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Muna Naash

Affiliations: 
University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States 
Area:
Neuroscience Biology, Pathology, Genetics
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"Muna Naash"
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Parents

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Robert E. Anderson grad student

Children

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Shannon M. Conley grad student (BME Tree)
May Nour grad student 2003 University of Oklahoma Health Sciences Center
Heidi M. Stricker grad student 2005 University of Oklahoma Health Sciences Center
Rafal A. Farjo grad student 2006 University of Oklahoma Health Sciences Center
Adarsha Koirala grad student 2012 University of Oklahoma Health Sciences Center

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Publications

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Lewis TR, Makia MS, Castillo CM, et al. (2023) ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Elife. 12
Crane R, Tebbe L, Mwoyosvi ML, et al. (2023) Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganization. Communications Biology. 6: 933
Ikelle L, Makia M, Lewis T, et al. (2023) Correction: Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones. Cellular and Molecular Life Sciences : Cmls. 80: 290
Lewis TR, Makia MS, Castillo CM, et al. (2023) ROM1 is redundant to PRPH2 as a molecular building block of photoreceptor disc rims. Biorxiv : the Preprint Server For Biology
Ikelle L, Makia M, Lewis T, et al. (2023) Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones. Cellular and Molecular Life Sciences : Cmls. 80: 214
Lewis TR, Al-Ubaidi MR, Naash MI, et al. (2023) The Role of Peripherin-2/ROM1 Complexes in Photoreceptor Outer Segment Disc Morphogenesis. Advances in Experimental Medicine and Biology. 1415: 277-281
Tebbe L, Mwoyosvi ML, Crane R, et al. (2023) The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1. Nature Communications. 14: 972
Zhao X, Tebbe L, Naash MI, et al. (2022) The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural Retina. Frontiers in Pharmacology. 13: 919667
Sinha T, Ikelle L, Makia MS, et al. (2022) Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasis. Redox Biology. 54: 102375
Tebbe L, Sakthivel H, Makia MS, et al. (2022) Prph2 disease mutations lead to structural and functional defects in the RPE. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 36: e22284
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