Lars Tebbe to Humans
This is a "connection" page, showing publications Lars Tebbe has written about Humans.
Connection Strength
0.345
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A Knockin Model with the Mouse Equivalent to the c.2299delG Mutation in Usherin Exhibits Early-Onset Hearing Loss and Progressive Retinal Degeneration. Adv Exp Med Biol. 2025; 1468:253-257.
Score: 0.094
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The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1. Nat Commun. 2023 02 21; 14(1):972.
Score: 0.083
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Prph2 disease mutations lead to structural and functional defects in the RPE. FASEB J. 2022 05; 36(5):e22284.
Score: 0.078
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The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases. Cells. 2020 03 24; 9(3).
Score: 0.068
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Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization. Commun Biol. 2023 09 12; 6(1):933.
Score: 0.022