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Rotational resonance for a heteronuclear spin pair under magic-angle spinning in solid-state NMR.

The Journal of chemical physics

Kamihara T, Takegoshi K.
PMID: 28433023
J Chem Phys. 2017 Apr 21;146(15):154202. doi: 10.1063/1.4980156.

Rotational resonance (R2) is one of the widely applied techniques in solid-state NMR for recoupling a homonuclear dipolar interaction under magic-angle spinning (MAS). R2 occurs as the result of interference between the difference of the chemical shifts and MAS....

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Kamihara T, Takegoshi K. Rotational resonance for a heteronuclear spin pair under magic-angle spinning in solid-state NMR. J Chem Phys. 2017;146(15):154202doi: 10.1063/1.4980156.
Kamihara, T., & Takegoshi, K. (2017). Rotational resonance for a heteronuclear spin pair under magic-angle spinning in solid-state NMR. The Journal of chemical physics, 146(15), 154202. https://doi.org/10.1063/1.4980156
Kamihara, Takayuki, and Takegoshi, K. "Rotational resonance for a heteronuclear spin pair under magic-angle spinning in solid-state NMR." The Journal of chemical physics vol. 146,15 (2017): 154202. doi: https://doi.org/10.1063/1.4980156
Kamihara T, Takegoshi K. Rotational resonance for a heteronuclear spin pair under magic-angle spinning in solid-state NMR. J Chem Phys. 2017 Apr 21;146(15):154202. doi: 10.1063/1.4980156. PMID: 28433023.
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Aneurysm growth after late conversion of thoracic endovascular aortic repair.

SAGE open medical case reports

Kasahara H, Hayashi I, Haijima N.
PMID: 27489673
SAGE Open Med Case Rep. 2015 Jan 08;3:2050313X14565422. doi: 10.1177/2050313X14565422. eCollection 2015.

A 69-year-old man underwent thoracic endovascular aortic repair of a descending aortic aneurysm. Three years later, he developed impending rupture due to aneurysmal expansion that included the proximal landing zone. Urgent open surgery was performed via lateral thoracotomy, and...

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Kasahara H, Hayashi I, Haijima N. Aneurysm growth after late conversion of thoracic endovascular aortic repair. SAGE Open Med Case Rep. 2015;3:2050313X14565422doi: 10.1177/2050313X14565422.
Kasahara, H., Hayashi, I., & Haijima, N. (2015). Aneurysm growth after late conversion of thoracic endovascular aortic repair. SAGE open medical case reports, 32050313X14565422. https://doi.org/10.1177/2050313X14565422
Kasahara, Hirofumi, et al. "Aneurysm growth after late conversion of thoracic endovascular aortic repair." SAGE open medical case reports vol. 3 (2015): 2050313X14565422. doi: https://doi.org/10.1177/2050313X14565422
Kasahara H, Hayashi I, Haijima N. Aneurysm growth after late conversion of thoracic endovascular aortic repair. SAGE Open Med Case Rep. 2015 Jan 08;3:2050313X14565422. doi: 10.1177/2050313X14565422. eCollection 2015. PMID: 27489673; PMCID: PMC4857313.
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Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia.

Neuropsychiatric disease and treatment

Oda Y, Kanahara N, Kimura H, Watanabe H, Hashimoto K, Iyo M.
PMID: 26251601
Neuropsychiatr Dis Treat. 2015 Jul 29;11:1845-51. doi: 10.2147/NDT.S86042. eCollection 2015.

BACKGROUND/AIM: Dopamine supersensitivity psychosis (DSP), clinically characterized by unstable and severe psychosis or tardive dyskinesia and often categorized as treatment-resistant schizophrenia, is promoted by long-term antipsychotic treatment. An upregulation of the dopamine D2 receptor caused by antipsychotic(s) is involved...

