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1                                          The unfractionated and fractionated samples were analyzed by
2 utralized the anticoagulant activity of both unfractionated and low molecular weight heparins and inh
3 is the primary receptor for the clearance of unfractionated and low molecular weight heparins in the
4 bes an emerging approach for the analysis of unfractionated and low molecular weight heparins, as wel
5      Although current anticoagulants such as unfractionated and low-molecular-weight heparins and the
6 IIIa receptor blockers), and anticoagulants (unfractionated and low-molecular-weight heparins).
7 e marrow transplantation, both HLA identical unfractionated and T cell-depleted HLA haploidentical, h
8  subducted uranium was probably isotopically unfractionated before full oceanic oxidation, about 600
9                Limiting dilution analysis of unfractionated blood demonstrated a SRC frequency of 1 i
10 l surface phenotyping and transplantation of unfractionated blood, that approximately 1-5% of the tot
11 t device that isolates live tumor cells from unfractionated blood.
12 acrophages, their specific BM precursors, or unfractionated BM cells were delivered during liver inju
13 s in cord blood mononuclear cells and in the unfractionated BM of healthy and Fanconi anemia donors,
14   We demonstrate that macrophages within the unfractionated BMCs are responsible for the production o
15 l without injury; a single i.v. injection of unfractionated BMCs in healthy mice.
16  the co-infusion of limited numbers of donor unfractionated BMCs with human amnion-derived multipoten
17                                              Unfractionated BMDSC from diabetic Lepr mice were incuba
18                                              Unfractionated BMMNCs were isolated from adult mice via
19 ntation of CD34(+) cells (n = 8 patients) or unfractionated bone marrow (BM) or peripheral blood mono
20                                  Autologous, unfractionated bone marrow cells or skeletal myoblasts w
21   Despite the frequent clinical use of adult unfractionated bone marrow mononuclear cells (BMMNCs) fo
22 en expression profile as compared to plating unfractionated CD34(+)/lin(-)-enriched bone marrow monon
23                                     Although unfractionated CD4(+) T cells have not been shown to be
24                                  Transfer of unfractionated CD4(+) T cells induced severe colitis in
25                                 Injection of unfractionated, CD4 or CD8 allogeneic human peripheral b
26 c analysis of the proteotypic peptides in an unfractionated cell lysate.
27                                  Then, using unfractionated cell lysates, a homogeneous kinase assay
28 hed for long-term repopulating EpiSCs versus unfractionated cells (3.9- and 5.2-fold, respectively).
29 deed, B6/Rag(-/-) recipients of dnTGFbetaRII unfractionated cells develop features of liver disease s
30 the sera of rabbits or horses immunized with unfractionated cells isolated from pediatric human thymi
31 pproach to measuring protein levels in total unfractionated cellular proteins, and we apply this appr
32 orm of STAT3 than either ALDH(-)/CD133(-) or unfractionated colon cancer cells.
33  of these pools, along with the complete EMD unfractionated compound and positive and negative contro
34 r greater in magnitude than that launched by unfractionated conventional T, invariant natural killer
35               In addition, OKT3 treatment of unfractionated cord blood resulted in robust engraftment
36             Exosomes, although isolated from unfractionated culture media, were absent in highly infe
37                              The transfer of unfractionated DBA/2J (DBA) splenocytes into B6D2F(1) (D
38 ity (EC50 13 +/- 0.6 mug Cu/L) than were the unfractionated dissolved FAs (EC50 39 +/- 0.4 and 41 +/-
39                  Using the breakthrough with unfractionated DOM as a baseline, on average, the water
40 regimen for the Ad5 vaccine did not increase unfractionated ELISpot responses compared with the Ad5 v
41 m liver replacement after transplantation of unfractionated embryonic day (ED) 14 fetal liver stem/pr
42                                        While unfractionated Epicor was inactive, the C18 resin-bindin
43 responses in the gut using intact tissues or unfractionated epithelial cells, thereby limiting conclu
44 (nanoparticle tracking analysis) analyses of unfractionated exosomes were also conducted to evaluate
45  all of the sharp peaks that were present in unfractionated extracts, along with some broad signal.
