Effect of 5' splice site mutations on splicing of the preceding intron.
about
Insensitivity to anti-müllerian hormone due to a mutation in the human anti-müllerian hormone receptorSpecies-specific alternative splicing of the epidermal growth factor-like domain 1 of cartilage aggrecanThe molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutationAssembly of splicing complexes on exon 11 of the human insulin receptor gene does not correlate with splicing efficiency in-vitroCross-kingdom patterns of alternative splicing and splice recognitionA donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidismDonor splice-site mutation in CUL4B is likely cause of X-linked intellectual disabilityDirect selection for mutations affecting specific splice sites in a hamster dihydrofolate reductase minigeneGeneration and analysis of the expressed sequence tags from the mycelium of Ganoderma lucidumIdentification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromesExon recognition in vertebrate splicingSplicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cellsAltered levels of the Drosophila HRB87F/hrp36 hnRNP protein have limited effects on alternative splicing in vivo.Exon skipping by overexpression of a Drosophila heterogeneous nuclear ribonucleoprotein in vivo.Gene discovery and transcript analyses in the corn smut pathogen Ustilago maydis: expressed sequence tag and genome sequence comparison.Impact of alternative initiation, splicing, and termination on the diversity of the mRNA transcripts encoded by the mouse transcriptome.Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defectsDeletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the youngDefective splicing of mRNA from one COL1A1 allele of type I collagen in nondeforming (type I) osteogenesis imperfecta.Multiple distinct splicing enhancers in the protein-coding sequences of a constitutively spliced pre-mRNA.Evidence for splice site pairing via intron definition in Schizosaccharomyces pombe.Mutations in the conserved loop of human U5 snRNA generate use of novel cryptic 5' splice sites in vivoThe role of SON in splicing, development, and diseaseA novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosisAn additional exon in the human vinculin gene specifically encodes meta-vinculin-specific difference peptide. Cross-species comparison reveals variable and conserved motifs in the meta-vinculin insert.Splicing enhancement in the yeast rp51b intron.Functional selection of splicing enhancers that stimulate trans-splicing in vitroRedefinition of exon 7 in the COL1A1 gene of type I collagen by an intron 8 splice-donor-site mutation in a form of osteogenesis imperfecta: influence of intron splice order on outcome of splice-site mutationMutations in the CHD7 gene: the experience of a commercial laboratoryThe role of evolutionarily conserved sequences in alternative splicing at the 3' end of Drosophila melanogaster myosin heavy chain RNAA simple model to explain evolutionary trends of eukaryotic gene architecture and expression: how competition between splicing and cleavage/polyadenylation factors may affect gene expression and splice-site recognition in eukaryotesCooperation of 5' and 3' processing sites as well as intron and exon sequences in calcitonin exon recognition.Cabeza, a Drosophila gene encoding a novel RNA binding protein, shares homology with EWS and TLS, two genes involved in human sarcoma formationAberrant pre-mRNA maturation is caused by LINE insertions into introns of the white gene of Drosophila melanogaster.Contrasted cis-acting effects of downstream 5' splice sites on the splicing of a retained intron: the adenoviral E1A pre-mRNA model.Regulation of human insulin receptor RNA splicing in vivo.Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase genePre-mRNA splicing during transcription in the mammalian system.Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.Spontaneous deletions in Ig heavy chain genes: flanking sequences influence splice site selection.
P2860
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P2860
Effect of 5' splice site mutations on splicing of the preceding intron.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Effect of 5' splice site mutations on splicing of the preceding intron.
@en
type
label
Effect of 5' splice site mutations on splicing of the preceding intron.
@en
prefLabel
Effect of 5' splice site mutations on splicing of the preceding intron.
@en
P2860
P356
P1476
Effect of 5' splice site mutations on splicing of the preceding intron.
@en
P2093
M Talerico
S M Berget
P2860
P304
P356
10.1128/MCB.10.12.6299
P407
P577
1990-12-01T00:00:00Z