Hu RM - Search Results

1

Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends upon Splice Variant Background and Intracellular Acidosis.

Hu RM, Tan BH, Tester DJ, Song C, He Y, Dovat S, Peterson BZ, Ackerman MJ, Makielski JC. Hu RM, et al. PLoS One. 2015 Apr 29;10(4):e0124921. doi: 10.1371/journal.pone.0124921. eCollection 2015. PLoS One. 2015. PMID: 25923670 Free PMC article.

2

Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients.

Hu RM, Tester DJ, Li R, Sun T, Peterson BZ, Ackerman MJ, Makielski JC, Tan BH. Hu RM, et al. Channels (Austin). 2018;12(1):176-186. doi: 10.1080/19336950.2018.1475794. Channels (Austin). 2018. PMID: 29983085 Free PMC article.

3

Expression defect of the rare variant/Brugada mutation R1512W depends upon the SCN5A splice variant background and can be rescued by mexiletine and the common polymorphism H558R.

Hu RM, Song EJ, Tester DJ, Deschenes I, Ackerman MJ, Makielski JC, Tan BH. Hu RM, et al. Channels (Austin). 2021 Dec;15(1):253-261. doi: 10.1080/19336950.2021.1875645. Channels (Austin). 2021. PMID: 33535892 Free PMC article.

4

Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I(Na) contributing to LQT syndrome.

Hu RM, Tan BH, Orland KM, Valdivia CR, Peterson A, Pu J, Makielski JC. Hu RM, et al. Am J Physiol Heart Circ Physiol. 2013 Apr 1;304(7):H994-H1001. doi: 10.1152/ajpheart.00705.2012. Epub 2013 Feb 1. Am J Physiol Heart Circ Physiol. 2013. PMID: 23376825 Free PMC article.

5

Comparison of read-through effects of aminoglycosides and PTC124 on rescuing nonsense mutations of HERG gene associated with long QT syndrome.

Yu H, Liu X, Huang J, Zhang Y, Hu R, Pu J. Yu H, et al. Int J Mol Med. 2014 Mar;33(3):729-35. doi: 10.3892/ijmm.2013.1601. Epub 2013 Dec 23. Int J Mol Med. 2014. PMID: 24366185

6

Activity-Based Protein Profiling of RHBDL4 Reveals Proteolysis of the Enzyme and a Distinct Inhibitor Profile.

Davies CC, Hu RM, Kamitsuka PJ, Morais GN, de Gonzalez RS, Bustin KA, Matthews ML, Parsons WH. Davies CC, et al. Among authors: hu rm. ACS Chem Biol. 2024 Aug 16;19(8):1674-1682. doi: 10.1021/acschembio.4c00273. Epub 2024 Jul 23. ACS Chem Biol. 2024. PMID: 39041925

7

Chemoproteomic strategy identified p120-catenin glutathionylation regulates E-cadherin degradation and cell migration.

Kukulage DSK, Yapa Abeywardana M, Matarage Don NNJ, Hu RM, Shishikura K, Matthews ML, Ahn YH. Kukulage DSK, et al. Among authors: hu rm. Cell Chem Biol. 2023 Dec 21;30(12):1542-1556.e9. doi: 10.1016/j.chembiol.2023.08.004. Epub 2023 Sep 14. Cell Chem Biol. 2023. PMID: 37714153

8

CA125 for the Diagnosis of Advanced Urothelial Carcinoma of the Bladder: A Systematic Review and Meta-Analysis.

Lin HJ, Hu RM, Chen HC, Lin CC, Lee CY, Chou CY. Lin HJ, et al. Among authors: hu rm. Cancers (Basel). 2023 Jan 28;15(3):813. doi: 10.3390/cancers15030813. Cancers (Basel). 2023. PMID: 36765770 Free PMC article. Review.

9

Established the first clinical prediction model regarding the risk of hyperuricemia in adult IgA nephropathy.

Geng YH, Zhang Z, Zhang JJ, Huang B, Guo ZS, Wang XT, Zhang LQ, Quan SX, Hu RM, Song CD, Duan FY, Liu YF. Geng YH, et al. Among authors: hu rm. Int Urol Nephrol. 2023 Jul;55(7):1787-1797. doi: 10.1007/s11255-023-03498-0. Epub 2023 Feb 8. Int Urol Nephrol. 2023. PMID: 36753014

10

MicroRNA-1246 Inhibits NFATc1 Phosphorylation and Regulates T Helper 17 Cell Activation in the Pathogenesis of Severe Alopecia Areata.

Qi SS, Miao Y, Sheng YY, Hu RM, Zhao J, Yang QP. Qi SS, et al. Among authors: hu rm. Ann Dermatol. 2023 Feb;35(1):46-55. doi: 10.5021/ad.22.126. Ann Dermatol. 2023. PMID: 36750458 Free PMC article.

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