| P50 | author | Marie-Laure Sobrier | Q55273215 |
| P2093 | author name string | Serge Amselem | |
| | Philippe Duquesnoy | |
| | Anne-Marie Fischer | |
| | Jacqueline Tapon-Bretaudière | |
| | Keren Borensztajn | |
| P2860 | cites work | Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation | Q22254871 |
| | Characterisation of a novel minisatellite that provides multiple splice donor sites in an interferon-induced transcript | Q24628850 |
| | RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression | Q24633499 |
| | Exon recognition in vertebrate splicing | Q29615088 |
| | Listening to silence and understanding nonsense: exonic mutations that affect splicing | Q29618493 |
| | Defining a 5' splice site by functional selection in the presence and absence of U1 snRNA 5' end. | Q30827740 |
| | Human genomic sequences that inhibit splicing | Q30910840 |
| | Multiple features contribute to efficient constitutive splicing of an unusually large exon | Q33938636 |
| | Factor VII gene intronic mutation in a lethal factor VII deficiency: effects on splice-site selection. | Q51838332 |
| | Repositioning of the reaction intermediate within the catalytic center of the spliceosome. | Q52568800 |
| | Are vertebrate exons scanned during splice-site selection? | Q59098666 |
| | RNA Splice Site Selection: Evidence for a 5′ → 3′ Scanning Model | Q67299051 |
| | Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7) | Q68214111 |
| | Construction of a novel database containing aberrant splicing mutations of mammalian genes | Q72375551 |
| | Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: a single nucleotide substitution in the second repeat prevents multiple alternate splicing | Q73459713 |
| | A repeated element in the human lamin B2 gene covers most of an intron and reiterates the exon/intron junction | Q73761628 |
| | Pre-mRNA splicing in the new millennium | Q33946020 |
| | Multiple splicing defects in an intronic false exon | Q33965191 |
| | Stop codons affect 5' splice site selection by surveillance of splicing | Q34024364 |
| | Factor VII deficiency and the FVII mutation database | Q34119225 |
| | Genomic variants in exons and introns: identifying the splicing spoilers | Q35787564 |
| | G triplets located throughout a class of small vertebrate introns enforce intron borders and regulate splice site selection | Q36570227 |
| | Scanning and competition between AGs are involved in 3' splice site selection in mammalian introns | Q36695561 |
| | Mutation of putative branchpoint consensus sequences in plant introns reduces splicing efficiency | Q38360757 |
| | Molecular analysis of factor VII deficiency in Italy: a frequent mutation (FVII Lazio) in a repeated intronic region. | Q38905795 |
| | An intronic splicing enhancer binds U1 snRNPs to enhance splicing and select 5' splice sites | Q39540203 |
| | U1 small nuclear RNA-promoted exon selection requires a minimal distance between the position of U1 binding and the 3' splice site across the exon | Q40024077 |
| | Intrinsic differences between authentic and cryptic 5' splice sites | Q40240461 |
| | PCR detection of a repeat polymorphism within the F7 gene | Q40506382 |
| | Mechanisms for selecting 5' splice sites in mammalian pre-mRNA splicing | Q40750224 |
| | Mutational analysis of 3' splice site selection during trans-splicing | Q40862425 |
| | Arabidopsis intron mutations and pre-mRNA splicing | Q41254418 |
| | Evidence against a scanning model of RNA splicing | Q41454583 |
| | An RNA switch at the 5' splice site requires ATP and the DEAD box protein Prp28p | Q41607972 |
| | Comparative analysis detects dependencies among the 5' splice-site positions | Q41807332 |
| | The role of branchpoint-3' splice site spacing and interaction between intron terminal nucleotides in 3' splice site selection in Saccharomyces cerevisiae | Q42611009 |
| | Conservation of an open-reading frame as an element affecting 5' splice site selection | Q42691129 |
| | A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels | Q43723747 |
| | The human factor VII gene is polymorphic due to variation in repeat copy number in a minisatellite | Q43777782 |
| | Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica | Q44702219 |
| | Unexpected point mutations activate cryptic 3' splice sites by perturbing a natural secondary structure within a yeast intron | Q46102390 |
| | Complex patterns of intragenic polymorphism at the PDGFA locus | Q47900898 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 9 | |
| P304 | page(s) | e138 | |
| P577 | publication date | 2006-07-20 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Oriented scanning is the leading mechanism underlying 5' splice site selection in mammals | |
| P478 | volume | 2 | |