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Matrix biology, ISSN 0945-053X, 2018, Volume 70, pp. 102 - 122
Intervertebral disc degeneration and associated low back and neck pain is a ubiquitous health condition that affects millions of people world-wide, and causes... 
Animal models | SM/J | LG/J | Intervertebral disc degeneration | Matrix degradation | Nucleus pulposus | Hypertrophy | LOW-BACK-PAIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | INBRED STRAINS | BONE MICROSTRUCTURE | MECHANICAL-PROPERTIES | LUMBAR | AGGRECAN | CELL BIOLOGY | NUCLEUS PULPOSUS CELLS | ARTICULAR-CARTILAGE | MICE | EXPRESSION | Annulus Fibrosus - metabolism | Humans | Alkaline Phosphatase - metabolism | Pyrophosphatases - genetics | Extracellular Matrix - metabolism | Male | Vascular Endothelial Growth Factor A - metabolism | Vascular Endothelial Growth Factor A - genetics | Wnt Proteins - metabolism | Core Binding Factor Alpha 1 Subunit - metabolism | Intervertebral Disc Degeneration - metabolism | Intervertebral Disc Degeneration - pathology | Collagen Type X - metabolism | Wnt Proteins - genetics | Annulus Fibrosus - pathology | Cell Death | Female | Chondrocytes - metabolism | Disease Models, Animal | Intervertebral Disc Degeneration - genetics | Chondrocytes - pathology | Alkaline Phosphatase - genetics | Phosphoric Diester Hydrolases - metabolism | Nucleus Pulposus - metabolism | Signal Transduction | Glycosaminoglycans - metabolism | Matrix Metalloproteinase 13 - genetics | Gene Expression Regulation | Nucleus Pulposus - pathology | Collagen Type X - genetics | Mice, Transgenic | Phosphoric Diester Hydrolases - genetics | Aggrecans - metabolism | Aggrecans - genetics | Matrix Metalloproteinase 13 - metabolism | Pyrophosphatases - metabolism | Animals | Connective Tissue Growth Factor - genetics | Mice | Extracellular Matrix - pathology | Connective Tissue Growth Factor - metabolism | Core Binding Factor Alpha 1 Subunit - genetics | Homeostasis - genetics | Physiological aspects | Endothelial growth factors | Cell death | Collagen | Analysis | Cells | intervertebral disc degeneration | matrix degradation | hypertrophy | nucleus pulposus
Journal Article
Fertility and Sterility, ISSN 0015-0282, 2015, Volume 104, Issue 6, pp. 1552 - 1560.e3
Objective To investigate the engraftment and proliferation of superparamagnetic iron oxide nanoparticles (SPIOs)-labeled human CD133+ bone marrow-derived stem... 
Internal Medicine | Obstetrics and Gynecology | Asherman syndrome | bone marrow-derived stem cells (BMDSCs) | CD133+cells | superparamagnetic iron oxide nanoparticles (SPIOs) | cells | CD133 | POPULATION | MOBILIZATION | REGENERATION | PHENOTYPE | MOUSE ENDOMETRIUM | CD133(+) cells | IDENTIFICATION | RAT MODEL | OBSTETRICS & GYNECOLOGY | REPRODUCTIVE BIOLOGY | THIN ENDOMETRIUM | DISEASE | DIFFERENTIATION | Cell Proliferation | Prospective Studies | Humans | Middle Aged | Cell Tracking - methods | Glycoproteins - metabolism | Ki-67 Antigen - metabolism | Insulin-Like Growth Factor I - genetics | Gynatresia - physiopathology | Stem Cells - metabolism | Gynatresia - genetics | Antigens, CD - metabolism | Atrophy | Stem Cell Transplantation | Peptides - metabolism | Thrombospondin 1 - genetics | Bone Marrow Transplantation | Adult | Female | Disease Models, Animal | Endometrium - metabolism | Biomarkers - metabolism | Gynatresia - surgery | Paracrine Communication | Cell Survival | Glycosaminoglycans - metabolism | Gene Expression Regulation | Graft Survival | Clinical Trials as Topic | Mice, SCID | AC133 Antigen | Collagen - metabolism | Animals | Gynatresia - metabolism | Endometrium - physiopathology | Mice, Inbred NOD | Mice | Thrombospondin 1 - metabolism | Endometrium - pathology | Gynatresia - pathology | Bone Marrow Cells - metabolism | Insulin-Like Growth Factor I - metabolism
Journal Article
The Journal of pathology, ISSN 0022-3417, 2014, Volume 233, Issue 3, pp. 294 - 307
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0165004
Osteoclasts are giant bone-resorbing cells originating from monocytes/macrophages. During their differentiation, they overexpress two lysosomal enzymes,... 
