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Stem Cells International, ISSN 1687-966X, 2014, Volume 2014, pp. 768391 - 12
The breakthrough of reprogramming human somatic cells was achieved in 2006 by the work of Yamanaka and Takahashi. From this point, fibroblasts are the most... 
PLURIPOTENT STEM-CELLS | DEFINED FACTORS | HAIR-FOLLICLES | EPIGENETIC MEMORY | SMALL-MOLECULE COMPOUNDS | EFFICIENT GENERATION | HUMAN CORD BLOOD | STROMAL CELLS | VIRAL VECTORS | HUMAN KERATINOCYTES | CELL & TISSUE ENGINEERING | Keratinocytes | Cell culture | Usage | Growth | Methods | Stem cells | Studies | Disease | Efficiency | Morphology | Bone marrow | Fibroblasts | Viruses | Genomes | Gene expression | Patients | Review
Journal Article
STEM CELLS, ISSN 1066-5099, 06/2016, Volume 34, Issue 6, pp. 1563 - 1575
Journal Article
Journal Article
Stem Cells International, ISSN 1687-966X, 2016, Volume 2016, pp. 6759343 - 7
TBX3 is amember of the T-box transcription factor family and is involved in the core pluripotency network. Despite this role in the pluripotency network, its... 
PLURIPOTENT STEM-CELLS | GENERATION | DIRECTS | CELL & TISSUE ENGINEERING | Stem cells | Studies | Transcription factors | Antibiotics | Efficiency | Fibroblasts | Infections
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2015, Volume 82, pp. 420 - 429
Abstract Autosomal-dominant mutations within the gene FUS (fused in sarcoma) are responsible for 5% of familial cases of amyotrophic lateral sclerosis (ALS).... 
Neurology | Aggregate prone disease | Motor neuron disease | iPSC | Amyotrophic lateral sclerosis | Fused in sarcoma | RNA granules | Stress granules | Disease spreading | Cortical neurodegeneration | FUS-FTLD | Translated in sarcoma | Human cell models | Frontotemporal dementia | IPSC | STEM-CELLS | RNA | INCLUSIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | WILD-TYPE FUS | FRONTOTEMPORAL LOBAR DEGENERATION | NUCLEAR-LOCALIZATION SIGNAL | NEUROSCIENCES | MUTANT FUS | FET PROTEINS | SARCOMA FUS | Neurons - pathology | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Middle Aged | Cerebral Cortex - pathology | Male | Motor Neurons - pathology | Cerebral Cortex - physiopathology | Spinal Cord - pathology | Neurons - physiology | Adult | Female | Induced Pluripotent Stem Cells - pathology | Severity of Illness Index | Motor Neurons - physiology | Induced Pluripotent Stem Cells - physiology | Amyotrophic Lateral Sclerosis - genetics | RNA-Binding Protein FUS - genetics | Inclusion Bodies - physiology | RNA-Binding Protein FUS - metabolism | Disease Progression | Amyotrophic Lateral Sclerosis - pathology | Phenotype | Animals | Inclusion Bodies - pathology | Spinal Cord - physiopathology | Mutation | Genetic aspects | Sarcoma | Neurons | Analysis | Medical research | Nervous system diseases | Disease transmission | Medicine, Experimental | Dementia
Journal Article
1997, Literatur, Kultur, Geschlecht. Grosse Reihe, ISBN 3412127965, Volume Bd. 8, xi, 327
Book
08/1992, Volume 75, Issue 10
Book Review
08/1992, Volume 75, Issue 10
Book Review
01/1995, Volume 103, Issue 1
Book Review
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