Staněk D - Search Results

1

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

Obuća M, Cvačková Z, Kubovčiak J, Kolář M, Staněk D. Obuća M, et al. Among authors: stanek d. PLoS One. 2022 Apr 6;17(4):e0265742. doi: 10.1371/journal.pone.0265742. eCollection 2022. PLoS One. 2022. PMID: 35385551 Free PMC article.

2

Pontin is localized in nucleolar fibrillar centers.

Cvacková Z, Albring KF, Koberna K, Ligasová A, Huber O, Raska I, Stanek D. Cvacková Z, et al. Among authors: stanek d. Chromosoma. 2008 Oct;117(5):487-97. doi: 10.1007/s00412-008-0170-8. Epub 2008 Jun 12. Chromosoma. 2008. PMID: 18548265 Free PMC article.

3

Chromatin position in human HepG2 cells: although being non-random, significantly changed in daughter cells.

Cvacková Z, Masata M, Stanĕk D, Fidlerová H, Raska I. Cvacková Z, et al. Among authors: stanek d. J Struct Biol. 2009 Feb;165(2):107-17. doi: 10.1016/j.jsb.2008.10.007. Epub 2008 Nov 12. J Struct Biol. 2009. PMID: 19056497 Free PMC article.

4

A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs.

Huranová M, Hnilicová J, Fleischer B, Cvacková Z, Stanek D. Huranová M, et al. Among authors: stanek d. Hum Mol Genet. 2009 Jun 1;18(11):2014-23. doi: 10.1093/hmg/ddp125. Epub 2009 Mar 17. Hum Mol Genet. 2009. PMID: 19293337

5

Histone deacetylase activity modulates alternative splicing.

Hnilicová J, Hozeifi S, Dušková E, Icha J, Tománková T, Staněk D. Hnilicová J, et al. Among authors: stanek d. PLoS One. 2011 Feb 2;6(2):e16727. doi: 10.1371/journal.pone.0016727. PLoS One. 2011. PMID: 21311748 Free PMC article.

6

Retinitis pigmentosa mutations of SNRNP200 enhance cryptic splice-site recognition.

Cvačková Z, Matějů D, Staněk D. Cvačková Z, et al. Among authors: stanek d. Hum Mutat. 2014 Mar;35(3):308-17. doi: 10.1002/humu.22481. Epub 2013 Dec 2. Hum Mutat. 2014. PMID: 24302620

7

Mutations in spliceosomal proteins and retina degeneration.

Růžičková Š, Staněk D. Růžičková Š, et al. Among authors: stanek d. RNA Biol. 2017 May 4;14(5):544-552. doi: 10.1080/15476286.2016.1191735. Epub 2016 Jun 14. RNA Biol. 2017. PMID: 27302685 Free PMC article. Review.

8

Assembly of the U5 snRNP component PRPF8 is controlled by the HSP90/R2TP chaperones.

Malinová A, Cvačková Z, Matějů D, Hořejší Z, Abéza C, Vandermoere F, Bertrand E, Staněk D, Verheggen C. Malinová A, et al. Among authors: stanek d. J Cell Biol. 2017 Jun 5;216(6):1579-1596. doi: 10.1083/jcb.201701165. Epub 2017 May 17. J Cell Biol. 2017. PMID: 28515276 Free PMC article.

9

PUF60-activated exons uncover altered 3' splice-site selection by germline missense mutations in a single RRM.

Královicová J, Ševcíková I, Stejskalová E, Obuca M, Hiller M, Stanek D, Vorechovský I. Královicová J, et al. Among authors: stanek d. Nucleic Acids Res. 2018 Jul 6;46(12):6166-6187. doi: 10.1093/nar/gky389. Nucleic Acids Res. 2018. PMID: 29788428 Free PMC article.

10

Splicing of long non-coding RNAs primarily depends on polypyrimidine tract and 5' splice-site sequences due to weak interactions with SR proteins.

Krchnáková Z, Thakur PK, Krausová M, Bieberstein N, Haberman N, Müller-McNicoll M, Stanek D. Krchnáková Z, et al. Among authors: stanek d. Nucleic Acids Res. 2019 Jan 25;47(2):911-928. doi: 10.1093/nar/gky1147. Nucleic Acids Res. 2019. PMID: 30445574 Free PMC article.

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