Pages that link to "Q40335651"

The following pages link to Variants in the human insulin gene that affect pre-mRNA splicing: is -23HphI a functional single nucleotide polymorphism at IDDM2? (Q40335651):

Displaying 24 items.

• DBASS3 and DBASS5: databases of aberrant 3'- and 5'-splice sites (Q24609035) ‎ (← links)
• Glial cell line-derived neurotrophic factor (GDNF) as a novel candidate gene of anxiety (Q28536350) ‎ (← links)
• Genome-wide survey of allele-specific splicing in humans (Q33339747) ‎ (← links)
• Dual effect of a single nucleotide polymorphism in the first intron of the porcine secreted phosphoprotein 1 gene: allele-specific binding of C/EBP beta and activation of aberrant splicing (Q33511672) ‎ (← links)
• Genome-wide data-mining of candidate human splice translational efficiency polymorphisms (STEPs) and an online database (Q33719164) ‎ (← links)
• Optimal antisense target reducing INS intron 1 retention is adjacent to a parallel G quadruplex (Q33843189) ‎ (← links)
• Allele-specific recognition of the 3' splice site of INS intron 1 (Q34127329) ‎ (← links)
• Both polymorphic variable number of tandem repeats and autoimmune regulator modulate differential expression of insulin in human thymic epithelial cells. (Q34448766) ‎ (← links)
• The insulin polymorphism -23Hph increases the risk for type 1 diabetes mellitus in the Romanian population (Q34562871) ‎ (← links)
• A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian population (Q35173404) ‎ (← links)
• Posttranscriptional regulation of insulin family ligands and receptors (Q37225291) ‎ (← links)
• Common polymorphic variation in the genetically diverse African insulin gene and its association with size at birth. (Q37385113) ‎ (← links)
• Alternative splicing of U2AF1 reveals a shared repression mechanism for duplicated exons (Q37577401) ‎ (← links)
• Aberrant 3' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization (Q39113625) ‎ (← links)
• Identification of U2AF(35)-dependent exons by RNA-Seq reveals a link between 3' splice-site organization and activity of U2AF-related proteins. (Q39771516) ‎ (← links)
• Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition (Q40078319) ‎ (← links)
• Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping (Q40114019) ‎ (← links)
• Aberrant 5' splice sites in human disease genes: mutation pattern, nucleotide structure and comparison of computational tools that predict their utilization (Q42430246) ‎ (← links)
• Disease-specific biases in alternative splicing and tissue-specific dysregulation revealed by multitissue profiling of lymphocyte gene expression in type 1 diabetes (Q45069924) ‎ (← links)
• Single-nucleotide polymorphism of INS, INSR, IRS1, IRS2, PPAR-G and CAPN10 genes in the pathogenesis of polycystic ovary syndrome (Q47809914) ‎ (← links)
• RNASEH1 gene variants are associated with autoimmune type 1 diabetes in Colombia (Q50075802) ‎ (← links)
• Thioflavin T Monitoring of Guanine Quadruplex Formation in the rs689-Dependent INS Intron 1. (Q64972698) ‎ (← links)
• PUF60-activated exons uncover altered 3' splice-site selection by germline missense mutations in a single RRM (Q88775001) ‎ (← links)
• DNA methylation near the INS gene is associated with INS genetic variation (rs689) and type 1 diabetes in the Diabetes Autoimmunity Study in the Young (Q89726293) ‎ (← links)