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Page 1
Reorganization of the nuclear lamina and cytoskeleton in adipogenesis.
Verstraeten VL, Renes J, Ramaekers FC, Kamps M, Kuijpers HJ, Verheyen F, Wabitsch M, Steijlen PM, van Steensel MA, Broers JL. Verstraeten VL, et al. Among authors: van steensel ma. Histochem Cell Biol. 2011 Mar;135(3):251-61. doi: 10.1007/s00418-011-0792-4. Epub 2011 Feb 25. Histochem Cell Biol. 2011. PMID: 21350821 Free PMC article.
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.
Verstraeten VL, Broers JL, van Steensel MA, Zinn-Justin S, Ramaekers FC, Steijlen PM, Kamps M, Kuijpers HJ, Merckx D, Smeets HJ, Hennekam RC, Marcelis CL, van den Wijngaard A. Verstraeten VL, et al. Among authors: van steensel ma, van den wijngaard a. Hum Mol Genet. 2006 Aug 15;15(16):2509-22. doi: 10.1093/hmg/ddl172. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825282
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress.
Verstraeten VL, Caputo S, van Steensel MA, Duband-Goulet I, Zinn-Justin S, Kamps M, Kuijpers HJ, Ostlund C, Worman HJ, Briedé JJ, Le Dour C, Marcelis CL, van Geel M, Steijlen PM, van den Wijngaard A, Ramaekers FC, Broers JL. Verstraeten VL, et al. Among authors: van steensel ma, van geel m, van den wijngaard a. J Cell Mol Med. 2009 May;13(5):959-71. doi: 10.1111/j.1582-4934.2009.00690.x. Epub 2009 Feb 11. J Cell Mol Med. 2009. PMID: 19220582 Free PMC article.
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies.
De Vos WH, Houben F, Kamps M, Malhas A, Verheyen F, Cox J, Manders EM, Verstraeten VL, van Steensel MA, Marcelis CL, van den Wijngaard A, Vaux DJ, Ramaekers FC, Broers JL. De Vos WH, et al. Among authors: van steensel ma, van den wijngaard a. Hum Mol Genet. 2011 Nov 1;20(21):4175-86. doi: 10.1093/hmg/ddr344. Epub 2011 Aug 10. Hum Mol Genet. 2011. PMID: 21831885
A new type of erythrokeratoderma.
van Steensel MA, van Geel M, Steijlen PM. van Steensel MA, et al. Among authors: van geel m. Br J Dermatol. 2005 Jan;152(1):155-8. doi: 10.1111/j.1365-2133.2005.06319.x. Br J Dermatol. 2005. PMID: 15656818
Molecular genetics of hereditary hair and nail disease.
van Steensel MA, van Geel M, Steijlen PM. van Steensel MA, et al. Among authors: van geel m. Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):52-60. doi: 10.1002/ajmg.c.30034. Am J Med Genet C Semin Med Genet. 2004. PMID: 15468149 Review.
217 results