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Characteristics of geoparks in China and Japan: similarities and differences

Cultural Transformation in the Geoscience Community AND Program Evaluation

Watanabe M.
GSID: NnTzmpztBXYJ
Y Cai, F Wu, M Watanabe, J Han - Geoheritage, 2021 - Springer

Abstract Both China and Japan have achieved considerable development of geoparks. This paper introduces the current status of geoparks and develops a comparative analysis of the legal system, management structure, and financial support of The United National Educational, Scientific...

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Cai, Y., Wu, F., Watanabe, M., & Han, J. (2021). Characteristics of geoparks in China and Japan: similarities and differences. Geoheritage, 13(4), 1-17.
Cai, Yinlu, et al. "Characteristics of geoparks in China and Japan: similarities and differences." Geoheritage 13.4 (2021): 1-17.
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[Nursing of tomorrow].

Kangogaku zasshi

Watanabe M, Suzuki T, Asakawa E, Iwasak Y, Minoda E, Matsuda M.
PMID: 4960512
Kangogaku Zasshi. 1967 Jan;31(1):26-32.

No abstract available.

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Watanabe M, Suzuki T, Asakawa E, et al. [Nursing of tomorrow]. Kangogaku Zasshi. 1967;31(1):26-32
Watanabe, M., Suzuki, T., Asakawa, E., Iwasak, Y., Minoda, E., & Matsuda, M. (1967). [Nursing of tomorrow]. Kangogaku zasshi, 31(1), 26-32.
Watanabe, M, et al. "[Nursing of tomorrow]." Kangogaku zasshi vol. 31,1 (1967): 26-32.
Watanabe M, Suzuki T, Asakawa E, Iwasak Y, Minoda E, Matsuda M. [Nursing of tomorrow]. Kangogaku Zasshi. 1967 Jan;31(1):26-32. Japanese. PMID: 4960512.
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Treatment of congenital absence of the mammary gland.

Case reports in surgery

Yazawa M, Watanabe M, So M, Kishi K.
PMID: 23476876
Case Rep Surg. 2013;2013:676573. doi: 10.1155/2013/676573. Epub 2013 Feb 12.

Breast reconstruction for breast deformity is significant not only for esthetic purposes but also from a psychological perspective. There have been a few reports on treatment of congenital simple absence of the mammary gland. For patients in puberty, even...

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Yazawa M, Watanabe M, So M, et al. Treatment of congenital absence of the mammary gland. Case Rep Surg. 2013;2013:676573doi: 10.1155/2013/676573.
Yazawa, M., Watanabe, M., So, M., & Kishi, K. (2013). Treatment of congenital absence of the mammary gland. Case reports in surgery, 2013676573. https://doi.org/10.1155/2013/676573
Yazawa, Masaki, et al. "Treatment of congenital absence of the mammary gland." Case reports in surgery vol. 2013 (2013): 676573. doi: https://doi.org/10.1155/2013/676573
Yazawa M, Watanabe M, So M, Kishi K. Treatment of congenital absence of the mammary gland. Case Rep Surg. 2013;2013:676573. doi: 10.1155/2013/676573. Epub 2013 Feb 12. PMID: 23476876; PMCID: PMC3583108.
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Full genome analysis of Philippine indigenous subgenotype IA hepatitis A virus strains from Japanese patients with imported acute hepatitis A.

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

Watanabe S, Isoda N, Ohtake T, Hirosawa T, Morimoto N, Aoki K, Ohnishi H, Takahashi M, Sugano K, Okamoto H.
PMID: 23607583
Hepatol Res. 2014 Mar;44(3):270-279. doi: 10.1111/hepr.12124. Epub 2013 Apr 29.

AIM: Hepatitis A virus (HAV) is the most common cause of infectious hepatitis worldwide. Although hepatitis A cases imported from South-East Asian countries, including the Philippines, have been reported in Japan, the molecular epidemiological data have been limited for...

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Watanabe S, Isoda N, Ohtake T, et al. Full genome analysis of Philippine indigenous subgenotype IA hepatitis A virus strains from Japanese patients with imported acute hepatitis A. Hepatol Res. 2013;44(3):270-279doi: 10.1111/hepr.12124.
Watanabe, S., Isoda, N., Ohtake, T., Hirosawa, T., Morimoto, N., Aoki, K., Ohnishi, H., Takahashi, M., Sugano, K., & Okamoto, H. (2014). Full genome analysis of Philippine indigenous subgenotype IA hepatitis A virus strains from Japanese patients with imported acute hepatitis A. Hepatology research : the official journal of the Japan Society of Hepatology, 44(3), 270-279. https://doi.org/10.1111/hepr.12124
Watanabe, Shunji, et al. "Full genome analysis of Philippine indigenous subgenotype IA hepatitis A virus strains from Japanese patients with imported acute hepatitis A." Hepatology research : the official journal of the Japan Society of Hepatology vol. 44,3 (2014): 270-279. doi: https://doi.org/10.1111/hepr.12124
Watanabe S, Isoda N, Ohtake T, Hirosawa T, Morimoto N, Aoki K, Ohnishi H, Takahashi M, Sugano K, Okamoto H. Full genome analysis of Philippine indigenous subgenotype IA hepatitis A virus strains from Japanese patients with imported acute hepatitis A. Hepatol Res. 2014 Mar;44(3):270-279. doi: 10.1111/hepr.12124. Epub 2013 Apr 29. PMID: 23607583.
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Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings.

