STEM CELLS, ISSN 1066-5099, 10/2019, Volume 37, Issue 10, pp. 1357 - 1368
Mesenchymal stromal cells (MSC) may exert their functions by the release of extracellular vesicles (EV). Our aim was to analyze changes induced in CD34+ cells...
Engraftment | Extracellular vesicles | Stem cell transplantation | Mesenchymal stromal cells | Hematopoietic stem cells | Bone marrow | Transplantation | Analysis | Flow cytometry | Phosphorylation | Incorporation | Mesenchyme | Genes | Reverse transcription | Confocal microscopy | Lodging | Macrophages | Kinases | Nanoparticles | Vesicles | CD44 antigen | Cell cycle | Janus kinase | CD34 antigen | Colonies | Diabetes mellitus | Immunodeficiency | Stat5 protein | Electron microscopy | Polymerase chain reaction | Microscopy | Human performance | Stromal cells | Stem cells | Leukocytes (granulocytic) | Apoptosis | Translational and Clinical Research
Engraftment | Extracellular vesicles | Stem cell transplantation | Mesenchymal stromal cells | Hematopoietic stem cells | Bone marrow | Transplantation | Analysis | Flow cytometry | Phosphorylation | Incorporation | Mesenchyme | Genes | Reverse transcription | Confocal microscopy | Lodging | Macrophages | Kinases | Nanoparticles | Vesicles | CD44 antigen | Cell cycle | Janus kinase | CD34 antigen | Colonies | Diabetes mellitus | Immunodeficiency | Stat5 protein | Electron microscopy | Polymerase chain reaction | Microscopy | Human performance | Stromal cells | Stem cells | Leukocytes (granulocytic) | Apoptosis | Translational and Clinical Research
Journal Article
PloS one, 2019, Volume 14, Issue 5, p. e0216674
CRISPR/Cas9 allows the generation of knockout cell lines and null zygotes by inducing site-specific double-stranded breaks. In most cases the DSB is repaired...
Journal Article
British Journal of Haematology, ISSN 0007-1048, 10/2019, Volume 187, Issue 1, pp. 93 - 104
Summary Patients with low‐risk myelodysplastic syndromes (MDS) usually develop iron overload. This leads to a high level of oxidative stress in the bone marrow...
iron overload | deferasirox | DNA damage | myelodysplastic syndromes | reactive oxygen species | Genetic research | Analysis | DNA | Flow cytometry | Oxidative stress | Bone marrow | Chelation | Iron | Oxidation | Intracellular | Damage | Differentiation | Deoxyribonucleic acid--DNA | Myelodysplastic syndrome
iron overload | deferasirox | DNA damage | myelodysplastic syndromes | reactive oxygen species | Genetic research | Analysis | DNA | Flow cytometry | Oxidative stress | Bone marrow | Chelation | Iron | Oxidation | Intracellular | Damage | Differentiation | Deoxyribonucleic acid--DNA | Myelodysplastic syndrome
Journal Article
PLOS ONE, ISSN 1932-6203, 05/2019, Volume 14, Issue 5, p. e0216674
CRISPR/Cas9 allows the generation of knockout cell lines and null zygotes by inducing site-specific double-stranded breaks. In most cases the DSB is repaired...
CONSEQUENCES | MUTATIONS | GENE | MULTIDISCIPLINARY SCIENCES | Gene therapy | Usage | CRISPR | Splicing | Exons | Frameshift mutation | Homology | Genomes | mRNA | Gene expression | Zygotes | Efficiency | Cell lines | Alleles | Cell cycle | Non-homologous end joining | Mutation | Deoxyribonucleic acid--DNA | Methods | Cancer | Deoxyribonucleic acid | DNA
CONSEQUENCES | MUTATIONS | GENE | MULTIDISCIPLINARY SCIENCES | Gene therapy | Usage | CRISPR | Splicing | Exons | Frameshift mutation | Homology | Genomes | mRNA | Gene expression | Zygotes | Efficiency | Cell lines | Alleles | Cell cycle | Non-homologous end joining | Mutation | Deoxyribonucleic acid--DNA | Methods | Cancer | Deoxyribonucleic acid | DNA
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2016, Volume 11, Issue 2, p. e0146722
Exosomes/microvesicles (MVs) provide a mechanism of intercellular communication. Our hypothesis was that mesenchymal stromal cells (MSC) from myelodysplastic...
