T. Mio

发表

Phosphoglucomutase 3 (= Phosphoacetylglucosamine Mutase) (PGM3)

H. Okabe, T. Mio, 2014 .

Saccharomyces cerevisiae GNA1, an Essential Gene Encoding a Novel Acetyltransferase Involved in UDP-N-acetylglucosamine Synthesis*

H. Yamada-Okabe, M. Arisawa, T. Yamada-Okabe, 1999, The Journal of Biological Chemistry.

Isolation of canCHS1A, a variant gene of Candida albicans chitin synthase.

H. Yamada-Okabe, S. Nagahashi, M. Arisawa, 1995, Microbiology.

Involvement of cell wall β‐glucan in the action of HM‐1 killer toxin

Y. Furuichi, S. B. Inoue, T. Nakajima, 1994 .

Functional cloning and mutational analysis of the human cDNA for phosphoacetylglucosamine mutase: identification of the amino acid residues essential for the catalysis.

M. Arisawa, T. Yamada-Okabe, T. Mio, 2000, Biochimica et biophysica acta.

Characterization of Chitin Synthase 2 of Saccharomyces cerevisiae.

S. Nagahashi, M. Arisawa, M. Takagi, 1995, The Journal of Biological Chemistry.

Phosphorylation of glucosamine-6-phosphate synthase is important but not essential for germination and mycelial growth of Candida albicans.

J. Kur, S. Milewski, I. Gabriel, 2004, FEMS microbiology letters.

Purification, crystallization and preliminary X-ray diffraction studies of UDP-N-acetylglucosamine pyrophosphorylase from Candida albicans.

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Isolation and characterization of the Candida albicans gene for mRNA 5′‐triphosphatase: association of mRNA 5′‐triphosphatase and mRNA 5′‐guanylyltransferase activities is essential for the function of mRNA 5′‐capping enzyme in vivo 1

M. Arisawa, T. Yamada-Okabe, Y. Kashima, 1998, FEBS letters.

Crystal Structures of N-Acetylglucosamine-phosphate Mutase, a Member of the α-d-Phosphohexomutase Superfamily, and Its Substrate and Product Complexes*

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2006, Journal of Biological Chemistry.

The Eukaryotic UDP-N-Acetylglucosamine Pyrophosphorylases

M. Arisawa, T Mio, T Yabe, 1998, The Journal of Biological Chemistry.

Cloning of the Candida albicans homolog of Saccharomyces cerevisiae GSC1/FKS1 and its involvement in beta-1,3-glucan synthesis

H. Tabuchi, T. Watanabe, M. Arisawa, 1997, Journal of bacteriology.

Identification and characterization of the genes for N-acetylglucosamine kinase and N-acetylglucosamine-phosphate deacetylase in the pathogenic fungus Candida albicans.

T. Yamada-Okabe, T. Mio, Y. Sakamori, 2001, European journal of biochemistry.

Tetracycline-Regulatable System To Tightly Control Gene Expression in the Pathogenic Fungus Candida albicans

Hironobu Nakayama, S. Nagahashi, M. Arisawa, 2000, Infection and Immunity.

Roles of Three Histidine Kinase Genes in Hyphal Development and Virulence of the Pathogenic Fungus Candida albicans

M. Arisawa, T. Yamada-Okabe, Y. Kashima, 1999, Journal of bacteriology.

UDP- N -Acetylglucosamine Pyrophosphorylase 1 (UAP1)

H. Okabe, T. Mio, 2014 .

Cloning of the Saccharomyces cerevisiae gene whose overexpression overcomes the effects of HM-1 killer toxin, which inhibits beta-glucan synthesis

C. Miyamoto, Y. Furuichi, T. Nakajima, 1994, Journal of bacteriology.

Candida albicans Fungus Control Gene Expression in the Pathogenic Tetracycline-Regulatable System To Tightly

Hironobu Nakayama, S. Nagahashi, M. Arisawa, 2000 .

Gene amplification and expression in lung cancer cells with acquired paclitaxel resistance.

K. Kitada, N. Yabuki, H. Terashima, 2007, Cancer genetics and cytogenetics.

YES1 is a targetable oncogene in cancers harboring YES1 gene amplification.

