ライフサイエンスコーパス: peripheral blood

1 pGs (CpG6772370/CpG6772811) in both PDAC and peripheral blood.

2 improved cellular immunity in the lungs and peripheral blood.

3 lin-like receptors compared with NK cells in peripheral blood.

4 and are detectable at low concentrations in peripheral blood.

5 a viral load and proviral copy number in the peripheral blood.

6 n, and HIV-1 coreceptor (CCR5) expression in peripheral blood.

7 tional NK cells in the mouse spleen or human peripheral blood.

8 d chemokine levels in placental and maternal peripheral blood.

9 exhibited increased CD4(+) TEM cells in the peripheral blood.

10 esions or activated CLA(+) T-cell subsets in peripheral blood.

11 n compared to the antibody repertoire of the peripheral blood.

12 was absent in nondiseased liver tissues and peripheral blood.

13 missing heritability for gene expression in peripheral blood.

14 cific to each, as well as their abundance in peripheral blood.

15 ve more Treg cells, IL-33 and IL-10 in their peripheral blood.

16 within noninvaded lymph nodes and absent in peripheral blood.

17 ene levels were measurable up to 780 days in peripheral blood.

18 red balance of lymphoid and myeloid cells in peripheral blood.

19 ansion of tumor-associated TCR clones in the peripheral blood 3 weeks after starting treatment (n = 2

20 (5-HT) system function, as well as elevated peripheral blood 5-HT levels.

21 Peripheral blood ADAM17 activity and soluble CD163 level

22 nown to what extent macrophages derived from peripheral blood adopt the phenotype of brain-resident m

23 Alloreactive CD4 T cells were isolated from peripheral blood after CD4 donor lymphocyte infusion and

24 Our results suggest that peripheral blood analysis may provide valuable insights

25 terferon (IFN) signatures identified in both peripheral blood and affected salivary gland tissues.

26 sess the association between TTV load in the peripheral blood and AMR, 715 kidney transplant recipien

27 e gene expression studies performed in human peripheral blood and animal models of PTSD, and review t

28 predominant stem cell source (n = 839; 84%); peripheral blood and cord blood progenitors were used in

29 effector memory phenotype in comparison with peripheral blood and display increased production of IFN

30 uding cancer cells, can be isolated from the peripheral blood and have been shown to be powerful mark

31 ype bone marrow (BM)-transplanted OS mice in peripheral blood and hematopoietic organs, such as the B

32 We have utilized primary human peripheral blood and hepatic mononuclear cells, mouse MA

33 ic adults was muted T-cell activation in the peripheral blood and inflammatory response in the nasal

34 output of effector memory CD4(+) T cells in peripheral blood and lymph nodes.

35 ffectively depleted CD20(+) B lymphocytes in peripheral blood and lymphoid tissues confirming that SG

36 v X5-transduced CD4 T cells were selected in peripheral blood and lymphoid tissues upon HIV-1 infecti

37 ells that occur in HIV infection both in the peripheral blood and lymphoid tissues, especially in the

38 ILC3s were isolated from peripheral blood and palatine tonsils, expanded, and coc

39 factors was analyzed in CD4(+) T cells from peripheral blood and the jejunum in rhesus macaques, rev

40 In both peripheral blood and the jejunum, memory CD4(+) T cells

41 to determine whether ILC2 numbers change in peripheral blood and the nasal mucosa during COX-1 inhib

42 rative potential is increased in cord versus peripheral blood and to define regulatory factors contro

43 ls, and CD8alphabeta T cells in lymph nodes, peripheral blood, and bronchoalveolar lavage fluid of AG

44 cells differing by proliferation, numbers in peripheral blood, and probably by their precursors witho

45 ne treatments that cause HSPC trafficking to peripheral blood are associated with an increase in dipe

46 successful deconvolution and that RGEPs from peripheral blood are insufficient.

