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1 BPI (bactericidal/permeability-increasing) is a potent a
2 BPI and BFI were completed for 7 consecutive days (days
3 BPI and LBP(N)-BPI(C) promote apparently CD14-independen
4 BPI binding to the bacterial surface rapidly triggers po
5 BPI could thus induce a p53-like response even in the pr
6 BPI gene transcript and protein were detected in airway
7 BPI has two domains with the same fold, but with little
8 BPI is based on the formulation of the original BrainPhy
9 BPI levels at 15 min of dialysis with CTA (10.91 +/- 3.6
10 BPI mRNA was detected in bovine retina; retinal pigment
11 BPI produced a dose-dependent increase (up to 3-fold) in
12 BPI was previously shown to retain aspects of its own fu
13 BPI, but not control protein thaumatin, activated extrac
14 BPI-CETP chimeras are inhibited by LPS but cannot be inh
15 BPI-derived peptide P2 rapidly halted oxygen consumption
16 BPI-enhanced delivery of the blebs to MDDC did not incre
17 BPI-inducible protein A (BipA) is a member of the family
18 BPI-reported pain reduction from baseline to 4 weeks aft
19 BPIs occurred in less than 1% of patients.
22 itiation factor (eIF) 4E-binding protein (4E-BPI), sensitizes fibroblasts to apoptosis in a manner st
25 xhibited IgG antibody autoreactivity against BPI in 64.7% and 46.7% of patients with positive blood c
26 how disrupted Shh signaling protects against BPI could uncover variants in the Shh pathway that cause
27 ectively demonstrated seropositivity against BPI fold containing family A member 1 (BPIFA1), BPI fold
30 in of LBP, COOH-terminal domain of BPI), and BPI(N)-LBP(C) with purified (3)H-LPS and, subsequently,
31 detailed clinical observations that EvC and BPI do not occur in the same individuals, led us to hypo
32 ctivities of combinations of cathepsin G and BPI were additive, as were those of combinations of cath
35 n the presence of Ca(2+) and Mg(2+), LBP and BPI each promote aggregation of LPS to protein-LPS aggre
36 human monocyte response to LPS, both LBP and BPI inhibited LPS-stimulated TNF-alpha production in mou
37 udy presented here, plasma levels of LBP and BPI were measured, predialysis, 15 min into dialysis and
38 6) Da), but only LPS associated with LBP and BPI(N)-LBP(C) is disaggregated in the presence of CD14.
39 ther, the association between LBP levels and BPI release during hemodialysis and clinical and laborat
40 nces, the physical properties of LBP-LPS and BPI-LPS complexes have been compared in this study by se
42 rt of bacteremic patient sera exhibited anti-BPI IgG responses in 23/154 (14.9%) patients with autore
43 status models (ASMs) were considered: ASM1 (BPI and schizoaffective disorder, BP cases (SABP) only),
44 with myeloid differentiation, such as AZU1, BPI, CTSG, LYZ and RNASE2 as well as of antiproliferativ
45 eptor, endothelin type A receptor, lamin B1, BPI fold-containing family B member 1, peroxisomal trans
49 fold containing family A member 1 (BPIFA1), BPI fold containing family A member 2 (BPIFA2)/parotid s
50 y meaningful pain progression as assessed by BPI-SF pain severity was longer with enzalutamide than w
56 e-N-propoxy bacteriopurpurinimide (dipropoxy-BPI), which was readily oxidized in oxygen atmosphere yi
57 a proband affected with bipolar I disorder (BPI) and at least one other member affected with BPI or
60 hrough a proband who had bipolar I disorder (BPI) were interviewed by a psychiatrist, assigned an all
64 ive bearing 3,4-ethylenedioxythiophene (EDOT-BPI) and its palladium complex (EDOT-PdBPI) were synthes
65 ns but produce profoundly different effects: BPI and a bioactive N-terminal fragment BPI-21 exert a s
68 , the Cohen kappa coefficients were 0.99 for BPI, 0.99 for BPII, and 0.98 for recurrent unipolar diso
70 ier in blood and exudate cells than mRNA for BPI, consistent with release of progressively less matur
71 that GPC4 is a specific binding protein for BPI on RPE to mediate the activation of ERK1/2, Akt, and
74 0 using the Brief Pain Inventory-Short Form (BPI-SF) were randomly assigned to receive either O3-FAs
75 nd were the Brief Pain Inventory-Short Form (BPI-SF), Brief Fatigue Inventory (BFI), Functional Asses
