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1 - 25 of 160 results for author:"Itoh M."Drop in Literature Citations

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NF-kappaB activation induced by Notch ligand stimulation in acute myeloid leukemia cells.

Itoh M., Fu L., Tohda S.

Oncol. Rep. 22:631-634(2009) · Mapped (3)

Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.

Kitamura K., Itou Y., Yanazawa M., Ohsawa M., Suzuki-Migishima R., Umeki Y., Hohjoh H., Yanagawa Y., Shinba T., Itoh M. et al.

Hum. Mol. Genet. 18:3708-3724(2009) · Mapped (40)

Characteristics of genes up-regulated and down-regulated after 24 h starvation in the head of Drosophila.

Fujikawa K., Takahashi A., Nishimura A., Itoh M., Takano-Shimizu T., Ozaki M.

Gene 446:11-17(2009) · Mapped (199)

Previously unrecognized amino acid substitutions in the hemagglutinin and fusion proteins of measles virus modulate cell-cell fusion, hemadsorption, virus growth, and penetration rate.

Okada H., Itoh M., Nagata K., Takeuchi K.

J. Virol. 83:8713-8721(2009) · UniProtKB (13)

An alternative spliced mouse presenilin-2 mRNA encodes a novel gamma-secretase inhibitor.

Suzuki Y., Ohta K., Itoh M., Sakoh-Sumitomo Y., Mitsuda T., Ueda M., Hayakawa-Yano Y., Li S., Hida Y., Inuzuka T. et al.

FEBS Lett. 583:1403-1408(2009) · Mapped (3)

Similar and distinct properties of MUPP1 and Patj, two homologous PDZ domain-containing tight-junction proteins.

Adachi M., Hamazaki Y., Kobayashi Y., Itoh M., Tsukita S., Furuse M., Tsukita S.

Mol. Cell. Biol. 29:2372-2389(2009) · Mapped (22)

Genetic screening for modifiers of the DREF pathway in Drosophila melanogaster: identification and characterization of HP6 as a novel target of DREF.

Ida H., Suzusho N., Suyari O., Yoshida H., Ohno K., Hirose F., Itoh M., Yamaguchi M.

Nucleic Acids Res. 37:1423-1437(2009) · Mapped (89)

Molecular spectrum of spontaneous de novo mutations in male and female germline cells of Drosophila melanogaster.

Watanabe Y., Takahashi A., Itoh M., Takano-Shimizu T.

Genetics 181:1035-1043(2009) · Mapped (16)

Both alleles of PSF1 are required for maintenance of pool size of immature hematopoietic cells and acute bone marrow regeneration.

Ueno M., Itoh M., Sugihara K., Asano M., Takakura N.

Blood 113:555-562(2009) · Mapped (18)

Reduced X-linked rare polymorphism in males in comparison to females of Drosophila melanogaster.

Takahashi K.H., Tanaka K., Itoh M., Takano-Shimizu T.

J. Hered. 100:97-105(2009) · UniProtKB (19)

Spinophilin inhibits the binding of RGS8 to M1-mAChR but enhances the regulatory function of RGS8.

Fujii S., Yamazoe G., Itoh M., Kubo Y., Saitoh O.

Biochem. Biophys. Res. Commun. 377:200-204(2008) · Mapped (8)

Rapid screening assay for KRAS mutations by the modified smart amplification process.

Tatsumi K., Mitani Y., Watanabe J., Takakura H., Hoshi K., Kawai Y., Kikuchi T., Kogo Y., Oguchi-Katayama A., Tomaru Y. et al.

J Mol Diagn 10:520-526(2008) · Mapped (8)

Increased brain histamine H1 receptor binding in patients with anorexia nervosa.

Yoshizawa M., Tashiro M., Fukudo S., Yanai K., Utsumi A., Kano M., Karahasi M., Endo Y., Morisita J., Sato Y. et al.

Biol. Psychiatry 65:329-335(2009) · Mapped (4)

Sensitive detection of EGFR mutations using a competitive probe to suppress background in the SMart Amplification Process.

Kawai Y., Kikuchi T., Mitani Y., Kogo Y., Itoh M., Usui K., Kanamori H., Kaiho A., Takakura H., Hoshi K. et al.

Biologicals 36:234-238(2008) · Mapped (15)

Deficiency of zonula occludens-1 causes embryonic lethal phenotype associated with defected yolk sac angiogenesis and apoptosis of embryonic cells.

Katsuno T., Umeda K., Matsui T., Hata M., Tamura A., Itoh M., Takeuchi K., Fujimori T., Nabeshima Y., Noda T. et al.

Mol. Biol. Cell 19:2465-2475(2008) · Mapped (3)

Novel mutations of the GLA gene in Japanese patients with Fabry disease and their functional characterization by active site specific chaperone.

Shimotori M., Maruyama H., Nakamura G., Suyama T., Sakamoto F., Itoh M., Miyabayashi S., Ohnishi T., Sakai N., Wataya-Kaneda M. et al.

Hum. Mutat. 29:331-331(2008) · Mapped (5)

Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.

Kanaumi T., Takashima S., Iwasaki H., Itoh M., Mitsudome A., Hirose S.

Brain Dev. 30:362-369(2008) · Mapped (13)

Structure of thymic cysts in congenital lymph nodes-lacking mice.

Nakamura Y., Qu N., Terayama H., Naito M., Yi S.Q., Moriyama H., Itoh M.

Anat Histol Embryol 37:126-130(2008) · Mapped (3)

A new test for detecting ongoing selection.

Inomata N., Itoh M., Kondo R., Ohshima M., Inoue Y., Takano-Shimizu T.

Genetica 133:321-334(2008) · Mapped (51)

Human chorionic gonadotropin induces nestin expression in endothelial cells of the ovary via vascular endothelial growth factor signaling.

Takahashi N., Itoh M.T., Ishizuka B.

Endocrinology 149:253-260(2008) · Mapped (1)

Human CYP2A6 is induced by estrogen via estrogen receptor.

Higashi E., Fukami T., Itoh M., Kyo S., Inoue M., Yokoi T., Nakajima M.

Drug Metab. Dispos. 35:1935-1941(2007) · Mapped (2)

Sequential histopathology of pancreatic tissues in aly/aly mice.

Nakamura Y., Yi S.Q., Terayama H., Naito M., Li J., Moriyama H., Tsuchida A., Itoh M.

Cells Tissues Organs (Print) 186:204-209(2007) · Mapped (3)

Short report: production of recombinant kinesin-related protein of Leishmania donovani and its application in the serodiagnosis of visceral leishmaniasis.

Takagi H., Islam M.Z., Itoh M., Islam A.U., Saifuddin Ekram A.R., Hussain S.M., Hashiguchi Y., Kimura E.

Am. J. Trop. Med. Hyg. 76:902-905(2007) · UniProtKB (1)

Gemin2 plays an important role in stabilizing the survival of motor neuron complex.

Ogawa C., Usui K., Aoki M., Ito F., Itoh M., Kai C., Kanamori-Katayama M., Hayashizaki Y., Suzuki H.

J. Biol. Chem. 282:11122-11134(2007) · Mapped (2)

Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains.

Itoh M., Ide S., Takashima S., Kudo S., Nomura Y., Segawa M., Kubota T., Mori H., Tanaka S., Horie H. et al.

J. Neuropathol. Exp. Neurol. 66:117-123(2007) · Mapped (5)

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