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2010 3
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Page 1
The nature of an ultra-faint galaxy in the cosmic dark ages seen with JWST.
Roberts-Borsani G, Treu T, Chen W, Morishita T, Vanzella E, Zitrin A, Bergamini P, Castellano M, Fontana A, Glazebrook K, Grillo C, Kelly PL, Merlin E, Nanayakkara T, Paris D, Rosati P, Yang L, Acebron A, Bonchi A, Boyett K, Bradač M, Brammer G, Broadhurst T, Calabró A, Diego JM, Dressler A, Furtak LJ, Filippenko AV, Henry A, Koekemoer AM, Leethochawalit N, Malkan MA, Mason C, Mercurio A, Metha B, Pentericci L, Pierel J, Rieck S, Roy N, Santini P, Strait V, Strausbaugh R, Trenti M, Vulcani B, Wang L, Wang X, Windhorst RA. Roberts-Borsani G, et al. Among authors: morishita t. Nature. 2023 Jun;618(7965):480-483. doi: 10.1038/s41586-023-05994-w. Epub 2023 May 17. Nature. 2023. PMID: 37198479 Free article.
Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.
Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K. Nozu K, et al. Among authors: morishita t. J Hum Genet. 2017 Jul;62(7):733-735. doi: 10.1038/jhg.2017.28. Epub 2017 Mar 9. J Hum Genet. 2017. PMID: 28275241
Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion.
Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K. Morisada N, et al. Among authors: morishita t. Pediatr Nephrol. 2010 Jul;25(7):1343-8. doi: 10.1007/s00467-010-1445-x. Epub 2010 Feb 4. Pediatr Nephrol. 2010. PMID: 20130917