ライフサイエンスコーパス: rib

1 ongation and the positioning of longitudinal ribs.

2 f hepatic function, and mild malformation of ribs.

3 polarity leading to fusions of vertebrae and ribs.

4 letal malformations with fused vertebrae and ribs.

5 There are 12 pairs of ribs.

6 6; 95% CI, 8.4-48.1), humerus, then vertebra/ribs.

7 e force coincident with the long axis of the ribs.

8 p solitary osteochondroma-like structures on ribs.

9 Left dorsal rib 7 (L7) and right dorsal rib 10 (R10) exhibit impacted fractures compressed 26 mm

10 addition to traumatic fractures, left dorsal rib 10 and possibly left phalanx I-1 have a morphology c

11 Left pedal phalanx I-1 and left dorsal rib 10 are both fractured with extensive callus formatio

12 Cartilage of rib 7 (21.3%, 47 of 221) was most commonly injured.

13 Left dorsal rib 7 (L7) and right dorsal rib 10 (R10) exhibit impacte

14 nal enzyme (riboflavin biosynthesis protein (RibD)), a putative functional analog of DHFR in a knock-

15 in riboflavin biosynthesis are catalyzed by RibD, a bifunctional protein with distinct pyrimidine de

16 ans show a positional shift of thoracolumbar ribs, a developmental variation that is controlled by Ho

17 Broadened ribs alone provide little protection [8] and confer sign

18 The displacements of the lower ribs along the craniocaudal and laterolateral axes and t

19 piration, and the displacements of the lower ribs along the craniocaudal and laterolateral axes were

20 he lack of both an attachment for the sacral rib and an ischium.

21 The harvest of the 6(th) or 7(th) rib and rectus abdominis muscle renders an acceptable do

22 ed to the silicon photonics devices based on rib and strip waveguides.

23 In patients with cystic fibrosis (CF), rib and thoracic vertebral fractures can have adverse ef

24 Matrilin-1 and epiphycan were specific for rib and trachea, whereas asporin was particularly abunda

25 ity of ribs, uncovers intrinsic laws linking ribbing and shell geometry, and provides new opportuniti

26 olutionary changes in bone microstructure in ribs and gastralia approaching the turtle condition and

27 ein alpha-subunit gene Gnai3 have fusions of ribs and lumbar vertebrae, indicating a requirement for

28 ved through a division of labour between the ribs and muscles of the trunk in which the abdominal mus

29 In rod-shaped cartilage structures (Meckel, ribs and skeletal elements in developing limbs), the tra

30 of rostral vertebrae, and reduced number of ribs and somites.

31 83 animals were phenotyped for the number of ribs and thoracolumbar vertebrae as well as successfully

32 Ribs and vertebrae are integral to this locomotor mode,

33 from osteoderms, but by contribution of the ribs and vertebrae that expand into the dermis to form p

34 d increased apoptosis of chondrocytes in the ribs and vertebrae.

35 .09; 95% confidence interval [CI], .04-.25), rib, and sternum; for pediatric patients (</=18 years) t

36 r cartilages, meniscus, intervertebral disc, rib, and tracheal cartilages on samples from 5-6 differe

37 abditis elegans as a model in which to study RIBEs, and identify the cysteine protease CPR-4, a homol

38 Our study provides crucial insights into RIBEs, and will facilitate the identification of additio

39 The vertebral column, ribs, and appendicular skeleton were all affected in the

40 hragm has an inspiratory action on the lower ribs, and current conventional wisdom maintains that thi

41 kdown evoked an extra pharyngeal arch, extra ribs, and extra somites, confirming endogenous roles of

42 stly preserved in situ, along its vertebrae, ribs, and forelimbs, as well as a row of flat, keeled ve

43 om the developing perichondral collar of the ribs, and paired gastralia that lack both lateral and me

44 as subtotal BMD and BMD of the extremities, ribs, and trunk subregions) was inversely associated wit

45 ng of all long bones, multiple contractures, rib anomalies, thoracic dysplasia, pulmonary hypoplasia

46 the shelled body plan was broadening of the ribs (approximately 50 my before the completed shell [5]

47 The ribs are a notable exception, yet the source of their re

48 These ribs are enriched with cellulose and lignin, molecules t

49 the ribs fluoroscopically and utilizing the rib as a conduit into the foramen provided an advantage

50 The sternum is fused with the ribs attaching on either side; however, unlike the ribs,

51 rib-bearing level, rather than the ultimate rib-bearing level, as in most humans and extant African

52 racic-like to lumbar-like at the penultimate rib-bearing level, rather than the ultimate rib-bearing

53 Au. sediba likely possessed five non-rib-bearing lumbar vertebrae and five sacral elements, t

54 n additive role in controlling the number of rib-bearing vertebra and positioning of the sacrum.

