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1                                              SPC activity in ONH lysate was significantly higher than
2                                              SPC films plasticized with 40-50% glycerol showed a time
3                                              SPC flow prior to Fontan measured 1.5+/-0.9 L/min/m(2),
4                                              SPC number and intracellular content of hypoxia-inducibl
5                                              SPC recruitment and protein changes were inhibited by si
6                                              SPC was extracted from soybean flour, produced during th
7                                              SPC-Cre(+) Vcan(-/-) mice demonstrated enhanced recruitm
8                                              SPC-IAP's high brightness (L* = 79.55), low redness (a*
9                                              SPC-Tert cKO mice did not develop pulmonary fibrosis spo
10                                              SPCs exhibit testicular repopulating activity in vivo an
11                                              SPCs performed only 18% of these operations (15,002).
12                                              SPCs were diagnosed in 16.8% of penile cancer patients a
13 tisfaction with SPC availability (P < .001), SPC acceptance of patients receiving chemotherapy (P < .
14 hosphoprotein 65 antigen SPCs were both >100 SPCs per 250 000 cells (cutoff 2), and a low CMV-CMI whe
15 ediatric appendectomies were performed in 21 SPCs and 183 DGHs in England.
16 any and 7,560 in Sweden, overall 752 and 349 SPCs were recorded, respectively.
17 sexD3 was recruited for biosynthesis of 3UFA SPCs in M. sexta lineage via gene duplication and neofun
18 (mean age, 60.4 years; 48.8% women), 156 442 SPC cases and 88 818 SPC deaths occurred during 11 197 8
19 ; 48.8% women), 156 442 SPC cases and 88 818 SPC deaths occurred during 11 197 890 person-years of fo
20 8.6 x 10,000 PY), and 22 of them developed a SPC (annual incidence: 3.9 x 10,000 PY).
21                    The annual incidence of a SPC in the transplanted patients who developed a first c
22 ype and presence of a fenestration, absolute SPC flow was significantly associated with hospital dura
23                                 In addition, SPC treatment, but not genistin treatment, significantly
24 or gene Trp53(F/F) mice infected with Adeno5-SPC-Cre and Adeno5-CC10-Cre viruses displayed difference
25 ounting for 31% to 33% of mortality from all SPCs.
26 to both small airway (CCSP(+)) and alveolar (SPC(+)) epithelial cells in three-dimensional (3D) organ
27 sing a bleomycin model of lung injury and an SPC-driven inducible cre to fate-map AECs, we found the
28 greater risk of developing and dying from an SPC, compared with the general population.
29 han that of retinal lysate; however, when an SPC inhibitor was added, activity in ONH decreased more
30              Risk for these genital and anal SPCs are high and a follow-up plan should be agreed at d
31 with SPC service availability (P < .001) and SPC service acceptance of patients on chemotherapy (P <
32                Combined absence of PAK-1 and SPC-1 induced complete axis retraction, owing to defecti
33 of ClayFF, constant-valence force field, and SPC water model.
34               Mice treated with genistin and SPC had reduced final tumor weights by 56% (P < 0.05) an
35 -transformed duration of hospitalization and SPC flow as a proportion of total aortic (rho=0.31, P=0.
36 Da secretory protein (CC10+) airway-like and SPC+ saccular structures within 6 days.
37 athology results (rho = 0.87; P < .001), and SPCs correlated with histopathology results (rho = 0.88;
38 s to observe and characterize Dirac WGMs and SPCs, and speculate that these features can potentially
39  when the IE-1 and phosphoprotein 65 antigen SPCs were both >100 SPCs per 250 000 cells (cutoff 2), a
40 isks were calculated bidirectionally for any SPC after skin cancer and for skin cancer as SPC.
