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Enantioselective Synthesis of Silacyclopentanes.

Angewandte Chemie (International ed. in English)

Igawa K, Yoshihiro D, Abe Y, Tomooka K.
PMID: 27037672
Angew Chem Int Ed Engl. 2016 May 04;55(19):5814-8. doi: 10.1002/anie.201511728. Epub 2016 Apr 01.

A variety of functionalized silacyclopentanes were synthesized by highly enantioselective β-eliminations of silacyclopentene oxides followed by stereospecific transformations. The reaction mechanism of the β-elimination was elucidated by DFT calculations. An in vitro biological assay with an oxy-functionalized silacyclopentane showed...

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Igawa K, Yoshihiro D, Abe Y, et al. Enantioselective Synthesis of Silacyclopentanes. Angew Chem Int Ed Engl. 2016;55(19):5814-8doi: 10.1002/anie.201511728.
Igawa, K., Yoshihiro, D., Abe, Y., & Tomooka, K. (2016). Enantioselective Synthesis of Silacyclopentanes. Angewandte Chemie (International ed. in English), 55(19), 5814-8. https://doi.org/10.1002/anie.201511728
Igawa, Kazunobu, et al. "Enantioselective Synthesis of Silacyclopentanes." Angewandte Chemie (International ed. in English) vol. 55,19 (2016): 5814-8. doi: https://doi.org/10.1002/anie.201511728
Igawa K, Yoshihiro D, Abe Y, Tomooka K. Enantioselective Synthesis of Silacyclopentanes. Angew Chem Int Ed Engl. 2016 May 04;55(19):5814-8. doi: 10.1002/anie.201511728. Epub 2016 Apr 01. PMID: 27037672.
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Cervical sympathectomy affects gonadotropin-releasing hormone, luteinizing hormone and testosterone in male rats.

Journal of anesthesia

Iwama H, Tase C, Tonosaki Y, Sugiura Y.
PMID: 28921287
J Anesth. 1995 Jun;9(2):166-169. doi: 10.1007/BF02479850.

To examine the effects of bilateral cervical sympathectomy on the secretion of gonadotropin-releasing hormone (GnRH), luteinizing hormone (LH) and testosterone (TS), 24 male rats were divided into four groups: control (C), light (L), sympathectomy (S), and light-sympathectomy (LS) groups....

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Iwama H, Tase C, Tonosaki Y, et al. Cervical sympathectomy affects gonadotropin-releasing hormone, luteinizing hormone and testosterone in male rats. J Anesth. 1995;9(2):166-169doi: 10.1007/BF02479850.
Iwama, H., Tase, C., Tonosaki, Y., & Sugiura, Y. (1995). Cervical sympathectomy affects gonadotropin-releasing hormone, luteinizing hormone and testosterone in male rats. Journal of anesthesia, 9(2), 166-169. https://doi.org/10.1007/BF02479850
Iwama, Hiroshi, et al. "Cervical sympathectomy affects gonadotropin-releasing hormone, luteinizing hormone and testosterone in male rats." Journal of anesthesia vol. 9,2 (1995): 166-169. doi: https://doi.org/10.1007/BF02479850
Iwama H, Tase C, Tonosaki Y, Sugiura Y. Cervical sympathectomy affects gonadotropin-releasing hormone, luteinizing hormone and testosterone in male rats. J Anesth. 1995 Jun;9(2):166-169. doi: 10.1007/BF02479850. PMID: 28921287.
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Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice.

Journal of oral & facial pain and headache

Maruno M, Shinoda M, Honda K, Ito R, Urata K, Watanabe M, Okada S, Lee J, Gionhaku N, Iwata K.
PMID: 28973050
J Oral Facial Pain Headache. 2017;31(4):372–380. doi: 10.11607/ofph.1849. Epub 2017 Oct 03.

AIMS: To develop a tongue pain model with no mucosal pathologic changes and to examine whether phosphorylation of p38 in trigeminal ganglion (TG) neurons innervating the tongue is associated with tongue heat hypersensitivity in mice.METHODS: Tongue heat sensitivity in...

