ライフサイエンスコーパス: fresh-frozen

1 n, deparaffinized, various stains, unstained fresh-frozen).

2 hin 24 to 36 hours of death, and immediately fresh frozen.

3 , stained with hematoxylin and eosin, and/or fresh frozen.

4 Each sample was divided into four parts: (1) fresh-frozen, (2) direct-fixed in formalin for 18 h, (3)

5 (2), ITB; 1.1 +/- 0.5 mm(2), DM) compared to fresh-frozen (5.8 +/- 2.1mm(2), ITB; 3.1 +/- 1.2mm(2), D

6 46 differentially expressed genes (DEGs) vs. fresh-frozen, 98% of which were down-regulated.

7 ical specimens, including paraffin-embedded, fresh frozen and chemically stained human tissues.

8 NanoCRCA classified fresh frozen and FFPE samples into all five CRCA subtype

9 We examined multiple fresh frozen and fixed tissues from 28 brains for the pr

10 e performed a pilot study that compared both fresh frozen and formalin-fixed paraffin-embedded health

11 Fresh frozen and formalin-fixed, paraffin-embedded sampl

12 serial mouse brain and liver sections, both fresh frozen and formalin-fixed.

13 We validate our method on cell-line data, fresh frozen and paraffin-embedded tumour tissue samples

14 dant potential of irradiated (0.5 and 1 kGy) fresh, frozen and dried samples were determined by chrom

15 f hematopoietic subsets in RNA mixtures from fresh, frozen and fixed tissues, including solid tumors,

16 hod can be applied to all kinds of products; fresh, frozen and processed, including those undergoing

17 essed the amount and type of PFAS present in fresh, frozen and ready-to-eat vegetables.

18 e cross-sectional area (CSA) measurements of fresh-frozen and Crosado-embalmed collagen-rich tissues,

19 on of DNA copy number alterations from small fresh-frozen and FFPE clinical tumor specimens, although

20 lon were recovered in comparable yields from fresh-frozen and FFPE preserved tissues of rodents treat

21 Here we performed ~ 1000 x WES on fresh-frozen and formalin-fixed paraffin-embedded (FFPE)

22 nd immunohistochemistry were performed using fresh-frozen and formalin-fixed tissue samples of tumor

23 s immune populations (n = 184,126 cells) and fresh-frozen and formalin-fixed, paraffin-embedded brain

24 Results on fresh-frozen and ground whole bone of several mammalian

25 er injection, and their hearts were excised, fresh frozen, and sectioned for histology and immunohist

26 iable prostate cancer cell lines and various fresh-frozen benign and malignant tissue specimens.

27 All five anti-PSMA mAbs reacted with fresh-frozen benign prostate secretory-acinar epithelium

28 g microarray gene expression data of matched fresh frozen biopsies as a gold standard.

29 adults and pediatric participants that used fresh frozen biopsies.

30 adverse events associated with placement of fresh-frozen bone allografts (FFBAs) during alveolar rid

31 ows for the detection of two mRNA species in fresh frozen brain tissue sections.

32 Immunoblot analysis of fresh frozen brain tissues revealed that tau was present

33 ously discarded cells in a nuclei hashing of fresh-frozen brain tissue.

34 mbers of apoptotic cells as well as in other fresh frozen brains.

35 Four fresh-frozen cadaver hip joints from two male donors, ag

36 omatic genetic variations were identified in fresh frozen clinical specimens by Illumina RNA-sequenci

37 ius) mince with different thermal histories (fresh, frozen, cooked) as affected by pH, water and NaCl

38 and endothelial cells) protein expression in fresh-frozen corneal tissue suggests that Fas ligand exp

39 man donors, aged stillborn to 85 years, were fresh frozen, cryostat sectioned, and prepared for indir

40 onors (age range, 6 months to 67 years) were fresh frozen, cryostat sectioned, and prepared for indir

41 mples (25 CIS and 5 muscle controls) from 26 fresh-frozen cystectomy specimens.

