Susann Meyer

30.03.2026

medrxiv

30.03.2026

FRMPD4, a causal gene for intellectual disability and epilepsy, is associated with X-linked non-syndromic hearing loss

Liedtke D, Rak K, Schrode KM, Hehlert P, Chamanrou N, Bengl D, Katana R, Heydaran S, Doll J, Han M, Nanda I, Senthilan PR, Jürgens L, Bieniussa L, Voelker J, Neuner C, Hofrichter MAH, Schröder J, Schellens RTW, de Vrieze E, van Wijk E, Zechner U, Herms S, Hoffmann P, Müller T, Dittrich M, Bartsch O, Krawitz PM, Klopocki E, Shehata-Dieler W, Maroofian R, Wang T, Worley PF, Göpfert MC, Galehdari H, Lauer AM, Haaf T, Vona B

30.03.2026

J Synchrotron Radiat

30.03.2026

Fast-scanning small-angle X-ray scattering of hydrated biological cells

Yu B, Sinha M, Da Silva RM, Rölleke U, Burghammer M, Köster S

28.03.2026

Nat Commun

28.03.2026

Generation of marmoset monkeys with a non-mosaic disruption of the OTOF gene as a model of human deafness

Kahland T, Lindenwald DL, Jeschke M, Kusch K, Tkachenko Eikel O, Uhl M, Rüger N, Drummer C, Wolf B, Benseler F, Brose N, Behr R, Moser T

26.03.2026

Sci Adv

26.03.2026

Dysferlin stabilizes membrane nanodomains of cardiomyocytes after myocardial infarction

Wegener JB, Zühlke Y, Fleischhacker C, Marks J, Foo B, Bader N, Riedemann GC, Wedemeyer J, Vu KC, Vergel Leon AM, Paulke NJ, Kohl T, Urlaub H, Schmidt C, Hasenfuß G, Moser T, Rog-Zielinska EA, Lenz C, Lehnart SE, Brandenburg S

25.03.2026

Neurobiol Dis

25.03.2026