46                             Fractionated and unfractionated FAs obtained from streamwater and suspend
47 mpare the quality of SELDI-TOF MS data using unfractionated, fractionated plasma samples and abundant
48  The three-copy construct, GST-HB3, detected unfractionated free heparin (UFH) as low as 39ng/ml (equ
49 was observed between GTPP constituents, with unfractionated GTPP more potently preconditioning cells
50 ow-molecular-weight heparin (73%, n=487) and unfractionated heparin (15%, n=97).
51 ing enoxaparin compared with those receiving unfractionated heparin (2.3% versus 1.4%; P=0.022) but s
52 oembolism for no chemical prophylaxis (33%), unfractionated heparin (29%), dalteparin (40%), or infer
53  found in death at 30 days for enoxaparin vs unfractionated heparin (3.0% vs 3.0%; odds ratio [OR], 1
54 ary intervention were randomized to low-dose unfractionated heparin (50 U/kg) or standard-dose unfrac
55 , or 0.175 [671] mg/kg/h) or to a control of unfractionated heparin (60 IU/kg intravenous bolus follo
56 ous thromboembolism), enoxaparin (n=666) and unfractionated heparin (669) were given for 10.5 days (S
57  venous thromboembolism by 43% compared with unfractionated heparin (68 [10%] vs 121 [18%]; relative
58 leeding was higher with enoxaparin than with unfractionated heparin (7 [1%] vs 0; p=0.015).
59 ing was similar with enoxaparin (69 [8%]) or unfractionated heparin (71 [8%]; p=0.83).
60 ctionated heparin (50 U/kg) or standard-dose unfractionated heparin (85 U/kg or 60 U/kg with glycopro
61 n or sterile saline containing 5000 units of unfractionated heparin (control).
62 th 184 (9.4%) of 1952 patients randomized to unfractionated heparin (hazard ratio [HR], 0.88; 95% con
63 fated hirugen (IC(50) = 1.2 +/- 0.2 microm), unfractionated heparin (IC(50) = 56.6 +/- 8.4 microg/ml)
64 gned randomly to eptifibatide + reduced dose unfractionated heparin (n = 298), eptifibatide + reduced
65 esigned to capture the desired attributes of unfractionated heparin (UFH) and low-molecular-weight he
66 py caused by antibodies to complexes between unfractionated heparin (UFH) and platelet factor 4 (PF4)
67 e most common pharmocoprevention strategies, unfractionated heparin (UFH) and the low-molecular-weigh
68 st effectiveness of enoxaparin compared with unfractionated heparin (UFH) as adjunctive therapy for f
69 ate whether enoxaparin (ENOX) is superior to unfractionated heparin (UFH) as adjunctive therapy for p
70 usted otamixaban regimens or weight-adjusted unfractionated heparin (UFH) before percutaneous coronar
71  safety and effectiveness of bivalirudin and unfractionated heparin (UFH) for carotid artery stenting
72 comparative outcomes between bivalirudin and unfractionated heparin (UFH) have not been well describe
73 icacy and safety of enoxaparin (ENOX) versus unfractionated heparin (UFH) in patients with ST-segment
74 all efficacy and safety of enoxaparin versus unfractionated heparin (UFH) in the SYNERGY (Superior Yi
75                                              Unfractionated heparin (UFH) is a widely used anticoagul
76                                   Monitoring unfractionated heparin (UFH) is crucial to prevent over-
77                                              Unfractionated heparin (UFH) is frequently administered
78                                              Unfractionated heparin (UFH) is the most widely used ant
79 rction patients that received abciximab with unfractionated heparin (UFH) or bivalirudin during percu
80 randomized to bivalirudin (n = 1,800) versus unfractionated heparin (UFH) plus a glycoprotein IIb/III
81 we characterized the interaction of PF4 with unfractionated heparin (UFH), its 16-, 8-, and 6-mer sub
82               All patients received aspirin, unfractionated heparin (UFH), or enoxaparin and early ca
83 normalized ratio (INR) affects the dosing of unfractionated heparin (UFH).
