ライフサイエンスコーパス: striate

1 These striated 2D crystals cannot be described by a typical un

2 The overall pattern of extra-striate activations is consistent with recent three-stre

3 ons share a common gain control mechanism in striate and extra-striate cortex.

4 organization of thalamocortical pathways in striate and extrastriate areas.

5 he pulvinar forms extensive connections with striate and extrastriate cortical areas, but the impact

6 ffect of enucleation on the surface areas of striate and extrastriate visual cortex by using magnetic

7 s was highly anomalous and the sizes of both striate and extrastriate visual cortex were significantl

8 t it still caused a reduction in the size of striate and extrastriate visual cortex.

9 salivary glands, be efficiently taken up by striated and excretory duct cells, and eventually secret

10 in decapods, such as size and characteristic striated and perpendicular layering.

11 have been described as a hybrid phenotype of striated and vascular smooth muscle cells (VSMCs), we pe

12 cardiac and skeletal myocytes their distinct striated appearance.

13 ture is first extracted in second-tier extra-striate areas and that responses over early visual areas

14 AWM exhibited a regular striated arrangement of the extracellular space.

15 male lethal mouse mutations bare patches and striated, as well as most cases of human CHILD syndrome.

16 tion into smooth mini-fibrils with the cross-striated banding pattern typical of fibrillar collagens.

17 ar lattice structure with intact vessels and striated basement membrane.

18 ganized as exaggerated multilamellar whorls, striated belts and 'fingerprint bodies'.

19 actile defect and mild fiber degeneration in striated body wall muscle.

20 min family, CYK-1 and FHOD-1, are present in striated body wall muscles near or on sarcomere Z lines,

21 The ZYX-1 protein is expressed in the striated body-wall muscles and localizes at dense bodies

22 diomyoblasts capable of differentiation into striated cardiomyocytes in vitro.

23 e dorsal root ganglion (hypermethylated) and striated cells (hypomethylated), was targeted with these

24 min during this period stunted growth of the striated contractile lattice, whereas their simultaneous

25 and that smooth myocytes later co-opted the striated contractile module repeatedly - for example, in

26 t, serum-free protocol for the generation of striated, contractile fibers from mouse and human plurip

27 a subtle change in the pattern of fine-scale striate correlations between hemispheres.

28 -field (7 T) fMRI, we find that responses in striate cortex (V1) best reflect stimulus position in th

29 bino rats, it has been reported that lateral striate cortex (V1) is highly binocular, and that input

30 columns (ODCs) have been well studied in the striate cortex (V1) of macaques, as well defined arrays

31 oxidase (CytOx)-rich patches (blobs) in the striate cortex (V1) of normally sighted Homo sapiens.

32 e shown that geniculate synapses are lost in striate cortex (V1).

33 Lesions of striate cortex [primary visual cortex (V1)] in adult pri

34 ength of long-range correlation between left striate cortex and Broca's area.

35 We examined the fine-scale pattern of striate cortex correlations within and between hemispher

36 We show that correlation-based cells in striate cortex do in fact signal depth here because they

37 cortical surface, however, the boundaries of striate cortex fall at a consistent location across indi

38 d to predict the retinotopic organization of striate cortex for an individual with accuracy equivalen

39 The tree shrew (Tupaia belangeri) striate cortex is reciprocally connected with the dorsal

40 rimates but are unique in that sublaminae of striate cortex layer IV respond preferentially to light

41 extent are spontaneous neural signals within striate cortex organized by vision?

42 In the Pv or the dLGN, striate cortex projections are thought to either strongl

43 rum, we compare the synaptic arrangements of striate cortex projections to the dLGN, Pv, and claustru

44 Attention-induced rate enhancement in striate cortex requires cholinergic mechanisms.

45 The striate cortex terminals were largest in the Pv (0.94 +/

46 Aergic terminals (0.34 +/- 0.01 mum(2) ) and striate cortex terminals were not significantly differen

47 trastriate visual cortex produced effects in striate cortex that were relatively weak, generally supp

48 geniculocortical terminals in the tree shrew striate cortex to compare directly the characteristics o

49 nucleus (LGN) and primary visual cortex (V1, striate cortex).

