- Ideology and nonsense in Czech Union of Chimney Climbers2020 | Publication without faculty affiliation
- Malý, Radek (ed.): Malé lalulá aneb Strašilet přes bibáseň a Iblise až k Niagááárským vodopááádům2015 | Faculty of Arts
- Medieval Nonsense Humour in Scribal Additions2023 | Faculty of Arts
- To the poectics of the children's books 'The tales of Doggie and Moggie' by Josef Čapek and 'Dasenka' by Karel Čapek2012 | Faculty of Education
- In the Realm of Politics, Nonsense, and the Absurd: The Myth of Antigone in West and South Slavic Drama in the Mid-Twentieth Century2019 | Faculty of Arts
- Quantitative analysis of CAPN3 transcripts in LGMD2A patients: Involvement of nonsense-mediated mRNA decay2007 | Second Faculty of Medicine
- Recurrent CYLD nonsense mutation associated with a severe, disfiguring phenotype in an African American family with multiple familial trichoepithelioma2011 | First Faculty of Medicine, Faculty of Medicine in Pilsen
- A novel nonsense mutation in the β-subunit of the epithelial sodium channel causing Liddle syndrome2021 | Faculty of Medicine in Pilsen
- Shadow Cabinet? A Nonsense in Our System.2005 | Faculty of Arts
- Seemingly unique devices...or nonsenses?2015 | Faculty of Mathematics and Physics
- Spontaneous nonsense mutation in the tuftelin 1 gene is associated with abnormal hair appearance and amelioration of glucose and lipid metabolism in the rat2024 | First Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine
- Dependence on the Internet: Disease, Symptom or Nonsense?Publication without faculty affiliation
- Lévinas: World and its Absurdity2020 | Faculty of Humanities
- Václav Havel in the element of absurdity and nonsense antinomy2014 | Faculty of Humanities
- SEEMINGLY UNIQUE DEVICES...HOW TO USE NONSENSES IN PHYSICS TEACHING2016 | Faculty of Mathematics and Physics
- Silence as an Absence is Nonsense : An Analysis of Silence and John Cage2012 | Faculty of Arts
- Interpreting Nonsense: The Challenge of Uniqueness in Medieval Latin Texts2009 | Publication without faculty affiliation
- Sense and Nonsense of Elevated Column Temperature in Proteomic Bottom-up LC-MS Analyses2021 | Faculty of Pharmacy in Hradec Králové
- A Recurrent VPS16 p.Arg187* Nonsense Variant in Early-Onset Generalized Dystonia2021 | First Faculty of Medicine
- Literature as reaction to the language crisis2001 | Faculty of Arts
- Detailed Assessment of Renal Function in a Proband with Harboyan Syndrome Caused by a Novel Homozygous SLC4A11 Nonsense Mutation2015 | First Faculty of Medicine
- The Early American History in the Czech History Writing and University Teaching after 1989: Example, Inspiration, Civic Education, or Nonsense?2001 | Faculty of Social Sciences
- Prosaposin deficiency due to 1BP deletion in SAP B domain: The evidence for functional SAP A deficiency due to nonsense-mediated decayPublication without faculty affiliation
- 1bp deletion in saposin B domain of the prosaposin gene leads to nonsense-mediated mRNA decay and prosaposin deficiencyPublication without faculty affiliation
- Prosaposin deficiency due to 1BP deletion in SAP B domain: the evidence for functional SAP A deficiency due to nonsense-mediated decayPublication without faculty affiliation
- In the Realm of Politics, Nonsense, and the Absurd : The Myth of Antigone in West and South Slavic Drama in the Mid-Twentieth Century2018 | Faculty of Arts
- Disease-associated nonsense and frame-shift variants resulting in the truncation of the GluN2A or GluN2B C-terminal domain decrease NMDAR surface expression and reduce potentiating effects of neurosteroids2024 | First Faculty of Medicine, Central Library of Charles University, Faculty of Science
- Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial2017 | Second Faculty of Medicine
- Prosaposin deficiency due to 1BP deletion in SAP B domain: the evidence for functional SAP A deficiency due to nonsense-mediated mRNA decayPublication without faculty affiliation
- The CYLD p.R758X worldwide recurrent nonsense mutation detected in patients with multiple familial trichoepithelioma type 1, Brooke-Spiegler syndrome and familial cylindromatosis represents a mutational hotspot in the gene2016 | Faculty of Medicine in Pilsen
