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Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.
Nat Genet. 2024 Aug;56(8):1644-1653. doi: 10.1038/s41588-024-01836-1. Epub 2024 Jul 22.
Nat Genet. 2024.
PMID: 39039281
Free PMC article.
Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany - a mixed-methods study.
Inhestern L, Otto R, Brandt M, Zybarth D, Oheim R, Schüler H, Mir TS, Tsiakas K, Dibaj P, Zschüntzsch J, Okun PM, Hegenbart U, Sommerburg O, Schramm C, Weiler-Normann C, Härter M, Bergelt C.
Inhestern L, et al. Among authors: okun pm.
Orphanet J Rare Dis. 2024 May 13;19(1):197. doi: 10.1186/s13023-024-03207-9.
Orphanet J Rare Dis. 2024.
PMID: 38741100
Free PMC article.
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Adenoviruses using the cancer marker EphA2 as a receptor in vitro and in vivo by genetic ligand insertion into different capsid scaffolds.
Behr M, Kaufmann JK, Ketzer P, Engelhardt S, Mück-Häusl M, Okun PM, Petersen G, Neipel F, Hassel JC, Ehrhardt A, Enk AH, Nettelbeck DM.
Behr M, et al. Among authors: okun pm.
PLoS One. 2014 Apr 23;9(4):e95723. doi: 10.1371/journal.pone.0095723. eCollection 2014.
PLoS One. 2014.
PMID: 24760010
Free PMC article.
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External alternative NADH:ubiquinone oxidoreductase redirected to the internal face of the mitochondrial inner membrane rescues complex I deficiency in Yarrowia lipolytica.
Kerscher SJ, Eschemann A, Okun PM, Brandt U.
Kerscher SJ, et al. Among authors: okun pm.
J Cell Sci. 2001 Nov;114(Pt 21):3915-21. doi: 10.1242/jcs.114.21.3915.
J Cell Sci. 2001.
PMID: 11719558
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