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1 d skeletal muscle dysfunction referred to as Emery Dreifuss muscular dystrophy.
2  may also be involved in the pathogenesis of Emery-Dreifuss muscular dystrophy.
3 with emerin, the protein mutated in X-linked Emery-Dreifuss muscular dystrophy.
4  H222P 'knock in' mice, a model of autosomal Emery-Dreifuss muscular dystrophy.
5  a knockin mouse model of autosomal dominant Emery-Dreifuss muscular dystrophy.
6 pment of heart disease in autosomal dominant Emery-Dreifuss muscular dystrophy.
7 scle atrophy, rigid spine syndrome (RSS) and Emery-Dreifuss muscular dystrophy.
8 use loss or mislocalization of emerin causes Emery-Dreifuss muscular dystrophy.
9 Mutations in emerin cause X-linked recessive Emery-Dreifuss muscular dystrophy.
10 rlapping functions, which may be relevant to Emery-Dreifuss muscular dystrophy.
11                        Loss of emerin causes Emery-Dreifuss muscular dystrophy.
12 duction-system disease or autosomal dominant Emery-Dreifuss muscular dystrophy.
13 hat exhibit tissue-specific defects, such as Emery-Dreifuss muscular dystrophy.
14 ein emerin, from an individual with X-linked Emery--Dreifuss muscular dystrophy.
15 y seen in limb-girdle type 1B, myotonic, and Emery-Dreifuss muscular dystrophies.
16 n and are closely linked to the pathology of Emery-Dreifuss muscular dystrophy 1 (EDMD1), a laminopat
17 n the head or tail domain of this gene cause Emery-Dreifuss muscular dystrophy, a childhood-onset dis
18                        Loss of emerin causes Emery-Dreifuss muscular dystrophy, a tissue-specific inh
19 tations result in laminopathies that include Emery-Dreifuss muscular dystrophy (AD-EDMD) and Hutchins
20  human diseases including autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD), which affec
21 ype lamins cause several diseases, including Emery-Dreifuss muscular dystrophy and Dunnigan-type fami
22 se a wide range of human diseases, including Emery-Dreifuss muscular dystrophy and Hutchinson-Gilford
23  rigidity is a nonspecific feature, found in Emery-Dreifuss muscular dystrophy and in some congenital
24 revent or delay heart failure in humans with Emery-Dreifuss muscular dystrophy and related disorders
25                                    Autosomal Emery-Dreifuss muscular dystrophy and related disorders
26 des epidemiological information for X-linked Emery-Dreifuss muscular dystrophy and the collagen VI di
27                 Each of the X-linked form of Emery-Dreifuss muscular dystrophy and Ullrich muscular d
28  strongly support gene expression models for Emery-Dreifuss muscular dystrophy by showing that emerin
29                                              Emery-Dreifuss muscular dystrophy can be caused by mutat
30       In the LmnaH222P/H222P murine model of Emery-Dreifuss muscular dystrophy caused by LMNA mutatio
31 a broad variety of human diseases, including Emery-Dreifuss muscular dystrophy, dilated cardiomyopath
32  cause a variety of human diseases including Emery-Dreifuss muscular dystrophy, dilated cardiomyopath
33 r neuromuscular disorder, autosomal dominant Emery-Dreifuss muscular dystrophy, DOK7 gene therapy lik
34  disrupted the expression of genes linked to Emery-Dreifuss muscular dystrophy (EDMD) and centronucle
35 ge of diseases, including autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) and related dis
36 en found in patients with autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) as well as dila
37                      Seventeen families with Emery-Dreifuss muscular dystrophy (EDMD) have been studi
38                                              Emery-Dreifuss muscular dystrophy (EDMD) is a geneticall
39                                              Emery-Dreifuss muscular dystrophy (EDMD) is a heterogene
40                                              Emery-Dreifuss muscular dystrophy (EDMD) is an inherited
41                                              Emery-Dreifuss muscular dystrophy (EDMD) is caused by va
42 ntified two patients with genetically proven Emery-Dreifuss muscular dystrophy (EDMD) who followed an
43 utations in nesprin-1/-2 are associated with Emery-Dreifuss muscular dystrophy (EDMD) with conduction
44        These abnormalities resemble those of Emery-Dreifuss muscular dystrophy (EDMD), caused by muta
45 ent a diverse group of diseases that include Emery-Dreifuss muscular dystrophy (EDMD), dilated cardio
46  protein, defects in which are implicated in Emery-Dreifuss muscular dystrophy (EDMD), one of the thr
47                      Using a murine model of Emery-Dreifuss muscular dystrophy (EDMD), we show here t
48 strophy, neuropathies and autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD).
49 domain nuclear protein, loss of which causes Emery-Dreifuss muscular dystrophy (EDMD).
50 utations in either emerin or lamin A/C cause Emery-Dreifuss muscular dystrophy (EDMD).
51 ane protein which is missing or defective in Emery-Dreifuss muscular dystrophy (EDMD).
52 etal muscle and heart abnormalities, such as Emery-Dreifuss muscular dystrophy (EDMD).
53                  Loss of human emerin causes Emery-Dreifuss muscular dystrophy (EDMD).
54                                Two of these, Emery-Dreifuss muscular dystrophy (EDMD-AD) and a form o
55 en shown to be altered in autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) and in dilat
56                                              Emery-Dreifuss muscular dystrophy (EDMD1) is caused by m
57  the overtly aphenotypical model of X-linked Emery-Dreifuss muscular dystrophy (Emd(-/y)) were also i
58                                              Emery-Dreifuss muscular dystrophy (EMD) is an X-linked d
59                                              Emery-Dreifuss muscular dystrophy (EMD) is an X-linked d
60                      A muscle biopsy from an Emery-Dreifuss muscular dystrophy (EMDM) patient showed
61                                              Emery-Dreifuss muscular dystrophy has some remarkably sp
62                                     X-linked Emery-Dreifuss muscular dystrophy is caused by loss of f
63 rd progeria syndrome (Lmna(L530P/L530P)) and Emery-Dreifuss muscular dystrophy (Lmna(-/-)).
64 he natural history of cardiac involvement in Emery-Dreifuss muscular dystrophy was described in detai
65 n LB3T-Ig (R454W; LB3T-IgRW), known to cause Emery-Dreifuss muscular dystrophy when present in lamin
66                                     X-linked Emery-Dreifuss muscular dystrophy (X-EDMD) is inherited