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

Year Number of Results
1960 1
1975 1
1977 1
1982 1
1984 1
1987 1
1988 1
1989 2
1990 2
1991 5
1992 14
1993 11
1994 13
1995 13
1996 3
1997 6
1998 6
1999 1
2000 4
2001 10
2002 9
2003 16
2004 14
2005 18
2006 22
2007 20
2008 29
2009 27
2010 31
2011 41
2012 52
2013 44
2014 54
2015 61
2016 69
2017 94
2018 111
2019 112
2020 125
2021 53
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Publication date

Search Results

974 results
Results by year
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Page 1
Molecular Genetics of Premature Ovarian Insufficiency.
Jiao X, Ke H, Qin Y, Chen ZJ. Jiao X, et al. Among authors: ke h. Trends Endocrinol Metab. 2018 Nov;29(11):795-807. doi: 10.1016/j.tem.2018.07.002. Epub 2018 Aug 2. Trends Endocrinol Metab. 2018. PMID: 30078697 Review.
Why are there hotspot mutations in the TP53 gene in human cancers?
Baugh EH, Ke H, Levine AJ, Bonneau RA, Chan CS. Baugh EH, et al. Among authors: ke h. Cell Death Differ. 2018 Jan;25(1):154-160. doi: 10.1038/cdd.2017.180. Epub 2017 Nov 3. Cell Death Differ. 2018. PMID: 29099487 Free PMC article. Review.
NLRP3 Inflammasome as a Molecular Marker in Diabetic Cardiomyopathy.
Luo B, Huang F, Liu Y, Liang Y, Wei Z, Ke H, Zeng Z, Huang W, He Y. Luo B, et al. Among authors: ke h. Front Physiol. 2017 Jul 25;8:519. doi: 10.3389/fphys.2017.00519. eCollection 2017. Front Physiol. 2017. PMID: 28790925 Free PMC article. Review.
Novel actions of sclerostin on bone.
Holdsworth G, Roberts SJ, Ke HZ. Holdsworth G, et al. Among authors: ke hz. J Mol Endocrinol. 2019 Feb 1;62(2):R167-R185. doi: 10.1530/JME-18-0176. J Mol Endocrinol. 2019. PMID: 30532996 Review.
FANCL gene mutations in premature ovarian insufficiency.
Yang Y, Guo T, Liu R, Ke H, Xu W, Zhao S, Qin Y. Yang Y, et al. Among authors: ke h. Hum Mutat. 2020 May;41(5):1033-1041. doi: 10.1002/humu.23997. Epub 2020 Feb 24. Hum Mutat. 2020. PMID: 32048394
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