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Usefulness of an Upright T-Wave in Lead aVR for Predicting the Short-Term Prognosis of Incident Hemodialysis Patients: A Potential Tool for Screening High-Risk Hemodialysis Patients.

Cardiorenal medicine

Matsukane A, Hayashi T, Tanaka Y, Iwasaki M, Kubo S, Asakawa T, Takahashi Y, Imamura Y, Hirahata K, Joki N, Hase H.
PMID: 26648943
Cardiorenal Med. 2015 Oct;5(4):267-77. doi: 10.1159/000433562. Epub 2015 Jul 28.

BACKGROUND/AIMS: An upright T-wave in lead aVR (aVRT) has recently been reported to be associated with cardiovascular death and mortality among the general population and patients with prior cardiovascular disease (CVD). However, evidence for the predictive ability of aVRT...

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Matsukane A, Hayashi T, Tanaka Y, et al. Usefulness of an Upright T-Wave in Lead aVR for Predicting the Short-Term Prognosis of Incident Hemodialysis Patients: A Potential Tool for Screening High-Risk Hemodialysis Patients. Cardiorenal Med. 2015;5(4):267-77doi: 10.1159/000433562.
Matsukane, A., Hayashi, T., Tanaka, Y., Iwasaki, M., Kubo, S., Asakawa, T., Takahashi, Y., Imamura, Y., Hirahata, K., Joki, N., & Hase, H. (2015). Usefulness of an Upright T-Wave in Lead aVR for Predicting the Short-Term Prognosis of Incident Hemodialysis Patients: A Potential Tool for Screening High-Risk Hemodialysis Patients. Cardiorenal medicine, 5(4), 267-77. https://doi.org/10.1159/000433562
Matsukane, Ai, et al. "Usefulness of an Upright T-Wave in Lead aVR for Predicting the Short-Term Prognosis of Incident Hemodialysis Patients: A Potential Tool for Screening High-Risk Hemodialysis Patients." Cardiorenal medicine vol. 5,4 (2015): 267-77. doi: https://doi.org/10.1159/000433562
Matsukane A, Hayashi T, Tanaka Y, Iwasaki M, Kubo S, Asakawa T, Takahashi Y, Imamura Y, Hirahata K, Joki N, Hase H. Usefulness of an Upright T-Wave in Lead aVR for Predicting the Short-Term Prognosis of Incident Hemodialysis Patients: A Potential Tool for Screening High-Risk Hemodialysis Patients. Cardiorenal Med. 2015 Oct;5(4):267-77. doi: 10.1159/000433562. Epub 2015 Jul 28. PMID: 26648943; PMCID: PMC4662279.
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Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease.

CEN case reports

Shimohata H, Maruyama H, Miyamoto Y, Takayasu M, Hirayama K, Kobayashi M.
PMID: 28593486
CEN Case Rep. 2017 Nov;6(2):148-151. doi: 10.1007/s13730-017-0262-5. Epub 2017 Jun 07.

Fabry disease is an X-linked lysosomal storage disorder caused by a lack of α-galactosidase A activity, which leads to the accumulation of globotriaosylceramide in various organs. A complete lack of α-galactosidase A activity in a hemizygous male is the...

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Shimohata H, Maruyama H, Miyamoto Y, et al. Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease. CEN Case Rep. 2017;6(2):148-151doi: 10.1007/s13730-017-0262-5.
Shimohata, H., Maruyama, H., Miyamoto, Y., Takayasu, M., Hirayama, K., & Kobayashi, M. (2017). Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease. CEN case reports, 6(2), 148-151. https://doi.org/10.1007/s13730-017-0262-5
Shimohata, Homare, et al. "Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease." CEN case reports vol. 6,2 (2017): 148-151. doi: https://doi.org/10.1007/s13730-017-0262-5
Shimohata H, Maruyama H, Miyamoto Y, Takayasu M, Hirayama K, Kobayashi M. Urinary mulberry cells and mulberry bodies are useful tool to detect late-onset Fabry disease. CEN Case Rep. 2017 Nov;6(2):148-151. doi: 10.1007/s13730-017-0262-5. Epub 2017 Jun 07. PMID: 28593486; PMCID: PMC5694400.
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Synthesis of novel selenium-containing donors as selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS).