50 ng from restricted loci in medial, acallosal striate cortex, and the overall pattern of callosal conn

51 region in V1 of albino rats includes lateral striate cortex, being therefore about 25% larger in area

52 ated in the superficial and middle layers of striate cortex, consistent with the known anatomy of thi

53 of striate-extrastriate, but not the size of striate cortex, ends by P6.

54 passage of ipsilateral eye input to lateral striate cortex, increasing its binocularity.

55 of direct subcortical inputs that may bypass striate cortex, such as input to V5/MT+.

56 rom geniculocortical recipient layers of the striate cortex.

57 lation-based computation that takes place in striate cortex.

58 the projection of the visual field upon the striate cortex.

59 gain control mechanism in striate and extra-striate cortex.

60 conditions did not differ in the calcarine (striate) cortex.

61 point-spread function across millimeters of striate cortical surface, rather than degrees of visual

62 ocal, vision-driven pattern synchrony of the striate cortices for long-range functional correlations

63 into a basal layer, a lamellar inner coat, a striated electrodense outer coat and a more external cru

64 nput plays on the development of ipsilateral striate-extrastriate connections and the interplay that

65 As in normal rats, striate-extrastriate projections in rats enucleated at b

66 Anomalies in patterns of striate-extrastriate projections were not observed in ra

67 which the eyes influence the development of striate-extrastriate, but not the size of striate cortex

68 t nuclear-associated Nesprin1 (dNesp1) forms striated F-actin-based filaments, which we dubbed "railr

69 Parasite striated fiber assemblins (SFA) polymerize into a dynami

70 is consistent with DisAp's similarity to the striated fiber protein SF-assemblin.

71 to the base of BB-appendage microtubules and striated fiber.

72 of the novel protein DisAp to T. thermophila striated fibers (kinetodesmal fibers; KFs), which is con

73 te and position cilia, whereby BB-associated striated fibers (SFs) promote BB anchorage and orientati

74 have attached auxiliary structures, such as striated fibers.

75 is the chemomechanical energy transducer in striated heart muscle.

76 V2 is thought to use its striate inputs as the basis for computations that are im

77 ase transformation mechanism for creating 2D striated lattice systems is revealed, where controlled t

78 ally organized their cytoskeleton in a cross-striated manner.

79 ferentiation protocol to efficiently produce striated, millimeter-long muscle fibers together with sa

80 t myosin isoforms in the sarcomeres of adult striated muscle (fast IIa, IId, the slow/cardiac isoform

81 outh opening during feeding, and oesophageal striated muscle (OSM), which is crucial for voluntary sw

82 STARS (STriated muscle Activator of Rho Signaling) is a sarcome

83 st that Wingless-mediated cross-talk between striated muscle and adipose tissue controls obesity in D

84 anization of the central contractile unit of striated muscle and also as a mechanosensitive signaling

85 carnitine palmitoyltransferase 1B (CPT1B) in striated muscle and BAT.

86 y of formins contributes to contractility of striated muscle and cell motility in several contexts.

87 s, fruits, legumes, and whole grains than by striated muscle and cow milk.

88 re of the 200 kDa alpha-actinin-2 dimer from striated muscle and explore its functional implications

89 adin (MYPN) is a Z-disc protein expressed in striated muscle and functions as a structural, signaling

90 However, cardiac muscle is also a subtype of striated muscle and is similarly affected in many of the

91 biomarker for a number of diseases affecting striated muscle and may also be a schizophrenia risk gen

92 cked neutrophils in vivo in venules of mouse striated muscle and revealed how endothelial permeabilit

93 keletal stiffness and mechanotransduction in striated muscle and that targeting this post-translation

94 assay and Western blot; AChR, MuSK, and anti-striated muscle antibodies were detected using a standar

95 Conditional deletion of LAP1 from striated muscle causes muscular dystrophy; this patholog

96 s troponin can be exchanged in permeabilized striated muscle cell preparations, and tested the hypoth

97 Caenorhabditis elegans striated muscle cells attach to basement membrane and tr

98 Here, we demonstrate that striated muscle cells form a continuous myofibrillar mat

99 Mitochondrial dynamism is rare in striated muscle cells, so cardiac-specific genetic manip

100 s Xin and XIRP2 are exclusively expressed in striated muscle cells, where they are believed to play a

101 ent of the cell membrane repair machinery in striated muscle cells.

