Worman HJ - Search Results

1

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.

Muchir A, Shan J, Bonne G, Lehnart SE, Worman HJ. Muchir A, et al. Among authors: worman hj. Hum Mol Genet. 2009 Jan 15;18(2):241-7. doi: 10.1093/hmg/ddn343. Epub 2008 Oct 16. Hum Mol Genet. 2009. PMID: 18927124 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. Among authors: worman hj. J Cell Sci. 2001 Dec;114(Pt 24):4435-45. doi: 10.1242/jcs.114.24.4435. J Cell Sci. 2001. PMID: 11792809

3

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: worman hj. Structure. 2002 Jun;10(6):811-23. doi: 10.1016/s0969-2126(02)00777-3. Structure. 2002. PMID: 12057196 Free article.

4

How do mutations in lamins A and C cause disease?

Worman HJ, Courvalin JC. Worman HJ, et al. J Clin Invest. 2004 Feb;113(3):349-51. doi: 10.1172/JCI20832. J Clin Invest. 2004. PMID: 14755330 Free PMC article. Review.

5

Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations.

Muchir A, Medioni J, Laluc M, Massart C, Arimura T, van der Kooi AJ, Desguerre I, Mayer M, Ferrer X, Briault S, Hirano M, Worman HJ, Mallet A, Wehnert M, Schwartz K, Bonne G. Muchir A, et al. Among authors: worman hj. Muscle Nerve. 2004 Oct;30(4):444-50. doi: 10.1002/mus.20122. Muscle Nerve. 2004. PMID: 15372542

6

The nuclear envelope and human disease.

Muchir A, Worman HJ. Muchir A, et al. Among authors: worman hj. Physiology (Bethesda). 2004 Oct;19:309-14. doi: 10.1152/physiol.00022.2004. Physiology (Bethesda). 2004. PMID: 15381760 Free article. Review.

7

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-beta signaling.

Lin F, Morrison JM, Wu W, Worman HJ. Lin F, et al. Among authors: worman hj. Hum Mol Genet. 2005 Feb 1;14(3):437-45. doi: 10.1093/hmg/ddi040. Epub 2004 Dec 15. Hum Mol Genet. 2005. PMID: 15601644

8

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy.

Boguslavsky RL, Stewart CL, Worman HJ. Boguslavsky RL, et al. Among authors: worman hj. Hum Mol Genet. 2006 Feb 15;15(4):653-63. doi: 10.1093/hmg/ddi480. Epub 2006 Jan 13. Hum Mol Genet. 2006. PMID: 16415042

9

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.

Wang Y, Herron AJ, Worman HJ. Wang Y, et al. Among authors: worman hj. Hum Mol Genet. 2006 Aug 15;15(16):2479-89. doi: 10.1093/hmg/ddl170. Epub 2006 Jul 6. Hum Mol Genet. 2006. PMID: 16825283

10

Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins.

Muchir A, Massart C, van Engelen BG, Lammens M, Bonne G, Worman HJ. Muchir A, et al. Among authors: worman hj. Biochem Biophys Res Commun. 2006 Dec 29;351(4):1011-7. doi: 10.1016/j.bbrc.2006.10.147. Epub 2006 Nov 3. Biochem Biophys Res Commun. 2006. PMID: 17097067 Free PMC article.

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