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Oda Y, Kanahara N, Kimura H, et al. Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia. Neuropsychiatr Dis Treat. 2015;11:1845-51doi: 10.2147/NDT.S86042.
Oda, Y., Kanahara, N., Kimura, H., Watanabe, H., Hashimoto, K., & Iyo, M. (2015). Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia. Neuropsychiatric disease and treatment, 111845-51. https://doi.org/10.2147/NDT.S86042
Oda, Yasunori, et al. "Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia." Neuropsychiatric disease and treatment vol. 11 (2015): 1845-51. doi: https://doi.org/10.2147/NDT.S86042
Oda Y, Kanahara N, Kimura H, Watanabe H, Hashimoto K, Iyo M. Genetic association between G protein-coupled receptor kinase 6/β-arrestin 2 and dopamine supersensitivity psychosis in schizophrenia. Neuropsychiatr Dis Treat. 2015 Jul 29;11:1845-51. doi: 10.2147/NDT.S86042. eCollection 2015. PMID: 26251601; PMCID: PMC4524575.
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Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions.

Annals of clinical and translational neurology

Fuke S, Kametani M, Yamada K, Kasahara T, Kubota-Sakashita M, Kujoth GC, Prolla TA, Hitoshi S, Kato T.
PMID: 25540805
Ann Clin Transl Neurol. 2014 Nov;1(11):909-20. doi: 10.1002/acn3.133. Epub 2014 Oct 22.

OBJECTIVE: Mutations in nuclear-encoded mitochondrial DNA (mtDNA) polymerase (POLG) are known to cause autosomal dominant chronic progressive external ophthalmoplegia (adCPEO) with accumulation of multiple mtDNA deletions in muscles. However, no animal model with a heterozygous Polg mutation representing mtDNA...

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Fuke S, Kametani M, Yamada K, et al. Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions. Ann Clin Transl Neurol. 2014;1(11):909-20doi: 10.1002/acn3.133.
Fuke, S., Kametani, M., Yamada, K., Kasahara, T., Kubota-Sakashita, M., Kujoth, G. C., Prolla, T. A., Hitoshi, S., & Kato, T. (2014). Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions. Annals of clinical and translational neurology, 1(11), 909-20. https://doi.org/10.1002/acn3.133
Fuke, Satoshi, et al. "Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions." Annals of clinical and translational neurology vol. 1,11 (2014): 909-20. doi: https://doi.org/10.1002/acn3.133
Fuke S, Kametani M, Yamada K, Kasahara T, Kubota-Sakashita M, Kujoth GC, Prolla TA, Hitoshi S, Kato T. Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions. Ann Clin Transl Neurol. 2014 Nov;1(11):909-20. doi: 10.1002/acn3.133. Epub 2014 Oct 22. PMID: 25540805; PMCID: PMC4265062.
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Erratum to: LC-MS-based quantification method for Achyranthes root saponins.

Journal of natural medicines

Kawahara Y, Hoshino T, Morimoto H, Shimizu T, Narukawa Y, Fuchino H, Kawahara N, Kiuchi F.
PMID: 26659596
J Nat Med. 2016 Apr;70(2):300. doi: 10.1007/s11418-015-0953-1.

No abstract available.

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Kawahara Y, Hoshino T, Morimoto H, et al. Erratum to: LC-MS-based quantification method for Achyranthes root saponins. J Nat Med. 2016;70(2):300doi: 10.1007/s11418-015-0953-1.
Kawahara, Y., Hoshino, T., Morimoto, H., Shimizu, T., Narukawa, Y., Fuchino, H., Kawahara, N., & Kiuchi, F. (2016). Erratum to: LC-MS-based quantification method for Achyranthes root saponins. Journal of natural medicines, 70(2), 300. https://doi.org/10.1007/s11418-015-0953-1
Kawahara, Yuki, et al. "Erratum to: LC-MS-based quantification method for Achyranthes root saponins." Journal of natural medicines vol. 70,2 (2016): 300. doi: https://doi.org/10.1007/s11418-015-0953-1
Kawahara Y, Hoshino T, Morimoto H, Shimizu T, Narukawa Y, Fuchino H, Kawahara N, Kiuchi F. Erratum to: LC-MS-based quantification method for Achyranthes root saponins. J Nat Med. 2016 Apr;70(2):300. doi: 10.1007/s11418-015-0953-1. PMID: 26659596.
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Arylation of diorganochalcogen compounds with diaryliodonium triflates: metal catalysts are unnecessary.