55 vertebra is distinct from and above the last rib-bearing vertebra in Au. sediba, resulting in a funct

56 nsition, one segment cranial to the ultimate rib-bearing vertebra, also occurs in all other early hom

57 ventilatory function, whereas the broadened ribs became the primary means of stabilizing the trunk.

58 ifocal bone pain, including pain in multiple ribs, bilateral shoulders, and bilateral hips.

59 Rib BM and all histologically negative LNs (N0) were exa

60 d tomography (CBCT) using an in vitro bovine rib bone model.

61 a near-complete loss of callus formation and rib bone regeneration.

62 hestrates large-scale regeneration of murine rib bones.

63 of South Africa, indicates the initiation of rib broadening was an adaptive response to fossoriality.

64 hragm has an inspiratory action on the lower ribs, but subjects with chronic obstructive pulmonary di

65 ponse to radiation, and CPR-4 seems to exert RIBEs by acting through the insulin-like growth factor r

66 ) indices including phase angle ( ), percent rib cage (RC %), breaths per minute (BPM), and labored b

67 alized along the entire vertebral column and rib cage and are linked to defective formation of cartil

68 thals and AMHs, such as the structure of the rib cage and supraorbital ridge development.

69 0.0015) and 48.7+/-4.3L/min with soft manual rib cage compression (p = 0.0002).

70 Hard manual rib cage compression improved mucus clearance in animals

71 the effects of two different types of manual rib cage compression on expiratory flow and mucus cleara

72 Soft manual rib cage compression slightly worsened static lung elast

73 reased to 28.4+/-5.2L/min during hard manual rib cage compression vs. 15.9+/-2.2 and 16.6+/-2.8L/min

74 Conversely, soft manual rib cage compression was not effective and potentially u

75 zed with early expiratory phase (hard manual rib cage compression) and soft and gradual rib cage comp

76 uring the late expiratory phase (soft manual rib cage compression).

77 he lungs during no treatment and soft manual rib cage compression, -0.28 +/- 0.61 and -0.15+/-0.95mm/

78 During hard manual rib cage compression, mucus moved toward the glottis (1.

79 /-2.8L/min without treatment and soft manual rib cage compression, respectively (p = 0.0006).

80 l rib cage compression) and soft and gradual rib cage compressions applied during the late expiratory

81 age compressions were tested: Hard and brief rib cage compressions synchronized with early expiratory

82 Two types of manual rib cage compressions were tested: Hard and brief rib ca

83 The normal decrease in the rib cage contribution to the tidal volume during phasic

84 acement of the lateral portions of the lower rib cage during inspiration.

85 nal motion (TAM) plot showed the abdomen and rib cage motion in synchrony.

86 arge frequencies of the SMUs were higher and rib cage movement greater during HF-SCS compared to spon

87 plitude during HF-SCS was adjusted such that rib cage movement matched (Protocol 2).

88 astic bands: one band (RC) placed around the rib cage under the upper armpit and another band (AB) ar

89 nk lesions (lateral abdominal wall below the rib cage, above the iliac crest).

90 otome, Kenya, along with its estimated adult rib cage, for comparison with H. sapiens and the Kebara

91 ity, supporting its role in the extension of rib cages.

92 elephants and manatees, which have extended rib cages.

93 in the tibia, humerus, sternebra, vertebrae, ribs, calvarium, mandible, and incisor.

94 Rib chondrocytes isolated from newborn AnxA6-/- mice sho

95 ion required for termination upstream of the ribD coding sequence.

96 ic curvature, we created multiplexed bilayer ribs composed of 4 materials, which enables us to encode

97 hragm contraction at FRC displaced the lower ribs cranially and outward, but this motion was progress

98 reasing volume, it continued to displace the ribs cranially and outward.

99 gh the force exerted by the diaphragm on the ribs decreased with increasing volume, it continued to d

100 estored riboflavin prototrophy to an E. coli ribD deletant strain when coexpressed with the correspon

101 Here, we combine genetic analysis of rib development with agent-based simulations to conclude

102 tional and appositional contributions to the rib displacement driven by transdiaphragmatic pressure.

