Mirna Mustapha

Affiliations: 
Stanford University, Palo Alto, CA 
Area:
Otolaryngology
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"Mirna Mustapha"
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Publications

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Mehawej C, Chouery E, Azar-Atallah S, et al. (2023) POLD3 deficiency is associated with severe combined immunodeficiency, neurodevelopmental delay, and hearing impairment. Clinical Immunology (Orlando, Fla.). 109326
Grandi FC, Tomasi LD, Mustapha M. (2020) Single-Cell RNA Analysis of Type I Spiral Ganglion Neurons Reveals a Lmx1a Population in the Cochlea. Frontiers in Molecular Neuroscience. 13: 83
Amor DJ, Stephenson SEM, Mustapha M, et al. (2019) Pathogenic Variants in GPC4 Cause Keipert Syndrome. American Journal of Human Genetics
Smeriglio P, Wangsawihardja FV, Leu R, et al. (2019) TSP1 and TSP2 Have Unique and Overlapping Roles in Protecting against Noise-Induced Auditory Synaptopathy. Neuroscience
Johnson SL, Safieddine S, Mustapha M, et al. (2019) Hair Cell Afferent Synapses: Function and Dysfunction. Cold Spring Harbor Perspectives in Medicine
Heimsath EG, Yim YI, Mustapha M, et al. (2017) Myosin-X knockout is semi-lethal and demonstrates that myosin-X functions in neural tube closure, pigmentation, hyaloid vasculature regression, and filopodia formation. Scientific Reports. 7: 17354
Sundaresan S, Balasubbu S, Mustapha M. (2015) Thyroid hormone is required for the pruning of afferent type II spiral ganglion neurons in the mouse cochlea. Neuroscience
Sundaresan S, Kong JH, Fang Q, et al. (2015) Thyroid hormone is required for pruning, functioning and long-term maintenance of afferent inner hair cell synapses. The European Journal of Neuroscience
Fang Q, Indzhykulian AA, Mustapha M, et al. (2015) The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing. Elife. 4
Calton MA, Lee D, Sundaresan S, et al. (2014) A lack of immune system genes causes loss in high frequency hearing but does not disrupt cochlear synapse maturation in mice. Plos One. 9: e94549
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