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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1998 | 1 |
2002 | 1 |
2003 | 1 |
2007 | 1 |
2009 | 1 |
2014 | 1 |
2019 | 1 |
2024 | 0 |
PubMed for id: 115527104
7 results
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Page 1
Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism.
Bone. 2019 May;122:193-198. doi: 10.1016/j.bone.2019.03.004. Epub 2019 Mar 5.
Bone. 2019.
PMID: 30849546
Bestrophin 3 ameliorates TNFα-induced inflammation by inhibiting NF-κB activation in endothelial cells.
Song W, Yang Z, He B.
Song W, et al.
PLoS One. 2014 Oct 20;9(10):e111093. doi: 10.1371/journal.pone.0111093. eCollection 2014.
PLoS One. 2014.
PMID: 25329324
Free PMC article.
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Bestrophin expression and function in the human pancreatic duct cell line, CFPAC-1.
Marsey LL, Winpenny JP.
Marsey LL, et al.
J Physiol. 2009 May 15;587(Pt 10):2211-24. doi: 10.1113/jphysiol.2008.159087. Epub 2009 Feb 23.
J Physiol. 2009.
PMID: 19237432
Free PMC article.
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Activation of bestrophin Cl- channels is regulated by C-terminal domains.
Qu ZQ, Yu K, Cui YY, Ying C, Hartzell C.
Qu ZQ, et al.
J Biol Chem. 2007 Jun 15;282(24):17460-7. doi: 10.1074/jbc.M701043200. Epub 2007 Apr 17.
J Biol Chem. 2007.
PMID: 17442670
Free article.
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Structure-function analysis of the bestrophin family of anion channels.
Tsunenari T, Sun H, Williams J, Cahill H, Smallwood P, Yau KW, Nathans J.
Tsunenari T, et al.
J Biol Chem. 2003 Oct 17;278(42):41114-25. doi: 10.1074/jbc.M306150200. Epub 2003 Aug 7.
J Biol Chem. 2003.
PMID: 12907679
Free PMC article.
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Three novel human VMD2-like genes are members of the evolutionary highly conserved RFP-TM family.
Stöhr H, Marquardt A, Nanda I, Schmid M, Weber BH.
Stöhr H, et al.
Eur J Hum Genet. 2002 Apr;10(4):281-4. doi: 10.1038/sj.ejhg.5200796.
Eur J Hum Genet. 2002.
PMID: 12032738
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Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).
Marquardt A, Stöhr H, Passmore LA, Krämer F, Rivera A, Weber BH.
Marquardt A, et al.
Hum Mol Genet. 1998 Sep;7(9):1517-25. doi: 10.1093/hmg/7.9.1517.
Hum Mol Genet. 1998.
PMID: 9700209
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