Organic letters

Racicot L, Kasahara T, Ciufolini MA.
PMID: 25493925
Org Lett. 2014 Dec 19;16(24):6382-5. doi: 10.1021/ol503177q. Epub 2014 Dec 10.

Diaryliodonium triflates transfer an aryl group to the chalcogen atom of organic sulfides, selenides, and tellurides (but not ethers), in the absence of transition-metal catalyst, simply upon heating in chloroform or dichloroethane solution.

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Racicot L, Kasahara T, Ciufolini MA. Arylation of diorganochalcogen compounds with diaryliodonium triflates: metal catalysts are unnecessary. Org Lett. 2014;16(24):6382-5doi: 10.1021/ol503177q.
Racicot, L., Kasahara, T., & Ciufolini, M. A. (2014). Arylation of diorganochalcogen compounds with diaryliodonium triflates: metal catalysts are unnecessary. Organic letters, 16(24), 6382-5. https://doi.org/10.1021/ol503177q
Racicot, Léanne, et al. "Arylation of diorganochalcogen compounds with diaryliodonium triflates: metal catalysts are unnecessary." Organic letters vol. 16,24 (2014): 6382-5. doi: https://doi.org/10.1021/ol503177q
Racicot L, Kasahara T, Ciufolini MA. Arylation of diorganochalcogen compounds with diaryliodonium triflates: metal catalysts are unnecessary. Org Lett. 2014 Dec 19;16(24):6382-5. doi: 10.1021/ol503177q. Epub 2014 Dec 10. PMID: 25493925.
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Ciliochoroidal Detachment Following Scleral Buckling Surgery for Rhegmatogenous Retinal Detachment.

Japanese journal of ophthalmology

Kawahara S, Nagai Y, Kawakami E, Ida RY, Takeuchi M, Uyama M.
PMID: 11094196
Jpn J Ophthalmol. 2000 Nov 01;44(6):692-693. doi: 10.1016/s0021-5155(00)00255-0.

Purpose and Methods: We observed the peripheral choroid, ciliary body, and depth of the anterior chamber by ultrasound biomicroscopy (UBM) in 31 eyes with rhegmatogenous retinal detachment before and after scleral buckling surgery. Scleral encircling was performed in 11...

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Kawahara S, Nagai Y, Kawakami E, et al. Ciliochoroidal Detachment Following Scleral Buckling Surgery for Rhegmatogenous Retinal Detachment. Jpn J Ophthalmol. 2000;44(6):692-693doi: 10.1016/s0021-5155(00)00255-0.
Kawahara, S., Nagai, Y., Kawakami, E., Ida, R. Y., Takeuchi, M., & Uyama, M. (2000). Ciliochoroidal Detachment Following Scleral Buckling Surgery for Rhegmatogenous Retinal Detachment. Japanese journal of ophthalmology, 44(6), 692-693. https://doi.org/10.1016/s0021-5155(00)00255-0
Kawahara, et al. "Ciliochoroidal Detachment Following Scleral Buckling Surgery for Rhegmatogenous Retinal Detachment." Japanese journal of ophthalmology vol. 44,6 (2000): 692-693. doi: https://doi.org/10.1016/s0021-5155(00)00255-0
Kawahara S, Nagai Y, Kawakami E, Ida RY, Takeuchi M, Uyama M. Ciliochoroidal Detachment Following Scleral Buckling Surgery for Rhegmatogenous Retinal Detachment. Jpn J Ophthalmol. 2000 Nov 01;44(6):692-693. doi: 10.1016/s0021-5155(00)00255-0. PMID: 11094196.
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Hepatitis C virus (HCV) genotype 1b sequences from fifteen patients with hepatocellular carcinoma: the 'progression score' revisited.

Hepatology research : the official journal of the Japan Society of Hepatology

Takahashi K, Iwata K, Matsumoto M, Matsumoto H, Nakao K, Hatahara T, Ohta Y, Kanai K, Maruo H, Baba K, Hijikata M, Mishiro S.
PMID: 11348851
Hepatol Res. 2001 Jun;20(2):161-171. doi: 10.1016/s1386-6346(00)00141-8.

