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Lars Tebbe

TitleResearch Assistant Professor
InstitutionUniversity of Houston
DepartmentBiomedical Engineering
Address4800 Calhoun Rd
Houston TX 77004
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Tebbe L, Al-Ubaidi MR, Naash MI. 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. PMID: 39930205.
      Citations:    Fields:    
    2. Crane R, Makia MS, Zeibak S, Tebbe L, Ikele L, Woods CR, Conley SM, Acharya G, Naash MI, Al-Ubaidi MR. Effective intravitreal gene delivery to retinal pigment epithelium with hyaluronic acid nanospheres. Mol Ther Nucleic Acids. 2024 Jun 11; 35(2):102222. PMID: 38868364; PMCID: PMC11168490.
      Citations: 2     
    3. Tebbe L, Kakakhel M, Al-Ubaidi MR, Naash MI. The role of syntaxins in retinal function and health. Front Cell Neurosci. 2024; 18:1380064. PMID: 38799985; PMCID: PMC11119284.
      Citations: 1     
    4. Crane R, Tebbe L, Mwoyosvi ML, Al-Ubaidi MR, Naash MI. 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. PMID: 37700068; PMCID: PMC10497539.
      Citations: 1     Translation:HumansAnimalsCells
    5. Tebbe L, Mwoyosvi ML, Crane R, Makia MS, Kakakhel M, Cosgrove D, Al-Ubaidi MR, Naash MI. The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1. Nat Commun. 2023 02 21; 14(1):972. PMID: 36810733; PMCID: PMC9944904.
      Citations: 3     Fields:    Translation:HumansAnimals
    6. Zhao X, Tebbe L, Naash MI, Al-Ubaidi MR. The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural Retina. Front Pharmacol. 2022; 13:919667. PMID: 35873559; PMCID: PMC9298789.
      Citations: 2     
    7. Tebbe L, Sakthivel H, Makia MS, Kakakhel M, Conley SM, Al-Ubaidi MR, Naash MI. Prph2 disease mutations lead to structural and functional defects in the RPE. FASEB J. 2022 05; 36(5):e22284. PMID: 35344225; PMCID: PMC10599796.
      Citations: 4     Fields:    Translation:HumansCells
    8. Kakakhel M, Tebbe L, Makia MS, Conley SM, Sherry DM, Al-Ubaidi MR, Naash MI. 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. PMID: 32778589; PMCID: PMC7456102.
      Citations: 15     Fields:    Translation:AnimalsCells
    9. Tebbe L, Kakakhel M, Makia MS, Al-Ubaidi MR, Naash MI. The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases. Cells. 2020 03 24; 9(3). PMID: 32213850; PMCID: PMC7140794.
      Citations: 12     Fields:    Translation:HumansAnimals
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