Introns Concept

subject area of

• A cell-specific regulatory region of the human ABO blood group gene regulates the neighborhood gene encoding odorant binding protein 2B  Journal Articles
• A spliceosomal intron in Giardia lamblia  Journal Articles
• Amplicon pyrosequencing late Pleistocene permafrost: the removal of putative contaminant sequences and small‐scale reproducibility  Journal Articles
• An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training‐induced muscle fiber hypertrophy in younger men  Journal Articles
• Antisense phosphorothioate oligonucleotides: selective killing of the intracellular parasite Leishmania amazonensis.  Journal Articles
• BCL11A is a major HbF quantitative trait locus in three different populations with β-hemoglobinopathies  Journal Articles
• Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 ( dip2 ), and its murine homolog  Journal Articles
• Cloning, physical mapping and structural characterization of the human α A -adaptin gene  Journal Articles
• Cloning, sequencing and characterization of the tilapia insulin gene  Journal Articles
• Comparison of mitochondrial genomes provides insights into intron dynamics and evolution in the caterpillar fungus Cordyceps militaris  Journal Articles
• Complex Exon-Intron Marking by Histone Modifications Is Not Determined Solely by Nucleosome Distribution  Journal Articles
• Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa  Journal Articles
• Development and use of a 293 cell line expressing lac repressor for the rescue of recombinant adenoviruses expressing high levels of rabies virus glycoprotein.  Journal Articles
• Evidence for intron capture: an unusual path for the evolution of proteins.  Journal Articles
• Evidence for intron capture: an unusual path for the evolution of proteins.  Journal Articles
• Exon 5 of the p53 gene is a target for deletions in ovarian cancer  Journal Articles
• Fungal mitochondrial genomes and genetic polymorphisms  Journal Articles
• Gene Structure for Adenosine Kinase in Chinese Hamster and Human: High-Frequency Mutants of CHO Cells Involve Deletions of Several Introns and Exons  Journal Articles
• Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population  Journal Articles
• Genome sequence of the Brown Norway rat yields insights into mammalian evolution  Journal Articles
• Genome structure and gene content in protist mitochondrial DNAs  Journal Articles
• Genomic organization and linkage via a bidirectional promoter of the AP-3 (adaptor protein-3) mu3A and AK (adenosine kinase) genes: deletion mutants of AK in Chinese hamster cells extend into the AP-3 mu3A gene  Journal Articles
• Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations  Journal Articles
• IRR: A Novel Member of the Insulin Receptor Family  Conferences
• Insertion of a Retrotransposon inMbpDisrupts mRNA Splicing and Myelination in a New Mutant Rat  Journal Articles
• Intron-specific patterns of divergence of lin-11 regulatory function in the C. elegans nervous system  Journal Articles
• Menin: The Protein Behind the MEN1 Syndrome  Journal Articles
• Mild β⁺-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)  Journal Articles
• Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis  Journal Articles
• Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression  Journal Articles
• Novel β-Thalassemia Mutation In Patients of Jewish Descent: [β30(B12)ARGGLY OR IVS-I (-2) (AG)]  Journal Articles
• Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis  Journal Articles
• Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutation  Journal Articles
• Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization  Journal Articles
• Plasticity of Animal Genome Architecture Unmasked by Rapid Evolution of a Pelagic Tunicate  Journal Articles
• Protein Z Gene Polymorphisms, Protein Z Concentrations, and Ischemic Stroke  Journal Articles
• Redesigned purification yields a fully functional PutA protein dimer from Escherichia coli.  Journal Articles
• SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects  Journal Articles
• Sudanese (δβ)⁰-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion  Journal Articles
• The 135 kbp mitochondrial genome of Agaricus bisporus is the largest known eukaryotic reservoir of group I introns and plasmid-related sequences  Journal Articles
• The Mechanisms of Codon Reassignments in Mitochondrial Genetic Codes  Journal Articles
• The Transcriptional Repressor ZEB Regulates p73 Expression at the Crossroad between Proliferation and Differentiation  Journal Articles
• The human telomerase catalytic subunit hTERT: organization of the gene and characterization of the promoter  Journal Articles
• The rat adenine phosphoribosyltransferase sequence shows evolutionary rate variation among exons in rodents  Journal Articles
• Tryptophan hydroxylase polymorphisms in suicide victims  Journal Articles
• WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations  Journal Articles
• α-Thalassemia Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)  Journal Articles