Splicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cells - Wikidata - wikimedia - TriplyDB

Splicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cells

Splicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cells

http://www.wikidata.org/entity/Q30450263

about

Genomic sequence, splicing, and gene annotation X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.Congenital end-plate acetylcholinesterase deficiency caused by a nonsense mutation and an A-->G splice-donor-site mutation at position +3 of the collagenlike-tail-subunit gene (COLQ): how does G at position +3 result in aberrant splicing?Sequence information for the splicing of human pre-mRNA identified by support vector machine classification Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type I Positive selection acting on splicing motifs reflects compensatory evolution Mutation of the PAX6 gene in patients with autosomal dominant keratitis Exon recognition in vertebrate splicing Human genomic sequences that inhibit splicing.Computational analysis of splicing errors and mutations in human transcripts.AT-AC pre-mRNA splicing mechanisms and conservation of minor introns in voltage-gated ion channel genes.Multiple splicing defects in an intronic false exon.A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis Evidence that the decay of nucleus-associated nonsense mRNA for human triosephosphate isomerase involves nonsense codon recognition after splicing.Premature termination codons do not affect the rate of splicing of neighboring introns.Context-dependent robustness to 5' splice site polymorphisms in human populations.When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.Splicing of designer exons informs a biophysical model for exon definition Coevolutionary networks of splicing cis-regulatory elements Splicing of internal large exons is defined by novel cis-acting sequence elements.Large exon size does not limit splicing in vivo Sequences homologous to 5' splice sites are required for the inhibitory activity of papillomavirus late 3' untranslated regions.Nonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.Synthetic intron improves transduction efficiency of trans-splicing adeno-associated viral vectors.Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection.Interactions between the terminal bases of mammalian introns are retained in inosine-containing pre-mRNAs.Context-dependent splicing regulation: exon definition, co-occurring motif pairs and tissue specificity Investigation of SCGB3A1 (UGRP2) gene arrays in patients with nasal polyposis.Phenotypic consequences of branch point substitutions.Exon inclusion is dependent on predictable exonic splicing enhancers Interaction between the first and last nucleotides of pre-mRNA introns is a determinant of 3' splice site selection in S. cerevisiae.Engineering the splice acceptor for improved gene expression and viral titer in an MLV-based retroviral vector.Spontaneous and MNNG-induced reversion of an EGFP construct in HeLa cells: an assay for observing mutations in living cells by fluorescent microscopy.Splice site and Germline variations of the MGMT gene in Esophageal cancer from Kashmir Valley: India.Dichotomous splicing signals in exon flanks.Splicing of designer exons reveals unexpected complexity in pre-mRNA splicing Identification of splicing silencers and enhancers in sense Alus: a role for pseudoacceptors in splice site repression.Intronic motif pairs cooperate across exons to promote pre-mRNA splicing.Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands.Dissection of splicing regulation at an endogenous locus by zinc-finger nuclease-mediated gene editing.

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P2860

Splicing mutants and their second-site suppressors at the dihydrofolate reductase locus in Chinese hamster ovary cells

http://www.wikidata.org/entity/Q30450263

description

1993 nî lūn-bûn

@nan

1993 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1993 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1993年の論文

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1993年論文

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1993年論文

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1993年論文

@zh-hk

1993年論文

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1993年論文

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1993年论文

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name

Splicing mutants and their sec ...... in Chinese hamster ovary cells

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Splicing mutants and their sec ...... in Chinese hamster ovary cells

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type

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Splicing mutants and their sec ...... in Chinese hamster ovary cells

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Splicing mutants and their sec ...... in Chinese hamster ovary cells

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prefLabel

Splicing mutants and their sec ...... in Chinese hamster ovary cells

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Splicing mutants and their sec ...... in Chinese hamster ovary cells

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Molecular and Cellular Biology

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Splicing mutants and their sec ...... in Chinese hamster ovary cells

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P2093

A M Carothers

http://www.w3.org/2001/XMLSchema#string

D Grunberger

http://www.w3.org/2001/XMLSchema#string

G Urlaub

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L A Chasin

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P2860

Isolation of Chinese hamster cell mutants deficient in dihydrofolate reductase activity

A catalogue of splice junction sequences

Scrambled exons

DNA strand-specific repair of (+-)-3 alpha,4 beta-dihydroxy-1 alpha,2 alpha-epoxy-1,2,3,4-tetrahydrobenzo[c]phenanthrene adducts in the hamster dihydrofolate reductase gene

DNA strand-specific mutations induced by (+/-)-3 alpha,4 beta-dihydroxy- 1 alpha,2 alpha-epoxy-1,2,3,4-tetrahydrobenzo[c]phenanthrene in the dihydrofolate reductase gene

Splicing mutations in the CHO DHFR gene preferentially induced by (+/-)-3 alpha,4 beta-dihydroxy-1 alpha,2 alpha-epoxy-1,2,3,4- tetrahydrobenzo[c]phenanthrene

Direct selection for mutations affecting specific splice sites in a hamster dihydrofolate reductase minigene

Improved free-energy parameters for predictions of RNA duplex stability

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

Mechanism for cryptic splice site activation during pre-mRNA splicing.

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10.1128/MCB.13.8.5085

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