The genome of hepatitis C virus (HCV) associated with hepatocellular carcinoma (HCC) may have some characteristics which would barely be found in those of HCV from asymptomatic carriers (ASC). We analyzed 15 HCC patients who were infected with HCV...

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Takahashi K, Iwata K, Matsumoto M, et al. Hepatitis C virus (HCV) genotype 1b sequences from fifteen patients with hepatocellular carcinoma: the 'progression score' revisited. Hepatol Res. 2001;20(2):161-171doi: 10.1016/s1386-6346(00)00141-8.
Takahashi, K., Iwata, K., Matsumoto, M., Matsumoto, H., Nakao, K., Hatahara, T., Ohta, Y., Kanai, K., Maruo, H., Baba, K., Hijikata, M., & Mishiro, S. (2001). Hepatitis C virus (HCV) genotype 1b sequences from fifteen patients with hepatocellular carcinoma: the 'progression score' revisited. Hepatology research : the official journal of the Japan Society of Hepatology, 20(2), 161-171. https://doi.org/10.1016/s1386-6346(00)00141-8
Takahashi, K, et al. "Hepatitis C virus (HCV) genotype 1b sequences from fifteen patients with hepatocellular carcinoma: the 'progression score' revisited." Hepatology research : the official journal of the Japan Society of Hepatology vol. 20,2 (2001): 161-171. doi: https://doi.org/10.1016/s1386-6346(00)00141-8
Takahashi K, Iwata K, Matsumoto M, Matsumoto H, Nakao K, Hatahara T, Ohta Y, Kanai K, Maruo H, Baba K, Hijikata M, Mishiro S. Hepatitis C virus (HCV) genotype 1b sequences from fifteen patients with hepatocellular carcinoma: the 'progression score' revisited. Hepatol Res. 2001 Jun;20(2):161-171. doi: 10.1016/s1386-6346(00)00141-8. PMID: 11348851.
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PRIMER NOTES: Isolation of microsatellite markers in Castanopsis cuspidata var. sieboldii Nakai from an enriched library.

Molecular ecology

Ueno S, Yoshimaru H, Kawahara T, Yamamoto S.
PMID: 10964247
Mol Ecol. 2000 Aug;9(8):1187-1189.

No abstract available.

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Ueno S, Yoshimaru H, Kawahara T, et al. PRIMER NOTES: Isolation of microsatellite markers in Castanopsis cuspidata var. sieboldii Nakai from an enriched library. Mol Ecol. 2000;9(8):1187-1189
Ueno, S., Yoshimaru, H., Kawahara, T., & Yamamoto, S. (2000). PRIMER NOTES: Isolation of microsatellite markers in Castanopsis cuspidata var. sieboldii Nakai from an enriched library. Molecular ecology, 9(8), 1187-1189.
Ueno, et al. "PRIMER NOTES: Isolation of microsatellite markers in Castanopsis cuspidata var. sieboldii Nakai from an enriched library." Molecular ecology vol. 9,8 (2000): 1187-1189.
Ueno S, Yoshimaru H, Kawahara T, Yamamoto S. PRIMER NOTES: Isolation of microsatellite markers in Castanopsis cuspidata var. sieboldii Nakai from an enriched library. Mol Ecol. 2000 Aug;9(8):1187-1189. PMID: 10964247.
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Diastereoselective 1,4-Addition of Stannyl Radical in the Presence of Lewis Acid: A Novel Synthetic Route to Optically Active beta-Stannyl Esters.

The Journal of organic chemistry

Nishida M, Nishida A, Kawahara N.
PMID: 11667194
J Org Chem. 1996 May 31;61(11):3574-3575. doi: 10.1021/jo952170d.

No abstract available.

