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1 d skeletal muscle dysfunction referred to as Emery Dreifuss muscular dystrophy.
2 with emerin, the protein mutated in X-linked Emery-Dreifuss muscular dystrophy.
3 H222P 'knock in' mice, a model of autosomal Emery-Dreifuss muscular dystrophy.
4 scle atrophy, rigid spine syndrome (RSS) and 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 use loss or mislocalization of emerin causes Emery-Dreifuss muscular dystrophy.
8 Mutations in emerin cause X-linked recessive Emery-Dreifuss muscular dystrophy.
9 rlapping functions, which may be relevant to Emery-Dreifuss muscular dystrophy.
10 Loss of emerin causes Emery-Dreifuss muscular dystrophy.
11 duction-system disease or autosomal dominant Emery-Dreifuss muscular dystrophy.
12 hat exhibit tissue-specific defects, such as Emery-Dreifuss muscular dystrophy.
13 may also be involved in the pathogenesis of 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 the head or tail domain of this gene cause Emery-Dreifuss muscular dystrophy, a childhood-onset dis
18 tations result in laminopathies that include Emery-Dreifuss muscular dystrophy (AD-EDMD) and Hutchins
19 human diseases including autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD), which affec
20 ype lamins cause several diseases, including Emery-Dreifuss muscular dystrophy and Dunnigan-type fami
21 se a wide range of human diseases, including Emery-Dreifuss muscular dystrophy and Hutchinson-Gilford
22 rigidity is a nonspecific feature, found in Emery-Dreifuss muscular dystrophy and in some congenital
23 revent or delay heart failure in humans with Emery-Dreifuss muscular dystrophy and related disorders
25 des epidemiological information for X-linked Emery-Dreifuss muscular dystrophy and the collagen VI di
27 strongly support gene expression models for Emery-Dreifuss muscular dystrophy by showing that emerin
29 a broad variety of human diseases, including Emery-Dreifuss muscular dystrophy, dilated cardiomyopath
30 cause a variety of human diseases including Emery-Dreifuss muscular dystrophy, dilated cardiomyopath
31 r neuromuscular disorder, autosomal dominant Emery-Dreifuss muscular dystrophy, DOK7 gene therapy lik
32 disrupted the expression of genes linked to Emery-Dreifuss muscular dystrophy (EDMD) and centronucle
33 ge of diseases, including autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) and related dis
34 en found in patients with autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD) as well as dila
38 ntified two patients with genetically proven Emery-Dreifuss muscular dystrophy (EDMD) who followed an
39 ent a diverse group of diseases that include Emery-Dreifuss muscular dystrophy (EDMD), dilated cardio
40 protein, defects in which are implicated in Emery-Dreifuss muscular dystrophy (EDMD), one of the thr
47 en shown to be altered in autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD-AD) and in dilat
49 the overtly aphenotypical model of X-linked Emery-Dreifuss muscular dystrophy (Emd(-/y)) were also i
56 he natural history of cardiac involvement in Emery-Dreifuss muscular dystrophy was described in detai
57 n LB3T-Ig (R454W; LB3T-IgRW), known to cause Emery-Dreifuss muscular dystrophy when present in lamin
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