84 occurring in up to 5% of patients exposed to unfractionated heparin (UFH).
85 harmacological and practical advantages over unfractionated heparin (UFH).
86  with anti-P-selectin monoclonal antibody or unfractionated heparin (UFH).
87 lecular weight heparin (LMWH) is superior to unfractionated heparin (UH) for venous thromboembolism (
88 noxaparin 40 mg subcutaneously once daily or unfractionated heparin 5000 U subcutaneously every 12 h
89 imilar between groups (enoxaparin 11 [1%] vs unfractionated heparin 6 [1%]; p=0.23).
90 ulfated, the inhibitors did not compete with unfractionated heparin alluding to a novel site of inter
91 ctivator over 15 hours (n=30; USAT group) or unfractionated heparin alone (n=29; heparin group).
92 ependently have shown superior efficacy over unfractionated heparin alone in patients with non-ST-ele
93 b/IIIa inhibitors, and 676 patients received unfractionated heparin alone.
94 ) occurred in 12.2 percent of patients given unfractionated heparin and 10.1 percent of those given e
95 n occurred in 14.5 percent of patients given unfractionated heparin and 11.7 percent of those given e
96 red in 4.5 percent of the patients receiving unfractionated heparin and 3.0 percent of those receivin
97      A total of 6055 patients received study unfractionated heparin and a fibrin-specific lytic and h
98 /LV) ratio >/=1.0 were randomized to receive unfractionated heparin and an USAT regimen of 10 to 20 m
99 on on noncovalent complexes formed by intact unfractionated heparin and antithrombin-III, interaction
100 he pharmacologic methods, including low-dose unfractionated heparin and low molecular weight heparin.
101  with low-molecular-weight heparin (LMWH) or unfractionated heparin and mortality, pulmonary embolism
102 MWH) prepared by partial depolymerization of unfractionated heparin are used globally to treat coagul
103 n when treated with enoxaparin compared with unfractionated heparin as adjunctive therapy with fibrin
104 eight heparin (LMWH) is modestly superior to unfractionated heparin at preventing recurrent DVT and i
105 hylaxis with low-molecular-weight heparin or unfractionated heparin at standard doses.
106 ivative has less anticoagulant activity than unfractionated heparin but retains the inherent anti-inf
107 arin Conjugate (CHC), a compound of multiple unfractionated heparin chains, coats cells with a glycoc
108                    A progressive increase in unfractionated heparin concentration results in a linear
109 ncreased from 77% to 84%, whereas the use of unfractionated heparin decreased from 22% to 8.4% (p < 0
110 w-molecular-weight heparin compared with bid unfractionated heparin decreases pulmonary embolism and
111 isk, P<0.001); 7.5 percent of patients given unfractionated heparin died, as did 6.9 percent of those
112  clotting time (ACT) is widely used to guide unfractionated heparin dosing during percutaneous corona
113                     In the Fondaparinux With Unfractionated Heparin During Revascularization in Acute
114 of TAVI has been empirically determined, and unfractionated heparin during the procedure followed by
115 go transfemoral TAVR with bivalirudin versus unfractionated heparin during the procedure.
116 e antithrombotic therapy with bivalirudin or unfractionated heparin during this procedure.
117 ospitalization is superior to treatment with unfractionated heparin for 48 hours but is associated wi
118 ute VTE treated with low-molecular-weight or unfractionated heparin for 5 to 11 days, we compared dab
119                          Patients were given unfractionated heparin for anticoagulation, as they woul
120 ut the index hospitalization or weight-based unfractionated heparin for at least 48 hours.
121 nitial therapy with open-label enoxaparin or unfractionated heparin for at least 5 days.
122 ficacy and safety of enoxaparin with that of unfractionated heparin for patients with stroke.
