Functional dissection of hnRNP D suggests that nuclear import is required before hnRNP D can modulate mRNA turnover in the cytoplasm

RNA

Volumn 10, Issue 4, 2004, Pages 669-680

  Chen, Chyi Ying A ^a   Xu, Nianhua ^a,b   Zhu, Wenmiao ^a   Shyu, Ann Bin ^a  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b LEXICON PHARMACEUTICALS INC   (United States)

Author keywords

ARE; AUF1; hnRNP D; Nuclear cytoplasmic shuttling; RNA turnover

Indexed keywords

HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN D; MESSENGER RNA;

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL COMPARTMENTALIZATION; CELL FATE; CELL FUNCTION; CELL TYPE; CONTROLLED STUDY; CYTOPLASM; GENE DELETION; GENETIC TRANSCRIPTION; HETEROKARYON; MESSENGER RNA SYNTHESIS; NONHUMAN; NUCLEAR IMPORT; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; RNA SPLICING;

ACTIVE TRANSPORT, CELL NUCLEUS; ANIMALS; CELL NUCLEUS; HETEROGENEOUS-NUCLEAR RIBONUCLEOPROTEIN D; MICE; NIH 3T3 CELLS; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; RNA, MESSENGER;

ANIMALIA;

EID: 1642488249     PISSN: 13558382     EISSN: None     Source Type: Journal    
DOI: 10.1261/rna.5269304     Document Type: Article

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