Ye B - Search Results

1

Common human SCN5A polymorphisms have altered electrophysiology when expressed in Q1077 splice variants.

Tan BH, Valdivia CR, Rok BA, Ye B, Ruwaldt KM, Tester DJ, Ackerman MJ, Makielski JC. Tan BH, et al. Among authors: ye b. Heart Rhythm. 2005 Jul;2(7):741-7. doi: 10.1016/j.hrthm.2005.04.021. Heart Rhythm. 2005. PMID: 15992732

2

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.

Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC. Valdivia CR, et al. Among authors: ye b. Cardiovasc Res. 2002 Aug 1;55(2):279-89. doi: 10.1016/s0008-6363(02)00445-5. Cardiovasc Res. 2002. PMID: 12123767

3

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation.

Ye B, Valdivia CR, Ackerman MJ, Makielski JC. Ye B, et al. Physiol Genomics. 2003 Feb 6;12(3):187-93. doi: 10.1152/physiolgenomics.00117.2002. Physiol Genomics. 2003. PMID: 12454206

4

A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels.

Makielski JC, Ye B, Valdivia CR, Pagel MD, Pu J, Tester DJ, Ackerman MJ. Makielski JC, et al. Among authors: ye b. Circ Res. 2003 Oct 31;93(9):821-8. doi: 10.1161/01.RES.0000096652.14509.96. Epub 2003 Sep 18. Circ Res. 2003. PMID: 14500339

5

Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current.

Cheng J, Van Norstrand DW, Medeiros-Domingo A, Valdivia C, Tan BH, Ye B, Kroboth S, Vatta M, Tester DJ, January CT, Makielski JC, Ackerman MJ. Cheng J, et al. Among authors: ye b. Circ Arrhythm Electrophysiol. 2009 Dec;2(6):667-76. doi: 10.1161/CIRCEP.109.891440. Circ Arrhythm Electrophysiol. 2009. PMID: 20009079 Free PMC article.

6

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation.

Valdivia CR, Medeiros-Domingo A, Ye B, Shen WK, Algiers TJ, Ackerman MJ, Makielski JC. Valdivia CR, et al. Among authors: ye b. Cardiovasc Res. 2010 Jun 1;86(3):392-400. doi: 10.1093/cvr/cvp417. Epub 2009 Dec 30. Cardiovasc Res. 2010. PMID: 20042427 Free PMC article.

7

The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current.

Cheng J, Tester DJ, Tan BH, Valdivia CR, Kroboth S, Ye B, January CT, Ackerman MJ, Makielski JC. Cheng J, et al. Among authors: ye b. Physiol Genomics. 2011 May 13;43(9):461-6. doi: 10.1152/physiolgenomics.00198.2010. Epub 2011 Mar 8. Physiol Genomics. 2011. PMID: 21385947 Free PMC article.

8

Rate-dependent QT shortening mechanism for the LQT3 deltaKPQ mutant.

Nagatomo T, January CT, Ye B, Abe H, Nakashima Y, Makielski JC. Nagatomo T, et al. Among authors: ye b. Cardiovasc Res. 2002 Jun;54(3):624-9. doi: 10.1016/s0008-6363(02)00265-1. Cardiovasc Res. 2002. PMID: 12031708

9

Function and distribution of the SUR isoforms and splice variants.

Shi NQ, Ye B, Makielski JC. Shi NQ, et al. Among authors: ye b. J Mol Cell Cardiol. 2005 Jul;39(1):51-60. doi: 10.1016/j.yjmcc.2004.11.024. Epub 2005 Feb 5. J Mol Cell Cardiol. 2005. PMID: 15978902 Review.

10

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Cronk LB, Ye B, Kaku T, Tester DJ, Vatta M, Makielski JC, Ackerman MJ. Cronk LB, et al. Among authors: ye b. Heart Rhythm. 2007 Feb;4(2):161-6. doi: 10.1016/j.hrthm.2006.11.030. Epub 2006 Dec 6. Heart Rhythm. 2007. PMID: 17275750 Free PMC article.

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