- Examination ofthe Gene for Connexin 26 in Czech Patients with Congenital Autosomal Recessive Non-SyndromicHearing Loss2002 | Second Faculty of Medicine
- Connnexin 26 in children with cochlear implant2002 | Second Faculty of Medicine, Central Library of Charles University
- Microphthalmia and cataract in rats with a novel point mutation in connexin 50-L7Q2008 | First Faculty of Medicine
- Charcot-Marie-Tooth gonosomal dominant type (CMTX1) - First findings of mutations in the gene for connexin 32 in the Czech Republic2000 | Second Faculty of Medicine
- The role of connexin 37 polymorphism in spontaneous abortion2021 | First Faculty of Medicine, Central Library of Charles University, Faculty of Physical Education and Sport
- Connexin 50 Mutation Lowers Blood Pressure in Spontaneously Hypertensive Rat2017 | First Faculty of Medicine, Third Faculty of Medicine
- Heterozygous connexin 50 mutation affects metabolic syndrome attributes in spontaneously hypertensive rat2016 | First Faculty of Medicine
- The role of connexin 37 gene polymorphism (1019C > T; pro319ser) in cardiovascular disease2011 | Second Faculty of Medicine
- The Connexin 37 (1019C > T) Gene Polymorphism Is Associated With Subclinical Atherosclerosis in Women With Type 1 and 2 Diabetes and in Women With Central Obesity2010 | Second Faculty of Medicine
- Expression of connexin 43 in the seminiferous epithelium of HD ratsPublication without faculty affiliation
- Pattern of expression of connexin 43 in the normal and damaged rat testisPublication without faculty affiliation
- Developmental mechanisms of arrhythmias - role of connexins in arrhythmogenesisPublication without faculty affiliation
- X-linked Charcot-Marie-Tooth disease: Phenotypic expression of a novel mutation IIe127Ser in the GJB1 (connexin 32) gene2005 | Second Faculty of Medicine
- Constitutional Monologues, Constitutional Dialogues or Constitutional Cacophony?2006 | Faculty of Law
- Expression of connexin -43 in the seminiferous epithelium of HD ratsPublication without faculty affiliation
- Spectrum of mutations in CX 26 gene in 142 patients with congenital nonsyndromic hearing loss2003 | Second Faculty of Medicine, Central Library of Charles University
- Spectrum of Mutations in the Connexin 26 Gene among 142 Patients with Congenital Deafness in Czech Republic.2003 | Second Faculty of Medicine
- Hereditary neuropathiesPublication without faculty affiliation
- Spontaneously Hypertensive Rat Chromosome 2 with Mutant Connexin 50 Triggers Divergent Effects on Metabolic Syndrome Components2017 | First Faculty of Medicine
- Inherited neuropathy-clinical and electrophysiological findings in the family with CMT X linked neuropathy2002 | Second Faculty of Medicine, Central Library of Charles University
- Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness2004 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Gap Junctional Communication via Connexin43 between Purkinje Fibers and Working Myocytes Explains the Epicardial Activation Pattern in the Postnatal Mouse Left Ventricle2021 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population2005 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Graphene monolayer as an appropriate substrate for mesenchymal stem cells support in regenerative medicine2023 | First Faculty of Medicine
- Magnetic resonance brain findings in Charcot-Marie-Tooth disease, type X12009 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
- Why Do We Have Purkinje Fibers Deep in Our Heart?2014 | First Faculty of Medicine
- EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus2013 | Second Faculty of Medicine
- Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease2010 | Second Faculty of Medicine
- Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene2009 | Second Faculty of Medicine
- Glucose Tightly Controls Morphological and Functional Properties of Astrocytes2016 | Second Faculty of Medicine