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Maruno M, Shinoda M, Honda K, et al. Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. J Oral Facial Pain Headache. 2017;31(4):372–380doi: 10.11607/ofph.1849.
Maruno, M., Shinoda, M., Honda, K., Ito, R., Urata, K., Watanabe, M., Okada, S., Lee, J., Gionhaku, N., & Iwata, K. (2017). Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. Journal of oral & facial pain and headache, 31(4), 372–380. https://doi.org/10.11607/ofph.1849
Maruno, Mitsuru, et al. "Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice." Journal of oral & facial pain and headache vol. 31,4 (2017): 372–380. doi: https://doi.org/10.11607/ofph.1849
Maruno M, Shinoda M, Honda K, Ito R, Urata K, Watanabe M, Okada S, Lee J, Gionhaku N, Iwata K. Phosphorylation of p38 in Trigeminal Ganglion Neurons Contributes to Tongue Heat Hypersensitivity in Mice. J Oral Facial Pain Headache. 2017;31(4):372–380. doi: 10.11607/ofph.1849. Epub 2017 Oct 03. PMID: 28973050.
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Molecular detection and characterization of infectious laryngotracheitis virus (Gallid herpesvirus-1) from clinical samples of commercial poultry flocks in India.

Virusdisease

Gowthaman V, Singh SD, Dhama K, Barathidasan R, Mathapati BS, Srinivasan P, Saravanan S, Ramakrishnan MA.
PMID: 25674602
Virusdisease. 2014;25(3):345-9. doi: 10.1007/s13337-014-0206-z. Epub 2014 Apr 01.

Although the existence of infectious laryngotracheitis virus (ILTV) in India was first reported in 1964, no reports are available regarding its molecular detection and characterization. The present study was aimed to detect and characterize ILTV from recent respiratory disease...

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Gowthaman V, Singh SD, Dhama K, et al. Molecular detection and characterization of infectious laryngotracheitis virus (Gallid herpesvirus-1) from clinical samples of commercial poultry flocks in India. Virusdisease. 2014;25(3):345-9doi: 10.1007/s13337-014-0206-z.
Gowthaman, V., Singh, S. D., Dhama, K., Barathidasan, R., Mathapati, B. S., Srinivasan, P., Saravanan, S., & Ramakrishnan, M. A. (2014). Molecular detection and characterization of infectious laryngotracheitis virus (Gallid herpesvirus-1) from clinical samples of commercial poultry flocks in India. Virusdisease, 25(3), 345-9. https://doi.org/10.1007/s13337-014-0206-z
Gowthaman, Vasudevan, et al. "Molecular detection and characterization of infectious laryngotracheitis virus (Gallid herpesvirus-1) from clinical samples of commercial poultry flocks in India." Virusdisease vol. 25,3 (2014): 345-9. doi: https://doi.org/10.1007/s13337-014-0206-z
Gowthaman V, Singh SD, Dhama K, Barathidasan R, Mathapati BS, Srinivasan P, Saravanan S, Ramakrishnan MA. Molecular detection and characterization of infectious laryngotracheitis virus (Gallid herpesvirus-1) from clinical samples of commercial poultry flocks in India. Virusdisease. 2014;25(3):345-9. doi: 10.1007/s13337-014-0206-z. Epub 2014 Apr 01. PMID: 25674602; PMCID: PMC4188208.
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Strategy of Revascularization for Critical Limb Ischemia Due to Infragenicular Lesions-Which Should Be Selected Firstly, Bypass Surgery or Endovascular Therapy?.

Annals of vascular diseases

Ohmine T, Iwasa K, Yamaoka T.
PMID: 26730251
Ann Vasc Dis. 2015;8(4):275-81. doi: 10.3400/avd.oa.15-00076. Epub 2015 Sep 11.

BACKGROUND AND OBJECTIVES: In patients with peripheral arterial diseases (PADs) due to infra-popliteal (below the knee; BTK) lesions, we often encounter situations requiring the immediate selection of either of two revascularization methods, namely bypass surgery or endovascular therapy (EVT)....