123 no differences in the association of LMWH vs unfractionated heparin for preventing mortality, pulmona
124 ter, followed by a VKA (LMWH and VKA); or 4) unfractionated heparin for the first trimester, followed
125               Subcutaneous LMWH has replaced unfractionated heparin for the initial treatment of VTE.
126  preferred drug-based approach over standard unfractionated heparin for the prevention of venous thro
127 l efficacy and improved safety over standard unfractionated heparin for the prevention of venous thro
128 w-molecular-weight heparin, enoxaparin, with unfractionated heparin for this purpose.
129 rin, enoxaparin is a suitable alternative to unfractionated heparin for treatment of non-ST-elevation
130 ecurrent DVT and is at least as effective as unfractionated heparin for treatment of pulmonary emboli
131 schaemic stroke, enoxaparin is preferable to unfractionated heparin for venous thromboembolism prophy
132                          The hypothesis that unfractionated heparin functions to decrease inflammator
133  occurred in 12.0 percent of patients in the unfractionated heparin group and 9.9 percent of those in
134 ic end points in the REG1 group and 1 in the unfractionated heparin group, with 1 major bleed in the
135 ted heparin group, with 1 major bleed in the unfractionated heparin group.
136 , a low-molecular-weight GAG C3 derived from unfractionated heparin has been reported to protect agai
137 ecent trials comparing use of enoxaparin and unfractionated heparin in ACS have yielded less robust e
138 d controlled trials comparing enoxaparin and unfractionated heparin in non-ST-segment elevation ACS w
139 ticoagulation with bivalirudin compared with unfractionated heparin in patients undergoing peripheral
140 3 randomized trial compared bivalirudin with unfractionated heparin in patients undergoing transfemor
141 um of ACS, enoxaparin is more effective than unfractionated heparin in preventing the combined end po
142 ular-weight heparin is more efficacious than unfractionated heparin in preventing VTE (0.25% vs 0.68%
143 e improved the efficacy and safety of dosing unfractionated heparin in ST-segment elevation myocardia
144 se findings should be considered when dosing unfractionated heparin in support of fibrinolytic therap
145 MI at 30 days was observed for enoxaparin vs unfractionated heparin in the overall trial populations
146 omen was reduced by enoxaparin compared with unfractionated heparin in women (15.4% versus 18.3%; P=0
147 ents are receiving preoperatively apart from unfractionated heparin include low-molecular-weight hepa
148 ycoprotein IIb/IIIa inhibitor tirofiban with unfractionated heparin independently have shown superior
149    Fondaparinux as compared with usual care (unfractionated heparin infusion or placebo) significantl
150                                              Unfractionated heparin is isolated from animal organs, p
151 ylaxis using low-molecular-weight heparin or unfractionated heparin is more likely in ICU patients wi
152                                              Unfractionated heparin is often used as adjunctive thera
153 hylaxis with low molecular weight heparin or unfractionated heparin is recommended in acute ischaemic
154                The use of bivalirudin versus unfractionated heparin monotherapy in patients without S
155 ous coronary intervention when compared with unfractionated heparin monotherapy was associated with l
156  [0.7% to -0.7%]; P=1.00) when compared with unfractionated heparin monotherapy.
157   Despite the use of a standard weight-based unfractionated heparin nomogram in ST-segment elevation
158                       Our study reveals that unfractionated heparin not only prolongs the onset of cl
159 rcutaneous coronary intervention with either unfractionated heparin or bivalirudin monotherapy.
160                        All patients received unfractionated heparin or enoxaparin before PCI and a 12
161 mes to one of three antithrombotic regimens: unfractionated heparin or enoxaparin plus a glycoprotein
162                              Substitution of unfractionated heparin or enoxaparin with bivalirudin re
163  to receive bivalirudin (n=1928) or heparin (unfractionated heparin or enoxaparin; n=1870) plus a GPI
164 EACS) treated with eptifibatide/reduced-dose unfractionated heparin or eptifibatide/reduced-dose enox
165                                     Low-dose unfractionated heparin or low molecular weight heparin i
166                 Periprocedural bridging with unfractionated heparin or low-molecular-weight heparin a
167 ologically mediated adverse drug reaction to unfractionated heparin or, less commonly, to low-molecul
168 ere randomized to bivalirudin (n = 1,800) or unfractionated heparin plus a glycoprotein IIb/IIIa inhi
169                                Compared with unfractionated heparin plus a glycoprotein IIb/IIIa inhi
170 ty in those taking bivalirudin compared with unfractionated heparin plus a glycoprotein IIb/IIIa inhi
171 (310 of 5466 patients) randomized to receive unfractionated heparin plus eptifibatide (adjusted relat
172 duce the rate of ischemic events relative to unfractionated heparin plus eptifibatide but did increas
173  events and have a safety profile similar to unfractionated heparin plus eptifibatide.
