- Distribution of Conventional and Nonconventional Introns in Tubulin (alpha and beta) Genes of Euglenids2014 | Přírodovědecká fakulta
- A case of Brooke-Spiegler syndrome with a novel germline deep intronic mutation in the CYLD gene leading to intronic exonization, diverse somatic mutations, and unusual histology2009 | 1. lékařská fakulta, Lékařská fakulta v Plzni
- The position of the longest intron is related to biological functions in some human genes2023 | Lékařská fakulta v Plzni
- Improved recovery and annotation of genes in metagenomes through the prediction of fungal introns2023 | Ústřední knihovna, Přírodovědecká fakulta
- Cloning of intronic sequence within DsRed2 increased the number of cells expressing red fluorescent protein2017 | Lékařská fakulta v Hradci Králové
- Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia2021 | Ústřední knihovna, Přírodovědecká fakulta, 1. lékařská fakulta
- Alternative intronic promoters in development and disease2017 | 1. lékařská fakulta
- Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia - A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variant2022 | 1. lékařská fakulta
- Role of intron 5 C/T polymorphism of the kalcium sensing receptor gene in the regulation of the serum FSH and LH in post-menopausal women.2005 | Přírodovědecká fakulta
- Intronic microduplications of RBFOX1 gene and their phenotypic consequencesPublikace bez příslušnosti k fakultě
- A case of Brooke-Spiegler syndrome with a novel germline deep intronic mutation in the CYLD gene leading to intronic exonization, diverse somatic mutations, and unusual histology2009 | Lékařská fakulta v Plzni
- A case of Brooke-Spiegler syndrome with a novel germline deep intronic mutation in the CYLD gene leading to intronic exonization, diverse somatic mutations, and unusual histology2009 | Ústřední knihovna
- Účinek nové intronické FBN1 mutace na sestřih odhalený metodou splicing minigene assayPublikace bez příslušnosti k fakultě
- Introns provide a platform for intergenic regulatory feedback of RPL22 paralogs in yeast2018 | Přírodovědecká fakulta
- Asymmetric pitx2 expression in medaka epithalamus is regulated by nodal signaling through an intronic enhancerPublikace bez příslušnosti k fakultě
- PPARA Intron Polymorphism Associated with Power Performance in 30-s Anaerobic Wingate Test2014 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu
- Hypervariabilní intronová oblast genu NCX1 obsahuje zvýšenou frekvenci inzerčního/delečního polymorfizmu a je spojena s kardiovaskulárními příznaky2010 | 1. lékařská fakulta
- PMD patient mutations reveal a long-distance intronic interaction that regulates PLP1/DM20 alternative splicing2014 | 2. lékařská fakulta
- Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction2023 | 1. lékařská fakulta
- Delece konzervované nekódující sekvence v intronu genu Plzf vede k snížení exprese Plzf v končetinových pupenech a k polydaktylii u potkana2009 | 1. lékařská fakulta
- Second intron in the protein-coding region of the fish parvalbumin gene – a promising platform for polymerase chain reaction-based discrimination of fish meat of various species2012 | Přírodovědecká fakulta
- The Intron 4 Polymorphism in the Calcium-Sensing Receptor Gene in Diabetes Mellitus and its Chronic Complications, Diabetic Nephropathy and Non-Diabetic Renal Disease2014 | 3. lékařská fakulta
- Genomic organizatiom of the mouse src gene. Sequencing of src inntrons revealed a new chromosome 2 microsatelite marker2002 | Publikace bez příslušnosti k fakultě
- ExOrthist: a tool to infer exon orthologies at any evolutionary distance2021 | Přírodovědecká fakulta
- PTPN22 intron polymorphism rs1310182 (c.2054-852T>C) is associated with type 1 diabetes mellitus in patients of Armenian descent2023 | 1. lékařská fakulta, 3. lékařská fakulta
- Migration distance is positively associated with sex-linked genetic diversity in passerine birds2016 | Přírodovědecká fakulta
- Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics2020 | 1. lékařská fakulta
- Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron I2007 | 1. lékařská fakulta
- The human rab GDI beta gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p131998 | 2. lékařská fakulta
- Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron I2007 | Fakulta tělesné výchovy a sportu