42 ral heads from five embalmed donors and five fresh-frozen donors were compared using Raman microspect

43 cies of vegetables and fruits in the form of fresh, frozen, dried and processed products.

44 We compared fresh frozen tissue, fresh frozen endoscopic brushings, and the Cytosponge de

45 tion mass spectrometry imaging (DESI-MSI) of fresh-frozen excision specimens, including cancer and pa

46 olytica/E. dispar, and C. parvum in fresh or fresh-frozen fecal specimens.

47 h for employing LCM of epithelial cells from fresh frozen fetal tissue that enables quantitative anal

48 Analysis of 56 fresh frozen (FF) and FFPE matched pairs demonstrates th

49 ody validation procedure and applied it onto fresh frozen (FF) and formalin-fixed and paraffin-embedd

50 titation of PTEN concentrations in cells and fresh frozen (FF) and formalin-fixed paraffin-embedded (

51 ide samples; 25 of these had direct FFPE vs. fresh frozen (FF) replicates, 57 were sequenced in 2 dif

52 ject, comparing 578 FFPE samples with 11,014 fresh frozen (FF) samples across multiple tumour types.

53 formalin-fixed paraffin embedded (FFPE) and fresh frozen (FF) sequential patient-matched breast tumo

54 DNA isolated from DFPE and fresh frozen (FF) tissues were sequenced by NGS.

55 steps were adapted to three tissue sources: fresh frozen (FF), optimal cutting temperature (OCT) com

56 cruited in Barcelona, Spain and included 112 fresh frozen (FF, median age 69, 44% women) and 163 form

57 onsistent classification of selected matched fresh frozen/FFPE samples.

58 Moreover, fresh/frozen fish consumption, longer birth intervals, a

59 s applied to examine protein localization in fresh frozen human cornea cells.

60 detected in each major corneal cell type in fresh frozen human cornea.

61 um x 200 um x 10 um (~100 cell region) from fresh frozen human spleen tissue, respectively.

62 we assessed the expression of SEPT9 in 7287 fresh frozen human tissue samples and 292 human cell lin

63 helial, keratocyte, and endothelial cells in fresh-frozen human cornea.

64 Protein expression in fresh-frozen human corneal sections was studied with imm

65 ng spatial transcriptomics and proteomics on fresh-frozen human MS brain tissue, we identified multic

66 )H-CBD-2115 (also known as (3)H-OXD-2115) in fresh-frozen human postmortem CTE brain tissue (stages I

67 .g., Crosado ITB PEG only 306 +/- 91 MPa vs. fresh-frozen ITB PEG only 108 +/- 31 MPa; mean +/- stand

68 e.g., Crosado ITB PEG only 46 +/- 15 MPa vs. fresh-frozen ITB PEG only 21 +/- 8 MPa; p < 0.001) when

69 hin human glomeruli from a normal portion of fresh-frozen kidney cancer nephrectomy tissue revealing

70 The specimens studied included fresh-frozen lesional tissues obtained from 16 patients

71 a component of a tissue lysate derived from fresh frozen lung tumor.

72 erns obtained directly from small amounts of fresh frozen lung-tumour tissue could be used to accurat

73 mune markers were assessed in parallel using fresh-frozen lung tissue from sibling rats of the same c

74 in 8-microm tissue sections obtained from a fresh frozen lymph node tumor infiltrated by metastatic

75 s for fresh plant tissue, formalin-fixed and fresh frozen mammalian tissue, fixed cells and biofluids

76 be used to interrogate DNA from cell lines, fresh frozen material and FFPE samples to assess copy nu

77 multiple sclerosis (n = 108, 34 males) with fresh frozen material available for genetic analyses and

78 iferation signature-using gene expression in fresh frozen material.

79 hival samples and the insufficient access to fresh-frozen material are partly the cause of the delaye

80 Therefore, many imaging approaches require fresh-frozen material to get meaningful results.

81 al antibodies were retrieved by selection on fresh-frozen MCB tissue sections.