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Ohmine T, Iwasa K, Yamaoka T. Strategy of Revascularization for Critical Limb Ischemia Due to Infragenicular Lesions-Which Should Be Selected Firstly, Bypass Surgery or Endovascular Therapy?. Ann Vasc Dis. 2015;8(4):275-81doi: 10.3400/avd.oa.15-00076.
Ohmine, T., Iwasa, K., & Yamaoka, T. (2015). Strategy of Revascularization for Critical Limb Ischemia Due to Infragenicular Lesions-Which Should Be Selected Firstly, Bypass Surgery or Endovascular Therapy?. Annals of vascular diseases, 8(4), 275-81. https://doi.org/10.3400/avd.oa.15-00076
Ohmine, Takahiro, et al. "Strategy of Revascularization for Critical Limb Ischemia Due to Infragenicular Lesions-Which Should Be Selected Firstly, Bypass Surgery or Endovascular Therapy?." Annals of vascular diseases vol. 8,4 (2015): 275-81. doi: https://doi.org/10.3400/avd.oa.15-00076
Ohmine T, Iwasa K, Yamaoka T. Strategy of Revascularization for Critical Limb Ischemia Due to Infragenicular Lesions-Which Should Be Selected Firstly, Bypass Surgery or Endovascular Therapy?. Ann Vasc Dis. 2015;8(4):275-81. doi: 10.3400/avd.oa.15-00076. Epub 2015 Sep 11. PMID: 26730251; PMCID: PMC4691500.
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Bipartite electronic superstructures in the vortex core of Bi2Sr2CaCu2O8+δ.

Nature communications

Machida T, Kohsaka Y, Matsuoka K, Iwaya K, Hanaguri T, Tamegai T.
PMID: 27230420
Nat Commun. 2016 May 27;7:11747. doi: 10.1038/ncomms11747.

The central issue in the physics of cuprate superconductivity is the mutual relationship among superconductivity, pseudogap and broken-spatial-symmetry states. A magnetic field B suppresses superconductivity, providing an opportunity to investigate the competition among these states. Although various B-induced electronic...

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Machida T, Kohsaka Y, Matsuoka K, et al. Bipartite electronic superstructures in the vortex core of Bi2Sr2CaCu2O8+δ. Nat Commun. 2016;7:11747doi: 10.1038/ncomms11747.
Machida, T., Kohsaka, Y., Matsuoka, K., Iwaya, K., Hanaguri, T., & Tamegai, T. (2016). Bipartite electronic superstructures in the vortex core of Bi2Sr2CaCu2O8+δ. Nature communications, 711747. https://doi.org/10.1038/ncomms11747
Machida, T, et al. "Bipartite electronic superstructures in the vortex core of Bi2Sr2CaCu2O8+δ." Nature communications vol. 7 (2016): 11747. doi: https://doi.org/10.1038/ncomms11747
Machida T, Kohsaka Y, Matsuoka K, Iwaya K, Hanaguri T, Tamegai T. Bipartite electronic superstructures in the vortex core of Bi2Sr2CaCu2O8+δ. Nat Commun. 2016 May 27;7:11747. doi: 10.1038/ncomms11747. PMID: 27230420; PMCID: PMC4895017.
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Multifocal BRAF(V600E)-Mutated Melanoma in situ on the Foot.

Case reports in dermatology

Iwama E, Fujimura T, Kusakari Y, Haga T, Aiba S.
PMID: 26594172
Case Rep Dermatol. 2015 Oct 30;7(3):322-7. doi: 10.1159/000441601. eCollection 2015.

Melanoma is an aggressive skin cancer that originates from melanocytes, and about one half of melanoma cases possess a BRAF mutation. Together with PD-L1 expression, the BRAF(V600E) mutation is one of the optimal therapeutic targets for the treatment of...

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Iwama E, Fujimura T, Kusakari Y, et al. Multifocal BRAF(V600E)-Mutated Melanoma in situ on the Foot. Case Rep Dermatol. 2015;7(3):322-7doi: 10.1159/000441601.
Iwama, E., Fujimura, T., Kusakari, Y., Haga, T., & Aiba, S. (2015). Multifocal BRAF(V600E)-Mutated Melanoma in situ on the Foot. Case reports in dermatology, 7(3), 322-7. https://doi.org/10.1159/000441601
Iwama, Eimei, et al. "Multifocal BRAF(V600E)-Mutated Melanoma in situ on the Foot." Case reports in dermatology vol. 7,3 (2015): 322-7. doi: https://doi.org/10.1159/000441601
Iwama E, Fujimura T, Kusakari Y, Haga T, Aiba S. Multifocal BRAF(V600E)-Mutated Melanoma in situ on the Foot. Case Rep Dermatol. 2015 Oct 30;7(3):322-7. doi: 10.1159/000441601. eCollection 2015. PMID: 26594172; PMCID: PMC4650989.
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Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen.

