Worman HJ - Search Results

1

Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene.

Le Dour C, Macquart C, Sera F, Homma S, Bonne G, Morrow JP, Worman HJ, Muchir A. Le Dour C, et al. Among authors: worman hj. Hum Mol Genet. 2017 Jan 15;26(2):333-343. doi: 10.1093/hmg/ddw389. Hum Mol Genet. 2017. PMID: 28069793 Free PMC article.

2

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

Bonne G, Capeau J, De Visser M, Duboc D, Merlini L, Morris GE, Muntoni F, Recan D, Sewry C, Squarzoni S, Stewart C, Talim B, van der Kooi A, Worman H, Schwartz K. Bonne G, et al. Neuromuscul Disord. 2002 Feb;12(2):187-94. doi: 10.1016/s0960-8966(01)00243-7. Neuromuscul Disord. 2002. PMID: 11738362 No abstract available.

3

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

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

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

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

8

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

9

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.

10

Emery-Dreifuss muscular dystrophy.

Muchir A, Worman HJ. Muchir A, et al. Among authors: worman hj. Curr Neurol Neurosci Rep. 2007 Jan;7(1):78-83. doi: 10.1007/s11910-007-0025-3. Curr Neurol Neurosci Rep. 2007. PMID: 17217858 Review.

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