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
2002 2
2003 1
2007 2
2008 3
2009 1
2011 4
2012 6
2013 5
2014 5
2015 4
2016 4
2017 9
2018 8
2019 13
2020 12
2021 13
2022 13
2023 5
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

99 results

Results by year

Filters applied: . Clear all
Page 1
BCS1L mutations produce Fanconi syndrome with developmental disability.
Kanako KI, Sakakibara N, Murayama K, Nagatani K, Murata S, Otake A, Koga Y, Suzuki H, Uehara T, Kosaki K, Yoshiura KI, Mishima H, Ichimiya Y, Mushimoto Y, Horinouchi T, Nagano C, Yamamura T, Iijima K, Nozu K. Kanako KI, et al. Among authors: mishima h. J Hum Genet. 2022 Mar;67(3):143-148. doi: 10.1038/s10038-021-00984-0. Epub 2021 Oct 15. J Hum Genet. 2022. PMID: 34650211
Patients with SATB2-associated syndrome exhibiting multiple odontomas.
Kikuiri T, Mishima H, Imura H, Suzuki S, Matsuzawa Y, Nakamura T, Fukumoto S, Yoshimura Y, Watanabe S, Kinoshita A, Yamada T, Shindoh M, Sugita Y, Maeda H, Yawaka Y, Mikoya T, Natsume N, Yoshiura KI. Kikuiri T, et al. Among authors: mishima h. Am J Med Genet A. 2018 Dec;176(12):2614-2622. doi: 10.1002/ajmg.a.40670. Epub 2018 Dec 21. Am J Med Genet A. 2018. PMID: 30575289
Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood.
Matsumoto M, Oyake M, Itonaga T, Maeda M, Suenobu S, Sato D, Sasahara Y, Mishima H, Yoshiura KI, Ihara K. Matsumoto M, et al. Among authors: mishima h. Eur J Med Genet. 2024 Apr 15;69:104939. doi: 10.1016/j.ejmg.2024.104939. Online ahead of print. Eur J Med Genet. 2024. PMID: 38614309 Free article.
Optimization of lymphapheresis for manufacturing autologous CAR-T cells.
Yamanaka I, Yamauchi T, Henzan T, Sakoda T, Miyamoto K, Mishima H, Ono H, Koga Y, Nakashima Y, Kato K, Miyamoto T, Mizuno S, Ogawa Y, Ohga S, Akashi K, Maeda T, Kunisaki Y. Yamanaka I, et al. Among authors: mishima h. Int J Hematol. 2021 Oct;114(4):449-458. doi: 10.1007/s12185-021-03191-x. Epub 2021 Jul 17. Int J Hematol. 2021. PMID: 34275066
Targeted deep sequencing analyses of long QT syndrome in a Japanese population.
Nagata Y, Watanabe R, Eichhorn C, Ohno S, Aiba T, Ishikawa T, Nakano Y, Aizawa Y, Hayashi K, Murakoshi N, Nakajima T, Yagihara N, Mishima H, Sudo T, Higuchi C, Takahashi A, Sekine A, Makiyama T, Tanaka Y, Watanabe A, Tachibana M, Morita H, Yoshiura KI, Tsunoda T, Watanabe H, Kurabayashi M, Nogami A, Kihara Y, Horie M, Shimizu W, Makita N, Tanaka T. Nagata Y, et al. Among authors: mishima h. PLoS One. 2022 Dec 8;17(12):e0277242. doi: 10.1371/journal.pone.0277242. eCollection 2022. PLoS One. 2022. PMID: 36480497 Free PMC article.
Germline mutations causing familial lung cancer.
Tomoshige K, Matsumoto K, Tsuchiya T, Oikawa M, Miyazaki T, Yamasaki N, Mishima H, Kinoshita A, Kubo T, Fukushima K, Yoshiura K, Nagayasu T. Tomoshige K, et al. Among authors: mishima h. J Hum Genet. 2015 Oct;60(10):597-603. doi: 10.1038/jhg.2015.75. Epub 2015 Jul 16. J Hum Genet. 2015. PMID: 26178433
99 results