R01 HL073817/HL/NHLBI NIH HHS/United States[Grants and Funding] - Search Results

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Subject: R01 HL073817/HL/NHLBI NIH HHS/United States[Grant - PubMed

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Year	Number of Results
2004	1
2005	3
2006	1
2007	1
2008	1
2011	2
2013	1
2019	1
2024	0

11 results

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SUMOylation of Vps34 by SUMO1 promotes phenotypic switching of vascular smooth muscle cells by activating autophagy in pulmonary arterial hypertension.

Yao Y, Li H, Da X, He Z, Tang B, Li Y, Hu C, Xu C, Chen Q, Wang QK. Yao Y, et al. Pulm Pharmacol Ther. 2019 Apr;55:38-49. doi: 10.1016/j.pupt.2019.01.007. Epub 2019 Jan 28. Pulm Pharmacol Ther. 2019. PMID: 30703554 Free PMC article.

Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.

Shen GQ, Girelli D, Li L, Olivieri O, Martinelli N, Chen Q, Topol EJ, Wang QK. Shen GQ, et al. Gene. 2013 May 25;521(1):78-81. doi: 10.1016/j.gene.2013.03.022. Epub 2013 Mar 21. Gene. 2013. PMID: 23524007 Free PMC article.

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population.

Yang Q, Li L, Chen Q, Foldvary-Schaefer N, Ondo WG, Wang QK. Yang Q, et al. Sleep Med. 2011 Sep;12(8):800-4. doi: 10.1016/j.sleep.2011.06.006. Sleep Med. 2011. PMID: 21925394 Free PMC article.

Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.

Wang AZ, Li L, Zhang B, Shen GQ, Wang QK. Wang AZ, et al. Ann Hum Genet. 2011 Jul;75(4):475-82. doi: 10.1111/j.1469-1809.2011.00646.x. Epub 2011 Apr 4. Ann Hum Genet. 2011. PMID: 21463265 Free PMC article.

Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.

Liu JY, Dai X, Sheng J, Cui X, Wang X, Jiang X, Tu X, Tang Z, Bai Y, Liu M, Wang QK. Liu JY, et al. Biochem Biophys Res Commun. 2008 Mar 7;367(2):420-6. doi: 10.1016/j.bbrc.2007.12.156. Epub 2008 Jan 3. Biochem Biophys Res Commun. 2008. PMID: 18177735 Free PMC article.

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.

Shen GQ, Li L, Girelli D, Seidelmann SB, Rao S, Fan C, Park JE, Xi Q, Li J, Hu Y, Olivieri O, Marchant K, Barnard J, Corrocher R, Elston R, Cassano J, Henderson S, Hazen SL, Plow EF, Topol EJ, Wang QK. Shen GQ, et al. Am J Hum Genet. 2007 Oct;81(4):780-91. doi: 10.1086/521581. Epub 2007 Aug 31. Am J Hum Genet. 2007. PMID: 17847002 Free PMC article.

Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.

Melamud A, Shen GQ, Chung D, Xi Q, Simpson E, Li L, Peachey NS, Zegarra H, Hagstrom SA, Wang QK, Traboulsi EI. Melamud A, et al. J Med Genet. 2006 Jun;43(6):e27. doi: 10.1136/jmg.2005.031518. J Med Genet. 2006. PMID: 16740911 Free PMC article.

Biomedicine and diseases: the Klippel-Trenaunay syndrome, vascular anomalies and vascular morphogenesis.

Timur AA, Driscoll DJ, Wang Q. Timur AA, et al. Cell Mol Life Sci. 2005 Jul;62(13):1434-47. doi: 10.1007/s00018-005-4523-7. Cell Mol Life Sci. 2005. PMID: 15905966 Free PMC article. Review.

Molecular genetics of coronary artery disease.

Wang Q. Wang Q. Curr Opin Cardiol. 2005 May;20(3):182-8. doi: 10.1097/01.hco.0000160373.77190.f1. Curr Opin Cardiol. 2005. PMID: 15861005 Free PMC article. Review.

Advances in the genetic basis of coronary artery disease.

Wang Q. Wang Q. Curr Atheroscler Rep. 2005 May;7(3):235-41. doi: 10.1007/s11883-005-0012-6. Curr Atheroscler Rep. 2005. PMID: 15811259 Free PMC article. Review.

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