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Keywords: Emery–Dreifuss muscular dystrophy (EDMD)
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Articles
Biochem Soc Trans (2011) 39 (6): 1683–1686.
Published: 21 November 2011
... avenues to be investigated and highlighted the signalling pathways suitable as therapeutic targets. 14 9 2011 © The Authors Journal compilation © 2011 Biochemical Society 2011 chromatin organization EmeryDreifuss muscular dystrophy (EDMD) Hutchinson–Gilford progeria syndrome (HGPS...
Articles
Biochem Soc Trans (2011) 39 (6): 1693–1697.
Published: 21 November 2011
... © The Authors Journal compilation © 2011 Biochemical Society 2011 EmeryDreifuss muscular dystrophy (EDMD) linker of nucleoskeleton and cytoskeleton complex (LINC complex) neuromuscular disorder Table 1 Patients identified with mutations in genes associated with EDMD Gene...
Articles
Biochem Soc Trans (2011) 39 (6): 1698–1704.
Published: 21 November 2011
... The Authors Journal compilation © 2011 Biochemical Society 2011 emerin EmeryDreifuss muscular dystrophy (EDMD) prelamin A progeroid laminopathy SUN1 SUN2 The LMNA gene (OMIM *150330), encoding the A-type lamins, was characterized in 1993 [ 1 ] and subsequently mapped to chromosome 1q21.2...
Articles
Biochem Soc Trans (2008) 36 (6): 1344–1349.
Published: 19 November 2008
... progression. 1 To whom correspondence should be addressed (email peter.zammit@kcl.ac.uk ). 7 7 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 emerin EmeryDreifuss muscular dystrophy (EDMD) lamin MyoD nuclear envelope retinoblastoma protein satellite...
Articles
Biochem Soc Trans (2008) 36 (6): 1354–1358.
Published: 19 November 2008
... emerin EmeryDreifuss muscular dystrophy (EDMD) hypertrophy lamin A/C To propose a role for emerin–β-catenin, we first summarize the known functions of β-catenin in the heart. β-Catenin is a key mediator of early heart development and is required for both physiological and pathological...
Articles
Biochem Soc Trans (2008) 36 (6): 1329–1334.
Published: 19 November 2008
... Biochemical Society 2008 EmeryDreifuss muscular dystrophy (EDMD) Hutchinson–Gilford progeria syndrome (HGPS) lamina nuclear envelope Probably the most intriguing disease that arises as a consequence of mutations in the LMNA gene is HGPS (Hutchinson–Gilford progeria syndrome). HGPS...
Articles
Biochem Soc Trans (2008) 36 (6): 1335–1338.
Published: 19 November 2008
... into the pathogenesis of this disorder, particularly that relating to the heart phenotype. 1 To whom correspondence should be addressed (email s.brown@imperial.ac.uk ). 8 7 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 emerin EmeryDreifuss muscular dystrophy (EDMD...