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1 rase (LE), an enzyme produced by leukocytes (white blood cells).
2 evere disability and high levels of infected white blood cells.
3 ion of disseminated cells with platelets and white blood cells.
4 gnetophoresis to remove magnetically-labeled white blood cells.
5 an in adjacent unaffected adrenal tissue and white blood cells.
6 e suggested that lipids increase activity of white blood cells.
7 of illegitimate transcripts from peripheral white blood cells.
8 e3 and H3K27me3 target sites in single human white blood cells.
10 macrophages engulf large numbers of red and white blood cells, a process called hemophagocytosis.
13 e size, we observed significant reduction of white blood cell and absolute lymphocyte count up to 1 y
15 ads to substantial increases in the clinical white blood cell and granulocyte count and is a well-doc
16 rval, fibrinogen level, factor VII level and white blood cell and platelet counts in 15 755 individua
17 CSF in immunocompetent hosts with normal CSF white blood cell and protein levels (</=5 cells/mm(3) an
18 inine clearance, calcium level, below-normal white blood cell and/or platelet count, polychemotherapy
19 leukocytes, we achieve 3.8-log depletion of white blood cells and a 97% yield of rare cells with a s
20 find more than 4,000 protein-coding mRNAs in white blood cells and adipose tissue to have seasonal ex
22 ur new method in the classification of OT-II white blood cells and SW-480 epithelial cancer cells wit
24 r aim was to determine the minimal number of white blood cells and the specific abilities of mononucl
25 pathogenesis; for example, they lyse red and white blood cells and trigger inflammatory responses.
30 hod to count red blood cells, platelets, and white blood cells, as well as to determine hemoglobin in
31 eads to a progressive increase in peripheral white blood cells, associated with increasing splenomega
32 e on average a reduced number of circulating white blood cells, because of the Duffy-null (CC) genoty
33 rmone (PTH), 25(OH)D, calcium and peripheral white blood cells broad gene expression were evaluated.
34 lineages by Pitx1, Pitx2, Barhl2, and Lmx1a; white blood cells by Myb, Etv2, and Tbx6, and ovary by P
36 g dd-cfDNA to the proportion of donor DNA in white blood cells can differentiate between relapse and
37 ived from red blood cells (RBCs), platelets, white blood cells, cancer cells, and bacteria, exhibit p
40 te >90 bpm, mean arterial pressure <60 mmHg, white blood cell count >/=15 000 cells/mL, age >60 years
41 onvert to 109 per liter, multiply by 0.001); white blood cell count >/=15000/microL, 27% (95% CI, 18%
42 High-risk patients (those presenting with a white blood cell count >10 x 10(9) cells per L) could re
43 aboratory abnormality, commonly defined by a white blood cell count >100,000/microL, caused by leukem
44 oups: temperature >=39 degrees C, peripheral white blood cell count >=20 000/mm3, C-reactive protein
45 liferative chronic myelomonocytic leukaemia (white blood cell count <13 000/muL), and had anaemia wit
46 ed, CMML is stratified into myelodysplastic (white blood cell count <13 x 10(9)/L) and proliferative
48 ia (26 [29%]), anaemia (26 [29%]), decreased white blood cell count (17 [19%]), and decreased lymphoc
52 (4.9 [4.0-5.8] vs 4.5 [3.7-5.5] mg/dL), and white blood cell count (7000 [5900-8200] vs 6600 [5600-7
53 eutropenia (31 [42%] vs 28 [39%]), decreased white blood cell count (8 [11%] vs 5 [7%]), and hypophos
54 ant was associated with a 29% lower baseline white blood cell count (95% confidence interval [CI], -7
55 prior skin infection (aOR 1.14), recent high white blood cell count (aOR 1.08), and genitourinary dis
56 02), bruising (aOR, 3.17; P=.0059), abnormal white blood cell count (aOR, 0.52; P=.0100), and prior a
57 s significantly higher in patients with high white blood cell count (HR 2.45, p 0.011), raised serum
58 s: age (hazard ratio [HR], 3.299; P < .001), white blood cell count (HR, 1.910; P = .017), platelet c
59 04 [95% CI, .006-.23], P < .0001); and lower white blood cell count (OR = 0.93 [95% CI, .89-.97], P <
60 ent of Model for End-Stage Liver Disease and white blood cell count (OR, 4.68; 95% CI, 1.80-12.17; P
62 ower body mass index (BMI; P = .003), higher white blood cell count (P = .005), and higher D-dimer le
64 eal inflammation, fluid, appendicoliths, and white blood cell count (WBC) were significantly correlat
67 ose episodes, 213 had data allowing complete white blood cell count analysis and were included in the
69 the mean value of several laboratory tests (white blood cell count and hepatic and lipid panels), ye
70 ence, waist-hip ratio, alanine transaminase, white blood cell count and lower high-density lipoprotei
72 ses by urbanicity and effect modification by white blood cell count as an inflammatory marker were al
74 te respiratory, cardiac, and liver function, white blood cell count at least 3 x 10(9) cells per L, p
75 36) and OS (HR, 0.64; P = .02), with initial white blood cell count being the only factor significant
76 In this large cohort of APL patients, high white blood cell count emerged as an independent predict
77 ven percent of patients with CDI had a serum white blood cell count greater than 12 000 cells per muL
79 al bilirubin level greater than 10 mg/dL and white blood cell count greater than 20000 cells/microL.