Organic & biomolecular chemistry

Shirahata T, Imakubo T.
PMID: 15188033
Org Biomol Chem. 2004 Jun 21;2(12):1685-7. doi: 10.1039/b406092j. Epub 2004 May 17.

Novel selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS) have been successfully derived from 1,3-diselenole-2-thione, which could be synthesized without the use of the highly toxic reagent CSe(2).

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Shirahata T, Imakubo T. Synthesis of novel selenium-containing donors as selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS). Org Biomol Chem. 2004;2(12):1685-7doi: 10.1039/b406092j.
Shirahata, T., & Imakubo, T. (2004). Synthesis of novel selenium-containing donors as selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS). Organic & biomolecular chemistry, 2(12), 1685-7. https://doi.org/10.1039/b406092j
Shirahata, Takashi, and Imakubo, Tatsuro. "Synthesis of novel selenium-containing donors as selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS)." Organic & biomolecular chemistry vol. 2,12 (2004): 1685-7. doi: https://doi.org/10.1039/b406092j
Shirahata T, Imakubo T. Synthesis of novel selenium-containing donors as selenium analogues of diiodo(ethylenedithio)diselenadithiafulvalene (DIETS). Org Biomol Chem. 2004 Jun 21;2(12):1685-7. doi: 10.1039/b406092j. Epub 2004 May 17. PMID: 15188033.
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Thioredoxin prevents thioacetamide-induced acute hepatitis.

Comparative hepatology

Okuyama H, Shimahara Y, Nakamura H, Araya S, Kawada N, Yamaoka Y, Yodoi J.
PMID: 14960158
Comp Hepatol. 2004 Jan 14;3:S6. doi: 10.1186/1476-5926-2-S1-S6.

No abstract available.

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Okuyama H, Shimahara Y, Nakamura H, et al. Thioredoxin prevents thioacetamide-induced acute hepatitis. Comp Hepatol. 2004;3:S6doi: 10.1186/1476-5926-2-S1-S6.
Okuyama, H., Shimahara, Y., Nakamura, H., Araya, S., Kawada, N., Yamaoka, Y., & Yodoi, J. (2004). Thioredoxin prevents thioacetamide-induced acute hepatitis. Comparative hepatology, 3S6. https://doi.org/10.1186/1476-5926-2-S1-S6
Okuyama, Hiroaki, et al. "Thioredoxin prevents thioacetamide-induced acute hepatitis." Comparative hepatology vol. 3 (2004): S6. doi: https://doi.org/10.1186/1476-5926-2-S1-S6
Okuyama H, Shimahara Y, Nakamura H, Araya S, Kawada N, Yamaoka Y, Yodoi J. Thioredoxin prevents thioacetamide-induced acute hepatitis. Comp Hepatol. 2004 Jan 14;3:S6. doi: 10.1186/1476-5926-2-S1-S6. PMID: 14960158; PMCID: PMC2410229.
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Molecular analysis of cross-reactive human monoclonal antibody AE6F4 generated by in vitro immunization: Epitope mapping of AE6F4 antibody on 14-3-3 family proteins and cytokeratin 8.

Cytotechnology

Ichikawa A, Shim SY, Katakura Y, Teruya K, Hashizume S, Shirahata S.
PMID: 19003320
Cytotechnology. 2001 Jul;36(1):101-7. doi: 10.1023/A:1014060113186.

We reported previously that adenocarcinoma-reactive human monoclonal antibody AE6F4, which had been generated by in vitro immunization method, recognizes both 14-3-3protein and cytokeratin 8 (CK8). In this study, to analyze the cross-reactivity of AE6F4 antibody, epitopes of AE6F4 antibody...