47 0.0218) and the proviral copy number in the peripheral blood as an indirect measure of partial viral

48 Flow cytometric analysis of peripheral blood B cells of 30 MC-negative HCV-infected

49 We show that in vitro-activated human peripheral blood B, CD4(+) T, and CD8(+) T lymphocytes a

50 Reactivity of CU patients' peripheral blood basophils (n=60) to specific anti-Fceps

51 ion of BDNF in SCZ, especially the decreased peripheral blood BDNF levels in SCZ patients validated b

52 t (TME), the presence of maternal T cells in peripheral blood before transplantation, is detectable i

53 ion at midlife and a concomitant increase in peripheral blood blast cells.

54 ncreased spleen size, and high leukocyte and peripheral-blood blast counts.

55 correlated with rapid clearance of virus in peripheral blood but remained undetectable in CSF for th

56 This evidence led us to identify a subset of peripheral blood CD14(+) CD1c(+) cells that expresses th

57 Mast cells were cultured from peripheral blood CD34(+) cells and examined for releasab

58 eveloped an ex vivo culture system to expand peripheral blood CD34(+) progenitor cells from patients

59 First, peripheral blood CD4(+) and CD8(+) T-cell activation lev

60 flammatory cytokine expression in stimulated peripheral blood CD4+ T cells and ex vivo human skin, an

61 sured cell surface ChR on HSV-specific human peripheral blood CD8 T cells and extended our studies to

62 cterized by abnormal blood cells, or reduced peripheral blood cell count.

63 also increased the inflammatory potential of peripheral blood cells after lunch.Compared with 3 meals

64 masome sensor for T. gondii in primary human peripheral blood cells and to define an upstream regulat

65 We collected peripheral blood cells from Framingham Heart Study parti

66 ayed by IFN-gamma ELISPOT for recognition in peripheral blood cells of CD patients and healthy contro

67 orresponding to C3 in freshly isolated human peripheral blood cells that was absent in corresponding

68 aberrant gene expression in brain as well as peripheral blood cells.

69 sequencing to detect the presence of CHIP in peripheral-blood cells and associated such presence with

70 The presence of CHIP in peripheral-blood cells was associated with nearly a doub

71 Xenogeneic peripheral blood chimerism was assessed after each infus

72 (ICN1) is detectable in approximately 50% of peripheral blood CLL cases lacking gene mutations.

73 ght to investigate immune gene signatures in peripheral blood collected after NAC under the setting o

74 number of CD4(+) T cell counts in patients' peripheral blood corresponds to the progression of HIV d

75 sfusion independence or complete recovery of peripheral blood counts in a proportion of patients.

76 LRP-1 expression on peripheral blood DCs was quantified by using flow cytome

77 se asthmatics is reflected in differences in peripheral blood dendritic cell subsets.

78 AIH/AISC we noted a substantial increase in peripheral blood-derived CD4(+) CD127(+) CD25(high) cell

79 mechanisms in human iPSC lines derived from peripheral blood-derived dendritic cells using a noninte

80 sing strategy might be the quantification of peripheral blood DNA levels of the highly prevalent and

81 We profiled peripheral blood DNA methylation levels of 384 CpGs in p

82 ovariates, high CXCL9 levels measured in the peripheral blood during pregnancy were associated with i

83 ompared the miRNA profiles of cord blood and peripheral blood ECFC-derived cells.