82 iant cell lines (UISO, MCC13, and MCC26) and fresh frozen MCC tumors.

83 he whole-genome sequencing (WGS) analysis of fresh-frozen metastatic biopsies from 197 mCRPC patients

84 s were derived from the IMS investigation of fresh frozen mouse liver and rabbit adrenal gland tissue

85 nable multimodal MALDI IMS of undecalcified, fresh-frozen murine femurs, allowing the distribution of

86 In this study, we analyzed 199 fresh-frozen OPSCC specimens for HPV DNA, viral load, RN

87 al contrast echocardiography and then either fresh frozen or embedded in paraffin were determined by

88 ylation of DNA extracted from microdissected fresh frozen or formalin-fixed paraffin-embedded tissue

89 Existing methods, developed based on fresh-frozen or similar-type samples, may cause suboptim

90 ng to search for somatic mosaic mutations in fresh, frozen, or fixed archival tissue from six affecte

91 nome analysis of DNA methylation profiles in fresh-frozen oropharyngeal squamous cell carcinoma (OPSC

92 es and/or p16 immunohistochemistry assays on fresh frozen paraffin-embedded tissue blocks.

93 cid compounds that have implications for the fresh-frozen pea industry.

94 med on a heterogenous set of 221 FFPE and 32 fresh frozen pediatric solid tumor and lymphoma specimen

95 platelets (0.86 U vs. 0.24 U, p = 0.001) and fresh frozen plasma (0.68 U vs. 0.24 U, p = 0.015).

96 ut also the proportion of patients requiring fresh frozen plasma (21.1% vs. 48.3%, P = 0.025).

97 , and albumin dissolvent (68.1%) compared to fresh frozen plasma (28.6%) and sterile water (20.0%) (P

98 s of platelets (10.0 versus 6.6 U, P<0.012), fresh frozen plasma (4.8 versus 3.1 U, P<0.03), and cryo

99 zard ratio = 1.55 [1.09-2.20]; p = 0.01) and fresh frozen plasma (cause-specific hazard ratio = 1.38

100 ns for use of other blood components such as fresh frozen plasma (FFP) and platelet transfusions are

101 sought to define the overall utilization of fresh frozen plasma (FFP) and platelets and the impact o

102 tments utilized in clinical practice include fresh frozen plasma (FFP) and prothrombin complex concen

103 ) and is used to justify preprocedure use of fresh frozen plasma (FFP) and/or platelets (PLT).

104 re in the critically ill, data on the use of fresh frozen plasma (FFP) are limited.

105 duct, human polyclonal antibody, obtained as fresh frozen plasma (FFP) from a HPS survivor.

106 from Iraq supporting early aggressive use of fresh frozen plasma (FFP) in a 1:1 ratio to packed red b

107 plasma volume was removed and replaced with fresh frozen plasma (FFP) or with 50% FFP and 50% albumi

108 Because the administration of fresh frozen plasma (FFP) prevents gastrointestinal blee

109 The practice of a high transfusion ratio of fresh frozen plasma (FFP) to red blood cells (RBCs) has

110 We assessed the safety and efficacy of fresh frozen plasma (FFP) versus prothrombin complex con

111 amounts of packed red blood cells (RBCs) and fresh frozen plasma (FFP) were recorded during hospital

112 raoperative aVWS received significantly more fresh frozen plasma (P = .016) and fibrinogen concentrat

113 ion of packed red blood cells (p = .442) and fresh frozen plasma (p = .063) were not different betwee

114 ess was developed to inactivate pathogens in fresh frozen plasma (PCT-FFP).