41 mong men, the overall risk of developing any SPCs was statistically significantly higher for 18 of th
42 ng women, the overall risk of developing any SPCs was statistically significantly higher for 21 of th
43 the 30 FPC types, and risk of dying from any SPCs was statistically significantly higher for 27 of 30
44 the 31 FPC types, and risk of dying from any SPCs was statistically significantly higher for 28 of 31
45 SPC after skin cancer and for skin cancer as SPC.
46 rranted to apply soy phytochemicals, such as SPC, as a potent prevention regimen for bladder cancer p
47 thetic templates, an approach we refer to as SPC-sequencing.
48 genital cancers might run in families and as SPCs are associated with human papilloma virus and smoki
49 were for invasive and in situ skin cancer as SPCs (14.59 and 16.71, respectively).
50 participate in an anonymous survey assessing SPC referral practices.
51 function may contribute to SPCs by assessing SPCs associated with known immune responsive skin cancer
52 ractor muscles and in the spicule-associated SPC and PCB cholinergic neurons.
53 r, only a few smoking- or obesity-associated SPCs, such as lung, urinary bladder, oral cavity/pharynx
54 ency included comprehensiveness of available SPC services (P = .004), satisfaction with SPC availabil
55 ck from mTORC1 to the GDNF receptor balances SPC growth with self-renewal.
56 plications in gas separation/storage because SPCs do not inherently suffer from the recyclability pro
57 e sought to evaluate the association between SPC flow and acute post-Fontan clinical outcomes using a
58                                           BM SPC recruitment is a repair response to dimethylnitrosam
59 uitment of SPCs was analyzed by examining BM SPC proliferation, mobilization to the circulation, engr
60 soidal endothelial cell progenitor cells (BM SPCs) repopulate the sinusoid as liver sinusoidal endoth
61 ays, 40% of all LSECs came from engrafted BM SPCs.
62                After partial hepatectomy, BM SPCs provide hepatocyte growth factor, promote hepatocyt
63 t, bone marrow progenitor cells of LSECs (BM SPCs), which are rich in HGF, are recruited to the liver
64 th factor (VEGF) regulates recruitment of BM SPCs and their effects on liver injury.
65 ethylnitrosamine-induced proliferation of BM SPCs and their mobilization to the circulation, reduced
66     Hepatic VEGF regulates recruitment of BM SPCs to liver and reduces this form of liver injury.
67 s in the bone marrow, and mobilization of BM SPCs to the circulation increased 2- to 4-fold by 24 hou
68                          Proliferation of BM SPCs, the number of SPCs in the bone marrow, and mobiliz
69 er regeneration from the perspective that BM SPCs that have been recruited to the liver, rather than
70 mong week-to-week assessments of blood-borne SPC HIF factors.
71  demonstrated that the number of blood-borne SPCs and the cellular content of HIFs at study entry and
72                        We conclude that both SPC-expressing alveolar type 2 cells and CC10-expressing
73 , migration, and tube formation through both SPC-dependent and -independent pathways.
74                            Furthermore, both SPCs and MASCs express GPR125, an orphan adhesion-type G
75 s and in them 45.9% of deaths were caused by SPC (other than penile cancer).
76 ce reduces processing time for genotyping by SPC-SBE and allows direct spotting of sample for rapid a
77  Oxidative stress from lactate metabolism by SPCs accelerated further SPC recruitment and differentia
78 -RasG12D expression in Surfactant Protein C (SPC)(+) alveolar type 2 cells and in Clara cell antigen
79 atic cancer, and sporadic pancreatic cancer (SPC) kindreds as families without such an affected pair.
80 ed the incidence of a second primary cancer (SPC) in 7,636 patients who underwent a kidney, liver, lu
81 a on the risk of subsequent primary cancers (SPCs) among survivors of adult-onset cancers are limited
82                      Second primary cancers (SPCs) are becoming a common cancer entity, which may int
83 ginal cancers and in second primary cancers (SPCs) following these cancers are limited.