174  in mortality with bivalirudin compared with unfractionated heparin plus glycoprotein IIb/IIIa inhibi
175 ortality and cardiac mortality compared with unfractionated heparin plus glycoprotein IIb/IIIa inhibi
176 ban (bolus and infusion, at 1 of 2 doses) or unfractionated heparin plus, at the time of percutaneous
177                                              Unfractionated heparin requirements to maintain a therap
178                                              Unfractionated heparin was administered in 33 (87%) and
179  myocardial uptake suppression protocol with unfractionated heparin was performed in all patients.
180 24 h before the examination, and 50 IU/kg of unfractionated heparin were administered intravenously 1
181  possibility to study interactions of intact unfractionated heparin with a client protein carried out
182 ctive as the current standard combination of unfractionated heparin with glycoprotein IIb/IIIa inhibi
183 -molecular-weight heparin (LMWH) or low dose unfractionated heparin with graded stockings has been va
184 were observed in the 14 trials that compared unfractionated heparin with low-molecular-weight heparin
185 both clotting and exogenous heparan sulfate (unfractionated heparin) released substantial amounts of
186 w-molecular-weight heparin (in comparison to unfractionated heparin) thromboprophylaxis lowered pulmo
187 1% of patients (23 for enoxaparin and 17 for unfractionated heparin).
188 ., aspirin, low-molecular-weight heparin, or unfractionated heparin).
189            These comprise studies with LMWH, unfractionated heparin, and vitamin K antagonists, with
190       The OSCS found in contaminated lots of unfractionated heparin, as well as a synthetically gener
191 ing a hirudin peptide (exosite 1 ligand) and unfractionated heparin, heparin octasaccharide, and gamm
192 ute ischaemic stroke that compared heparins (unfractionated heparin, heparinoids, or low-molecular-we
193                                Compared with unfractionated heparin, low-molecular-weight heparin red
194                                   Parenteral unfractionated heparin, low-molecular-weight heparin, an
195 icoagulation therapy (initial treatment with unfractionated heparin, low-molecular-weight heparin, or
196 sion stockings, pneumatic compression boots, unfractionated heparin, low-molecular-weight heparin, or
197 tic dosages of low-molecular weight heparin, unfractionated heparin, or fondaparinux at admission.
198 nt of VTE with low-molecular-weight heparin, unfractionated heparin, or fondaparinux in hospitalized
199 favorable in-hospital outcomes compared with unfractionated heparin, the current standard of care.
200  infarction were randomized to enoxaparin or unfractionated heparin, the latter dosed according to th
201                               In contrast to unfractionated heparin, this synthetic pentasaccharide t
202 not been compared with warfarin, aspirin, or unfractionated heparin.
203 eeding, and despite the use of preprocedural unfractionated heparin.
204 ndard management for pulmonary embolism with unfractionated heparin.
205 llowed by 2 groups randomized 5:1 to REG1 or unfractionated heparin.
206  who were treated with either bivalirudin or unfractionated heparin.
207  cost-saving or cost-effective compared with unfractionated heparin.
208 s with planned fibrinolysis to enoxaparin or unfractionated heparin.
209 anticipated to receive either bivalirudin or unfractionated heparin.
210 affinity with TGFbeta1 compared to low MW or unfractionated heparin.
211 gnificantly lower with bivalirudin than with unfractionated heparin.
