ライフサイエンスコーパス: necropsy

1 ression lasting over 6 months (tumor free at necropsy).

2 against culture for M. bovis (n = 1,464) at necropsy.

3 ding to tumor regression that is verified at necropsy.

4 well as in lung and lymph nodes collected at necropsy.

5 nalysis of brain tissue sections obtained at necropsy.

6 n all animals in which virus was detected at necropsy.

7 Macroscopic analysis was performed at necropsy.

8 s from pulmonary tissue extracts obtained at necropsy.

9 ymphoid and nonlymphoid tissues collected at necropsy.

10 ficacy of medications and/or vaccine without necropsy.

11 a the PCR method at 6 and 10 months prior to necropsy.

12 Oral tumors were resected at necropsy.

13 ic vascular rejection changes at the time of necropsy.

14 graphy was performed at 2 weeks, followed by necropsy.

15 colonization and lesions were recorded after necropsy.

16 wine bioassay of tissue samples collected at necropsy.

17 ale heart at least 9 months before death and necropsy.

18 rrelated with infarction and area at risk at necropsy.

19 4-year old man in whom diagnosis was made at necropsy.

20 e drug concentrations and graft histology at necropsy.

21 lateaus of cynomolgus monkeys at the time of necropsy.

22 nimals demonstrated features of renal TMA at necropsy.

23 as an incidental lesion in adult animals at necropsy.

24 Fgf8b transgenic mice had lung metastases at necropsy.

25 8 months of age that were grossly visible at necropsy.

26 17E, and the renal pathology was examined at necropsy.

27 d either experimental or control diets until necropsy.

28 n, miscarried, or aborted fetuses by MRI and necropsy.

29 liver, kidneys, and spleen were harvested at necropsy.

30 c B cells were measured by flow cytometry at necropsy.

31 LI correlated with that generated by PET and necropsy.

32 o VZV DNA was detected in sensory ganglia at necropsy.

33 m plasma over time and from brain tissues at necropsy.

34 use yielded more visible ablation lesions at necropsy.

35 idated by histopathological evaluation after necropsy.

36 re harvested for histopathologic analysis at necropsy.

37 r and a region attributed to the pancreas by necropsy.

38 rate reflection of the pathology findings at necropsy.

39 mall but significant differences with LVM at necropsy.

40 phy (echo) and an ex vivo standard of LVM at necropsy.

41 olymer was confirmed by visual assessment at necropsy.

42 y the culture method at the time of moribund necropsy.

43 d histologically confirmed ablation zones at necropsy.

44 4 days, after which they were euthanized and necropsied.

45 sed with CHD and some CHD-negative pups were necropsied.

46 Between 1996 and 2016, we necropsied 127 apparently healthy pelagic olive ridley t

47 Two were euthanized and necropsied 19-22 h after injection, and 6 received autol

48 capillary density (per mm2) was measured at necropsy (252 +/- 12 versus 183 +/- 10 (P < 0.005) for p

49 ger than the mean size of true infarction at necropsy (29% +/- 3) but smaller than the mean size of t

50 CD8(hCXCR5) and untransduced CD8 T cells and necropsied 48 h later.

51 nfected piglet was still excreting spores at necropsy 50 days after an oral challenge.

52 Bone marrow was examined at necropsy 6, 10, or 15 days postinfection.

53 f tissues from RhCMV/SIV vector-protected RM necropsied 69-172 weeks after challenge did not detect S

54 nimals were monitored through death and were necropsied; 94% developed multiple neurofibromas, with 7

55 On necropsy, a large number of necrotic polymorphonuclear l

56 At necropsy, a small retroperitoneal hematoma along the ste

57 Upon necropsy after 10 days of infection, fungal burden in lu

58 On necropsy, all dolphins were in good nutritive status wit

59 At necropsy, all tissues were assessed for levels of radioa

60 After 6 to 8 weeks, 2 underwent direct necropsy analysis for histology, 3 underwent primary x-r

61 Necropsy analysis of animals that received DiI-labeled V

62 pathologies in Caenorhabditis elegans with a necropsy analysis of worms that have died of old age.

