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Search for publications relevant for "mutační analýza"
mutační analýza
Publication
Class
Person
Publication
Programmes
publication
Controversial impact of mutational analysis on thyroid fine-needle aspiration biopsies - pilot Study
2018 |
Faculty of Medicine in Hradec Králové
publication
Mutation analysis in Bartter and Gitelman syndrome in Czech republic
Publication without faculty affiliation
publication
Mutation analysis of TNNT gene in Czech patients with hypertrophic cardiomyopathy
2003 |
Faculty of Science
publication
The mutation analysis of gene BRCA 1 in families with genetic risk of breast and ovarian carcinoma
2000 |
First Faculty of Medicine
publication
Mutation analysis in patients with gitelman's syndrome
2006 |
First Faculty of Medicine
publication
Mutation analysis of the genes coding for fluoropyrimidines' catabolizing enzymes in prediction of fluoropyrimidines-associated toxicity in cancer patients
Publication without faculty affiliation
publication
Mutation Analysis of COL4A5 and COL4A3 Genes in Alport´s Syndrome
1999 |
Central Library of Charles University, Second Faculty of Medicine
publication
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome
2012 |
First Faculty of Medicine
publication
Mucopolysaccharidosis Type I in 21 Czech and Slovak Patients: Mutation Analysis Suggests a Functional Importance of C-Terminus of the IDUA Protein
2009 |
First Faculty of Medicine
publication
Mutační analýza vybraných genů pomocí High resolution meeting analysis
Publication without faculty affiliation
publication
Mutační analýza genů APC a MYH u pacientů s familiární adenomatózní polypózou
Publication without faculty affiliation
publication
Mutační analýza genů replikace MTDNA- využití ''High resolution melting analysis''
Publication without faculty affiliation
publication
Clinical characteristics of three Czech families with catecholaminergic polymorphic ventricular tachycardia and pilot results of RyR2 gene mutation analysis
2010 |
First Faculty of Medicine, Faculty of Physical Education and Sport
publication
Arginin519 -cystein COL2A1 gene mutation in czech osteoarthritis population.
2005 |
Faculty of Science
publication
Fluoropyrimidines toxicity prediction based on mutation analysis of dihydropyrimidin dehydrogease (DPD) coding sequence
Publication without faculty affiliation
publication
Vazebná a mutační analýza genů PKD1 a PKD2 v rodinách s autosomálně dominantní polycystickou chorobou ledvin
Publication without faculty affiliation
publication
Mutation analysis of APC and MYH gene in FAP families
Publication without faculty affiliation
publication
Mutations in the non-duplicated region of the PKD1 gene in families with autosomal dominant polycystic kidney disease (ADPKD)
Publication without faculty affiliation
publication
Occurrence of CHEK2 1100delC mutation in breast cancer patients and control cohort in the Czech Republic
2005 |
First Faculty of Medicine
publication
Molecular-pathologic and genetic diagnostics of limb girdle muscular dystrophy LGMD2A: presentation of first cases diagnosed in the Czech republik
2004 |
First Faculty of Medicine
publication
Contribution of mutations in ATM to breast cancer development in the Czech population
2008 |
First Faculty of Medicine
publication
Familial adenomatous polyposis and genetic testing
2007 |
First Faculty of Medicine
publication
Program DPD online - program for fluoropyrimidines' toxicity prediction
Publication without faculty affiliation
publication
Hereditary forms of colorectal adenomatous polyposis
2006 |
First Faculty of Medicine
publication
CHEK2 gene alterations in the forkhead-associated domain, 1100delC and del5395 do not modify the risk of sporadic pancreatic cancer.
2010 |
First Faculty of Medicine
publication
Familial adenomatous polyposis - novel molecular diagnostic techniques
2006 |
First Faculty of Medicine
publication
Project 'DPD online': the possibility of toxicity prediction of 5-fluorouracil and its derivates
2003 |
First Faculty of Medicine
publication
Hepatitis C virus internal ribosome entry site initiates protein synthesis at the authentic initiation codon in yeast
2007 |
Faculty of Science
publication
The Role of ABCB4 Gene Variation in Etiology of Idiopathic Cholelithiasis at the Child Age
2009 |
First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine
publication
Hereditary form of thrombotic thrombocytopenic purpura
2006 |
Second Faculty of Medicine