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Page 1
Influenza A virus exploits transferrin receptor recycling to enter host cells.
Mazel-Sanchez B, Niu C, Williams N, Bachmann M, Choltus H, Silva F, Serre-Beinier V, Karenovics W, Iwaszkiewicz J, Zoete V, Kaiser L, Hartley O, Wehrle-Haller B, Schmolke M. Mazel-Sanchez B, et al. Among authors: iwaszkiewicz j. Proc Natl Acad Sci U S A. 2023 May 23;120(21):e2214936120. doi: 10.1073/pnas.2214936120. Epub 2023 May 16. Proc Natl Acad Sci U S A. 2023. PMID: 37192162 Free PMC article.
Influenza A viruses balance ER stress with host protein synthesis shutoff.
Mazel-Sanchez B, Iwaszkiewicz J, Bonifacio JPP, Silva F, Niu C, Strohmeier S, Eletto D, Krammer F, Tan G, Zoete V, Hale BG, Schmolke M. Mazel-Sanchez B, et al. Among authors: iwaszkiewicz j. Proc Natl Acad Sci U S A. 2021 Sep 7;118(36):e2024681118. doi: 10.1073/pnas.2024681118. Proc Natl Acad Sci U S A. 2021. PMID: 34479996 Free PMC article.
Actin assembly requirements of the formin Fus1 to build the fusion focus.
Billault-Chaumartin I, Michon L, Anderson CA, Yde SE, Suarez C, Iwaszkiewicz J, Zoete V, Kovar DR, Martin SG. Billault-Chaumartin I, et al. Among authors: iwaszkiewicz j. J Cell Sci. 2022 Jul 1;135(13):jcs260289. doi: 10.1242/jcs.260289. Epub 2022 Jul 8. J Cell Sci. 2022. PMID: 35673994 Free PMC article.
Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature.
Ansar M, Ebstein F, Özkoç H, Paracha SA, Iwaszkiewicz J, Gesemann M, Zoete V, Ranza E, Santoni FA, Sarwar MT, Ahmed J, Krüger E, Bachmann-Gagescu R, Antonarakis SE. Ansar M, et al. Among authors: iwaszkiewicz j. Hum Mol Genet. 2020 May 8;29(7):1132-1143. doi: 10.1093/hmg/ddaa032. Hum Mol Genet. 2020. PMID: 32129449
Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.
Antonarakis SE, Holoubek A, Rapti M, Rademaker J, Meylan J, Iwaszkiewicz J, Zoete V, Wilson C, Taylor J, Ansar M, Borel C, Menzel O, Kuželová K, Santoni FA. Antonarakis SE, et al. Among authors: iwaszkiewicz j. Hum Mol Genet. 2021 Dec 17;31(1):1-9. doi: 10.1093/hmg/ddab026. Hum Mol Genet. 2021. PMID: 33693784
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature.
Ansar M, Paracha SA, Serretti A, Sarwar MT, Khan J, Ranza E, Falconnet E, Iwaszkiewicz J, Shah SF, Qaisar AA, Santoni FA, Zoete V, Megarbane A, Ahmed J, Colombo R, Makrythanasis P, Antonarakis SE. Ansar M, et al. Among authors: iwaszkiewicz j. Hum Mol Genet. 2019 Mar 15;28(6):972-979. doi: 10.1093/hmg/ddy406. Hum Mol Genet. 2019. PMID: 30481285 Free PMC article.
Disulfide-Linked Peptides for Blocking BTLA/HVEM Binding.
Spodzieja M, Kuncewicz K, Sieradzan A, Karczyńska A, Iwaszkiewicz J, Cesson V, Węgrzyn K, Zhukov I, Maszota-Zieleniak M, Michielin O, Speiser DE, Zoete V, Derré L, Rodziewicz-Motowidło S. Spodzieja M, et al. Among authors: iwaszkiewicz j. Int J Mol Sci. 2020 Jan 18;21(2):636. doi: 10.3390/ijms21020636. Int J Mol Sci. 2020. PMID: 31963646 Free PMC article.
68 results