CEN case reports

Uchida A, Watanabe M, Nawata A, Ikari Y, Sasaki M, Shigemoto K, Hisano S, Nakashima H.
PMID: 28849361
CEN Case Rep. 2017 Nov;6(2):169-174. doi: 10.1007/s13730-017-0269-y. Epub 2017 Aug 28.

Immune-checkpoint inhibitor nivolumab (anti-PD-1 antibody) blocks T cell inhibition and stimulate immunologic response toward cancer cells. It was also revealed that PD-1/PD-L1 interaction crucially controls the effector differentiation of auto-reactive T cells to maintain self-tolerance. Therefore, potential autoimmunological side-effect...

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Uchida A, Watanabe M, Nawata A, et al. Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings. CEN Case Rep. 2017;6(2):169-174doi: 10.1007/s13730-017-0269-y.
Uchida, A., Watanabe, M., Nawata, A., Ikari, Y., Sasaki, M., Shigemoto, K., Hisano, S., & Nakashima, H. (2017). Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings. CEN case reports, 6(2), 169-174. https://doi.org/10.1007/s13730-017-0269-y
Uchida, Ai, et al. "Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings." CEN case reports vol. 6,2 (2017): 169-174. doi: https://doi.org/10.1007/s13730-017-0269-y
Uchida A, Watanabe M, Nawata A, Ikari Y, Sasaki M, Shigemoto K, Hisano S, Nakashima H. Tubulointerstitial nephritis as adverse effect of programmed cell death 1 inhibitor, nivolumab, showed distinct histological findings. CEN Case Rep. 2017 Nov;6(2):169-174. doi: 10.1007/s13730-017-0269-y. Epub 2017 Aug 28. PMID: 28849361; PMCID: PMC5694406.
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Enabling Ambipolar to Heavy n-Type Transport in PbS Quantum Dot Solids through Doping with Organic Molecules.

ACS applied materials & interfaces

Nugraha MI, Kumagai S, Watanabe S, Sytnyk M, Heiss W, Loi MA, Takeya J.
PMID: 28472887
ACS Appl Mater Interfaces. 2017 May 31;9(21):18039-18045. doi: 10.1021/acsami.7b02867. Epub 2017 May 16.

PbS quantum dots (QDs) are remarkable semiconducting materials, which are compatible with low-cost solution-processed electronic device fabrication. Understanding the doping of these materials is one of the great research interests, as it is a necessary step to improve the...

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Nugraha MI, Kumagai S, Watanabe S, et al. Enabling Ambipolar to Heavy n-Type Transport in PbS Quantum Dot Solids through Doping with Organic Molecules. ACS Appl Mater Interfaces. 2017;9(21):18039-18045doi: 10.1021/acsami.7b02867.
Nugraha, M. I., Kumagai, S., Watanabe, S., Sytnyk, M., Heiss, W., Loi, M. A., & Takeya, J. (2017). Enabling Ambipolar to Heavy n-Type Transport in PbS Quantum Dot Solids through Doping with Organic Molecules. ACS applied materials & interfaces, 9(21), 18039-18045. https://doi.org/10.1021/acsami.7b02867
Nugraha, Mohamad Insan, et al. "Enabling Ambipolar to Heavy n-Type Transport in PbS Quantum Dot Solids through Doping with Organic Molecules." ACS applied materials & interfaces vol. 9,21 (2017): 18039-18045. doi: https://doi.org/10.1021/acsami.7b02867
Nugraha MI, Kumagai S, Watanabe S, Sytnyk M, Heiss W, Loi MA, Takeya J. Enabling Ambipolar to Heavy n-Type Transport in PbS Quantum Dot Solids through Doping with Organic Molecules. ACS Appl Mater Interfaces. 2017 May 31;9(21):18039-18045. doi: 10.1021/acsami.7b02867. Epub 2017 May 16. PMID: 28472887; PMCID: PMC5499821.
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Overexpression of REIC/Dkk-3 suppresses the expression of CD147 and inhibits the proliferation of human bladder cancer cells.