102 ate meshwork that organizes myofibers within striated muscle cells.

103 the Ca(2+) activation of myofilaments during striated muscle contraction and relaxation.

104 tropomyosin's Ca(2+)-triggered regulation of striated muscle contraction has advanced greatly, partic

105 Striated muscle contraction involves sliding of actin th

106 Striated muscle contraction is a highly cooperative proc

107 Regulation of striated muscle contraction is achieved by Ca2+ -depende

108 Striated muscle contraction is regulated by Ca(2+) -depe

109 Striated muscle contraction is regulated by the transloc

110 Striated muscle contraction is the result of sarcomeres,

111 Striated muscle contraction occurs when myosin thick fil

112 n in regulating actin-myosin interactions in striated muscle contraction, and dephosphorylation of Ml

113 EGF receptor signaling, circadian exercise, striated muscle contraction, and lipid and carbohydrate

114 MyBP-C is a multidomain modulator of striated muscle contraction, interacting with myosin, ti

115 olling the troponin I switching mechanism of striated muscle contraction.

116 The Z-band in vertebrate striated muscle crosslinks actin filaments of opposite p

117 ity with exercise lead to protection against striated muscle damage, oxidative stress and injury.

118 In addition to striated muscle defects, double-null animals and LEM-2-n

119 The demonstration that both types of striated muscle derive from common progenitors comes fro

120 critical determinant of cardiac and skeletal striated muscle development and function, with misexpres

121 Striated muscle development requires the coordinated exp

122 ing and mechanosensor and has been linked to striated muscle disease.

123 Striated muscle enables movement in all animals by the c

124 ropose that neurons secrete vMSPs to promote striated muscle energy production and metabolism, in par

125 eceptor channels (RyR) are key components of striated muscle excitation-contraction coupling, and alt

126 of the key characteristics of the different striated muscle fiber types, including maximum shortenin

127 Striated muscle fibers are characterized by their tightl

128 In striated muscle fibres, the binding of myosin motors to

129 the cytoplasmic surface of the sarcolemma of striated muscle fibres.

130 We propose that striated muscle force is generated by a singular, mesh-l

131 hich in turn anchors IFs, both essential for striated muscle formation and function.

132 While Thbs4 is known to protect striated muscle from disease by enhancing sarcolemmal st

133 Recent proteomics studies of vertebrate striated muscle have identified lysine acetylation at se

134 rs transduced liver and kidney in GSD Ia and striated muscle in GSD II mice to replace the deficient

135 sarcomeric protein exclusively localized in striated muscle in humans.

136 Striated muscle is activated by myosin- and actin-linked

137 hese results suggest that fast relaxation of striated muscle is an emergent property that reflects mu

138 Tarantula striated muscle is an outstanding system for understandi

139 The scallop's large striated muscle is energy-dynamic but not fully differen

140 Contraction of striated muscle is tightly regulated by the release and

141 nds of contiguous tropomyosin (Tm) dimers in striated muscle is unknown.

142 l iPSC-derived progenitors (MiPs) toward the striated muscle lineages.

143 nuclear membrane that has been implicated in striated muscle maintenance.

144 Striated muscle mitochondria form connected networks cap

145 gs are circulating hormones that pattern the striated muscle mitochondrial reticulum.

146 erone UNC-45B is required for the folding of striated muscle myosin II.

147 nd image processing of nucleotide-free (apo) striated muscle myosin-2 subfragment-1 (S1), possessing

148 Striated muscle myosins are encoded by a large gene fami

149 schistosome myosin II heavy chain and known striated muscle myosins.

