Gaysinskaya V[au] - Search Results

Year	Number of Results
2003	1
2004	1
2007	2
2008	1
2009	2
2010	2
2011	2
2012	1
2014	1
2015	1
2017	1
2018	1
2019	1
2020	1
2021	1
2023	1
2025	0

1

Gaysinskaya V, Bortvin A. Gaysinskaya V, et al. Curr Protoc Cytom. 2015 Apr 1;72:7.44.1-7.44.24. doi: 10.1002/0471142956.cy0744s72. Curr Protoc Cytom. 2015. PMID: 25827485

2

T cell immune deficiency rather than chromosome instability predisposes patients with short telomere syndromes to squamous cancers.

Schratz KE, Flasch DA, Atik CC, Cosner ZL, Blackford AL, Yang W, Gable DL, Vellanki PJ, Xiang Z, Gaysinskaya V, Vonderheide RH, Rooper LM, Zhang J, Armanios M. Schratz KE, et al. Cancer Cell. 2023 Apr 10;41(4):807-817.e6. doi: 10.1016/j.ccell.2023.03.005. Epub 2023 Apr 2. Cancer Cell. 2023. PMID: 37037617 Free PMC article.

3

Optimized flow cytometry isolation of murine spermatocytes.

Gaysinskaya V, Soh IY, van der Heijden GW, Bortvin A. Gaysinskaya V, et al. Cytometry A. 2014 Jun;85(6):556-65. doi: 10.1002/cyto.a.22463. Epub 2014 Mar 24. Cytometry A. 2014. PMID: 24664803 Free PMC article.

4

Intact piRNA pathway prevents L1 mobilization in male meiosis.

Newkirk SJ, Lee S, Grandi FC, Gaysinskaya V, Rosser JM, Vanden Berg N, Hogarth CA, Marchetto MCN, Muotri AR, Griswold MD, Ye P, Bortvin A, Gage FH, Boeke JD, An W. Newkirk SJ, et al. Proc Natl Acad Sci U S A. 2017 Jul 11;114(28):E5635-E5644. doi: 10.1073/pnas.1701069114. Epub 2017 Jun 19. Proc Natl Acad Sci U S A. 2017. PMID: 28630288 Free PMC article.

5

Somatic reversion impacts myelodysplastic syndromes and acute myeloid leukemia evolution in the short telomere disorders.

Schratz KE, Gaysinskaya V, Cosner ZL, DeBoy EA, Xiang Z, Kasch-Semenza L, Florea L, Shah PD, Armanios M. Schratz KE, et al. J Clin Invest. 2021 Sep 15;131(18):e147598. doi: 10.1172/JCI147598. J Clin Invest. 2021. PMID: 34343137 Free PMC article.

6

Transient reduction of DNA methylation at the onset of meiosis in male mice.

Gaysinskaya V, Miller BF, De Luca C, van der Heijden GW, Hansen KD, Bortvin A. Gaysinskaya V, et al. Epigenetics Chromatin. 2018 Apr 4;11(1):15. doi: 10.1186/s13072-018-0186-0. Epigenetics Chromatin. 2018. PMID: 29618374 Free PMC article.

7

Synonymous Mutation in DKC1 Causes Telomerase RNA Insufficiency Manifesting as Familial Pulmonary Fibrosis.

Gaysinskaya V, Stanley SE, Adam S, Armanios M. Gaysinskaya V, et al. Chest. 2020 Dec;158(6):2449-2457. doi: 10.1016/j.chest.2020.07.025. Epub 2020 Jul 22. Chest. 2020. PMID: 32710892 Free PMC article.

8

Persistent hepatitis C virus infection in microscale primary human hepatocyte cultures.

Ploss A, Khetani SR, Jones CT, Syder AJ, Trehan K, Gaysinskaya VA, Mu K, Ritola K, Rice CM, Bhatia SN. Ploss A, et al. Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3141-5. doi: 10.1073/pnas.0915130107. Epub 2010 Feb 1. Proc Natl Acad Sci U S A. 2010. PMID: 20133632 Free PMC article.

9

ZCCHC8, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturation.

Gable DL, Gaysinskaya V, Atik CC, Talbot CC Jr, Kang B, Stanley SE, Pugh EW, Amat-Codina N, Schenk KM, Arcasoy MO, Brayton C, Florea L, Armanios M. Gable DL, et al. Genes Dev. 2019 Oct 1;33(19-20):1381-1396. doi: 10.1101/gad.326785.119. Epub 2019 Sep 5. Genes Dev. 2019. PMID: 31488579 Free PMC article.

10

Human occludin is a hepatitis C virus entry factor required for infection of mouse cells.

Ploss A, Evans MJ, Gaysinskaya VA, Panis M, You H, de Jong YP, Rice CM. Ploss A, et al. Nature. 2009 Feb 12;457(7231):882-6. doi: 10.1038/nature07684. Epub 2009 Jan 28. Nature. 2009. PMID: 19182773 Free PMC article.

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