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Volumn 7, Issue 12, 2001, Pages 1753-1767
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A 250-nucleotide UA-rich element in the 3′ untranslated region of Xenopus laevis Vg1 mRNA represses translation both in vivo and in vitro
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Author keywords
3 UTR; Cap; Oogenesis; Poly(A); Translational control
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Indexed keywords
ADENINE;
CELL PROTEIN;
CIS ACTING ELEMENT;
GENE PRODUCT;
LUCIFERASE;
MESSENGER RNA;
POLYADENYLIC ACID;
PROTEIN P42;
PROTEIN P45;
PROTEIN P60;
PROTEIN VG1;
PROTEIN VTE;
UNCLASSIFIED DRUG;
URIDINE;
3' UNTRANSLATED REGION;
ANALYTIC METHOD;
ANIMAL CELL;
ARTICLE;
BINDING SITE;
CELL MATURATION;
CODON USAGE;
CONTROLLED STUDY;
GENE DELETION;
NONHUMAN;
OOCYTE DEVELOPMENT;
PESTIVIRUS;
POLYADENYLATION;
PRIORITY JOURNAL;
PROTEIN CROSS LINKING;
PROTEIN LOCALIZATION;
RACE PAT METHOD;
REPRESSOR GENE;
RNA TRANSLATION;
TRANSLATION REGULATION;
XENOPUS LAEVIS;
3' UNTRANSLATED REGIONS;
ADENINE;
ANIMALS;
BASE SEQUENCE;
GENE EXPRESSION REGULATION;
GENES, REPORTER;
GLYCOPROTEINS;
MOLECULAR SEQUENCE DATA;
OOGENESIS;
PROTEIN BIOSYNTHESIS;
REGULATORY SEQUENCES, NUCLEIC ACID;
RNA PROCESSING, POST-TRANSCRIPTIONAL;
RNA-BINDING PROTEINS;
TRANSFORMING GROWTH FACTOR BETA;
URIDINE;
XENOPUS LAEVIS;
XENOPUS PROTEINS;
AMPHIBIA;
ANIMALIA;
CLASSICAL SWINE FEVER VIRUS;
PESTIVIRUS;
REPTILIA;
SUS SCROFA;
XENOPUS LAEVIS;
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EID: 0035678561
PISSN: 13558382
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (38)
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References (70)
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