84 tic tool to quantify L. loa microfilariae in peripheral blood, enables rapid, point-of-care identific

85 osections were incubated with purified human peripheral blood eosinophils with or without activation

86 We evaluated aeroallergen sensitization, peripheral blood eosinophils, and serum periostin as pot

87 ded for 11-color flow cytometric analysis of peripheral blood for IgG4-expressing B cells and TH subs

88 sitively with living on a farm and increased peripheral blood forkhead box protein 3 expression and c

89 We obtained tumor samples and matched peripheral blood from 14 patients with HNC.

90 We compared peripheral blood from 32 moderate-to-severe AA adults wi

91 eased CXCR2 expression compared with that in peripheral blood from BC patients or healthy controls (P

92 Peripheral blood gene expression to identify subjects wi

93 tantial enrichments for distal regulation of peripheral-blood gene expression: coding regions (4.47x)

94 Mobilized peripheral blood hematopoietic cells from transgenic swi

95 Peripheral blood histone acetylation and HDAC2 gene expr

96 reduced intensity conditioning and mobilized peripheral blood HSCT in unrelated, fully MHC-matched Ma

97 Here we show that human peripheral blood IFN-gamma(+)IL-17(+) (TH1/17) and IFN-g

98 Thus, there is a need to evaluate the peripheral blood immune environment and to conduct detai

99 mosaic LOY was detected in DNA isolated from peripheral blood in 9.6% of them, and was the only recur

100 e likely role of DNA methylation measured in peripheral blood in the etiology of type 2 diabetes.

101 exhibit increased presence of MDSCs in their peripheral blood, in comparison with normal controls.

102 COR1DeltaID ameliorated abnormalities in the peripheral blood indices, and corrected the defective di

103 Peripheral blood iNKTs were quantitatively and qualitati

104 The presence and degree of peripheral blood involvement in patients with cutaneous

105 s (HSPCs) from the bone marrow (BM) into the peripheral blood is a complex process that is enhanced d

106 To compare peripheral blood leucocyte populations using flow cytome

107 and TOLLIP rs5743890) and telomere length in peripheral blood leucocytes, and assessed their associat

108 We analyzed: (1) peripheral blood leukocyte levels and immune responses;

109 lergic rhinoconjunctivitis symptoms; and (2) peripheral blood leukocyte levels/responses and gene exp

110 med genome-wide gene expression profiling in peripheral blood leukocytes of adult patients admitted t

111 Several studies report reduced peripheral blood levels of BDNF in AD, but findings are

112 ofluidic device that isolates and enumerates peripheral blood lymphoblasts using affinity separations

113 efficacy in HIV-1-infected humanized [human peripheral blood lymphocyte (Hu-PBL)] mice by completely

114 , SOCE measurements, immunologic analysis of peripheral blood lymphocyte populations by using flow cy

115 fluorescent InsB10-23:DQ8 tetramers, stained peripheral blood lymphocytes directly ex vivo, and show

116 Mutational analyses of CTCL patient peripheral blood malignant cell samples suggested the an

117 performed conditional eQTL analysis in 4,896 peripheral blood microarray gene expression samples.

118 ced both serum C-reactive protein levels and peripheral blood monocyte secretion of IL-6 and TNF-alph

119 We reported previously that a high peripheral blood monocyte turnover rate was predictive f

120 time; Mf1 and Mf2, phenotypically similar to peripheral blood monocytes (PBMos), were largely replace

121 n also regulated cell death in primary human peripheral blood monocytes (PBMs).

122 pon infection of human THP-1 macrophages and peripheral blood monocytes but does not occur during inf

123 Peripheral blood monocytes play a role in sarcoidosis in

124 of the HCV genome in either liver tissue or peripheral blood monocytes, despite constant negative re

125 ll subjects remained off ERT with normalized peripheral blood mononuclear cell (PBMC) ADA activity, i

126 ing to profile DENV-3 intrahost diversity in peripheral blood mononuclear cell (PBMC) and plasma samp

127 liferation and the secretion of cytokines in Peripheral blood mononuclear cell (PBMC) culture from CM

128 sample with whole blood concentration of the peripheral blood mononuclear cell (PBMC) fraction were e

129 n delaying time to viral rebound or reducing peripheral blood mononuclear cell (PBMC) or lymph node p

130 Suppression of parasite-specific peripheral blood mononuclear cell (PBMC) proliferation w

131 ctions, an ex vivo co-culture model of human peripheral blood mononuclear cell (PBMC) responses to Es

132 SCs deliver miR-9 to the injured pancreas or peripheral blood mononuclear cell (PBMC), which can targ

133 d D-dimer levels were associated with higher peripheral blood mononuclear cell and gut integrated HIV

134 Neutralizing antibodies were detected in a peripheral blood mononuclear cell assay, and moderate an

135 stress/depression to recurrent wheezing and peripheral blood mononuclear cell cytokine responses at

136 d an allogeneic HCT and had archived pre-HCT peripheral blood mononuclear cell samples.

