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Items: 36

1.

Exosome-associated Shiga toxin 2 is released from cells and causes severe toxicity in mice.

Watanabe-Takahashi M, Yamasaki S, Murata M, Kano F, Motoyama J, Yamate J, Omi J, Sato W, Ukai H, Shimasaki K, Ikegawa M, Tamura-Nakano M, Yanoshita R, Nishino Y, Miyazawa A, Natori Y, Toyama-Sorimachi N, Nishikawa K.

Sci Rep. 2018 Jul 17;8(1):10776. doi: 10.1038/s41598-018-29128-9.

2.

Immediate effects of maternal separation on the development of interneurons derived from medial ganglionic eminence in the neonatal mouse hippocampus.

Katahira T, Miyazaki N, Motoyama J.

Dev Growth Differ. 2018 Jun;60(5):278-290. doi: 10.1111/dgd.12540.

PMID:
29878325
3.

The role of sonic hedgehog-Gli2 pathway in the masculinization of external genitalia.

Miyagawa S, Matsumaru D, Murashima A, Omori A, Satoh Y, Haraguchi R, Motoyama J, Iguchi T, Nakagata N, Hui CC, Yamada G.

Endocrinology. 2011 Jul;152(7):2894-903. doi: 10.1210/en.2011-0263. Epub 2011 May 17.

4.

Genetic analysis of Hedgehog signaling in ventral body wall development and the onset of omphalocele formation.

Matsumaru D, Haraguchi R, Miyagawa S, Motoyama J, Nakagata N, Meijlink F, Yamada G.

PLoS One. 2011 Jan 20;6(1):e16260. doi: 10.1371/journal.pone.0016260.

5.

Ptch1-mediated dosage-dependent action of Shh signaling regulates neural progenitor development at late gestational stages.

Shikata Y, Okada T, Hashimoto M, Ellis T, Matsumaru D, Shiroishi T, Ogawa M, Wainwright B, Motoyama J.

Dev Biol. 2011 Jan 15;349(2):147-59. doi: 10.1016/j.ydbio.2010.10.014. Epub 2010 Oct 20.

6.

Mouse Shh is required for prechordal plate maintenance during brain and craniofacial morphogenesis.

Aoto K, Shikata Y, Imai H, Matsumaru D, Tokunaga T, Shioda S, Yamada G, Motoyama J.

Dev Biol. 2009 Mar 1;327(1):106-20. doi: 10.1016/j.ydbio.2008.11.022. Epub 2008 Dec 7.

7.

Size dependent heat generation of magnetite nanoparticles under AC magnetic field for cancer therapy.

Motoyama J, Hakata T, Kato R, Yamashita N, Morino T, Kobayashi T, Honda H.

Biomagn Res Technol. 2008 Oct 20;6:4. doi: 10.1186/1477-044X-6-4.

8.

FGF8 signaling patterns the telencephalic midline by regulating putative key factors of midline development.

Okada T, Okumura Y, Motoyama J, Ogawa M.

Dev Biol. 2008 Aug 1;320(1):92-101. doi: 10.1016/j.ydbio.2008.04.034. Epub 2008 May 8.

9.

Regulation of apoptosis and neurite extension by FKBP38 is required for neural tube formation in the mouse.

Shirane M, Ogawa M, Motoyama J, Nakayama KI.

Genes Cells. 2008 Jun;13(6):635-51. doi: 10.1111/j.1365-2443.2008.01194.x. Epub 2008 May 4.

10.

Fetal ethanol exposure activates protein kinase A and impairs Shh expression in prechordal mesendoderm cells in the pathogenesis of holoprosencephaly.

Aoto K, Shikata Y, Higashiyama D, Shiota K, Motoyama J.

Birth Defects Res A Clin Mol Teratol. 2008 Apr;82(4):224-31. doi: 10.1002/bdra.20447.

PMID:
18338389
11.

Hyperthermic treatment of DMBA-induced rat mammary cancer using magnetic nanoparticles.

Motoyama J, Yamashita N, Morino T, Tanaka M, Kobayashi T, Honda H.

Biomagn Res Technol. 2008 Feb 25;6:2. doi: 10.1186/1477-044X-6-2.

12.

Molecular analysis of coordinated bladder and urogenital organ formation by Hedgehog signaling.

Haraguchi R, Motoyama J, Sasaki H, Satoh Y, Miyagawa S, Nakagata N, Moon A, Yamada G.

Development. 2007 Feb;134(3):525-33. Epub 2007 Jan 3.

13.
14.

Mice with a targeted mutation of patched2 are viable but develop alopecia and epidermal hyperplasia.

Nieuwenhuis E, Motoyama J, Barnfield PC, Yoshikawa Y, Zhang X, Mo R, Crackower MA, Hui CC.

Mol Cell Biol. 2006 Sep;26(17):6609-22.

