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Journal Article
FEBS Journal, ISSN 1742-464X, 05/2016, Volume 283, Issue 9, pp. 1689 - 1700
Intervertebral discs ( IVD s) provide stability and flexibility to the spinal column; however, IVD s, and in particular the nucleus pulposus ( NP ), undergo a... 
intervertebral disc degeneration | Smad | BMP | mesenchymal stem cells | nucleus pulposus | BMP7 | REGENERATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | MESENCHYMAL STEM-CELLS | TRANSPLANTATION | CROSS-TALK | LUMBAR-SPINE | IN-VITRO | NUCLEUS PULPOSUS CELLS | DISEASE | GROWTH | DIFFERENTIATION | RNA, Small Interfering - genetics | Bone Morphogenetic Protein 7 - genetics | Humans | Extracellular Matrix - metabolism | Intervertebral Disc Degeneration - metabolism | Intervertebral Disc Degeneration - therapy | Collagen Type II - metabolism | Intervertebral Disc Degeneration - pathology | Lentivirus - metabolism | Glucuronosyltransferase - genetics | Mesenchymal Stromal Cells - cytology | Smad1 Protein - genetics | Lentivirus - genetics | Intervertebral Disc - pathology | Chondrocytes - metabolism | Disease Models, Animal | Intervertebral Disc Degeneration - genetics | SOX9 Transcription Factor - metabolism | Chondrocytes - pathology | Rabbits | Genetic Vectors - chemistry | Signal Transduction | Bone Marrow Cells - cytology | Glycosaminoglycans - metabolism | Keratin-8 - genetics | Gene Expression Regulation | Genetic Vectors - metabolism | Mesenchymal Stromal Cells - metabolism | Intervertebral Disc - metabolism | Aggrecans - metabolism | Smad1 Protein - antagonists & inhibitors | Aggrecans - genetics | Collagen Type II - genetics | Keratin-19 - genetics | Animals | Glucuronosyltransferase - metabolism | Keratin-8 - metabolism | Bone Morphogenetic Protein 7 - metabolism | Smad1 Protein - metabolism | Keratin-19 - metabolism | Extracellular Matrix - pathology | SOX9 Transcription Factor - genetics | Bone Marrow Cells - metabolism | Mesenchymal Stem Cell Transplantation | RNA, Small Interfering - metabolism | Physiological aspects | Bone morphogenetic proteins | Cell differentiation | Analysis | Stem cells | Extracellular matrix | Spine | Rodents | Keratins | Therapy | Surgical implants | Smad protein | Mesenchyme | Collagen (type II) | Sox9 protein | Medical services | Differentiation (biology) | Electrochemical machining | Homeostasis | Nucleus pulposus | Remodeling | Intervertebral discs | Nuclei | Flexibility | Bone marrow | Degeneration | Effectiveness | Stability | Markers | Feasibility studies | Implantation | Columns (process) | Survival | Diseases | Overexpression | Disks | Feasibility | Chondroitin sulfate | Sulfate | Aggrecan | Viability | Bone morphogenetic protein 7 | Index Medicus
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 | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, pp. e0165004 - 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 | Trafficking | 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 | Index Medicus | Biomedical materials
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2000, Volume 275, Issue 40, pp. 31226 - 31232
Journal Article
The Journal of Pathology, ISSN 0022-3417, 07/2014, Volume 233, Issue 3, pp. 294 - 307
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 | CELLS | CARDIAC & CARDIOVASCULAR SYSTEMS | differentiation | MESENCHYMAL PROGENITORS | pericytes | ARTERY WALL | CHONDROCYTE DIFFERENTIATION | BETA | STEM | ATHEROSCLEROTIC PLAQUE DEVELOPMENT | IN-VITRO | vascular disease | CALCIFICATION | PERIPHERAL VASCULAR DISEASE | chondrogenesis | 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 | Index Medicus
Journal Article
Science, ISSN 0036-8075, 7/2009, 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 | CELLS | PROTEIN | FIBRILS | GLYCOSAMINOGLYCANS | MOLECULAR-ORGANIZATION | PROLACTIN GRANULES | BIOGENESIS | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | ALPHA-SYNUCLEIN | AMYLOIDOGENESIS | 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 | Index Medicus | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2016, 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 | Proteins | Peptides | Cytoplasm | Binding sites | Stem cells | Index Medicus | Biological Sciences | PNAS Plus
Journal Article
Journal Article