ライフサイエンスコーパス: PSF

1 PSF (a.k.a. SFPQ) is a ubiquitously expressed, essential

2 PSF also contains two RNA-binding domains (RBD) that for

3 PSF also stimulates early steps of HR in vitro.

4 PSF and p54(nrb) are RNA recognition motif-containing pr

5 PSF binds PGC-1alpha and suppresses its transcriptional

6 PSF enhances N30 inclusion in a UGCAUG-dependent manner,

7 PSF is phosphorylated at two sites by the Mnks.

8 PSF represses transcription of the insulin-like growth f

9 paralogs and that the B. fragilis NCTC 9343 PSF repeat unit contains xylose.

10 in the endogenous NMHC II-B transcript in a PSF-dependent manner.

11 notype, but deletion of both genes abrogates PSF synthesis, strongly suggesting that they are functio

12 In the patient study, again, PSF increased the detected activity in the patient's les

13 Although PSF-TFE3 has no effect on the nuclear localization of wi

14 Here we show that DJ-1 and PSF bind and regulate the human tyrosine hydroxylase (TH

15 ins and provides evidence that the Fox-3 and PSF interaction is an integral part of the mechanism by

16 O-binding proteins such as FUS/TLS (FUS) and PSF/SFPQ (PSF).

17 nagement strategies for patients with HF and PSF.

18 The associations of hnRNP L and PSF with the ESS1 complex are largely independent of eac

19 on of TFE3 chimeras of PRCC, RCC17, NonO and PSF (PTB-associated splicing factor).

20 onsistent to this, we show that p54(nrb) and PSF induce CoAM splice variant through the cis-regulatin

21 Our finding that both p54(nrb) and PSF, which bind the C-terminal domain of the largest sub

22 P54nrb and PSF belong to Drosophila behavior/human splicing (DBHS)

23 Thus, p54nrb and PSF have properties of key factors mediating INS functio

24 to cells can reduce the levels of P54nrb and PSF proteins through proteasome-mediated degradation.

25 alization of heterodimer proteins P54nrb and PSF to nucleoli is an early event in the pathway that ex

26 ator that may act in concert with p54nrb and PSF to regulate the expression of a neuroprotective gene

27 a complex that includes RNase H1, P54nrb and PSF; but RNase H1/P54nrb complexes were observed in only

28 teomics and metabolomics profiles of PLF and PSF groups were acquired for the hippocampus and plasma

29 pathway activity differences between PLF and PSF mice.

30 eudosylvian and suprasylvian fields (PPF and PSF), suggesting that these connections are frequency sp

31 targeting the posterior bank fields PPF and PSF, which in turn project to the ventral posterior fiel

32 on of the splicing factors RBM8A, SRSF9, and PSF as well as the nucleolar proteins NPM1 and PHF6, and

33 t cubic splines can capture the shape of any PSF with high accuracy and that they can be used for fit

34 in vitro, and identified one such protein as PSF (the PTB (polypyrimidine tract-binding protein)-asso

35 e several proteins identified so far such as PSF (PTB associated splicing factor), NonO, PRCC, CLTC a

36 ther transcription/splicing factors, such as PSF and TLS, as well as transcription factors that inter

37 ion involving formation of a complex between PSF protein and mouse VL30 (mVL30) retrotransposon RNA.

38 NA; however, in resting cells, TRAP150 binds PSF and prevents access to the CD45 RNA, though the mech

39 Use of both PSF+TOF together provided a cumulative benefit in lesion

40 odel (PSF), baseline plus TOF, and with both PSF+TOF.

41 e presence of ligand, the levels of TR-bound PSF and Sin3A appear to remain unchanged, indicating tha

42 nificant difference between intact and burnt PSF with a modern signature for both CO(2) and CH(4) flu

43 cteristics in an intact and a degraded burnt PSF in Brunei Darussalam affected by seven fires over th

44 ll patient-level metrics was not affected by PSF reconstruction.

