Characterization and prediction of alternative splice sites.
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NMNAT1 mutations cause Leber congenital amaurosisA dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvementSurvey of Programs Used to Detect Alternative Splicing Isoforms from Deep Sequencing Data In SilicoSkipping of exons by premature termination of transcription and alternative splicing within intron-5 of the sheep SCF gene: a novel splice variantAlternative splicing of human and mouse NPFF2 receptor genes: Implications to receptor expressionAxial Spondylometaphyseal Dysplasia Is Caused by C21orf2 MutationsMECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis DisorderEfficient disruption of Zebrafish genes using a Gal4-containing gene trapProfound human/mouse differences in alpha-dystrobrevin isoforms: a novel syntrophin-binding site and promoter missing in mouse and rat.New perspectives on the renal slit diaphragm protein podocin.A new densovirus in cerebrospinal fluid from a case of anti-NMDA-receptor encephalitis.The emergence of alternative 3' and 5' splice site exons from constitutive exonsA remarkable depletion of both naïve CD4+ and CD8+ with high proportion of memory T cells in an IPEX infant with a FOXP3 mutation in the forkhead domain.Allelic gene structure variations in Anopheles gambiae mosquitoesThe 5'UTR in human adenoviruses: leader diversity in late gene expression.Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.Prediction of alternatively spliced exons using support vector machinesFLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.Common susceptibility variants examined for association with dilated cardiomyopathy.New splice site acceptor mutation in AIRE gene in autoimmune polyendocrine syndrome type 1.Abnormal retinal development associated with FRMD7 mutations.Natural history of SLC11 genes in vertebrates: tales from the fish worldSplice Site Variants in the KCNQ1 and SCN5A Genes: Transcript Analysis as a Tool in Supporting Pathogenicity.A bioinformatic and computational study of myosin phosphatase subunit diversity.The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmusSpliceAid 2: a database of human splicing factors expression data and RNA target motifs.Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing?Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population.Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease.Identification of the gene defect responsible for severe hypercholesterolaemia using whole-exome sequencing.An intronic mutation in MLH1 associated with familial colon and breast cancer.Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosaAssociation and linkage of allelic variants of the dopamine transporter gene in ADHD.Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population.Genetic association of the tachykinin receptor 1 TACR1 gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndromeDeleterious mutations in the essential mRNA metabolism factor, hGle1, in amyotrophic lateral sclerosis.Identification of alternative 5'/3' splice sites based on the mechanism of splice site competition.Identification of a Novel C-Terminal Truncated WT1 Isoform with Antagonistic Effects against Major WT1 Isoforms.Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutationsAbnormal Localization of STK17A in Bile Canaliculi in Liver Allografts: An Early Sign of Chronic Rejection.
P2860
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P2860
Characterization and prediction of alternative splice sites.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Characterization and prediction of alternative splice sites.
@en
type
label
Characterization and prediction of alternative splice sites.
@en
prefLabel
Characterization and prediction of alternative splice sites.
@en
P1433
P1476
Characterization and prediction of alternative splice sites.
@en
P2093
Antonio Marín
Magnus Wang
P304
P356
10.1016/J.GENE.2005.07.015
P407
P577
2005-10-13T00:00:00Z