137 athway-based signature derived from grouping peripheral blood mononuclear cell transcriptomes disting

138 n brain regions (BP case/control: 45/50) and peripheral blood mononuclear cells (BP case/control: 193

139 ients) or unfractionated bone marrow (BM) or peripheral blood mononuclear cells (n = 10) resulted in

140 elated with proviral HIV-DNA copy numbers in peripheral blood mononuclear cells (PBMC) (Rho = 0.4011;

141 al human MCF10A mammary epithelial and human peripheral blood mononuclear cells (PBMC) by MTT assay.

142 ntibodies in ex vivo cultures of naive human peripheral blood mononuclear cells (PBMC) exposed to P.

143 Mycobacterial growth in peripheral blood mononuclear cells (PBMC) from both huma

144 f CCR5 does not prevent ex vivo infection of peripheral blood mononuclear cells (PBMC) from SM or ver

145 ed to examine transcriptional differences in peripheral blood mononuclear cells (PBMC), and in purifi

146 city (CEC) and changes in gene expression in peripheral blood mononuclear cells (PBMC).

147 V-1 DNA longitudinally for up to 14 years in peripheral blood mononuclear cells (PBMCs) among 61 peri

148 irus (CMV)-pp65-specific T-cell responses in peripheral blood mononuclear cells (PBMCs) and breast mi

149 We used ex vivo stimulations of peripheral blood mononuclear cells (PBMCs) and monocytes

150 luding plasma HIV RNA and nested PCR on bulk peripheral blood mononuclear cells (PBMCs) and sigmoid b

151 c induction in freshly isolated B cells from peripheral blood mononuclear cells (PBMCs) and that acti

152 L-17-positive T cells were sorted from human peripheral blood mononuclear cells (PBMCs) by intracellu

153 In this study, we screened peripheral blood mononuclear cells (PBMCs) from donors v

154 Peripheral blood mononuclear cells (PBMCs) from infectio

155 SCC spheroids were co-cultured in vitro with peripheral blood mononuclear cells (PBMCs) in the presen

156 Here, we analyse ZIKV infectivity of peripheral blood mononuclear cells (PBMCs) in vitro and

157 d DNA methylation at baseline and 3 hours in peripheral blood mononuclear cells (PBMCs) using the Inf

158 Human peripheral blood mononuclear cells (PBMCs) were isolated

159 this barrier, we isolated mRNAs from feline peripheral blood mononuclear cells (PBMCs), and used ava

160 s applied for the quantitation of HIV RNA in peripheral blood mononuclear cells (PBMCs; n = 72), semi

161 and the results were further validated with peripheral blood mononuclear cells (PBMNCs) isolated fro

162 unoCloak treatment was evaluated using human peripheral blood mononuclear cells and by testing for an

163 , induced proinflammatory responses in human peripheral blood mononuclear cells and in monocolonized

164 ere mainly of a memory phenotype, present in peripheral blood mononuclear cells and intestinal tissue

165 In an analysis of peripheral blood mononuclear cells and intestinal tissue

166 Patient's and father's peripheral blood mononuclear cells and macrophages demon

167 Vdelta2(neg) gammadelta T-cell subset within peripheral blood mononuclear cells and other annexin A2-

168 showed enhanced histone (H3) acetylation in peripheral blood mononuclear cells and reduced interleuk

169 Peripheral blood mononuclear cells and sera were obtaine

170 Cryopreserved peripheral blood mononuclear cells and serum samples col

171 al and noncanonical pathways was examined in peripheral blood mononuclear cells and transfected HEK29

172 ytometry in a mimetic cell mixture and human peripheral blood mononuclear cells as model systems.