IN-VITRO | CATHEPSIN-K | MULTIDISCIPLINARY SCIENCES | MACROPHAGE MANNOSE RECEPTOR | LIVER LYSOSOMES | H+-ATPASE | MICE | PLASMA-MEMBRANE | PROCESSED FORMS | EXPRESSION | BONE-RESORPTION | Mannose-Binding Lectins - metabolism | Up-Regulation | Chondroitin Sulfates - metabolism | RANK Ligand - metabolism | Hyaluronoglucosaminidase - metabolism | Monocytes - cytology | Monocytes - metabolism | Exocytosis | Osteoclasts - cytology | Endosomes - metabolism | Lectins, C-Type - metabolism | Hyaluronoglucosaminidase - deficiency | Lysosomes - metabolism | Cell Differentiation | Bone Marrow Cells - cytology | Cells, Cultured | Receptors, Cell Surface - metabolism | Macrophages - cytology | Osteoclasts - metabolism | GPI-Linked Proteins - metabolism | Mice, Knockout | Macrophages - metabolism | Animals | Cathepsin K - metabolism | Hyaluronic Acid - metabolism | Tartrate-Resistant Acid Phosphatase - metabolism | RAW 264.7 Cells | Mice | Hyaluronoglucosaminidase - genetics | Osteogenesis | GPI-Linked Proteins - genetics | Hydrolysis | Cathepsins | Physiological aspects | RNA | Hyaluronic acid | Macrophages | Glycosaminoglycans | Lysosomes | Acidification | Mannose | Phosphatase | Cell surface | Degradation | Proteins | Bone resorption | Lysosomal enzymes | Bone marrow | Biocompatibility | Bone matrix | Enzymes | Fractionation | Cathepsin K | Hydrolase | Secretion | Bone remodelling | Metabolism | Gene expression | Osteoclastogenesis | Monocytes | Acids | Osteoclasts | Acid phosphatase (tartrate-resistant) | Chondroitin sulfate | Sulfate | Differentiation | Endosomes
Journal Article
Journal Article
The Journal of biological chemistry, ISSN 1083-351X, 2000, Volume 275, Issue 40, pp. 31226 - 31232
Journal Article
Science (American Association for the Advancement of Science), ISSN 1095-9203, 2009, Volume 325, Issue 5938, pp. 328 - 332
Amyloids are highly organized cross--β-sheet--rich protein or peptide aggregates that are associated with pathological conditions including Alzheimer's disease... 
Aggregation | Secretory vesicles | Neurons | Cell aggregates | Antibodies | Fluorescence | Reports | Amyloids | Hormones | Solar fibrils | Monomers | PATHWAYS | PROTEIN | GLYCOSAMINOGLYCANS | FIBRILS | MOLECULAR-ORGANIZATION | PROLACTIN GRANULES | BIOGENESIS | MULTIDISCIPLINARY SCIENCES | SYNUCLEIN | ATT-20 | HEPARIN | Humans | Secretory Vesicles - metabolism | Neurons - cytology | Pituitary Gland - chemistry | Amyloid - chemistry | Pituitary Gland, Anterior - metabolism | Pituitary Hormones - chemistry | Peptide Hormones - metabolism | Urocortins - metabolism | beta-Endorphin - metabolism | Amyloid - metabolism | Neurons - physiology | Pituitary Hormones - metabolism | Peptide Hormones - chemistry | Adrenocorticotropic Hormone - metabolism | beta-Endorphin - chemistry | Secretory Vesicles - chemistry | Adrenocorticotropic Hormone - chemistry | Cell Survival | Pituitary Gland, Posterior - chemistry | Heparin, Low-Molecular-Weight - chemistry | Rats | Corticotropin-Releasing Hormone - chemistry | Urocortins - chemistry | Corticotropin-Releasing Hormone - metabolism | Animals | Pituitary Gland, Posterior - metabolism | Protein Conformation | Sheep | Mice | Pituitary Gland, Anterior - chemistry | Hydrogen-Ion Concentration | Glycoproteins | Research | Properties | Peptide hormones | Proteins | Pituitary gland | Physiology | Peptides | Cellular biology
Journal Article
British journal of clinical pharmacology, ISSN 0306-5251, 2015, Volume 80, Issue 3, pp. 389 - 402
Journal Article
Journal Article
Circulation Research, ISSN 0009-7330, 09/2007, Volume 101, Issue 6, pp. 581 - 589
The aberrant differentiation of pericytes along the adipogenic, chondrogenic, and osteogenic lineages may contribute to the development and progression of... 