115 95% confidence interval [CI], 0.57 to 0.99), fresh frozen plasma (RR, 0.37; 95% CI, 0.21 to 0.64), an

116 8 U blood products (red blood cells [RBCs] + fresh frozen plasma [FFP] + platelets) had a median (int

117 transfused with all three blood components (fresh frozen plasma [FFP], PLTs, and cryoprecipitate) ve

118 Transfusions of platelets and fresh frozen plasma account for risk factors of ICU-acqu

119 es, we found no association between ARDS and fresh frozen plasma administration.

120 ents who received a total of 46,101 units of fresh frozen plasma and 6,251 units of apheresis platele

121 The relative risk for transfusion of fresh frozen plasma and all infections was 2.99 (2.28-3.

122 ransfusion of high plasma volume components, fresh frozen plasma and apheresis platelets, from potent

123 tive RAR parameters predicted transfusion of fresh frozen plasma and cryoprecipitate with modest to h

124 ) of 65 received blood products (15 received fresh frozen plasma and eight received red blood cell co

125 Fresh frozen plasma and immunoglobulins were administere

126 analysis to evaluate the association between fresh frozen plasma and infectious complication, control

127 gnificant dose-response relationship between fresh frozen plasma and infectious complications (p = .0

128 The association between fresh frozen plasma and infectious complications remaine

129 ine concentrations, the amount of platelets, fresh frozen plasma and packed erythrocytes used, and th

130 nd anemia were corrected with transfusion of fresh frozen plasma and packed red blood cells.

131 Fresh frozen plasma and packed red cells were the most f

132 or the continued unbridled administration of fresh frozen plasma and platelets without objective evid

133 ave shown to reduce bleeding, transfusion of fresh frozen plasma and platelets, and possibly mortalit

134 ns to platelets is the highest compared with fresh frozen plasma and red blood cells.

135 When compared to fresh frozen plasma and regular convalescent plasma, pat

136 association was found between transfusion of fresh frozen plasma and ventilator-associated pneumonia

137 C1 inhibitor concentrates and fresh frozen plasma are available for acute intervention

138 an COVID-19 convalescent plasma and standard fresh frozen plasma are not different.

139 for whom prothrombin complex concentrates or fresh frozen plasma are, to date, the only option.

140 Tranexamic acid or virally inactivated fresh frozen plasma can be used for long-term prophylaxi

141 The value of fresh frozen plasma components, both standard and steril

142 Treatment with alteplase and fresh frozen plasma during NESLiP was associated with si

143 otal of 380 non-trauma patients who received fresh frozen plasma from 2004 to 2005 were compared with

144 ncreased risk of VTE, whereas transfusion of fresh frozen plasma had no effect.

145 ciation between infection and transfusion of fresh frozen plasma in patients who did not receive conc

146 Transfusion of fresh frozen plasma is associated with an increased risk

147 cation of these patients is critical so that fresh frozen plasma may be avoided.

148 o >1.5) or clinical (transfusion >2 units of fresh frozen plasma or >1 pack of platelets in 6 hours)

149 red blood cells, platelet concentrates, and fresh frozen plasma over the routine storage time.

150 The mean packed red blood cells to fresh frozen plasma ratio changed from 2.6:1 during the

151 hemorrhagic shock; however, the exact RBC to fresh frozen plasma ratio is still unclear.

152 io-based transfusion (packed red blood cells:fresh frozen plasma ratio of 1:1 to 2:1) and were treate

153 Higher fresh frozen plasma ratios (> 1:2) were not associated w

154 Higher fresh frozen plasma ratios were associated with lower 24

155 BEST PRACTICE ADVICE 6: The large volume of fresh frozen plasma required to reach an arbitrary inter

156 ction without prior PVE demonstrated a lower fresh frozen plasma requirement (P = 0.01), a lower peak

157 ence of reactions to platelets compared with fresh frozen plasma suggests that a platelet-related fac

158 with an odds ratio of infection per unit of fresh frozen plasma transfused equal to 1.039 (1.013-1.0

159 -test allowed comparison of average units of fresh frozen plasma transfused to patients with and with

160 [0-4] versus 1.1 units [0-3]; P = 0.21), or fresh frozen plasma transfusion requirements (0 unit [0-

161 rative packed red cells (r=0.28, P=.049) and fresh frozen plasma transfusions (r=0.42, P=.004), highe

162 RBC, platelet, and fresh frozen plasma transfusions collected up to 24 hour

163 e likely to have received RBC, platelet, and fresh frozen plasma transfusions.

