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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2022 | 2 |
2023 | 1 |
Search Results
6
results
Results by year
Page 1
Janus Hydrogel Microbeads for Glucose Sensing with pH Calibration.
Sensors (Basel). 2021 Jul 15;21(14):4829. doi: 10.3390/s21144829.
Sensors (Basel). 2021.
PMID: 34300568
Free PMC article.
Shared decision making between patients with Fabry disease and physicians in Japan: An online survey.
Inagaki N, Tsuchiya M, Otani K, Nakayama T.
Inagaki N, et al. Among authors: tsuchiya m.
Mol Genet Metab Rep. 2022 Aug 10;32:100899. doi: 10.1016/j.ymgmr.2022.100899. eCollection 2022 Sep.
Mol Genet Metab Rep. 2022.
PMID: 36046392
Free PMC article.
Item in Clipboard
Eye-recognizable and repeatable biochemical flexible sensors using low angle-dependent photonic colloidal crystal hydrogel microbeads.
Tsuchiya M, Kurashina Y, Onoe H.
Tsuchiya M, et al.
Sci Rep. 2019 Nov 19;9(1):17059. doi: 10.1038/s41598-019-53499-2.
Sci Rep. 2019.
PMID: 31745154
Free PMC article.
Item in Clipboard
Influence of MILR1 promoter polymorphism on expression levels and the phenotype of atopy.
Nanatsue K, Ninomiya T, Tsuchiya M, Tahara-Hanaoka S, Shibuya A, Masuko H, Sakamoto T, Hizawa N, Arinami T, Noguchi E.
Nanatsue K, et al. Among authors: tsuchiya m.
J Hum Genet. 2014 Sep;59(9):480-3. doi: 10.1038/jhg.2014.57. Epub 2014 Jul 10.
J Hum Genet. 2014.
PMID: 25007884
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Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan.
Tsuchiya M, Yamada T, Akaishi R, Hamanoue H, Hirasawa A, Hyodo M, Imoto I, Kosho T, Kurosawa K, Murakami H, Nakatani K, Nomura F, Sasaki A, Shimizu K, Tamai M, Umemura H, Watanabe A, Yoshida A, Yoshihashi H, Yotsumoto J, Kosugi S.
Tsuchiya M, et al.
J Hum Genet. 2020 Dec;65(12):1045-1053. doi: 10.1038/s10038-020-0802-2. Epub 2020 Jul 13.
J Hum Genet. 2020.
PMID: 32661284
Free article.
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Challenges of secondary finding disclosure in genomic medicine in rare diseases: A nation-wide survey of Japanese facilities outsourcing comprehensive genetic testing.
Hiromoto K, Yamada T, Tsuchiya M, Kawame H, Nanba E, Goto Y, Kosugi S.
Hiromoto K, et al. Among authors: tsuchiya m.
J Hum Genet. 2023 Jan;68(1):1-9. doi: 10.1038/s10038-022-01084-3. Epub 2022 Oct 3.
J Hum Genet. 2023.
PMID: 36192516
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