ライフサイエンスコーパス: girdle

1 pically mild and located around the shoulder girdle.

2 ed microfibrils that we termed the fibrillar girdle.

3 verify high expression of IL-22 in chorionic girdle.

4 eurocranium, pharyngeal arches, and pectoral girdle.

5 the reconstruction of the skull and shoulder girdle.

6 Odontochelys in various features of the limb girdles.

7 posture within a girdle and between the two girdles.

8 elongate dorsal vertebrae, and modified limb girdles.

9 ed below 0.5 MPa and was inhibited by phloem girdling.

10 transpiring flowers were unaffected by bark girdling.

11 number of vertebrae posterior to the pelvic girdle (65-68); thoracolumbar synarcual extending backwa

12 The pelvic girdle and appendage of tetrapods is dramatically larger

13 extent, the coordination of posture within a girdle and between the two girdles.

14 The limb girdle and congenital muscular dystrophies (LGMD and CMD

15 Becker muscular dystrophy and forms of limb-girdle and congenital muscular dystrophies, and 21 patie

16 opathies with broad severity, including limb-girdle and congenital muscular dystrophy.

17 pods in expressing a high degree of pectoral girdle and forelimb functional diversity associated with

18 Its shoulder girdle and limbs show fossorial features similar to thos

19 rast, reductions in the length of the pelvic girdle and pelvic spines resulted from directional shift

20 rs characterized by weakness in the shoulder-girdle and peroneal muscles.

21 ep length through the rotation of the pelvic girdle and retraction of the femur.

22 Hip girdle and shoulder girdle weakness appeared later in th

23 s severely atrophic and weak in his shoulder girdle and the entire paraspinal musculature.

24 basal and intermediate snakes retain pelvic girdles and small rudiments of the femur.

25 ransfer of recently assimilated C using stem girdling and root trenching and measured soil CO2 efflux

26 uration, a more vertically oriented pectoral girdle, and low torsion of the femoral head relative to

27 Patient 1 had cervical, limb girdle, and respiratory muscle weakness and died of resp

28 tening injuries, stabilization of the pelvic girdle, and timely insinuation of pelvic angiography and

29 spine and thoracic wall, pelvic and shoulder girdles, and peripheral entheses and joints.

30 isease that affects the shoulder, the pelvic girdles, and the neck, usually in individuals older than

31 duced belowground C supply to soils via tree girdling, and contrasted responses in control and girdle

32 ar sling or loosely attached to the pectoral girdle anteriorly.

33 Analogous cation-pai bonds and the girdle are seen in many closed TRP channel structures.

34 cluded by four cytoplasmic loops that form a girdle around the central pore (G-loop).

35 progressive weakness of the hip and shoulder girdles, as well as a distinctive dysarthric pattern of

36 our S4-S5 linker helices together, forming a girdle backing the closed gate.

37 e basal layer of the frustule as well as the girdle band and show that these components display simil

38 ponents, VHA(B) -eGFP first localized in the girdle band SDVs, and subsequently in valve SDVs.

39 sely resemble characteristic features of the girdle band silica nanopatterns.

40 ciated with the silicon-starvation response, girdle bands and valve synthesis, suggesting that many g

41 microrings are specifically associated with girdle bands, which constitute a substantial part of dia

42 hat IL-22 cytokine produced by the chorionic girdle binds IL-22R1 on endometrium, serving as a mechan

43 Girdling birches reduced total soil CO(2) efflux in the

44 pulative investigations (e.g. starvation via girdling) combined with Delta(14) C measurements of this

45 GFPT1) cause the neuromuscular disorder limb-girdle congenital myasthenic syndrome (LG-CMS).

46 ished by rotation of the pectoral and pelvic girdles creating a standing wave of the axial body.

47 In ECM-dominated plots, girdling decreased the activity of enzymes that break do

48 trast with the known requirement for Tbx5 in girdle development in forelimbs.

49 Islet1 and Pitx1 function in parallel during girdle development in hindlimbs, which is in contrast wi

50 f the Hand2-Shh pathway and contributions to girdle development.

51 genes has suggested their potential roles in girdle development.