173 microarray gene expression data derived from peripheral blood mononuclear cells as well as 16S riboso

174 -induced cytokine responses) from stimulated peripheral blood mononuclear cells at age 3 years.

175 ug, exerts anti-HIV-1 activity in TZM-bl and peripheral blood mononuclear cells at low nanomolar conc

176 n and activity of ADAM-10 and ADAM-17 in old peripheral blood mononuclear cells compared with those o

177 of telomeres was measured longitudinally in peripheral blood mononuclear cells during human aging, i

178 OLM-4, THP-1 or primary AML cells with donor peripheral blood mononuclear cells elicited a cell conta

179 DNA double-strand breaks were determined in peripheral blood mononuclear cells from 13 pSS patients,

180 observed in 7% and 56% of tax sequences from peripheral blood mononuclear cells from animals 12141 an

181 criptome microarray data were generated from peripheral blood mononuclear cells from Chinese children

182 Peripheral blood mononuclear cells from chronic lymphocy

183 ized to the responses previously observed in peripheral blood mononuclear cells from donors from regi

184 immunogenicity in A2-transgenic mice and on peripheral blood mononuclear cells from ESO-vaccinated m

185 Peripheral blood mononuclear cells from healthy controls

186 inhibited IFN-gamma and IL-17A production in peripheral blood mononuclear cells from HIV-infected ART

187 Peripheral blood mononuclear cells from HIV-infected wom

188 sy samples and Leishmania antigen-stimulated peripheral blood mononuclear cells from patients infecte

189 Peripheral blood mononuclear cells from SLA identical wi

190 Conversely, addition of sialidases to human peripheral blood mononuclear cells induces accumulation

191 Peripheral blood mononuclear cells isolated from CHIKV-i

192 ve TLR7 agonist, GS-9620, activated HIV from peripheral blood mononuclear cells isolated from HIV-inf

193 than intra-arterial infusion, and mobilized peripheral blood mononuclear cells may outperform bone m

194 al activity of RXRalpha is down-modulated in peripheral blood mononuclear cells of patients with lung

195 activated B cells and A20 were diminished in peripheral blood mononuclear cells of sepsis patients, w

196 , combined delivery of ICOVIR-15K-cBiTE with peripheral blood mononuclear cells or T cells enhanced t

197 Peripheral blood mononuclear cells or whole blood were c

198 By contrast, the patient's peripheral blood mononuclear cells responded normally to

199 Peripheral blood mononuclear cells samples were stained

200 We profiled 68k peripheral blood mononuclear cells to demonstrate the sy

201 In vitro secretion of these miRNAs by peripheral blood mononuclear cells was also significantl

202 Plasma and peripheral blood mononuclear cells were collected at mul

203 Human primary TEC and peripheral blood mononuclear cells were infected with BK

204 To analyze the level of DNA DSBs, peripheral blood mononuclear cells were isolated from bl

205 Peripheral blood mononuclear cells were obtained at week

206 DNA genotyping and mRNA expression levels in peripheral blood mononuclear cells were quantified via m

207 We observed that pretreatment of human peripheral blood mononuclear cells with HMBA led to a ma

208 wide range of cancers, does not bind normal peripheral blood mononuclear cells, and can activate imm

209 s by reprogramming microglia-like cells from peripheral blood mononuclear cells, and combining them w

210 o against Daudi cells with cynomolgus monkey peripheral blood mononuclear cells, and had minimal comp

211 Human IgG, eluted from human and pig peripheral blood mononuclear cells, interacted across sp

212 mmadelta T-cell clones could be derived from peripheral blood mononuclear cells.

