Haploinsufficiency screen highlights two distinct groups of ribosomal protein genes essential for embryonic stem cell fate

Proceedings of the National Academy of Sciences of the United States of America

Volumn 112, Issue 7, 2015, Pages 2127-2132

  Fortier, Simon ^a   MacRaea, Tara ^a   Bilodeau, Mélanie ^a   Sargeant, Tobias ^a,b,c   Sauvageau, Guy ^a  

^a INSTITUTE FOR RESEARCH IN IMMUNOLOGY AND CANCER   (Canada)

^b WALTER AND ELIZA HALL INSTITUTE OF MEDICAL RESEARCH   (Australia)

^c UNIVERSITY OF MELBOURNE   (Australia)

Author keywords

Differentiation; Embryoid body; Embryonic stem cells; Ribosomal proteins

Indexed keywords

COMPLEMENTARY DNA; MESSENGER RNA; RIBOSOME PROTEIN; RPS14 PROTEIN; RPS28 PROTEIN; RPS5 PROTEIN; UNCLASSIFIED DRUG; PROTEIN P53; TP53 PROTEIN, HUMAN;

ANIMAL EXPERIMENT; ARTICLE; CELL DIFFERENTIATION; CELL FATE; CHROMOSOME DELETION; EMBRYOID BODY; EMBRYONIC STEM CELL; ESSENTIAL GENE; GENE EXPRESSION; GENE ONTOLOGY; HAPLOINSUFFICIENCY; MESODERM; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; ANIMAL; CELL LINE; CELL LINEAGE; CYTOLOGY; GENETICS; HUMAN; MALE;

ANIMALS; CELL LINE; CELL LINEAGE; EMBRYONIC STEM CELLS; HAPLOINSUFFICIENCY; HUMANS; MALE; MICE; RIBOSOMAL PROTEINS; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84923169838     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1418845112     Document Type: Article

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