Brodsky GL - Search Results

1

Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.

Brodsky GL, Muntoni F, Miocic S, Sinagra G, Sewry C, Mestroni L. Brodsky GL, et al. Circulation. 2000 Feb 8;101(5):473-6. doi: 10.1161/01.cir.101.5.473. Circulation. 2000. PMID: 10662742

2

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.

Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, Bohlmeyer TJ, Ferguson DA, Brodsky GL, Boucek MM, Lascor J, Moss AC, Li WL, Stetler GL, Muntoni F, Bristow MR, Mestroni L; Familial Dilated Cardiomyopathy Registry Research Group. Taylor MR, et al. Among authors: brodsky gl. J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. doi: 10.1016/s0735-1097(02)02954-6. J Am Coll Cardiol. 2003. PMID: 12628721 Free article.

3

Current perspective new insights into the molecular basis of familial dilated cardiomyopathy.

Sinagra G, Di Lenarda A, Brodsky GL, Taylor MR, Muntoni F, Pinamonti B, Carniel E, Driussi M, Bristow MR, Mestroni L; Heart Muscle Disease Study Group. Sinagra G, et al. Among authors: brodsky gl. Ital Heart J. 2001 Apr;2(4):280-6. Ital Heart J. 2001. PMID: 11374497 Review.

4

The prelamin A pre-peptide induces cardiac and skeletal myoblast differentiation.

Brodsky GL, Bowersox JA, Fitzgerald-Miller L, Miller LA, Maclean KN. Brodsky GL, et al. Biochem Biophys Res Commun. 2007 May 18;356(4):872-9. doi: 10.1016/j.bbrc.2007.03.062. Epub 2007 Mar 19. Biochem Biophys Res Commun. 2007. PMID: 17389141

5

Hypoplastic left heart syndrome myocytes are differentiated but possess a unique phenotype.

Bohlmeyer TJ, Helmke S, Ge S, Lynch J, Brodsky G, Sederberg JH, Robertson AD, Minobe W, Bristow MR, Perryman MB. Bohlmeyer TJ, et al. Cardiovasc Pathol. 2003 Jan-Feb;12(1):23-31. doi: 10.1016/s1054-8807(02)00127-8. Cardiovasc Pathol. 2003. PMID: 12598014

6

A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2.

Noetzli L, Sanz PG, Brodsky GL, Hinckley JD, Giugni JC, Giannaula RJ, Gonzalez-Alegre P, Di Paola J. Noetzli L, et al. Among authors: brodsky gl. Gene. 2014 Jan 1;533(1):447-50. doi: 10.1016/j.gene.2013.09.076. Epub 2013 Oct 5. Gene. 2014. PMID: 24103481

7

Constitutive induction of pro-inflammatory and chemotactic cytokines in cystathionine beta-synthase deficient homocystinuria.

Keating AK, Freehauf C, Jiang H, Brodsky GL, Stabler SP, Allen RH, Graham DK, Thomas JA, Van Hove JL, Maclean KN. Keating AK, et al. Among authors: brodsky gl. Mol Genet Metab. 2011 Aug;103(4):330-7. doi: 10.1016/j.ymgme.2011.04.012. Epub 2011 May 5. Mol Genet Metab. 2011. PMID: 21601502 Free PMC article.

8

A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment.

Maclean KN, Sikora J, Kožich V, Jiang H, Greiner LS, Kraus E, Krijt J, Overdier KH, Collard R, Brodsky GL, Meltesen L, Crnic LS, Allen RH, Stabler SP, Elleder M, Rozen R, Patterson D, Kraus JP. Maclean KN, et al. Among authors: brodsky gl. Mol Genet Metab. 2010 Oct-Nov;101(2-3):153-62. doi: 10.1016/j.ymgme.2010.06.010. Epub 2010 Jun 23. Mol Genet Metab. 2010. PMID: 20638879 Free PMC article.

9

Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice.

Tomberg K, Khoriaty R, Westrick RJ, Fairfield HE, Reinholdt LG, Brodsky GL, Davizon-Castillo P, Ginsburg D, Di Paola J. Tomberg K, et al. Among authors: brodsky gl. PLoS One. 2016 Mar 7;11(3):e0150852. doi: 10.1371/journal.pone.0150852. eCollection 2016. PLoS One. 2016. PMID: 26950939 Free PMC article.

10

Mutations in the Chinese hamster ovary cell GART gene of de novo purine synthesis.

Knox AJ, Graham C, Bleskan J, Brodsky G, Patterson D. Knox AJ, et al. Gene. 2009 Jan 15;429(1-2):23-30. doi: 10.1016/j.gene.2008.10.007. Epub 2008 Oct 21. Gene. 2009. PMID: 19007868 Free PMC article.

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