52 ineate novel regulatory networks in shoulder girdle development.

53 nce skeletal abnormalities, including pelvic girdle dysgenesis, skull bone fusions and polydactyly.

54 ing congenital muscular dystrophies and limb-girdle dystrophies), strokes and stroke-like episodes, e

55 and autopod) and the less prominent proximal girdle elements (scapula and clavicle) that brace the li

56 AR-domain superfamily proteins are touted to girdle eukaryotic phospholipid bilayers into narrow tubu

57 es in belowground C dynamics, we conducted a girdling experiment with plots distributed across 1 km(2

58 Stem-girdling experiments, which leave xylem vessels intact b

59 dials proximally fused to each other; pelvic girdle extremely small and strongly arched; dorsal and c

60 low spinose sclerites, and a smooth, ventral girdle flanks an extensive mantle cavity.

61 f the M2 helices that disrupts a hydrophobic girdle formed by 9' and 13' residues.

62 crease in IL-22 mRNA expression in chorionic girdle from days 32 to 35 and an absence of IL-22 expres

63 In AM-dominated plots, girdling had little effect on SOM-degrading enzymes, but

64 By contrast, JA treatments, branching and girdling had little or no impact on (1)(5)N import.

65 ue (SVT) regeneration after large-scale bark girdling in trees.

66 Our discovery of IL-22 in the chorionic girdle is a novel finding, as this cytokine has been pre

67 tion of the underlying soft body, the scaled girdle is an excellent model for multifunctional armor d

68 Unlike terrestrial theropods, the pelvic girdle is downsized, the hindlimbs are short, and all of

69 This girdle is not observed in the cryo-EM structure of amphi

70 ggesting the possibility of an intracellular girdle just below the mouth of the ENaC pore.

71 ors covered include vein cutting, trenching, girdling, leaf clipping, and application of fluids from

72 rp residues are essential for gating and the girdle-like structure that lines the intracellular mouth

73 mb, as well as input from limbs of the other girdle made a much smaller contribution to the PTN modul

74 AAV treatments for Duchenne MD, various limb girdle MDs, myotonic dystrophy 1, facioscapulohumeral MD

75 g different experimental methods (trenching, girdling, microcosms), as well as considering different

76 netic mechanism that reoriented the shoulder girdle more laterally.

77 ) involved in the control of head, trunk and girdle movements, while the other, lateral set of fibres

78 plexus MR imaging, brachial plexus and limb-girdle muscle abnormalities were evaluated in 23 patient

79 Nerve root and limb-girdle muscle abnormalities were visually evaluated by t

80 Limb-girdle muscle alterations (ie, T2 signal intensity alter

81 dependent proteinase that is mutated in Limb Girdle Muscle Dystrophy type 2A.

82 f the peripheral nervous system and the limb-girdle muscle may be useful for monitoring the evolution

83 In contrast, the deeper girdle muscles (e.g. rhomboideus profundus and serratus

84 The more superficial girdle muscles (pectoral and latissimus dorsi) develop b

85 friction, and alternate contractions of the girdle muscles provided propulsion during bidirectional

86 opic suckers bearing two paired fins and two girdle muscles.

87 Limb-girdle muscular dystrophies (LGMD) are a heterogeneous g

88 y which has long been recognized in the limb-girdle muscular dystrophies (LGMD) has been shown to rel

89 nts with sarcoglycanopathies, which are limb-girdle muscular dystrophies (LGMD2C-2F) caused by mutati

90 se four subtypes of autosomal recessive limb-girdle muscular dystrophies (LGMDR3, LGMDR4, LGMDR5 and

91 nother group of MD's referred to as the limb-girdle muscular dystrophies (LGMDs) can affect boys or g

92 ate analysis of current knowledge about limb-girdle muscular dystrophies (LGMDs).

93 ypes of muscular dystrophies, including limb-girdle muscular dystrophies (LGMDs).

94 Autosomal recessive limb girdle muscular dystrophies 2C-2F represent a family of

95 Limb-girdle muscular dystrophies 2C-F represent a family of a

96 Limb-girdle muscular dystrophies are a genetically diverse gr

97 The limb-girdle muscular dystrophies are a group of disorders wit

98 ecialist Commissioning Team service for limb-girdle muscular dystrophies at Newcastle (UK).

