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Molecular Design, Characterization, and Application of Multiinformation Dyes (MIDs) for Optical Chemical Sensings. 3. Application of MIDs for λ(max)-Tunable Ion-Selective Optodes.

Analytical chemistry

Hisamoto H, Tani M, Mori S, Yamada T, Ishigaki T, Tohma H, Suzuki K.
PMID: 21662947
Anal Chem. 1999 Jan 01;71(1):259-64. doi: 10.1021/ac980757x.

By utilizing "multiinformation dyes (MIDs)", which have plural spectral change characteristics such as an absorption maximum wavelength (λ(max)) shift based on a polarity change and an absorbance change due to protonation, novel λ(max)-tunable ion-selective optodes were proposed and prepared...

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Hisamoto H, Tani M, Mori S, et al. Molecular Design, Characterization, and Application of Multiinformation Dyes (MIDs) for Optical Chemical Sensings. 3. Application of MIDs for λ(max)-Tunable Ion-Selective Optodes. Anal Chem. 1999;71(1):259-64doi: 10.1021/ac980757x.
Hisamoto, H., Tani, M., Mori, S., Yamada, T., Ishigaki, T., Tohma, H., & Suzuki, K. (1999). Molecular Design, Characterization, and Application of Multiinformation Dyes (MIDs) for Optical Chemical Sensings. 3. Application of MIDs for λ(max)-Tunable Ion-Selective Optodes. Analytical chemistry, 71(1), 259-64. https://doi.org/10.1021/ac980757x
Hisamoto, H, et al. "Molecular Design, Characterization, and Application of Multiinformation Dyes (MIDs) for Optical Chemical Sensings. 3. Application of MIDs for λ(max)-Tunable Ion-Selective Optodes." Analytical chemistry vol. 71,1 (1999): 259-64. doi: https://doi.org/10.1021/ac980757x
Hisamoto H, Tani M, Mori S, Yamada T, Ishigaki T, Tohma H, Suzuki K. Molecular Design, Characterization, and Application of Multiinformation Dyes (MIDs) for Optical Chemical Sensings. 3. Application of MIDs for λ(max)-Tunable Ion-Selective Optodes. Anal Chem. 1999 Jan 01;71(1):259-64. doi: 10.1021/ac980757x. PMID: 21662947.
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E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity.

International journal of Alzheimer's disease

Suzuki T, Murakami K, Izuo N, Kume T, Akaike A, Nagata T, Nishizaki T, Tomiyama T, Takuma H, Mori H, Irie K.
PMID: 21234376
Int J Alzheimers Dis. 2010 Dec 19;2011:431320. doi: 10.4061/2011/431320.

Oligomers of 40- or 42-mer amyloid β-protein (Aβ40, Aβ42) cause cognitive decline and synaptic dysfunction in Alzheimer's disease. We proposed the importance of a turn at Glu22 and Asp23 of Aβ42 to induce its neurotoxicity through the formation of...

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Suzuki T, Murakami K, Izuo N, et al. E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity. Int J Alzheimers Dis. 2010;2011:431320doi: 10.4061/2011/431320.
Suzuki, T., Murakami, K., Izuo, N., Kume, T., Akaike, A., Nagata, T., Nishizaki, T., Tomiyama, T., Takuma, H., Mori, H., & Irie, K. (2010). E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity. International journal of Alzheimer's disease, 2011431320. https://doi.org/10.4061/2011/431320
Suzuki, Takayuki, et al. "E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity." International journal of Alzheimer's disease vol. 2011 (2010): 431320. doi: https://doi.org/10.4061/2011/431320
Suzuki T, Murakami K, Izuo N, Kume T, Akaike A, Nagata T, Nishizaki T, Tomiyama T, Takuma H, Mori H, Irie K. E22Δ Mutation in Amyloid β-Protein Promotes β-Sheet Transformation, Radical Production, and Synaptotoxicity, But Not Neurotoxicity. Int J Alzheimers Dis. 2010 Dec 19;2011:431320. doi: 10.4061/2011/431320. PMID: 21234376; PMCID: PMC3017891.
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Esterification of N-benzyloxycarbonyldipeptides in ethanol-water with immobilized papain.

Biotechnology and bioengineering

Kawashiro K, Ishizaki H, Sugiyama S, Hayashi H.
PMID: 18613014
Biotechnol Bioeng. 1993 Jul;42(3):309-14. doi: 10.1002/bit.260420307.