76 ales of the Brief Pain Inventory-short form (BPI-sf), length of Intensive Care Unit stay and postoper
77 ncluded the Brief Pain Inventory-Short Form (BPI-SF), Western Ontario and McMaster Universities Osteo
80 ssed by the Brief Pain Inventory Short Form [BPI-SF] questionnaire) and health-related quality of lif
81 hree of the Brief Pain Inventory Short Form [BPI-SF] questionnaire) or mildly symptomatic (score of 2
82 em 3 on the Brief Pain Inventory-Short Form [BPI-SF]) and symptomatic skeletal events, alongside prep
83 cts: BPI and a bioactive N-terminal fragment BPI-21 exert a selective and potent antibacterial effect
89 ecombinant 21-kDa modified fragment of human BPI (rBPI21), containing the active antimicrobial and en
90 fragments and the crystal structure of human BPI have established that BPI consists of two functional
91 .4 angstroms, the crystal structure of human BPI shows a boomerang-shaped molecule formed by two simi
93 etic studies of BP disorder since bipolar I (BPI) and BPII disorders often cluster in the same famili
94 gation of high numbers of EvC and Bipolar I (BPI) cases in several large Amish families descending fr
98 a neuromedium called BrainPhys(TM) Imaging (BPI) in which we optimize the concentrations of fluoresc
99 results localize the site of LPS binding in BPI to a region no larger than the amino terminal 155 am
100 rical pain responder (> or = 30% decrease in BPI) than the 137 patients in the usual-care group (P <
103 existence of an anatomic disconnectivity in BPI and further underscore a role for interhemispheric d
104 tervention group had greater improvements in BPI pain severity over the 12 months of the trial whethe
110 The bactericidal/permeability increasing (BPI) and lipopolysaccharide (LPS)-binding (LBP) proteins
111 er of the bacterial/permeability increasing (BPI) fold-containing protein family, which shares struct
112 er of the bacterial/permeability-increasing (BPI) family of antimicrobial proteins but was first iden
113 of the bactericidal/permeability-increasing (BPI) fold-containing (BPIF) protein family, sharing stru
114 own as bactericidal/permeability-increasing (BPI) fold-containing protein, family A, member 1 (BPIFA1
115 of the bactericidal/permeability-increasing (BPI) gene with pulmonary function in a cohort of patient
116 donor bactericidal/permeability-increasing (BPI) haplotypes were associated with a 2-fold to 3-fold
119 ne effects on the Behavioral Problems Index (BPI) and Home Observation Measurement of the Environment
120 index [BDI] versus bronchoprotection index [BPI]: 1.62 +/- 0.21 versus 2.02 +/- 0.40 [mean +/- SEM],
125 nal 10% time on boosted protease inhibitors (BPIs) was associated with reduced KS incidence in the th
126 seroma, paresthesia, brachial plexus injury (BPI), and lymphedema was available for 821 patients.
128 fter treatment, by the Brief Pain Inventory (BPI) and the M D Anderson Symptom Inventory (MDASI).
129 utcome measure was the Brief Pain Inventory (BPI) average pain severity score (range 0-10, where 0=no
132 al (FACT-G) scale, the Brief Pain Inventory (BPI), the Medical Outcomes Study (MOS) questionnaire, an
137 that the resting state of the catalyst is [(BPI)Cu(O2CPh)] (1-O2CPh), formed from [(BPI)Cu(PPh3)2],
138 The tridentate bipyridylimino isoindoline (BPI) ligands of these complexes were designed to enable
139 ptors, we have compared interactions of LBP, BPI, LBP(N)-BPI(C) (NH(2)-terminal domain of LBP, COOH-t
140 Lower KS incidence was observed with longer BPI use, after accounting for potential IRIS and other f
141 primary end point was the difference in mean BPI-SF worst pain scores at 6 weeks, which was lower for
142 et of N-substituted benzoperylene monoimide (BPI) fluorophores was synthesized and characterized stru
143 udy examines the feasibility of using murine BPI (mBPI) expressed on halophilic Archaeal gas vesicle
144 ve compared interactions of LBP, BPI, LBP(N)-BPI(C) (NH(2)-terminal domain of LBP, COOH-terminal doma
146 respectively) was similar to the neutrophil BPI content of normal controls (163+/-35 ng per 106 neut
147 studies led to the identification of nickel BPI complexes that could undergo stable charge-discharge