99 lycan causes an array of congenital and limb girdle muscular dystrophies known as dystroglycanopathie

100 of the cardiac involvement in forms of limb girdle muscular dystrophies secondary to abnormal glycos

101 ar dystrophies ranging from adult onset limb girdle muscular dystrophies to severe congenital forms w

102 ar dystrophies ranging from adult onset limb girdle muscular dystrophies to severe congenital forms w

103 in any of the sarcoglycan genes lead to limb-girdle muscular dystrophies type 2C-2F.

104 Limb Girdle Muscular Dystrophies type 2I (LGMD2I), a recessiv

105 facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophies types 2A and 2B, Miyoshi myo

106 spectrum of GMPPB mutations to include limb-girdle muscular dystrophies with adult onset with or wit

107 ions are responsible for congenital and limb-girdle muscular dystrophies with hypoglycosylation of al

108 s and intellectual delay to adult-onset limb-girdle muscular dystrophies without mental retardation.

109 ying the molecular mechanism of several limb-girdle muscular dystrophies, particularly those where in

110 te promising therapeutic strategies for limb-girdle muscular dystrophies.

111 hasis on animal models for Duchenne and limb-girdle muscular dystrophies.

112 in the encoding genes cause congenital/limb-girdle muscular dystrophies.

113 absence is common to both Duchenne and limb girdle muscular dystrophies.

114 rcoglycan result in autosomal recessive limb girdle muscular dystrophy (AR-LGMD).

115 Duchenne muscular dystrophy (DMD) and limb girdle muscular dystrophy (LGMD) 2C-F result from the lo

116 Limb girdle muscular dystrophy (LGMD) 2F is caused by mutatio

117 ncluding Walker-Warburg syndrome (WWS), limb girdle muscular dystrophy (LGMD) 2I and congenital muscu

118 POMT2 have also been linked to a milder limb-girdle muscular dystrophy (LGMD) phenotype, named LGMD t

119 PTP dysregulation is found in limb girdle muscular dystrophy (LGMD) type 2B myoblasts but n

120 tary inclusion body myopathy (hIBM) and limb-girdle muscular dystrophy (LGMD), are a genetically hete

121 LGMD2L is a subtype of limb-girdle muscular dystrophy (LGMD), caused by recessive mu

122 lvement, to relatively mild adult onset limb girdle muscular dystrophy (LGMD).

123 family of 4 with cardiac arrhythmia and limb-girdle muscular dystrophy (LGMD).

124 Autosomal dominant limb-girdle muscular dystrophy (LGMD-1C) in humans is due to

125 fied a novel autosomal dominant form of limb-girdle muscular dystrophy (LGMD-1C) in humans that is du

126 regulated in patients with this form of limb girdle muscular dystrophy (LGMD-1C).

127 xpressing an autosomal dominant form of limb girdle muscular dystrophy (LGMD1A).

128 including Emery-Dreifuss (EDMD2/3) and Limb-Girdle muscular dystrophy (LGMD1B).

129 The other 18 had limb girdle muscular dystrophy (LGMD2I).

130 Limb-girdle muscular dystrophy 1A (LGMD1A [MIM 159000]) is an

131 1 (DYX1) and TMOD4 a candidate gene for limb girdle muscular dystrophy 1B (LGMD1B).

132 Of these, Emery-Dreifuss and Limb-Girdle muscular dystrophy 1B mainly affect striated musc

133 Limb girdle muscular dystrophy 1D/1E (OMIM nomenclature LGMD1

134 Limb girdle muscular dystrophy 2A is due to loss-of-function

135 amily member calpain 3 (CAPN3) underlie limb-girdle muscular dystrophy 2A.