The esterification of some N-benzyloxycarbonyl (Z)-dipeptides in ethanol-containing water was investigated using papain as a catalyst. The esterification took place in ethanol containing a small amount of water (2% v/v, pH 9) with free papain at room temperature. The...

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Kawashiro K, Ishizaki H, Sugiyama S, et al. Esterification of N-benzyloxycarbonyldipeptides in ethanol-water with immobilized papain. Biotechnol Bioeng. 1993;42(3):309-14doi: 10.1002/bit.260420307.
Kawashiro, K., Ishizaki, H., Sugiyama, S., & Hayashi, H. (1993). Esterification of N-benzyloxycarbonyldipeptides in ethanol-water with immobilized papain. Biotechnology and bioengineering, 42(3), 309-14. https://doi.org/10.1002/bit.260420307
Kawashiro, K, et al. "Esterification of N-benzyloxycarbonyldipeptides in ethanol-water with immobilized papain." Biotechnology and bioengineering vol. 42,3 (1993): 309-14. doi: https://doi.org/10.1002/bit.260420307
Kawashiro K, Ishizaki H, Sugiyama S, Hayashi H. Esterification of N-benzyloxycarbonyldipeptides in ethanol-water with immobilized papain. Biotechnol Bioeng. 1993 Jul;42(3):309-14. doi: 10.1002/bit.260420307. PMID: 18613014.
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Fucoidan, a major component of brown seaweed, prohibits the growth of human cancer cell lines in vitro.

Molecular medicine reports

Fukahori S, Yano H, Akiba J, Ogasawara S, Momosaki S, Sanada S, Kuratomi K, Ishizaki Y, Moriya F, Yagi M, Kojiro M.
PMID: 21479446
Mol Med Rep. 2008 Jul-Aug;1(4):537-42.

Fucoidan, the general term for sulfated polysaccharides, is reported to engage in various biological activities having anti-tumor, anti-coagulation and anti-viral effects. Though it has been investigated, the mechanism of its anti-tumor effects remains elusive. The current study examined the...

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Fukahori S, Yano H, Akiba J, et al. Fucoidan, a major component of brown seaweed, prohibits the growth of human cancer cell lines in vitro. Mol Med Rep. 2008;1(4):537-42
Fukahori, S., Yano, H., Akiba, J., Ogasawara, S., Momosaki, S., Sanada, S., Kuratomi, K., Ishizaki, Y., Moriya, F., Yagi, M., & Kojiro, M. (2008). Fucoidan, a major component of brown seaweed, prohibits the growth of human cancer cell lines in vitro. Molecular medicine reports, 1(4), 537-42.
Fukahori, Suguru, et al. "Fucoidan, a major component of brown seaweed, prohibits the growth of human cancer cell lines in vitro." Molecular medicine reports vol. 1,4 (2008): 537-42.
Fukahori S, Yano H, Akiba J, Ogasawara S, Momosaki S, Sanada S, Kuratomi K, Ishizaki Y, Moriya F, Yagi M, Kojiro M. Fucoidan, a major component of brown seaweed, prohibits the growth of human cancer cell lines in vitro. Mol Med Rep. 2008 Jul-Aug;1(4):537-42. PMID: 21479446.
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Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene.

Comparative biochemistry and physiology. Part D, Genomics & proteomics

Ishizaki S, Yokoyama Y, Oshiro N, Teruya N, Nagashima Y, Shiomi K, Watabe S.
PMID: 20483244
Comp Biochem Physiol Part D Genomics Proteomics. 2006 Mar;1(1):139-44. doi: 10.1016/j.cbd.2005.09.004. Epub 2005 Nov 09.

This study amplified the mitochondrial 16S rRNA gene using polymerase chain reaction (PCR) with a template of total DNA from muscle tissues of nine pufferfish species collected from the coastal area of Okinawa Islands in Japan: Pleuranacanthus sceleratus, Triodon...

