Bibliotecas PUC-SP - Busca Integrada

Coilin and Cajal bodies

per David Staněk
Publicat a Nucleus (2023-12-01)

Probing Nucleic Acid Interactions and Pre-mRNA Splicing by Förster Resonance Energy Transfer (FRET) Microscopy

per David Staněk, Eva Šimková
Publicat a International Journal of Molecular Sciences (2012-11-01)

Sequences of Groups, Hypergroups and Automata of Linear Ordinary Differential Operators

per Jan Chvalina, Michal Novák, Bedřich Smetana, David Staněk
Publicat a Mathematics (2021-02-01)

Retinitis pigmentosa-linked mutation in DHX38 modulates its splicing activity.

per Mina Obuća, Zuzana Cvačková, Jan Kubovčiak, Michal Kolář, David Staněk
Publicat a PLoS ONE (2022-01-01)

Estimation of Nitrate Trends in the Groundwater of the Zagreb Aquifer

per Zoran Kovač, Zoran Nakić, Drago Špoljarić, David Stanek, Andrea Bačani
Publicat a Geosciences (2018-05-01)

Histone deacetylase activity modulates alternative splicing.

per Jarmila Hnilicová, Samira Hozeifi, Eva Dušková, Jaroslav Icha, Tereza Tománková, David Staněk
Publicat a PLoS ONE (2011-01-01)

TSSC4 is a component of U5 snRNP that promotes tri-snRNP formation

per Klára Klimešová, Jitka Vojáčková, Nenad Radivojević, Franck Vandermoere, Edouard Bertrand, Celine Verheggen, David Staněk
Publicat a Nature Communications (2021-06-01)

Detection rate of causal variants in severe childhood epilepsy is highest in patients with seizure onset within the first four weeks of life

per David Staněk, Petra Laššuthová, Katalin Štěrbová, Markéta Vlčková, Jana Neupauerová, Marcela Krůtová, Pavel Seeman
Publicat a Orphanet Journal of Rare Diseases (2018-05-01)

SART3-Dependent Accumulation of Incomplete Spliceosomal snRNPs in Cajal Bodies

per Ivan Novotný, Anna Malinová, Eva Stejskalová, Daniel Matějů, Klára Klimešová, Adriana Roithová, Martin Švéda, Zdeněk Knejzlík, David Staněk
Publicat a Cell Reports (2015-01-01)

The SMN complex drives structural changes in human snRNAs to enable snRNP assembly

per Josef Pánek, Adriana Roithová, Nenad Radivojević, Michal Sýkora, Archana Bairavasundaram Prusty, Nicholas Huston, Han Wan, Anna Marie Pyle, Utz Fischer, David Staněk
Publicat a Nature Communications (2023-10-01)

BRAT1 links Integrator and defective RNA processing with neurodegeneration

per Zuzana Cihlarova, Jan Kubovciak, Margarita Sobol, Katerina Krejcikova, Jana Sachova, Michal Kolar, David Stanek, Cyril Barinka, Grace Yoon, Keith W. Caldecott, Hana Hanzlikova
Publicat a Nature Communications (2022-08-01)

The Cause of Hereditary Hearing Loss in <i>GJB2</i> Heterozygotes—A Comprehensive Study of the <i>GJB2</i>/DFNB1 Region

per Dana Safka Brozkova, Anna Uhrova Meszarosova, Petra Lassuthova, Lukáš Varga, David Staněk, Silvia Borecká, Jana Laštůvková, Vlasta Čejnová, Dagmar Rašková, Filip Lhota, Daniela Gašperíková, Pavel Seeman
Publicat a Genes (2021-05-01)

A 5‐year‐old boy with super‐refractory status epilepticus and RANBP2 variant warranting life‐saving hemispherotomy

per Barbora Straka, Miroslav Koblížek, Barbora Splítková, Radka Valkovičová, Lenka Krsková, Markéta Kalinová, Markéta Vlčková, Josef Zámečník, Petra Laššuthová, Lucie Sedláčková, David Staněk, Alice Maulisová, Michal Tichý, Martin Kynčl, Pavel Kršek
Publicat a Epilepsia Open (2024-02-01)

A novel SATB1 protein isoform with different biophysical properties

per Tomas Zelenka, Tomas Zelenka, Dionysios-Alexandros Papamatheakis, Dionysios-Alexandros Papamatheakis, Petros Tzerpos, Giorgos Panagopoulos, Konstantinos C. Tsolis, Vassilis M. Papadakis, Dimitris Mariatos Metaxas, George Papadogkonas, George Papadogkonas, Eleftherios Mores, Manouela Kapsetaki, Joseph Papamatheakis, Joseph Papamatheakis, David Stanek, Charalampos Spilianakis, Charalampos Spilianakis
Publicat a Frontiers in Cell and Developmental Biology (2023-08-01)