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Results: 1 to 20 of 907

1.

Biodegradation of bisphenol A by an algal-bacterial system.

Eio EJ, Kawai M, Niwa C, Ito M, Yamamoto S, Toda T.

Environ Sci Pollut Res Int. 2015 May 28. [Epub ahead of print]

PMID:
26013738
2.

The Msd1-Wdr8-Pkl1 complex anchors microtubule minus ends to fission yeast spindle pole bodies.

Yukawa M, Ikebe C, Toda T.

J Cell Biol. 2015 May 25;209(4):549-62. doi: 10.1083/jcb.201412111. Epub 2015 May 18.

PMID:
25987607
3.

Distinct cardiac phenotype between two homozygotes born in a village with accumulation of a genetic deficiency of adipose triglyceride lipase.

Higashi M, Hirano KI, Kobayashi K, Ikeda Y, Issiki A, Otsuka T, Suzuki A, Yamaguchi S, Zaima N, Hamada S, Hanada H, Suzuki C, Nakamura H, Nagasaka H, Miyata T, Miyamoto Y, Kobayashi K, Naito H, Toda T.

Int J Cardiol. 2015 May 6;192:30-32. doi: 10.1016/j.ijcard.2015.05.004. [Epub ahead of print] No abstract available.

PMID:
25985012
4.

Variants associated with Gaucher disease in multiple system atrophy.

Mitsui J, Matsukawa T, Sasaki H, Yabe I, Matsushima M, Dürr A, Brice A, Takashima H, Kikuchi A, Aoki M, Ishiura H, Yasuda T, Date H, Ahsan B, Iwata A, Goto J, Ichikawa Y, Nakahara Y, Momose Y, Takahashi Y, Hara K, Kakita A, Yamada M, Takahashi H, Onodera O, Nishizawa M, Watanabe H, Ito M, Sobue G, Ishikawa K, Mizusawa H, Kanai K, Hattori T, Kuwabara S, Arai K, Koyano S, Kuroiwa Y, Hasegawa K, Yuasa T, Yasui K, Nakashima K, Ito H, Izumi Y, Kaji R, Kato T, Kusunoki S, Osaki Y, Horiuchi M, Kondo T, Murayama S, Hattori N, Yamamoto M, Murata M, Satake W, Toda T, Filla A, Klockgether T, Wüllner U, Nicholson G, Gilman S, Tanner CM, Kukull WA, Stern MB, Lee VM, Trojanowski JQ, Masliah E, Low PA, Sandroni P, Ozelius LJ, Foroud T, Tsuji S.

Ann Clin Transl Neurol. 2015 Apr;2(4):417-26. doi: 10.1002/acn3.185. Epub 2015 Feb 28.

5.

Centriolar satellites- and hMsd1/SSX2IP-dependent microtubule anchoring is critical for centriole assembly.

Hori A, Peddie CJ, Collinson LM, Toda T.

Mol Biol Cell. 2015 Apr 1. pii: mbc.E14-11-1561. [Epub ahead of print]

PMID:
25833712
6.

ABCG2 variant has opposing effects on onset ages of Parkinson's disease and gout.

Matsuo H, Tomiyama H, Satake W, Chiba T, Onoue H, Kawamura Y, Nakayama A, Shimizu S, Sakiyama M, Funayama M, Nishioka K, Shimizu T, Kaida K, Kamakura K, Toda T, Hattori N, Shinomiya N.

Ann Clin Transl Neurol. 2015 Mar;2(3):302-6. doi: 10.1002/acn3.167. Epub 2015 Jan 19.

7.

Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients.

Yang H, Kobayashi K, Wang S, Jiao H, Xiao J, Toda T, Wu X, Xiong H.

Brain Dev. 2015 Mar 23. pii: S0387-7604(15)00035-2. doi: 10.1016/j.braindev.2015.02.010. [Epub ahead of print]

PMID:
25814170
8.

[A case of true neurogenic thoracic outlet syndrome accompanied by an aberrant right subclavian artery].

Sekiguchi K, Saito T, Yokota I, Kowa H, Kanda F, Toda T.

Rinsho Shinkeigaku. 2015;55(3):155-9. doi: 10.5692/clinicalneurol.55.155. Japanese.

PMID:
25786751
9.

[Medial longitudinal fasciculus (MLF) syndrome in a patient with giant cell arteritis].

Uenaka T, Hamaguchi H, Sekiguchi K, Kowa H, Kanda F, Toda T.