84 ribution and risk of second primary cancers (SPCs) in multiple myeloma (MM) survivors in Germany and
85 uencing method using solid-phase capturable (SPC) dideoxynucleotides and MALDI-TOF mass spectrometry
86                                      CD34(+) SPCs from lactate-supplemented Matrigel exhibited signif
87          There were over one million CD34(+) SPCs per Matrigel plug 18 h after Matrigel implantation,
88 ab-on-a-screen-printed electrochemical cell (SPC) based on iron-sparked graphite working electrode mo
89       Using spermatogonial progenitor cells (SPCs) as a model system, we show that mTORC1 impairs ste
90 ative adult spermatogonial progenitor cells (SPCs) can be efficiently obtained by cultivation on mito
91 iation of circulating stem/progenitor cells (SPCs) in subcutaneous Matrigel in mice was assessed.
92 sized that studies of stem/progenitor cells (SPCs) in the early weeks of standard wound management co
93  We observed that CML stem/progenitor cells (SPCs) produce tumor necrosis factor-alpha (TNF-alpha) in
94 rvival signals to CML stem/progenitor cells (SPCs) with contradictory results.
95 f postnatal spermatogonial progenitor cells (SPCs).
96  models [i.e., extended simple point charge (SPC/E) vs. four-site transferrable intermolecular potent
97 ding yeast, the spindle position checkpoint (SPC) delays mitotic exit until the mitotic spindle moves
98             The spindle position checkpoint (SPC) ensures correct mitotic spindle position before all
99 ay known as the spindle position checkpoint (SPC) to ensure the arrival of one end of the mitotic spi
100 ircuit components, including the cholinergic SPC and PCB and the glutamatergic PCA sensory-motor neur
101 d on the concept of split proximity circuit (SPC) to achieve both high sequence selectivity and assay
102                    The tunable binary citrem/SPC nanoplatform holds promise for future development of
103 hway as a relevant therapeutic target in CML SPCs and endorse the current use of nilotinib in combina
104      Furthermore, we demonstrate that in CML SPCs, inhibition of autocrine TNF-alpha signaling via a
105  highlight a novel survival mechanism of CML SPCs and suggest a new putative therapeutic target for t
106 a and found that it supports survival of CML SPCs by promoting nuclear factor kappaB/p65 pathway acti
107 s correlated with increased apoptosis of CML SPCs in vitro and a reduction in primitive quiescent CML
108 1A1+ airway cell population that coexpresses SPC, a marker for type II alveolar cells that promotes a
109 f systemic-to-pulmonary arterial collateral (SPC) vessels in single ventricle patients are poorly und
110               Systemic-pulmonary collateral (SPC) flow occurs commonly in single ventricle patients a
111 bjected to a supervised principal component (SPC) analysis to predict progression-free survival (PFS)
112 RCC-specific supervised principal component (SPC) risk score prognostic gene signature was constructe
113 y the molecular basis of novel SP component (SPC) acquisition, we used the tobacco hornworm (Manduca
114 with individual sparse principal components (SPCs) are also reported, showing that both high- and low
115                Availability of comprehensive SPC, especially for patients receiving chemotherapy, and
116 oflavone-rich soy phytochemical concentrate (SPC) on the growth and metastasis of 253J B-V tumors in
117 coacervation of soybean protein concentrate (SPC) by using calcium salts and spray-drying.
118 l properties of soybean protein concentrate (SPC) films, plasticized with varying levels of glycerol
119 sing that the isolated protein concentrates (SPC-IAP) show high protein content (69.08% d.b) as well
120  (ML) for monitoring soluble pectin content (SPC) changes in orange juice.
121 d inhibited spontaneous phasic contractions (SPCs) of colonic muscle through activation of a SK condu
122 proach based on statistical process control (SPC), which is able to monitor the response to a treatme
123 luated by using statistical process control (SPC).
124  by a subtilisin-like proprotein convertase (SPC).
125      Subtilisin-like proprotein convertases (SPCs) are a family of calcium-dependent cleavage enzymes
126 y of subtilisin-like proprotein convertases (SPCs).