45 Here we demonstrate that in resting T cells PSF is directly phosphorylated by GSK3, thus promoting i

46 In stimulated T cells, PSF binds to and suppresses the inclusion of CD45 exon 4

47 PSF) engineering is in use to create complex PSF shapes.

48 n a large nuclear-protein complex containing PSF-NonO (polypyrimidine-tract-binding-protein-associate

49 trate that the obtained background-corrected PSF images, for both simulated and experimental data, le

50 olution was applied to the PSF +/- TOF data (PSF +/- TOF.EQ) to harmonize SUVs with the OSEM values.

51 In contrast, a SUMOylation-deficient PSF mutant exhibits reduced binding to PGC-1alpha and pr

52 small interfering RNA (siRNA) that degrades PSF transcripts.

53 h fovea on and off) that did not demonstrate PSF after surgery (non-PSF group).

54 reattachment on funduscopy and demonstrated PSF after surgery (PSF group) were compared with 62 eyes

55 (2 microm) by finding the center of the 2 DH-PSF lobes.

56 repeated imaging of sparse subsets with a DH-PSF microscope provides superresolution imaging of high

57 its a double-helix point spread function (DH-PSF).

58 The DH-PSF design features high and uniform Fisher information

59 odel in which TRAP150 interacts with dimeric PSF to block access of RNA to RRM2, thereby regulating t

60 formance, significantly outperforming either PSF or TOF alone (P < 0.002).

61 ework for noisy, aberrated and/or engineered PSF imaging.

62 hood estimator using a particular engineered PSF microscope demonstrates unmatched low-photon-count 3

63 This experimental PSF allows the approach to take into account the laser b

64 carcinoma cells, which endogenously express PSF-TFE3, siRNA complementary to the PSF-TFE3 fusion jun

65 ma-derived cells, which endogenously express PSF-TFE3.

66 ed high cytotoxicity but the floret extract (PSF) found to be most effective with IC(5)(0) value of 2

67 In affected eyes, PSF tends to persist for more than 1 year and results in

68 the heterogeneous capsular polysaccharide F (PSF) biosynthesis locus.

69 More importantly, the splicing factor PSF is recruited to the ESS1 complex in an activation-de

70 inding protein p54(nrb), the splicing factor PSF, and the inner nuclear matrix structural protein mat

71 -binding protein-associated splicing factor (PSF) and a 54-kDa nuclear RNA-binding protein (p54(nrb))

72 binding protein-associated splicing factor (PSF) as an interacting protein with Fox-3 by affinity-ch

73 -binding protein-associated splicing factor (PSF) as OEE-binding factors, which was confirmed by ChIP

74 onO(p54)-protein-associated splicing factor (PSF), multifunctional proteins involved in several nucle

75 -binding protein-associated splicing factor (PSF), two multifunctional regulators of transcription an

76 -binding protein-associated splicing factor (PSF).

77 -binding protein-associated splicing factor (PSF).

78 the past 25 years, the plant-soil feedback (PSF) framework has catalyzed our understanding of how be

79 Plant-soil feedback (PSF) theory provides a powerful framework for understand

80 ical studies show that plant-soil feedbacks (PSF) can generate negative density dependent (NDD) recru

81 and paroxetine-treated short-time floating (PSF) groups were stratified as proxies for drug non-resp

82 tivity and 1.3 cm(3) in volume estimates for PSF images and up to 20% and 2.5 cm(3) for the SFS-RR im

83 f corresponding blurred and sharp images for PSF estimation, avoiding the need to perform parameter o

84 s in human cell lines, indicating a role for PSF as a human tumor-suppressor protein.

85 air-entry suction in the pore-solid fractal (PSF) model, which additionally considered the hysteresis

86 ptical-bench-measured point spread function (PSF) and glare sources were compared.

