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MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss.
Bademci G, Abad C, Incesulu A, Rad A, Alper O, Kolb SM, Cengiz FB, Diaz-Horta O, Silan F, Mihci E, Ocak E, Najafi M, Maroofian R, Yilmaz E, Nur BG, Duman D, Guo S, Sant DW, Wang G, Monje PV, Haaf T, Blanton SH, Vona B, Walz K, Tekin M. Bademci G, et al. Among authors: monje pv. Hum Genet. 2018 Jul;137(6-7):479-486. doi: 10.1007/s00439-018-1901-4. Epub 2018 Jul 7. Hum Genet. 2018. PMID: 29982980 Free PMC article.
Oscillatory cAMP signaling rapidly alters H3K4 methylation.
Huff TC, Camarena V, Sant DW, Wilkes Z, Van Booven D, Aron AT, Muir RK, Renslo AR, Chang CJ, Monje PV, Wang G. Huff TC, et al. Among authors: monje pv. Life Sci Alliance. 2019 Dec 27;3(1):e201900529. doi: 10.26508/lsa.201900529. Print 2020 Jan. Life Sci Alliance. 2019. PMID: 31882444 Free PMC article.
Fluorescent Detection of Merlin-deficient Schwann Cells and Primary Human Vestibular Schwannoma Cells Using Sodium Fluorescein.
Perez ER, Bracho O, Ein L, Szczupak M, Monje PV, Fernandez-Valle C, Alshaiji A, Ivan M, Morcos J, Liu XZ, Hoffer M, Eshraghi A, Angeli S, Telischi F, Dinh CT. Perez ER, et al. Among authors: monje pv. Otol Neurotol. 2018 Sep;39(8):1053-1059. doi: 10.1097/MAO.0000000000001895. Otol Neurotol. 2018. PMID: 30001282 Free PMC article.
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