127 d by subtilisin-like proprotein convertases (SPCs).
128 y of subtilisin-like proprotein convertases (SPCs).
129 opsy samples using stereologic point counts (SPCs).
130 rmediate-early 1 (IE-1) antigen spot counts (SPCs) were >100 (cutoff 1) or when the IE-1 and phosphop
131                        Soft porous crystals (SPCs) that exhibit stimuli-responsive dynamic sorption b
132 e an emerging class of soft porous crystals (SPCs) with potential for high working capacity for gas s
133 ), also referred to as soft porous crystals (SPCs), show reversible structural transitions dependent
134                      The sneak path current (SPC) problem is one of the main difficulties in crossbar
135 enceforth the term superpersistent currents (SPCs).
136 p-angle cycled (SFC), rf pulse phase cycled (SPC), and pulsed field gradient (PFG) strength cycled (S
137 thesized that embolization acutely decreases SPC flow and increases systemic blood flow (Q(S)).
138                           In differentiating SPCs, Sall4 levels transiently increase and Sall4 physic
139  substrate-based assay was used to elucidate SPC enzyme activity within human retina and optic nerve
140 cle embolization of angiographically evident SPC vessels.
141 1b+ cells give rise to adenomas that express SPC and TTF1.
142 e show that surfactant protein C-expressing (SPC-expressing) alveolar epithelial type II cells (AECII
143 d solid phase capture-single base extension (SPC-SBE) method.
144 vitro assays indicated that MMP8 facilitated SPC migration across endothelial cells and through Matri
145 arrows of ApoE(-/-)/MMP8(-/-) mice had fewer SPCs in atheromas and smaller lesions than ApoE(-/-)/MMP
146                   In addition, a fluorogenic SPC substrate-based assay was used to elucidate SPC enzy
147 zed with GLY had the highest EE (74.54%) for SPC-GLY-0.25%HC (P < 0.05).
148  groups were different at 95% confidence for SPC average values.
149 sponse to GDNF, a growth factor critical for SPC self-renewal, via negative feedback at the level of
150 g Plzf, a transcription factor essential for SPC maintenance, have enhanced mTORC1 activity.
151               Similar associations exist for SPC flow as a percentage of total aortic (OR=1.09, P=0.0
152 ointestinal track model system was found for SPC-CHO-0.5%HC.
153 an intrachain disulfide bond is required for SPC-mediated cleavage and that SPC-mediated cleavage is
154 cer in family members; additionally risk for SPCs was calculated.
155        The biological effects resulting from SPC/GPR4 interactions involve the activation of both pho
156  of such cells with culture supernatant from SPCs without MMP8 knockdown, and this compensatory effec
157 ctate metabolism by SPCs accelerated further SPC recruitment and differentiation through Trx1-mediate
158                Long-term cultures of GPR125+ SPCs (GSPCs) also converted into GPR125+ MASC colonies.
159                         All patients who had SPC flow quantified by CMR imaging before Fontan were re
160                 An important question is how SPC activity is coordinated with mother-daughter polarit
161                       These results identify SPC and its receptor, GPR4, as critical regulators of th
162 , showing that both high- and low-importance SPCs were associated with cell death pathways, though th
163 ion, demonstrating a significant decrease in SPC flow and Q(P):Q(S) and increase in Q(SVC) and Q(S).
164 lization, we found a significant decrease in SPC flow of 0.9 (range, 0.6-1.3) L/(min.m(2)) (P=0.03);
165 t encapsulation efficiency (EE) was found in SPC-CHO-0.5%HC (P < 0.05) (85.42%), while liposome stabi
166 he spontaneous lung inflammation observed in SPC-TSLP mice reflects a TSLP-driven predisposition towa
167  metalloproteinase-8 (MMP8) played a role in SPC migration and their recruitment into atheromas.