82 cholesterol in men, and with higher BMI and white blood cell count in women (differences 0.03-0.06 s
87 roup (ECOG) performance status of 3 or less, white blood cell count less than 10 x 10(9) per L, and a
88 plete blood cell count parameter thresholds: white blood cell count less than 5000/microL, 10% (95% C
89 4 vs 0-2 and 5.20 (95% CI, 2.70-10.02) for a white blood cell count of >/=20 000/muL vs <20 000/muL.
90 esenting features (age >= 1 and < 10 years), white blood cell count of <50 x109/L, lack of extramedul
91 of 133 mg/L (normal range, 0.2-0.9 mg/L), a white blood cell count of 11.69 x10(9)/L (normal range,
93 inent blood test results showed an increased white blood cell count of 13 000/muL (13 x10(9)/L) (norm
94 inent blood test results showed an increased white blood cell count of 13,000/uL (13 x 109/L) (normal
95 ratory studies revealed leukocytosis, with a white blood cell count of 15.1 x 10(3)/uL (15.1 x 10(9)/
96 ratory studies revealed leukocytosis, with a white blood cell count of 15.1 x 103/muL (15.1 x 109/L)
97 oratory analyses were notable for a complete white blood cell count of 17000/muL (31% blast cells), a
98 vel of 206 mg/L (normal range, 0-10 mg/L), a white blood cell count of 24.5 x 10(9)/L (normal range,
100 tologic laboratory investigations revealed a white blood cell count of 6.7 x 10(9), a C-reactive prot
102 analysis of the validation cohort confirmed white blood cell count of more than 20000 cells/microL (
104 globulins vs. late immunotherapy), and a low white blood cell count on the first cerebrospinal examin
105 significant interaction between PM(2.5) and white blood cell count only in the model of lung functio
108 r both for clinical examination findings and white blood cell count parameters compared with a valid
109 uppression, defined as a decline in absolute white blood cell count to 2.5 x 109/L or less or a decli
118 elevated total protein and a mildly elevated white blood cell count with lymphocytic predominance.
119 atients with eosinophil counts (out of total white blood cell count) of 2% or greater (rate ratio 1.2
121 /m(2) on day 1) added to high-risk patients (white blood cell count, >10 x 10(9)/L), as well as low-r
122 Laboratory evaluation revealed leukocytosis (white blood cell count, 15.4 x 10(9)/L; normal range, [3
123 atase, 88.35 U/L (58.94-117.76 U/L); and for white blood cell count, 6890/microL (5700/microL-8030/mi
127 subset of patients with FLT3-ITD, only age, white blood cell count, and < 4-log reduction in PB-MRD,
129 core, red blood cell transfusion dependency, white blood cell count, and marrow blasts retained indep
130 cases had normal, the other two had elevated white blood cell count, but all of them had elevated CRP
131 lycerides, waist circumference), and immune (white blood cell count, C-reactive protein) markers.
133 is of hematological cancer requires complete white blood cell count, followed by flow cytometry with
134 th poor outcome (CSF culture positivity, CSF white blood cell count, hemoglobin, Glasgow Coma Scale,
135 performance status of two or more, increased white blood cell count, high-risk IPSS score, and higher
136 tors using tricuspid regurgitation velocity, white blood cell count, history of acute chest syndrome,
137 or 3 AKI included initial respiratory rate, white blood cell count, neutrophil/lymphocyte ratio, and
138 and >60 years and for high vs lower initial white blood cell count, no significant differences betwe
139 hypertension, C-reactive protein level, and white blood cell count, this association remained signif
140 ion, serum levels of albumin and sodium, and white blood cell count, to identify metabolites that dif
141 iles (C-reactive protein, plasma fibrinogen, white blood cell count, vitamin D, high-density lipoprot
142 ted prediction highlighted by our tool: that white blood cell count--a quantitative trait of the immu
145 ore (age, creatinine clearance, haemoglobin, white-blood-cell count, and previous spontaneous bleedin
147 >=1 day (43.9% vs 36.6%; P < .0001), and had white blood cell counts >=15 000 cells/uL (31.4% vs 21.4
148 atients with severe COVID-19 had higher peak white blood cell counts (15.8 vs 7 x 10(3) /uL, P = .019
149 ep fragmentation raises inflammatory-related white blood cell counts (neutrophils and monocytes), the