136 Adipogenic muscle loss is a feature of limb girdle muscular dystrophy 2B (LGMD2B) - a disease caused

137 Mutations in the dysferlin gene cause limb girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopat

138 Deficiency of dysferlin leads to limb-girdle muscular dystrophy 2B (LGMD2B) and Miyoshi myopat

139 y in a mouse model of the human disease limb girdle muscular dystrophy 2B (LGMD2B), caused by a mutat

140 gnaling offers a therapeutic avenue for limb girdle muscular dystrophy 2B and Miyoshi myopathy patien

141 Limb girdle muscular dystrophy 2B and Miyoshi myopathy were r

142 Dysferlinopathies, most commonly limb girdle muscular dystrophy 2B and Miyoshi myopathy, are d

143 INTS: Dysferlin, the protein missing in limb girdle muscular dystrophy 2B and Miyoshi myopathy, conce

144 ve developed a new diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy, which

145 ations in dysferlin are responsible for limb girdle muscular dystrophy 2B and Miyoshi myopathy.

146 sulting in dysferlin-deficiency lead to limb-girdle muscular dystrophy 2B and Myoshi myopathy in huma

147 ysferlin, underlie Miyoshi myopathy and limb-girdle muscular dystrophy 2B in humans and produce a slo

148 In our analysis of 12 patients with limb girdle muscular dystrophy 2B or Miyoshi myopathy, the fi

149 muscular dystrophies Miyoshi myopathy, limb girdle muscular dystrophy 2B, and distal anterior compar

150 Limb-girdle muscular dystrophy 2B, Miyoshi myopathy, and dist

151 6 and dysferlin, the protein mutated in limb girdle muscular dystrophy 2B.

152 s mutations in patients presenting with limb-girdle muscular dystrophy 2B.

153 Limb girdle muscular dystrophy 2C is caused by mutations in t

154 a sarcoglycan (Sgca), a mouse model for limb girdle muscular dystrophy 2D.

155 , congenital muscular dystrophy 1A, and limb girdle muscular dystrophy 2D.

156 s unclear why mutations in Tcap lead to limb-girdle muscular dystrophy 2G (LGMD2G) in human patients.

157 TRIM32) are responsible for the disease limb-girdle muscular dystrophy 2H (LGMD2H).

158 Limb girdle muscular dystrophy 2H is caused by mutations in t

159 tal muscular dystrophy type 1C (MDC1C), limb girdle muscular dystrophy 2I (LGMD2I) and congenital mus

160 Limb-girdle muscular dystrophy 2I (LGMD2I) is caused by mutat

161 e a wide range of pathologies from mild limb girdle muscular dystrophy 2I (LGMD2I), severe congenital

162 448L-mutant mouse representing moderate limb-girdle muscular dystrophy 2I.

163 e clinical phenotypes, most commonly as limb-girdle muscular dystrophy 2I.

164 y in FKRP P448Lneo(-) mice, a model for limb girdle muscular dystrophy 2I.

165 Human tibial muscular dystrophy and limb-girdle muscular dystrophy 2J are caused by mutations in

166 of two previously identified disorders, limb-girdle muscular dystrophy 2L and non-dysferlin Miyoshi m

167 we have identified an important case of limb girdle muscular dystrophy and cardiomyopathy with normal

168 wild type (WT) Cav3 and associates with limb-girdle muscular dystrophy and cardiomyopathy.

169 mutation (Thr192-->Met) in a woman with limb-girdle muscular dystrophy and cognitive impairment.

170 trate that FLN2 protein localization in limb-girdle muscular dystrophy and Duchenne muscular dystroph

171 g from congenital muscular dystrophy to limb-girdle muscular dystrophy and identified allelic ISPD va

172 l vectors have recently started, one in limb-girdle muscular dystrophy and one in Duchenne muscular d

173 ster is a naturally occurring model for limb-girdle muscular dystrophy caused by a primary deficiency

174 ar dystrophy type 2A is the most common limb girdle muscular dystrophy form worldwide.

175 rmalities were not found, we identified limb-girdle muscular dystrophy gene mutations affecting DYSF,

176 Limb-girdle muscular dystrophy is a class of disorders encomp

177 n that may be a good candidate gene for limb-girdle muscular dystrophy or other neuromuscular disorde

178 ep in the diagnostic algorithm of adult limb-girdle muscular dystrophy patients.