103 From these data, the separate effects on rib displacement of Ppl and of the force exerted by the

104 pressure and transdiaphragmatic pressure on rib displacement were determined.

105 ray scattering, suggests that variability in Rib domain number would result in differential projectio

106 mportance in infection, the structure of the Rib domain was previously unknown.

107 Rib domain-containing surface proteins are found associa

108 the extensive structural malleability of the Rib domain.

109 Structures of single Rib domains of differing length reveal a rare case of do

110 viously, observed variation in the number of Rib domains within these bacterial cell wall-attached pr

111 fy the relative motions of the vertebrae and ribs during slow treadmill locomotion in three savannah

112 ivision, the structures remain as orthogonal ribs, encoding the location of past division planes in t

113 d post-mortem CT methods were used to assess rib end morphology, auricular surfaces, pubic symphyseal

114 extrapleural soft tissue lesions that cause rib expansion and destruction and appear on imaging as c

115 The ease of identifying the ribs fluoroscopically and utilizing the rib as a conduit

116 ents the first quantitative model to explain rib formation.

117 till interact with Hoxb6 and Pax3 to promote rib formation.

118 ting that these proteins are unable to block rib formation.

119 .27-9.38 vs 4.05%; 95% CI, 3.87%-4.24%), and rib fracture (4.53%; 95% CI, 3.63%-5.64% vs 3.62%; 95% C

120 as used to estimate patients' probability of rib fracture after ablation as a function of time.

121 7 patients (30.5%) presented with at least 1 rib fracture and 59 subjects (12.2%) with delayed hemoth

122 s also increase with increments of number of rib fracture detected on radiograph.

123 determine the optimal views and to simplify rib fracture diagnostics.

124 tients with solely delayed hemothorax and no rib fracture had the lowest global physical health score

125 Rib fracture is the most common thoracic injury.

126 Nerve blocks are instrumental in treating rib fracture pain along with utilization of opioids and

127 ence of delayed hemothorax and the number of rib fracture were associated with increased functional l

128 dyspnoea or cough, and one [3%] fatigue and rib fracture).

129 ons (32.3%) of the lung, as well as multiple rib fractures (29.6%).

130 Pain management for traumatic rib fractures has been described in literature, but ther

131 truction of radiographic images of traumatic rib fractures in order to determine the optimal views an

132 8)F-NaF PET was superior in the detection of rib fractures in particular.

133 Rib fractures in proximity to the ablation zone were fou

134 Bilateral multiple consecutive rib fractures occurred in 36% (41 of 114) versus 14% (64

135 No patients with rib fractures that were apparently induced by RFA and MW

136 nagement regimen for geriatric patients with rib fractures to decrease the morbidity and mortality as

137 Rib fractures were present in 13.5% of patients after pe

138 rted as being associated with PPIs, such as 'rib fractures', where signals were detected for overall

139 scapula), 93% for the detection of posterior rib fractures, and 67% for the detection of classic meta

140 ractures, 73% for the detection of posterior rib fractures, and 80% for the detection of CMLs.

141 phenotypes, including osteolytic lesions and rib fractures, osteoporosis, slow growth and reduced sur

142 ax, aortic or great vessel injury, 2 or more rib fractures, ruptured diaphragm, sternal fracture, and

143 signs of fracture, e.g. evaluation of lower rib fractures, while 45 degrees oblique view during fast

144 se to the chest wall should be monitored for rib fractures.

145 ed radiologists to determine the presence of rib fractures.

146 debridement, laceration repair, and multiple rib fractures.

147 n zone characteristics had on development of rib fractures.

148 rly, let alone pain resulting from traumatic rib fractures.

149 diagnostics and interpretation of traumatic rib fractures.

150 breathing is recommended for suspected upper rib fractures.

151 ma and often occur with multiple consecutive rib fractures.

152 Penetrance and expressivity of the rib fusion phenotype is altered in mice with a mixed C57

153 the iliac process of a hypertrophied sacral rib; fusion of these bones in tetrapods creates an aceta

154 o genes increases the number and severity of rib fusions without affecting the lumbar fusions.

155 riboswitches in Bacillus subtilis, allowing rib gene expression even in the presence of high levels

156 to FMN riboswitches leads to a reduction of rib gene expression.