150 reversed the established pathologies in the striated muscle of the KO mouse.

151 ostnatal cardiac function and reinforces the striated muscle phenotype by regulating both transcripti

152 Hoip is expressed in striated muscle precursors within the muscle lineage and

153 Striated muscle preferentially expressed protein kinase

154 Striated muscle preferentially expressed protein kinase

155 e role of newly identified JMC protein SPEG (striated muscle preferentially expressed protein kinase)

156 ght the functional relevance of a smooth and striated muscle progenitor dialogue for ESM patterning.

157 gene delivery intervention with tropism for striated muscle reduced the serum concentrations of Acti

158 ely induced apoptosis, we report evidence of striated muscle regeneration in vivo in mice by human Mi

159 etween calcium and the regulatory site(s) of striated muscle regulatory protein troponin switches on

160 ebulin to reinforce and temporally fine-tune striated muscle relaxation-contraction cycles.

161 Therefore, TnT potentially contributes to striated muscle relaxation; however, the in vivo functio

162 Physiologically, loss of Lmods in striated muscle results in cardiomyopathy or nemaline my

163 butes to the mechanical stabilization of the striated muscle sarcomere and cell contacts within the c

164 sponges found to induce Ca(2+) release from striated muscle sarcoplasmic reticulum (SR).

165 function, the authors generated and compared striated muscle specific knockouts (KOs) with progressiv

166 rotein C (MyBP-C) is an accessory protein of striated muscle thick filaments and a modulator of cardi

167 hat has been implicated in the regulation of striated muscle thin filament assembly; its physiologica

168 The striated muscle thin filament comprises actin, tropomyos

169 Vertebrate striated muscle thin filaments are thought to be thermod

170 at mechanically stabilizes the sarcolemma of striated muscle through interaction with the cortical ac

171 nd that loss of Fer1l6 led to deformation of striated muscle tissues, delayed development of the hear

172 ucose-regulated protein 94 (GRP94) in murine striated muscle to test the necessity of local IGFs for

173 Missense mutations K15N and R21H in striated muscle tropomyosin are linked to dilated cardio

174 dge) an atomic-level structure of alphaalpha-striated muscle tropomyosin bound to an actin filament t

175 e of cardiac leiomodin and the N-terminus of striated muscle tropomyosin.

176 rived progenitors (MiPs) can regenerate both striated muscle types simultaneously in mice.

177 Strategies to target multiple striated muscle types would provide a much-needed improv

178 es that enable regeneration of both of these striated muscle types.

179 Striated muscle was indeed found later in development su

180 scular dystrophy is a severe and progressive striated muscle wasting disorder that leads to premature

181 ophy (DMD) is a uniformly fatal condition of striated muscle wasting resulting in premature death fro

182 e 427-kDa protein dystrophin is expressed in striated muscle where it physically links the interior o

183 ant protein titin is expressed in vertebrate striated muscle where it spans half a sarcomere from the

184 KBTBD13 is a protein expressed in striated muscle whose precise function is unknown.

185 ignalosomes for regulating MEF2D activity in striated muscle, affirming mAKAPbeta as a nodal regulato

186 eres, the functional units of contraction in striated muscle, are composed of an array of interdigita

187 s," mainly affect mesenchymal tissues (e.g., striated muscle, bone, and fibrous tissue).

188 In striated muscle, desmin intermediate filaments interlink

189 We identified mCRP in inflamed human striated muscle, human atherosclerotic plaque, and infar

190 is the principal regulator of contraction in striated muscle, in vitro evidence suggests that some ac

191 In striated muscle, including involuntary cardiac muscle, T

192 tomyosin-based force production mechanism in striated muscle, it was originally proposed that contrac

193 h Sco1 was specifically deleted in heart and striated muscle, respectively.

