Makishima T - Search Results

1

The Importance of Lassa Fever and Its Disease Management in West Africa.

Reyna RA, Littlefield KE, Shehu N, Makishima T, Maruyama J, Paessler S. Reyna RA, et al. Among authors: makishima t. Viruses. 2024 Feb 7;16(2):266. doi: 10.3390/v16020266. Viruses. 2024. PMID: 38400041 Free PMC article. Review.

2

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

Makishima T, Kurima K, Brewer CC, Griffith AJ. Makishima T, et al. Otol Neurotol. 2004 Sep;25(5):714-9. doi: 10.1097/00129492-200409000-00011. Otol Neurotol. 2004. PMID: 15354000

3

Topology of transmembrane channel-like gene 1 protein.

Labay V, Weichert RM, Makishima T, Griffith AJ. Labay V, et al. Among authors: makishima t. Biochemistry. 2010 Oct 5;49(39):8592-8. doi: 10.1021/bi1004377. Epub 2010 Sep 8. Biochemistry. 2010. PMID: 20672865 Free PMC article.

4

Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.

Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ. Kitajiri SI, et al. Among authors: makishima t. Clin Genet. 2007 Dec;72(6):546-50. doi: 10.1111/j.1399-0004.2007.00895.x. Epub 2007 Sep 17. Clin Genet. 2007. PMID: 17877751

5

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

Makishima T, Rodriguez CI, Robertson NG, Morton CC, Stewart CL, Griffith AJ. Makishima T, et al. Hum Genet. 2005 Oct;118(1):29-34. doi: 10.1007/s00439-005-0001-4. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16078052

6

Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.

Kawashima Y, Géléoc GS, Kurima K, Labay V, Lelli A, Asai Y, Makishima T, Wu DK, Della Santina CC, Holt JR, Griffith AJ. Kawashima Y, et al. Among authors: makishima t. J Clin Invest. 2011 Dec;121(12):4796-809. doi: 10.1172/JCI60405. Epub 2011 Nov 21. J Clin Invest. 2011. PMID: 22105175 Free PMC article.

7

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.

Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF Jr, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ. Kurima K, et al. Among authors: makishima t. Nat Genet. 2002 Mar;30(3):277-84. doi: 10.1038/ng842. Epub 2002 Feb 19. Nat Genet. 2002. PMID: 11850618

8

Otolaryngologic markers for the early diagnosis of Turner syndrome.

Makishima T, King K, Brewer CC, Zalewski CK, Butman J, Bakalov VK, Bondy C, Griffith AJ. Makishima T, et al. Int J Pediatr Otorhinolaryngol. 2009 Nov;73(11):1564-7. doi: 10.1016/j.ijporl.2009.08.005. Epub 2009 Sep 3. Int J Pediatr Otorhinolaryngol. 2009. PMID: 19732968 Free PMC article.

9

Analysis of auditory phenotype and karyotype in 200 females with Turner syndrome.

King KA, Makishima T, Zalewski CK, Bakalov VK, Griffith AJ, Bondy CA, Brewer CC. King KA, et al. Among authors: makishima t. Ear Hear. 2007 Dec;28(6):831-41. doi: 10.1097/AUD.0b013e318157677f. Ear Hear. 2007. PMID: 17982369

10

Animal Model of Sensorineural Hearing Loss Associated with Lassa Virus Infection.

Yun NE, Ronca S, Tamura A, Koma T, Seregin AV, Dineley KT, Miller M, Cook R, Shimizu N, Walker AG, Smith JN, Fair JN, Wauquier N, Bockarie B, Khan SH, Makishima T, Paessler S. Yun NE, et al. Among authors: makishima t. J Virol. 2015 Dec 30;90(6):2920-7. doi: 10.1128/JVI.02948-15. J Virol. 2015. PMID: 26719273 Free PMC article.

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