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Independent loss events of a functional tetherin gene in galliform birds.
J Virol. 2023 Oct 31;97(10):e0080323. doi: 10.1128/jvi.00803-23. Epub 2023 Sep 15.
J Virol. 2023.
PMID: 37712707
Free PMC article.
Heterologous avian system for quantitative analysis of Syncytin-1 interaction with ASCT2 receptor.
Štafl K, Trávníček M, Kučerová D, Pecnová Ľ, Krchlíková V, Gáliková E, Stepanets V, Hejnar J, Trejbalová K.
Štafl K, et al. Among authors: pecnova l.
Retrovirology. 2021 Jun 22;18(1):15. doi: 10.1186/s12977-021-00558-0.
Retrovirology. 2021.
PMID: 34158079
Free PMC article.
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Epigenetic regulation of transcription and splicing of syncytins, fusogenic glycoproteins of retroviral origin.
Trejbalová K, Blazková J, Matousková M, Kucerová D, Pecnová L, Vernerová Z, Herácek J, Hirsch I, Hejnar J.
Trejbalová K, et al. Among authors: pecnova l.
Nucleic Acids Res. 2011 Nov 1;39(20):8728-39. doi: 10.1093/nar/gkr562. Epub 2011 Jul 19.
Nucleic Acids Res. 2011.
PMID: 21771862
Free PMC article.
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Topologically Associated Domains Delineate Susceptibility to Somatic Hypermutation.
Senigl F, Maman Y, Dinesh RK, Alinikula J, Seth RB, Pecnova L, Omer AD, Rao SSP, Weisz D, Buerstedde JM, Aiden EL, Casellas R, Hejnar J, Schatz DG.
Senigl F, et al. Among authors: pecnova l.
Cell Rep. 2019 Dec 17;29(12):3902-3915.e8. doi: 10.1016/j.celrep.2019.11.039.
Cell Rep. 2019.
PMID: 31851922
Free PMC article.
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OmniPlex--a new QF-PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population.
Putzova M, Pecnova L, Dvorakova L, Soldatova I, Goetz P, Stejskal D.
Putzova M, et al. Among authors: pecnova l.
Prenat Diagn. 2008 Dec;28(13):1214-20. doi: 10.1002/pd.2151.
Prenat Diagn. 2008.
PMID: 19012274
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QF-PCR-based prenatal detection of common aneuploidies in the Czech population: five years of experience.
Putzova M, Soldatova I, Pecnova L, Dvorakova L, Jencikova N, Goetz P, Stejskal D.
Putzova M, et al. Among authors: pecnova l.
Eur J Med Genet. 2008 May-Jun;51(3):209-18. doi: 10.1016/j.ejmg.2008.02.003. Epub 2008 Feb 19.
Eur J Med Genet. 2008.
PMID: 18378202
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Preimplantation genetic diagnosis of X-linked diseases examined by indirect linkage analysis.
Borgulova I, Putzova M, Soldatova I, Krautova L, Pecnova L, Mika J, Kren R, Potuznikova P, Stejskal D.
Borgulova I, et al. Among authors: pecnova l.
Bratisl Lek Listy. 2015;116(9):542-6. doi: 10.4149/bll_2015_103.
Bratisl Lek Listy. 2015.
PMID: 26435019
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