ACUTE KIDNEY INJURY | STEM-CELLS | EXTRACELLULAR VESICLES | HEMATOPOIESIS | MECHANISM | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | EXOSOMES | MYELOID-LEUKEMIA PATIENTS | MICRORNAS | EXPRESSION | Antigens, CD34 | Exosomes - metabolism | Gene Expression | Myelodysplastic Syndromes - metabolism | Cell Survival | Humans | Middle Aged | Cell Communication | Cellular Microenvironment | Mesenchymal Stromal Cells - metabolism | Male | MicroRNAs - metabolism | Hematopoietic Stem Cells - metabolism | Hematopoietic Stem Cells - immunology | Aged, 80 and over | Adult | Female | Aged | Myelodysplastic Syndromes - genetics | Stem cells | Physiological aspects | Gas vesicles | Development and progression | Genetic aspects | Research | Myelodysplastic syndromes | Flow cytometry | Intercellular signalling | Mesenchyme | p53 Protein | Leukemia | Crosstalk | Fluorescence | Ultracentrifugation | Confocal | Exosomes | Myelodysplastic syndrome | Cell cycle | DNA methylation | Bone marrow | Communication | CD34 antigen | MDM2 protein | Risk groups | CD63 antigen | MiRNA | Electron microscopy | Gene expression | Patients | Hemopoiesis | Polymerase chain reaction | Cytometry | Properties (attributes) | Transmission electron microscopy | Stromal cells | MicroRNAs | Epigenetics | Viability | Fluorescence microscopy
ACUTE KIDNEY INJURY | STEM-CELLS | EXTRACELLULAR VESICLES | HEMATOPOIESIS | MECHANISM | MULTIDISCIPLINARY SCIENCES | BONE-MARROW | EXOSOMES | MYELOID-LEUKEMIA PATIENTS | MICRORNAS | EXPRESSION | Antigens, CD34 | Exosomes - metabolism | Gene Expression | Myelodysplastic Syndromes - metabolism | Cell Survival | Humans | Middle Aged | Cell Communication | Cellular Microenvironment | Mesenchymal Stromal Cells - metabolism | Male | MicroRNAs - metabolism | Hematopoietic Stem Cells - metabolism | Hematopoietic Stem Cells - immunology | Aged, 80 and over | Adult | Female | Aged | Myelodysplastic Syndromes - genetics | Stem cells | Physiological aspects | Gas vesicles | Development and progression | Genetic aspects | Research | Myelodysplastic syndromes | Flow cytometry | Intercellular signalling | Mesenchyme | p53 Protein | Leukemia | Crosstalk | Fluorescence | Ultracentrifugation | Confocal | Exosomes | Myelodysplastic syndrome | Cell cycle | DNA methylation | Bone marrow | Communication | CD34 antigen | MDM2 protein | Risk groups | CD63 antigen | MiRNA | Electron microscopy | Gene expression | Patients | Hemopoiesis | Polymerase chain reaction | Cytometry | Properties (attributes) | Transmission electron microscopy | Stromal cells | MicroRNAs | Epigenetics | Viability | Fluorescence microscopy
Journal Article
Journal of Tissue Engineering and Regenerative Medicine, ISSN 1932-6254, 03/2018, Volume 12, Issue 3, pp. e1450 - e1460
Biocompatibility studies, especially innate immunity induction, in vitro and in vivo cytotoxicity, and fibrosis, are often lacking for many novel biomaterials...
