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

Year Number of Results
1951 1
1960 1
1961 1
1970 1
1975 1
1976 3
1977 1
1978 2
1979 2
1981 1
1982 1
1984 4
1985 6
1986 5
1987 5
1988 2
1989 4
1990 3
1991 6
1992 4
1993 16
1994 11
1995 6
1996 5
1997 3
1998 10
1999 5
2000 7
2001 54
2002 8
2003 6
2004 9
2005 16
2006 21
2007 10
2008 12
2009 12
2010 21
2011 24
2012 16
2013 22
2014 23
2015 38
2016 28
2017 32
2018 38
2019 44
2020 44
2021 24
Text availability
Article attribute
Article type
Publication date

Search Results

554 results
Results by year
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Page 1
PKM1 Confers Metabolic Advantages and Promotes Cell-Autonomous Tumor Cell Growth.
Morita M, Sato T, Nomura M, Sakamoto Y, Inoue Y, Tanaka R, Ito S, Kurosawa K, Yamaguchi K, Sugiura Y, Takizaki H, Yamashita Y, Katakura R, Sato I, Kawai M, Okada Y, Watanabe H, Kondoh G, Matsumoto S, Kishimoto A, Obata M, Matsumoto M, Fukuhara T, Motohashi H, Suematsu M, Komatsu M, Nakayama KI, Watanabe T, Soga T, Shima H, Maemondo M, Tanuma N. Morita M, et al. Among authors: kurosawa k. Cancer Cell. 2018 Mar 12;33(3):355-367.e7. doi: 10.1016/j.ccell.2018.02.004. Cancer Cell. 2018. PMID: 29533781 Free article.
Practical guidance in echocardiographic assessment of global longitudinal strain.
Negishi K, Negishi T, Kurosawa K, Hristova K, Popescu BA, Vinereanu D, Yuda S, Marwick TH. Negishi K, et al. Among authors: kurosawa k. JACC Cardiovasc Imaging. 2015 Apr;8(4):489-492. doi: 10.1016/j.jcmg.2014.06.013. Epub 2014 Aug 13. JACC Cardiovasc Imaging. 2015. PMID: 25129519 Free article. No abstract available.
Update of the genotype and phenotype of KMT2D and KDM6A by genetic screening of 100 patients with clinically suspected Kabuki syndrome.
Murakami H, Tsurusaki Y, Enomoto K, Kuroda Y, Yokoi T, Furuya N, Yoshihashi H, Minatogawa M, Abe-Hatano C, Ohashi I, Nishimura N, Kumaki T, Enomoto Y, Naruto T, Iwasaki F, Harada N, Ishikawa A, Kawame H, Sameshima K, Yamaguchi Y, Kobayashi M, Tominaga M, Ishikiriyama S, Tanaka T, Suzumura H, Ninomiya S, Kondo A, Kaname T, Kosaki K, Masuno M, Kuroki Y, Kurosawa K. Murakami H, et al. Among authors: kurosawa k. Am J Med Genet A. 2020 Oct;182(10):2333-2344. doi: 10.1002/ajmg.a.61793. Epub 2020 Aug 17. Am J Med Genet A. 2020. PMID: 32803813
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome.
Aoki Y, Niihori T, Banjo T, Okamoto N, Mizuno S, Kurosawa K, Ogata T, Takada F, Yano M, Ando T, Hoshika T, Barnett C, Ohashi H, Kawame H, Hasegawa T, Okutani T, Nagashima T, Hasegawa S, Funayama R, Nagashima T, Nakayama K, Inoue S, Watanabe Y, Ogura T, Matsubara Y. Aoki Y, et al. Among authors: kurosawa k. Am J Hum Genet. 2013 Jul 11;93(1):173-80. doi: 10.1016/j.ajhg.2013.05.021. Epub 2013 Jun 20. Am J Hum Genet. 2013. PMID: 23791108 Free PMC article.
[Anencephaly].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):191-2. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462395 Review. Japanese. No abstract available.
[Anorchia].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):204. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462400 Review. Japanese. No abstract available.
[Aniridia].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):199-201. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462398 Review. Japanese. No abstract available.
[ATR-16].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(33):242-3. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462420 Review. Japanese. No abstract available.
[Nose].
Kurosawa K. Kurosawa K. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):328-9. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11528764 Review. Japanese. No abstract available.
554 results
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