164 of platelet units (4.3 vs. 1.7, p =.05) and fresh frozen plasma units (1.1 vs. 0.6, p =.08) also was

165 tests) and the transfusion (blood units and fresh frozen plasma units) during the operative period w

166 id infusion volume (6.1-3.2 L) and increased fresh frozen plasma use (3.2-10.1 U) (both P < .05) in t

167 unoglobulin (4 cases), interferon (3 cases), fresh frozen plasma with WNV IgG (2 cases), and ribaviri

168 ood products (red blood cells, platelets, or fresh frozen plasma) administered during transplantation

169 platelets, 12.5 +/- 5.4 U vs. 8.6 +/- 6.4 U; fresh frozen plasma, 9.6 +/- 4.9 U vs. 4.9 +/- 3.6 U; an

170 core analysis adjusting by use of platelets, fresh frozen plasma, and cryoprecipitate; and adjusting

171 h a 68%, 56%, and 58% reduction in platelet, fresh frozen plasma, and packed erythrocyte usage, respe

172 used patients, pooled platelet concentrates, fresh frozen plasma, and packed red cells collected usin

173 ed significantly less volume of packed RBCs, fresh frozen plasma, and platelet transfusion (p < 0.001

174 ng administration of packed red blood cells, fresh frozen plasma, and platelets in ratios approximati

175 gulation factor assays were compared between fresh frozen plasma, COVID-19 convalescent plasma, and p

176 ent between COVID-19 convalescent plasma and fresh frozen plasma, except for protein C antigen.

177 The administration of coagulation factors (fresh frozen plasma, prothrombin complex concentrates or

178 ontinued, and treatment with plasmapheresis, fresh frozen plasma, steroids, and OKT3 was begun.

179 apy and treatment with lactulose, vitamin K, fresh frozen plasma, ventilatory assistance, and intensi

180 Fresh frozen plasma-to-packed RBCs and platelets-to-pack

181 The benefits of higher ratios of fresh frozen plasma-to-packed RBCs and platelets-to-pack

182 2,058 nontrauma patients who did not receive fresh frozen plasma.

183 o did receive red blood cells in addition to fresh frozen plasma.

184 ion for patients receiving and not receiving fresh frozen plasma.

185 sate, which could be quenched by addition of fresh frozen plasma.

186 between CCP, intravenous immunoglobulin, and fresh frozen plasma.

187 and avoidance of preemptive transfusions of fresh frozen plasma.

188 r bias improved survival outcome with higher fresh frozen plasma: red blood cell ratios.

189 Ratios of fresh frozen plasma:packed RBC and platelet:packed RBC.

190 high (>= 1:1) and medium (>= 1:2 and < 1:1) fresh frozen plasma:packed RBC ratio groups, respectivel

191 ts (0.1 [0.04] vs 1.9 U [4.5] p=0.0001), and fresh-frozen plasma (0.1 [0.07] vs 0.75 U [0.21] p=0.000

192 Fresh-frozen plasma (FFP) and intermediate purity factor

193 ross as a virally inactivated alternative to fresh-frozen plasma (FFP).

194 nesthetized mice were transfused with murine fresh-frozen plasma (mFFP), PCC, mixtures of human vitam

195 use of a combination of packed red cells and fresh-frozen plasma (reconstituted blood) for priming of

196 The dose of fresh-frozen plasma administered was highly variable (me

197 ulopathy unresponsive to vitamin K requiring fresh-frozen plasma after the first 24 hours postresecti

198 both platelets and coagulant products (e.g., fresh-frozen plasma and recombinant-activated factor VII

199 Transfused red cells, platelets, and fresh-frozen plasma can transmit West Nile virus.

200 use of a combination of packed red cells and fresh-frozen plasma during surgery for congenital heart

201 anticoagulation, and/or plasmapheresis with fresh-frozen plasma exchange, resolved TMA in most patie

202 The severe group required more fresh-frozen plasma intraoperatively than the mild group

203 six allografts lost, despite treatment with fresh-frozen plasma or plasmapheresis.

