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Hasan MM, Konishi S, Tanaka M, Izawa T, Yamate J, Kuwamura M.  2023. Disrupted neurogenesis, gliogenesis, and ependymogenesis in the <i>Ccdc85c<\/i> knockout rat for hydrocephalus model. <i>Cells Dev<\/i> 175: 203858.","DOI":"10.1016\/j.cdev.2023.203858"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Hinz B.  2010. The myofibroblast: paradigm for a mechanically active cell. <i>J Biomech<\/i> 43: 146\u2013155.","DOI":"10.1016\/j.jbiomech.2009.09.020"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Hol EM, Pekny M.  2015. Glial fibrillary acidic protein (GFAP) and the astrocyte intermediate filament system in diseases of the central nervous system. <i>Curr Opin Cell Biol<\/i> 32: 121\u2013130.","DOI":"10.1016\/j.ceb.2015.02.004"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Hou CC, Li D, Berry BC, Zheng S, Carroll RS, Johnson MD, Yang HW.  2023. Heterozygous <i>FOXJ1<\/i> mutations cause incomplete ependymal cell differentiation and communicating hydrocephalus. <i>Cell Mol Neurobiol<\/i> 43: 4103\u20134116.","DOI":"10.1007\/s10571-023-01398-6"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Jannat N, Hasan MM, Tokuno H, Tanaka M, Izawa T, Yamate J, Kuwamura M.  2025. Aberrant alpha-smooth muscle actin expression in the lateral ventricle of <i>Ccdc85C<\/i> knockout rats. <i>Vet Pathol<\/i> 62: 364\u2013370.","DOI":"10.1177\/03009858241312611"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Konishi S, Tanaka N, Mashimo T, Yamamoto T, Sakuma T, Kaneko T, Tanaka M, Izawa T, Yamate J, Kuwamura M.  2020. Pathological characteristics of <i>Ccdc85c<\/i> knockout rats: a rat model of genetic hydrocephalus. <i>Exp Anim<\/i> 69: 26\u201333.","DOI":"10.1538\/expanim.19-0005"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Kuwamura M, Kinoshita A, Okumoto M, Yamate J, Mori N.  2004. Hemorrhagic hydrocephalus (<i>hhy<\/i>): a novel mutation on mouse chromosome 12. <i>Brain Res Dev Brain Res<\/i> 152: 69\u201372.","DOI":"10.1016\/j.devbrainres.2004.05.006"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Makihara N, Arimura K, Ago T, Tachibana M, Nishimura A, Nakamura K, Matsuo R, Wakisaka Y, Kuroda J, Sugimori H, Kamouchi M, Kitazono T.  2015. Involvement of platelet-derived growth factor receptor \u03b2 in fibrosis through extracellular matrix protein production after ischemic stroke. <i>Exp Neurol<\/i> 264: 127\u2013134.","DOI":"10.1016\/j.expneurol.2014.12.007"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Mori N, Kuwamura M, Tanaka N, Hirano R, Nabe M, Ibuki M, Yamate J.  2012. <i>Ccdc85c<\/i> encoding a protein at apical junctions of radial glia is disrupted in hemorrhagic hydrocephalus (<i>hhy<\/i>) mice. <i>Am J Pathol<\/i> 180: 314\u2013327.","DOI":"10.1016\/j.ajpath.2011.09.014"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Morimoto Y, Yoshida S, Kinoshita A, Satoh C, Mishima H, Yamaguchi N, Matsuda K, Sakaguchi M, Tanaka T, Komohara Y, Imamura A, Ozawa H, Nakashima M, Kurotaki N, Kishino T, Yoshiura KI, Ono S.  2019. Nonsense mutation in <i>CFAP43<\/i> causes normal-pressure hydrocephalus with ciliary abnormalities. <i>Neurology<\/i> 92: e2364\u2013e2374.","DOI":"10.1212\/WNL.0000000000007505"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Okamoto N, Wada Y, Kawabata H, Ishikiriyama S, Takahashi S.  1996. 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In: Pediatric Hydrocephalus (Cinalli G, \u00d6zek M, Sainte-Rose C eds.), Springer, Cham.","DOI":"10.1007\/978-3-319-27250-4_36"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Shapiro AJ, Kaspy K, Daniels MLA, Stonebraker JR, Nguyen VH, Joyal L, Knowles MR, Zariwala MA.  2021. Autosomal dominant variants in <i>FOXJ1<\/i> causing primary ciliary dyskinesia in two patients with obstructive hydrocephalus. <i>Mol Genet Genomic Med<\/i> 9: e1726.","DOI":"10.1002\/mgg3.1726"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Sharma V, Ling TW, Rewell SS, Hare DL, Howells DW, Kourakis A, Wookey PJ.  2012. A novel population of \u03b1-smooth muscle actin-positive cells activated in a rat model of stroke: an analysis of the spatio-temporal distribution in response to ischemia. <i>J Cereb Blood Flow Metab<\/i> 32: 2055\u20132065.","DOI":"10.1038\/jcbfm.2012.107"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Silson M, Robinson R.  1969. Hereditary hydrocephalus in the cat. <i>Vet Rec<\/i> 84: 477.","DOI":"10.1136\/vr.84.19.477"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Takano T, Rutka JT, Becker LE.  1996. Overexpression of nestin and vimentin in ependymal cells in hydrocephalus. <i>Acta Neuropathol<\/i> 92: 90\u201397.","DOI":"10.1007\/s004010050493"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Talele NP, Fradette J, Davies JE, Kapus A, Hinz B.  2015. Expression of \u03b1-smooth muscle actin determines the fate of mesenchymal stromal cells. <i>Stem Cell Reports<\/i> 4: 1016\u20131030.","DOI":"10.1016\/j.stemcr.2015.05.004"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Tully HM, Dobyns WB.  2014. Infantile hydrocephalus: a review of epidemiology, classification and causes. <i>Eur J Med Genet<\/i> 57: 359\u2013368.","DOI":"10.1016\/j.ejmg.2014.06.002"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Wallmeier J, Frank D, Shoemark A, N\u00f6the-Menchen T, Cindric S, Olbrich H, Loges NT, Aprea I, Dougherty GW, Pennekamp P, Kaiser T, Mitchison HM, Hogg C, Carr SB, Zariwala MA, Ferkol T, Leigh MW, Davis SD, Atkinson J, Dutcher SK, Knowles MR, Thiele H, Altm\u00fcller J, Krenz H, W\u00f6ste M, Brentrup A, Ahrens F, Vogelberg C, Morris-Rosendahl DJ, Omran H.  2019. 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