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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 1 |
2008 | 2 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
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Decreased SH3BP2 inhibits osteoclast differentiation and function.
J Orthop Res. 2011 Oct;29(10):1521-7. doi: 10.1002/jor.21408. Epub 2011 Mar 29.
J Orthop Res. 2011.
PMID: 21448930
Free PMC article.
Cloning and characterization of the human SH3BP2 promoter.
Fan C, Gaivin RJ, Marth TA, Willard B, Levine MA, Lietman SA.
Fan C, et al.
Biochem Biophys Res Commun. 2012 Aug 17;425(1):25-32. doi: 10.1016/j.bbrc.2012.07.043. Epub 2012 Jul 17.
Biochem Biophys Res Commun. 2012.
PMID: 22820184
Free PMC article.
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Preimplantation genetic diagnosis for severe albright hereditary osteodystrophy.
Lietman SA, Goldfarb J, Desai N, Levine MA.
Lietman SA, et al.
J Clin Endocrinol Metab. 2008 Mar;93(3):901-4. doi: 10.1210/jc.2007-2040. Epub 2007 Dec 18.
J Clin Endocrinol Metab. 2008.
PMID: 18089698
Free PMC article.
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SH3BP2 is an activator of NFAT activity and osteoclastogenesis.
Lietman SA, Yin L, Levine MA.
Lietman SA, et al.
Biochem Biophys Res Commun. 2008 Jul 11;371(4):644-8. doi: 10.1016/j.bbrc.2008.04.080. Epub 2008 Apr 25.
Biochem Biophys Res Commun. 2008.
PMID: 18440306
Free PMC article.
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SH3BP2 mutations potentiate osteoclastogenesis via PLCγ.
Lietman SA, Yin L, Levine MA.
Lietman SA, et al.
J Orthop Res. 2010 Nov;28(11):1425-30. doi: 10.1002/jor.21164.
J Orthop Res. 2010.
PMID: 20872577
Free PMC article.
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