1 Here, we choose
facioscapulohumeral dystrophy (FSHD) as a model to deter
2 Facioscapulohumeral dystrophy (FSHD) is associated with
3 Facioscapulohumeral dystrophy (FSHD) is caused by decrea
4 Facioscapulohumeral dystrophy (FSHD) is caused by the mi
5 Facioscapulohumeral dystrophy (FSHD) is one of the most
6 pecifically, the 4q35 subtelomere mutated in
facioscapulohumeral dystrophy (FSHD).
7 Facioscapulohumeral dystrophy (FSHD; MIM158900, MIM15890
8 Facioscapulohumeral dystrophy is an autosomal dominant m
9 ular dystrophies (Becker muscular dystrophy,
facioscapulohumeral dystrophy, and limb-girdle muscular
10 ms, electrocardiograms, and in subjects with
facioscapulohumeral dystrophy, funduscopic and audiometr
11 o critically involved in the pathogenesis of
facioscapulohumeral dystrophy.
12 myodystrophy (myd), is a candidate model for
facioscapulohumeral dystrophy.
13 muscles with iliopsoas sparing is common in
facioscapulohumeral muscular dystrophy (67% of the patie
14 SP syndromes can resemble
facioscapulohumeral muscular dystrophy (FSH) due to scap
15 Facioscapulohumeral muscular dystrophy (FSHD) involves s
16 Facioscapulohumeral muscular dystrophy (FSHD) is a commo
17 Facioscapulohumeral muscular dystrophy (FSHD) is a muscu
18 Facioscapulohumeral muscular dystrophy (FSHD) is a neuro
19 Facioscapulohumeral muscular dystrophy (FSHD) is a preva
20 Facioscapulohumeral muscular dystrophy (FSHD) is a progr
21 Facioscapulohumeral muscular dystrophy (FSHD) is a uniqu
22 Facioscapulohumeral muscular dystrophy (FSHD) is an auto
23 Facioscapulohumeral muscular dystrophy (FSHD) is an auto
24 Facioscapulohumeral muscular dystrophy (FSHD) is an auto
25 Facioscapulohumeral muscular dystrophy (FSHD) is an auto
26 Facioscapulohumeral muscular dystrophy (FSHD) is an auto
27 Facioscapulohumeral muscular dystrophy (FSHD) is associa
28 Facioscapulohumeral muscular dystrophy (FSHD) is caused
29 Facioscapulohumeral muscular dystrophy (FSHD) is caused
30 In most cases
facioscapulohumeral muscular dystrophy (FSHD) is caused
31 Facioscapulohumeral muscular dystrophy (FSHD) is caused
32 Facioscapulohumeral muscular dystrophy (FSHD) is caused
33 Facioscapulohumeral muscular dystrophy (FSHD) is charact
34 Facioscapulohumeral muscular dystrophy (FSHD) is linked
35 Facioscapulohumeral muscular dystrophy (FSHD) is linked
36 Facioscapulohumeral muscular dystrophy (FSHD) is one of
37 Facioscapulohumeral muscular dystrophy (FSHD) may be a n
38 ce places the subtelomeric defect underlying
facioscapulohumeral muscular dystrophy (FSHD) much close
39 The neuromuscular disorder
facioscapulohumeral muscular dystrophy (FSHD) results fr
40 ons in SMCHD1 that have been associated with
facioscapulohumeral muscular dystrophy (FSHD) type 2.
41 subtelomeric region of chromosome 4q causes
facioscapulohumeral muscular dystrophy (FSHD) when occur
42 Facioscapulohumeral muscular dystrophy (FSHD), a common
43 ubtelomeric region, 4q35.2, is implicated in
facioscapulohumeral muscular dystrophy (FSHD), a dominan
44 Facioscapulohumeral muscular dystrophy (FSHD), the most
45 ce best supports an epigenetic mechanism for
facioscapulohumeral muscular dystrophy (FSHD), whereby d
46 DUX4 is associated with the pathogenesis of
Facioscapulohumeral muscular dystrophy (FSHD).
47 homeodomain transcription factor DUX4 causes
facioscapulohumeral muscular dystrophy (FSHD).
48 the underlying molecular genetic changes in
facioscapulohumeral muscular dystrophy (FSHD).
49 f human chromosome 4q contains the locus for
facioscapulohumeral muscular dystrophy (FSHD).
50 chromosome 4q contains the locus involved in
facioscapulohumeral muscular dystrophy (FSHD1).
51 olemma of skeletal muscle from patients with
facioscapulohumeral muscular dystrophy (FSHD1A) to learn
52 ted with the age-associated genetic disease,
facioscapulohumeral muscular dystrophy (FSHD1A, MIM 1589
53 Facioscapulohumeral muscular dystrophy (FSHD: MIM#158900
54 ations of chromatin structure: ICF syndrome,
facioscapulohumeral muscular dystrophy and a case of alp
55 are consistent with a model that configures
facioscapulohumeral muscular dystrophy as a "muscle-by-m
56 scle MRI can be also used for distinguishing
facioscapulohumeral muscular dystrophy from other myopat
57 rs in facioscapulohumeral muscular dystrophy.
Facioscapulohumeral muscular dystrophy is a severe myopa
58 Facioscapulohumeral muscular dystrophy is a slowly progr
59 he validity of the human graft as a model of
facioscapulohumeral muscular dystrophy is demonstrated i
60 ctive X chromosome, imprinted genes, and the
facioscapulohumeral muscular dystrophy locus.
61 most frequent are the dystrophinopathies and
facioscapulohumeral muscular dystrophy making up 22.9% (
62 fficient, and use this finding to develop an
facioscapulohumeral muscular dystrophy mouse model with
63 SMCHD1 mutations cause
facioscapulohumeral muscular dystrophy type 2 (FSHD2) vi
64 ic inheritance and an epigenetic modifier in
facioscapulohumeral muscular dystrophy type 2.
65 ular dystrophy: Duchenne muscular dystrophy,
facioscapulohumeral muscular dystrophy, and myotonic dys
66 beginning of this disease-associated array (
facioscapulohumeral muscular dystrophy, FSHD) despite se
67 5 near the heterochromatic region mutated in
facioscapulohumeral muscular dystrophy, indicating a pos
68 dystrophy (DMD), Becker muscular dystrophy,
facioscapulohumeral muscular dystrophy, limb-girdle musc
69 Here we show that the endogenous
facioscapulohumeral muscular dystrophy-specific DUX4 pol
70 ate the degree of pathology in patients with
facioscapulohumeral muscular dystrophy.
71 on chromosome 4 that is partially deleted in
facioscapulohumeral muscular dystrophy.
72 wn-regulation of ALP does not participate in
facioscapulohumeral muscular dystrophy.
73 e 4q35 and was identified as a candidate for
facioscapulohumeral muscular dystrophy.
74 nvolvement of fibroadipogenic progenitors in
facioscapulohumeral muscular dystrophy.Facioscapulohumer
75 lated to be affected by mutations that cause
facioscapulohumeral muscular dystrophy; thus, the charac
76 Duchenne and Becker; Emery-Dreifuss; distal;
facioscapulohumeral;
oculopharyngeal; and limb-girdle wh