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introns
Publication
Class
Person
Publication
Programmes
publication
Distribution of Conventional and Nonconventional Introns in Tubulin (alpha and beta) Genes of Euglenids
2014 |
Faculty of Science
publication
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 histology
2009 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
The position of the longest intron is related to biological functions in some human genes
2023 |
Faculty of Medicine in Pilsen
publication
Improved recovery and annotation of genes in metagenomes through the prediction of fungal introns
2023 |
Central Library of Charles University, Faculty of Science
publication
Cloning of intronic sequence within DsRed2 increased the number of cells expressing red fluorescent protein
2017 |
Faculty of Medicine in Hradec Králové
publication
Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia
2021 |
Central Library of Charles University, Faculty of Science, First Faculty of Medicine
publication
Alternative intronic promoters in development and disease
2017 |
First Faculty of Medicine
publication
Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia - A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variant
2022 |
First Faculty of Medicine
publication
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 |
Faculty of Science
publication
Intronic microduplications of RBFOX1 gene and their phenotypic consequences
Publication without faculty affiliation
publication
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 histology
2009 |
Faculty of Medicine in Pilsen
publication
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 histology
2009 |
Central Library of Charles University
publication
Effect of a novel intronic FBN1 mutation on splicing revealed by splicing minigene assay
Publication without faculty affiliation
publication
Introns provide a platform for intergenic regulatory feedback of RPL22 paralogs in yeast
2018 |
Faculty of Science
publication
Asymmetric pitx2 expression in medaka epithalamus is regulated by nodal signaling through an intronic enhancer
Publication without faculty affiliation
publication
PPARA Intron Polymorphism Associated with Power Performance in 30-s Anaerobic Wingate Test
2014 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits
2010 |
First Faculty of Medicine
publication
PMD patient mutations reveal a long-distance intronic interaction that regulates PLP1/DM20 alternative splicing
2014 |
Second Faculty of Medicine
publication
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
2023 |
First Faculty of Medicine
publication
Deletion of a Conserved Noncoding Sequence in Plzf Intron Leads to Plzf Down-regulation in Limb Bud and Polydactyly in the Rat
2009 |
First Faculty of Medicine
publication
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 species
2012 |
Faculty of Science
publication
The Intron 4 Polymorphism in the Calcium-Sensing Receptor Gene in Diabetes Mellitus and its Chronic Complications, Diabetic Nephropathy and Non-Diabetic Renal Disease
2014 |
Third Faculty of Medicine
publication
Genomic organizatiom of the mouse src gene. Sequencing of src inntrons revealed a new chromosome 2 microsatelite marker
2002 |
Publication without faculty affiliation
publication
ExOrthist: a tool to infer exon orthologies at any evolutionary distance
2021 |
Faculty of Science
publication
PTPN22 intron polymorphism rs1310182 (c.2054-852T>C) is associated with type 1 diabetes mellitus in patients of Armenian descent
2023 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Migration distance is positively associated with sex-linked genetic diversity in passerine birds
2016 |
Faculty of Science
publication
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
2020 |
First Faculty of Medicine
publication
Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron I
2007 |
First Faculty of Medicine
publication
The human rab GDI beta gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13
1998 |
Second Faculty of Medicine
publication
Resequencing PNMT in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron I
2007 |
Faculty of Physical Education and Sport