157 The berries from Ribes genera showed a high diversity and concentration o

158 berries, especially the berries of Rubus and Ribes genera, had high cupric reducing antioxidant capac

159 biosynthesis and/or transport of riboflavin (rib genes).

160 r normal musculoskeletal development and for rib growth and mineralization in zebrafish.

161 o undergo proteolytic cleavage in the bovine rib growth plate, but this was not explored further.

162 istological analysis of femoral, tibial, and rib growth plates from newborn mice revealed that the hy

163 Thoracic vertebrae and ribs had abnormal morphology, lumbar and sacral vertebra

164 Although RIBEs have important implications for radioprotection, r

165 While the ribs have been shown to arise from the somites, little i

166 CaM binds to the rib helix of TRPC4, which results in the ordering of a p

167 Plants have two diverged RibD homologs, PyrD and PyrR; PyrR proteins have an extr

168 We show that the choice of large bovid ribs in an archaeological layer dominated by reindeer (R

169 ass transfer caused by vortices along d-type ribs in crossflow is applicable to filter-feeding duck b

170 At juvenile and adult stages, ribs in scxa mutants fail to mineralize and/or are small

171 Then external forces were applied to the ribs in the cranial and the lateral direction to simulat

172 el near the treatment area or heating of the ribs in the transcostal applications.

173 Eighty implants were placed in bovine ribs in which small and large bone defects were created

174 at recognize receptor-induced binding sites (RIBS) in Glu-plasminogen and, therefore, preferentially

175 y recognized receptor-induced binding sites (RIBS) in Glu-plasminogen were obtained.

176 unk vertebrae (nine), nine pairs of T-shaped ribs, inferred loss of intercostal muscles, reorganizati

177 Incorporation of the ribs into the turtle shell negates the costal movements

178 he force applied by the muscle fibres on the ribs into which they insert (insertional force) and the

179 carbon dating and DNA analysis show that the rib is associated with the other remains and dates to 13

180 Hemangioma of the rib is rarely seen.

181 ive cartilage from the nasal septum, ear, or rib is the standard material for surgical reconstruction

182 fect of the diaphragmatic force on the lower ribs is equal to the expiratory effect of pleural pressu

183 A pooled analysis of the RIBS IV (Restenosis Intra-Stent of Drug-Eluting Stents:

184 This patient-level pooled analysis of the RIBS IV and RIBS V randomized clinical trials suggests t

185 Then, the Rheum ribes L. ethanol extract (RE) was added to the films in

186 nta, Karat and Black Negus and five currant (Ribes L.) cultivars of NS 11, Focus, Ben Gairn, Otelo an

187 re-operative embolization of such a vascular rib lesion before surgically removing the lesion by thor

188 We reported on a case of a rib lesion which had a classic imaging pattern of hemang

189 canal raised on a keel (wing), supported by rib like braces (fenestral bars) and tube-like portulae;

190 epitopes recognized by the anti-plasminogen-RIBS mAbs: a linear epitope within a domain linking krin

191 The wild Chilean currants Ribes magellanicum and R. punctatum are a good source of

192 During locomotion, every rib measured in both species rotated substantially aroun

193 CLV1 signaling in the rib meristem (RM) of the shoot apical meristem is necess

194 anscription factor WUSCHEL, expressed in the rib meristem (RM), located beneath the CZ, has been show

195 ining different levels of WUS protein in the rib meristem and adjacent cells.

196 factor, accumulates at a higher level in the rib meristem and at a lower level in the central zone wh

197 higher nuclear levels of WUS in cells of the rib meristem and lower nuclear levels in adjacent cells.

198 veals that a higher level of WUS outside the rib meristem leads to protein destabilization, suggestin

199 e in the adjacent peripheral zone and in the rib meristem located just beneath the CZ.

200 domain transcription factor expressed in the rib meristem of the Arabidopsis SAM, is a key regulatory

201 is thaliana WUS, which is synthesized in the rib meristem, migrates and accumulates at lower levels i

202 cell-cycle inhibitor KRP2 in the underlying rib meristem, without affecting the canonical WUSCHEL-CL

203 WUS expression and activity, but only in the rib meristem.

204 entilation, suggesting a new hypothesis that rib motion during locomotion may have been an exaptation

205 ork is needed to establish what causes these rib motions, active contraction of the hypaxial musculat

206 Unilateral locomotor rib movements are remarkably similar to the bilateral pa

207 1386-1349 BC), a balm associated with a beef rib mummy containing a high abundance of Pistacia resin

208 (mud crab--Panopeus herbstii) and resource (ribbed musse--Geukensia demissa).

