RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
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Exon first nucleotide mutations in splicing: evaluation of in silico prediction toolsEpigenetic inactivation and aberrant transcription of CSMD1 in squamous cell carcinoma cell lines.Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS).Coexpression of the KCNA3B gene product with Kv1.5 leads to a novel A-type potassium channelGenomic analysis of a murine cell-surface sialomucin, MGC-24/CD164Characterization of human RhCG and mouse Rhcg as novel nonerythroid Rh glycoprotein homologues predominantly expressed in kidney and testisType III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi JewsComplex regulation of the human gene for the Z-DNA binding protein DLM-1.The GLI-Kruppel family of human genesPBX2 and PBX3, new homeobox genes with extensive homology to the human proto-oncogene PBX1Molecular cloning, gene organization and expression of the human UDP-GalNAc:Neu5Acalpha2-3Galbeta-R beta1,4-N-acetylgalactosaminyltransferase responsible for the biosynthesis of the blood group Sda/Cad antigen: evidence for an unusual extended cytopCloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brainA CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.Abnormal type III collagen produced by an exon-17-skipping mutation of the COL3A1 gene in Ehlers-Danlos syndrome type IV is not incorporated into the extracellular matrixSequence and regulation of a gene encoding a human 89-kilodalton heat shock proteinCharacterization of the second type of human beta-galactoside alpha 2,6-sialyltransferase (ST6Gal II), which sialylates Galbeta 1,4GlcNAc structures on oligosaccharides preferentially. Genomic analysis of human sialyltransferase genesThe BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribedComplete exon-intron organization of the human gene for the alpha1 chain of type XV collagen (COL15A1) and comparison with the homologous COL18A1 geneMutant U5A cells are complemented by an interferon-alpha beta receptor subunit generated by alternative processing of a new member of a cytokine receptor gene clusterExpression and alternative splicing of the cytochrome P-450 CYP2A7Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patientIsolation and characterization of cDNAs corresponding to two human calcium, calmodulin-regulated, 3',5'-cyclic nucleotide phosphodiesterasesMolecular cloning and characterization of CIDE-3, a novel member of the cell-death-inducing DNA-fragmentation-factor (DFF45)-like effector familyAn alternate promoter directs expression of a truncated, muscle-specific isoform of the human ankyrin 1 geneSplicing factor SRSF6 promotes hyperplasia of sensitized skinPhosphoglucomutase 1: a gene with two promoters and a duplicated first exonIsolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignmentHuman peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humansMolecular cloning and functional expression of a novel CC chemokine receptor cDNA from a human basophilic cell lineA third member of the synapsin gene familyClustered organization of homologous KRAB zinc-finger genes with enhanced expression in human T lymphoid cellsCharacterization of a human ubiquitin-conjugating enzyme gene UBE2L3Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeCarbamyl phosphate synthetase I deficiency. One base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicingCloning, characterization, and expression of cDNAs encoding human delta 1-pyrroline-5-carboxylate dehydrogenaseFunctional consequences of PRODH missense mutationsMolecular cloning and predicted full-length amino acid sequence of the type I beta isozyme of cGMP-dependent protein kinase from human placenta. Tissue distribution and developmental changes in ratA 5' splice site mutation in fucosidosisThe structure of the human gene encoding protein gene product 9.5 (PGP9.5), a neuron-specific ubiquitin C-terminal hydrolaseCharacterization of three types of human alpha s1-casein mRNA transcripts
P2860
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P2860
RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression
description
1987 nî lūn-bûn
@nan
1987 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
RNA splice junctions of differ ...... mplications in gene expression
@ast
RNA splice junctions of differ ...... mplications in gene expression
@en
RNA splice junctions of differ ...... mplications in gene expression
@nl
type
label
RNA splice junctions of differ ...... mplications in gene expression
@ast
RNA splice junctions of differ ...... mplications in gene expression
@en
RNA splice junctions of differ ...... mplications in gene expression
@nl
prefLabel
RNA splice junctions of differ ...... mplications in gene expression
@ast
RNA splice junctions of differ ...... mplications in gene expression
@en
RNA splice junctions of differ ...... mplications in gene expression
@nl
P2860
P3181
P356
P1476
RNA splice junctions of differ ...... mplications in gene expression
@en
P2093
M B Shapiro
P Senapathy
P2860
P304
P3181
P356
10.1093/NAR/15.17.7155
P407
P577
1987-09-11T00:00:00Z