Temat: "Human iPSC-derived chondrocytes" - OpacWWW

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Tytuł:: Human iPSC-derived chondrocytes mimic juvenile chondrocyte function for the dual advantage of increased proliferation and resistance to IL-1β.
Autorzy:: Lee J; Department of Orthopaedic Surgery, Stanford University School of Medicine, 300 Pasteur Drive, Edwards Bldg., R164, Stanford, CA, 94305-5341, USA.
Smeriglio P; Department of Orthopaedic Surgery, Stanford University School of Medicine, 300 Pasteur Drive, Edwards Bldg., R164, Stanford, CA, 94305-5341, USA.
Chu CR; Department of Orthopaedic Surgery, Stanford University School of Medicine, 300 Pasteur Drive, Edwards Bldg., R164, Stanford, CA, 94305-5341, USA.; Veterans Administration Palo Alto Health Care System, Palo Alto, CA, USA.
Bhutani N; Department of Orthopaedic Surgery, Stanford University School of Medicine, 300 Pasteur Drive, Edwards Bldg., R164, Stanford, CA, 94305-5341, USA. .; Pokaż więcej
Źródło:: Stem cell research & therapy [Stem Cell Res Ther] 2017 Nov 02; Vol. 8 (1), pp. 244. Date of Electronic Publication: 2017 Nov 02.
Typ publikacji:: Journal Article
MeSH Terms:: CD24 Antigen/*genetics
Chondrocytes/*drug effects
Induced Pluripotent Stem Cells/*drug effects
Interleukin-1beta/*pharmacology
Adult ; Age Factors ; CD24 Antigen/immunology ; Cartilage, Articular/cytology ; Cartilage, Articular/immunology ; Cell Differentiation/drug effects ; Cell Proliferation/drug effects ; Chondrocytes/cytology ; Chondrocytes/immunology ; Female ; Fetus ; Gene Expression Profiling ; Gene Expression Regulation ; Gene Ontology ; Humans ; Induced Pluripotent Stem Cells/cytology ; Induced Pluripotent Stem Cells/immunology ; Infant ; Interleukin-1beta/immunology ; Molecular Mimicry ; Molecular Sequence Annotation ; Regeneration/immunology

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