209 This ecosystem service, provided by the ribbed mussel (Geukensia demissa), was studied in animal

210 Naturally occurring populations of ribbed mussels were observed to be healthy and resilient

211 -forming marsh cordgrass and aggregations of ribbed mussels.

212 f several blackcurrant cultivars, highlining Ribes 'Myuryucheene' with 20.2% GLA of total FA.

213 = 12), cervical rib (n = 6), abnormal first rib (n = 3), and/or history of embolization (n = 2).

214 abduction by duplex scan (n = 12), cervical rib (n = 6), abnormal first rib (n = 3), and/or history

215 0 Gb genome and transcriptome of the Iberian ribbed newt Pleurodeles waltl, a tractable species suita

216 ects of sucrose ingested with blackcurrants (Ribes nigrum) and lingonberries (Vaccinium vitis-idaea)

217 rries used as ingredients were blackcurrant (Ribes nigrum), sea buckthorn (Hippophae rhamnoides), bil

218 point made of mastodon bone is embedded in a rib of a single disarticulated mastodon at the Manis sit

219 ilar to extant fossorial taxa [8], the broad ribs of Eunotosaurus provide an intrinsically stable bas

220 etermined that the lissoirs were produced on ribs of medium-sized ungulates.

221 sap-conducting tubes kept open by thickened ribs of secondary cell wall that provide the major struc

222 In culture, RNAi knockdown caused ribs of secondary cell wall, surrounded by microtubules,

223 e report that amyloid fibrils constitute the ribs of the buoyancy organelles of Anabaena flos-aquae.

224 n of the primaxial domain (vertebrae, dorsal ribs) of the skeleton in snake-like body forms has never

225 Ac substitution at the ribitiol 5-phosphate (Rib-ol-5-P), and (iii) the length of (i.e. the number of

226 and molecular evidence including meridional ribs on the cell wall, pigment production, and its 18S r

227 ctures (backward-facing steps forming d-type ribs on the porous surface of a cone) cause fluid dynami

228 l gland is located well superior to the 12th rib, on the anterior surface of the kidney, or in the re

229 sion Vertical expandable prosthetic titanium rib operation was associated with postoperative increase

230 , the deletion of the endogenous riboflavin (rib) operon and presence of four putative plasmids harbo

231 resence of four putative plasmids harbouring rib operons.

232 Clinical parameters (ie, pain in ribs or chest, organ damage caused by fractured rib) wer

233 acic vertebra, diminutive thoracic or lumbar rib, os centrale carpi and bipartite scaphoid, tripartit

234 f PAS-resistant clinical isolates encoding a RibD overexpression mutation displaying cross-resistance

235 All three rib pathologies and the pathological left phalanx I-1 ar

236 defining feature is the spiral geometry and ribbing pattern through which palaeontologists infer phy

237 including an elongated axis and the loss of ribs, pelvic fins, and teeth.

238 ding the T7 vertebral body and left pedicle, ribs, pelvis, and calvarium.

239 anted 3D-printed in vivo bioreactors against rib periosteum and utilized biomaterial-based space main

240 s: humerus, handplate, fibula, tibia, femur, ribs, petrous part, scapula and head mesenchyme.

241 The short-rib polydactyly (SRP) group of disorders are among the m

242 yxiating thoracic dystrophy (JATD) and short rib polydactyly (SRP) type III.

243 two families with autosomal-recessive short-rib polydactyly syndrome Majewski type to identify mutat

244 Short-rib polydactyly syndromes (SRPS) and Asphyxiating thorac

245 The short rib polydactyly syndromes (SRPS) are a group of recessiv

246 The short-rib polydactyly syndromes (SRPS) encompass a radiographi

247 The short rib polydactyly syndromes (SRPSs) are a heterogeneous gr

248 rol the evolution of these high-shear-stress ribs, potentially causing migration of the grounding lin

249 dulating its response to rib-suppressing and rib-promoting Hox proteins.

250 , by the dominant effect of Ppl on the lower ribs, rather than an inward pull from the diaphragm.

251 horacic to lumbar vertebrae because of their rib-repressing activity.

252 how that this is not a result of the loss of rib-repressing properties by the snake proteins, but rat

253 (HR 8.43; p = 0.003) and increased number of ribs resected (HR 1.78; p = 0.02).

