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1 n all animals in which virus was detected at necropsy.
2 Macroscopic analysis was performed at necropsy.
3 s from pulmonary tissue extracts obtained at necropsy.
4 ymphoid and nonlymphoid tissues collected at necropsy.
5 ficacy of medications and/or vaccine without necropsy.
6 a the PCR method at 6 and 10 months prior to necropsy.
7 Oral tumors were resected at necropsy.
8 ic vascular rejection changes at the time of necropsy.
9 graphy was performed at 2 weeks, followed by necropsy.
10 wine bioassay of tissue samples collected at necropsy.
11 ale heart at least 9 months before death and necropsy.
12 rrelated with infarction and area at risk at necropsy.
13 o VZV DNA was detected in sensory ganglia at necropsy.
14 4-year old man in whom diagnosis was made at necropsy.
15 e drug concentrations and graft histology at necropsy.
16 lateaus of cynomolgus monkeys at the time of necropsy.
17 nimals demonstrated features of renal TMA at necropsy.
18 as an incidental lesion in adult animals at necropsy.
19 Fgf8b transgenic mice had lung metastases at necropsy.
20 8 months of age that were grossly visible at necropsy.
21 17E, and the renal pathology was examined at necropsy.
22 d either experimental or control diets until necropsy.
23 n, miscarried, or aborted fetuses by MRI and necropsy.
24 n filtered air for 0, 4, 16, and 40 h before necropsy.
25 fection but was not cultured from tissues at necropsy.
26 radic Alzheimer's disease (AD) who underwent necropsy.
27 o information previously available only from necropsy.
28 m plasma over time and from brain tissues at necropsy.
29 n; no isolates were obtained from tissues at necropsy.
30 ion was more extensive than that obtained at necropsy.
31 rdance with our protocol, immediately before necropsy.
32 use yielded more visible ablation lesions at necropsy.
33 idated by histopathological evaluation after necropsy.
34 liver, kidneys, and spleen were harvested at necropsy.
35 re harvested for histopathologic analysis at necropsy.
36 r and a region attributed to the pancreas by necropsy.
37 rate reflection of the pathology findings at necropsy.
38 mall but significant differences with LVM at necropsy.
39 phy (echo) and an ex vivo standard of LVM at necropsy.
40 olymer was confirmed by visual assessment at necropsy.
41 y the culture method at the time of moribund necropsy.
42 c B cells were measured by flow cytometry at necropsy.
43 d histologically confirmed ablation zones at necropsy.
44 LI correlated with that generated by PET and necropsy.
45 against culture for M. bovis (n = 1,464) at necropsy.
46 ding to tumor regression that is verified at necropsy.
47 well as in lung and lymph nodes collected at necropsy.
48 nalysis of brain tissue sections obtained at necropsy.
49 4 days, after which they were euthanized and necropsied.
50 sed with CHD and some CHD-negative pups were necropsied.
52 capillary density (per mm2) was measured at necropsy (252 +/- 12 versus 183 +/- 10 (P < 0.005) for p
53 ger than the mean size of true infarction at necropsy (29% +/- 3) but smaller than the mean size of t
54 el, E. coli infected rabbits were imaged and necropsied 4 hr after administration of 99mTc-P483H.
58 f tissues from RhCMV/SIV vector-protected RM necropsied 69-172 weeks after challenge did not detect S
59 nimals were monitored through death and were necropsied; 94% developed multiple neurofibromas, with 7
69 pathologies in Caenorhabditis elegans with a necropsy analysis of worms that have died of old age.
80 plaque extent (determined subsequently after necropsy) and plasma lipoproteins did not alter the resu
82 SHIV T cell responses in blood or tissues at necropsy, and no virus emerged after CD8(+) T cell deple
83 s were isolated from the spleen and liver at necropsy, and propidium iodide labeled target-specific c
84 entire SIV genome from tissues collected at necropsy, and the course of viral evolution was assessed
89 ferrets were biopsied at 12 and 15 weeks and necropsied at 18 weeks after infection, the levels of ba
98 or at gestational day (gd) 11 or 14 and were necropsied at gd 11, 14, or 18 or within 24 h of parturi
99 e inoculated with broth or H. bilis and were necropsied at several time points postinoculation to ass
105 s and microscopic lesions were assessed upon necropsy at 3, 7, 14, and 21 days following SIV inoculat
106 d from the time of experimental infection to necropsy at 5 or 7 months and were similar among all exp
109 direct viral assay of lung tissues taken by necropsy at the peak of viral replication demonstrated a
112 targeting by PET correlated with traditional necropsy-based analysis at all time points analyzed.