148 Compared with baseline, the mean observed BPI-SF score decreased by 1.74 points at 12 weeks and 2.
150 roup analyses revealed similar activation of BPI and control subjects during passive viewing but sign
152 and at least one post-baseline assessment of BPI-SF item 3, and patient-reported outcomes (PROs) were
155 uthors have extended the characterization of BPI interaction with membrane proteins from bovine RPE.
156 rophil extracts were analyzed for content of BPI by Western blotting and ELISA and for defensin pepti
157 minal domain of LBP, COOH-terminal domain of BPI), and BPI(N)-LBP(C) with purified (3)H-LPS and, subs
158 omain, corresponding to the active domain of BPI, thus creating the notion of a BPI/PLUNC structural
160 ability of E. coli to tolerate low doses of BPI and escape the progression of sublethal to lethal da
161 esicles ("blebs"), we examined the effect of BPI on interactions of metabolically labeled ([(14)C]-ac
162 racterized the previously unknown effects of BPI in the eye and the molecular mechanisms involved in
165 inant 21-kDa modified N-terminal fragment of BPI (rBPI(21)), which has the biological properties of t
166 t 21 kDa modified amino-terminal fragment of BPI (rBPI21) reduced H2O2-induced apoptosis in RPE and i
167 n a recombinant 21-kDa bioactive fragment of BPI, rBPI21, and the gram-positive pathogen Streptococcu
169 possibility that supplementing the levels of BPI in plasma might enhance newborn antibacterial defens
170 nome-wide significant evidence of linkage of BPI to a candidate region of approximately 10 cM in 5q31
176 electron microscopy confirmed the storage of BPI in primary granules and showed that p15s are stored
180 rmeability, the mechanistic understanding of BPI's action may provide novel therapeutic opportunities
185 phorylation was not reduced by either LBP or BPI under conditions that result in selective TNF-alpha
189 Secondary outcomes were improvement in other BPI subscales and at other time points, FACT-Hep and EOR
190 rences occurred over time in sustained pain (BPI mean pain, 0.07 point [CI, -0.23 to 0.37 points]; BP
192 pain, 0.07 point [CI, -0.23 to 0.37 points]; BPI worst pain, -0.14 point [CI, -0.59 to 0.31 points]),
193 s itself related to the host defense protein BPI (bactericidal/permeability-increasing protein).
194 actericidal-permeability-increasing protein (BPI) also mediated fungistasis against H. capsulatum in
195 actericidal permeability-increasing protein (BPI) and lipopolysaccharide (LPS)-binding protein, have
196 actericidal/permeability-increasing protein (BPI) and lipopolysaccharide-binding protein (LBP), which
197 actericidal permeability increasing protein (BPI) differs from LBP by inhibiting LPS-induced human mo
198 actericidal/permeability-increasing protein (BPI) fold-containing family B, member 3 (BPIFB3) is an e
199 actericidal/permeability-increasing protein (BPI) fold-containing family B, member 6 (BPIFB6), whose
200 actericidal/permeability-increasing protein (BPI) had been shown to possess anti-inflammatory and end
201 actericidal/permeability-increasing protein (BPI) has been shown to induce various effects in retinal
202 actericidal/permeability-increasing protein (BPI) is a natural protein, stored within the neutrophil
203 actericidal/permeability-increasing protein (BPI) is found in the primary granules of adult neutrophi
204 actericidal/permeability-increasing protein (BPI) is strongly associated with Pseudomonas aeruginosa
205 actericidal/permeability-increasing protein (BPI) is thought to play an important role in killing and
206 actericidal/permeability-increasing protein (BPI) of neutrophils is a lipopolysaccharide (LPS)-bindin
207 actericidal/permeability-increasing protein (BPI) released from polymorphonuclear leukocytes (PMNs) i
209 actericidal/permeability-increasing protein (BPI) was originally identified as a lipopolysaccharide (
210 actericidal/permeability-increasing protein (BPI), a member of a genomically conserved lipid-interact
211 actericidal/permeability-increasing protein (BPI), an antibacterial and lipopolysaccharide-neutralizi
214 actericidal/permeability-increasing protein (BPI)-derived peptide P2 and the murine alpha-defensin cr
221 bactericidal/permeability inducing protein (BPI), and lipopolysaccharide binding protein (LBP) are m
226 ide, retroinverso BCL6 peptide inhibitor (RI-BPI) selectively killed BCR rather than OxPhos-type DLBC
230 t (ICE) and Brief Pain Inventory pain score (BPI-PS), is associated with patient perception of benefi
235 olipase C, and anti-GPC4 antibody suppressed BPI-induced ERK and Akt phosphorylation in bovine RPE.