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Ichikawa A, Shim SY, Katakura Y, et al. Molecular analysis of cross-reactive human monoclonal antibody AE6F4 generated by in vitro immunization: Epitope mapping of AE6F4 antibody on 14-3-3 family proteins and cytokeratin 8. Cytotechnology. 2001;36(1):101-7doi: 10.1023/A:1014060113186.
Ichikawa, A., Shim, S. Y., Katakura, Y., Teruya, K., Hashizume, S., & Shirahata, S. (2001). Molecular analysis of cross-reactive human monoclonal antibody AE6F4 generated by in vitro immunization: Epitope mapping of AE6F4 antibody on 14-3-3 family proteins and cytokeratin 8. Cytotechnology, 36(1), 101-7. https://doi.org/10.1023/A:1014060113186
Ichikawa, A, et al. "Molecular analysis of cross-reactive human monoclonal antibody AE6F4 generated by in vitro immunization: Epitope mapping of AE6F4 antibody on 14-3-3 family proteins and cytokeratin 8." Cytotechnology vol. 36,1 (2001): 101-7. doi: https://doi.org/10.1023/A:1014060113186
Ichikawa A, Shim SY, Katakura Y, Teruya K, Hashizume S, Shirahata S. Molecular analysis of cross-reactive human monoclonal antibody AE6F4 generated by in vitro immunization: Epitope mapping of AE6F4 antibody on 14-3-3 family proteins and cytokeratin 8. Cytotechnology. 2001 Jul;36(1):101-7. doi: 10.1023/A:1014060113186. PMID: 19003320; PMCID: PMC3449674.
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Immobilization of gold nanoparticles onto silicon surfaces by Si-C covalent bonds.

Langmuir : the ACS journal of surfaces and colloids

Yamanoi Y, Yonezawa T, Shirahata N, Nishihara H.
PMID: 15803677
Langmuir. 2004 Feb 17;20(4):1054-6. doi: 10.1021/la036437c.

No abstract available.

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Yamanoi Y, Yonezawa T, Shirahata N, et al. Immobilization of gold nanoparticles onto silicon surfaces by Si-C covalent bonds. Langmuir. 2004;20(4):1054-6doi: 10.1021/la036437c.
Yamanoi, Y., Yonezawa, T., Shirahata, N., & Nishihara, H. (2004). Immobilization of gold nanoparticles onto silicon surfaces by Si-C covalent bonds. Langmuir : the ACS journal of surfaces and colloids, 20(4), 1054-6. https://doi.org/10.1021/la036437c
Yamanoi, Yoshinori, et al. "Immobilization of gold nanoparticles onto silicon surfaces by Si-C covalent bonds." Langmuir : the ACS journal of surfaces and colloids vol. 20,4 (2004): 1054-6. doi: https://doi.org/10.1021/la036437c
Yamanoi Y, Yonezawa T, Shirahata N, Nishihara H. Immobilization of gold nanoparticles onto silicon surfaces by Si-C covalent bonds. Langmuir. 2004 Feb 17;20(4):1054-6. doi: 10.1021/la036437c. PMID: 15803677.
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Effect of inhalation anesthetics on swimming activity of artemia salina.

Journal of anesthesia

Takasaki M, Tatara T, Suezaki Y, Shirahama K, Kamaya H, Ueda I, Totoki T.
PMID: 15278632
J Anesth. 1991 Jul;5(3):287-93. doi: 10.1007/s0054010050287.

The swimming movement of artemia salina in the artificial sea water was measured by using the video camera system in the absence and presence of anesthetics, i.e. enflurane, halothane, and isoflurane. The movement of artemia looked random at a...

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Takasaki M, Tatara T, Suezaki Y, et al. Effect of inhalation anesthetics on swimming activity of artemia salina. J Anesth. 1991;5(3):287-93doi: 10.1007/s0054010050287.
Takasaki, M., Tatara, T., Suezaki, Y., Shirahama, K., Kamaya, H., Ueda, I., & Totoki, T. (1991). Effect of inhalation anesthetics on swimming activity of artemia salina. Journal of anesthesia, 5(3), 287-93. https://doi.org/10.1007/s0054010050287
Takasaki, M, et al. "Effect of inhalation anesthetics on swimming activity of artemia salina." Journal of anesthesia vol. 5,3 (1991): 287-93. doi: https://doi.org/10.1007/s0054010050287
Takasaki M, Tatara T, Suezaki Y, Shirahama K, Kamaya H, Ueda I, Totoki T. Effect of inhalation anesthetics on swimming activity of artemia salina. J Anesth. 1991 Jul;5(3):287-93. doi: 10.1007/s0054010050287. PMID: 15278632.
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Microwave-resonance-induced resistivity: evidence of ultrahot surface-state electrons on liquid 3He.