113 /neu C6.5 diabody PET data and compared with necropsy biodistribution data from the same tumor-bearin
115 c mouse model of Huntington's disease and in necropsy brain tissue of patients with Huntington's dise
118 enhanced green fluorescent protein model, at necropsy, can provide an opportunity to locate or assess
119 D8(+) or CD4(+) lymphocyte depletion and, at necropsy, cell-associated SIV was only occasionally meas
120 ucting time-dependent (124)I diabody PET and necropsy comparative studies with larger numbers of mice
121 less than 20.0 x 10(9)/L (20,000/microL) at necropsy, compared with only 8% of imatinib mesylate-tre
132 Imaging (including small-animal PET) and necropsy data were collected at several intervals over 2
135 at least two of the following features in 23 necropsies: dermatitis, severe pan-nephritis, and/or sev
143 better diagnostic sensitivity than internal necropsy examination; in 18 (90%) of the 20 cases the tw
149 Cardiovascular structures were examined at necropsy for rupture, perforation, dissection, or hemorr
150 tonsil biopsy specimens and surveillance by necropsy for the screening of farmed deer which have bee
151 eplication in jejunum and colon collected at necropsy from 12 SIV-infected (group 1), or 10 uninfecte
152 ction of seven PTMs with plasma collected at necropsy from a rapid-progressor PTM was consistently hi
153 d histologically normal thyroids obtained at necropsy from eight women who died from unrelated condit
155 ression of the complexins in tissue taken at necropsy from human medial temporal lobe (hippocampus, p
156 pleens, and 40 lymph nodes) were obtained at necropsy from patients affected by prion disease and fro
157 All lymphoreticular tissues obtained at necropsy from patients with neuropathologically confirme
159 3 pathway in jejunum and colon, collected at necropsy, from 10 SIV-infected macaques with diarrhea (g
160 ir musculoskeletal allografts at the time of necropsy (>100 days) regardless of the status of the epi
161 organ parts from deceased infants undergoing necropsy had been kept for several years without parenta
165 side effect of SWNTs to mice was observed in necropsy, histology, and blood chemistry measurements.
169 distention and brain edema were observed at necropsy in a few mice, while histology showed multifoca
170 discretely stained LV sites were observed at necropsy in each pig, corresponding to the injection sit
172 untreated until 70 days of age (the time of necropsy in the previous experiments) and then treated t
174 hrombi are detected histologically following necropsy in untreated sph/sph mice of various ages and a
181 n immunodeficiency virus (SIV) infection, we necropsied male rhesus macaques at 1, 3, 7, and 14 days
183 s; and polymerase chain reaction analysis of necropsy material, using probes specific for kinetoplast
192 raphy was performed at 1-month intervals and necropsy of graft-containing animals at 1, 2, 3, 4, and
196 nef sequences in brain tissues, collected at necropsy of two animals with detectable infection in the
197 ately or kept at 4 degrees C for 30 h before necropsy of two monkeys inoculated with simian varicella
199 mice were identified at gross examination on necropsy, of which 30 measured 2-5 mm and 11 measured <2
200 sues of the animals that were euthanized and necropsied on day 14 were prepared for histopathologic e
205 ulated with PCV2 VP120 at both day 21 and 42 necropsies (P = 0.0032 and P = 0.0274, respectively).
206 infection (5.4% and 6.7%, respectively); at necropsy, PCR was positive in none of 17 patients from v
213 r Mrp6 expression in the liver, and complete necropsies revealed profound mineralization of several t
217 kin punch biopsies and multiple tissues from necropsy samples remained PCR positive and B. burgdorfer
218 fy and sequence this same region of pag from necropsy samples taken from victims of the 1979 Sverdlov
220 e dog, and subsequent analysis of biopsy and necropsy samples, demonstrated in vivo repair of the GRM
223 We studied lymphoreticular tissues from a necropsy series and assessed tonsillar biopsy samples as
224 firmed non-AD patients in other longitudinal necropsy series will allow the predictive value of APOE
235 ng tissues of historical adult bighorn sheep necropsy specimens supported the association of this age
246 t weights, leptin levels, and body weight at necropsy tended to map to the same locations and were re
247 ificantly more likely to have lung tumors at necropsy than age-matched non-transgenic littermates (9
249 patients in whom PE was first discovered at necropsy, the mortality rate at 3 months was 15.3% (365
256 aling 15 to 30% of the genomes from blood or necropsy tissue from eight different cases, we have dete
257 notype analyses by partial PCR sequencing of necropsy tissue from five asymptomatic African elephants
258 sed DNA sequencing to detect EEHV genomes in necropsy tissue from five healthy adult African elephant
259 ysis of GPD1-L on genomic DNA extracted from necropsy tissue of 83 unrelated cases of sudden unexplai
260 by direct targeted PCR from blood samples or necropsy tissue samples from six viremic elephants.
261 ents of DNA amplified directly from blood or necropsy tissue samples of six more selected cases of he
262 rions by mucosal routes and performed serial necropsies to assess PrP(CWD) tissue distribution by rea
263 g (MRI) of the fetus with internal perinatal necropsy to assess whether MRI examination is a feasible
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
271 women who continued with their pregnancies; necropsy was done in two cases of pregnancy termination.
275 ce were killed at 3, 6, 9, 12 and 15 months; necropsy was performed and serum thyroid stimulating hor
284 g disease progression, and after death, when necropsies were performed and lung samples were collecte
287 To study the long-term fate of these MSCs, necropsies were performed between 9 and 21 months follow
291 eads retrieved from the peritoneal cavity at necropsy were found to secrete insulin, C-peptide, and g
295 ascular perfusion to prevent collapse during necropsy were used for morphometry evaluations of mucus
297 mpression (repair) and continued daily until necropsy, when liver underwent morphometric analysis, im
299 -old female crossbred puppy was submitted to necropsy with a history of weakness and vomiting for sev
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