The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
about
Optimization of oligonucleotide arrays and RNA amplification protocols for analysis of transcript structure and alternative splicingReevaluating human gene annotation: a second-generation analysis of chromosome 22A transcript finishing initiative for closing gaps in the human transcriptomeThe Human Anatomic Gene Expression Library (H-ANGEL), the H-Inv integrative display of human gene expression across disparate technologies and platformsA genome-wide survey demonstrates widespread non-linear mRNA in expressed sequences from multiple speciesIntronic alternative splicing regulators identified by comparative genomics in nematodesEvidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humansGene discovery and transcript analyses in the corn smut pathogen Ustilago maydis: expressed sequence tag and genome sequence comparison.Comparative genomics in cyprinids: common carp ESTs help the annotation of the zebrafish genomeEvidence of functional selection pressure for alternative splicing events that accelerate evolution of protein subsequences.An expectation-maximization algorithm for probabilistic reconstructions of full-length isoforms from splice graphs.Large-scale identification and characterization of alternative splicing variants of human gene transcripts using 56,419 completely sequenced and manually annotated full-length cDNAsSignatures of domain shuffling in the human genome.Selecting for functional alternative splices in ESTs.The multiassembly problem: reconstructing multiple transcript isoforms from EST fragment mixtures.The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tagsIntegrated analysis of differential expression and alternative splicing of non-small cell lung cancer based on RNA sequencing.Alu-containing exons are alternatively spliced.Exon repetition: a major pathway for processing mRNA of some genes is allele-specific.Computational discovery of internal micro-exonsEvolution of alternative splicing after gene duplication.
P2860
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P2860
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
description
2001 nî lūn-bûn
@nan
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
The contribution of exon-skipping events on chromosome 22 to protein coding diversity
@nl
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@ast
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@en
type
label
The contribution of exon-skipping events on chromosome 22 to protein coding diversity
@nl
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@ast
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@en
prefLabel
The contribution of exon-skipping events on chromosome 22 to protein coding diversity
@nl
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@ast
The contribution of exon-skipping events on chromosome 22 to protein coding diversity.
@en
P2860
P50
P356
P1433
P1476
The contribution of exon-skipping events on chromosome 22 to protein coding diversity
@en
P2093
V N Babenko
P2860
P304
P356
10.1101/GR.188001
P407
P577
2001-11-01T00:00:00Z