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Ishizaki S, Yokoyama Y, Oshiro N, et al. Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene. Comp Biochem Physiol Part D Genomics Proteomics. 2005;1(1):139-44doi: 10.1016/j.cbd.2005.09.004.
Ishizaki, S., Yokoyama, Y., Oshiro, N., Teruya, N., Nagashima, Y., Shiomi, K., & Watabe, S. (2006). Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene. Comparative biochemistry and physiology. Part D, Genomics & proteomics, 1(1), 139-44. https://doi.org/10.1016/j.cbd.2005.09.004
Ishizaki, Shoichiro, et al. "Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene." Comparative biochemistry and physiology. Part D, Genomics & proteomics vol. 1,1 (2006): 139-44. doi: https://doi.org/10.1016/j.cbd.2005.09.004
Ishizaki S, Yokoyama Y, Oshiro N, Teruya N, Nagashima Y, Shiomi K, Watabe S. Molecular identification of pufferfish species using PCR amplification and restriction analysis of a segment of the 16S rRNA gene. Comp Biochem Physiol Part D Genomics Proteomics. 2006 Mar;1(1):139-44. doi: 10.1016/j.cbd.2005.09.004. Epub 2005 Nov 09. PMID: 20483244.
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A comparison between low-flow leak test and oxygen flush leak test.

Journal of anesthesia

Tokumine J, Iha H, Okuda Y, Nitta K, Ishigaki K, Oshiro M, Shimabukuro T.
PMID: 14564564
J Anesth. 2000;14(4):191-3. doi: 10.1007/s005400070004.

PURPOSE: The clinical efficacy of two methods of preanesthetic leak test,namely the oxygen flush leak test (OFLT) and the low-flow leak test (LFLT), was compared regarding their ability to detect leakage in the anesthesia circuit and their accuracy.METHODS: Examinees...

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Tokumine J, Iha H, Okuda Y, et al. A comparison between low-flow leak test and oxygen flush leak test. J Anesth. 2000;14(4):191-3doi: 10.1007/s005400070004.
Tokumine, J., Iha, H., Okuda, Y., Nitta, K., Ishigaki, K., Oshiro, M., & Shimabukuro, T. (2000). A comparison between low-flow leak test and oxygen flush leak test. Journal of anesthesia, 14(4), 191-3. https://doi.org/10.1007/s005400070004
Tokumine, J, et al. "A comparison between low-flow leak test and oxygen flush leak test." Journal of anesthesia vol. 14,4 (2000): 191-3. doi: https://doi.org/10.1007/s005400070004
Tokumine J, Iha H, Okuda Y, Nitta K, Ishigaki K, Oshiro M, Shimabukuro T. A comparison between low-flow leak test and oxygen flush leak test. J Anesth. 2000;14(4):191-3. doi: 10.1007/s005400070004. PMID: 14564564.
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Primary malignant melanoma of the esophagogastric junction: Report of a case.

International journal of surgery case reports

Ishizaki M, Aibara Y, Furuya K.
PMID: 23810918
Int J Surg Case Rep. 2013;4(8):700-3. doi: 10.1016/j.ijscr.2013.04.037. Epub 2013 May 22.

INTRODUCTION: Primary malignant melanoma of the gastrointestinal tract is very rare, especially in the stomach. We report an extremely rare case of primary malignant melanoma of the esophagogastric junction mainly situated in the stomach.PRESENTATION OF CASE: The patient was...

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Ishizaki M, Aibara Y, Furuya K. Primary malignant melanoma of the esophagogastric junction: Report of a case. Int J Surg Case Rep. 2013;4(8):700-3doi: 10.1016/j.ijscr.2013.04.037.
Ishizaki, M., Aibara, Y., & Furuya, K. (2013). Primary malignant melanoma of the esophagogastric junction: Report of a case. International journal of surgery case reports, 4(8), 700-3. https://doi.org/10.1016/j.ijscr.2013.04.037
Ishizaki, Masahiro, et al. "Primary malignant melanoma of the esophagogastric junction: Report of a case." International journal of surgery case reports vol. 4,8 (2013): 700-3. doi: https://doi.org/10.1016/j.ijscr.2013.04.037
Ishizaki M, Aibara Y, Furuya K. Primary malignant melanoma of the esophagogastric junction: Report of a case. Int J Surg Case Rep. 2013;4(8):700-3. doi: 10.1016/j.ijscr.2013.04.037. Epub 2013 May 22. PMID: 23810918; PMCID: PMC3710912.
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Distribution of pathogenic vibrios and other bacteria in imported frozen shrimps and their decontamination by gamma-irradiation.

World journal of microbiology & biotechnology

Rashid HO, Ito H, Ishigaki I.
PMID: 24425563
World J Microbiol Biotechnol. 1992 Sep;8(5):494-9. doi: 10.1007/BF01201947.

