R01 DC012564/DC/NIDCD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2012	1
2013	4
2014	4
2015	14
2016	5
2017	2
2018	4
2019	1
2020	1
2021	2
2023	3
2024	0

1

Dual AAV-based PCDH15 gene therapy achieves sustained rescue of visual function in a mouse model of Usher syndrome 1F.

Riaz S, Sethna S, Duncan T, Naeem MA, Redmond TM, Riazuddin S, Riazuddin S, Carvalho LS, Ahmed ZM. Riaz S, et al. Mol Ther. 2023 Dec 6;31(12):3490-3501. doi: 10.1016/j.ymthe.2023.10.017. Epub 2023 Oct 20. Mol Ther. 2023. PMID: 37864333

2

An Open-Source Tool for Automated Human-Level Circling Behavior Detection.

Stanley OR, Swaminathan A, Wojahn E, Ahmed ZM, Cullen KE. Stanley OR, et al. bioRxiv [Preprint]. 2023 May 30:2023.05.30.540066. doi: 10.1101/2023.05.30.540066. bioRxiv. 2023. PMID: 37398316 Free PMC article. Preprint.

3

Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channels.

Giese APJ, Weng WH, Kindt KS, Chang HHV, Montgomery JS, Ratzan EM, Beirl AJ, Rivera RA, Lotthammer JM, Walujkar S, Foster MP, Zobeiri OA, Holt JR, Riazuddin S, Cullen KE, Sotomayor M, Ahmed ZM. Giese APJ, et al. bioRxiv [Preprint]. 2023 May 30:2023.05.26.542533. doi: 10.1101/2023.05.26.542533. bioRxiv. 2023. PMID: 37398045 Free PMC article. Preprint.

4

Putting the Pieces Together: the Hair Cell Transduction Complex.

Holt JR, Tobin M, Elferich J, Gouaux E, Ballesteros A, Yan Z, Ahmed ZM, Nicolson T. Holt JR, et al. J Assoc Res Otolaryngol. 2021 Dec;22(6):601-608. doi: 10.1007/s10162-021-00808-0. Epub 2021 Oct 6. J Assoc Res Otolaryngol. 2021. PMID: 34617206 Free PMC article. Review.

5

CIB2 regulates mTORC1 signaling and is essential for autophagy and visual function.

Sethna S, Scott PA, Giese APJ, Duncan T, Jian X, Riazuddin S, Randazzo PA, Redmond TM, Bernstein SL, Riazuddin S, Ahmed ZM. Sethna S, et al. Nat Commun. 2021 Jun 23;12(1):3906. doi: 10.1038/s41467-021-24056-1. Nat Commun. 2021. PMID: 34162842 Free PMC article.

6

Myosins and Hearing.

Friedman TB, Belyantseva IA, Frolenkov GI. Friedman TB, et al. Adv Exp Med Biol. 2020;1239:317-330. doi: 10.1007/978-3-030-38062-5_13. Adv Exp Med Biol. 2020. PMID: 32451864 Review.

7

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.

Richard EM, Santos-Cortez RLP, Faridi R, Rehman AU, Lee K, Shahzad M, Acharya A, Khan AA, Imtiaz A, Chakchouk I, Takla C, Abbe I, Rafeeq M, Liaqat K, Chaudhry T, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics; Schrauwen I, Khan SN, Morell RJ, Zafar S, Ansar M, Ahmed ZM, Ahmad W, Riazuddin S, Friedman TB, Leal SM, Riazuddin S. Richard EM, et al. Hum Mutat. 2019 Jan;40(1):53-72. doi: 10.1002/humu.23666. Epub 2018 Nov 18. Hum Mutat. 2019. PMID: 30303587 Free PMC article.

8

Mutations in Diphosphoinositol-Pentakisphosphate Kinase PPIP5K2 are associated with hearing loss in human and mouse.

Yousaf R, Gu C, Ahmed ZM, Khan SN, Friedman TB, Riazuddin S, Shears SB, Riazuddin S. Yousaf R, et al. PLoS Genet. 2018 Mar 28;14(3):e1007297. doi: 10.1371/journal.pgen.1007297. eCollection 2018 Mar. PLoS Genet. 2018. PMID: 29590114 Free PMC article.

9

Inframe deletion of human ESPN is associated with deafness, vestibulopathy and vision impairment.

Ahmed ZM, Jaworek TJ, Sarangdhar GN, Zheng L, Gul K, Khan SN, Friedman TB, Sisk RA, Bartles JR, Riazuddin S, Riazuddin S. Ahmed ZM, et al. J Med Genet. 2018 Jul;55(7):479-488. doi: 10.1136/jmedgenet-2017-105221. Epub 2018 Mar 23. J Med Genet. 2018. PMID: 29572253 Free PMC article.

10

Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.

Yousaf R, Ahmed ZM, Giese AP, Morell RJ, Lagziel A, Dabdoub A, Wilcox ER, Riazuddin S, Friedman TB, Riazuddin S. Yousaf R, et al. J Clin Invest. 2018 Apr 2;128(4):1509-1522. doi: 10.1172/JCI97350. Epub 2018 Mar 12. J Clin Invest. 2018. PMID: 29408807 Free PMC article.

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