168              MMP8 plays an important role in SPC migration and their recruitment into atherosclerotic
169   Postoperative length of stay was double in SPCs compared with DGHs (median, 4 vs 2 days).
170 ve appendectomy rates than those operated in SPCs.
171 ons, and 11% more readmissions than those in SPCs.
172                                   Increasing SPC flow before Fontan, as measured by CMR imaging, is a
173  by crossing floxed Tert mice with inducible SPC-driven Cre mice.
174 own-regulation of GPR4 specifically inhibits SPC-, but not sphingosine-1-phosphate-, or vascular endo
175  forms a noncovalent latent complex with its SPC-cleaved prodomain and that this latent complex is ac
176  (AECII)-specific TERT conditional knockout (SPC-Tert cKO) mice by crossing floxed Tert mice with ind
177                          Primary GPR125-LacZ SPC lines retained GPR125 expression, underwent clonal e
178 on of mouse oocytes with the GPR3/12 ligands SPC and S1P delayed spontaneous oocyte maturation.
179 mbedded human posterior sections to localize SPC family members.
180 More detailed analysis of Adora2b(loxP/loxP) SPC Cre(+) mice confirmed elevated lung inflammation and
181 disease susceptibility in Adora2b(loxP/loxP) SPC Cre(+) mice.
182 lveolar epithelial cells (Adora2b(loxP/loxP) SPC Cre(+)) revealed a selective increase in disease sus
183                        After lyophilization, SPC-CHO-0.5%HC had higher EE than SPC-GLY-0.25%HC (P < 0
184                                  Lyophilized SPC-CHO-0.5%HC exhibited higher stability than lyophiliz
185  exhibited higher stability than lyophilized SPC-GLY-0.25%HC during storage at 25 degrees C for 28 da
186 epithelial cell-specific Cre transgenic mice SPC-rtTA/TetO-Cre and floxed-Alk3 mice.
187 epithelial-specific versican-deficient mice [SPC-Cre(+) Vcan(-/-)] demonstrated that RSV infection le
188                                         More SPCs entered the bloodstream in the first 2 weeks of car
189 type MMTV mice and a triple transgenic mouse SPC-rtTA(+/-)TetoCre(+/-)LoxP-VEGF-A(+/+) to conditional
190           A degree of toxicity toward normal SPCs was observed with the combination treatment, althou
191  of a Sca1 promoter yielded CC10(+), but not SPC(+), hyperplasias, and adenomas.
192 njugation of low-molecular-mass O-SP-core (O-SPC) fragments.
193 ced in young outbred mice by the S. sonnei O-SPC conjugates were significantly higher then those elic
194                                        The O-SPC conjugates used oxime linkages between the terminal
195                                        The O-SPC fragments were bound by their reducing ends similar
196 ECT 475) in order to evaluate the ability of SPC to encapsulate and protect bacteria from stress cond
197 ction of GPR4 fully restores the activity of SPC.
198 hesis of the first photoaffinity analogue of SPC.
199           Here, we report the application of SPC-sequencing in characterizing frameshift mutations by
200 uitable strategy for the quick assessment of SPC trends in orange juices.
201 e amino group at C2 of the sphingoid base of SPC analogue 2.
202                     Moreover, the effects of SPC on EC require SPC induced trans-phosphorylation and
203 R4 is required for the biological effects of SPC on endothelial cells (EC).
204                        The acute efficacy of SPC embolization has not been demonstrated in a quantifi
205    We sought to assess the acute efficacy of SPC embolization on blood flow as quantified by phase co
206           We report on the acute efficacy of SPC embolization, demonstrating a significant decrease i
207  and adenomas, but not for the generation of SPC(+) ATII lesions.
208                 Current reference methods of SPC in orange juice are laborious, requiring several ext
209 he simple rapid screening of a wide range of SPC mediated organic reactions.