The distribution of pathogenic vibrios and other bacteria in eight samples of imported frozen shrimps and the effect of irradiation on these bacteria were investigated. Total aerobic bacteria were at 2×10(4) to 4×10(6)/g. Coliforms consisted mainly ofEnterobacter. No salmonella...

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Rashid HO, Ito H, Ishigaki I. Distribution of pathogenic vibrios and other bacteria in imported frozen shrimps and their decontamination by gamma-irradiation. World J Microbiol Biotechnol. 1992;8(5):494-9doi: 10.1007/BF01201947.
Rashid, H. O., Ito, H., & Ishigaki, I. (1992). Distribution of pathogenic vibrios and other bacteria in imported frozen shrimps and their decontamination by gamma-irradiation. World journal of microbiology & biotechnology, 8(5), 494-9. https://doi.org/10.1007/BF01201947
Rashid, H O, et al. "Distribution of pathogenic vibrios and other bacteria in imported frozen shrimps and their decontamination by gamma-irradiation." World journal of microbiology & biotechnology vol. 8,5 (1992): 494-9. doi: https://doi.org/10.1007/BF01201947
Rashid HO, Ito H, Ishigaki I. Distribution of pathogenic vibrios and other bacteria in imported frozen shrimps and their decontamination by gamma-irradiation. World J Microbiol Biotechnol. 1992 Sep;8(5):494-9. doi: 10.1007/BF01201947. PMID: 24425563.
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Dermoscopic Features of Pigmented Bowen's Disease in a Japanese Female Mimicking Malignant Melanoma.

Dermatology research and practice

Inoue T, Kobayashi K, Sawada M, Ishizaki S, Ito H, Fujibayashi M, Tanaka M.
PMID: 20811602
Dermatol Res Pract. 2010;2010. doi: 10.1155/2010/543091. Epub 2010 Aug 02.

Various structures have been reported for dermoscopic features of pigmented Bowen's disease (BD), which could be a mimic of various pigmented skin lesions. A 79-year-old Japanese woman presented with a 3-year history of brown-black macule on her right upper...

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Inoue T, Kobayashi K, Sawada M, et al. Dermoscopic Features of Pigmented Bowen's Disease in a Japanese Female Mimicking Malignant Melanoma. Dermatol Res Pract. 2010;2010doi: 10.1155/2010/543091.
Inoue, T., Kobayashi, K., Sawada, M., Ishizaki, S., Ito, H., Fujibayashi, M., & Tanaka, M. (2010). Dermoscopic Features of Pigmented Bowen's Disease in a Japanese Female Mimicking Malignant Melanoma. Dermatology research and practice, 2010. https://doi.org/10.1155/2010/543091
Inoue, Takayuki, et al. "Dermoscopic Features of Pigmented Bowen's Disease in a Japanese Female Mimicking Malignant Melanoma." Dermatology research and practice vol. 2010 (2010). doi: https://doi.org/10.1155/2010/543091
Inoue T, Kobayashi K, Sawada M, Ishizaki S, Ito H, Fujibayashi M, Tanaka M. Dermoscopic Features of Pigmented Bowen's Disease in a Japanese Female Mimicking Malignant Melanoma. Dermatol Res Pract. 2010;2010. doi: 10.1155/2010/543091. Epub 2010 Aug 02. PMID: 20811602; PMCID: PMC2929512.
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The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems: a survey of the perceptions of Japanese pediatricians and child health nurses.

BioPsychoSocial medicine

Ishizaki Y, Maru M, Higashino H, Katsumoto S, Egawa K, Yanagimoto Y, Nagahama T.
PMID: 22433283
Biopsychosoc Med. 2012 Mar 20;6:8. doi: 10.1186/1751-0759-6-8.

BACKGROUND: Advances in medical science have enabled many children with chronic diseases to survive to adulthood. The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems has received attention in Europe and the United...