87 A point spread function (PSF) could be derived from topography maps of single pul

88 t accuracy, even when point-spread function (PSF) engineering is in use to create complex PSF shapes.

89 These techniques use point spread function (PSF) fitting methods borrowed from single-molecule fluor

90 onally, the effect of point-spread function (PSF) image reconstruction on the repeatability of uptake

91 orrected SPECT versus point-spread function (PSF) model-based and time-of-flight (TOF) PET.

92 struction algorithms, point-spread function (PSF) modeling increases SUVs significantly in tumors but

93 e impact of including point-spread function (PSF) modeling into the process of iterative PET image re

94 ion (OSEM), OSEM with point-spread function (PSF) modeling, and the Q.Clear algorithm (which also inc

95 that reshapes the 3D point spread function (PSF) of an XYZ image stack into a narrow Gaussian profil

96 that approximates the point spread function (PSF) of the microscope.

97 technology using the point-spread function (PSF) of the scanner in the reconstruction procedure.

98 reconstructed with a point spread function (PSF) or PSF + time-of-flight (TOF) for optimal tumor det

99 scale, and the system point-spread function (PSF) serves as the key for encryption and decryption.

100 hree-dimensional (3D) point spread function (PSF) through additional optics has been demonstrated to

101 and that of the axial point spread function (PSF) was 115 microm.

102 gical tissue, and the point spread function (PSF) was assessed off the reflector.

103 ution to the measured point spread function (PSF), and can retrieve the 3D subpixel position of the f

104 vity of fMRI, unknown point spread function (PSF), and lack of comparison with independent techniques

105 the conjugate of the point spread function (PSF), is studied to further enhance lateral resolution a

106 esolved" images using point spread function (PSF)-based deconvolution, where the point conductor play

107 s, of the microscope point spread function (PSF).

108 techniques, including point-spread-function (PSF) engineering(5-9) -namely, encoding the axial (z) po

109 rt failure with preserved systolic function (PSF) is common but not well understood.

110 ilure (HF) with preserved systolic function (PSF).

111 ues with complicated point spread functions (PSF) such as differential interference contrast (DIC) mi

112 with truly invariant point spread functions (PSF), a property critical for accurate deconvolution.

113 Phosphate solubilizing fungi (PSF) have huge potentials in enhancing release of phosph

114 mortality in both systolic function groups (PSF: 4.8%; systolic dysfunction: 8.4%; p < 0.0001), and

115 tation maps, suggesting that the hemodynamic PSF is narrower than intercolumn distances.

116 recognition motif domains in the heteromeric PSF.p54(nrb) complex cooperate to align separate DNA mol

117 similar lesion detectability between (124)I PSF TOF PET/CT and (131)I SPECT/CT for small spheres (</

118 s purified from mouse tissues and identified PSF (polypyrimidine tract-binding protein-associated spl

119 This study is the first to identify PSF as a coactivator of Fox proteins and provides eviden

120 In whole-body PET/MR hybrid imaging, PSF-based PET reconstructions can improve activity recov

121 Thus, the DBD and RBD in PSF are linked by a mechanism of reversible gene regulat

122 TFE3 fusion junction leads to a reduction in PSF-TFE3 and redistribution of endogenous TFE3 and p53 f

123 d the Q.Clear algorithm (which also includes PSF modeling).

124 conserved RVxF PP1-binding motif (including PSF/SFPQ, Tra2-beta1 and SF2/ASF).

125 om was measured, and the impact of including PSF modeling in ordinary Poisson ordered-subset expectat

126 weight sumoylated protein species, including PSF, accumulate in the lymphoblast cells from the patien

127 Indeed, PSF associates specifically with the TNFalpha mRNA in li

128 32 +/- 83 mg CO(2) m(-2) hr(-1) ) and intact PSF (359 +/- 76 mg CO(2) m(-2) hr(-1) ).

