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Volumn 15, Issue 5, 2014, Pages 634-642

Comparable frequencies of coding mutations and loss of imprinting in human pluripotent cells derived by nuclear transfer and defined factors

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CELL CLONE; CELL CULTURE; CELL NUCLEUS TRANSPLANTATION; CELLS BY BODY ANATOMY; CONTROLLED STUDY; DNA METHYLATION; EMBRYONIC STEM CELL; EPIGENETICS; GENE EXPRESSION; GENE MUTATION; GENETIC CODE; GENETIC HETEROGENEITY; GENETIC STABILITY; GENETICS; HUMAN; HUMAN CELL; ISOGENIC INDUCED PLURIPOTENT STEM CELL; NUCLEAR REPROGRAMMING; NUCLEAR TRANSFER EMBRYONIC STEM CELL; PARTHENOGENESIS; PLURIPOTENT STEM CELL; PRIORITY JOURNAL; SOMATIC CELL; ADULT; CYTOLOGY; GENE EXPRESSION REGULATION; GENE LOCUS; GENOME IMPRINTING; MALE; METABOLISM; MOLECULAR GENETICS; MUTATION RATE; NUCLEOTIDE SEQUENCE; OPEN READING FRAME;

EID: 84922637049     PISSN: 19345909     EISSN: 18759777     Source Type: Journal    
DOI: 10.1016/j.stem.2014.10.002     Document Type: Article
Times cited : (102)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.