H. Koyano, N. Ishii, Haruhiko Sato, 2019, Cancer research.

Enhanced antitumor activity of erlotinib in combination with the Hsp90 inhibitor CH5164840 against non‐small‐cell lung cancer

N. Ishii, Y. Aoki, O. Kondoh, 2013, Cancer science.

Acquired JHDM1D–BRAF Fusion Confers Resistance to FGFR Inhibition in FGFR2-Amplified Gastric Cancer

M. Aoki, N. Ishii, T. Mio, 2018, Molecular Cancer Therapeutics.

The Fibroblast Growth Factor Receptor Genetic Status as a Potential Predictor of the Sensitivity to CH5183284/Debio 1347, a Novel Selective FGFR Inhibitor

K. Morikami, H. Shindoh, N. Ishii, 2014, Molecular Cancer Therapeutics.

Small Molecule Therapeutics The Fibroblast Growth Factor Receptor Genetic Status as a Potential Predictor of the Sensitivity to CH 5183284 / Debio 1347 , a Novel Selective FGFR Inhibitor

K. Morikami, H. Shindoh, N. Ishii, 2014 .

Role of three chitin synthase genes in the growth of Candida albicans

M. Arisawa, T. Nakajima, M. Sudoh, 1996, Journal of bacteriology.

The Candida albicans gene for mRNA 5-cap methyltransferase: identification of additional residues essential for catalysis.

M. Arisawa, T. Yamada-Okabe, Y. Kashima, 1999, Microbiology.

Characterization and gene cloning of 1,3-beta-D-glucan synthase from Saccharomyces cerevisiae.

T. Watanabe, M. Arisawa, C. Miyamoto, 1995, European journal of biochemistry.

Reduced virulence of Candida albicans mutants lacking the GNA1 gene encoding glucosamine-6-phosphate acetyltransferase.

M. Arisawa, T. Mio, H. Yamada‐Okabe, 2000, Microbiology.

Isolation of the Candida albicans homologs of Saccharomyces cerevisiae KRE6 and SKN1: expression and physiological function

M. Arisawa, T. Nakajima, T. Yamada-Okabe, 1997, Journal of bacteriology.

Isolation of theCandida albicansHomologs ofSaccharomyces cerevisiae KRE6andSKN1: Expression and Physiological Function

M. Arisawa, T. Nakajima, T. Yamada-Okabe, 1997 .

Yuji Candida albicans Pathogenic Fungus Hyphal Development and Virulence of the Roles of Three Histidine Kinase Genes in

M. Arisawa, T. Yamada-Okabe, Y. Kashima, 1999 .

Isolation of CaSLN1 and CaNIK1, the genes for osmosensing histidine kinase homologues, from the pathogenic fungus Candida albicans.

H. Bussey, S. Nagahashi, M. Arisawa, 1998, Microbiology.

Isolation and characterization of the Candida albicans gene for mRNA 5'-triphosphatase: association of mRNA 5'-triphosphatase and mRNA 5'-guanylyltransferase activities is essential for the function of mRNA 5'-capping enzyme in vivo.

M. Arisawa, T. Yamada-Okabe, Y. Kashima, 1998, FEBS Letters.

Selective TRK Inhibitor CH7057288 against TRK Fusion-Driven Cancer

Miyuki Yoshida, Kenji Takanashi, A. Higashida, 2018, Molecular Cancer Therapeutics.

Preclinical antitumor activity of the novel heat shock protein 90 inhibitor CH5164840 against human epidermal growth factor receptor 2 (HER2)‐overexpressing cancers

Shigeo Sato, N. Ishii, Y. Aoki, 2012, Cancer science.

Crystal Structure of Uridine-diphospho-N-acetylglucosamine Pyrophosphorylase from Candida albicans and Catalytic Reaction Mechanism*

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2007, Journal of Biological Chemistry.

Purification, crystallization and preliminary X-ray diffraction studies of N-acetylglucosamine-phosphate mutase from Candida albicans

K. Miki, Y. Nishitani, T. Fukami, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Enhanced antitumor activity of erlotinib in combination with the Hsp90 inhibitor CH5164840 against non‐small‐cell lung cancer

Y. Aoki, O. Kondoh, A. Suda, 2013, Cancer science.