129 CH(4) m(-2) hr(-1) ) compared to the intact PSF (4.0 +/- 2.0 mg CH(4) m(-2) hr(-1) ) due to prolonge

130 Likewise, PSF-TFE3 and NONO-TFE3 also bind this promoter.

131 The modified pore-solid fractal (M-PSF) model was tested using 26 soil samples from Yanglin

132 The M-PSF model demonstrated good performance particularly at

133 The derivation results showed that the M-PSF model is user-friendly and flexible for a wide range

134 Furthermore, the M-PSF model, used the fractal dimension of the particle si

135 PSF of any microscope and uses the measured PSF to perform 3D single molecule localization microscop

136 lt, variation in reconstruction methodology (PSF +/- TOFPET1/OSEMPET2 or OSEM PET1/PSF +/- TOFPET2) l

137 algorithm plus point spread function model (PSF), baseline plus TOF, and with both PSF+TOF.

138 ee of four species experienced weak negative PSF whereas, in contrast, all four species experienced s

139 We find that net PSF effects vary as a function of both host abundance an

140 To model the experimental z-scan data, a new PSF model had to be introduced.

141 Lastly, for all 20 patients, when PSF and no-PSF reconstructions were compared, an identical number o

142 For no-PSF no-TOF PET, DEP was 3.6%, 2.1%, 3.5%, 7.8%, 15.1%, a

143 bility for large lesions (>10 mm) and for no-PSF no-TOF PET, since DEPs are greater than 1%.

144 5% for lesion diameters of up to 17 mm on no-PSF no-TOF PET, (124)I activities as high as 170 MBq may

145 tions was rated better when compared with no-PSF data.

146 t did not demonstrate PSF after surgery (non-PSF group).

147 ively, and 87.1%, 11.3%, and 1.6% in the non-PSF group, respectively.

148 p54(nrb), PSF, and PSP1 alpha are all expressed in hESCs, but para

149 complexes containing the proteins p54(nrb), PSF, and PSP1 alpha.

150 p forest biomass dynamics across 96 km(2) of PSF in Kalimantan, Indonesia.

151 to RRM2, thereby regulating the activity of PSF toward a broad set of splicing events in T cells.

152 imes in which the fundamental assumptions of PSF fitting hold and where they begin to break down.

153 ted phosphorylation increases the binding of PSF to the TNFalpha mRNA in living cells.

154 Identification of possible causes of PSF abnormalities and solutions to improve microscope pe

155 The diagnosis of PSF was made by the detection of subretinal fluid pocket

156 es not appear to inhibit the dimerization of PSF with other Drosophila Behavior, Human Splicing (DBHS

157 -TFE3 became evident by stable expression of PSF-TFE3 in NIH-3T3 mouse fibroblast cells, which leads

158 In addition, the expression of PSF-TFE3 in normal renal proximal tubular epithelial cel

159 This suggests that the expression of PSF-TFE3 in renal epithelial cells plays an important ro

160 FDG PET/MR) were selected, and the impact of PSF on lesion activity concentration and image noise for

161 d; and for all 20 patients, the influence of PSF modeling was investigated on visual image quality an

162 We show that the inhibition of PSF-TFE3 expression through siRNA or shRNA leads to impa

163 0's PID directly inhibits the interaction of PSF RRMs with RNA, which is mediated through RRM2.

164 However, interaction of PSF with TRAP150 does not appear to inhibit the dimeriza

165 lated by GSK3, thus promoting interaction of PSF with TRAP150, which prevents PSF from binding CD45 p

166 st that the Mnk-catalyzed phosphorylation of PSF may regulate the fate of specific mRNAs by modulatin

167 The oncogenic potential of PSF-TFE3 became evident by stable expression of PSF-TFE3

168 icant factor associated with the presence of PSF (adjusted odds ratio [AOR], 13.4; 95% CI, 3.1-34.7 [

169 nclusion by Fox-3 depends on the presence of PSF.