tissue engineering | catalyst‐free click gels | biocompatibility | regenerative medicine | cytocompatibility | elastin‐like recombinamers | silk‐elastin multiblock corecombinamers | elastin-like recombinamers | silk-elastin multiblock corecombinamers | catalyst-free click gels | POLYMERS | STEM-CELLS | CYTOKINES | ARG-GLY-ASP | ENGINEERING, BIOMEDICAL | CELL-ADHESION | DELIVERY | CELL & TISSUE ENGINEERING | CELL BIOLOGY | HEART | BIOMATERIAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | PROTEINS | Proteins | Nuclear magnetic resonance spectroscopy | Biological products | Tissue engineering | Mass spectrometry | Luciferase | Cell proliferation | Bioluminescence | Hydrogels | Toxicity | Cytotoxicity | Inflammatory response | Innate immunity | Immunity | Regeneration (physiology) | Biomaterials | Engineering | Biomedical materials | Biocompatibility | Extracellular matrix | Recombinant | Elastin | Inflammation | Tumor necrosis factor-α | IL-1β | Substrates | Endothelial cells | Medicine | Regeneration | Fibrosis | Mice | In vivo methods and tests | Umbilical vein
tissue engineering | catalyst‐free click gels | biocompatibility | regenerative medicine | cytocompatibility | elastin‐like recombinamers | silk‐elastin multiblock corecombinamers | elastin-like recombinamers | silk-elastin multiblock corecombinamers | catalyst-free click gels | POLYMERS | STEM-CELLS | CYTOKINES | ARG-GLY-ASP | ENGINEERING, BIOMEDICAL | CELL-ADHESION | DELIVERY | CELL & TISSUE ENGINEERING | CELL BIOLOGY | HEART | BIOMATERIAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | IN-VIVO | PROTEINS | Proteins | Nuclear magnetic resonance spectroscopy | Biological products | Tissue engineering | Mass spectrometry | Luciferase | Cell proliferation | Bioluminescence | Hydrogels | Toxicity | Cytotoxicity | Inflammatory response | Innate immunity | Immunity | Regeneration (physiology) | Biomaterials | Engineering | Biomedical materials | Biocompatibility | Extracellular matrix | Recombinant | Elastin | Inflammation | Tumor necrosis factor-α | IL-1β | Substrates | Endothelial cells | Medicine | Regeneration | Fibrosis | Mice | In vivo methods and tests | Umbilical vein
Journal Article
Haematologica, ISSN 0390-6078, 08/2012, Volume 97, Issue 8, pp. 1218 - 1224
Background Recent findings suggest that a specific deletion of Dicer1 in mesenchymal stromal cell-derived osteoprogenitors triggers several features of...
DROSHA | DICER | Myelodysplastic syndrome | Mesenchymal stem cells | STEM-CELLS | HEMATOPOIESIS | PATHWAY | mesenchymal stem cells | BONE-MARROW | MDS PATIENTS | myelodysplastic syndrome | HEMATOLOGY | Myelodysplastic Syndromes - metabolism | Ribonuclease III - genetics | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Mesenchymal Stromal Cells - metabolism | Male | Gene Expression Profiling | Case-Control Studies | Proteins - genetics | DEAD-box RNA Helicases - genetics | Aged, 80 and over | Female | Aged | MicroRNAs - genetics | Myelodysplastic Syndromes - genetics | Original and Brief Reports
DROSHA | DICER | Myelodysplastic syndrome | Mesenchymal stem cells | STEM-CELLS | HEMATOPOIESIS | PATHWAY | mesenchymal stem cells | BONE-MARROW | MDS PATIENTS | myelodysplastic syndrome | HEMATOLOGY | Myelodysplastic Syndromes - metabolism | Ribonuclease III - genetics | Humans | Middle Aged | Gene Expression Regulation, Neoplastic | Mesenchymal Stromal Cells - metabolism | Male | Gene Expression Profiling | Case-Control Studies | Proteins - genetics | DEAD-box RNA Helicases - genetics | Aged, 80 and over | Female | Aged | MicroRNAs - genetics | Myelodysplastic Syndromes - genetics | Original and Brief Reports
Journal Article
Journal of Materials Science: Materials in Medicine, ISSN 0957-4530, 8/2017, Volume 28, Issue 8, pp. 1 - 11
Over the last decades, novel therapeutic tools for osteochondral regeneration have arisen from the combination of mesenchymal stromal cells (MSCs) and highly...