BMC clinical pathology

Hamada S, Horiguchi A, Kuroda K, Ito K, Asano T, Miyai K, Iwaya K.
PMID: 25972764
BMC Clin Pathol. 2015 May 13;15:7. doi: 10.1186/s12907-015-0007-3. eCollection 2015.

[This corrects the article DOI: 10.1186/1472-6890-14-3.].

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Hamada S, Horiguchi A, Kuroda K, et al. Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen. BMC Clin Pathol. 2015;15:7doi: 10.1186/s12907-015-0007-3.
Hamada, S., Horiguchi, A., Kuroda, K., Ito, K., Asano, T., Miyai, K., & Iwaya, K. (2015). Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen. BMC clinical pathology, 157. https://doi.org/10.1186/s12907-015-0007-3
Hamada, Shinsuke, et al. "Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen." BMC clinical pathology vol. 15 (2015): 7. doi: https://doi.org/10.1186/s12907-015-0007-3
Hamada S, Horiguchi A, Kuroda K, Ito K, Asano T, Miyai K, Iwaya K. Erratum: Increased fatty acid synthase expression in prostate biopsy cores predicts higher Gleason score in radical prostatectomy specimen. BMC Clin Pathol. 2015 May 13;15:7. doi: 10.1186/s12907-015-0007-3. eCollection 2015. PMID: 25972764; PMCID: PMC4430029.
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Planar-chiral [7]orthocyclophanes.

Angewandte Chemie (International ed. in English)

Tomooka K, Iso C, Uehara K, Suzuki M, Nishikawa-Shimono R, Igawa K.
PMID: 22976842
Angew Chem Int Ed Engl. 2012 Oct 08;51(41):10355-8. doi: 10.1002/anie.201204484. Epub 2012 Sep 13.

No abstract available.

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Tomooka K, Iso C, Uehara K, et al. Planar-chiral [7]orthocyclophanes. Angew Chem Int Ed Engl. 2012;51(41):10355-8doi: 10.1002/anie.201204484.
Tomooka, K., Iso, C., Uehara, K., Suzuki, M., Nishikawa-Shimono, R., & Igawa, K. (2012). Planar-chiral [7]orthocyclophanes. Angewandte Chemie (International ed. in English), 51(41), 10355-8. https://doi.org/10.1002/anie.201204484
Tomooka, Katsuhiko, et al. "Planar-chiral [7]orthocyclophanes." Angewandte Chemie (International ed. in English) vol. 51,41 (2012): 10355-8. doi: https://doi.org/10.1002/anie.201204484
Tomooka K, Iso C, Uehara K, Suzuki M, Nishikawa-Shimono R, Igawa K. Planar-chiral [7]orthocyclophanes. Angew Chem Int Ed Engl. 2012 Oct 08;51(41):10355-8. doi: 10.1002/anie.201204484. Epub 2012 Sep 13. PMID: 22976842.
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Germline and somatic mutations of the .

Oncology letters

Kumamoto K, Ishida H, Ohsawa T, Ishibashi K, Ushiama M, Yoshida T, Iwama T.
PMID: 26622826
Oncol Lett. 2015 Oct;10(4):2239-2243. doi: 10.3892/ol.2015.3578. Epub 2015 Aug 06.

Patients with familial adenomatous polyposis (FAP), which is caused by the dysfunction of the adenomatous polyposis coli (APC) protein, have the possibility of developing extracolonic manifestations, including thyroid cancer (TC), congenital hypertrophy of the retinal pigment epithelium, desmoid tumors,...