254 ibs were resected (IQR = 1-3), and number of ribs resected did not correlate with margin status (p =

255 Scoliosis was associated with posterior rib resection (HR 8.43; p = 0.003) and increased number

256 Surgical intervention by means of first rib resection and anterior scalenectomy is an effective

257 n and scalenectomy (FRRS) (n = 15), cervical rib resection and FRRS (n = 6), or FRRS and second rib r

258 All patients received immediate first rib resection and scalenectomy (FRRS) (n = 15), cervical

259 ith hypercoagulability do as well with first rib resection and scalenectomy for SVT as those without

260 ercoagulability in patients undergoing first rib resection and scalenectomy presenting with SVT.

261 section and FRRS (n = 6), or FRRS and second rib resection due to fusion (n = 1).

262 rterial TOS should undergo cervical or first rib resection with or without arterial reconstruction to

263 NusG-dependent pausing in the ribD riboswitch provides time for cotranscriptional bind

264 ll individuals from both species, the middle ribs rotated cranially through bucket and pump-handle mo

265 Rib rotations can be decomposed into bucket-handle rotat

266 w grouping species as botanical criteria for Ribes sections do.

267 ies and R. nigrum-based cultivars from eight Ribes sections were surveyed for gamma-linolenic acid (G

268 characterized primarily by short, horizontal ribs, short limbs and polydactyly.

269 l disorders primarily characterized by short ribs, shortened long bones, varying types of polydactyly

270 Here, we examine the development of the ribs, simple structures that in most terrestrial vertebr

271 coil domain for the 'pole' and four helical 'ribs' spanning the N-terminal TRPM homology regions (MHR

272 Fifty Ribes species and R. nigrum-based cultivars from eight R

273 92% for the detection of thoracic fractures (ribs, sternum, clavicle, and scapula), 93% for the detec

274 a skilled-nursing facility ranged from 28% (ribs/sternum) to 47% (pelvis/hip).

275 spiratory muscles to the ventral side of the ribs, (sub)dermal outgrowth of bone from the developing

276 ne by differently modulating its response to rib-suppressing and rib-promoting Hox proteins.

277 ree taxa share anteroposteriorly broad trunk ribs that are T-shaped in cross-section and bear sculptu

278 ttaching on either side; however, unlike the ribs, the sternal precursors do not originate from the s

279 se, as well as in the genetic diseases short-rib thoracic dysplasia, Mohr-syndrome and amyotrophic la

280 sia of the mandible and asymmetric fusion of ribs to the sternum.

281 insertional and appositional forces, and the rib trajectories for these external forces were used as

282 ubiquitous presence of ornamentation such as ribs, tubercles, or spines presents yet another level of

283 ation for the morphogenesis and diversity of ribs, uncovers intrinsic laws linking ribbing and shell

284 dicating myocardial uptake absent, less than rib uptake, equal to rib uptake, or more than rib uptake

285 ptake absent, less than rib uptake, equal to rib uptake, or more than rib uptake, respectively).

286 ib uptake, equal to rib uptake, or more than rib uptake, respectively).

287 Berries of four gooseberry (Ribes uva-crispa L.) cultivars of Invicta, Rixanta, Kara

288 ing Balloon vs Everolimus-Eluting Stent) and RIBS V (Restenosis Intra-Stent of Bare Metal Stents: Pac

289 ent-level pooled analysis of the RIBS IV and RIBS V randomized clinical trials suggests that EES prov

290 sing vertical expandable prosthetic titanium rib (VEPTR).

291 basal endochondral axial skeletal elements (ribs, vertebrae) and plates of bone, which are overlain

292 RibD was shown to act as a functional analog of DHFR, an

293 of the force exerted by the diaphragm on the ribs were determined.

294 ight different plain radiography pictures of ribs were performed with the patient in an erect positio

295 A median of 2 ribs were resected (IQR = 1-3), and number of ribs resec

296 A median of 3 (range: 1-5) contiguous ribs were resected.

297 s or chest, organ damage caused by fractured rib) were evaluated for patients with confirmed fracture

298 in the form of lattices with curved bilayer ribs whose geometry is individually programmed to achiev

299 myocutaneous component and a 6(th) or 7(th) rib with adjacent muscle and skin to restore bone defect

300 gion of the shoot apical meristem called the rib zone (RZ).