Prediction of human mRNA donor and acceptor sites from the DNA sequence.
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L1 antisense promoter drives tissue-specific transcription of human genesPurification and characterization of a novel 13 S hetero-oligomeric protein complex that stimulates in vitro Golgi transportGenomic organization and functional characterization of the chemokine receptor CXCR4, a major entry co-receptor for human immunodeficiency virus type 1Structural analysis and tissue localization of human C4.4A: a protein homologue of the urokinase receptorOrganisation of the human PAX4 gene and its exclusion as a candidate for the Wolcott-Rallison syndromeInactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation.Birth of a chimeric primate gene by capture of the transposase gene from a mobile elementA hidden Markov model that finds genes in E. coli DNAMutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)Identification of ribosome binding sites in Escherichia coli using neural network modelsHomozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairmentAHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeCharacterization of the endokinins: human tachykinins with cardiovascular activityMonoclonal antibody-mediated enhancement of dengue virus infection in vitro and in vivo and strategies for preventionSurvey of Programs Used to Detect Alternative Splicing Isoforms from Deep Sequencing Data In SilicoRNA-Binding Proteins: Splicing Factors and DiseaseIn silico tools for splicing defect prediction: a survey from the viewpoint of end usersGNAO1 encephalopathy: further delineation of a severe neurodevelopmental syndrome affecting females.C. elegans germ cells show temperature and age-dependent expression of Cer1, a Gypsy/Ty3-related retrotransposonSTAT2 deficiency and susceptibility to viral illness in humansExon/intron organisation of human proteasome PROS-27 K geneTargeting cells with single vectors using multiple-feature Boolean logicGermline mutations in RAD51D confer susceptibility to ovarian cancerDiagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relativesRare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease familiesSystematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateExon recognition in vertebrate splicingChloroP, a neural network-based method for predicting chloroplast transit peptides and their cleavage sitesAb initio gene finding in Drosophila genomic DNACan correct protein models be identified?Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABATNAMPT and NAPRT1: novel polymorphisms and distribution of variants between normal tissues and tumor samples.Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney diseaseA frequent splicing mutation and novel missense mutations color the updated mutational spectrum of classic galactosemia in Portugal.Kcnq1-5 (Kv7.1-5) potassium channel expression in the adult zebrafish.Functional consequences of novel connexin 26 mutations associated with hereditary hearing lossIdentification of novel point mutations in splicing sites integrating whole-exome and RNA-seq data in myeloproliferative diseasesTargeted and genomewide NGS data disqualify mutations in MYO1A, the "DFNA48 gene", as a cause of deafness.Splice site identification using probabilistic parameters and SVM classification.DNA splice site detection: a comparison of specific and general methods.
P2860
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P2860
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年学术文章
@wuu
1991年学术文章
@zh
1991年学术文章
@zh-cn
1991年学术文章
@zh-hans
1991年学术文章
@zh-my
1991年学术文章
@zh-sg
1991年學術文章
@yue
1991年學術文章
@zh-hant
name
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@en
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@nl
type
label
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@en
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@nl
prefLabel
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@en
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@nl
P1476
Prediction of human mRNA donor and acceptor sites from the DNA sequence.
@en
P2093
Engelbrecht J
P356
10.1016/0022-2836(91)90380-O
P407
P50
P577
1991-07-01T00:00:00Z