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For: Morell RJ, Olszewski R, Tona R, Leitess S, Wafa TT, Taukulis I, Schultz JM, Thomason EJ, Richards K, Whitley BN, Hill C, Saunders T, Starost MF, Fitzgerald T, Wilson E, Ohyama T, Friedman TB, Hoa M. Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39. J Neurosci 2020;40:2976-92. [PMID: 32152201 DOI: 10.1523/JNEUROSCI.2278-19.2020] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Naz S. Molecular genetic landscape of hereditary hearing loss in Pakistan. Hum Genet 2021. [PMID: 34308486 DOI: 10.1007/s00439-021-02320-0] [Reference Citation Analysis]
2 Shuster B, Casserly R, Lipford E, Olszewski R, Milon B, Viechweg S, Davidson K, Enoch J, McMurray M, Rutherford MA, Ohlemiller KK, Hoa M, Depireux DA, Mong JA, Hertzano R. Estradiol Protects against Noise-Induced Hearing Loss and Modulates Auditory Physiology in Female Mice. Int J Mol Sci 2021;22:12208. [PMID: 34830090 DOI: 10.3390/ijms222212208] [Reference Citation Analysis]
3 Taukulis IA, Olszewski RT, Korrapati S, Fernandez KA, Boger ET, Fitzgerald TS, Morell RJ, Cunningham LL, Hoa M. Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene Targets. Front Mol Neurosci 2021;14:718241. [PMID: 34566577 DOI: 10.3389/fnmol.2021.718241] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Fu J, Su X, Li Z, Deng L, Liu X, Feng X, Peng J. HGF/c-MET pathway in cancer: from molecular characterization to clinical evidence. Oncogene 2021;40:4625-51. [PMID: 34145400 DOI: 10.1038/s41388-021-01863-w] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Nicolson T. Navigating Hereditary Hearing Loss: Pathology of the Inner Ear. Front Cell Neurosci 2021;15:660812. [PMID: 34093131 DOI: 10.3389/fncel.2021.660812] [Reference Citation Analysis]
6 Renauld JM, Khan V, Basch ML. Intermediate Cells of Dual Embryonic Origin Follow a Basal to Apical Gradient of Ingression Into the Lateral Wall of the Cochlea. Front Cell Dev Biol 2022;10:867153. [PMID: 35372344 DOI: 10.3389/fcell.2022.867153] [Reference Citation Analysis]
7 Gu S, Olszewski R, Taukulis I, Wei Z, Martin D, Morell RJ, Hoa M. Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea. Sci Rep 2020;10:18100. [PMID: 33093630 DOI: 10.1038/s41598-020-75238-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
8 Avraham KB, Khalaily L, Noy Y, Kamal L, Koffler-Brill T, Taiber S. The noncoding genome and hearing loss. Hum Genet 2021. [PMID: 34491412 DOI: 10.1007/s00439-021-02359-z] [Reference Citation Analysis]
9 Mei X, Zhou Y, Amjad M, Yang W, Zhu R, Asif M, Hussain HMJ, Yang T, Iqbal F, Hu H. Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. Neural Plast 2021;2021:5528434. [PMID: 33976695 DOI: 10.1155/2021/5528434] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Renauld JM, Basch ML. Congenital Deafness and Recent Advances Towards Restoring Hearing Loss. Curr Protoc 2021;1:e76. [PMID: 33780161 DOI: 10.1002/cpz1.76] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Gu S, Olszewski R, Nelson L, Gallego-Martinez A, Lopez-Escamez JA, Hoa M. Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis. Front Neurol 2021;12:630561. [PMID: 33613436 DOI: 10.3389/fneur.2021.630561] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
12 Tona R, Lopez IA, Fenollar-Ferrer C, Faridi R, Anselmi C, Khan AA, Shahzad M, Morell RJ, Gu S, Hoa M, Dong L, Ishiyama A, Belyantseva IA, Riazuddin S, Friedman TB. Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness. Genes (Basel) 2020;11:E1122. [PMID: 32987832 DOI: 10.3390/genes11101122] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 2.5] [Reference Citation Analysis]
13 Kremer H. Novel gene discovery for hearing loss and other routes to increased diagnostic rates. Hum Genet 2021. [PMID: 34599370 DOI: 10.1007/s00439-021-02374-0] [Reference Citation Analysis]