Physical review letters

Konstantinov D, Isshiki H, Monarkha Y, Akimoto H, Shirahama K, Kono K.
PMID: 17677914
Phys Rev Lett. 2007 Jun 08;98(23):235302. doi: 10.1103/PhysRevLett.98.235302. Epub 2007 Jun 07.

Measurements of the dc resistivity of surface-state electrons on liquid helium exposed to microwave radiation are reported. It is shown that the resonant microwave excitation of surface-state electrons is accompanied by a strong increase in their resistivity, which is...

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Konstantinov D, Isshiki H, Monarkha Y, et al. Microwave-resonance-induced resistivity: evidence of ultrahot surface-state electrons on liquid 3He. Phys Rev Lett. 2007;98(23):235302doi: 10.1103/PhysRevLett.98.235302.
Konstantinov, D., Isshiki, H., Monarkha, Y., Akimoto, H., Shirahama, K., & Kono, K. (2007). Microwave-resonance-induced resistivity: evidence of ultrahot surface-state electrons on liquid 3He. Physical review letters, 98(23), 235302. https://doi.org/10.1103/PhysRevLett.98.235302
Konstantinov, Denis, et al. "Microwave-resonance-induced resistivity: evidence of ultrahot surface-state electrons on liquid 3He." Physical review letters vol. 98,23 (2007): 235302. doi: https://doi.org/10.1103/PhysRevLett.98.235302
Konstantinov D, Isshiki H, Monarkha Y, Akimoto H, Shirahama K, Kono K. Microwave-resonance-induced resistivity: evidence of ultrahot surface-state electrons on liquid 3He. Phys Rev Lett. 2007 Jun 08;98(23):235302. doi: 10.1103/PhysRevLett.98.235302. Epub 2007 Jun 07. PMID: 17677914.
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Interfacial observation of an alkylsilane self-assembled monolayer on hydrogen-terminated Si.

Langmuir : the ACS journal of surfaces and colloids

Shirahata N, Seo WS, Kinoshita T, Yonezawa T, Hozumi A, Yokogawa Y, Kameyama T, Masuda Y, Koumoto K.
PMID: 15379531
Langmuir. 2004 Sep 28;20(20):8942-6. doi: 10.1021/la036362c.

No abstract available.

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Shirahata N, Seo WS, Kinoshita T, et al. Interfacial observation of an alkylsilane self-assembled monolayer on hydrogen-terminated Si. Langmuir. 2004;20(20):8942-6doi: 10.1021/la036362c.
Shirahata, N., Seo, W. S., Kinoshita, T., Yonezawa, T., Hozumi, A., Yokogawa, Y., Kameyama, T., Masuda, Y., & Koumoto, K. (2004). Interfacial observation of an alkylsilane self-assembled monolayer on hydrogen-terminated Si. Langmuir : the ACS journal of surfaces and colloids, 20(20), 8942-6. https://doi.org/10.1021/la036362c
Shirahata, Naoto, et al. "Interfacial observation of an alkylsilane self-assembled monolayer on hydrogen-terminated Si." Langmuir : the ACS journal of surfaces and colloids vol. 20,20 (2004): 8942-6. doi: https://doi.org/10.1021/la036362c
Shirahata N, Seo WS, Kinoshita T, Yonezawa T, Hozumi A, Yokogawa Y, Kameyama T, Masuda Y, Koumoto K. Interfacial observation of an alkylsilane self-assembled monolayer on hydrogen-terminated Si. Langmuir. 2004 Sep 28;20(20):8942-6. doi: 10.1021/la036362c. PMID: 15379531.
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JAACT Issue. Preface.

Cytotechnology

Sasaki R, Ikura K, Shirahata S.
PMID: 19002804
Cytotechnology. 2000 Jul;33(1):1. doi: 10.1023/A:1008161418546.

No abstract available.

