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Items: 1 to 20 of 37

1.

The role of GABAB receptors in the vestibular oculomotor system in mice.

Shimizu N, Wood S, Kushiro K, Perachio A, Makishima T.

Behav Brain Res. 2016 Apr 1;302:152-9. doi: 10.1016/j.bbr.2016.01.017. Epub 2016 Jan 8.

PMID:
26778789
2.

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.

J Virol. 2015 Dec 30;90(6):2920-7. doi: 10.1128/JVI.02948-15.

3.

Preserved otolith organ function in caspase-3-deficient mice with impaired horizontal semicircular canal function.

Armstrong PA, Wood SJ, Shimizu N, Kuster K, Perachio A, Makishima T.

Exp Brain Res. 2015 Jun;233(6):1825-35. doi: 10.1007/s00221-015-4254-4. Epub 2015 Apr 1.

4.

Dynamic characteristics of otolith ocular response during counter rotation about dual yaw axes in mice.

Shimizu N, Wood S, Kushiro K, Yanai S, Perachio A, Makishima T.

Neuroscience. 2015 Jan 29;285:204-14. doi: 10.1016/j.neuroscience.2014.11.022. Epub 2014 Nov 20.

5.

Encapsulation of poorly water-soluble drugs into organic nanotubes for improving drug dissolution.

Moribe K, Makishima T, Higashi K, Liu N, Limwikrant W, Ding W, Masuda M, Shimizu T, Yamamoto K.

Int J Pharm. 2014 Jul 20;469(1):190-6. doi: 10.1016/j.ijpharm.2014.04.005. Epub 2014 Apr 16.

PMID:
24746412
6.

Phialemonium infection complicating chronic suppurative otitis media.

Pong DL, Marom T, Makishima T.

Med Mycol Case Rep. 2014 Jan 27;4:5-7. doi: 10.1016/j.mmcr.2014.01.001. eCollection 2014 Apr.

7.

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.

J Clin Invest. 2011 Dec;121(12):4796-809. doi: 10.1172/JCI60405. Epub 2011 Nov 21.

8.

Inner ear dysfunction in caspase-3 deficient mice.

Makishima T, Hochman L, Armstrong P, Rosenberger E, Ridley R, Woo M, Perachio A, Wood S.

BMC Neurosci. 2011 Oct 12;12:102. doi: 10.1186/1471-2202-12-102.

9.

Topology of transmembrane channel-like gene 1 protein.

Labay V, Weichert RM, Makishima T, Griffith AJ.

Biochemistry. 2010 Oct 5;49(39):8592-8. doi: 10.1021/bi1004377. Epub 2010 Sep 8.

10.

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.

Int J Pediatr Otorhinolaryngol. 2009 Nov;73(11):1564-7. doi: 10.1016/j.ijporl.2009.08.005. Epub 2009 Sep 3.

11.

Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss.

Kelly B, Lozano A, Altenberg G, Makishima T.

Int J Dermatol. 2008 May;47(5):443-7. doi: 10.1111/j.1365-4632.2008.03603.x.

PMID:
18412859
12.

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.

Ear Hear. 2007 Dec;28(6):831-41.

PMID:
17982369
13.

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.

Clin Genet. 2007 Dec;72(6):546-50. Epub 2007 Sep 17.

PMID:
17877751
14.

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ.

Am J Med Genet A. 2007 Jul 15;143A(14):1592-8.

PMID:
17567890
15.
16.

Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.

Noguchi Y, Kurima K, Makishima T, de Angelis MH, Fuchs H, Frolenkov G, Kitamura K, Griffith AJ.

Genetics. 2006 Aug;173(4):2111-9. Epub 2006 Apr 28.

17.

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.

Hum Genet. 2005 Oct;118(1):29-34. Epub 2005 Oct 28.

PMID:
16078052
18.

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

Makishima T, Kurima K, Brewer CC, Griffith AJ.

Otol Neurotol. 2004 Sep;25(5):714-9.

PMID:
15354000
20.

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, Menon PS, Deshmukh D, Griffith AJ, Riazuddin S, Friedman TB, Wilcox ER.

Hum Genet. 2002 Jun;110(6):527-31. Epub 2002 May 3.

PMID:
12107438
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