Toward a bioartificial kidney: Will embryonic stem cells be the answer?

Kidney International

Volumn 83, Issue 4, 2013, Pages 543-545

  Pollock, Carol A ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOKINE; GROWTH FACTOR; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 2; TRANSCRIPTION FACTOR;

ACUTE KIDNEY FAILURE; ARTICLE; ARTIFICIAL KIDNEY; BIOARTIFICIAL KIDNEY; CELL ACTIVATION; CELL DIFFERENTIATION; CELL FUNCTION; CELL TRANSDIFFERENTIATION; CHRONIC KIDNEY FAILURE; CONTROLLED STUDY; EMBRYO; EMBRYONIC STEM CELL; FOOD AND DRUG ADMINISTRATION; GENE EXPRESSION PROFILING; GLOMERULUS; HENLE LOOP; HUMAN; HUMAN CELL; KIDNEY FUNCTION; KIDNEY TUBULE CELL; MESENCHYMAL STEM CELL; PLURIPOTENT STEM CELL; PRACTICE GUIDELINE; PRIORITY JOURNAL; REGENERATION; RENAL REPLACEMENT THERAPY;

EID: 84875729373     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2012.461     Document Type: Note

References (9)

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9. Feng Q, Lu SJ, Klimanskaya I et al. Hemangioblastic derivatives from human induced pluripotent stem cells exhibit limited expansion and early senescence. Stem Cells 2010; 28: 704-712.