Markova D - Search Results

1

Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.

Zhang RZ, Zou Y, Pan TC, Markova D, Fertala A, Hu Y, Squarzoni S, Reed UC, Marie SKN, Bönnemann CG, Chu ML. Zhang RZ, et al. Among authors: markova d. J Biol Chem. 2010 Mar 26;285(13):10005-10015. doi: 10.1074/jbc.M109.093666. Epub 2010 Jan 27. J Biol Chem. 2010. PMID: 20106987 Free PMC article.

2

COL6A3 protein deficiency in mice leads to muscle and tendon defects similar to human collagen VI congenital muscular dystrophy.

Pan TC, Zhang RZ, Markova D, Arita M, Zhang Y, Bogdanovich S, Khurana TS, Bönnemann CG, Birk DE, Chu ML. Pan TC, et al. Among authors: markova d. J Biol Chem. 2013 May 17;288(20):14320-14331. doi: 10.1074/jbc.M112.433078. Epub 2013 Apr 5. J Biol Chem. 2013. PMID: 23564457 Free PMC article.

3

Genetic heterogeneity of cutis laxa: a heterozygous tandem duplication within the fibulin-5 (FBLN5) gene.

Markova D, Zou Y, Ringpfeil F, Sasaki T, Kostka G, Timpl R, Uitto J, Chu ML. Markova D, et al. Am J Hum Genet. 2003 Apr;72(4):998-1004. doi: 10.1086/373940. Epub 2003 Feb 28. Am J Hum Genet. 2003. PMID: 12618961 Free PMC article.

4

Forelimb contractures and abnormal tendon collagen fibrillogenesis in fibulin-4 null mice.

Markova DZ, Pan TC, Zhang RZ, Zhang G, Sasaki T, Arita M, Birk DE, Chu ML. Markova DZ, et al. Cell Tissue Res. 2016 Jun;364(3):637-646. doi: 10.1007/s00441-015-2346-x. Epub 2015 Dec 28. Cell Tissue Res. 2016. PMID: 26711913 Free PMC article.

5

Zinc finger protein Zac1 is expressed in chondrogenic sites of the mouse.

Tsuda T, Markova D, Wang H, Evangelisti L, Pan TC, Chu ML. Tsuda T, et al. Among authors: markova d. Dev Dyn. 2004 Feb;229(2):340-8. doi: 10.1002/dvdy.10439. Dev Dyn. 2004. PMID: 14745959 Free article.

6

Fibulin-2 is dispensable for mouse development and elastic fiber formation.

Sicot FX, Tsuda T, Markova D, Klement JF, Arita M, Zhang RZ, Pan TC, Mecham RP, Birk DE, Chu ML. Sicot FX, et al. Among authors: markova d. Mol Cell Biol. 2008 Feb;28(3):1061-7. doi: 10.1128/MCB.01876-07. Epub 2007 Dec 10. Mol Cell Biol. 2008. PMID: 18070922 Free PMC article.

7

Loss of fibulin-2 protects against progressive ventricular dysfunction after myocardial infarction.

Tsuda T, Wu J, Gao E, Joyce J, Markova D, Dong H, Liu Y, Zhang H, Zou Y, Gao F, Miller T, Koch W, Ma X, Chu ML. Tsuda T, et al. Among authors: markova d. J Mol Cell Cardiol. 2012 Jan;52(1):273-82. doi: 10.1016/j.yjmcc.2011.11.001. Epub 2011 Nov 9. J Mol Cell Cardiol. 2012. PMID: 22100229 Free PMC article.

8

A comparative analysis of the fibulin protein family. Biochemical characterization, binding interactions, and tissue localization.

Kobayashi N, Kostka G, Garbe JH, Keene DR, Bächinger HP, Hanisch FG, Markova D, Tsuda T, Timpl R, Chu ML, Sasaki T. Kobayashi N, et al. Among authors: markova d. J Biol Chem. 2007 Apr 20;282(16):11805-16. doi: 10.1074/jbc.M611029200. Epub 2007 Feb 26. J Biol Chem. 2007. PMID: 17324935 Free article.

9

Post-ischemic myocardial fibrosis occurs independent of hemodynamic changes.

Tsuda T, Gao E, Evangelisti L, Markova D, Ma X, Chu ML. Tsuda T, et al. Among authors: markova d. Cardiovasc Res. 2003 Oct 1;59(4):926-33. doi: 10.1016/s0008-6363(03)00519-4. Cardiovasc Res. 2003. PMID: 14553832

10

Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa.

Dasouki M, Markova D, Garola R, Sasaki T, Charbonneau NL, Sakai LY, Chu ML. Dasouki M, et al. Among authors: markova d. Am J Med Genet A. 2007 Nov 15;143A(22):2635-41. doi: 10.1002/ajmg.a.31980. Am J Med Genet A. 2007. PMID: 17937443

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