204 re frequent recurrences, and prescription of fresh-frozen plasma prophylaxis.

205 VE than the PVE group, as were postoperative fresh-frozen plasma requirements.

206 Fresh-frozen plasma should be given for documented defic

207 nternational normalized ratios, 33% received fresh-frozen plasma transfusions during their intensive

208 Wide variation in fresh-frozen plasma treatment exists suggesting clinical

209 Fifty-one percent of fresh-frozen plasma treatments were to nonbleeding patie

210 from 7.8% to 92.8% for RBCs, 0% to 97.5% for fresh-frozen plasma, and 0.4% to 90.4% for platelets.

211 s and infusing those with abnormalities with fresh-frozen plasma, coagulation factor concentrates, or

212 e vWf-cleaving metalloprotease is present in fresh-frozen plasma, in cryoprecipitate-depleted plasma

213 ive bleeding disorder treated by infusion of fresh-frozen plasma, plasma-derived FVII concentrates an

214 and nonleukoreduced red cells, platelets, or fresh-frozen plasma.

215 cluded sample type comparisons (whole blood, fresh/frozen plasma, and capillary finger prick) and pre

216 In brief, we use fresh-frozen rat spines and a system of carboxyl methylc

217 s of the latter molecules using MALDI-MSI in fresh-frozen rodent brain tissue samples.

218 From the fresh frozen samples (n = 237), a subset had matched mic

219 n profiling was performed in 140 samples, 47 fresh frozen samples and 93 FFPE samples, on HU133_Plus_

220 nt data sets that used similar platforms and fresh frozen samples, the average differences were 11% t

221 are currently limited by the availability of fresh frozen samples.

222 values were comparable to those observed in fresh frozen samples.

223 performed comprehensive genomic analyses on fresh-frozen samples from 348 patients affected by prima

224 imens are concordant with ChIP-seq data from fresh-frozen samples of the same tumors.

225 genome-wide expression profiling studies of fresh-frozen samples were validated in the formalin-fixe

226 in reaction (qRT-PCR) from 114 corresponding fresh-frozen samples.

227 ted by the need for non-embedded, non-fixed, fresh-frozen samples.

228 Fresh-frozen sections of corneas from an 18-year-old and

229 ied to detect Fas and Fas ligand proteins in fresh-frozen sections of normal human cornea.

230 estigated by immunohistochemical analysis of fresh frozen skin specimens using multiple lymphocytic m

231 e-transcription polymerase chain reaction in fresh-frozen skin biopsies and whole-genome sequencing.

232 is based on the low temperature embedding of fresh frozen specimens into a hydrogel matrix composed o

233 tide polymorphism microarray platform, of 60 fresh-frozen specimens that represent the main salivary

234 ue imaging using a variety of samples, using fresh frozen surgical prostate resections and formalin-f

235 trans-pedicular access to the vertebra using fresh-frozen thoraco-lumbar vertebrae from two female bo

236 We performed total RNA sequencing with fresh frozen thyroid tissues from a cohort of three cate

237 tic study, the MSPen was used to analyze 184 fresh-frozen thyroid, parathyroid, and lymph node tissue

238 Fresh frozen tissue from 232 patients (T3-4, N0, M0) wit

239 Mass spectra are acquired directly from fresh frozen tissue sections using matrix-assisted laser

240 We compared fresh frozen tissue, fresh frozen endoscopic brushings,

241 s of photoreceptors were microdissected from fresh frozen tissue, RNA was purified, and quantitative

242 ings demonstrate for the first time that, in fresh frozen tissue, that the anatomical distribution of

243 alyses have been restricted to patients with fresh-frozen tissue and limited follow-up.