210 study does not indicate an increased risk of SPC in transplanted subjects who already suffered a firs
211              Herein, we report a new type of SPC based on a [2 + 3] imide-based organic cage (NKPOC-1
212 pecific types of FPCs with specific types of SPC risk; however, only a few smoking- or obesity-associ
213 lveolar hyperplasias, exclusively made up of SPC(+) ATII cells, progressed to yield malignant adenoca
214 hat MMP8 deficiency inhibited the ability of SPCs to migrate from the arterial lumen and the adventit
215         The decrease in migratory ability of SPCs with MMP8 knockdown was reduced by incubation of su
216 he expression, localization, and activity of SPCs in the human retina and optic nerve head.
217                   We conclude that assays of SPCs during the first weeks of care in patients with DFU
218  NKPOC-1 supports the further development of SPCs for applications in gas separation/storage because
219                   Incidence and mortality of SPCs per 10 000 person-years; standardized incidence rat
220 actate concentration increased the number of SPCs by 3.6-fold.
221      Proliferation of BM SPCs, the number of SPCs in the bone marrow, and mobilization of BM SPCs to
222 uman testis could enrich for a population of SPCs for derivation of GPR125+ MASCs, which may be emplo
223                               Recruitment of SPCs was analyzed by examining BM SPC proliferation, mob
224 chanism contributing to an increased risk of SPCs.
225         However, the design and synthesis of SPCs is challenging.
226 eden to provide etiological understanding of SPCs and insight into their incidence rates and recordin
227 sintegrin-and-metalloproteinase-domain-10 on SPCs.
228 r GI254023X decreased E-cadherin shedding on SPCs.
229                                However, only SPC(+) alveolar type II (ATII) cells were able to form h
230                 However, in adult mice, only SPC(+) ATII cells were able to yield malignant adenocarc
231 comprised substantial proportions of overall SPC incidence and mortality among all survivors and high
232 xture of citrem and soy phosphatidylcholine (SPC) at different weight ratios, we describe a library o
233 somes prepared from soy phosphatidylcholine (SPC) with various stabilizers (cholesterol (CHO) or glyc
234            The semiconductor photocatalyzed (SPC) oxidation of toluene is performed inside an NMR spe
235      Aberrant mTORC1 activation in Plzf(-/-) SPCs inhibits their response to GDNF, a growth factor cr
236  with self-rectifying behavior are potential SPC solutions.
237 ed recombined, GFP+ cells were predominantly SPC+.
238 eta4, but little or no pro-surfactant C (pro-SPC), is endowed with regenerative potential.
239 ession of the type II epithelial marker, pro-SPC.
240 LP transgene (surfactant protein C promoter (SPC)-TSLP) develop a spontaneous and progressive asthma-
241 outcomes using a novel method of quantifying SPC flow by cardiac magnetic resonance (CMR) imaging.
242 and that MMP8 knockout significantly reduced SPC numbers in atherosclerotic lesions in apolipoprotein
243   Moreover, the effects of SPC on EC require SPC induced trans-phosphorylation and activation of the
244                          Allogeneic resident SPCs, infused 24 hours after injection of dimethylnitros
245                                      Results SPC analysis allowed stratification based on 11 features
246 ed free-running single photon counting (SEFR-SPC), excitation pulses from inexpensive laser diodes (p
247                       We also show that SEFR-SPC provides state-of-the-art sensitivity in the SWIR sp
248                                     The SEFR-SPC method will be a valuable tool for studies of weak,
249 SIRs) were used to assess risk of a specific SPC compared to risk of the same first cancer in the cor
250                A SOMA for the CCRCC-specific SPC prognostic gene signature that is predictive of dise
251 nder the control of lung epithelial-specific SPC promoter was produced.
252      Significantly elevated SIRs of specific SPCs were observed for acute myeloid leukemia (AML; SIR
253 hway, thereby identifying the alpha-spectrin SPC-1.
254  that the lipid sphingosylphosphorylcholine (SPC) induces angiogenesis in vivo and GPR4 is required f
255  lipid mediator sphingosylphosphorylcholine (SPC) has not yet been identified.