170 rolled, in large part, by the recruitment of PSF to the pre-mRNA substrate upon T cell activation; ho

171 stoperative vision and time to resolution of PSF.

172 In this study, we explored the role of PSF-TFE3 fusion protein in mediating cell transformation

173 present study documents the central role of PSF-TFE3 in oncogenic transformation.

174 passing the RNA recognition motifs (RRMs) of PSF using a previously uncharacterized, 70 residue regio

175 f host species, to the strength and scale of PSF and overall plant community diversity.

176 expression by inhibiting the sumoylation of PSF and preventing its sumoylation-dependent recruitment

177 Specifically, the use of PSF is not an issue in routine clinical processes or in

178 The use of PSF reconstruction affected classification of tumor resp

179 They are dependent on PSF/SFPQ, whose phosphorylation is regulated by PyrCer.

180 The combination of optical PSF design and digital postprocessing with photoactivata

181 ely 3 x 10(-3) times the size of the optical PSF.

182 ructed with a point spread function (PSF) or PSF + time-of-flight (TOF) for optimal tumor detection a

183 Unlike wild-type TFE3 or PSF, which are nuclear proteins, PSF-TFE3 is not a nucle

184 Conversely, OSEM PSF was ranked second highest for lesion detectability i

185 Poor lesion detectability on OSEM PSF was seen in cases of mildly (18)F-FDG-avid mediastin

186 CT scans were reconstructed using OSEM, OSEM PSF, and Q.Clear using B values of 200, 300, 400, and 50

187 The least preferred reconstruction was OSEM PSF in all cases.

188 9 of 15 (67%) and 10 of 15 (73%), with OSEM PSF ranked lowest.

189 laudin-5, and barrier induction, and the p54/PSF heterodimer may contribute to normal blood-retinal b

190 with paraspeckle proteins, including P54nrb, PSF, PSPC1 and hnRNPK.

191 gag mRNA is a high-affinity ligand of p54nrb/PSF, a heterodimeric transcription/splicing factor.

192 Together, our data indicate that p54nrb/PSF functions in recruitment of XRN2 to facilitate pre-m

193 h PSF using a meta-analysis of 1038 pairwise PSF measures.

194 tly because of a failure to analyse pairwise PSF, the metric directly linked to plant species coexist

195 l image data of the microspheres and perform PSF measurements.

196 peatability than features extracted from PET(PSF) images (P < 0.001).

197 maximization with point-spread function (PET(PSF)).

198 ology (PSF +/- TOFPET1/OSEMPET2 or OSEM PET1/PSF +/- TOFPET2) led to 13 of 86 (15%) and 17 of 86 (20%

199 3 (hTIM3) and its ligand phosphatidylserine (PSF).

200 e binding of the C2 domains to phospholipid (PSF) has been modeled and provides an insight into the l

201 Mnks phosphorylate PSF at two sites in vitro, and our data show that PSF is

202 ethered diffusion around their anchor point, PSF fitting cannot be extended to arbitrarily fast frame

203 as identified a complex of two polypeptides, PSF and p54(nrb), as a stimulatory factor in a reconstit

204 biofilm-forming bacterium, and polysulfone (PSF) ultrafiltration (UF) membranes to unravel the mecha

205 eraction of PSF with TRAP150, which prevents PSF from binding CD45 pre-mRNA.

206 The mammalian protein PSF contains a DNA-binding domain (DBD) that coordinatel

207 achinery through the multifunctional protein PSF.

208 ype TFE3 or PSF, which are nuclear proteins, PSF-TFE3 is not a nuclear protein and is targeted to the

209 tion, reduced GSK3 activity leads to reduced PSF phosphorylation, releasing PSF from TRAP150 and allo

210 The complex with mVL30 RNA releases PSF, allowing transcription to proceed.

211 ds to reduced PSF phosphorylation, releasing PSF from TRAP150 and allowing it to bind CD45 splicing r

212 a noncoding VL30 retroelement RNA, releasing PSF from a gene and reversing repression.