213 n human cell lines, primary macrophages, and peripheral blood mononuclear cells.

214 ce the activation of in vitro-cultured human peripheral blood mononuclear cells.

215 and acutely HIV-1 infected T cells by human peripheral blood mononuclear cells.

216 ses were studied in 42 vaccinees using fresh peripheral blood mononuclear cells.

217 ntiation of CD4+ T cells isolated from human peripheral blood mononuclear cells.

218 vo than either GG or AG (p < 0.001) in total peripheral blood mononuclear cells.

219 phatase-1 were determined in neutrophils and peripheral blood mononuclear cells.

220 cyte-derived dendritic cells [moDCs], PBMCs [peripheral blood mononuclear cells] and epithelial and i

221 Knockdown of LY6E in human peripheral blood mononuclear, SupT1, and THP-1 cells dim

222 o did not achieve a 4-log reduction in NPM1m peripheral blood-MRD (PB-MRD) had a higher cumulative in

223 The pattern of involvement of peripheral blood myeloid cells was indistinguishable bet

224 Human peripheral blood myeloid DC subsets from patients with e

225 of the developing brain and that a subset of peripheral blood myeloid mononuclear cells represent a k

226 For many years, human peripheral blood natural killer (NK) cells have been div

227 taxonomic units, as well as with lavage and peripheral blood neutrophilia.

228 cient to induce OSM production (P < .001) in peripheral blood neutrophils in vitro.

229 eta-analysis to quantitatively summarize the peripheral blood NGF data in SCZ patients compared with

230 ts with SCZ are accompanied by the decreased peripheral blood NGF levels, strengthening the clinical

231 Peripheral blood NK cells from individuals with GATA2 mu

232 Peripheral blood NK cells from patients with STAT1 GOF m

233 ge Melan-A-specific T-cell repertoire in the peripheral blood of 9 melanoma patients before and after

234 ted in children, detection of BRAF(V600E) in peripheral blood of adults was a marker of active multis

235 accumulation of T-bet(+)CD21(low) B cells in peripheral blood of affected patients.

236 in tonsil tissue of allergic patients and in peripheral blood of allergic asthmatic patients.

237 lating tumour cells (CTCs) selected from the peripheral blood of cancer patients.

238 lpha, whereas IL-10 levels were increased in peripheral blood of clinical responders after 12 wk of t

239 vIL-10 was detected in peripheral blood of healthy blood donors.

240 ation in left-ventricular biopsies and whole peripheral blood of living probands.

241 Basophils were isolated from the peripheral blood of patient.

242 ysis of osteoclast progenitors isolated from peripheral blood of patients revealed that stimulation w

243 fic TR1 cells can be generated in vitro from peripheral blood of patients with PA at baseline or duri

244 /TH17CM) cells were selectively increased in peripheral blood of patients with relapsing-remitting MS

245 A9, MMP8, and ARG1, were up-regulated in the peripheral blood of patients with sepsis.

246 ur study was to ascertain if HCMV DNA in the peripheral blood of pregnant women with primary HCMV inf

247 s were restored in the spleen of C57BL/6 and peripheral blood of SJL/J mice along with a decreased TH

248 icance of islet Ag-reactive T cells found in peripheral blood of type 1 diabetes (T1D) subjects is un

249 e analyzed CD4(+) helper T-cell subsets from peripheral blood or cerebrospinal fluid for cytokine pro

250 No differences in either peripheral blood or local lymphocyte populations were fo

251 n in this study, individuals must have had a peripheral blood or mononuclear cell sample collected be

252 e accessibility of tumor cells obtained from peripheral blood or through bone marrow aspirates, toget

253 found to influence ADCY2 gene expression in peripheral blood (P = 4.50 x 10(-4)).

