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Human Gene Therapy, ISSN 1043-0342, 10/2008, Volume 19, Issue 10, pp. 979 - 990
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 02/2013, Volume 14, Issue 1, pp. 21 - 21
Journal Article
Journal Article
Journal Article
Cell Reports, ISSN 2211-1247, 07/2014, Volume 8, Issue 2, pp. 327 - 337
Although transcriptome analysis can uncover the molecular changes that occur during induced reprogramming, the functional requirements for a given factor... 
SOMATIC-CELLS | MIR-302 | BARRIER | HUMAN FIBROBLASTS | TARGETS | PLURIPOTENCY | GENERATION | INDUCTION | MICRORNAS | EXPRESSION | CELL BIOLOGY | Embryonic Stem Cells - metabolism | NF-E2 Transcription Factor, p45 Subunit - metabolism | Embryonic Stem Cells - cytology | Membrane Glycoproteins - metabolism | Protein Disulfide-Isomerases - metabolism | Homeodomain Proteins - metabolism | Transcriptome | Otx Transcription Factors - metabolism | Neoplasm Proteins - metabolism | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Otx Transcription Factors - genetics | Tumor Suppressor Proteins - genetics | Trans-Activators - genetics | Induced Pluripotent Stem Cells - cytology | Neoplasm Proteins - genetics | Cellular Reprogramming - genetics | Induced Pluripotent Stem Cells - metabolism | NF-E2 Transcription Factor, p45 Subunit - genetics | Hepatocyte Nuclear Factor 4 - metabolism | Tumor Suppressor Proteins - metabolism | Chromosomal Proteins, Non-Histone - metabolism | Signal Transduction | Epidermal Growth Factor - genetics | Cells, Cultured | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Suppressor of Cytokine Signaling Proteins - genetics | Epidermal Growth Factor - metabolism | Hepatocyte Nuclear Factor 4 - genetics | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | Membrane Glycoproteins - genetics | Nerve Tissue Proteins - metabolism | Transcription Factors - metabolism | Protein Disulfide-Isomerases - genetics | Transcription Factors, TFII - genetics | Animals | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Transcription Factors, TFII - metabolism | Trans-Activators - metabolism | Mice | Suppressor of Cytokine Signaling Proteins - metabolism | Genome | Inositol 1,4,5-Trisphosphate Receptors - genetics | Index Medicus
Journal Article
Journal Article
Journal Article
Gene, ISSN 0378-1119, 10/2014, Volume 550, Issue 1, pp. 136 - 140
Inherited diseases are the result of DNA sequence changes. In recessive diseases, the clinical phenotype results from the combined functional effects of... 
ACAD8 | AUH | FKBP14 | LOVD 3.0 | ROGDI | DHCR7 | HMGCS2 | ACADSB | HSD17B10 | LEMLI-OPITZ-SYNDROME | GENETICS & HEREDITY | MUTATIONS | LSDBS | Enoyl-CoA Hydratase - genetics | Mitochondrial Diseases - pathology | Rare Diseases - genetics | RNA-Binding Proteins - genetics | Smith-Lemli-Opitz Syndrome - pathology | Lipid Metabolism, Inborn Errors - genetics | Smith-Lemli-Opitz Syndrome - genetics | Humans | Hydroxymethylglutaryl-CoA Synthase - genetics | Databases, Genetic | Hypoglycemia - pathology | Acyl-CoA Dehydrogenases - genetics | Amelogenesis Imperfecta - genetics | Dementia - genetics | Ehlers-Danlos Syndrome - pathology | Ehlers-Danlos Syndrome - genetics | Amino Acid Metabolism, Inborn Errors - genetics | Lipid Metabolism, Inborn Errors - pathology | Genetic Association Studies - statistics & numerical data | Epilepsy - genetics | Oxidoreductases Acting on CH-CH Group Donors - genetics | Rare Diseases - pathology | Amelogenesis Imperfecta - pathology | Amino Acid Metabolism, Inborn Errors - pathology | Peptidylprolyl Isomerase - genetics | Hydroxymethylglutaryl-CoA Synthase - deficiency | Nuclear Proteins - genetics | Acyl-CoA Dehydrogenase - genetics | Hypoglycemia - genetics | Mitochondrial Diseases - genetics | Dementia - pathology | Membrane Proteins - genetics | 3-Hydroxyacyl CoA Dehydrogenases | Genetic Association Studies - methods | Genotype | Metabolism, Inborn Errors - genetics | Phenotype | Acyl-CoA Dehydrogenase - deficiency | Apolipoproteins E - genetics | Internet | Mutation | Metabolism, Inborn Errors - pathology | Epilepsy - pathology | ATP Binding Cassette Transporter 1 - genetics | Apolipoproteins | Genetic polymorphisms | Index Medicus
Journal Article
Nature Cell Biology, ISSN 1465-7392, 2012, Volume 14, Issue 12, pp. 1295 - 1304
Journal Article