179 trophin-glycoprotein complex, produce a limb-girdle muscular dystrophy phenotype; however, the precis

180 in these genes might also cause milder limb-girdle muscular dystrophy phenotypes.

181 Limb-girdle muscular dystrophy R1 (LGMD R1) is caused by muta

182 oad spectrum of disorders, ranging from limb girdle muscular dystrophy to Walker-Warburg syndrome.

183 ns have been described in patients with limb-girdle muscular dystrophy type 1A (LGMD1A), myofibrillar

184 fforts for several disorders, including limb-girdle muscular dystrophy type 1A and the genes deleted

185 Limb-girdle muscular dystrophy type 1D (LGMD1D) is caused by

186 One such example recently discovered is limb-girdle muscular dystrophy type 1D (LGMD1D), which is cau

187 e protein dysferlin, the product of the Limb Girdle Muscular Dystrophy type 2 locus, has been shown t

188 pain-3 (CAPN3) the product of the human limb-girdle muscular dystrophy type 2A (LGMD2A) gene.

189 calpain 3 (CAPN3) result in the disease limb girdle muscular dystrophy type 2A (LGMD2A).

190 somal cysteine protease calpain 3 cause limb-girdle muscular dystrophy type 2A (LGMD2A).

191 athological signs in a murine model for limb-girdle muscular dystrophy type 2A after intramuscular an

192 Diagnosis of limb girdle muscular dystrophy type 2A can be complex due to

193 Limb girdle muscular dystrophy type 2A is the most common lim

194 tic defects in calpain3 (CAPN3) lead to limb-girdle muscular dystrophy type 2A, a disease of the skel

195 s patients deficient in calpain 3 as in limb girdle muscular dystrophy type 2A, albeit in a milder fo

196 s was generally milder than observed in limb girdle muscular dystrophy type 2A, but affected the same

197 esult in an autosomal recessive form of limb girdle muscular dystrophy type 2A.

198 unction, since mutations in CAPN3 cause limb girdle muscular dystrophy type 2A.

199 calpain 3 (C3), the protein mutated in limb girdle muscular dystrophy type 2A.

200 identified as a novel gene involved in limb-girdle muscular dystrophy type 2B (LGMD2B) and its allel

201 , a gene which is also mutated in human limb-girdle muscular dystrophy type 2B (LGMD2B).

202 Dysferlin deficiency causes limb-girdle muscular dystrophy type 2B (LGMD2B; proximal weak

203 Limb girdle muscular dystrophy type 2B and Miyoshi myopathy a

204 Defects in dysferlin result in limb-girdle muscular dystrophy type 2B and Miyoshi myopathy i

205 ncy of the dysferlin protein results in limb girdle muscular dystrophy type 2B and Miyoshi myopathy,

206 wo clinically distinct muscle diseases, limb-girdle muscular dystrophy type 2B and Miyoshi myopathy,

207 Mutations in the dysferlin gene cause limb girdle muscular dystrophy type 2B and Miyoshi myopathy.

208 a member of the ferlin family, lead to limb girdle muscular dystrophy type 2B and Myoshi myopathy.

209 The dysferlin gene is mutated in limb-girdle muscular dystrophy type 2B, Miyoshi myopathy, and

210 herapeutically useful for patients with limb girdle muscular dystrophy type 2B.

211 gamma-sarcoglycan-null mice, a model of limb-girdle muscular dystrophy type 2C, with a Col6a2-deficie

212 enne muscular dystrophy (DMD) patients, limb-girdle muscular dystrophy type 2D (LGMD2D) and their res

213 Limb-girdle muscular dystrophy type 2D (LGMD2D) is caused by

214 in a severe form of muscular dystrophy (limb-girdle muscular dystrophy type 2D [LGMD2D]) without trea

215 Limb-girdle muscular dystrophy type 2E (LGMD 2E) is caused by

216 an (delta sgc), a mouse model for human limb girdle muscular dystrophy type 2F.

