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Results: 1 to 20 of 33

1.

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
[PubMed - in process]
2.

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.

PMID:
24596671
[PubMed]
Free PMC Article
3.

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.

PMID:
22105175
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
21988729
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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.

PMID:
20672865
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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.

PMID:
19732968
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

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
[PubMed - indexed for MEDLINE]
8.

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
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

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
[PubMed - indexed for MEDLINE]
11.

A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.

Kitajiri S, Makishima T, Friedman TB, Griffith AJ.

Clin Genet. 2007 Feb;71(2):148-52.

PMID:
17250663
[PubMed - indexed for MEDLINE]
12.

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.

PMID:
16648588
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

Col11a1 and Col11a2 mRNA expression in the developing mouse cochlea: implications for the correlation of hearing loss phenotype with mutant type XI collagen genotype.

Shpargel KB, Makishima T, Griffith AJ.

Acta Otolaryngol. 2004 Apr;124(3):242-8.

PMID:
15141750
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

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.

Nat Genet. 2002 Mar;30(3):277-84. Epub 2002 Feb 19.

PMID:
11850618
[PubMed - indexed for MEDLINE]
18.

Deafness due to degeneration of cochlear neurons in caspase-3-deficient mice.

Morishita H, Makishima T, Kaneko C, Lee YS, Segil N, Takahashi K, Kuraoka A, Nakagawa T, Nabekura J, Nakayama K, Nakayama KI.

Biochem Biophys Res Commun. 2001 Jun 1;284(1):142-9.

PMID:
11374883
[PubMed - indexed for MEDLINE]
19.

A subunit of the mammalian oligosaccharyltransferase, DAD1, interacts with Mcl-1, one of the bcl-2 protein family.

Makishima T, Yoshimi M, Komiyama S, Hara N, Nishimoto T.

J Biochem. 2000 Sep;128(3):399-405.

PMID:
10965038
[PubMed - indexed for MEDLINE]
Free Article
20.

An Arabidopsis thaliana cDNA complementing a hamster apoptosis suppressor mutant.

Gallois P, Makishima T, Hecht V, Despres B, Laudié M, Nishimoto T, Cooke R.

Plant J. 1997 Jun;11(6):1325-31.

PMID:
9225471
[PubMed - indexed for MEDLINE]

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