237 come was associated with improved short-term BPI scores (per $1,000, beta = -0.47; P = 0.01) and medi
239 of addition of recombinant 21-kDa N-terminal BPI fragment (rBPI(21)) on the growth and tumor necrosis
241 structure of human BPI have established that BPI consists of two functionally distinct domains: a pot
243 Scanning electron microscopy revealed that BPI treatment produced greater membrane perturbations in
244 hmark available neuronal media and show that BPI enhances fluorescence signals, reduces phototoxicity
246 he results of the present study suggest that BPI is tightly regulated and functionally expressed by e
250 ain from bone metastases, as measured by the BPI, increased from 39 of 149 (26%) before SBRT to 55 of
251 with placebo also significantly improved the BPI average pain interference score, the Fibromyalgia Im
252 d a significantly greater improvement in the BPI average pain severity score (P=0.015; estimated diff
254 nically significant change at 1 month in the BPI subscale of symptom on average in the past 24 hours.
256 a combination of systematic variation of the BPI ligand and the metal center along with mechanistic i
257 ents had superior scores on all items of the BPI-FI (ie, general activity, mood, walking ability, nor
258 nically meaningful (mean 3.4 [SD 2.9] on the BPI pain-at-its-worst item at baseline, 2.1 [2.4] at 4 w
259 were mostly asymptomatic at baseline: on the BPI-SF pain severity scale of 0-10, median pain scores (
260 s remains elusive, our data suggest that the BPI peptide sensitivity of OmpU-deficient V. cholerae is
262 Similar results were obtained using the BPI-PS; observed improvements were typically of lesser m
265 larity searches have shown homology with the BPI-like family of innate immune genes, particularly wit
271 related LPS-binding protein, in contrast to BPI, did not increase association of the blebs with MDDC
272 suggest that the fate of E. coli exposed to BPI depends on both OmpR-independent mechanisms engaged
273 y depends on the high molar ratio of p15s to BPI in the extracellular fluid (approximately 50:1), whi
275 a indicate that low-avidity IgG responses to BPI can arise acutely in response to bacteremia and that
278 ction was significantly stronger (BDI versus BPI: 3.40 +/- 0.43 versus 6.98 +/- 1.42, p = 0.02).
281 d proteins in CP compared with controls were BPI, ITGAM, CAP37, PCM1, MMP-9, MZB1, UGTT1, PLG, RAB1B,
282 es (RPC), and endothelial cells (REC); while BPI protein was measured in human vitreous and plasma.
283 ts with BP (13 males and 26 females; 28 with BPI and 11 with BPII) and 35 healthy controls were inves
284 and at least one other member affected with BPI or bipolar II disorder (BPII), we identified four re
286 infection with S. aureus was associated with BPI antibody autoreactivity in 2/15 patients (13.3%).
290 rum symptoms in this sample of patients with BPI disorder was associated with greater levels of depre
291 ment strategies are needed for patients with BPI disorder who endorse lifetime panic spectrum feature
296 ne the association of EITC payment size with BPI and HOME scores; in the second, we used EITC payment
299 oCAP18, exhibited antibacterial synergy with BPI, and the p15s also displayed synergy with CAP18p in