194 ffraction to study the contraction in living striated muscle, taking advantage of the paracrystalline

195 In striated muscle, the archetype P-type ATPase, SERCA (sar

196 similar in organization to the sarcomeres of striated muscle, there are intriguing differences in the

197 st that because of high expression levels in striated muscle, TRIC-A produces most of the counterion

198 rther understand the function of myospryn in striated muscle, we searched for additional myospryn par

199 In striated muscle, X-ROS is the mechanotransduction pathwa

200 endent activation is a universal property of striated muscle, yet the molecular mechanisms that under

201 NA-1 (miR-1) is an evolutionarily conserved, striated muscle-enriched miRNA.

202 schistosome muscles are hybrids, containing striated muscle-like myosin filaments and smooth muscle-

203 uscle-like contractile apparatuses, it has a striated muscle-like regulatory mechanism through tropon

204 early myogenesis, but the functions of this striated muscle-specific enzyme in more differentiated s

205 Xin is a striated muscle-specific protein that is localized to th

206 ion of an unrelated peptide derived from the striated muscle-specific protein titin.

207 phosphorylation state of two Z-disc kinases (striated muscle-specific serine/threonine protein kinase

208 ociated with CNM, and it has been shown that striated muscle-specific Speg-knockout (KO) mice have de

209 ferentiation of myogenic cells obtained from striated muscle-specific Speg-KO mice and compared them

210 metabolic demand and functional dynamics of striated muscle.

211 pal regulator of the contractile behavior of striated muscle.

212 xtend our understanding of titin function in striated muscle.

213 allowing excitation-contraction coupling in striated muscle.

214 ding protein that is abundantly expressed in striated muscle.

215 h, which are also expressed in the body-wall striated muscle.

216 drolysis to generate force and shortening in striated muscle.

217 ter of the sarcomere, the structural unit of striated muscle.

218 C is a thick filament protein of vertebrate striated muscle.

219 sly reported to be specifically expressed in striated muscle.

220 indistinguishable from those in an arthropod striated muscle.

221 ve stress in a variety of tissues, including striated muscle.

222 filament pointed-end dynamics and length in striated muscle.

223 n, a major actin-binding filament protein of striated muscle.

224 b-Girdle muscular dystrophy 1B mainly affect striated muscle.

225 for excitation-contraction (EC) coupling in striated muscle.

226 RLC) also controls contraction of vertebrate striated muscle.

227 of length dependence of force generation in striated muscle.

228 (SR), the major calcium storage organelle in striated muscle.

229 response factor (SRF) regulatory axis within striated muscle.

230 in contraction and regulation of vertebrate striated muscle.

231 growth cone guidance receptors expressed in striated muscle.

232 eads to sarcomere disassembly and atrophy in striated muscle.

233 e assembly of ryanodine receptor clusters in striated muscle.

234 A striated-muscle myosin (UNC-54) appears to provide parti

235 le-like myosin filaments containing MYO-3, a striated-muscle myosin isoform.

236 Masticatory and esophagus striated muscles (ESM) share a common cardiopharyngeal m

237 is caused by the progressive degeneration of striated muscles aggravated by sterile inflammation.

238 and challenges the paradigm that smooth and striated muscles always have distinctly different compon

239 hesion plaques and dense bodies (Z-disks) of striated muscles and attachment plaques of smooth muscle

240 orm lengths, including the thin filaments of striated muscles and the spectrin-based membrane skeleto

241 (CPM) origin, however ESM are unusual among striated muscles as they are established in the absence

242 ribe a novel mechanism of nuclear spacing in striated muscles controlled by the cooperative activity

243 dystrophin protein function and stability in striated muscles in vivo.

244 g the dystrophin protein to be long-lived in striated muscles in vivo; however, more rigorous quantit

245 The smallest contractile unit in striated muscles is the sarcomere.

246 PMO) dramatically enhanced ASO delivery into striated muscles of DM1 mice following systemic administ

247 The mechanisms that limit the speed at which striated muscles relax are poorly understood.

248 Genetic inactivation of murine E4f1 in striated muscles results in viable animals that show low

249 t constitute a novel regulatory mechanism in striated muscles that acts independently of the well-kno

250 Striated muscles that enable mouth opening and swallowin

251 toskeletal proteins originally identified in striated muscles with structural and regulatory roles.