254 inal studies by immunophenotyping cells from peripheral blood (particularly T lymphocytes) derived fr

255 was investigated in Treg cells isolated from peripheral blood (PB) and from pancreatic draining lymph

256 After RA SF and peripheral blood (PB) CD14+ monocytes were treated with

257 MRD was measured in peripheral blood (PB) from treatment-naive patients in t

258 opoietic stem cell (HSC) mobilization to the peripheral blood (PB).

259 lower in other human TILs and in many human peripheral blood populations.

260 rculating tumor cells (CTCs) in preoperative peripheral blood (PPB) and intraoperative pulmonary veno

261 factor expression in this subset relative to peripheral blood prior to infection.

262 little cytotoxicity against normal mobilized peripheral blood progenitor cells.

263 taining of reticulocytes enriched from adult peripheral blood reveals 4 distinct reticulocyte populat

264 d the relationship between RUNX1 and PCTP in peripheral blood RNA and PCTP and death or myocardial in

265 For each patient, a peripheral blood sample was collected at baseline for th

266 n levels of candidate genes were measured in peripheral blood sampled from ischemic stroke patients a

267 Assessing peripheral blood samples at steady-state and during the

268 RNA-seq analysis of peripheral blood samples collected just prior to experim

269 Peripheral blood samples from patients with ALF had a hi

270 acute peanut allergic reactions using serial peripheral blood samples obtained from 19 children befor

271 ases, we detected clonal haemopoiesis in the peripheral blood samples of ten (71%) patients.

272 e sequencing of 32 genes on the pretreatment peripheral blood samples to detect clonal haemopoiesis.

273 Thymic function was quantified in peripheral blood samples using the sj/beta-TREC ratio.

274 Peripheral blood samples were obtained for HIV antibody

275 mor-free liver tissues (control tissues) and peripheral blood samples.

276 -associated signature transcript profiles in peripheral blood samples.

277 A peripheral blood smear revealed anemia, thrombocytopenia

278 nulocyte colony-stimulating factor-mobilized peripheral blood stem cell donor grafts and successful t

279 ers of erythroblasts are recorded in patient peripheral blood, suggesting that interferon might have

280 ion, we show that mast cell progenitors from peripheral blood survive, mature, and proliferate withou

281 CAR T cells are generated from the patient's peripheral blood T cells and expand in the recipient to

282 ht a potential for IL6 signaling response in peripheral blood T cells at diagnosis as a predictive bi

283 onal Kv1.3 channels in TILs as compared with peripheral blood T cells from paired patients, which was

284 y results in uniform CAR expression in human peripheral blood T cells, but also enhances T-cell poten

285 air transmigration of freshly isolated human peripheral blood T lymphocytes, but not neutrophils or B

286 g clinical symptoms and biospecimens such as peripheral blood to be collected.

287 methylation (DNAm) data from cord blood and peripheral blood to identify SNPs associated with DNA me

288 tion state of eosinophils and neutrophils in peripheral blood to phenotype and monitor asthma.

289 promoted the recruitment of Treg cells from peripheral blood to the tumor site in vitro and in vivo.

290 Interestingly, most ( approximately 60%) peripheral blood Treg cells express CCR6, and CCR6(+) Tr

291 encing on 5,063 single T cells isolated from peripheral blood, tumor, and adjacent normal tissues fro

292 CTL019 levels in peripheral blood typically peaked at 10 to 14 days posti

293 0 bioactive mediators and pathway markers in peripheral blood using established criteria for arachido

294 Patients with higher peripheral blood viral loads in primary infection and gr

295 Peripheral blood was collected before and after challeng

296 Peripheral blood was collected from 70 virally suppresse

297 iomarker to track a self-reactive H chain in peripheral blood, we found evidence of similarly enhance

298 s, basophils, lymphocytes, and monocytes) in peripheral blood were measured by using Coulter Counter

299 tablish endothelial cell cultures from human peripheral blood, with an ultimate goal of examining int

300 ed CCR2-expressing Ly6C(hi) monocytes in the peripheral blood, without affecting overall number of ki