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Items: 1 to 20 of 37

1.

A simple microfluidic device for live-imaging of the vertical section of epithelial cells.

Araki S, Nakano M, Tsugane M, Sunaga F, Hattori M, Nakano M, Nagai T, Suzuki H.

Analyst. 2019 Dec 4. doi: 10.1039/c9an02165e. [Epub ahead of print]

PMID:
31799546
2.

Cooperative interaction among BMAL1, HSF1, and p53 protects mammalian cells from UV stress.

Kawamura G, Hattori M, Takamatsu K, Tsukada T, Ninomiya Y, Benjamin I, Sassone-Corsi P, Ozawa T, Tamaru T.

Commun Biol. 2018 Nov 22;1:204. doi: 10.1038/s42003-018-0209-1. eCollection 2018.

3.

A genetic screen to discover SUMOylated proteins in living mammalian cells.

Komiya M, Ito A, Endo M, Hiruma D, Hattori M, Saitoh H, Yoshida M, Ozawa T.

Sci Rep. 2017 Dec 12;7(1):17443. doi: 10.1038/s41598-017-17450-7.

4.

Spatiotemporal analysis with a genetically encoded fluorescent RNA probe reveals TERRA function around telomeres.

Yamada T, Yoshimura H, Shimada R, Hattori M, Eguchi M, Fujiwara TK, Kusumi A, Ozawa T.

Sci Rep. 2016 Dec 13;6:38910. doi: 10.1038/srep38910.

5.

Bioluminescent Indicator for Highly Sensitive Analysis of Estrogenic Activity in a Cell-Based Format.

Takenouchi O, Kanno A, Takakura H, Hattori M, Ozawa T.

Bioconjug Chem. 2016 Nov 16;27(11):2689-2694. Epub 2016 Oct 18.

PMID:
27690388
6.

Live Cell Bioluminescence Imaging in Temporal Reaction of G Protein-Coupled Receptor for High-Throughput Screening and Analysis.

Hattori M, Ozawa T.

Methods Mol Biol. 2016;1461:195-202. doi: 10.1007/978-1-4939-3813-1_16.

PMID:
27424906
7.

Confocal Bioluminescence Imaging for Living Tissues with a Caged Substrate of Luciferin.

Hattori M, Kawamura G, Kojima R, Kamiya M, Urano Y, Ozawa T.

Anal Chem. 2016 Jun 21;88(12):6231-8. doi: 10.1021/acs.analchem.5b04142. Epub 2016 Jun 2.

PMID:
27216493
8.

CRY Drives Cyclic CK2-Mediated BMAL1 Phosphorylation to Control the Mammalian Circadian Clock.

Tamaru T, Hattori M, Honda K, Nakahata Y, Sassone-Corsi P, van der Horst GT, Ozawa T, Takamatsu K.

PLoS Biol. 2015 Nov 12;13(11):e1002293. doi: 10.1371/journal.pbio.1002293. eCollection 2015.

9.

Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.

Tsukada K, Nishio SY, Hattori M, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:61S-76S. doi: 10.1177/0003489415575060. Review.

PMID:
25999548
11.

Demonstration of pollinator-mediated competition between two native Impatiens species, Impatiens noli-tangere and I. textori (Balsaminaceae).

Tokuda N, Hattori M, Abe K, Shinohara Y, Nagano Y, Itino T.

Ecol Evol. 2015 Mar;5(6):1271-7. doi: 10.1002/ece3.1431. Epub 2015 Feb 25.

12.

Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.

Nishio SY, Hattori M, Moteki H, Tsukada K, Miyagawa M, Naito T, Yoshimura H, Iwasa Y, Mori K, Shima Y, Sakuma N, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:6S-48S. doi: 10.1177/0003489415575549. Epub 2015 Mar 26. Review.

PMID:
25814645
13.

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.

Miyagawa M, Nishio SY, Hattori M, Moteki H, Kobayashi Y, Sato H, Watanabe T, Naito Y, Oshikawa C, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:158S-68S. doi: 10.1177/0003489415575058. Epub 2015 Mar 19.

PMID:
25792667
14.

Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritance.

Ichinose A, Moteki H, Hattori M, Nishio SY, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:142S-7S. doi: 10.1177/0003489415575043. Epub 2015 Mar 18.

PMID:
25788562
15.

Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.

Moteki H, Azaiez H, Booth KT, Hattori M, Sato A, Sato Y, Motobayashi M, Sloan CM, Kolbe DL, Shearer AE, Smith RJ, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:177S-83S. doi: 10.1177/0003489415575045. Epub 2015 Mar 18.

16.

Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients.

Iwasa Y, Moteki H, Hattori M, Sato R, Nishio SY, Takumi Y, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:111S-7S. doi: 10.1177/0003489415575044. Epub 2015 Mar 16.

PMID:
25780254
17.

Germinal mosaicism in a family with BO syndrome.

Miyagawa M, Nishio SY, Hattori M, Takumi Y, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:118S-22S. doi: 10.1177/0003489415575062. Epub 2015 Mar 16.

PMID:
25780253
18.

Detailed hearing and vestibular profiles in the patients with COCH mutations.

Tsukada K, Ichinose A, Miyagawa M, Mori K, Hattori M, Nishio SY, Naito Y, Kitajiri S, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:100S-10S. doi: 10.1177/0003489415573074. Epub 2015 Mar 16.

PMID:
25780252
19.

The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.

Miyagawa M, Nishio SY, Sakurai Y, Hattori M, Tsukada K, Moteki H, Kojima H, Usami S.

Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:193S-204S. doi: 10.1177/0003489415575056. Epub 2015 Mar 13.

PMID:
25770132
20.

Simultaneous time-lamination imaging of protein association using a split fluorescent timer protein.

Takamura A, Hattori M, Yoshimura H, Ozawa T.

Anal Chem. 2015 Mar 17;87(6):3366-72. doi: 10.1021/ac504583t. Epub 2015 Feb 26.

PMID:
25679333

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