Veronika Barešová
Charles University(CZ)
Publications by Year
Research Areas
Biochemical and Molecular Research, Cytomegalovirus and herpesvirus research, Lysosomal Storage Disorders Research, Renal Diseases and Glomerulopathies, Adenosine and Purinergic Signaling
Most-Cited Works
- → Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing(2013)306 cited
- → Mutations in DNAJC5, Encoding Cysteine-String Protein Alpha, Cause Autosomal-Dominant Adult-Onset Neuronal Ceroid Lipofuscinosis(2011)261 cited
- → Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy(2019)193 cited
- → Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure(2009)163 cited
- → Increased level of cytokines and matrix metalloproteinases in osteoarthritic subchondral bone(2007)158 cited
- → Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia(2016)155 cited
- → Mutation of Nogo-B Receptor, a Subunit of cis-Prenyltransferase, Causes a Congenital Disorder of Glycosylation(2014)139 cited
- → Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome(2006)125 cited
- → Nanoscale topography of nanocrystalline diamonds promotes differentiation of osteoblasts(2009)94 cited
- → Mutations in ANTXR1 Cause GAPO Syndrome(2013)92 cited