217 Autosomal recessive limb-girdle muscular dystrophy type 2G (LGMD2G) is an adult-o

218 nt-derived cell lines for two diseases: limb-girdle muscular dystrophy type 2G (LGMD2G)(1) and Herman

219 igase-ubiquitin ligase mutated in human limb-girdle muscular dystrophy type 2H (LGMD2H) and Bardet-Bi

220 Limb-girdle muscular dystrophy type 2H (LGMD2H) and sarcotubu

221 ) cause two seemingly diverse diseases: limb-girdle muscular dystrophy type 2H (LGMD2H) or sarcotubul

222 veral hereditary disorders that include limb girdle muscular dystrophy type 2H (LGMD2H), sarcotubular

223 ally separate diseases, one of which is Limb-girdle muscular dystrophy type 2H (LGMD2H).

224 two forms of muscular dystrophy called limb girdle muscular dystrophy type 2H and sarcotubular myopa

225 muscle and is orthologous to the human limb-girdle muscular dystrophy type 2H disease gene Trim32.

226 , mutations in the FKRP gene also cause limb-girdle muscular dystrophy type 2I (LGMD2I), a considerab

227 muscular dystrophy type 1C (MDC1C) and limb girdle muscular dystrophy type 2I (LGMD2I).

228 ngenital muscular dystrophy type 1C and limb girdle muscular dystrophy type 2I are allelic, both bein

229 ted with FKRP mutations range from mild limb-girdle muscular dystrophy type 2I with predominantly mus

230 es in biopsies of 6 patients, 3 with an limb-girdle muscular dystrophy type 2J (LGMD2J) phenotype.

231 both Walker-Warburg syndrome (WWS) and limb girdle muscular dystrophy type 2K (LGMD2K).

232 o several clinical phenotypes including limb-girdle muscular dystrophy type 2L and Miyoshi myopathy t

233 ause a late-onset muscle disease termed limb-girdle muscular dystrophy type D1 (LGMDD1), which is cha

234 Limb-girdle muscular dystrophy types 2E and F are characteriz

235 Here we review each form of limb-girdle muscular dystrophy with attention to molecular ge

236 t severe form of dystroglycanopathy, to limb-girdle muscular dystrophy with cognitive defects.

237 tructural eye defects to a mild form of limb-girdle muscular dystrophy with onset in adult life and n

238 phy, facioscapulohumeral dystrophy, and limb-girdle muscular dystrophy).

239 y (EDMD), dilated cardiomyopathy (DCM), limb-girdle muscular dystrophy, and Hutchison-Gilford progeri

240 s of muscular dystrophy, including DM1, limb-girdle muscular dystrophy, congenital merosin-deficient

241 esented as an adult or adolescent-onset limb-girdle muscular dystrophy, one presented with isolated e

242 Limb-girdle muscular dystrophy, type 2A (LGMD 2A), is an auto

243 ng alpha-sarcoglycan gene expression in limb-girdle muscular dystrophy, type 2D (LGMD2D) subjects med

244 Limb girdle muscular dystrophy, which was described for the f

245 ent with the mild phenotype observed in Limb-girdle muscular dystrophy-1C (LGMD-1C) in humans, charac

246 Cav-3-related muscle diseases, such as limb-girdle muscular dystrophy-1C, distal myopathy, and rippl

247 expression in skeletal muscle resembles limb-girdle muscular dystrophy-1C.

248 ystrophy resembling what is observed in limb girdle muscular dystrophy.

249 syndrome, to mild forms of adult-onset limb-girdle muscular dystrophy.

250 mice accelerates muscle loss and causes limb girdle muscular dystrophy.

251 ase calpain-3 cause autosomal recessive limb girdle muscular dystrophy.

252 oglycan-null (scgd(-/-)) mouse model of limb-girdle muscular dystrophy.

253 delta-sarcoglycan (scgd-/-), a model of limb-girdle muscular dystrophy.

254 in dysferlin, whose gene is mutated in limb girdle muscular dystrophy.

255 for the development of gene therapy for limb-girdle muscular dystrophy.

256 olemma and produce one of four types of limb-girdle muscular dystrophy.

257 for a novel type of autosomal recessive limb girdle muscular dystrophy.