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Sasaki R, Ikura K, Shirahata S. JAACT Issue. Preface. Cytotechnology. 2000;33(1):1doi: 10.1023/A:1008161418546.
Sasaki, R., Ikura, K., & Shirahata, S. (2000). JAACT Issue. Preface. Cytotechnology, 33(1), 1. https://doi.org/10.1023/A:1008161418546
Sasaki, R, et al. "JAACT Issue. Preface." Cytotechnology vol. 33,1 (2000): 1. doi: https://doi.org/10.1023/A:1008161418546
Sasaki R, Ikura K, Shirahata S. JAACT Issue. Preface. Cytotechnology. 2000 Jul;33(1):1. doi: 10.1023/A:1008161418546. PMID: 19002804; PMCID: PMC3466732.
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Properties of ras-amplified recombinant BHK-21 cells in protein-free culture.

Cytotechnology

Inoue Y, Kawamoto S, Shoji M, Hashizume S, Teruya K, Katakura Y, Shirahata S.
PMID: 19002807
Cytotechnology. 2000 Jul;33(1):21-6. doi: 10.1023/A:1008163312841.

We compared serum and protein-free cultures ofa ras-amplified recombinant BHK-21 cell line(ras-rBHK-IgG), which hyperproduces a lungcancer specific recombinant human monoclonal antibody. Ras-rBHK-IgG cells were shown to grow well, evenin protein-free medium and to be morphologicallysimilar to cells cultured in...

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Inoue Y, Kawamoto S, Shoji M, et al. Properties of ras-amplified recombinant BHK-21 cells in protein-free culture. Cytotechnology. 2000;33(1):21-6doi: 10.1023/A:1008163312841.
Inoue, Y., Kawamoto, S., Shoji, M., Hashizume, S., Teruya, K., Katakura, Y., & Shirahata, S. (2000). Properties of ras-amplified recombinant BHK-21 cells in protein-free culture. Cytotechnology, 33(1), 21-6. https://doi.org/10.1023/A:1008163312841
Inoue, Y, et al. "Properties of ras-amplified recombinant BHK-21 cells in protein-free culture." Cytotechnology vol. 33,1 (2000): 21-6. doi: https://doi.org/10.1023/A:1008163312841
Inoue Y, Kawamoto S, Shoji M, Hashizume S, Teruya K, Katakura Y, Shirahata S. Properties of ras-amplified recombinant BHK-21 cells in protein-free culture. Cytotechnology. 2000 Jul;33(1):21-6. doi: 10.1023/A:1008163312841. PMID: 19002807; PMCID: PMC3466723.
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Purification and characterization of alpha-D-galactosidase produced by ADG cell line established from abalon digestive gland.

Cytotechnology

Kusumoto K, Shirahata S, Kamei Y.
PMID: 19002810
Cytotechnology. 2000 Jul;33(1):47-52. doi: 10.1023/A:1008175226819.

ADG cell line was established from an abalonedigestive gland and previously characterized. ADGcells have the potential to grow in protein-freeculture and secrete l3 types of glycosidases. Inthis article, we determined the origin of ADG cell line,using electron microscopy, and...

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Kusumoto K, Shirahata S, Kamei Y. Purification and characterization of alpha-D-galactosidase produced by ADG cell line established from abalon digestive gland. Cytotechnology. 2000;33(1):47-52doi: 10.1023/A:1008175226819.
Kusumoto, K., Shirahata, S., & Kamei, Y. (2000). Purification and characterization of alpha-D-galactosidase produced by ADG cell line established from abalon digestive gland. Cytotechnology, 33(1), 47-52. https://doi.org/10.1023/A:1008175226819
Kusumoto, K, et al. "Purification and characterization of alpha-D-galactosidase produced by ADG cell line established from abalon digestive gland." Cytotechnology vol. 33,1 (2000): 47-52. doi: https://doi.org/10.1023/A:1008175226819
Kusumoto K, Shirahata S, Kamei Y. Purification and characterization of alpha-D-galactosidase produced by ADG cell line established from abalon digestive gland. Cytotechnology. 2000 Jul;33(1):47-52. doi: 10.1023/A:1008175226819. PMID: 19002810; PMCID: PMC3466711.
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Showing 1 to 12 of 314 entries