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fragmentation analysis
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Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene
2004 |
Third Faculty of Medicine
publication
Fluorescence-based automated fragment analysis of microsatellite polymorphism within the transmembrane region of the MIC-A gene
2004 |
Central Library of Charles University
publication
10. Quantification of the finds and deposition analysis
2023 |
Faculty of Arts
publication
A novel high-resolution chipCE assay for rapid detection of EGFR gene mutations and amplifications in lung cancer therapy by a combination of fragment analysis, denaturing CE and MLPA
2010 |
Faculty of Science
publication
Detection of microsatellite instability in Czech HNPCC patients
2008 |
Second Faculty of Medicine
publication
A novel high-resolution chipCE assay for rapid detection of EGFR gene mutations and amplifications in lung cancer therapy by a combination of fragment analysis, denaturing CE and MLPA
2010 |
Faculty of Medicine in Pilsen
publication
A novel high-resolution chipCE assay for rapid detection of EGFR gene mutations and amplifications in lung cancer therapy by a combination of fragment analysis, denaturing CE and MLPA
2010 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Polymerase chain reaction
2014 |
Faculty of Medicine in Hradec Králové
publication
9. Artefacts in contexts
2023 |
Faculty of Arts
publication
Charcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsies (HNPP): Reliable detection of the CMT1A duplication and HNPP deletion using 8 microsatellite markers in 2 multiplex PCRs
2000 |
Second Faculty of Medicine
publication
Facultative promiscuity in a presumably monogamous mouse Apodemus microps
2005 |
Faculty of Science
publication
Simultaneous genotyping of microsatellite variations in HMOX1 and UGT1A1 genes using multicolored capillary electrophoresis
2010 |
First Faculty of Medicine
publication
Evaluation of microsatellite amplifications at chromosomal locus 3q26 as surrogate marker for premalignant changes in mucosa surrounding head and neck squamous cell carcinoma
2006 |
Central Library of Charles University
publication
Preimplantation genetic diagnostics of monogenic-based diseases: possibilities, pitfalls and first accomplishments in the Czech Republic
2008 |
Second Faculty of Medicine
publication
Dynamic roll call analysis of parties' ideological positions in the Czech Republic
2020 |
Faculty of Social Sciences
publication
Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening
2005 |
Second Faculty of Medicine
publication
DNA Analysis of Ancient Skeletal Remains
2010 |
Faculty of Science
publication
No association of promoter variations of HMOX1 and UGT1A1 genes with liver injury in chronic hepatitis C
2011 |
First Faculty of Medicine
publication
Molecular phenotyping of colorectal tumors in clinical practice: Assignment of extended prognostic subtypes by direct testing of endoscopic specimens
Publication without faculty affiliation
publication
Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients
2021 |
Second Faculty of Medicine
publication
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness
2004 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Determination of body fluid based on analysis of nucleic acids
2015 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Association of Serum Bilirubin and Functional Variants of Heme Oxygenase 1 and Bilirubin UDP-Glucuronosyl Transferase Genes in Czech Adult Patients with Non-Alcoholic Fatty Liver Disease
2021 |
First Faculty of Medicine
publication
The characterization of four gene expression analysis in circulating tumor cells made by Multiplex-PCR from the AdnaTest kit on the lab-on-a-chip Agilent DNA 1000 platform
2016 |
First Faculty of Medicine
publication
Characterization of telomeres and telomerase from the single-celled eukaryote Giardia intestinalis
2017 |
First Faculty of Medicine
publication
Serum Bilirubin Levels and Promoter Variations in HMOX1 and UGT1A1 Genes in Patients with Fabry Disease
2017 |
First Faculty of Medicine
publication
The Relationship Between Serum Bilirubin and Crohn's Disease
2014 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Pharmacy in Hradec Králové
publication
CRISPR/Cas9-targeted enrichment and long-read sequencing of the Fuchs endothelial corneal dystrophy-associated TCF4 triplet repeat
2019 |
First Faculty of Medicine
publication
Combined Targeted and Untargeted Profiling of HeLa Cells Deficient in Purine De Novo Synthesis
2022 |
First Faculty of Medicine
publication
Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2
2016 |
First Faculty of Medicine