150 This C. difficile variant elicited higher white blood cell counts and caused disease in younger pa
151 A content is also influenced by platelet and white blood cell counts and estroprogestogen intake.
152 AST and ALT, and negatively correlated with white blood cell counts and fibrinogen in free-ranging d
153 emonstrated severe thrombocytopenia, reduced white blood cell counts and high fever with 93% mortalit
154 ents, from oncology to psychiatry, can lower white blood cell counts and thus access to these treatme
156 high-dose group had significantly lower mean white blood cell counts at months 5 and 6; however, prem
159 lenged mice, UFP-exposed offspring had lower white blood cell counts in bronchoalveolar lavage fluid
161 e protected against viremia, fever, elevated white blood cell counts, and CHIKF-associated cytokine c
163 nical information, complete and differential white blood cell counts, and lymphocyte subsets for 301
165 al use of G-CSF in these patients to support white blood cell counts, and suggest that direct targeti
166 telomere length increased red blood cell and white blood cell counts, decreased mean corpuscular hemo
167 etry, blood samples analyzed for hemoglobin, white blood cell counts, eosinophil counts and total ser
168 lmonary disease and had significantly higher white blood cell counts, lower lymphocyte counts, and in
173 e were no significant changes in hemoglobin, white blood cells, creatinine, or tubular extraction rat
175 to be significant independent predictors for white blood cell cystine levels in patients of all ages
176 extrarenal complications and was superior to white blood cell cystine levels in predicting the presen
177 om poor therapeutic control (on the basis of white blood cell cystine levels of <2 nmol 1/2 cystine/m
178 decreased (ten [16%] vs four [6%]; p=0.09), white blood cell decreased (15 [24%] vs seven [11%]; p=0
179 r depressed flows, endothelial inflammation, white blood cell-derived tissue factor, and ample red bl
180 Assessment of red blood cell integrity, white blood cell differential counts, and plasma biochem
181 approach yields 1) a quantitative five-part white blood cell differential, 2) quantitative red blood
184 ensity sequencing assay of cfDNA and matched white blood cell DNA covering a large genomic region (50
185 enic exposure and gene-specific differential white blood cell DNA methylation, suggesting that epigen
187 ed and fixed cells, such as red blood cells, white blood cells, DU-145 prostate cancer cells, MCF-7 b
190 reduced ubiquitination activity in vitro and white blood cells from affected individuals exhibited si
195 ed by a simultaneous increase in circulating white blood cells, granulocytes, and interleukin 17A (IL
196 major blood cells (i.e., red blood cells and white blood cells) have a size distribution of 3-5 and 6
197 atures derived from genome-wide profiling in white blood cells, identifying 26 expression probes and
198 also demonstrate that accurate estimates of white blood cell images can be recovered from extremely
199 Neutrophils are the predominant circulating white blood cell in humans, and contain an arsenal of to
200 device proved effective to retain >99.9% of white blood cells in 100 mul of WB without affecting pla
201 sing this platform, we were able to quantify white blood cells in 15 muL of blood, and visually diffe
202 ormed a genome-wide DNA methylation study of white blood cells in a population-based study (N = 717).
203 For proof of principle, enumeration of the white blood cells in human blood samples on the RDM prov
204 fection marks neutrophils (the most abundant white blood cells in humans) as vital immune defenders.
207 al fluid opening pressure of 28 mm H2O and 8 white blood cells, including 1 atypical plasma cell.