Biomedical Engineering | Polymer Sciences | Materials Science | Regenerative Medicine/Tissue Engineering | Ceramics, Glass, Composites, Natural Materials | Surfaces and Interfaces, Thin Films | Biomaterials | OSTEOCHONDRAL DEFECT REPAIR | STEM-CELLS | RABBITS | XENOTRANSPLANTATION | MATERIALS SCIENCE, BIOMATERIALS | IMPLANTATION | ENGINEERING, BIOMEDICAL | MODEL | SCAFFOLDS | TECHNOLOGY | IN-SITU | TRANSPLANTATION | Elastin | Biological products | Resveratrol | Knee | Surgical implants | Hydrogels | Mesenchyme | Sectioning | Cartilage | Mitochondria | Biomedical materials | Computed tomography | Biocompatibility | Lesions | Rabbits | Statistical analysis | Knee (anatomy) | Bone healing | Bone (subchondral) | Biological activity | Regeneration | Magnetic resonance imaging | Stromal cells | Skin & tissue grafts | Resonance | Immunofluorescence
Biomedical Engineering | Polymer Sciences | Materials Science | Regenerative Medicine/Tissue Engineering | Ceramics, Glass, Composites, Natural Materials | Surfaces and Interfaces, Thin Films | Biomaterials | OSTEOCHONDRAL DEFECT REPAIR | STEM-CELLS | RABBITS | XENOTRANSPLANTATION | MATERIALS SCIENCE, BIOMATERIALS | IMPLANTATION | ENGINEERING, BIOMEDICAL | MODEL | SCAFFOLDS | TECHNOLOGY | IN-SITU | TRANSPLANTATION | Elastin | Biological products | Resveratrol | Knee | Surgical implants | Hydrogels | Mesenchyme | Sectioning | Cartilage | Mitochondria | Biomedical materials | Computed tomography | Biocompatibility | Lesions | Rabbits | Statistical analysis | Knee (anatomy) | Bone healing | Bone (subchondral) | Biological activity | Regeneration | Magnetic resonance imaging | Stromal cells | Skin & tissue grafts | Resonance | Immunofluorescence
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2017, Volume 12, Issue 8, p. e0182470
There is evidence of continuous bidirectional cross-talk between malignant cells and bone marrow-derived mesenchymal stromal cells (BM-MSC), which favors the...
ORGANIZATION | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | BONE-MARROW NICHE | CORD BLOOD | MYELOID-LEUKEMIA | DIFFERENTIATION | LARGE GENE LISTS | PRIMARY MYELOFIBROSIS | EXPRESSION | MYELODYSPLASTIC SYNDROMES | Gene Expression | Coculture Techniques | Humans | Middle Aged | Male | Hematologic Neoplasms - enzymology | Hematologic Neoplasms - pathology | Cell Cycle | Hematologic Neoplasms - blood | Hematopoiesis | Janus Kinase 2 - metabolism | Biomarkers, Tumor - metabolism | Cell Line, Tumor | Adult | Female | Aged | Biomarkers, Tumor - genetics | Mesenchymal Stromal Cells - physiology | Apoptosis | Mesenchyme | Genes | Fluorescence | Colony-forming cells | Neoplasms | CD90 antigen | CD44 antigen | Janus kinase 2 | Bone marrow | Fibroblasts | Extracellular matrix | CD73 antigen | CD105 antigen | NF-κB protein | Medical research | Cell survival | Colonies | Maintenance | Gene expression | Patients | Hemopoiesis | Stromal cells | Medical prognosis | Cells (biology) | Stem cells | Mutation | Differentiation | Tumors
