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2002 2
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2013 1
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Ein neues Forum für seltene Hauterkrankungen.
Emmert S, Iben S, Fischer J, Komlosi K, Betz RC, Frank J J, Has C. Emmert S, et al. Among authors: iben s. J Dtsch Dermatol Ges. 2019 Jun;17(6):672-673. doi: 10.1111/ddg.13863. J Dtsch Dermatol Ges. 2019. PMID: 31241841 No abstract available.
Intranuclear inclusions of polyQ-expanded ATXN1 sequester RNA molecules.
Gkekas I, Vagiona AC, Pechlivanis N, Kastrinaki G, Pliatsika K, Iben S, Xanthopoulos K, Psomopoulos FE, Andrade-Navarro MA, Petrakis S. Gkekas I, et al. Among authors: iben s. Front Mol Neurosci. 2023 Dec 6;16:1280546. doi: 10.3389/fnmol.2023.1280546. eCollection 2023. Front Mol Neurosci. 2023. PMID: 38125008 Free PMC article.
TFIIH mutations can impact on translational fidelity of the ribosome.
Khalid F, Phan T, Qiang M, Maity P, Lasser T, Wiese S, Penzo M, Alupei M, Orioli D, Scharffetter-Kochanek K, Iben S. Khalid F, et al. Among authors: iben s. Hum Mol Genet. 2023 Mar 20;32(7):1102-1113. doi: 10.1093/hmg/ddac268. Hum Mol Genet. 2023. PMID: 36308430 Free PMC article.
Loss of Proteostasis Is a Pathomechanism in Cockayne Syndrome.
Alupei MC, Maity P, Esser PR, Krikki I, Tuorto F, Parlato R, Penzo M, Schelling A, Laugel V, Montanaro L, Scharffetter-Kochanek K, Iben S. Alupei MC, et al. Among authors: iben s. Cell Rep. 2018 May 8;23(6):1612-1619. doi: 10.1016/j.celrep.2018.04.041. Cell Rep. 2018. PMID: 29742419 Free article.
Nucleolar TFIIE plays a role in ribosomal biogenesis and performance.
Phan T, Maity P, Ludwig C, Streit L, Michaelis J, Tsesmelis M, Scharffetter-Kochanek K, Iben S. Phan T, et al. Among authors: iben s. Nucleic Acids Res. 2021 Nov 8;49(19):11197-11210. doi: 10.1093/nar/gkab866. Nucleic Acids Res. 2021. PMID: 34581812 Free PMC article.
29 results