252 a lineage (including giant axons innervating striated muscles) strongly support an extensive and wide

253 ed acute deleterious effects of tamoxifen on striated muscles, including a transient down regulation

254 usually not seen as endocrine ones, bone and striated muscles, influence several physiological proces

255 a sarcomeric protein expressed primarily in striated muscles, is responsible for maintaining the str

256 In striated muscles, the actin filaments are anchored at Z-

257 In striated muscles, Tmods prevent actin filaments from ove

258 n binding protein C (MyBP-C) is expressed in striated muscles, where it plays key roles in the modula

259 standing of the development and mechanics of striated muscles.

260 he smallest functional unit of myofibrils in striated muscles.

261 are the primary actin isoforms expressed in striated muscles.

262 mooth muscles is also different from that in striated muscles.

263 rganization of the sarcoplasmic reticulum in striated muscles.

264 ement controlling active force generation in striated muscles.

265 oviding structural support and located under striated muscles.

266 that were co-opted for a similar purpose in striated muscles.

267 During these smooth-to-striated myocyte conversions, the core regulatory comple

268 phin(1), a rod-like protein(2) that protects striated myocytes from contraction-induced injury(3,4).

269 z-line architecture should be used to assess striated myocytes has not been fully explored.

270 The dichotomy between smooth and striated myocytes is fundamental for bilaterian musculat

271 uggest that both visceral smooth and somatic striated myocytes were present in the protostome-deutero

272 bit aligned architecture, multinucleated and striated myofibers, and a Pax7(+) cell pool.

273 ted shrinkage and rightward asymmetry of the striate nucleus was found in healthy adults and there we

274 The striated organelle (SO), a cytoskeletal structure locate

275 enuating MAPK/ERK signaling and is linked to striate palmoplantar keratoderma (SPPK).

276 echanisms leading to keratinopathies such as striate palmoplantar keratoderma, as reported in this st

277 e bursts of ultrasonic clicks perpetually; a striated patch in their hind wing clicks as the beating

278 ortex (V1) is damaged, the dominant geniculo-striate pathway can no longer convey visual information

279 f subcortical auditory input to the geniculo-striate pathway.

280 n that the signal change driven by these non-striate pathways can be measured, and suggest that model

281 lso permitted immunostaining of CD38, with a striated pattern in WT myocytes, whereas CD38(-/-) myocy

282 lated ventricular myocytes and confirmed the striated pattern of Na(V)1.6 fluorescence in myocytes.

283 lusters of GFP-RyR2 organized in rows with a striated pattern.

284 Its striated, periodic appearance in electron micrographs le

285 Striated preferentially expressed gene (Speg) is a membe

286 SPEG (striated preferentially expressed protein kinase) has be

287 gray matter, suggesting that highly variable striate projections patterns do not result from anomalou

288 esulting in an increase in the divergence of striate projections.

289 ns associate with the basal bodies and their striated rootlets and form complexes named ciliary adhes

290 rbonate ejecta represented by large polished striated rounded pebbles and cobbles, henceforth, called

291 that PYROXD1 localizes to the nucleus and to striated sarcomeric compartments.

292 -dependent stiffening is associated with the striated sheet matrix (SSM).

293 TECTB levels are reduced, a clearly defined striated-sheet matrix does not develop, and Hensen's str

294 TECTB are both required for formation of the striated-sheet matrix within which collagen fibrils of t

295 fibrils and accessory structures typical of striated skeletal muscle fibers.

296 of the apical region in type I hair cells--a striated structure restricting a cluster of large mitoch

297 we present evidence that fin mesenchyme and striated tail muscle in both animals are derived solely

298 The affinity of Tmod1 to skeletal striated TM (stTM) is higher than that of Tmod3 and Tmod

299 rough areas between these ridges forming the Striated Unit (SU).

300 suppression on neuronal activity in primary (striate) visual cortex, the pattern of cytochrome oxidas