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Nishida M, Nishida A, Kawahara N. Diastereoselective 1,4-Addition of Stannyl Radical in the Presence of Lewis Acid: A Novel Synthetic Route to Optically Active beta-Stannyl Esters. J Org Chem. 1996;61(11):3574-3575doi: 10.1021/jo952170d.
Nishida, M., Nishida, A., & Kawahara, N. (1996). Diastereoselective 1,4-Addition of Stannyl Radical in the Presence of Lewis Acid: A Novel Synthetic Route to Optically Active beta-Stannyl Esters. The Journal of organic chemistry, 61(11), 3574-3575. https://doi.org/10.1021/jo952170d
Nishida, Mayumi, et al. "Diastereoselective 1,4-Addition of Stannyl Radical in the Presence of Lewis Acid: A Novel Synthetic Route to Optically Active beta-Stannyl Esters." The Journal of organic chemistry vol. 61,11 (1996): 3574-3575. doi: https://doi.org/10.1021/jo952170d
Nishida M, Nishida A, Kawahara N. Diastereoselective 1,4-Addition of Stannyl Radical in the Presence of Lewis Acid: A Novel Synthetic Route to Optically Active beta-Stannyl Esters. J Org Chem. 1996 May 31;61(11):3574-3575. doi: 10.1021/jo952170d. PMID: 11667194.
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Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation.

Organic letters

Tanaka M, Imai M, Yamamoto Y, Tanaka K, Shimowatari M, Nagumo S, Kawahara N, Suemune H.
PMID: 12688760
Org Lett. 2003 Apr 17;5(8):1365-7. doi: 10.1021/ol034343o.

[reaction: see text] Rh-Catalyzed intermolecular hydroacylation between salicylaldehydes and 1,5-hexadienes proceeded under remarkably mild reaction conditions to afford a mixture of iso- and normal-hydroacylated products in good yields. The experiments using deuterated salicylaldehyde-d revealed that "double chelation" of salicylaldehyde...

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Tanaka M, Imai M, Yamamoto Y, et al. Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation. Org Lett. 2003;5(8):1365-7doi: 10.1021/ol034343o.
Tanaka, M., Imai, M., Yamamoto, Y., Tanaka, K., Shimowatari, M., Nagumo, S., Kawahara, N., & Suemune, H. (2003). Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation. Organic letters, 5(8), 1365-7. https://doi.org/10.1021/ol034343o
Tanaka, Masakazu, et al. "Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation." Organic letters vol. 5,8 (2003): 1365-7. doi: https://doi.org/10.1021/ol034343o
Tanaka M, Imai M, Yamamoto Y, Tanaka K, Shimowatari M, Nagumo S, Kawahara N, Suemune H. Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation. Org Lett. 2003 Apr 17;5(8):1365-7. doi: 10.1021/ol034343o. PMID: 12688760.
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First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester.

Inorganic chemistry

Kato S, Niyomura O, Nakaiida S, Kawahara Y, Kanda T, Yamada R, Hori S.
PMID: 11673957
Inorg Chem. 1999 Feb 08;38(3):519-530. doi: 10.1021/ic980815x.

The first synthesis and characterization of sodium and potassium tellurocarboxylates were achieved by the reaction of acyl chlorides with the corresponding alkali metal tellurides. The salts are yellow to red solids or oils. The aliphatic derivatives are very sensitive...

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Kato S, Niyomura O, Nakaiida S, et al. First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester. Inorg Chem. 1999;38(3):519-530doi: 10.1021/ic980815x.
Kato, S., Niyomura, O., Nakaiida, S., Kawahara, Y., Kanda, T., Yamada, R., & Hori, S. (1999). First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester. Inorganic chemistry, 38(3), 519-530. https://doi.org/10.1021/ic980815x
Kato, Shinzi, et al. "First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester." Inorganic chemistry vol. 38,3 (1999): 519-530. doi: https://doi.org/10.1021/ic980815x
Kato S, Niyomura O, Nakaiida S, Kawahara Y, Kanda T, Yamada R, Hori S. First Isolation and Characterization of Sodium and Potassium Tellurocarboxylates: Structural Analysis of Te-Alkyl Telluroester. Inorg Chem. 1999 Feb 08;38(3):519-530. doi: 10.1021/ic980815x. PMID: 11673957.
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Showing 25 to 36 of 1151 entries