63 Necropsy analysis revealed hepatic microvesicular steato

64 Necropsy and histology ruled out hemorrhage and hypovole

65 Furthermore, gross necropsy and histopathology did not show any significant

66 Both necropsy and histopathology revealed the presence of int

67 Confirmation with analysis by necropsy and histopathology showed excellent diagnostic

68 Upon killing, careful necropsy and tissue histology show age-related changes o

69 ue extent of atherosclerosis is supported by necropsy and transplant donor studies.

70 Our study provides necropsy and ultrasonographic evidence of the dynamic as

71 Whole brains were snap-frozen at necropsy and were subsequently sectioned prior to analys

72 plaque extent (determined subsequently after necropsy) and plasma lipoproteins did not alter the resu

73 Five weeks post-BMT, mice were necropsied, and lung and GI tissue were analyzed.

74 SHIV T cell responses in blood or tissues at necropsy, and no virus emerged after CD8(+) T cell deple

75 s were isolated from the spleen and liver at necropsy, and propidium iodide labeled target-specific c

76 entire SIV genome from tissues collected at necropsy, and the course of viral evolution was assessed

77 tissues and organs were collected from each necropsied animal.

78 r, HSV-2 DNA was detected in ganglia in most necropsied animals.

79 Paralleling these results, at necropsy, animals immunized with the recombinant BCG vac

80 Two chickens from each group were necropsied at 1, 3, 5, 7, 10, 13, 16, 20, 24, 28, 35, an

81 ferrets were biopsied at 12 and 15 weeks and necropsied at 18 weeks after infection, the levels of ba

82 and 0.24 microg/kg/week subcutaneously) and necropsied at 2 or 10 weeks postsurgery.

83 Piglets were necropsied at 2 to 10 days after inoculation, and intest

84 Animals were necropsied at 2 weeks postinoculation; 100% of F344, 42%

85 ive doses of Yersinia pestis strain CO92 and necropsied at 24-h intervals postexposure (p.e.).

86 Two pigs from each group were necropsied at 3, 7, 14, 20, 27, and 55 days postinoculat

87 Two to four pigs from each group were necropsied at 3, 7, 14, 20, 27, or 55 days postinoculati

88 ation (dpi), and the remaining chickens were necropsied at 56 dpi.

89 8) of IL-10-deficient mice was genotyped and necropsied at 6 weeks of age.

90 e inoculated with broth or H. bilis and were necropsied at several time points postinoculation to ass

91 Necropsies at 5 and 7 months postinfection included hist

92 ells in the peripheral blood and heart until necropsy at > or = 11 months of age.

93 y rats to CB11 via nose-only inhalation with necropsy at 0, 4, and 8 h post exposure.

94 Rumen epithelial tissues were collected at necropsy at 17 weeks of age.

95 d rumen epithelial tissues were collected at necropsy at 17 weeks of age.

96 Necropsy at 24 h revealed that the popliteal node on the

97 ing at 3 weeks postinoculation and ending at necropsy at 3 months postinoculation.

98 s and microscopic lesions were assessed upon necropsy at 3, 7, 14, and 21 days following SIV inoculat

99 d from the time of experimental infection to necropsy at 5 or 7 months and were similar among all exp

100 Macroscopic pneumonia on necropsy at days 3 and 7 was greatest in both SIV-infect

101 rand HEV RNA in each tissue collected during necropsy at different DPI.

102 direct viral assay of lung tissues taken by necropsy at the peak of viral replication demonstrated a

103 Necropsy at the time of natural death revealed an associ

104 At necropsy, bacteria were present in mammary lymph nodes o

105 Diagnosis was confirmed at necropsy based on histopathologic evaluation of multiple

106 targeting by PET correlated with traditional necropsy-based analysis at all time points analyzed.