258 minant involvement of the pelvic or shoulder girdle musculature.

259 n, and DOK7 mutations underlie familial limb-girdle myasthenia (DOK7 myasthenia), a neuromuscular dis

260 cting primarily proximal limb muscles ['limb-girdle myasthenia' (LGM)].

261 he phenotype can be distinguished from 'limb-girdle' myasthenia associated with tubular aggregates, w

262 In contrast, the pelvic girdle of Cryptotora is a large, broad puboischiadic pla

263 smonate (JA) treatment, branching and phloem girdling on (1)(3)C and (1)(5)N import, invertase activi

264 competing branches, treated with JA or not, girdled or not, had no impact on carbohydrate (CHO) impo

265 Soil CO2 efflux was not influenced by girdling or trenching through the 14-month observation p

266 henic syndrome (CMS) characterized by a limb-girdle pattern of muscle weakness.

267 ng defect in patients with an inherited limb-girdle pattern of myasthenic weakness.

268 group of individuals with an inherited limb-girdle pattern of myasthenic weakness.

269 S patients have a recessively inherited limb-girdle pattern of weakness caused by mutations in DOK7.

270 oup of patients shows a characteristic "limb girdle" pattern of muscle weakness, in which the muscles

271 ore affected than distal, leading to a 'limb-girdle' pattern of weakness; although ptosis was often p

272 the avian furculum, and they retain shoulder girdle plesiomorphies of mammaliaforms and monotremes.

273 ing, and contrasted responses in control and girdled plots for three consecutive growing seasons.

274 efects progress from preaxial polydactyly to girdle reduction combined with hypoplasia, aplasia or mi

275 th and involving the neck, shoulders, or hip girdle regions; and an erythrocyte sedimentation rate (E

276 RNA encoding the cytokine IL-22 in chorionic girdle relative to noninvasive chorion.

277 interspecific structural diversity of chiton girdle scales.

278 Comparative analysis of the upper girdle scan in 181 of these subjects was also performed.

279 eurocranium, pharyngeal arches, and pectoral girdle similar to humans with campomelic dysplasia.

280 loss of Dok-7 activity cause a distinct limb-girdle subtype of the inherited NMJ disorder congenital

281 narcual extending backward beyond the pelvic girdle; tail extremely short not protruding from the pos

282 equence gait and has evolved a robust pelvic girdle that shares morphological features associated wit

283 mall, mineralized scales arrayed on the soft girdle that surrounds their overlapping shell plates.

284 dimeric apoA-I(Milano) on 78 A diameter rHDL girdles the edge of a phospholipid disk assuming a "belt

285 In the shoulder girdle, the type of resection and soft-tissue reconstruc

286 o stabilize three ligands in the metallocene girdle to form saturated (C(5)H(5))(2)ML(3) species, in

287 xcised panicle stems subjected to a +/- stem-girdling treatment during grain fill.

288 abolism on photosynthesis in cassava, a heat-girdling treatment was applied to petioles of cassava le

289 er muscular dystrophy (BMD, n = 14) and limb-girdle type 2I muscular dystrophy (LGMD2I, n = 11), befo

290 ects affecting the palatal shelves, shoulder girdle, vertebrae, and sternum.

291 The fibrillar girdle was located directly above the transition zone, a

292 Patients have prominent limb girdle weakness and minimal craniobulbar symptoms.

293 Hip girdle and shoulder girdle weakness appeared later in the disease course.

294 reened 1,500 patients with unclassified limb girdle weakness or hyperCKemia for pathogenic POPDC3 var

295 inical spectrum varied from mild static limb-girdle weakness to severe generalized progressive diseas

296 All patients had prominent limb-girdle weakness with minimal or absent craniobulbar mani

297 from childhood very slowly progressive limb-girdle weakness with rigid spine and disabling contractu

298 e phenotype with facial weakness or scapular girdle weakness, 6.7% display minor signs such as winged

299 cioscapulohumeral; oculopharyngeal; and limb-girdle which is the most heterogeneous group.

300 ead onto the anterior lining of the shoulder girdle, while a Hox-gene-controlled mesoderm links trunk