ライフサイエンスコーパス: striate

1 organization of thalamocortical pathways in striate and extrastriate areas.

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

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

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

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

6 n all muscle lineages, SRF may regulate many striated- and smooth-muscle genes that lack known SRF co

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

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

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

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

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

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

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

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

15 the sex myoblast fate, over a differentiated striated bodywall muscle fate.

16 diomyoblasts capable of differentiation into striated cardiomyocytes in vitro.

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

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

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

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

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

22 blindsight, which results from damage to the striate cortex (area V1) of the brain that is sufficient

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

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

25 In striate cortex (V1), the frontal eye fields (FEF), and t

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

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

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

29 tems of the retina that provide input to the striate cortex are now well described, although certain

30 redict the internal, retinotopic function of striate cortex as well.

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

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

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

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

35 hrome oxidase in patches or blobs of primate striate cortex has never been explained.

36 Functional architecture of the striate cortex is known mostly at the tissue level--how

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

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

39 vity and tissue oxygen concentrations in the striate cortex of anaesthetized cats while using visual

40 d with linear array multielectrodes from the striate cortex of two macaque monkeys performing an inte

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

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

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

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

55 on the first stage of cortical processing in striate cortex.

56 rom geniculocortical recipient layers of the striate cortex.

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

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

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

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

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

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

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

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

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

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

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

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

69 have attached auxiliary structures, such as striated fibers.

70 is the chemomechanical energy transducer in striated heart muscle.

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

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

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

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

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

76 Adjacent myosin filaments in striated muscle A-bands are cross-linked by the M-band.

77 Furthermore, striated muscle activator of Rho signaling (STARS), an a

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

79 development and pregnancy mediate smooth and striated muscle adaptations through SMTNL1 and MYPT1.

80 heptad repeat positions were mutated in rat striated muscle alphaTm and expressed in Escherichia col

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

82 ies, that affect distinct tissues, including striated muscle and adipose tissue.

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

84 The ancient MYH7b gene, expressed in striated muscle and brain, encodes a sarcomeric myosin a

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

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

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

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

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

90 eal the first direct mRNA targets of FXR1 in striated muscle and support translational repression as

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

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

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

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

95 length dependence of tension differs between striated muscle cell types during submaximal activations

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

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

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

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

100 ate meshwork that organizes myofibers within striated muscle cells.

101 on actin are important for the regulation of striated muscle contraction and could also be important

102 The molecular regulation of striated muscle contraction couples the binding and diss

103 The regulation of vertebrate striated muscle contraction involves a number of differe

104 Striated muscle contraction is a highly cooperative proc

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

106 Striated muscle contraction is regulated by the actin bi

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

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

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

110 units of the troponin complex that regulates striated muscle contraction.

111 central to the control of calcium-regulated striated muscle contraction.

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

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

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

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

116 scular dystrophy (DMD) is a fatal disease of striated muscle deterioration caused by lack of the cyto

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

118 Striated muscle development requires the coordinated exp

119 lamins, or expression of variants that cause striated muscle disease, did not affect assembly of nesp

120 We find that LMNA mutations causing striated muscle diseases block actin-dependent nuclear m

121 remature aging syndromes, lipodystrophy, and striated muscle disorders.

122 provides stability to the plasma membrane of striated muscle during muscle contraction.

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

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

125 Striated muscle fibers are characterized by their tightl

126 Striated muscle fibres in the urethral rhabdosphincter a

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

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

129 role in some mammalian cellular systems, but striated muscle generally is not considered to be among

130 sarcomeric protein exclusively localized in striated muscle in humans.

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

132 Tarantula striated muscle is an outstanding system for understandi

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

134 evelopment and early postnatal adaptation of striated muscle is largely unknown.

135 arcoplasmic reticulum (SR) Ca(2+) release in striated muscle is mediated by a multiprotein complex th

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

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

138 e indispensable for normal morphogenesis and striated muscle lineage specification.

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

140 The mechanism by which striated muscle loss occurs is the tumor release of pro-

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

142 redictably affect the calcium sensitivity of striated muscle mechanics, providing a novel A-M kinetic

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

144 Vertebrate striated muscle myosin filaments have a 3-fold rotationa

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

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

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

148 Activation of thin filaments in striated muscle occurs when tropomyosin exposes myosin b

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

150 he outer edge of the A-band in the obliquely striated muscle of the nematode.

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

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

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

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

158 Excitation-contraction coupling in striated muscle requires proper communication of plasmal

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

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

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

162 and the importance of the proteins in normal striated muscle structure and function.

