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ARVO Annual Meeting Abstract July 2018

Ataluren-mediated read-through of a nonsense mutation in FAM161A gene which causes retinitis pigmentosa

Avigail Beryozkin; Ananya Samanta; Samer Khateb; Eyal Banin; Dror Sharon; Uwe Wolfrum; Kerstin Nagel-Wolfrum

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5324. doi:

ARVO Annual Meeting Abstract September 2016

Small molecules for targeting nonsense mutations causing ciliopathies

Fabian Möller; Ananya Samanta; Inessa Penner; Timor Baasov; Uwe Wolfrum; Kerstin Nagel-Wolfrum

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):1184. doi:

ARVO Annual Meeting Abstract June 2015

The SANS-USH2a-whirlin ternary complex of Usher syndrome type 1 and type 2 proteins is disrupted by pathogenic mutations

Uwe Wolfrum; Katharina Bauss; Barbara Knapp; Ananya Samanta; Kerstin Nagel-Wolfrum; Nasrin Sorusch; Biochemistry

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4626. doi:

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