LET-418/Mi2 and SPR-5/LSD1 cooperatively prevent somatic reprogramming of C. Elegans germline stem cells

Stem Cell Reports

Volumn 2, Issue 4, 2014, Pages 547-559

  Käser Pébernard, Stéphanie ^a   Müller, Fritz ^a   Wicky, Chantal ^a  

^a UNIVERSITY OF FRIBOURG   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

HELMINTH PROTEIN; HISTONE DEMETHYLASE; LET 418 PROTEIN; LSD1 PROTEIN; MI2 PROTEIN; SPR 5 PROTEIN; UNCLASSIFIED DRUG; HISTONE H3; LSD2 PROTEIN; LYSINE; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR LET 418; TRANSCRIPTION FACTOR MI2; CAENORHABDITIS ELEGANS PROTEIN; CHROMATIN; DNA BINDING PROTEIN; HISTONE; HISTONE DEACETYLASE; LET-418 PROTEIN, C ELEGANS; N DEMETHYLASE; PROTEIN BINDING; SPR-5 PROTEIN, C ELEGANS;

ARTICLE; CAENORHABDITIS ELEGANS; CARCINOGENESIS; CELL COUNTING; CELL DIFFERENTIATION; CELL DIVISION; CELL FATE; CELL FUNCTION; CELL MATURATION; CHROMATIN ASSEMBLY AND DISASSEMBLY; CONTROLLED STUDY; DOWN REGULATION; EMBRYO; EPIGENETICS; GAMETOGENESIS; GENE TARGETING; GERM CELL SOMATIC REPROGRAMMING; GERMLINE STEM CELL; HISTONE METHYLATION; MOLECULAR PHYLOGENY; NERVE CELL DIFFERENTIATION; NERVE FIBER; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; WORM; ANIMAL CELL; CELL STRUCTURE; CHROMATIN STRUCTURE; IN VITRO STUDY; MUTANT; NERVE CELL; NUCLEAR REPROGRAMMING; SOMATIC CELL; ANIMAL; CELL TRANSFORMATION; CHROMATIN; CYTOLOGY; FEMALE; GENE EXPRESSION REGULATION; GENETICS; GERM CELL; MALE; METABOLISM; METHYLATION; MUTATION; NEOPLASM; STEM CELL;

CAENORHABDITIS ELEGANS;

ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; CELL DIFFERENTIATION; CELL DIVISION; CELL TRANSFORMATION, NEOPLASTIC; CELLULAR REPROGRAMMING; CHROMATIN; DNA-BINDING PROTEINS; DOWN-REGULATION; FEMALE; GENE EXPRESSION REGULATION; GERM CELLS; HISTONES; MALE; METHYLATION; MI-2 NUCLEOSOME REMODELING AND DEACETYLASE COMPLEX; MUTATION; NEOPLASMS, GERM CELL AND EMBRYONAL; NEURONS; OXIDOREDUCTASES, N-DEMETHYLATING; PROTEIN BINDING; STEM CELLS;

EID: 84898419025     PISSN: 22136711     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.stemcr.2014.02.007     Document Type: Article

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