212 uction in ischemic events with standard-dose unfractionated heparin.
213 that Robo1 binds more tightly to full-length unfractionated heparin.
214 d to determine the constituents of GAGs from unfractionated heparin/HS from various bovine and porcin
215 g were low (3.0% for enoxaparin and 2.2% for unfractionated heparin; P =.13).
216                                      Either (unfractionated) heparin or low molecular weight heparin
217 S) of active pharmaceutical ingredient (API) unfractionated heparins (UFHs) from six different manufa
218           In vitro, low-molecular weight and unfractionated heparins stimulated sFlt-1 release from p
219 s derived from Asp-N and Glu-C digestions of unfractionated histones from calf thymus and acid-extrac
220                The primary end point was the unfractionated HIV-1 gag-specific interferon gamma enzym
221 development of infections permits lifesaving unfractionated HLA-identical or T cell-depleted haploide
222 novel approach to the analysis of glycans in unfractionated human biospecimens has been developed tha
223  dendritic cell coculture system, which uses unfractionated human PBMCs as the starting material.
224                    In a previous study using unfractionated human peripheral blood mononuclear cells,
225 lly all of the misTTR hydrolytic activity of unfractionated human serum.
226                                              Unfractionated iMPC-Heps did not form tumours, most prob
227 uantitative comparison with the proteomes of unfractionated leaves, thylakoids, and stroma.
228 ls possess regulatory activity, whereas both unfractionated LP lymphocytes and purified LP CD4(+) T c
229 bust, Dectin-1-dependent IL-22 production by unfractionated lung digest cells.
230                                           In unfractionated lymphocytes, this effect was seen in all
231 liver, and blood, but was rarely detected in unfractionated lymphoid tissues.
232     We demonstrate that targeted analysis of unfractionated lysates (2 hr) accurately reproduces the
233          Two years later, brother B received unfractionated marrow from brother A after reduced-inten
234 also inhibited the farnesylation of HDJ-2 in unfractionated mononuclear cells and purified myeloma ce
235 mature myotubes, as observed previously with unfractionated MPCs containing both SP and MP cells.
236                                  Conversely, unfractionated MSCs and CD146(-) cells induce differenti
237 D146(+) perivascular cells, as compared with unfractionated MSCs and CD146(-) cells, to sustain human
238                   For a low concentration of unfractionated NOM (10 ppm), both fractions contributed
239  contribute to the stabilizing effect of the unfractionated NOM even in small proportions.
240                               In many cases, unfractionated NOM provided better stability than its se
241 weight-average molecular weight, Mw, for the unfractionated NOM was 23,300 g/mol, determined by size
242                                       In the unfractionated NOM, the relative importance of the two c
243                              By contrast, an unfractionated nuclear extract-based system in which Med
244                                     With the unfractionated OprF, we saw only rare channel formation.
245 .S. patients were randomized to: 1) heparin (unfractionated or enoxaparin) + GPI; 2) bivalirudin + GP
246  syndromes (ACS) were randomized to heparin (unfractionated or enoxaparin) plus glycoprotein IIb/IIIa
247 tively randomly assigned to receive heparin (unfractionated or enoxaparin) plus glycoprotein IIb/IIIa
248 nd high-risk ACS were randomized to heparin (unfractionated or enoxaparin) plus glycoprotein IIb/IIIa
249                      Treatment with heparin (unfractionated or low molecular weight) prevented comple
250 ect of bivalirudin monotherapy compared with unfractionated or low-molecular-weight heparin plus opti
251 ) in ambulance to bivalirudin monotherapy vs unfractionated or low-molecular-weight heparin plus opti
252 primary PCI to receive either bivalirudin or unfractionated or low-molecular-weight heparin with opti
253 tic therapy, including aspirin, clopidogrel, unfractionated or low-molecular-weight heparin, and glyc
254 erated coagulation in the presence of either unfractionated or low-molecular-weight heparins more pot
255 44+ CD4+ T cells would induce less GVHD than unfractionated or naive CD4+ T cells.