Rinsho Shinkeigaku. 2015;55(2):107-10. doi: 10.5692/clinicalneurol.55.107. Japanese.

PMID:
25746074
10.

[A case of neurologic muscle weakness, ataxia, and retinitis pigmentosa (NARP) syndrome with a novel mitochondrial mutation m.8729 G>A].

Miyawaki T, Koto S, Ishihara H, Goto Y, Nishino I, Kanda F, Toda T.

Rinsho Shinkeigaku. 2015;55(2):91-5. doi: 10.5692/clinicalneurol.55.91. Japanese.

PMID:
25746071
11.

Successful recovery from an acute kidney injury due to amniotic fluid embolism.

Ihara K, Naito S, Okado T, Rai T, Mori Y, Toda T, Uchida S, Sasaki S, Matsui N.

Intern Med. 2015;54(1):49-54. doi: 10.2169/internalmedicine.54.2348. Epub 2015 Jan 1.

12.

Comparison between Long- and Short-Acting Erythropoiesis-Stimulating Agents in the Period Required for Haemoglobin Stabilisation in Treatment of Anaemia in Patients with Chronic Kidney Disease.

Hayashi T, Nagamatsu T, Matsushita A, Mizuno T, Nishibe S, Noguchi A, Kato R, Toda T, Tanaka J, Takahashi H, Hayashi H, Yuzawa Y, Yamada S.

Biol Pharm Bull. 2015 May 1;38(5):740-5. doi: 10.1248/bpb.b14-00844. Epub 2015 Feb 25.

13.

Genetic testing for spinocerebellar ataxias in patients diagnosed as Parkinson's disease in Bangladesh.

Rahman MS, Sarkar MA, Rahman MF, Paul SK, Nagai SY, Uddin MJ, Toda T.

Mymensingh Med J. 2015 Jan;24(1):44-51.

PMID:
25725667
14.

Casein Kinase 1γ Ensures Monopolar Growth Polarity under Incomplete DNA Replication Downstream of Cds1 and Calcineurin in Fission Yeast.

Koyano T, Konishi M, Martin SG, Ohya Y, Hirata D, Toda T, Kume K.

Mol Cell Biol. 2015 May 1;35(9):1533-42. doi: 10.1128/MCB.01465-14. Epub 2015 Feb 17.

15.

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.

Funayama M, Ohe K, Amo T, Furuya N, Yamaguchi J, Saiki S, Li Y, Ogaki K, Ando M, Yoshino H, Tomiyama H, Nishioka K, Hasegawa K, Saiki H, Satake W, Mogushi K, Sasaki R, Kokubo Y, Kuzuhara S, Toda T, Mizuno Y, Uchiyama Y, Ohno K, Hattori N.

Lancet Neurol. 2015 Mar;14(3):274-82. doi: 10.1016/S1474-4422(14)70266-2. Epub 2015 Feb 4.

PMID:
25662902
16.

Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression.

Ohtsuka Y, Kanagawa M, Yu CC, Ito C, Chiyo T, Kobayashi K, Okada T, Takeda S, Toda T.

Sci Rep. 2015 Feb 9;5:8316. doi: 10.1038/srep08316.

17.

MAPping the Ndc80 loop in cancer: A possible link between Ndc80/Hec1 overproduction and cancer formation.

Tang NH, Toda T.

Bioessays. 2015 Mar;37(3):248-56. doi: 10.1002/bies.201400175. Epub 2015 Jan 2.

18.

Down-regulation of KCC2 expression and phosphorylation in motoneurons, and increases the number of in primary afferent projections to motoneurons in mice with post-stroke spasticity.

Toda T, Ishida K, Kiyama H, Yamashita T, Lee S.

PLoS One. 2014 Dec 29;9(12):e114328. doi: 10.1371/journal.pone.0114328. eCollection 2014.

19.

Alp7/TACC recruits kinesin-8-PP1 to the Ndc80 kinetochore protein for timely mitotic progression and chromosome movement.

Tang NH, Toda T.

J Cell Sci. 2015 Jan 15;128(2):354-63. doi: 10.1242/jcs.160036. Epub 2014 Dec 3.

20.

Drug-drug Interaction between Losartan and Paclitaxel in Human Liver Microsomes with Different CYP2C8 Genotypes.

Mukai Y, Senda A, Toda T, Hayakawa T, Eliasson E, Rane A, Inotsume N.

Basic Clin Pharmacol Toxicol. 2015 Jun;116(6):493-8. doi: 10.1111/bcpt.12355. Epub 2014 Dec 23.

PMID:
25424246
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