Fate by RNA methylation: m6A steers stem cell pluripotency

Genome Biology

Volumn 16, Issue 1, 2015, Pages

  Zhao, Boxuan Simen ^a,b   He, Chuan ^a,b  

^a THE UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

6 N METHYLADENOSINE; BINDING PROTEIN; DIOXYGENASE; MESSENGER RNA; METHYLTRANSFERASE; METHYLTRANSFERASE METTL14; METHYLTRANSFERASE METTL3; OCTAMER TRANSCRIPTION FACTOR 4; RNA DEMETHYLASE ALKBH5; TRANSCRIPTION FACTOR NANOG; UNCLASSIFIED DRUG; YTHDF2 PROTEIN; ADENOSINE; N(6)-METHYLADENOSINE;

ARTICLE; CELL DEATH; CELL DIFFERENTIATION; CELL RENEWAL; EMBRYONIC STEM CELL; GENE EXPRESSION; METTL3 GENE; NANOG GENE; NONHUMAN; PLURIPOTENT STEM CELL; POU5F1 GENE; PROTEIN DEPLETION; PROTEIN FUNCTION; RNA METHYLATION; RNA SPLICING; RNA STABILITY; RNA TRANSLATION; STOP CODON; TRANSCRIPTION INITIATION SITE; ANALOGS AND DERIVATIVES; ANIMAL; CYTOLOGY; GENETICS; METABOLISM; METHYLATION; MOUSE; PHENOTYPE;

MURINAE;

ADENOSINE; ANIMALS; CELL DIFFERENTIATION; EMBRYONIC STEM CELLS; METHYLATION; MICE; PHENOTYPE; PLURIPOTENT STEM CELLS; RNA, MESSENGER;

EID: 84939131103     PISSN: 14747596     EISSN: 1474760X     Source Type: Journal    
DOI: 10.1186/s13059-015-0609-1     Document Type: Article

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