256    Surprisingly, we found that incubation of unfractionated PBMC with IL-15 for 48 h resulted in the
257 ESI-MS/MS analyses, each using 250 ng of the unfractionated peptide mixture, at 95% confidence (FDR <
258     As observed by other investigators using unfractionated peripheral blood cells from patients with
259 K cells (P = .02), overall K562 cytolysis by unfractionated peripheral blood mononuclear cells was no
260 eration sequencing of HIV-1 DNA derived from unfractionated peripheral blood mononuclear cells, ex vi
261  in activated CD4(+) T cells, monocytes, and unfractionated peripheral blood mononuclear cells.
262                Full-donor chimerism (FDC) in unfractionated peripheral blood was 42%; no patient achi
263                 The peaks detected using the unfractionated plasma samples have the highest reproduci
264 roteins, present in complex materials (e.g., unfractionated plasma); (ii) select ligands to multiple
265 tive to low mug/ml protein concentrations in unfractionated plasma.
266          To identify the DC-SIGN ligand from unfractionated PNAg, we expressed the extracellular port
267 s less than that of the unbound fraction and unfractionated product, respectively.
268                                              Unfractionated properdin contains aggregates or high-ord
269             Recently, commercially available unfractionated properdin was shown to bind to certain bi
270 observations, preincubation of bacteria with unfractionated properdin, followed by the addition of pr
271 gonorrhoeae specifically using native versus unfractionated properdin.
272   Quantitative comparisons with proteomes of unfractionated proplastids and chloroplasts facilitated
273  the purified 170-kDa ZmpB/ZmpC fraction and unfractionated S. pneumoniae culture supernatant generat
274  also directly observed in the ESI MS of the unfractionated sample of the heat-stressed AT.
275  2/3, and 19 glycoforms of IgG4) directly in unfractionated samples of human plasma and we detect tra
276                                              Unfractionated samples were randomized into sets for tra
277  new and known peptides in both enriched and unfractionated samples.
278 nerate high-throughput proteomic profiles of unfractionated serum samples using an immobilized metal
279 increase in genotoxicity was measured in the unfractionated soil extract, as well as in four polar so
280  only one-third of all SL-ICs present in the unfractionated specimen.
281 tive transfer studies, transferring Ly5.1(+) unfractionated spleen cell CD4(+) or CD8(+) T cells from
282                             The treatment of unfractionated splenic cells with ConA plus CT induced B
283                             The treatment of unfractionated splenic cells with CT, LT-IIa, or LT-IIb
284 e developed a simplified technique that used unfractionated splenocytes as a precursor population and
285                                              Unfractionated splenocytes from donor mice without prote
286                    In vitro proliferation of unfractionated splenocytes from tumor-bearing mice, as a
287  kinase 1 [JNK-1], and p38 MAPK) from either unfractionated splenocytes or purified donor CD4+ T cell
288 found that Treg expansion occurred only with unfractionated splenocytes, suggesting that accessory ce
289 lls with either purified Treg cells, or with unfractionated splenocytes.
290            Rag2(-/-) mice reconstituted with unfractionated STAT1(-/-) splenocytes (B cells and T cel
291                 Separations are made of both unfractionated SWNTs and SWNT fractions made by use of s
292 ulations, the majority of ACT trials utilize unfractionated T cell subsets.
293 erefore represent a potential alternative to unfractionated T cells for promotion of allogeneic engra
294     PIT effectively suppressed AAI driven by unfractionated Th2 cells.
295 nd IL-13 mRNA and protein when compared with unfractionated (total) CD4+ Th2 cells.
296                                   Binding of unfractionated tRNA establishes that these molecules are
297 enriched 16.8-fold in tumorigenic cells over unfractionated (UNF) cells, such that 1 in 21,000 cells
298  use of NMR spectroscopy to characterize the unfractionated venom was central to the discovery of thi
299                  Furthermore, transfusion of unfractionated wild-type blood into unconditioned, nonir
300                     NanoLC-FAIMS-MS/MS of an unfractionated yeast tryptic digest using the modified F

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