Csoka AB - Search Results

1

Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.

Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS. Eriksson M, et al. Among authors: csoka ab. Nature. 2003 May 15;423(6937):293-8. doi: 10.1038/nature01629. Epub 2003 Apr 25. Nature. 2003. PMID: 12714972 Free PMC article.

2

Hyaluronan is not elevated in urine or serum in Hutchinson-Gilford Progeria Syndrome.

Gordon LB, Harten IA, Calabro A, Sugumaran G, Csoka AB, Brown WT, Hascall V, Toole BP. Gordon LB, et al. Among authors: csoka ab. Hum Genet. 2003 Jul;113(2):178-87. doi: 10.1007/s00439-003-0958-9. Epub 2003 May 1. Hum Genet. 2003. PMID: 12728312

3

Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis.

Csoka AB, English SB, Simkevich CP, Ginzinger DG, Butte AJ, Schatten GP, Rothman FG, Sedivy JM. Csoka AB, et al. Aging Cell. 2004 Aug;3(4):235-43. doi: 10.1111/j.1474-9728.2004.00105.x. Aging Cell. 2004. PMID: 15268757 Free article.

4

Signaling pathway activation drift during aging: Hutchinson-Gilford Progeria Syndrome fibroblasts are comparable to normal middle-age and old-age cells.

Aliper AM, Csoka AB, Buzdin A, Jetka T, Roumiantsev S, Moskalev A, Zhavoronkov A. Aliper AM, et al. Among authors: csoka ab. Aging (Albany NY). 2015 Jan;7(1):26-37. doi: 10.18632/aging.100717. Aging (Albany NY). 2015. PMID: 25587796 Free PMC article.

5

Defective DSB repair correlates with abnormal nuclear morphology and is improved with FTI treatment in Hutchinson-Gilford progeria syndrome fibroblasts.

Constantinescu D, Csoka AB, Navara CS, Schatten GP. Constantinescu D, et al. Among authors: csoka ab. Exp Cell Res. 2010 Oct 15;316(17):2747-59. doi: 10.1016/j.yexcr.2010.05.015. Epub 2010 Jun 25. Exp Cell Res. 2010. PMID: 20599958

6

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes.

Csoka AB, Cao H, Sammak PJ, Constantinescu D, Schatten GP, Hegele RA. Csoka AB, et al. J Med Genet. 2004 Apr;41(4):304-8. doi: 10.1136/jmg.2003.015651. J Med Genet. 2004. PMID: 15060110 Free PMC article. No abstract available.

7

A mouse model of human mucopolysaccharidosis IX exhibits osteoarthritis.

Martin DC, Atmuri V, Hemming RJ, Farley J, Mort JS, Byers S, Hombach-Klonisch S, Csoka AB, Stern R, Triggs-Raine BL. Martin DC, et al. Among authors: csoka ab. Hum Mol Genet. 2008 Jul 1;17(13):1904-15. doi: 10.1093/hmg/ddn088. Epub 2008 Mar 15. Hum Mol Genet. 2008. PMID: 18344557

8

Lamin A/C expression is a marker of mouse and human embryonic stem cell differentiation.

Constantinescu D, Gray HL, Sammak PJ, Schatten GP, Csoka AB. Constantinescu D, et al. Among authors: csoka ab. Stem Cells. 2006 Jan;24(1):177-85. doi: 10.1634/stemcells.2004-0159. Epub 2005 Sep 22. Stem Cells. 2006. PMID: 16179429

9

Hypotheses on the evolution of hyaluronan: a highly ironic acid.

Csoka AB, Stern R. Csoka AB, et al. Glycobiology. 2013 Apr;23(4):398-411. doi: 10.1093/glycob/cws218. Epub 2013 Jan 12. Glycobiology. 2013. PMID: 23315448 Free PMC article. Review.

10

Pro-fibrotic pathway activation in trabecular meshwork and lamina cribrosa is the main driving force of glaucoma.

Zhavoronkov A, Izumchenko E, Kanherkar RR, Teka M, Cantor C, Manaye K, Sidransky D, West MD, Makarev E, Csoka AB. Zhavoronkov A, et al. Among authors: csoka ab. Cell Cycle. 2016 Jun 17;15(12):1643-52. doi: 10.1080/15384101.2016.1170261. Cell Cycle. 2016. PMID: 27229292 Free PMC article.

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