Vera CD - Search Results

1

Treating Duchenne Muscular Dystrophy: The Promise of Stem Cells, Artificial Intelligence, and Multi-Omics.

Vera CD, Zhang A, Pang PD, Wu JC. Vera CD, et al. Front Cardiovasc Med. 2022 Mar 10;9:851491. doi: 10.3389/fcvm.2022.851491. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35360042 Free PMC article. Review.

2

Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants.

Manhas A, Jahng JWS, Vera CD, Shenoy SP, Knowles JW, Wu JC. Manhas A, et al. Among authors: vera cd. Stem Cell Res. 2022 May;61:102774. doi: 10.1016/j.scr.2022.102774. Epub 2022 Mar 31. Stem Cell Res. 2022. PMID: 35413566 Free PMC article.

3

Intersectionality and genetic ancestry: New methods to solve old problems.

Vera CD, Mullen M, Minhas N, Wu JC. Vera CD, et al. EBioMedicine. 2022 Jun;80:104049. doi: 10.1016/j.ebiom.2022.104049. Epub 2022 May 10. EBioMedicine. 2022. PMID: 35561454 Free PMC article. No abstract available.

4

Generation of two induced pluripotent stem cell lines carrying the phospholamban R14del mutation for modeling ARVD/C.

Vera CD, Manhas A, Shenoy SP, Wheeler MT, Sallam K, Wu JC. Vera CD, et al. Stem Cell Res. 2022 Aug;63:102834. doi: 10.1016/j.scr.2022.102834. Epub 2022 Jun 6. Stem Cell Res. 2022. PMID: 35700631 Free PMC article.

5

Generation of human induced pluripotent stem cell lines carrying heterozygous PLN mutation from dilated cardiomyopathy patients.

Caudal A, Mondejar-Parreño G, Vera CD, Williams DR, Shenoy SP, Liang D, Wu JC. Caudal A, et al. Among authors: vera cd. Stem Cell Res. 2022 Aug;63:102855. doi: 10.1016/j.scr.2022.102855. Epub 2022 Jul 11. Stem Cell Res. 2022. PMID: 35853412 Free PMC article.

6

Modulating fast skeletal muscle contraction protects skeletal muscle in animal models of Duchenne muscular dystrophy.

Russell AJ, DuVall M, Barthel B, Qian Y, Peter AK, Newell-Stamper BL, Hunt K, Lehman S, Madden M, Schlachter S, Robertson B, Van Deusen A, Rodriguez HM, Vera C, Su Y, Claflin DR, Brooks SV, Nghiem P, Rutledge A, Juehne TI, Yu J, Barton ER, Luo YE, Patsalos A, Nagy L, Sweeney HL, Leinwand LA, Koch K. Russell AJ, et al. J Clin Invest. 2023 May 15;133(10):e153837. doi: 10.1172/JCI153837. J Clin Invest. 2023. PMID: 36995778 Free PMC article.

7

Myosin motor domains carrying mutations implicated in early or late onset hypertrophic cardiomyopathy have similar properties.

Vera CD, Johnson CA, Walklate J, Adhikari A, Svicevic M, Mijailovich SM, Combs AC, Langer SJ, Ruppel KM, Spudich JA, Geeves MA, Leinwand LA. Vera CD, et al. J Biol Chem. 2019 Nov 15;294(46):17451-17462. doi: 10.1074/jbc.RA119.010563. Epub 2019 Oct 3. J Biol Chem. 2019. PMID: 31582565 Free PMC article.

8

Dilated cardiomyopathy myosin mutants have reduced force-generating capacity.

Ujfalusi Z, Vera CD, Mijailovich SM, Svicevic M, Yu EC, Kawana M, Ruppel KM, Spudich JA, Geeves MA, Leinwand LA. Ujfalusi Z, et al. Among authors: vera cd. J Biol Chem. 2018 Jun 8;293(23):9017-9029. doi: 10.1074/jbc.RA118.001938. Epub 2018 Apr 17. J Biol Chem. 2018. PMID: 29666183 Free PMC article.

9

The hypertrophic cardiomyopathy myosin mutation R453C alters ATP binding and hydrolysis of human cardiac β-myosin.

Bloemink M, Deacon J, Langer S, Vera C, Combs A, Leinwand L, Geeves MA. Bloemink M, et al. J Biol Chem. 2014 Feb 21;289(8):5158-67. doi: 10.1074/jbc.M113.511204. Epub 2013 Dec 16. J Biol Chem. 2014. PMID: 24344137 Free PMC article.

10

The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects.

Walklate J, Vera C, Bloemink MJ, Geeves MA, Leinwand L. Walklate J, et al. J Biol Chem. 2016 May 6;291(19):10318-31. doi: 10.1074/jbc.M115.707489. Epub 2016 Mar 4. J Biol Chem. 2016. PMID: 26945064 Free PMC article.

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