15.

Expression of the mouse Fgf15 gene is directly initiated by Sonic hedgehog signaling in the diencephalon and midbrain.

Saitsu H, Komada M, Suzuki M, Nakayama R, Motoyama J, Shiota K, Ishibashi M.

Dev Dyn. 2005 Feb;232(2):282-92.

16.

Differential activities of Sonic hedgehog mediated by Gli transcription factors define distinct neuronal subtypes in the dorsal thalamus.

Hashimoto-Torii K, Motoyama J, Hui CC, Kuroiwa A, Nakafuku M, Shimamura K.

Mech Dev. 2003 Oct;120(10):1097-111.

17.

Differential requirement for Gli2 and Gli3 in ventral neural cell fate specification.

Motoyama J, Milenkovic L, Iwama M, Shikata Y, Scott MP, Hui CC.

Dev Biol. 2003 Jul 1;259(1):150-61.

18.

Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud.

Aoto K, Nishimura T, Eto K, Motoyama J.

Dev Biol. 2002 Nov 15;251(2):320-32.

19.

Patched and smoothened mRNA expression in human astrocytic tumors inversely correlates with histological malignancy.

Katayam M, Yoshida K, Ishimori H, Katayama M, Kawase T, Motoyama J, Kamiguchi H.

J Neurooncol. 2002 Sep;59(2):107-15.

PMID:
12241103
20.

Unique functions of Sonic hedgehog signaling during external genitalia development.

Haraguchi R, Mo R, Hui C, Motoyama J, Makino S, Shiroishi T, Gaffield W, Yamada G.

Development. 2001 Nov;128(21):4241-50.

21.

Shh and Ptc are associated with taste bud maintenance in the adult mouse.

Miura H, Kusakabe Y, Sugiyama C, Kawamatsu M, Ninomiya Y, Motoyama J, Hino A.

Mech Dev. 2001 Aug;106(1-2):143-5.

22.

[Analyses of Gli genes functions using mutant mice].

Motoyama J.

Seikagaku. 2001 Jan;73(1):35-8. Review. Japanese. No abstract available.

PMID:
11244740
24.

Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human.

Crackower MA, Sinasac DS, Xia J, Motoyama J, Prochazka M, Rommens JM, Scherer SW, Tsui LC.

Genomics. 1999 Feb 1;55(3):257-67.

PMID:
10049579
25.

Overlapping and non-overlapping Ptch2 expression with Shh during mouse embryogenesis.

Motoyama J, Heng H, Crackower MA, Takabatake T, Takeshima K, Tsui LC, Hui C.

Mech Dev. 1998 Nov;78(1-2):81-4.

26.

Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse.

Crackower MA, Motoyama J, Tsui LC.

Dev Biol. 1998 Sep 1;201(1):78-89.

27.

Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus.

Motoyama J, Liu J, Mo R, Ding Q, Post M, Hui CC.

Nat Genet. 1998 Sep;20(1):54-7.

PMID:
9731531
28.

Diminished Sonic hedgehog signaling and lack of floor plate differentiation in Gli2 mutant mice.

Ding Q, Motoyama J, Gasca S, Mo R, Sasaki H, Rossant J, Hui CC.

Development. 1998 Jul;125(14):2533-43.

29.

Ptch2, a second mouse Patched gene is co-expressed with Sonic hedgehog.

Motoyama J, Takabatake T, Takeshima K, Hui C.

Nat Genet. 1998 Feb;18(2):104-6. No abstract available.

PMID:
9462734
30.

Organogenesis of the liver, thymus and spleen is affected in jumonji mutant mice.

Motoyama J, Kitajima K, Kojima M, Kondo S, Takeuchi T.

Mech Dev. 1997 Aug;66(1-2):27-37.

31.

The presence of a magnocellular defect depends on the type of dyslexia.

Borsting E, Ridder WH 3rd, Dudeck K, Kelley C, Matsui L, Motoyama J.

Vision Res. 1996 Apr;36(7):1047-53.

32.

[The mouse embryogenesis of jumonji mutant obtained by gene-trap method].

Motoyama J, Takeuchi T.

Tanpakushitsu Kakusan Koso. 1995 Oct;40(14):2152-61. Review. Japanese. No abstract available.

PMID:
8532871
33.

Gene trap capture of a novel mouse gene, jumonji, required for neural tube formation.

Takeuchi T, Yamazaki Y, Katoh-Fukui Y, Tsuchiya R, Kondo S, Motoyama J, Higashinakagawa T.

Genes Dev. 1995 May 15;9(10):1211-22.

36.

[Studies on determination of urinary sugar content by the 3,6-dinitrophthalic acid method (Momose's method)].

YAKATA M, TSUCHIDA M, MOTOYAMA J.

Rinsho Byori. 1963 Apr;11:211-4. Japanese. No abstract available.

PMID:
14002213

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