Heterogeneity in polyadenylation cleavage sites in mammalian mRNA sequences: Implications for SAGE analysis

Nucleic Acids Research

Volumn 29, Issue 8, 2001, Pages 1690-1694

  Pauws, E ^a   Van Kampen, A H C ^a   Van De Graaf, S A R ^a   De Vijlder, J J M ^a   Ris Stalpers, C ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; THYROGLOBULIN;

ARTICLE; CALCULATION; DATA ANALYSIS; GENE EXPRESSION; GENE LIBRARY; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC TRANSCRIPTION; HUMAN; IN VIVO STUDY; MOLECULAR CLONING; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYADENYLATION; PRIORITY JOURNAL; RAT; RNA CLEAVAGE; RNA SEQUENCE; SCREENING; SEQUENCE HOMOLOGY; SIGNAL TRANSDUCTION; THYROID GLAND;

MAMMALIA; SALVIA;

EID: 0035870688     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/29.8.1690     Document Type: Article

References (15)

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5. In silico detection of control signals: mRNA 3′-end-processing sequences in diverse species
6. Cleavage site determinants in the mammalian polyadenylation signal
7. Point mutation in AAUAAA and the poly(A) addition site: Effects on the accuracy and efficiency of cleavage and polyadenylation in vitro
8. The upstream sequence element of the C2 complement poly(A) signal activates mRNA 3′ end formation by two distinct mechanisms
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14. Genomic organization of the 39 region of the human thyroglobulin gene
15. Control of cleavage site selection during mRNA 3′ end formation by a yeast hnRNP