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Items: 1 to 20 of 30

1.

Pro-death signaling of cytoprotective heat shock factor 1: upregulation of NOXA leading to apoptosis in heat-sensitive cells.

Janus P, Toma-Jonik A, Vydra N, Mrowiec K, Korfanty J, Chadalski M, Widłak P, Dudek K, Paszek A, Rusin M, Polańska J, Widłak W.

Cell Death Differ. 2020 Jan 29. doi: 10.1038/s41418-020-0501-8. [Epub ahead of print]

PMID:
31996779
2.

PHLDA1 Does Not Contribute Directly to Heat Shock-Induced Apoptosis of Spermatocytes.

Janus P, Mrowiec K, Vydra N, Widłak P, Toma-Jonik A, Korfanty J, Smolarczyk R, Widłak W.

Int J Mol Sci. 2019 Dec 30;21(1). pii: E267. doi: 10.3390/ijms21010267.

3.

17β-Estradiol Activates HSF1 via MAPK Signaling in ERα-Positive Breast Cancer Cells.

Vydra N, Janus P, Toma-Jonik A, Stokowy T, Mrowiec K, Korfanty J, Długajczyk A, Wojtaś B, Gielniewski B, Widłak W.

Cancers (Basel). 2019 Oct 11;11(10). pii: E1533. doi: 10.3390/cancers11101533.

4.

Interplay between HSF1 and p53 signaling pathways in cancer initiation and progression: non-oncogene and oncogene addiction.

Toma-Jonik A, Vydra N, Janus P, Widłak W.

Cell Oncol (Dordr). 2019 Oct;42(5):579-589. doi: 10.1007/s13402-019-00452-0. Epub 2019 Jun 10. Review.

PMID:
31183804
5.

RRAD, IL4I1, CDKN1A, and SERPINE1 genes are potentially co-regulated by NF-κB and p53 transcription factors in cells exposed to high doses of ionizing radiation.

Szołtysek K, Janus P, Zając G, Stokowy T, Walaszczyk A, Widłak W, Wojtaś B, Gielniewski B, Cockell S, Perkins ND, Kimmel M, Widlak P.

BMC Genomics. 2018 Nov 12;19(1):813. doi: 10.1186/s12864-018-5211-y.

6.

SPEN protein expression and interactions with chromatin in mouse testicular cells.

Korfanty J, Stokowy T, Chadalski M, Toma-Jonik A, Vydra N, Widłak P, Wojtaś B, Gielniewski B, Widlak W.

Reproduction. 2018 Sep;156(3):195-206. doi: 10.1530/REP-18-0046. Epub 2018 Jun 7.

PMID:
29880719
7.

Quantitative analysis reveals crosstalk mechanisms of heat shock-induced attenuation of NF-κB signaling at the single cell level.

Kardyńska M, Paszek A, Śmieja J, Spiller D, Widłak W, White MRH, Paszek P, Kimmel M.

PLoS Comput Biol. 2018 Apr 30;14(4):e1006130. doi: 10.1371/journal.pcbi.1006130. eCollection 2018 Apr.

8.

Pro-inflammatory cytokine and high doses of ionizing radiation have similar effects on the expression of NF-kappaB-dependent genes.

Janus P, Szołtysek K, Zając G, Stokowy T, Walaszczyk A, Widłak W, Wojtaś B, Gielniewski B, Iwanaszko M, Braun R, Cockell S, Perkins ND, Kimmel M, Widlak P.

Cell Signal. 2018 Jun;46:23-31. doi: 10.1016/j.cellsig.2018.02.011. Epub 2018 Feb 21.

PMID:
29476964
9.

The Role of Heat Shock Factors in Mammalian Spermatogenesis.

Widlak W, Vydra N.

Adv Anat Embryol Cell Biol. 2017;222:45-65. doi: 10.1007/978-3-319-51409-3_3. Review.

PMID:
28389750
10.

BRAFV600E-Associated Gene Expression Profile: Early Changes in the Transcriptome, Based on a Transgenic Mouse Model of Papillary Thyroid Carcinoma.