Oncology letters

Horikawa Y, Watanabe M, Sadahira T, Ariyoshi Y, Kobayashi Y, Araki M, Wada K, Ochiai K, Li SA, Nasu Y.
PMID: 28927069
Oncol Lett. 2017 Sep;14(3):3223-3228. doi: 10.3892/ol.2017.6548. Epub 2017 Jul 08.

Our group previously developed an adenoviral vector encoding the REIC/Dkk-3 gene (Ad-REIC), a tumor suppressor, for cancer gene therapy. The Ad-REIC agent induces apoptosis and inhibits invasion in a number of cancer cell lines; however, the molecular mechanisms underlying...

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Horikawa Y, Watanabe M, Sadahira T, et al. Overexpression of REIC/Dkk-3 suppresses the expression of CD147 and inhibits the proliferation of human bladder cancer cells. Oncol Lett. 2017;14(3):3223-3228doi: 10.3892/ol.2017.6548.
Horikawa, Y., Watanabe, M., Sadahira, T., Ariyoshi, Y., Kobayashi, Y., Araki, M., Wada, K., Ochiai, K., Li, S. A., & Nasu, Y. (2017). Overexpression of REIC/Dkk-3 suppresses the expression of CD147 and inhibits the proliferation of human bladder cancer cells. Oncology letters, 14(3), 3223-3228. https://doi.org/10.3892/ol.2017.6548
Horikawa, Yuhei, et al. "Overexpression of REIC/Dkk-3 suppresses the expression of CD147 and inhibits the proliferation of human bladder cancer cells." Oncology letters vol. 14,3 (2017): 3223-3228. doi: https://doi.org/10.3892/ol.2017.6548
Horikawa Y, Watanabe M, Sadahira T, Ariyoshi Y, Kobayashi Y, Araki M, Wada K, Ochiai K, Li SA, Nasu Y. Overexpression of REIC/Dkk-3 suppresses the expression of CD147 and inhibits the proliferation of human bladder cancer cells. Oncol Lett. 2017 Sep;14(3):3223-3228. doi: 10.3892/ol.2017.6548. Epub 2017 Jul 08. PMID: 28927069; PMCID: PMC5588074.
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Complicated adult right-sided Bochdalek hernia with Chilaiditi's syndrome: a case report.

Surgical case reports

Watanabe M, Ishibashi O, Watanabe M, Kondo T, Ohkohchi N.
PMID: 26943419
Surg Case Rep. 2015 Dec;1(1):95. doi: 10.1186/s40792-015-0100-y. Epub 2015 Oct 06.

An extremely rare adult case that underwent surgery for ileus caused by Bochdalek hernia associated with Chilaiditi's syndrome is presented. A 65-year-old woman complaining of upper abdominal pain presented to our hospital. Abdominal plain radiography showed increased intestinal gas,...

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Watanabe M, Ishibashi O, Watanabe M, et al. Complicated adult right-sided Bochdalek hernia with Chilaiditi's syndrome: a case report. Surg Case Rep. 2015;1(1):95doi: 10.1186/s40792-015-0100-y.
Watanabe, M., Ishibashi, O., Watanabe, M., Kondo, T., & Ohkohchi, N. (2015). Complicated adult right-sided Bochdalek hernia with Chilaiditi's syndrome: a case report. Surgical case reports, 1(1), 95. https://doi.org/10.1186/s40792-015-0100-y
Watanabe, Motonobu, et al. "Complicated adult right-sided Bochdalek hernia with Chilaiditi's syndrome: a case report." Surgical case reports vol. 1,1 (2015): 95. doi: https://doi.org/10.1186/s40792-015-0100-y
Watanabe M, Ishibashi O, Watanabe M, Kondo T, Ohkohchi N. Complicated adult right-sided Bochdalek hernia with Chilaiditi's syndrome: a case report. Surg Case Rep. 2015 Dec;1(1):95. doi: 10.1186/s40792-015-0100-y. Epub 2015 Oct 06. PMID: 26943419; PMCID: PMC4595410.
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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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Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation.

BioResearch open access

Umebayashi M, Sumita Y, Kawai Y, Watanabe S, Asahina I.
PMID: 26309793
Biores Open Access. 2015 Feb 01;4(1):164-74. doi: 10.1089/biores.2014.0057. eCollection 2015.

To date, therapeutic method for in vivo gene delivery has not been established on bone engineering though its potential usefulness has been suggested. For clinical applications, an effective condition should be developed to transfer the genes in vivo without...