ORGANIZATION | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | BONE-MARROW NICHE | CORD BLOOD | MYELOID-LEUKEMIA | DIFFERENTIATION | LARGE GENE LISTS | PRIMARY MYELOFIBROSIS | EXPRESSION | MYELODYSPLASTIC SYNDROMES | Gene Expression | Coculture Techniques | Humans | Middle Aged | Male | Hematologic Neoplasms - enzymology | Hematologic Neoplasms - pathology | Cell Cycle | Hematologic Neoplasms - blood | Hematopoiesis | Janus Kinase 2 - metabolism | Biomarkers, Tumor - metabolism | Cell Line, Tumor | Adult | Female | Aged | Biomarkers, Tumor - genetics | Mesenchymal Stromal Cells - physiology | Apoptosis | Mesenchyme | Genes | Fluorescence | Colony-forming cells | Neoplasms | CD90 antigen | CD44 antigen | Janus kinase 2 | Bone marrow | Fibroblasts | Extracellular matrix | CD73 antigen | CD105 antigen | NF-κB protein | Medical research | Cell survival | Colonies | Maintenance | Gene expression | Patients | Hemopoiesis | Stromal cells | Medical prognosis | Cells (biology) | Stem cells | Mutation | Differentiation | Tumors
Journal Article
Stem Cells International, ISSN 1687-966X, 2018, Volume 2018, pp. 7089484 - 10
Significant research efforts have been undertaken during the last decades to treat musculoskeletal disorders and improve patient's mobility and quality of...
TISSUE-ENGINEERED BONE | CRITICAL-SIZE DEFECTS | STEM-CELLS | REPAIR | XENOTRANSPLANTATION | CALCIUM PHOSPHATES | IN-VIVO | ANIMAL-MODELS | BIOMATERIALS | TRICALCIUM PHOSPHATE | CELL & TISSUE ENGINEERING | Surgical implants | Femur | Neurosciences | Osteointegration | Spinal cord | Transplants & implants | Disease | Mesenchyme | Heart surgery | Xenotransplantation | Differentiation (biology) | Defects | Tricalcium phosphate | Bone growth | Biomedical materials | Xenografts | Bone marrow | Biocompatibility | Growth factors | Implantation | Inflammation | Calcium phosphates | Quality of life | Regeneration | Granular materials | Stromal cells | Skin & tissue grafts | Stem cells | Granules | Laboratory animals | Viability
TISSUE-ENGINEERED BONE | CRITICAL-SIZE DEFECTS | STEM-CELLS | REPAIR | XENOTRANSPLANTATION | CALCIUM PHOSPHATES | IN-VIVO | ANIMAL-MODELS | BIOMATERIALS | TRICALCIUM PHOSPHATE | CELL & TISSUE ENGINEERING | Surgical implants | Femur | Neurosciences | Osteointegration | Spinal cord | Transplants & implants | Disease | Mesenchyme | Heart surgery | Xenotransplantation | Differentiation (biology) | Defects | Tricalcium phosphate | Bone growth | Biomedical materials | Xenografts | Bone marrow | Biocompatibility | Growth factors | Implantation | Inflammation | Calcium phosphates | Quality of life | Regeneration | Granular materials | Stromal cells | Skin & tissue grafts | Stem cells | Granules | Laboratory animals | Viability
Journal Article
Haematologica, ISSN 0390-6078, 07/2011, Volume 96, Issue 7, pp. 1072 - 1076
This trial evaluated the feasibility and efficacy of the infusion of mesenchymal stem cells expanded using human serum for the treatment of refractory acute or...
