Ostlund C - Search Results

1

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: ostlund c. 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.

2

Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy.

Ostlund C, Bonne G, Schwartz K, Worman HJ. Ostlund C, et al. J Cell Sci. 2001 Dec;114(Pt 24):4435-45. doi: 10.1242/jcs.114.24.4435. J Cell Sci. 2001. PMID: 11792809

3

1H, 13C and 15N resonance assignments of the C-terminal domain of human lamin A/C.

Krimm I, Couprie J, Ostlund C, Worman HJ, Zinn-Justin S. Krimm I, et al. Among authors: ostlund c. J Biomol NMR. 2002 Apr;22(4):371-2. doi: 10.1023/a:1014943122068. J Biomol NMR. 2002. PMID: 12018485 No abstract available.

4

The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy.

Krimm I, Ostlund C, Gilquin B, Couprie J, Hossenlopp P, Mornon JP, Bonne G, Courvalin JC, Worman HJ, Zinn-Justin S. Krimm I, et al. Among authors: ostlund c. Structure. 2002 Jun;10(6):811-23. doi: 10.1016/s0969-2126(02)00777-3. Structure. 2002. PMID: 12057196 Free article.

5

Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.

Favreau C, Dubosclard E, Ostlund C, Vigouroux C, Capeau J, Wehnert M, Higuet D, Worman HJ, Courvalin JC, Buendia B. Favreau C, et al. Among authors: ostlund c. Exp Cell Res. 2003 Jan 1;282(1):14-23. doi: 10.1006/excr.2002.5669. Exp Cell Res. 2003. PMID: 12490190

6

Nuclear envelope proteins and neuromuscular diseases.

Ostlund C, Worman HJ. Ostlund C, et al. Muscle Nerve. 2003 Apr;27(4):393-406. doi: 10.1002/mus.10302. Muscle Nerve. 2003. PMID: 12661041 Review.

7

The carboxyl-terminal region common to lamins A and C contains a DNA binding domain.

Stierlé V, Couprie J, Ostlund C, Krimm I, Zinn-Justin S, Hossenlopp P, Worman HJ, Courvalin JC, Duband-Goulet I. Stierlé V, et al. Among authors: ostlund c. Biochemistry. 2003 May 6;42(17):4819-28. doi: 10.1021/bi020704g. Biochemistry. 2003. PMID: 12718522

8

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo.

Holt I, Ostlund C, Stewart CL, Man Nt, Worman HJ, Morris GE. Holt I, et al. Among authors: ostlund c. J Cell Sci. 2003 Jul 15;116(Pt 14):3027-35. doi: 10.1242/jcs.00599. Epub 2003 Jun 3. J Cell Sci. 2003. PMID: 12783988

9

Altered protein dynamics of disease-associated lamin A mutants.

Gilchrist S, Gilbert N, Perry P, Ostlund C, Worman HJ, Bickmore WA. Gilchrist S, et al. Among authors: ostlund c. BMC Cell Biol. 2004 Dec 13;5(1):46. doi: 10.1186/1471-2121-5-46. BMC Cell Biol. 2004. PMID: 15596010 Free PMC article.

10

Lamin-associated proteins.

Ostlund C, Worman HJ. Ostlund C, et al. Methods Cell Biol. 2004;78:829-59. Methods Cell Biol. 2004. PMID: 15646641 No abstract available.

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