ライフサイエンスコーパス: rib

1 anti-TB drug isoniazid, inhibits the E. coli RibD.

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 p solitary osteochondroma-like structures on ribs.

8 f the somite-derived vertebrae and vertebral ribs.

9 ongation and the positioning of longitudinal ribs.

10 effect lethality were found in sqv-1, sqv-8, rib-1 and rib-2 mutants, which affect enzymes involved i

11 closely related to the lux genes of the lux-rib(2) operon of P. leiognathi.

12 closely related to the lux genes of the lux-rib(2) operon of Photobacterium leiognathi; and (iv) a s

13 hality were found in sqv-1, sqv-8, rib-1 and rib-2 mutants, which affect enzymes involved in heparan

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

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

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

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

18 engel deformity of scapula, fusion of spine, rib abnormities, pectus excavatum, and pes planus repres

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

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

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

22 thoraco-lumbar transition and unfused lumbar ribs among early mammals.

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

24 r tissue, specifically the phloem of the mid-rib and minor veins of leaves, roots and flowers.

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

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

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

28 ese include Uncx, a somite gene required for rib and vertebral patterning, and Nrarp, a regulator of

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

30 diate electron density at the surface of the ribs and longitudinal columns of the fibrous sheath.

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

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

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

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

35 d intervertebral discs, as well as adjoining ribs and sternum.

36 83 animals were phenotyped for the number of ribs and thoracolumbar vertebrae as well as successfully

37 of intestinal IgA were detected to half the rIBs and to both commensal flagellins.

38 h small body size, and develop fusion of the ribs and vertebrae, abnormal spinal curvatures, and dysm

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

40 three dorsal-open group genes [raw, ribbon (rib), and puckered (puc)] indicate that these gene produ

41 .09; 95% confidence interval [CI], .04-.25), rib, and sternum; for pediatric patients (</=18 years) t

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

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

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

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

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

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

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

49 soderm, which forms the vertebral bodies and ribs, and from lateral plate mesoderm, which forms the s

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

51 with loss of vertebral identity, rudimentary ribs, and rostral hindlimb shifts.

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

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

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

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

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

57 ation, with complete bilateral fusion of the ribs at the costovertebral junction producing a "crab-li

58 splay cleft palate, incomplete fusion of the ribs at the midline and bifid sternum as well as delayed

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 ns regarding the nature of the ;Hox code' in rib cage and axial skeleton development are revealed.

75 Other defects in the skull, lung, rib cage and long bones are likely to be the result of t

76 0.0015) and 48.7+/-4.3L/min with soft manual rib cage compression (p = 0.0002).

77 Hard manual rib cage compression improved mucus clearance in animals

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

79 Soft manual rib cage compression slightly worsened static lung elast

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

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

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

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

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

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

86 /-2.8L/min without treatment and soft manual rib cage compression, respectively (p = 0.0006).

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

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

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

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

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

92 ely from somitic mesoderm, patterning of the rib cage is complicated by its derivation from two disti

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

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

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

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

97 elephants and manatees, which have extended rib cages.

98 rsus the two substrates, we propose that the RibD-catalyzed reduction step follows a kinetic scheme s

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

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

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

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

103 role in rib development, suggested by severe rib defects upon ablating the myf5 lineage.

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

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

106 ge within ribs that has an important role in rib development, suggested by severe rib defects upon ab

107 ed during successive stages of vertebral and rib development.

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

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

110 pressure and transdiaphragmatic pressure on rib displacement were determined.

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

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

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

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

115 and is required for palatogenesis, skeletal rib formation and perinatal viability.

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 ecursors also produces patterning defects of rib formation.

120 .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

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

122 7 patients (30.5%) presented with at least 1 rib fracture and 59 subjects (12.2%) with delayed hemoth

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

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

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

126 Rib fracture is the most common thoracic injury.

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

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

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

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 ed body weight curves, reduced the number of rib fractures, and improved bone mineralization and bone

142 Age, gender, number of rib fractures, Injury Severity Score, comorbidities, pne

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

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

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

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

147 ed radiologists to determine the presence of rib fractures.

148 debridement, laceration repair, and multiple rib fractures.

