Role of Inosine–Uracil Base Pairs in the Canonical RNA Duplexes

por Špačková, Naďa, Réblová, Kamila
Publicado 2018

Structure and mechanical properties of the ribosomal L1 stalk three-way junction

por Réblová, Kamila, Šponer, Jiří, Lankaš, Filip
Publicado 2012

Novel Evolutionary Lineages Revealed in the Chaetothyriales (Fungi) Based on Multigene Phylogenetic Analyses and Comparison of ITS Secondary Structure

por Réblová, Martina, Untereiner, Wendy A., Réblová, Kamila
Publicado 2013

Correction: Novel Evolutionary Lineages Revealed in the Chaetothyriales (Fungi) Based on Multigene Phylogenetic Analyses and Comparison of ITS Secondary Structure

por Réblová, Martina, Untereiner, Wendy A., Réblová, Kamila
Publicado 2013

Initiation of apoptosis by photodynamic therapy on MCF7 cells

por Kolacaronova, Hana, Reblova, Kamila, Strnad, Miroslav, Lenobel, R.
Publicado 2001

Molecular dynamics simulations suggest that RNA three-way junctions can act as flexible RNA structural elements in the ribosome

por Beššeová, Ivana, Réblová, Kamila, Leontis, Neocles B., Šponer, Jiří
Publicado 2010

Phylogenetic Reconstruction of the Calosphaeriales and Togniniales Using Five Genes and Predicted RNA Secondary Structures of ITS, and Flabellascus tenuirostris gen. et sp. nov.

por Réblová, Martina, Jaklitsch, Walter M., Réblová, Kamila, Štěpánek, Václav
Publicado 2015

Importance of base-pair opening for mismatch recognition

por Bouchal, Tomáš, Durník, Ivo, Illík, Viktor, Réblová, Kamila, Kulhánek, Petr
Publicado 2020

Dynamics of the base of ribosomal A-site finger revealed by molecular dynamics simulations and Cryo-EM

por Réblová, Kamila, Rázga, Filip, Li, Wen, Gao, Haixiao, Frank, Joachim, Šponer, Jiří
Publicado 2010

Bending of DNA duplexes with mutation motifs

por Růžička, Michal, Souček, Přemysl, Kulhánek, Petr, Radová, Lenka, Fajkusová, Lenka, Réblová, Kamila
Publicado 2019

DNA mutation motifs in the genes associated with inherited diseases

por Růžička, Michal, Kulhánek, Petr, Radová, Lenka, Čechová, Andrea, Špačková, Naďa, Fajkusová, Lenka, Réblová, Kamila
Publicado 2017

Conformations of Flanking Bases in HIV-1 RNA DIS Kissing Complexes Studied by Molecular Dynamics

por Réblová, Kamila, Fadrná, Eva, Sarzynska, Joanna, Kulinski, Tadeusz, Kulhánek, Petr, Ennifar, Eric, Koča, Jaroslav, Šponer, Jiří
Publicado 2007

Phylogenetic Reassessment, Taxonomy, and Biogeography of Codinaea and Similar Fungi

por Réblová, Martina, Kolařík, Miroslav, Nekvindová, Jana, Réblová, Kamila, Sklenář, František, Miller, Andrew N., Hernández-Restrepo, Margarita
Publicado 2021

Structural and Functional Impact of Seven Missense Variants of Phenylalanine Hydroxylase

por Pecimonova, Martina, Kluckova, Daniela, Csicsay, Frantisek, Reblova, Kamila, Krahulec, Jan, Procházkova, Dagmar, Skultety, Ludovit, Kadasi, Ludevit, Soltysova, Andrea
Publicado 2019

Low Density Lipoprotein Receptor Variants in the Beta-Propeller Subdomain and Their Functional Impact

por Dušková, Lucie, Nohelová, Lucie, Loja, Tomáš, Fialová, Jana, Zapletalová, Petra, Réblová, Kamila, Tichý, Lukáš, Freiberger, Tomáš, Fajkusová, Lenka
Publicado 2020

CLCN1 Mutations in Czech Patients with Myotonia Congenita, In Silico Analysis of Novel and Known Mutations in the Human Dimeric Skeletal Muscle Chloride Channel

por Skálová, Daniela, Zídková, Jana, Voháňka, Stanislav, Mazanec, Radim, Mušová, Zuzana, Vondráček, Petr, Mrázová, Lenka, Kraus, Josef, Réblová, Kamila, Fajkusová, Lenka
Publicado 2013

Inherited ichthyoses: molecular causes of the disease in Czech patients

por Borská, Romana, Pinková, Blanka, Réblová, Kamila, Bučková, Hana, Kopečková, Lenka, Němečková, Jitka, Puchmajerová, Alena, Malíková, Marcela, Hermanová, Markéta, Fajkusová, Lenka
Publicado 2019

P602: SINGLE-CELL RNA-SEQUENCING ENABLES TRACKING AND CHARACTERIZATION OF RARE CLL CELLS WITH THE POTENTIAL TO CAUSE REFRACTORINESS.

por Kurucová, Terézia, Réblová, Kamila, Vališová, Martina, Paweł Porc, Jakub, Navrkalová, Veronika, Pavlová, Šárka, Malčíková, Jitka, Plevová, Karla, Tichý, Boris, Doubek, Michael, Kotašková, Jana, Pospíšilová, Šárka
Publicado 2023

A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia

por Doubková, Martina, Staňo Kozubík, Kateřina, Radová, Lenka, Pešová, Michaela, Trizuljak, Jakub, Pál, Karol, Svobodová, Klára, Réblová, Kamila, Svozilová, Hana, Vrzalová, Zuzana, Pospíšilová, Šárka, Doubek, Michael
Publicado 2019

A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome

por Skalníková, Magdalena, Staňo Kozubík, Kateřina, Trizuljak, Jakub, Vrzalová, Zuzana, Radová, Lenka, Réblová, Kamila, Holbová, Radka, Kurucová, Terézia, Svozilová, Hana, Štika, Jiří, Blaháková, Ivona, Dvořáčková, Barbara, Prudková, Marie, Stehlíková, Olga, Šmída, Michal, Křen, Leoš, Smejkal, Petr, Pospíšilová, Šárka, Doubek, Michael
Publicado 2022