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Kumamoto K, Ishida H, Ohsawa T, et al. Germline and somatic mutations of the . Oncol Lett. 2015;10(4):2239-2243doi: 10.3892/ol.2015.3578.
Kumamoto, K., Ishida, H., Ohsawa, T., Ishibashi, K., Ushiama, M., Yoshida, T., & Iwama, T. (2015). Germline and somatic mutations of the . Oncology letters, 10(4), 2239-2243. https://doi.org/10.3892/ol.2015.3578
Kumamoto, Kensuke, et al. "Germline and somatic mutations of the ." Oncology letters vol. 10,4 (2015): 2239-2243. doi: https://doi.org/10.3892/ol.2015.3578
Kumamoto K, Ishida H, Ohsawa T, Ishibashi K, Ushiama M, Yoshida T, Iwama T. Germline and somatic mutations of the . Oncol Lett. 2015 Oct;10(4):2239-2243. doi: 10.3892/ol.2015.3578. Epub 2015 Aug 06. PMID: 26622826; PMCID: PMC4579915.
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MK-801 treatment affects glycolysis in oligodendrocytes more than in astrocytes and neuronal cells: insights for schizophrenia.

Frontiers in cellular neuroscience

Guest PC, Iwata K, Kato TA, Steiner J, Schmitt A, Turck CW, Martins-de-Souza D.
PMID: 26029051
Front Cell Neurosci. 2015 May 12;9:180. doi: 10.3389/fncel.2015.00180. eCollection 2015.

Schizophrenia is a debilitating mental disorder, affecting more than 30 million people worldwide. As a multifactorial disease, the underlying causes of schizophrenia require analysis by multiplex methods such as proteomics to allow identification of whole protein networks. Previous post-mortem...

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Guest PC, Iwata K, Kato TA, et al. MK-801 treatment affects glycolysis in oligodendrocytes more than in astrocytes and neuronal cells: insights for schizophrenia. Front Cell Neurosci. 2015;9:180doi: 10.3389/fncel.2015.00180.
Guest, P. C., Iwata, K., Kato, T. A., Steiner, J., Schmitt, A., Turck, C. W., & Martins-de-Souza, D. (2015). MK-801 treatment affects glycolysis in oligodendrocytes more than in astrocytes and neuronal cells: insights for schizophrenia. Frontiers in cellular neuroscience, 9180. https://doi.org/10.3389/fncel.2015.00180
Guest, Paul C, et al. "MK-801 treatment affects glycolysis in oligodendrocytes more than in astrocytes and neuronal cells: insights for schizophrenia." Frontiers in cellular neuroscience vol. 9 (2015): 180. doi: https://doi.org/10.3389/fncel.2015.00180
Guest PC, Iwata K, Kato TA, Steiner J, Schmitt A, Turck CW, Martins-de-Souza D. MK-801 treatment affects glycolysis in oligodendrocytes more than in astrocytes and neuronal cells: insights for schizophrenia. Front Cell Neurosci. 2015 May 12;9:180. doi: 10.3389/fncel.2015.00180. eCollection 2015. PMID: 26029051; PMCID: PMC4429244.
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Peer-assisted learning--beyond teaching: How can medical students contribute to the undergraduate curriculum?.

Medical teacher

Furmedge DS, Iwata K, Gill D.
PMID: 25020139
Med Teach. 2014 Sep;36(9):812-7. doi: 10.3109/0142159X.2014.917158. Epub 2014 Jul 14.

INTRODUCTION: Peer-assisted learning (PAL) has become increasingly popular over recent years with many medical schools now formally incorporating peer-teaching programs into the curriculum. PAL has a sound evidence base with benefit to both peer-teacher and peer-learner. Aside from in...

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Furmedge DS, Iwata K, Gill D. Peer-assisted learning--beyond teaching: How can medical students contribute to the undergraduate curriculum?. Med Teach. 2014;36(9):812-7doi: 10.3109/0142159X.2014.917158.
Furmedge, D. S., Iwata, K., & Gill, D. (2014). Peer-assisted learning--beyond teaching: How can medical students contribute to the undergraduate curriculum?. Medical teacher, 36(9), 812-7. https://doi.org/10.3109/0142159X.2014.917158
Furmedge, Daniel S, et al. "Peer-assisted learning--beyond teaching: How can medical students contribute to the undergraduate curriculum?." Medical teacher vol. 36,9 (2014): 812-7. doi: https://doi.org/10.3109/0142159X.2014.917158
Furmedge DS, Iwata K, Gill D. Peer-assisted learning--beyond teaching: How can medical students contribute to the undergraduate curriculum?. Med Teach. 2014 Sep;36(9):812-7. doi: 10.3109/0142159X.2014.917158. Epub 2014 Jul 14. PMID: 25020139.
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Showing 1 to 12 of 1105 entries