Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1979 1
1982 2
1983 3
1984 1
1985 7
1986 5
1987 4
1989 1
1990 1
1992 2
1993 2
1994 2
1995 2
1996 8
1997 2
1998 6
1999 3
2000 2
2001 1
2002 1
2004 2
2005 3
2006 3
2007 6
2008 4
2009 2
2011 2
2012 9
2013 9
2014 1
2016 1
2017 2
2018 1
2019 2
2020 5
2021 2
2022 4
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

107 results

Results by year

Filters applied: . Clear all
Page 1
Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole-exome sequencing.
Suga A, Yoshitake K, Minematsu N, Tsunoda K, Fujinami K, Miyake Y, Kuniyoshi K, Hayashi T, Mizobuchi K, Ueno S, Terasaki H, Kominami T, Nao-I N, Mawatari G, Mizota A, Shinoda K, Kondo M, Kato K, Sekiryu T, Nakamura M, Kusuhara S, Yamamoto H, Yamamoto S, Mochizuki K, Kondo H, Matsushita I, Kameya S, Fukuchi T, Hatase T, Horiguchi M, Shimada Y, Tanikawa A, Yamamoto S, Miura G, Ito N, Murakami A, Fujimaki T, Hotta Y, Tanaka K, Iwata T. Suga A, et al. Hum Mutat. 2022 Dec;43(12):2251-2264. doi: 10.1002/humu.24492. Epub 2022 Nov 7. Hum Mutat. 2022. PMID: 36284460
[Epidemiology of glaucoma].
Nao-i N. Nao-i N. Nihon Rinsho. 1993 Jan;51 Suppl:1003-6. Nihon Rinsho. 1993. PMID: 8459523 Review. Japanese. No abstract available.
CLEC3B is a novel causative gene for macular-retinal dystrophy.
Zhou R, Mawatari G, Cai XB, Shen RJ, Wang YH, Wang YT, Guo YM, Guo FY, Yuan J, Pan D, Nao-I N, Jin ZB. Zhou R, et al. Genet Med. 2022 Jun;24(6):1249-1260. doi: 10.1016/j.gim.2022.02.012. Epub 2022 Mar 22. Genet Med. 2022. PMID: 35331648 Free article.
Studies on auromomycin.
Yamashita T, Naoi N, Hidaka T, Watanabe K, Kumada Y, Takeuchi T, Umezawa H. Yamashita T, et al. Among authors: naoi n. J Antibiot (Tokyo). 1979 Apr;32(4):330-9. doi: 10.7164/antibiotics.32.330. J Antibiot (Tokyo). 1979. PMID: 468720 Free article.
Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan.
Oishi A, Fujinami K, Mawatari G, Naoi N, Ikeda Y, Ueno S, Kuniyoshi K, Hayashi T, Kondo H, Mizota A, Shinoda K, Kusuhara S, Nakamura M, Iwata T, Tsujikawa A, Tsunoda K. Oishi A, et al. Among authors: naoi n. Genes (Basel). 2021 Nov 18;12(11):1817. doi: 10.3390/genes12111817. Genes (Basel). 2021. PMID: 34828423 Free PMC article.
Further purification and characterization of macromomycin.
Yamashita T, Naoi N, Watanabe K. Yamashita T, et al. Among authors: naoi n. J Antibiot (Tokyo). 1976 Apr;29(4):415-23. doi: 10.7164/antibiotics.29.415. J Antibiot (Tokyo). 1976. PMID: 931811 Free article.
Comparison of combination therapy of prednisolone and cyclosporine with corticosteroid pulse therapy in Vogt-Koyanagi-Harada disease.
Ono T, Goto H, Sakai T, Nitta F, Mizuki N, Takase H, Kaneko Y, Hori J, Nakano S, Nao-I N, Ohguro N, Miyata K, Tomita M, Mochizuki M; Japan VKH Disease Treatment Study Group. Ono T, et al. Jpn J Ophthalmol. 2022 Mar;66(2):119-129. doi: 10.1007/s10384-021-00878-w. Epub 2021 Oct 24. Jpn J Ophthalmol. 2022. PMID: 34689288 Clinical Trial.
107 results