244 Typically, fresh-frozen tissue preparations are considered optimal

245 Fresh-frozen tissue samples and touch imprints were anal

246 Fresh-frozen tissue samples were collected for genomic a

247 ly quenched activity-based probes (qABPs) to fresh-frozen tissue samples.

248 trometry profiles from 10-microm sections of fresh-frozen tissue samples: 25 normal lung, 29 normal b

249 We describe the preparation of a fresh-frozen tissue section for both histological imagin

250 mal setup for the analysis of cell cultures, fresh-frozen tissue sections and in vivo experiments on

251 In this method, fresh-frozen tissue sections are fixed, incubated with t

252 ass of in situ probes that can be applied to fresh-frozen tissue sections in a manner analogous to im

253 (PLC) to near-quantitatively degrade PCs in fresh-frozen tissue sections.

254 hnical differences (e.g., formalin-fixed vs. fresh-frozen tissue), the distribution of mutations and

255 Fresh-frozen tissue, microsatellite instability status,

256 hylation-Specific PCR (MSP), performed using fresh-frozen tissue, was used to determine the methylati

257 issue; (2) blood and its components; and (3) fresh/frozen tissue from breast cancer trials.

258 eveloped for blood, serum, plasma, FFPE, and fresh/frozen tissue.

259 tion from complex clinical specimens such as fresh frozen tissues or FFPE.

260 ing human lung cancer tissue microarrays and fresh frozen tissues, we found that the overexpression o

261 ed and purified from 134 tissue samples from fresh-frozen tissues (n = 87) or formalin-fixed, paraffi

262 By using microdissection of fresh-frozen tissues and recombinant isolation of RNA se

263 As high-quality fresh-frozen tissues are limited in their availability,

264 in human studies is often restricted because fresh-frozen tissues are not available.

265 Fresh-frozen tissues available from seven patients and C

266 Importantly, oxidative degradation of fresh-frozen tissues begins within the normal time scale

267 I-MSI analysis typically involves sectioning fresh-frozen tissues or, less commonly, embedding sample

268 Fresh-frozen tissues were analyzed in a laboratory.

269 Of the analyses performed on 184 fresh-frozen tissues, 131 were included based on suffici

270 roof-of-concept examples of MSI for FFPE and fresh-frozen tissues, with no post-sectioning sample pre

271 formalin-fixed, paraffin-embedded (FFPE) and fresh-frozen tissues.

272 abolite and lipid classes from both FFPE and fresh-frozen tissues.

273 tic remanence measurements of 147 samples of fresh/frozen tissues, from Alzheimer's disease (AD) and

274 dy epigenetics in clear-cell ovarian cancer, fresh frozen tumor DNA (n = 485) was assayed on Illumina

275 number and LOH profiles from paired FFPE and fresh frozen tumor samples.

276 Therefore, we examined B7-H4 expression in fresh-frozen tumor specimens from 259 renal cell carcino

277 64 primary, 41 metastatic, and 17 recurrent fresh-frozen tumors from 77 patients along with matched

278 , copy number profiling was limited to large fresh-frozen tumors where intact DNA could be readily ex

279 spar, and Cryptosporidium parvum in fresh or fresh, frozen, unfixed human fecal specimens.

280 n aqueous extracts of human fecal specimens (fresh, frozen, unfixed, or fixed in 5 or 10% formalin or

281 cedures used in pathology, we selected small fresh frozen uterine tissue samples to investigate how t

282 STmut is tested on fresh-frozen Visium data, formalin-fixed paraffin-embedd

283 was performed on genomic DNA extracted from fresh-frozen whole blood and patient-matched tumor pairs

284 zed from isolated pancreatic islets and from fresh-frozen whole pancreatic tissue using PCR and seque