Graft-versus-host disease | Allogeneic stem cell transplant | Mesenchymal stem cells | MARROW | SUBSTITUTE | PLATELET LYSATE | THERAPY | mesenchymal stem cells | CULTURE-CONDITIONS | ANIMAL SERUM | EXPANSION | OPTIMIZATION | REFRACTORY ACUTE GVHD | STROMAL CELLS | HEMATOLOGY | graft-versus-host disease | allogeneic stem cell transplant | Graft vs Host Disease - therapy | Cell Proliferation | Culture Techniques | Humans | Middle Aged | Cells, Cultured | Mesenchymal Stromal Cells - metabolism | Male | Treatment Outcome | Transplantation, Homologous | Young Adult | Mesenchymal Stromal Cells - cytology | Graft vs Host Disease - mortality | Adult | Female | Serum | Aged | Mesenchymal Stem Cell Transplantation | Brief Reports
Graft-versus-host disease | Allogeneic stem cell transplant | Mesenchymal stem cells | MARROW | SUBSTITUTE | PLATELET LYSATE | THERAPY | mesenchymal stem cells | CULTURE-CONDITIONS | ANIMAL SERUM | EXPANSION | OPTIMIZATION | REFRACTORY ACUTE GVHD | STROMAL CELLS | HEMATOLOGY | graft-versus-host disease | allogeneic stem cell transplant | Graft vs Host Disease - therapy | Cell Proliferation | Culture Techniques | Humans | Middle Aged | Cells, Cultured | Mesenchymal Stromal Cells - metabolism | Male | Treatment Outcome | Transplantation, Homologous | Young Adult | Mesenchymal Stromal Cells - cytology | Graft vs Host Disease - mortality | Adult | Female | Serum | Aged | Mesenchymal Stem Cell Transplantation | Brief Reports
Journal Article
Journal of Translational Medicine, ISSN 1479-5876, 08/2016, Volume 14, Issue 1, p. 246
Background: Mesenchymal stromal cells are a promising option to treat knee osteoarthritis. Their safety and usefulness must be confirmed and the optimal dose...
Non-surgical management | Knee osteoarthritis | Stem cell therapy | Bone marrow-mesenchymal stromal cells | CRITERIA | MEDICINE, RESEARCH & EXPERIMENTAL | FOLLOW-UP | IDENTIFICATION | CARTILAGE DEFECTS | THERAPY | ARTICULAR-CARTILAGE | CHONDROCYTE IMPLANTATION | REGENERATIVE MEDICINE | STROMAL CELLS | EXPRESSION | Hyaluronic Acid - administration & dosage | Demography | Humans | Middle Aged | Visual Analog Scale | Hyaluronic Acid - pharmacology | Male | Treatment Outcome | Combined Modality Therapy | Osteoarthritis, Knee - therapy | Osteoarthritis, Knee - diagnostic imaging | Mesenchymal Stem Cell Transplantation - adverse effects | Range of Motion, Articular - drug effects | Magnetic Resonance Imaging | Osteoarthritis, Knee - pathology | Injections, Intra-Articular | Female | Aged | Osteoarthritis, Knee - physiopathology | Hyaluronic Acid - adverse effects | Care and treatment | Usage | Stem cells | Clinical trials | Bone marrow | Transplantation | Research | Osteoarthritis
Non-surgical management | Knee osteoarthritis | Stem cell therapy | Bone marrow-mesenchymal stromal cells | CRITERIA | MEDICINE, RESEARCH & EXPERIMENTAL | FOLLOW-UP | IDENTIFICATION | CARTILAGE DEFECTS | THERAPY | ARTICULAR-CARTILAGE | CHONDROCYTE IMPLANTATION | REGENERATIVE MEDICINE | STROMAL CELLS | EXPRESSION | Hyaluronic Acid - administration & dosage | Demography | Humans | Middle Aged | Visual Analog Scale | Hyaluronic Acid - pharmacology | Male | Treatment Outcome | Combined Modality Therapy | Osteoarthritis, Knee - therapy | Osteoarthritis, Knee - diagnostic imaging | Mesenchymal Stem Cell Transplantation - adverse effects | Range of Motion, Articular - drug effects | Magnetic Resonance Imaging | Osteoarthritis, Knee - pathology | Injections, Intra-Articular | Female | Aged | Osteoarthritis, Knee - physiopathology | Hyaluronic Acid - adverse effects | Care and treatment | Usage | Stem cells | Clinical trials | Bone marrow | Transplantation | Research | Osteoarthritis
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2014, Volume 20, Issue 10, pp. 1580 - 1585
Abstract We evaluated the feasibility, safety, and efficacy of the administration of 4 sequential doses (intravenously administered on days 1, 4, 11, and 18)...