209 the model were: prothrombin activity, urea, white blood cell, interleukin-2 receptor, indirect bilir
211 nce that transcript abundance in circulating white blood cells is associated with fertility in heifer
213 ic loss of chromosome Y (LOY) in circulating white blood cells is the most common form of clonal mosa
215 mmune system through activation of a type of white blood cell known as natural killer T cell (NKT cel
216 helial cells/low-power field [lpf] and >/=25 white blood cells/lpf or a quality score [q-score] defin
219 asts could also be distinguished from benign white blood cells (notably these also lacked MDR activit
220 s (Siglecs) are expressed on the majority of white blood cells of the immune system and play critical
221 rine culture) plus pyuria (ie, any number of white blood cells on urinalysis) assessed every 2 months
222 h they showed significantly lower peripheral white blood cell (P = 0.014) and absolute lymphocyte (P
223 tification of an ESBL gene; (3) pyuria (>=10 white blood cells per high powered field in the urine);
227 reted by Staphylococcus aureus, which target white blood cells preferentially and consist of an S- an
228 tricted to individuals with normal levels of white blood cells, principally in order to minimize risk
229 regulated genes were linked to activation of white blood cells, production of cytokines, and inhibiti
230 There were concomitant increases in CSF white blood cells, protein, interferon-gamma (IFNgamma),
231 protein-coding genes expressed in peripheral white blood cells (PWBCs), and circulating micro RNAs in
232 perm from the original sample while removing white blood cells, replacing the seminal plasma, and red
234 rrelation between PPP1R11 and TLR2 levels in white blood cell samples isolated from patients with Sta
236 ues such as positron emission tomography and white blood cell scintigraphy have been shown to reduce
237 o compared with available bone scintigraphy, white blood cell scintigraphy, and (18)F-FDG PET/CT resu
238 emphasizing the importance of matched cfDNA-white blood cell sequencing for accurate variant interpr
240 Patient bone marrow-derived neutrophils and white blood cells showed a severely impaired chemotactic
242 yglucose positron emission tomography/CT and white blood cell single photon emission CT/CT in a time
243 yglucose positron emission tomography/CT and white blood cell single photon emission CT/CT scans were
245 hy/computed tomography (CT) and radiolabeled white blood cells single photon emission CT/CT in a coho
246 Autoimmune diseases mediated by a type of white blood cell-T lymphocytes-are currently treated usi
247 of 115) and decreased neutrophil (16 [14%]), white blood cell (ten [9%]), and platelet (nine [8%]) co
249 ay produce interacting epigenetic effects in white blood cells that influence immune function and hea
250 s (CACs) are an exercise-inducible subset of white blood cells that maintain vascular integrity.
251 od CD14(+) monocytes are bone marrow-derived white blood cells that sense and respond to pathogens.
252 sity of gold nanoparticles on the surface of white blood cells that were trapped in the paper mesh.
253 After filtering alterations from matched white blood cells, the presence of ctDNA predicts recurr
254 L and monocytes accounting for >/=10% of the white blood cells, this aging-associated disease combine
256 nally interrogating the lipid metabolism and white blood cell transcriptomic markers in healthy, norm
257 We studied the relationship between major white blood cell types and blood pressure in the UK Biob
259 s the processing of a semen sample to remove white blood cells, wash away seminal plasma, and reduce
263 An abnormal CSF diagnosis was defined as a white blood cell (WBC) count >20/uL, a CSF protein readi
265 e negative predictive values of a normal CSF white blood cell (WBC) count for ME panel targets were 1
267 avy marijuana use and HIV disease markers or white blood cell (WBC) count were examined using mixed-e
268 say, C-reactive protein (CRP) concentration, white blood cell (WBC) count, and absolute neutrophil ce
269 reactive protein (hsCRP), lipid profile, and white blood cell (WBC) count, at baseline and 1, 3, and
271 L) patients with >30% bone marrow blasts and white blood cell (WBC) counts </=15 x 109/L (AZA-AML-001
272 ting, though CT-toxin(+) patients had higher white blood cell (WBC) counts (12.5 x 10(3) versus 9.3 x
274 lyses of phenotypic variation in circulating white blood cell (WBC) counts from large samples of othe
275 ariability (HRV) with electrocardiogram, and white blood cell (WBC) counts with hematology analyzer.
276 r 2 induction cycles were ELN risk group and white blood cell (WBC) counts; treatment with midostauri
278 ps between periodontitis, hours of sleep and white blood cell (WBC) markers among a nationally repres
279 brary consisting of over one quarter-million white blood cell (WBC) nuclei together with CD15/CD16 pr
280 ematocrit, hemoglobin, red blood cell (RBC), white blood cell (WBC), and platelet counts with an accu
283 ous titer, the intravenous administration of white blood cells (WBC) resulted in efficient disease tr
284 r confounders, in particular distribution of white blood cells (WBC), as well as random effects.
287 of Treponema pallidum 16S RNA in CSF or CSF white blood cells (WBCs) >20/uL or a reactive CSF-Venere
291 l blood mononuclear cells (PBMCs) and of CSF white blood cells (WBCs) that were activated monocytes (
293 ed high iron intensities, whereas individual white blood cells were characterized by their high phosp
295 ndividuals reflected nucleosomal patterns of white blood cells, whereas patients with cancer had alte
296 sidual disease negativity with CLL <1/10 000 white blood cells, which persisted even after ibrutinib
297 0% with a contamination of 0.6 +/- 0.1% from white blood cells with a 23.8 +/- 1.3-fold concentration
298 +/- 2.1% with 0.2 +/- 0.04% contamination of white blood cells with a 9.6 +/- 0.4-fold concentration
300 , and produce an ultrapure buffy coat (96.6% white blood cell yield, 0.0059% red blood cell carryover