256 ed for their ability to effectively suppress SPC in RRAM arrays.
257 ilization, SPC-CHO-0.5%HC had higher EE than SPC-GLY-0.25%HC (P < 0.05).
258  required for SPC-mediated cleavage and that SPC-mediated cleavage is essential to protein function.
259 preexisting type II AECs, demonstrating that SPC- progenitor cells replenished type II AECs during re
260 ally HIF-1 null myeloid cells indicated that SPC recruitment and lactate-mediated effects were depend
261            Ninety-four percent reported that SPC was available to them, but only 37% reported that th
262                            Results show that SPC is a feasible material for the development of probio
263 like growth factor-I levels, suggesting that SPC may contain other bioactive ingredients that have an
264                                 We find that SPCs lacking Plzf, a transcription factor essential for
265                                We found that SPCs in atheromas expressed MMP8 and that MMP8 knockout
266 med the relationship between the RRS and the SPC gene signature (R = 0.45, P < .001, classification a
267 we identified bud2Delta as deficient for the SPC.
268  based on the X -S charts generated from the SPC charts.
269 d-type males, GAR-3(mAChR) expression in the SPC and PCB neurons is required for the male to sustain
270 ings reveal a novel function for Elm1 in the SPC and suggest how checkpoint activity may be linked to
271 nce interval (CI), 4.5-16.1], but not in the SPC kindreds (1.8; 95% CI., 0.22-6.4).
272                       The performance of the SPC analysis (OS: IBS, 0.149; C index, 0.654; PFS: IBS,
273                       The performance of the SPC analysis model was further improved when combined wi
274                       mRNA expression of the SPC family in the human retina and optic nerve head tiss
275       We discussed the design aspects of the SPC recognition regions and demonstrated its plug-and-pl
276  This result shows that the incidence of the SPC was the same as the incidence of a first cancer.
277  kinase Elm1 is an obligate regulator of the SPC, and this function requires localization of Elm1 to
278 nstringent assay condition requirements, the SPC retained good analytical performance to detect subna
279 t dataset to confirm its relationship to the SPC gene signature (n = 70) and determination of patient
280  of the human p53 gene in one tube using the SPC-SBE method.
281 te IR and isotropic Raman spectra, using the SPC/E simulation model, and the results are in good agre
282 of a Cox proportional hazards model with the SPC analysis predictor was assessed with C index and int
283 , Spn4.1 forms SDS-stable complexes with the SPC furin and directly inhibits it.
284                      The RRS scaled with the SPC gene signature (R = 0.57, P < .001, classification a
285              These results indicate that the SPCs are expressed in distinct patterns throughout the h
286               A striking finding is that the SPCs can be attributed to a robust type of relativistic
287 orm noncovalent, latent complexes with their SPC-cleaved prodomains.
288                                        Thus, SPC-CHO liposome could be used as a promising carrier of
289 tients with SPC, 36.4% of deaths were due to SPC.
290  Oncologists referred patients frequently to SPC, but generally late in the disease course for patien
291                     One third would refer to SPC earlier if it was renamed supportive care.
292 is that immune dysfunction may contribute to SPCs by assessing SPCs associated with known immune resp
293  cavopulmonary connection patients underwent SPC flow quantification by phase contrast magnetic reson
294 000 cells (cutoff 2), and a low CMV-CMI when SPCs were below these thresholds.
295 reased neutrophils in the lung compared with SPC-Cre(-) RSV-infected littermates.
296       In vulvar/vaginal cancer patients with SPC, 36.4% of deaths were due to SPC.
297 e SPC services (P = .004), satisfaction with SPC availability (P < .001), SPC acceptance of patients
298 ather than later, included satisfaction with SPC service availability (P < .001) and SPC service acce
299 d to interact directly and specifically with SPC and in the definition of the ligand-binding sites.
300 e correlated the (1)H-MRS PDFF findings with SPCs (r = 0.92; P < .001).

 
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