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Class-specific interactions between Sis1 J-domain protein and Hsp70 chaperone potentiate disaggregation of misfolded proteins.
Proc Natl Acad Sci U S A. 2021 Dec 7;118(49):e2108163118. doi: 10.1073/pnas.2108163118.
Proc Natl Acad Sci U S A. 2021.
PMID: 34873058
Free PMC article.
Selective Hsp70-Dependent Docking of Hsp104 to Protein Aggregates Protects the Cell from the Toxicity of the Disaggregase.
Chamera T, Kłosowska A, Janta A, Wyszkowski H, Obuchowski I, Gumowski K, Liberek K.
Chamera T, et al. Among authors: wyszkowski h.
J Mol Biol. 2019 May 17;431(11):2180-2196. doi: 10.1016/j.jmb.2019.04.014. Epub 2019 Apr 24.
J Mol Biol. 2019.
PMID: 31026451
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CLPB (caseinolytic peptidase B homolog), the first mitochondrial protein refoldase associated with human disease.
Mróz D, Wyszkowski H, Szablewski T, Zawieracz K, Dutkiewicz R, Bury K, Wortmann SB, Wevers RA, Ziętkiewicz S.
Mróz D, et al. Among authors: wyszkowski h.
Biochim Biophys Acta Gen Subj. 2020 Apr;1864(4):129512. doi: 10.1016/j.bbagen.2020.129512. Epub 2020 Jan 7.
Biochim Biophys Acta Gen Subj. 2020.
PMID: 31917998
Free article.
No abstract available.
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Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.
Wortmann SB, Ziętkiewicz S, Guerrero-Castillo S, Feichtinger RG, Wagner M, Russell J, Ellaway C, Mróz D, Wyszkowski H, Weis D, Hannibal I, von Stülpnagel C, Cabrera-Orefice A, Lichter-Konecki U, Gaesser J, Windreich R, Myers KC, Lorsbach R, Dale RC, Gersting S, Prada CE, Christodoulou J, Wolf NI, Venselaar H, Mayr JA, Wevers RA.
Wortmann SB, et al. Among authors: wyszkowski h.
Genet Med. 2021 Sep;23(9):1705-1714. doi: 10.1038/s41436-021-01194-x. Epub 2021 Jun 17.
Genet Med. 2021.
PMID: 34140661
Free article.
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Correction to: Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.
Wortmann SB, Ziętkiewicz S, Guerrero-Castillo S, Feichtinger RG, Wagner M, Russell J, Ellaway C, Mróz D, Wyszkowski H, Weis D, Hannibal I, von Stülpnagel C, Cabrera-Orefice A, Lichter-Konecki U, Gaesser J, Windreich R, Myers KC, Lorsbach R, Dale RC, Gersting S, Prada CE, Christodoulou J, Wolf NI, Venselaar H, Mayr JA, Wevers RA.
Wortmann SB, et al. Among authors: wyszkowski h.
Genet Med. 2021 Sep;23(9):1789. doi: 10.1038/s41436-021-01280-0.
Genet Med. 2021.
PMID: 34302123
Free article.
No abstract available.
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