Rusinek D, Swierniak M, Chmielik E, Kowal M, Kowalska M, Cyplinska R, Czarniecka A, Piglowski W, Korfanty J, Chekan M, Krajewska J, Szpak-Ulczok S, Jarzab M, Widlak W, Jarzab B.

PLoS One. 2015 Dec 1;10(12):e0143688. doi: 10.1371/journal.pone.0143688. eCollection 2015.

11.

Cross talk between cytokine and hyperthermia-induced pathways: identification of different subsets of NF-κB-dependent genes regulated by TNFα and heat shock.

Janus P, Stokowy T, Jaksik R, Szoltysek K, Handschuh L, Podkowinski J, Widlak W, Kimmel M, Widlak P.

Mol Genet Genomics. 2015 Oct;290(5):1979-90. doi: 10.1007/s00438-015-1055-1. Epub 2015 May 6.

12.

Crosstalk between HSF1 and HSF2 during the heat shock response in mouse testes.

Korfanty J, Stokowy T, Widlak P, Gogler-Piglowska A, Handschuh L, Podkowiński J, Vydra N, Naumowicz A, Toma-Jonik A, Widlak W.

Int J Biochem Cell Biol. 2014 Dec;57:76-83. doi: 10.1016/j.biocel.2014.10.006. Epub 2014 Oct 19.

13.

Active heat shock transcription factor 1 supports migration of the melanoma cells via vinculin down-regulation.

Toma-Jonik A, Widlak W, Korfanty J, Cichon T, Smolarczyk R, Gogler-Piglowska A, Widlak P, Vydra N.

Cell Signal. 2015 Feb;27(2):394-401. doi: 10.1016/j.cellsig.2014.11.029. Epub 2014 Nov 27.

14.

Pleiotropic role of HSF1 in neoplastic transformation.

Vydra N, Toma A, Widlak W.

Curr Cancer Drug Targets. 2014;14(2):144-55. Review.

15.

Overexpression of Heat Shock Transcription Factor 1 enhances the resistance of melanoma cells to doxorubicin and paclitaxel.

Vydra N, Toma A, Glowala-Kosinska M, Gogler-Piglowska A, Widlak W.

BMC Cancer. 2013 Oct 29;13:504. doi: 10.1186/1471-2407-13-504.

16.

Impact of heat shock transcription factor 1 on global gene expression profiles in cells which induce either cytoprotective or pro-apoptotic response following hyperthermia.

Kus-Liśkiewicz M, Polańska J, Korfanty J, Olbryt M, Vydra N, Toma A, Widłak W.

BMC Genomics. 2013 Jul 8;14:456. doi: 10.1186/1471-2164-14-456.

17.

Identification of a new mouse sperm acrosome-associated protein.

Korfanty J, Toma A, Wojtas A, Rusin A, Vydra N, Widlak W.

Reproduction. 2012 Jun;143(6):749-57. doi: 10.1530/REP-11-0270. Epub 2012 Apr 11.

PMID:
22495889
18.

NF-κB signaling pathway is inhibited by heat shock independently of active transcription factor HSF1 and increased levels of inducible heat shock proteins.

Janus P, Pakuła-Cis M, Kalinowska-Herok M, Kashchak N, Szołtysek K, Pigłowski W, Widlak W, Kimmel M, Widlak P.

Genes Cells. 2011 Dec;16(12):1168-75. doi: 10.1111/j.1365-2443.2011.01560.x. Epub 2011 Nov 13.

19.

The expression patterns of heat shock genes and proteins and their role during vertebrate's development.

Rupik W, Jasik K, Bembenek J, Widłak W.

Comp Biochem Physiol A Mol Integr Physiol. 2011 Aug;159(4):349-66. doi: 10.1016/j.cbpa.2011.04.002. Epub 2011 Apr 17. Review.

PMID:
21527352
20.

[Finding targets of transcriptional regulators--chromatin immunoprecipitation assay (ChIP)].

Kus-Liśkiewicz M, Widłak W.

Postepy Biochem. 2011;57(4):418-24. Review. Polish.

PMID:
22568174

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