Vascular disease | Pericytes | Wnt signaling | Chondrogenesis | Differentiation | PATHWAYS | CELLS | CARDIAC & CARDIOVASCULAR SYSTEMS | differentiation | pericytes | MECHANISMS | CHONDROCYTE DIFFERENTIATION | BETA | STEM | vascular disease | OSTEOBLASTS | CALCIFICATION | PERIPHERAL VASCULAR DISEASE | chondrogenesis | WNT | HEMATOLOGY | EXPRESSION | LDL-Receptor Related Proteins - metabolism | Transcription, Genetic - drug effects | Chondrogenesis - drug effects | Chondrogenesis - genetics | Adipogenesis - drug effects | RNA, Messenger - metabolism | Wnt Proteins - metabolism | Transforming Growth Factor beta3 - metabolism | Collagen Type II - metabolism | TCF Transcription Factors - metabolism | Wnt Proteins - genetics | Cattle | Lithium Chloride - pharmacology | Adipogenesis - genetics | Transduction, Genetic | High Mobility Group Proteins - metabolism | Glycosaminoglycans - metabolism | Pericytes - metabolism | Cells, Cultured | Frizzled Receptors - metabolism | Proteoglycans - metabolism | Vascular Diseases - genetics | Lipid Metabolism | Signal Transduction - genetics | Vascular Diseases - physiopathology | Aggrecans - metabolism | beta Catenin - metabolism | beta Catenin - genetics | Transcription Factors - metabolism | Animals | Signal Transduction - drug effects | Wnt3 Protein | SOX9 Transcription Factor | Vascular Diseases - metabolism
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2016, Volume 113, Issue 3, pp. E291 - E299
Protein transduction domains (PTDs) are powerful nongenetic tools that allow intracellular delivery of conjugated cargoes to modify cell behavior. Their use in... 
Human embryonic stem cells | Transduction | Cell-penetrating peptides | Differentiation | Heparin-binding domain | differentiation | transduction | MULTIDISCIPLINARY SCIENCES | MECHANISMS | HEPARIN | MAMMALIAN-CELLS | IPS CELLS | PLURIPOTENT STEM-CELLS | cell-penetrating peptides | heparin-binding domain | MACROPINOCYTOSIS | GROWTH-FACTOR | PROTEINS | human embryonic stem cells | NIH 3T3 Cells | Homeodomain Proteins - metabolism | Human Embryonic Stem Cells - cytology | Humans | Mouse Embryonic Stem Cells - cytology | Mouse Embryonic Stem Cells - drug effects | Mouse Embryonic Stem Cells - metabolism | Drug Delivery Systems | Nanoparticles | Human Embryonic Stem Cells - drug effects | Integrases - metabolism | Cell Membrane - metabolism | Cell Membrane - drug effects | Cell-Penetrating Peptides - chemistry | Induced Pluripotent Stem Cells - metabolism | Protein Structure, Tertiary | Detergents - pharmacology | Human Embryonic Stem Cells - metabolism | Nanog Homeobox Protein | Induced Pluripotent Stem Cells - drug effects | Glycosaminoglycans - metabolism | Endocytosis - drug effects | Solubility | MyoD Protein - metabolism | Nucleic Acids - metabolism | Trypsin - metabolism | Amino Acid Motifs | Animals | Muscle Development - drug effects | Cell Differentiation - drug effects | Cell Proliferation - drug effects | Mice | Genome | Cell-Penetrating Peptides - metabolism | Physiological aspects | Physiological research | Cellular signal transduction | Glycosaminoglycans | Research | Biological Sciences | PNAS Plus
Journal Article