Co-Authors
This is a "connection" page, showing publications co-authored by Lars Tebbe and Muayyad Al-Ubaidi.
Connection Strength
1.621
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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: 0.246
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Effective intravitreal gene delivery to retinal pigment epithelium with hyaluronic acid nanospheres. Mol Ther Nucleic Acids. 2024 Jun 11; 35(2):102222.
Score: 0.235
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The role of syntaxins in retinal function and health. Front Cell Neurosci. 2024; 18:1380064.
Score: 0.235
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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: 0.216
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The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural Retina. Front Pharmacol. 2022; 13:919667.
Score: 0.207
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Prph2 disease mutations lead to structural and functional defects in the RPE. FASEB J. 2022 05; 36(5):e22284.
Score: 0.204
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The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases. Cells. 2020 03 24; 9(3).
Score: 0.177
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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: 0.056
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Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survival. Proc Natl Acad Sci U S A. 2020 08 25; 117(34):20615-20624.
Score: 0.045