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coding sequences
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Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism
2006 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Analysis of dihydropyrimidine dehydrogenase (DPD) coding sequence variants in patients with serious fluoropyrimidines toxicity
Publication without faculty affiliation
publication
A large-scale study of the random variability of a coding sequence: a study on the CFTR gene
2005 |
Second Faculty of Medicine
publication
Fluoropyrimidines toxicity prediction based on mutation analysis of dihydropyrimidin dehydrogease (DPD) coding sequence
Publication without faculty affiliation
publication
Regulation of Plzf expression but not the protein coding sequence is altered in rat polydactyly-luxate syndrome
Publication without faculty affiliation
publication
Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism
2006 |
Faculty of Medicine in Pilsen
publication
Influence of dihydropyrimidine dehydrogenase gene (DPYD) coding sequence variants on the development of fluoropyrimidine-related toxicity in patients with high-grade toxicity and patients with excellent tolerance of fluoropyrimidine-based chemotherapy
2009 |
First Faculty of Medicine
publication
Influence of dihydropyrimidine dehydrogenase gene (DPYD) coding sequence variants on the development of fluoropyrimidine-related toxicity in patients with high-grade toxicity and patients with excellent tolerance of fluoropyrimidine-based chemotherapy
2009 |
Publication without faculty affiliation
publication
Hepatitis C virus internal ribosome entry site initiates protein synthesis at the authentic initiation codon in yeast
2007 |
Faculty of Science
publication
Cloning, expression and purification of AKR1C3
Publication without faculty affiliation
publication
Transcriptome, proteome and draft genome of Euglena gracilis
2019 |
Faculty of Science, Central Library of Charles University
publication
Exome sequencing for identification of disease genes for rare syndromes. Experiences from Hamburg
2014 |
Second Faculty of Medicine
publication
Identification of GC-rich LAT genes in birds
2023 |
Faculty of Science
publication
Saccharomyces cerevisiae can secrete Sapp1p proteinase of Candida parapsilosis but cannot use it for efficient nitrogen acquisition
2013 |
Central Library of Charles University
publication
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant
2022 |
Second Faculty of Medicine
publication
Identification of a novel, transactivation-defective splicing variant of p53 gene in patients with chronic lymphocytic leukemia
2008 |
First Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
AGAMOUS regulates various target genes via cell cycle–coupled H3K27me3 dilution in floral meristems and stamens
2023 |
Faculty of Science
publication
Upregulation of asparagine synthetase and cell cycle arrest in t(12;21)-positive ALL - Reply
2005 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma
2015 |
First Faculty of Medicine
publication
Contribution of dihydropyrimidinase gene alterations to the development of serious toxicity in fluoropyrimidine-treated cancer patients.
2010 |
First Faculty of Medicine
publication
Mutations in Czech LGMD2A patients revealed by analysis of calpain3 mRNA and their phenotypic outcome
2004 |
Second Faculty of Medicine
publication
Haplotype block structure study of the CFTR gene. Most variants are associated with the M470 allele in several European populations
2006 |
Second Faculty of Medicine
publication
Three metallothionein isoforms and sequestration of intracellular silver in the hyperaccumulator Amanita strobiliformis
2011 |
Faculty of Science
publication
Alterations of CHEK2 gene in non-Hodgkin lymphoma patients
Publication without faculty affiliation
publication
Renal Cell Carcinoma With Leiomyomatous Stroma: A Group of Tumors With Indistinguishable Histopathologic Features, But 2 Distinct Genetic Profiles: Next-Generation Sequencing Analysis of 6 Cases Negative for Aberrations Related to the VHL gene
2018 |
Faculty of Medicine in Pilsen
publication
SMED-TLX-1 (NR2E1) Is Critical for Tissue and Body Plan Maintenance in Schmidtea mediterranea in Fasting/Feeding Cycles
2011 |
First Faculty of Medicine, Third 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
Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma
2014 |
Second Faculty of Medicine
publication
Somatic mutations of KIT in familial testicular germ cell tumours
2004 |
Publication without faculty affiliation
publication
A rapid approach for in locus overexpression of Trypanosoma brucei proteins
2020 |
Faculty of Science