Hematology, Oncology and Palliative Medicine | Mesenchymal stromal cells (MSC) | Graft-versus-host disease (GVHD) | STEM-CELLS | STEROID-RESISTANT | ACUTE GVHD | IMMUNOLOGY | SOCIETY | TRANSPLANTATION | TRIAL | CULTURE-CONDITIONS | OPTIMIZATION | HEMATOLOGY | BLOOD | Graft vs Host Disease - therapy | Hematologic Neoplasms - therapy | Prospective Studies | Cell Count | Hematologic Neoplasms - mortality | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Drug Resistance, Neoplasm | Male | Antineoplastic Agents - therapeutic use | Hematologic Neoplasms - pathology | Graft vs Host Disease - immunology | Transplantation, Homologous | Mesenchymal Stromal Cells - immunology | Mesenchymal Stromal Cells - cytology | Graft vs Host Disease - mortality | Cryopreservation | Adult | Female | Unrelated Donors | Steroids - therapeutic use | Transplantation Conditioning - methods | Acute Disease | Blood Platelets - chemistry | Treatment Outcome | Graft vs Host Disease - pathology | Survival Analysis | Hematologic Neoplasms - immunology | Mesenchymal Stem Cell Transplantation | Political corruption | Stem cells | Index Medicus
Hematology, Oncology and Palliative Medicine | Mesenchymal stromal cells (MSC) | Graft-versus-host disease (GVHD) | STEM-CELLS | STEROID-RESISTANT | ACUTE GVHD | IMMUNOLOGY | SOCIETY | TRANSPLANTATION | TRIAL | CULTURE-CONDITIONS | OPTIMIZATION | HEMATOLOGY | BLOOD | Graft vs Host Disease - therapy | Hematologic Neoplasms - therapy | Prospective Studies | Cell Count | Hematologic Neoplasms - mortality | Humans | Immunosuppressive Agents - therapeutic use | Middle Aged | Drug Resistance, Neoplasm | Male | Antineoplastic Agents - therapeutic use | Hematologic Neoplasms - pathology | Graft vs Host Disease - immunology | Transplantation, Homologous | Mesenchymal Stromal Cells - immunology | Mesenchymal Stromal Cells - cytology | Graft vs Host Disease - mortality | Cryopreservation | Adult | Female | Unrelated Donors | Steroids - therapeutic use | Transplantation Conditioning - methods | Acute Disease | Blood Platelets - chemistry | Treatment Outcome | Graft vs Host Disease - pathology | Survival Analysis | Hematologic Neoplasms - immunology | Mesenchymal Stem Cell Transplantation | Political corruption | Stem cells | Index Medicus
Journal Article
Experimental Hematology, ISSN 0301-472X, 2008, Volume 36, Issue 8, pp. 1014 - 1021
Objective Optimization of the mesenchymal stem cells (MSC) isolation and expansion method. Materials and Methods Mononuclear cells (MNC) from bone marrow...
Hematology, Oncology and Palliative Medicine | Advanced Basic Science | PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | SUBSTITUTE | CORD BLOOD | TISSUE | HUMAN-BONE-MARROW | FETAL CALF SERUM | PERIPHERAL-BLOOD | HYPOXIA | HEMATOLOGY |
Hematology, Oncology and Palliative Medicine | Advanced Basic Science | PROGENITOR CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | SUBSTITUTE | CORD BLOOD | TISSUE | HUMAN-BONE-MARROW | FETAL CALF SERUM | PERIPHERAL-BLOOD | HYPOXIA | HEMATOLOGY |