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Michaela Vorlíčková

Researcher at Academy of Sciences of the Czech Republic

Publications -  82
Citations -  4491

Michaela Vorlíčková is an academic researcher from Academy of Sciences of the Czech Republic. The author has contributed to research in topics: DNA & G-quadruplex. The author has an hindex of 28, co-authored 80 publications receiving 3954 citations. Previous affiliations of Michaela Vorlíčková include Central European Institute of Technology.

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Revealing structural peculiarities of homopurine GA repetition stuck by i-motif clip.

TL;DR: In this article, a series of DNA oligonucleotides comprising GAGA segment and C3 clip is analyzed by NMR and CD spectroscopies to understand the sequence-structure-stability relationships.
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Spectroscopic insights into quadruplexes of five-repeat telomere DNA sequences upon G-block damage.

TL;DR: Lesion in one guanine tract of a more than four repeats long human telomere DNA sequence may cause re-positioning of its quadruplex arrangement associated with a shift of the structure to less common quadruplex conformations.
Posted ContentDOI

Stability of Two-quartet G-quadruplexes and Their Dimers in Atomistic Simulations

TL;DR: The simulations suggest that a minimum of three quartets are needed to form an intrinsically stable all-anti parallel-stranded DNA GQ in the presence of Na+ or K+ ions, and predict that isolated RNA two-quartet parallel GQs may form, albeit being weakly stable.
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Diversity of Parallel Guanine Quadruplexes Induced by Guanine Substitutions

TL;DR: It is shown that parallel quadruplexes are significantly more sensitive towards guanine substitutions than antiparallel ones, and Guanine-substituted variants, which in principle might correspond to native genomic sequences, distinctly differ in their biophysical properties, indicating that the four guanines in each tetrad of parallel quadru Plexes are not equal.
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Comparative Electrochemical and Spectroscopic Studies of I‐motif‐forming DNA Nonamers

TL;DR: In this article, the structural diversity of cytosine (C)-rich oligodeoxynucleotides (ODNs) arising from their detail nucleotide sequence and experimental conditions was analyzed.