Diverse diseases from a ubiquitous process: The ribosomopathy paradox

FEBS Letters

Volumn 588, Issue 9, 2014, Pages 1491-1500

  Armistead, Joy ^a   Triggs Raine, Barbara ^a,b  

^a UNIVERSITY OF MANITOBA   (Canada)

^b MANITOBA INSTITUTE OF CHILD HEALTH   (Canada)

Author keywords

IRES elements; Ribosome biogenesis; Ribosomopathy; Tissue specificity

Indexed keywords

MAMMALIAN TARGET OF RAPAMYCIN; MESSENGER RNA; MYC PROTEIN; PROTEIN P53;

ANAUXETIC DYSPLASIA; BINDING AFFINITY; BLACKFAN DIAMOND ANEMIA; CANCER SUSCEPTIBILITY; CARTILAGE HAIR HYPOPLASIA; CELL CYCLE REGULATION; CLINICAL FEATURE; DWARFISM; DYSKERATOSIS CONGENITA; DYSPLASIA; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; HUMAN; INTERNAL RIBOSOME ENTRY SITE; LIVER CIRRHOSIS; MANDIBULOFACIAL DYSOSTOSIS; MOLECULAR PATHOLOGY; NONHUMAN; NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN SYNTHESIS; REVIEW; RIBOSOME; RIBOSOMOPATHY; RNA TRANSPORT; SHORT STATURE; SHWACHMAN SYNDROME; SIGNAL TRANSDUCTION; TISSUE SPECIFICITY; TRANSLATION REGULATION;

IRES ELEMENTS; RIBOSOME BIOGENESIS; RIBOSOMOPATHY; TISSUE SPECIFICITY;

ANIMALS; BINDING SITES; GENES, MYC; GENETIC DISEASES, INBORN; HUMANS; MUTATION; ORGAN SPECIFICITY; PROTEIN BIOSYNTHESIS; RIBOSOMES; TOR SERINE-THREONINE KINASES; TUMOR SUPPRESSOR PROTEIN P53;

EID: 84899656943     PISSN: 00145793     EISSN: 18733468     Source Type: Journal    
DOI: 10.1016/j.febslet.2014.03.024     Document Type: Review

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