Structure, mechanics and material properties of claw cuticle from mole cricket Gryllotalpaorientalis von Zhang, Zhifeng, Zhang, Yan, Zhang, Junxia, Zhu, Yueying

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Imperfect and askew: A review of asymmetric genitalia in araneomorph spiders (Araneae: Araneomorphae) von Rivera-Quiroz, Francisco Andres, Schilthuizen, Menno, Petcharad, Booppa, Miller, Jeremy A

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Long-term in vivo cochlear transgene expression mediated by recombinant adeno-associated virus von LALWANI, A. K, WALSH, B. J, REILLY, P. G, CARVALHO, G. J, ZOLOTUKHIN, S, MUZYCZKA, N, MHATRE, A. N

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Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9 von Lalwani, Anil K., Goldstein, Jayne A., Kelley, Michael J., Luxford, William, Castelein, Caley M., Mhatre, Anand N.

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Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment von Mhatre, AN, Weld, E, Lalwani, AK

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Wastewater Testing and Detection of Poliovirus Type 2 Genetically Linked to Virus Isolated from a Paralytic Polio Case - New York, March 9-October 11, 2022 von Ryerson, A Blythe, Lang, Daniel, Alazawi, Mohammed A, Neyra, Milagros, Hill, Dustin T, St George, Kirsten, Fuschino, Meghan, Lutterloh, Emily, Backenson, Bryon, Rulli, Samuel, Ruppert, Patricia Schnabel, Lawler, Jacqueline, McGraw, Nancy, Knecht, Andrew, Gelman, Irina, Zucker, Jane R, Omoregie, Enoma, Kidd, Sarah, Sugerman, David E, Jorba, Jaume, Gerloff, Nancy, Ng, Terry Fei Fan, Lopez, Adriana, Masters, Nina B, Leung, Jessica, Burns, Cara C, Routh, Janell, Bialek, Stephanie R, Oberste, M Steven, Rosenberg, Eli S

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Cochlear gene delivery through an intact round window membrane in mouse von JERO, Jussi, MHATRE, Anand N, TSENG, Charles J, STERN, Ryan E, COLING, Donald E, GOLDSTEIN, Jayne A, KEELUNG HONG, WEI WEN ZHENG, HOQUE, A. T. M. Shamsul, LALWANI, Anil K

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MYH9 mutant alleles: Effects upon MDA-MB-231 cell phenotype von Wei, Calvin, Lalwani, Anil, Mhatre, An

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Localization in stereocilia, plasma membrane, and mitochondria suggests diverse roles for NMHC-IIa within cochlear hair cells von Lalwani, Anil K, Atkin, Graham, Li, Yan, Lee, Jennifer Y, Hillman, Dean E, Mhatre, Anand N

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Aquaporin 4 expression in the mammalian inner ear and its role in hearing von Mhatre, Anand N, Stern, Ryan E, Li, Jiang, Lalwani, Anil K

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Windows Server 2012 R2 administrator cookbook: over 80 hands-on recipes to effectively administer and manage your Windows Server 2012 R2 infrastructure in enterprise environments von Krause, Jordan

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Reduced transcriptional regulatory competence of the androgen receptor in X-linked spinal and bulbar muscular atrophy von Mhatre, Anand N, Trifiro, Mark A, Kaufman, Morris, Kazemi-Esfarjani, Parsa, Figlewicz, Denise, Rouleau, Guy, Pinsky, Leonard

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Effect of SOD1 overexpression on age- and noise-related hearing loss von Coling, Donald E, Yu, Kenneth C.Y, Somand, David, Satar, Bulent, Bai, Uma, Huang, Ting-Ting, Seidman, Michael D, Epstein, Charles J, Mhatre, Anand N, Lalwani, Anil K

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Detection of Fungi in the Nasal Mucosa Using Polymerase Chain Reaction von Catten, Michael D., Murr, Andrew H., Goldstein, Jayne A., Mhatre, Anand N., Lalwani, Anil K.

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Safety of Adeno-Associated Virus as Cochlear Gene Transfer Vector: Analysis of Distant Spread Beyond Injected Cochleae von Kho, Soochuen T., Pettis, Robert M., Mhatre, Anand N., Lalwani, Anil K.

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A surgical approach appropriate for targeted cochlear gene therapy in the mouse von JERO, Jussi, TSENG, Charles J, MHATRE, Anand N, LALWANI, Anil K

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Aquaporin-2 expression in the mammalian cochlea and investigation of its role in Meniere’s disease von Mhatre, Anand N, Jero, Jussi, Chiappini, Ilaria, Bolasco, Giulia, Barbara, Maurizio, Lalwani, Anil K

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Transgene expression in the guinea pig cochlea mediated by a lentivirus-derived gene transfer vector von HAN, J. J, MHATRE, A. N, WAREING, M, PETTIS, R, GAO, W.-Q, ZUFFEREY, R. N, TRONO, D, LALWANI, A. K

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Audiologic Testing and Molecular Analysis of 12S rRNA in Patients Receiving Aminoglycosides von Gürtler, Nicolas, Schmuziger, Nicolas, Kim, Yuil, Mhatre, Anand N., Jungi, Manuel, Lalwani, Anil K.

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SDHB, SDHC, and SDHD mutation screen in sporadic and familial head and neck paragangliomas von Mhatre, AN, Li, Y, Feng, L, Gasperin, A, Lalwani, AK

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