163 ( approximately 800-kDa), modular protein of striated muscle that concentrates around the M-bands and

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

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

166 The striated muscle thin filament comprises actin, tropomyos

167 quantified for the first time the levels of striated muscle TM isoforms in human heart, including a

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

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

170 MW overlap complex that is homologous to the striated muscle tropomyosin complex in which the ends ar

171 long the shaft of rotary-shadowed smooth and striated muscle tropomyosin molecules are equivalent to

172 Here, 40 nm long smooth and striated muscle tropomyosin molecules were rotary-shadow

173 Electron microscopy shows that striated muscle tropomyosin primarily consists of single

174 ccurs despite their weaker interactions with striated muscle tropomyosins.

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

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

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

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

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

180 Titin is a giant protein of striated muscle with important roles in the assembly, in

181 n complex in the Ca(2+)-regulatory system of striated muscle, and among their muscle type-specific is

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

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

184 In striated muscle, desmin intermediate filaments interlink

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

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

187 In striated muscle, including involuntary cardiac muscle, T

188 Troponin C (TnC), present in all striated muscle, is the Ca(2+)-activated trigger that in

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

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

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

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

193 Smooth muscle, striated muscle, their central and peripheral innervatio

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

195 mine the specific role of Cypher isoforms in striated muscle, we generated two mouse lines in which e

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

197 ivotal role in the structure and function of striated muscle, whereas the role of Enigma homolog prot

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

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

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

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

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

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

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

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

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

207 We have identified a novel striated muscle-specific splice variant of the formin FH

208 The striated muscle-specific tripartite motif (TRIM) protein

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

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

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

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

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

214 RLC) also controls contraction of vertebrate striated muscle.

215 of length dependence of force generation in striated muscle.

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

217 in contraction and regulation of vertebrate striated muscle.

218 growth cone guidance receptors expressed in striated muscle.

219 soforms play overlapping and unique roles in striated muscle.

220 ll death known to be abundantly expressed in striated muscle.

221 (myosin containing) filaments of vertebrate striated muscle.

222 pal regulator of the contractile behavior of striated muscle.

223 itical role in regulating the contraction of striated muscle.

224 xtend our understanding of titin function in striated muscle.

225 pregnancy induced adaptations in smooth and striated muscle.

226 otein associated with the thick filaments of striated muscle.

227 periodic sarcomeric organization similar to striated muscle.

228 omponent of the membrane repair machinery in striated muscle.

229 allowing excitation-contraction coupling in striated muscle.

230 ding protein that is abundantly expressed in striated muscle.

231 e assembly of ryanodine receptor clusters in striated muscle.

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

233 drolysis to generate force and shortening in striated muscle.

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

235 sly reported to be specifically expressed in striated muscle.

236 indistinguishable from those in an arthropod striated muscle.

237 pen ER ryanodine-receptor Ca(2+) channels in striated-muscle cells.

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

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

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

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

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

243 in protein present in the thick filaments of striated muscles and is involved in both sarcomere forma

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

245 Striated muscles are relaxed under low Ca(2+) concentrat

246 ficantly after PNT, indicating that urethral striated muscles contribute significantly to continence.

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

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

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

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

251 Striated muscles that enable mouth opening and swallowin

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

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

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

255 libut tissues, whereas capn3 was detected in striated muscles, spleen and ovary, but absent or relati

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

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

258 rganization of the sarcoplasmic reticulum in striated muscles.

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

260 ement controlling active force generation in striated muscles.

261 processes, including the pathophysiology of striated muscles.

262 ure proper sarcomere-membrane interaction in striated muscles.

263 he smallest functional unit of myofibrils in striated muscles.

264 are the primary actin isoforms expressed in striated muscles.

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

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

267 Although normally expressed in striated myocytes and neurons, ARC is markedly induced i

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

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

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

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

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

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

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

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

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

277 ce as an alternative to the primary geniculo-striate pathway.

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

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

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

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

282 Its striated, periodic appearance in electron micrographs le

283 Striated preferentially expressed gene (Speg) is a membe

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

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

286 KD forms in a non-nuclear, Z-line localized, striated reticular pattern, suggesting the importance of

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

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

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

290 The striated sheet matrix is believed to contribute to shear

291 ncodes for the alpha-tectorin protein in the striated sheet matrix, causes a 60-dB threshold shift in

292 ade up of the radial collagen fibers and the striated sheet matrix.

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 ted beta-tectorin composition, and disrupted striated-sheet matrix.

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

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

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

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

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