References
- Geigy CA, Heid S, Steffen F, Danielson K, Jaggy A, Gaillard C. Does a pleiotropic gene explain deafness and blue irises in white cats? Vet J 2007; 173:548-53; PMID:16956778; https://doi.org/10.1016/j.tvjl.2006.07.021
- Heid S, Hartmann R, Klinke R. A model for prelingual deafness, the congenitally deaf white cat–population statistics and degenerative changes. Hear Res 1998; 115:101-12; PMID:9472739; https://doi.org/10.1016/S0378-5955(97)00182-2
- Kral A, Lomber SG. Deaf white cats. Curr Biol 2015; 25:R351-3; PMID:25942543; https://doi.org/10.1016/j.cub.2015.02.040
- Locher H, de Groot JCMJ, van Iperen L, Huisman MA, Frijns JHM, Chuva de Sousa Lopes SM. Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss. Dev Neurobiol 2015; 75:1219-40; PMID:25663387; https://doi.org/10.1002/dneu.22279
- Mair IW, Elverland HH. Hereditary deafness in the cat. An electron microscopic study of the stria vascularis and Reissner's membrane. Arch Otorhinolaryngol 1977; 217:199-217; PMID:303094; https://doi.org/10.1007/BF00665540
- Mayor R, Theveneau E. The neural crest. Development 2013; 140:2247-51; PMID:23674598; https://doi.org/10.1242/dev.091751
- Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S. A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. J Med Genet 2015; 52:548-52; PMID:25941349; https://doi.org/10.1136/jmedgenet-2015-103023
- Naldini L, Weidner KM, Vigna E, Gaudino G, Bardelli A, Ponzetto C, Narsimhan RP, Hartmann G, Zarnegar R, Michalopoulos GK. Scatter factor and hepatocyte growth factor are indistinguishable ligands for the MET receptor. EMBO J 1991; 10:2867-78; PMID:1655405
- Neng L, Zhang F, Kachelmeier A, Shi X. Endothelial cell, pericyte, and perivascular resident macrophage-type melanocyte interactions regulate cochlear intrastrial fluid-blood barrier permeability. J Assoc Res Otolaryngol 2013; 14:175-185; PMID:23247886; https://doi.org/10.1007/s10162-012-0365-9
- Patuzzi R. Ion flow in stria vascularis and the production and regulation of cochlear endolymph and the endolymphatic potential. Hear Res 2011; 277:4-19; PMID:21329750; https://doi.org/10.1016/j.heares.2011.01.010
- Peinado H, Alečković M, Lavotshkin S, Matei I, Costa-Silva B, Moreno-Bueno G, Hergueta-Redondo M, Williams C, García-Santos G, Ghajar C, et al. Melanoma exosomes educate bone marrow progenitor cells toward a pro-metastatic phenotype through MET. Nat Med 2012; 18:883-91; PMID:22635005; https://doi.org/10.1038/nm.2753
- Pingault V, Ente D, Dastot-Le Moal F, Goossens M, Marlin S, Bondurand N. Review and update of mutations causing Waardenburg syndrome. Hum Mutat 2010; 31:391-406; PMID:20127975; https://doi.org/10.1002/humu.21211
- Schultz JM, Khan SN, Ahmed ZM, Riazuddin S, Waryah AM, Chhatre D, Starost MF, Ploplis B, Buckley S, Velásquez D, et al. Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39. Am J Hum Genet 2009; 85:25-39; PMID:19576567; https://doi.org/10.1016/j.ajhg.2009.06.003
- Shibata S, Miwa T, Wu H-H, Levitt P, Ohyama T. Hepatocyte growth factor-c-MET signaling mediates the development of nonsensory structures of the mammalian cochlea and hearing. J Neurosci 2016; 36:8200-09; PMID:27488639; https://doi.org/10.1523/JNEUROSCI.4410-15.2016
- Trusolino L, Bertotti A, Comoglio PM. MET signalling: principles and functions in development, organ regeneration and cancer. Nat Rev Mol Cell Biol 2010; 11:834-48; PMID:21102609; https://doi.org/10.1038/nrm3012
- Waardenburg PJ. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness. Am J Hum Genet 1951; 3:195-253; PMID:14902764
- Zhang W, Dai M, Fridberger A, Hassan A, Degagne J, Neng L, Zhang F, He W, Ren T, Trune D, Auer M, Shi X. Perivascular-resident macrophage-like melanocytes in the inner ear are essential for the integrity of the intrastrial fluid-blood barrier. Proc Natl Acad Sci U S A 2012; 109:10388-93; PMID:22689949; https://doi.org/10.1073/pnas.1205210109