107 /neu C6.5 diabody PET data and compared with necropsy biodistribution data from the same tumor-bearin

108 At necropsy, blood, lung, kidney, and spleen samples were c

109 c mouse model of Huntington's disease and in necropsy brain tissue of patients with Huntington's dise

110 At necropsy, bronchoalveolar lavage was performed and the r

111 Brain viral RNA was undetectable at necropsy, but viral DNA levels were not different from t

112 enhanced green fluorescent protein model, at necropsy, can provide an opportunity to locate or assess

113 D8(+) or CD4(+) lymphocyte depletion and, at necropsy, cell-associated SIV was only occasionally meas

114 ucting time-dependent (124)I diabody PET and necropsy comparative studies with larger numbers of mice

115 less than 20.0 x 10(9)/L (20,000/microL) at necropsy, compared with only 8% of imatinib mesylate-tre

116 Necropsy confirmed severe aortic vegetative endocarditis

117 Necropsy confirmed the presence of EAC in 50% of treatme

118 Data from hundreds of necropsy-confirmed non-AD patients in other longitudinal

119 ian gerbils were infected with H. pylori and necropsied continuously during 18 months.

120 that the amount of normal liver remaining at necropsy correlated best with survival.

121 ensity in the ischemic limb was performed at necropsy (D40).

122 Imaging and necropsy data for tumor-bearing animals given the anti-C

123 Twenty-four-hour necropsy data in the DU145 model showed significantly hi

124 Necropsy data indicated that the signal in tumor-bearing

125 A comprehensive survey of necropsy data was performed across 36 mammalian species

126 Imaging (including small-animal PET) and necropsy data were collected at several intervals over 2

127 Analyses of tracheal rings obtained at necropsy (day 12) documented widespread infection of ind

128 The four individuals who had necropsies demonstrated the neuropathological hallmarks

129 at least two of the following features in 23 necropsies: dermatitis, severe pan-nephritis, and/or sev

130 Results Swine gross necropsy did not show any extracardiac damage related to

131 At necropsy, disease was quantified with respect to patholo

132 failure was unsuccessfully implemented, and necropsy evaluation of the dog was not permitted.

133 m a total of four premises were subjected to necropsy evaluation.

134 After euthanization on day 28, necropsy examination disclosed that capillary density wa

135 Necropsy examination findings included enlarged pulmonar

136 No significant changes were noted in post necropsy examination of internal organs and organ-to-bod

137 ble toxicity as evaluated by weight gain and necropsy examination.

138 uminescence imaging, caliper measurement and necropsy examination.

139 Necropsy examinations confirmed DLIT measurements.

140 luation of influenza virus pathogenicity, as necropsy findings can provide important information rega

141 MR imaging and necropsy findings confirmed stent position.

142 eath was determined and tissues collected at necropsy for histologic examination.

143 r and spleen samples, were collected at each necropsy for pathological and virological testing.

144 Cardiovascular structures were examined at necropsy for rupture, perforation, dissection, or hemorr

145 tonsil biopsy specimens and surveillance by necropsy for the screening of farmed deer which have bee

146 eplication in jejunum and colon collected at necropsy from 12 SIV-infected (group 1), or 10 uninfecte

147 ction of seven PTMs with plasma collected at necropsy from a rapid-progressor PTM was consistently hi

148 d histologically normal thyroids obtained at necropsy from eight women who died from unrelated condit

149 We obtained tissues at necropsy from four patients with neuropathologically con

150 ression of the complexins in tissue taken at necropsy from human medial temporal lobe (hippocampus, p

151 pleens, and 40 lymph nodes) were obtained at necropsy from patients affected by prion disease and fro

152 All lymphoreticular tissues obtained at necropsy from patients with neuropathologically confirme

153 ologic sections of lung tissue were taken at necropsy from the injury group.

