shown that pericytes can differentiate into osteoblasts and form bone. This study investigated whether pericytes can also... 
Microcirculation | Cardiovascular diseases | Cells | Stem cells | Vasculature | vasculature | stem cells | CARDIAC & CARDIOVASCULAR SYSTEMS | ANGIOGENESIS | BONE-MARROW | VASCULAR CALCIFICATION | OSTEOGENESIS | cardiovascular diseases | microcirculation | MESENCHYMAL STEM-CELLS | IN-VITRO | cells | DIFFUSION-CHAMBERS | PERIPHERAL VASCULAR DISEASE | DIFFERENTIATION | OSSIFICATION | HEMATOLOGY | EXPRESSION | Chondrocytes - cytology | Extracellular Matrix Proteins - biosynthesis | Cells, Cultured - cytology | Pericytes - cytology | Extracellular Matrix - metabolism | Adipocytes - cytology | Gene Expression Profiling | Cattle | Aggrecans | Cartilage - cytology | Cell Differentiation | Chondrocytes - metabolism | Collagen Type II - biosynthesis | PPAR gamma - genetics | Extracellular Matrix Proteins - genetics | Lectins, C-Type | Pericytes - metabolism | Proteoglycans - biosynthesis | Transcription Factors - biosynthesis | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Collagen Type II - genetics | PPAR gamma - biosynthesis | Animals | Diffusion Chambers, Culture | Mice, Nude | Adipocytes - metabolism | Biomarkers | High Mobility Group Proteins - biosynthesis | Cells, Cultured - metabolism | Mice | SOX9 Transcription Factor | Proteoglycans - genetics | High Mobility Group Proteins - genetics
Journal Article
Biochemical Journal, ISSN 0264-6021, 05/2014, Volume 460, Issue 1, pp. 25 - 34
Growth factors inactivate the FOXO (forkhead box O) transcription factors through PI3K (phosphoinositide 3-kinase) and PKB (protein kinase B). By comparing... 
Cell proliferation | Akt/protein kinase B (PKB) | High-mobility group-box protein 1 (HBP1) | Forkhead box O (FOXO) | Transcriptional regulation | Growth factor | FORKHEAD TRANSCRIPTION FACTOR | CELL-CYCLE REGULATION | HMG-BOX | cell proliferation | high-mobility group-box protein 1 (HBP1) | transcriptional regulation | PHOSPHATIDYLINOSITOL 3-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | INDUCED PREMATURE SENESCENCE | growth factor | C-MYC EXPRESSION | forkhead box O (FOXO) | REPRESSOR HBP1 | RETINOBLASTOMA PROTEIN | BINDING PROTEINS | GENE-EXPRESSION | NIH 3T3 Cells | Protein Binding - genetics | Cricetulus | High Mobility Group Proteins - antagonists & inhibitors | Humans | Gene Expression Regulation, Neoplastic | Male | Proto-Oncogene Proteins c-akt - genetics | Repressor Proteins - antagonists & inhibitors | MCF-7 Cells | HEK293 Cells | Conserved Sequence | CHO Cells | Fibroblasts - metabolism | Forkhead Transcription Factors - biosynthesis | Promoter Regions, Genetic | Cricetinae | Phosphatidylinositol 3-Kinase - biosynthesis | Cells, Cultured | Intercellular Signaling Peptides and Proteins - genetics | Repressor Proteins - genetics | Signal Transduction - genetics | Forkhead Transcription Factors - genetics | Down-Regulation - genetics | Proto-Oncogene Proteins c-akt - biosynthesis | Animals | Repressor Proteins - biosynthesis | Phosphatidylinositol 3-Kinase - genetics | Fibroblasts - drug effects | High Mobility Group Proteins - biosynthesis | Forkhead Box Protein O1 | Mice | High Mobility Group Proteins - genetics
Journal Article
Developmental Biology, ISSN 0012-1606, 2007, Volume 302, Issue 2, pp. 683 - 693
Journal Article
Blood, ISSN 0006-4971, 01/2008, Volume 111, Issue 2, pp. 800 - 805
Mantle cell lymphoma (MCL) is defined pathologically by the detection of CD20, CD5, and most importantly cyclin D1 (CCND1). Its distinction from other... 
CD5 Antigens - genetics | Central Nervous System - metabolism | Oligonucleotide Array Sequence Analysis | Humans | Brain Neoplasms - pathology | Cyclins - genetics | Lymphoma, Mantle-Cell - pathology | Lymphopoiesis - genetics | Central Nervous System - pathology | Gene Expression Profiling | Central Nervous System - embryology | Brain Neoplasms - metabolism | Embryo, Mammalian - metabolism | Glioma - metabolism | Brain - metabolism | Glioma - genetics | Lymphoma, Mantle-Cell - diagnosis | Cell Nucleus - metabolism | Cyclins - metabolism | Cell Transformation, Neoplastic - genetics | Gene Expression Regulation, Developmental | Glioma - pathology | Trans-Activators - genetics | Trans-Activators - biosynthesis | B-Lymphocytes - pathology | Cyclin D | Neoplasm Proteins - genetics | Lymphoma, Mantle-Cell - genetics | Lymphoma, Mantle-Cell - metabolism | Embryo, Mammalian - pathology | Neoplasm Proteins - biosynthesis | Brain Neoplasms - genetics | Antigens, CD20 - metabolism | Gene Expression Regulation, Leukemic | CD5 Antigens - metabolism | Organ Specificity | Cell Transformation, Neoplastic - metabolism | Antigens, CD20 - genetics | Sequence Homology, Amino Acid | Cell Nucleus - genetics | Brain - pathology | High Mobility Group Proteins - biosynthesis | Biomarkers, Tumor - genetics | SOXC Transcription Factors | Cell Transformation, Neoplastic - pathology | Biomarkers, Tumor - biosynthesis | High Mobility Group Proteins - genetics | Clinical Medicine | Hematologi | Medical and Health Sciences | Hematology | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 07/2016, Volume 12, Issue 7, p. e1006221
Journal Article