213 ation with co-activator p54nrb and repressor PSF.

214 We examined hemodynamic response PSF by comparing these CBV-based signals with oxygen met

215 images were compared with the manufacturer's PSF-based reconstruction using the standardized uptake v

216 We designed a side-lobe-free SB-PSF and implemented a two-channel detection scheme to en

217 uce a self-bending point spread function (SB-PSF) based on Airy beams for three-dimensional (3D) supe

218 gation-dependent lateral bending make the SB-PSF well suited for precise 3D localization of molecules

219 licing (DBHS) family include mammalian SFPQ (PSF), NONO (p54nrb), PSPC1, and invertebrate NONA and Hr

220 proteins such as FUS/TLS (FUS) and PSF/SFPQ (PSF).

221 oteomics screen, we recently identified SFPQ/PSF as an interacting partner with the RAD51 paralogs, R

222 In addition, the transcriptional silencer PSF induces neuronal apoptosis, which can be reversed by

223 We demonstrate this method, named in situ PSF retrieval (INSPR), across a range of cellular and ti

224 In the phantom study, PSF modeling significantly improved activity recovery an

225 nduscopy and demonstrated PSF after surgery (PSF group) were compared with 62 eyes with macula-off RR

226 and resulting TFE3 gene fusions (PRCC-TFE3, PSF-TFE3, NONO-TFE3, ASPL-TFE3), encoding related aberra

227 ally associated with p54nrb in vivo and that PSF inhibited its expression, acting via INS.

228 ndependent studies, our results confirm that PSF may play a key role in plant species coexistence, sp

229 We also demonstrate that PSF, together with its partner, p54(nrb), binds RNAs tha

230 We find that PSF fundamentally alters the electrostatic environment w

231 an infectious molecular clone, we found that PSF affected specifically the INS-containing, Rev-depend

232 Our results indicate that PSF-TFE3 acts through a novel mechanism, and exports TFE

233 This indicates that PSF likely belongs to the pachychoroid spectrum.

234 Our analysis indicates that PSF within the PER complex recruits SIN3A, a scaffold fo

235 t two sites in vitro, and our data show that PSF is an Mnk substrate in vivo.

236 The PSF geometry is used as an indicator to identify problem

237 The PSF group demonstrated a greater proportion of RPE chang

238 The PSF was determined in the presence of no ultrasound, pul

239 The PSF-NonO complex is involved in the regulation of many c

240 The PSF.p54(nrb) complex cooperates with Ku protein to form

241 rm up), whereas collecting and analyzing the PSF images require an additional 2-3 h.

242 ordance (Cohen unweighted kappa) between the PSF and the PSFEARL DS was 0.82 (95% confidence interval

243 inexpensive, may not accurately capture the PSF shape leading to reduced fitting accuracy.

244 al functions that can accurately capture the PSF shape, such as those based on pupil functions, can b

245 cy and that they can be used for fitting the PSF with only a 2-3x increase in computation time as com

246 tinopexy were 71.4%, 14.3%, and 14.3% in the PSF group, respectively, and 87.1%, 11.3%, and 1.6% in t

247 understand the function of hysteresis in the PSF theory, the role of allowable and accessible pores m

248 ethers mCF to mPSF, and we have named it the PSF interaction motif (PIM).

249 en-source software package that measures the PSF of any microscope and uses the measured PSF to perfo

250 simulations showed reduced broadening of the PSF due to collimator penetration for the PC collimator

251 Extension of the PSF framework to the phyllosphere is needed to more full

252 The analysis of the PSF is used to determine the resolution of the microscop

253 The overall image quality of the PSF reconstructions was rated better when compared with

254 emaining greater than 5-10% (5-10 nm) of the PSF size.

255 on with a Taylor series approximation of the PSF.

256 he transcriptional silencing activity of the PSF.