154 3 pathway in jejunum and colon, collected at necropsy, from 10 SIV-infected macaques with diarrhea (g

155 ir musculoskeletal allografts at the time of necropsy (>100 days) regardless of the status of the epi

156 organ parts from deceased infants undergoing necropsy had been kept for several years without parenta

157 F344 rats without struvite stones at necropsy had milder bladder lesions and significantly lo

158 2110 (86.0%) patients had PE proven by necropsy, high-probability lung scan, pulmonary angiogra

159 terferon-gamma(-/-) mice were assessed using necropsy, histologic examination, IHC analysis, flow cyt

160 At necropsy, histologic lesions of OA were graded, and the

161 side effect of SWNTs to mice was observed in necropsy, histology, and blood chemistry measurements.

162 Echocardiography, necropsy, histology, and molecular phenotype confirm a d

163 detection by any routine BTB tests (BOVIGAM, necropsy, histology, culture, PCR) that are regularly pe

164 We report ultrasonographic visualization, necropsy, histopathologic and ultrastructural findings o

165 Comprehensive necropsy, histopathology, and metabolomic analysis revea

166 Necropsy identified a widespread ALK+ lymphoma in lymph

167 distention and brain edema were observed at necropsy in a few mice, while histology showed multifoca

168 discretely stained LV sites were observed at necropsy in each pig, corresponding to the injection sit

169 of stent graft-induced injury at surgery or necropsy in half of the patients.

170 untreated until 70 days of age (the time of necropsy in the previous experiments) and then treated t

171 luded or severely stenotic at venography and necropsy in the remaining six animals.

172 hrombi are detected histologically following necropsy in untreated sph/sph mice of various ages and a

173 ion loss in 6 studies measured by antigen or necropsy, indicating transient serological responses and

174 IL-8 levels were elevated in necropsy lavages of animals with significant lung infect

175 At necropsy, lymphoid tissues and vaginal mucosa were virus

176 At necropsy, macaques with SIVE had more infected macrophag

177 n immunodeficiency virus (SIV) infection, we necropsied male rhesus macaques at 1, 3, 7, and 14 days

178 At necropsy, mammary tumors and blood were collected for ev

179 s; and polymerase chain reaction analysis of necropsy material, using probes specific for kinetoplast

180 Necropsy measurements of cardiac mass indexed for body w

181 At necropsy, monkeys with active disease had more lung T ce

182 At necropsy, more lesions were found using needle versus co

183 At necropsy, multiple markers (CD44v6, CCR2, and CCR5 on bl

184 On necropsy, no PFA animals (0 of 6, 0%) demonstrated esoph

185 Empirical data from necropsies of deceased animals were then utilised to ass

186 Necropsy of 2 eyes of 1 patient revealed prominent granu

187 Finally, upon necropsy of a WSU5-infected horse 4 years postinfection,

188 raphy was performed at 1-month intervals and necropsy of graft-containing animals at 1, 2, 3, 4, and

189 Necropsy of nmd mice in end-stage heart failure revealed

190 by computed axial tomography of the head and necropsy of the brain when possible.

191 duction abnormalities could be detected upon necropsy of the null mice.

192 nef sequences in brain tissues, collected at necropsy of two animals with detectable infection in the

193 ately or kept at 4 degrees C for 30 h before necropsy of two monkeys inoculated with simian varicella

194 ned and bacterial species were identified by necropsy of various tissues.

195 This is especially true for scheduled necropsy of virus-infected ferrets, a standard component

196 model, and optimal sample collection during necropsy of virus-infected ferrets.

197 mice were identified at gross examination on necropsy, of which 30 measured 2-5 mm and 11 measured <2

198 sues of the animals that were euthanized and necropsied on day 14 were prepared for histopathologic e

199 ommendations) from 60 d before conception to necropsy on d 135 of pregnancy.

200 ytometry, tissue culture, adoptive transfer, necropsies, or histologic examination.

201 mor xenografts for scintigraphic imaging and necropsy organ counting.