149 n zone characteristics had on development of rib fractures.

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

151 diagnostics and interpretation of traumatic rib fractures.

152 breathing is recommended for suspected upper rib fractures.

153 ma and often occur with multiple consecutive rib fractures.

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

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

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

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

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

159 loned and solubly expressed the bifunctional ribD gene from Escherichia coli, whose three-dimensional

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

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

162 s the first report of merodiploidy of lux or rib genes in a luminous bacterium and the first indicati

163 each other than either one is to the lux and rib genes of other bacterial species, which rules out in

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

165 these polymer chains by the enzyme poly(ADP-Rib) glycohydrolase (PARG).

166 ADP-Rib groups are removed from these polymer chains by the

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

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

169 per two-thirds and lower one-third of rabbit rib growth plates were microsurgically isolated and proc

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

171 Although RIBEs have important implications for radioprotection, r

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

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

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

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

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

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

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

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

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

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

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

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

184 Hemangioma of the rib is rarely seen.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 t the geographic sampling range, whereas lux-rib merodiploid strains were found only in coastal water

206 1386-1349 BC), a balm associated with a beef rib mummy containing a high abundance of Pistacia resin

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

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

209 of gene-expression changes in the California ribbed mussel (Mytilus californianus) at different phase

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

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

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

213 0 Gb genome and transcriptome of the Iberian ribbed newt Pleurodeles waltl, a tractable species suita

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

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

216 of four candidate genes for QTL relating to rib number and eye size.

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

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

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

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

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

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

223 (1-->3)alpha-d-Glcp(1-->3)alpha-l-Rhap(1-->3)Rib-ol and alpha-d-Glcp(1-->3)alpha-l-Rhap(1-->3)Rib-ol

224 ol and alpha-d-Glcp(1-->3)alpha-l-Rhap(1-->3)Rib-ol but did not bind alpha-l-Rhap(1-->3)Rib-ol.

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

226 3)Rib-ol but did not bind alpha-l-Rhap(1-->3)Rib-ol.

227 y using a tissue-simulating gel phantom with ribs on one side and without ribs on the other.

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

229 el phantom with ribs on one side and without ribs on the other.

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

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

232 ied 106 strains that carry only a single lux-rib operon and 68 that carry multiple lux-rib operons.

233 Strains bearing a single lux-rib operon were obtained throughout the geographic sampl

234 tent, organization, and sequence of each lux-rib operon, we constructed a fosmid library of genomic D

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

236 resence of four putative plasmids harbouring rib operons.

237 ux-rib operon and 68 that carry multiple lux-rib operons.

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

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

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

241 nd assessed both vertebral and nonvertebral (rib, pelvic, and femur) fractures in a protocolized fash

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

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

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

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

246 The short-rib polydactyly (SRP) syndromes are a heterogeneous grou

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

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

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

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

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

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

253 Cellular levels of ADP-Rib polymer increase after infection with avirulent Pseu

254 NAD(+) are attached to proteins by poly(ADP-Rib) polymerase (PARP) enzymes.

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

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

257 hose observed in Korean melons, silk gourds, ribbed pumpkins, striped cavern tomatoes, and cantaloupe

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

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

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

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

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

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

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

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

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

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

268 evelop an EvC-like syndrome, including short ribs, short limbs and dental abnormalities.

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

270 g heart defects, cleft palate, fusion of the ribs, short limbs, distal colon aganglionosis, abnormal

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

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

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

274 my as specifically defined with avoidance of rib spreading is feasible.

275 e and a traditional hilar dissection without rib spreading.

276 92% for the detection of thoracic fractures (ribs, sternum, clavicle, and scapula), 93% for the detec

277 ergent situations, such as assessment of the ribs, sternum, pelvis, hips, and joints, should be guide

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

279 Merodiploid lux-rib strains of P. leiognathi were detected during sequen

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

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

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

283 istence of a significant myf5 lineage within ribs that has an important role in rib development, sugg

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

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

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

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

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

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

290 rotein modification in which ADP-ribose (ADP-Rib) units derived from NAD(+) are attached to proteins

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

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

293 Somites are embryonic precursors of the ribs, vertebrae and certain dermis tissue.

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

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

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

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

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

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).