257 onsidered the hysteresis effect based on the PSF theory.

258 For example, taking the PSF +/- TOFPET1/OSEMPET2 scenario increased the apparent

259 erized, 70 residue region we have termed the PSF-interacting domain (PID).

260 human blastocyst cells, indicating that the PSF-VL30 RNA regulatory mechanism also could function in

261 of DSBs in vivo in human cells and that the PSF.p54(nrb) complex may thus be a potential target for

262 rietary software solution was applied to the PSF +/- TOF data (PSF +/- TOF.EQ) to harmonize SUVs with

263 E3 transcription factor becomes fused to the PSF and NonO pre-mRNA splicing factors and most commonly

264 express PSF-TFE3, siRNA complementary to the PSF-TFE3 fusion junction leads to a reduction in PSF-TFE

265 e use the intensity z scan together with the PSF model to determine the geometry of the sample and th

266 mprovement similar to that obtained with the PSF model.

267 rate that the interaction of N-WASP with the PSF-NonO complex can couple N-WASP with RNA polymerase I

268 wn, and show that for the majority of these, PSF's effect is antagonized by TRAP150.

269 nvironmental factors for coexistence through PSF using a meta-analysis of 1038 pairwise PSF measures.

270 Thus, PSF-TFE3 is a promising target for the treatment for a s

271 Additionally, a 6-mm filter was applied to PSF images to meet the requirements of the EANM Research

272 pecific mRNAs by modulating their binding to PSF.p54(nrb).

273 ic small interfering RNA sensitizes cells to PSF-induced apoptosis.

274 ately 40 T cell splicing events sensitive to PSF knockdown, and show that for the majority of these,

275 Two PSF (NJDL-03 and NJDL-12) were isolated and identified a

276 ect on the nuclear localization of wild-type PSF, it sequesters wild-type TFE3 as well as p53 in the

277 data were reconstructed with the unfiltered PSF method.

278 For Eot-PET, patients were classified using PSF and PSFEARL as responders and nonresponders in 69 an

279 For i-PET, using PSF and PSFEARL, we classified patients as responders an

280 Lastly, for all 20 patients, when PSF and no-PSF reconstructions were compared, an identic

281 his work also highlights strategies by which PSF-mediated conformational change could be controlled,

282 atient scans reconstructed with PSF and with PSF+TOF.

283 er mVL30 RNA tracts that form a complex with PSF or a small interfering RNA (siRNA) that degrades PSF

284 Eyes with PSF showed significantly thicker subfoveal choroid than

285 Heart failure with PSF is common and is characterized by a unique patient p

286 Heart failure with PSF was present in 50.4% of patients with in-hospital as

287 processes of mice, by complex formation with PSF.

288 registry reveal a high prevalence of HF with PSF, and these patients have a similar post-discharge mo

289 The SUVs of the detected lesions with PSF were substantially increased in the range of 6%-75%,

290 ospital mortality was lower in patients with PSF (EF > or =40%) (2.9% vs. 3.9%; p < 0.0001).

291 -day post-discharge follow-up, patients with PSF (EF > or =40%) had a similar mortality risk (9.5% vs

292 Patients with PSF (EF > or =40%) were more likely to be older, female,

293 dysfunction (LVSD) and 21,149 patients with PSF (left ventricular ejection fraction [EF] > or =40%).

294 ospital mortality was lower in patients with PSF compared with patients with systolic dysfunction (2.

295 Analyses of patients with PSF defined as EF >50% were also performed for compariso

296 nts with systolic dysfunction, patients with PSF were more likely to be older, women, and hypertensiv

297 and rehospitalization rates in patients with PSF.

298 llustrative patient scans reconstructed with PSF and with PSF+TOF.

299 Findings were comparable with those with PSF defined as EF >50%.

300 thicker subfoveal choroid than eyes without PSF (305+/-61 mum vs. 200+/-70 mum, respectively; adjust