202 HGE agent-infected C3H/HeJ mice were necropsied over 21 days.

203 ulated with PCV2 VP120 at both day 21 and 42 necropsies (P = 0.0032 and P = 0.0274, respectively).

204 infection (5.4% and 6.7%, respectively); at necropsy, PCR was positive in none of 17 patients from v

205 Necropsies performed 8 to 55 weeks after the initiation

206 after inoculation and brain virus burden at necropsy (r = -0.614; P < 0.01).

207 Plasma virus loads at necropsy ranged from 11 to 28 copies of vRNA per ml.

208 At necropsy, remdesivir-treated animals had lower lung vira

209 e done, and permission for neuropathological necropsy requested, in suspected cases.

210 Necropsy results showed the animal suffered from feline

211 ction, clinical signs were minimal and gross necropsy results were unremarkable.

212 r Mrp6 expression in the liver, and complete necropsies revealed profound mineralization of several t

213 Necropsy revealed at least two of the following features

214 Necropsy revealed no gross vascular injury.

215 Necropsy revealed patent ductus arteriosus with normal i

216 kin punch biopsies and multiple tissues from necropsy samples remained PCR positive and B. burgdorfer

217 fy and sequence this same region of pag from necropsy samples taken from victims of the 1979 Sverdlov

218 clonal pattern in paired splenic biopsy and necropsy samples was correlated with progression.

219 e dog, and subsequent analysis of biopsy and necropsy samples, demonstrated in vivo repair of the GRM

220 The necropsy sampling was weighted in that we preferentially

221 At necropsy, selected organs were weighed and prepared for

222 We studied lymphoreticular tissues from a necropsy series and assessed tonsillar biopsy samples as

223 firmed non-AD patients in other longitudinal necropsy series will allow the predictive value of APOE

224 e used as controls, and histology after full necropsy served as the gold standard.

225 Electrocardiograph profiles and necropsies showed the cause of death to be the developme

226 Follow-up catheterization and necropsy showed accurate stent deployment, durable gradi

227 Necropsy showed expansive PFA lesions without stenosis i

228 Necropsy showed prominent meningitis with vasculitis ext

229 At necropsy, similar brain nef sequences were found in diff

230 a profound reduction in brain mass of 30% at necropsy, similar to alterations observed in human patie

231 by light (LM) and electron (EM) microscopy; necropsy specimens by LM.

232 Necropsy specimens from 4 sources were studied: (1) hear

233 ere compared with postinjection MRI and with necropsy specimens obtained 24 hours later.

234 on of "arterial remodeling" was confirmed in necropsy specimens of human coronary arteries.

235 ng tissues of historical adult bighorn sheep necropsy specimens supported the association of this age

236 Necropsy specimens were taken of both expanded and non-e

237 trunk in 86 patients were supplemented by 16 necropsy specimens.

238 0.4) compared well with those obtained from necropsy studies (5.1).

239 Necropsy studies from Africa have shown that Pneumocysti

240 Necropsy studies have outlined the morphological charact

241 Serial angiographic and necropsy studies suggest that the risk of plaque rupture

242 Here, by detailed necropsy studies, we show that the virus can rapidly dis

243 therosclerosis at young ages is derived from necropsy studies, which have inherent limitations.

244 then be further evaluated using traditional necropsy studies.

245 Subsets of animals underwent a necropsy study at 4, 7, 14 and 28 days after injury; inj

246 Analysis of necropsies suggests that the analog was well tolerated.

247 , a large scale, high-throughput prospective necropsy survey was conducted spanning 2013-2016.

248 t weights, leptin levels, and body weight at necropsy tended to map to the same locations and were re

249 ificantly more likely to have lung tumors at necropsy than age-matched non-transgenic littermates (9

250 patients in whom PE was first discovered at necropsy, the mortality rate at 3 months was 15.3% (365

251 At necropsy, the mutant mice had very small thymuses and sp

252 At necropsy, the rear paws were either fixed in formalin an

253 At necropsy, the small, and occasionally the large, intesti

254 At necropsy, the urogenital system and periaortic lymph nod

255 ine (PBS) (n = 15) or PBS alone (n = 10) and necropsied them at 7 weeks postinfection.