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Ishizaki Y, Maru M, Higashino H, et al. The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems: a survey of the perceptions of Japanese pediatricians and child health nurses. Biopsychosoc Med. 2012;6:8doi: 10.1186/1751-0759-6-8.
Ishizaki, Y., Maru, M., Higashino, H., Katsumoto, S., Egawa, K., Yanagimoto, Y., & Nagahama, T. (2012). The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems: a survey of the perceptions of Japanese pediatricians and child health nurses. BioPsychoSocial medicine, 68. https://doi.org/10.1186/1751-0759-6-8
Ishizaki, Yuko, et al. "The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems: a survey of the perceptions of Japanese pediatricians and child health nurses." BioPsychoSocial medicine vol. 6 (2012): 8. doi: https://doi.org/10.1186/1751-0759-6-8
Ishizaki Y, Maru M, Higashino H, Katsumoto S, Egawa K, Yanagimoto Y, Nagahama T. The transition of adult patients with childhood-onset chronic diseases from pediatric to adult healthcare systems: a survey of the perceptions of Japanese pediatricians and child health nurses. Biopsychosoc Med. 2012 Mar 20;6:8. doi: 10.1186/1751-0759-6-8. PMID: 22433283; PMCID: PMC3383542.
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A new role of multi scaffold protein Liprin-α: Liprin-α suppresses Rho-mDia mediated stress fiber formation.

Bioarchitecture

Sakamoto S, Narumiya S, Ishizaki T.
PMID: 22754629
Bioarchitecture. 2012 Feb 01;2(2):43-49. doi: 10.4161/bioa.20442.

Regulation of the actin cytoskeleton is crucial for cell morphology and migration. One of the key molecules that regulates actin remodeling is the small GTPase Rho. Rho shuttles between the inactive GDP-bound form and the active GTP-bound form, and...

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Sakamoto S, Narumiya S, Ishizaki T. A new role of multi scaffold protein Liprin-α: Liprin-α suppresses Rho-mDia mediated stress fiber formation. Bioarchitecture. 2012;2(2):43-49doi: 10.4161/bioa.20442.
Sakamoto, S., Narumiya, S., & Ishizaki, T. (2012). A new role of multi scaffold protein Liprin-α: Liprin-α suppresses Rho-mDia mediated stress fiber formation. Bioarchitecture, 2(2), 43-49. https://doi.org/10.4161/bioa.20442
Sakamoto, Satoko, et al. "A new role of multi scaffold protein Liprin-α: Liprin-α suppresses Rho-mDia mediated stress fiber formation." Bioarchitecture vol. 2,2 (2012): 43-49. doi: https://doi.org/10.4161/bioa.20442
Sakamoto S, Narumiya S, Ishizaki T. A new role of multi scaffold protein Liprin-α: Liprin-α suppresses Rho-mDia mediated stress fiber formation. Bioarchitecture. 2012 Feb 01;2(2):43-49. doi: 10.4161/bioa.20442. PMID: 22754629; PMCID: PMC3383721.
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Sensitivity of hepatocellular carcinoma to nine anticancer drugs is unchanged after administration of epirubicin suspended in lipiodol.

International journal of oncology

Nishizaki T, Takenaka K, Yanaga K, Kishikawa K, Maehara Y, Shimada M, Sugimachi K.
PMID: 21544464
Int J Oncol. 1996 Jun;8(6):1059-62. doi: 10.3892/ijo.8.6.1059.

Multidrug resistance is a major obstacle to the successful chemotherapy for human cancers. The chemosensitivities of hepatocellular carcinoma (HCC) treated with preoperative lipiodolization (LPD) to anticancer agents were compared to those without chemotherapy. Data on 22 patients with HCC...

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Nishizaki T, Takenaka K, Yanaga K, et al. Sensitivity of hepatocellular carcinoma to nine anticancer drugs is unchanged after administration of epirubicin suspended in lipiodol. Int J Oncol. 1996;8(6):1059-62doi: 10.3892/ijo.8.6.1059.
Nishizaki, T., Takenaka, K., Yanaga, K., Kishikawa, K., Maehara, Y., Shimada, M., & Sugimachi, K. (1996). Sensitivity of hepatocellular carcinoma to nine anticancer drugs is unchanged after administration of epirubicin suspended in lipiodol. International journal of oncology, 8(6), 1059-62. https://doi.org/10.3892/ijo.8.6.1059
Nishizaki, T, et al. "Sensitivity of hepatocellular carcinoma to nine anticancer drugs is unchanged after administration of epirubicin suspended in lipiodol." International journal of oncology vol. 8,6 (1996): 1059-62. doi: https://doi.org/10.3892/ijo.8.6.1059
Nishizaki T, Takenaka K, Yanaga K, Kishikawa K, Maehara Y, Shimada M, Sugimachi K. Sensitivity of hepatocellular carcinoma to nine anticancer drugs is unchanged after administration of epirubicin suspended in lipiodol. Int J Oncol. 1996 Jun;8(6):1059-62. doi: 10.3892/ijo.8.6.1059. PMID: 21544464.
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