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Umebayashi M, Sumita Y, Kawai Y, et al. Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation. Biores Open Access. 2015;4(1):164-74doi: 10.1089/biores.2014.0057.
Umebayashi, M., Sumita, Y., Kawai, Y., Watanabe, S., & Asahina, I. (2015). Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation. BioResearch open access, 4(1), 164-74. https://doi.org/10.1089/biores.2014.0057
Umebayashi, Mayumi, et al. "Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation." BioResearch open access vol. 4,1 (2015): 164-74. doi: https://doi.org/10.1089/biores.2014.0057
Umebayashi M, Sumita Y, Kawai Y, Watanabe S, Asahina I. Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation. Biores Open Access. 2015 Feb 01;4(1):164-74. doi: 10.1089/biores.2014.0057. eCollection 2015. PMID: 26309793; PMCID: PMC4497668.
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Bone morphogenetic protein-4 modulates proliferation and terminal differentiation of fetal hepatic stem/progenitor cells.

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

Goto F, Kakinuma S, Miyoshi M, Tsunoda T, Kaneko S, Sato A, Asano Y, Otani S, Azuma S, Nagata H, Kawai-Kitahata F, Murakawa M, Nitta S, Itsui Y, Nakagawa M, Asahina Y, Watanabe M.
PMID: 27670640
Hepatol Res. 2017 Aug;47(9):941-952. doi: 10.1111/hepr.12823. Epub 2016 Oct 31.

Fetal hepatic stem/progenitor cells, called hepatoblasts, play central roles in liver organogenesis; however, molecular mechanisms regulating proliferation and terminal differentiation of such cells have not been completely elucidated. Bone morphogenetic protein-4 (BMP-4) is essential for the development of stem...

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Goto F, Kakinuma S, Miyoshi M, et al. Bone morphogenetic protein-4 modulates proliferation and terminal differentiation of fetal hepatic stem/progenitor cells. Hepatol Res. 2016;47(9):941-952doi: 10.1111/hepr.12823.
Goto, F., Kakinuma, S., Miyoshi, M., Tsunoda, T., Kaneko, S., Sato, A., Asano, Y., Otani, S., Azuma, S., Nagata, H., Kawai-Kitahata, F., Murakawa, M., Nitta, S., Itsui, Y., Nakagawa, M., Asahina, Y., & Watanabe, M. (2017). Bone morphogenetic protein-4 modulates proliferation and terminal differentiation of fetal hepatic stem/progenitor cells. Hepatology research : the official journal of the Japan Society of Hepatology, 47(9), 941-952. https://doi.org/10.1111/hepr.12823
Goto, Fumio, et al. "Bone morphogenetic protein-4 modulates proliferation and terminal differentiation of fetal hepatic stem/progenitor cells." Hepatology research : the official journal of the Japan Society of Hepatology vol. 47,9 (2017): 941-952. doi: https://doi.org/10.1111/hepr.12823
Goto F, Kakinuma S, Miyoshi M, Tsunoda T, Kaneko S, Sato A, Asano Y, Otani S, Azuma S, Nagata H, Kawai-Kitahata F, Murakawa M, Nitta S, Itsui Y, Nakagawa M, Asahina Y, Watanabe M. Bone morphogenetic protein-4 modulates proliferation and terminal differentiation of fetal hepatic stem/progenitor cells. Hepatol Res. 2017 Aug;47(9):941-952. doi: 10.1111/hepr.12823. Epub 2016 Oct 31. PMID: 27670640.
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Data on individual metabolites of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunninghamella elegans.

Data in brief

Watanabe S, Kuzhiumparambil U, Winiarski Z, Fu S.
PMID: 26977432
Data Brief. 2016 Feb 23;7:332-40. doi: 10.1016/j.dib.2016.02.039. eCollection 2016 Jun.

Synthetic cannabinoids JWH-018, JWH-073 and AM2201 were metabolised by the fungus Cunninghamella elegans. In this article, data on individual metabolites of their retention times, mass accuracies, major product ions and structures indicated by product ions are presented. The data...

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Watanabe S, Kuzhiumparambil U, Winiarski Z, et al. Data on individual metabolites of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunninghamella elegans. Data Brief. 2016;7:332-40doi: 10.1016/j.dib.2016.02.039.
Watanabe, S., Kuzhiumparambil, U., Winiarski, Z., & Fu, S. (2016). Data on individual metabolites of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunninghamella elegans. Data in brief, 7332-40. https://doi.org/10.1016/j.dib.2016.02.039
Watanabe, Shimpei, et al. "Data on individual metabolites of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunninghamella elegans." Data in brief vol. 7 (2016): 332-40. doi: https://doi.org/10.1016/j.dib.2016.02.039
Watanabe S, Kuzhiumparambil U, Winiarski Z, Fu S. Data on individual metabolites of synthetic cannabinoids JWH-018, JWH-073 and AM2201 by Cunninghamella elegans. Data Brief. 2016 Feb 23;7:332-40. doi: 10.1016/j.dib.2016.02.039. eCollection 2016 Jun. PMID: 26977432; PMCID: PMC4781962.
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Showing 1 to 12 of 3249 entries