256 estinal content collected at three different necropsy times.

257 aling 15 to 30% of the genomes from blood or necropsy tissue from eight different cases, we have dete

258 notype analyses by partial PCR sequencing of necropsy tissue from five asymptomatic African elephants

259 sed DNA sequencing to detect EEHV genomes in necropsy tissue from five healthy adult African elephant

260 ysis of GPD1-L on genomic DNA extracted from necropsy tissue of 83 unrelated cases of sudden unexplai

261 by direct targeted PCR from blood samples or necropsy tissue samples from six viremic elephants.

262 ents of DNA amplified directly from blood or necropsy tissue samples of six more selected cases of he

263 rions by mucosal routes and performed serial necropsies to assess PrP(CWD) tissue distribution by rea

264 fter phases 2 and 3 with the use of detailed necropsy to detect pigs with live, nondegenerated cysts

265 es and tissues taken during infection and at necropsy to determine viral load and tissue tropism.

266 d viral load was measured in brain tissue at necropsy to examine the relationship of systemic and cen

267 At necropsy, tumors were harvested, and the relative enzyme

268 cerebrospinal fluid nor in neural tissues at necropsy two weeks after infection.

269 At necropsy, up to 7.1% of CD3(+) cells in tissues were GFP

270 yields improved CMR agreement with echo and necropsy-verified LVM.

271 Tumor uptake measured at necropsy was 3- to 15-fold higher and tumor-to-blood rat

272 women who continued with their pregnancies; necropsy was done in two cases of pregnancy termination.

273 Necropsy was done on surviving animals 100-200 d after t

274 Necropsy was done on two patients who died; there was ly

275 Upon animal death and/or 72 hrs, necropsy was followed by histopathologic evaluation of o

276 ce were killed at 3, 6, 9, 12 and 15 months; necropsy was performed and serum thyroid stimulating hor

277 t venography was performed at 5-8 weeks, and necropsy was performed at 7-8 weeks.

278 cultation and angiography for up to 1 month; necropsy was performed in all animals.

279 Necropsy was performed on all cats, and a complete set o

280 Necropsy was performed on Day 14.

281 s were sacrificed between 2 and 4 weeks, and necropsy was performed.

282 th blood sampling until they were killed and necropsy was performed.

283 At necropsy we determined tumor and ulcer numbers, tumor si

284 During this period, 519 necropsies were conducted in 155 young/subadult koalas,

285 g disease progression, and after death, when necropsies were performed and lung samples were collecte

286 in the hind limb with 100 B. pahangi L3, and necropsies were performed at various times.

287 Necropsies were performed between 12 hours and 28 days a

288 To study the long-term fate of these MSCs, necropsies were performed between 9 and 21 months follow

289 In the original study, necropsies were performed on 714 adult blacks from south

290 each of the genotypes throughout the gut at necropsy were determined.

291 Tissues collected at necropsy were examined for disease-associated prion prot

292 eads retrieved from the peritoneal cavity at necropsy were found to secrete insulin, C-peptide, and g

293 Isolates collected at necropsy were not tested for antimicrobial susceptibilit

294 dure, after follow-up splenic venography and necropsy were performed.

295 Skeletal muscles removed at necropsy were studied by (i) microscopic examination of

296 ascular perfusion to prevent collapse during necropsy were used for morphometry evaluations of mucus

297 The mice were necropsied when the control mice became moribund.

298 mpression (repair) and continued daily until necropsy, when liver underwent morphometric analysis, im

299 Animals were necropsied while immunosuppressed on day 50 (two animals

300 Animals also underwent necropsy with quantitative bacterial cultures from multi