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1 RVF is caused by Rift Valley fever virus (RVFV; family B
2 RVF is exotic to the United States; however, mosquito sp
3 RVF was associated with significantly reduced RV ejectio
4 and efficacy of the Rift Valley fever MP-12 (RVF MP-12) vaccine, 9 healthy adult Rhesus macaques, wei
5 ed the model using data from the recent 2010 RVF outbreak in South Africa as a case study; mapping th
6 ent sequence was obtained from a total of 31 RVF virus specimens spanning the entire known outbreak p
8 tem for the reverse genetics generation of a RVF virus replicon particle (VRP(RVF)) vaccine candidate
12 .8 mL/s, range 2.5-5.7 mL/s; P < 0.001), and RVF (45%, range 32.5-51.5%; P = 0.006), and clinical imp
13 1, OF4), calf muscle pump function (EF), and RVF of the stented limbs did not differ significantly fr
14 ose immunization regimen induced robust anti-RVF virus immunoglobulin G antibodies (titer, approximat
20 ve implications for further studies of basic RVF virus ecology and the design of future surveillance/
23 -12 vaccine is one of the best-characterized RVF vaccines for safety and efficacy and is currently co
26 ration continuous mechanical assist devices, RVF after implantation of LVAD is still associated with
27 genome sequence was achieved for 33 diverse RVF virus strains collected from throughout Africa and S
29 ecent insights on right-ventricular failure (RVF) following left-ventricular assist device (LVAD) imp
30 hypertension and right ventricular failure (RVF) in left ventricular systolic dysfunction (LVSD) is
41 ue-forming units (pfu) of Rift Valley fever (RVF) MP-12 vaccine by oral, intranasal drops, or small p
51 for the first time to a rapid vertical flow (RVF) immunotechnology for detection of anti-HCV antibodi
53 he existing nonhuman primate (NHP) model for RVF utilizes an intravenous (i.v.) exposure route in rhe
58 and hypertension [Residual Venous Fraction (RVF) in %], were examined before and after successful ve
59 lling index [VFI], residual volume fraction [RVF]) and venous duplex, treadmill (3.5 km/h, 10%) to de
61 et model more closely resembles severe human RVF disease and is therefore an ideal model for the eval
62 and anthropogenic factors are implicated in RVF spread, the multidisciplinary One Health approach wa
63 was associated with a greater improvement in RVF (DeltaRV fractional area change 8.1% versus 5.4%; P<
65 toms, CRT was associated with improvement in RVF, which improved in parallel with improvement in left
70 dies of the LV in rats with pressure-induced RVF (monocrotaline [MCT] injection, n = 25; controls wit
74 ic assays is illustrated by testing of known RVF case materials obtained during the Saudi Arabia outb
79 l provide a basis for further development of RVF virus marker vaccines for use in endemic regions or
81 nvironmental factors are the main drivers of RVF infection in humans can be used to design better pre
82 o insights into the evolution and ecology of RVF virus, these genomic data also provide a foundation
85 We propose a new compartmentalized model of RVF and the related ordinary differential equations to a
86 mate data predicted areas where outbreaks of RVF in humans and animals were expected and occurred in
87 ans to better understand the pathogenesis of RVF and to use for evaluation of medical countermeasures
89 dies have tried to better define the risk of RVF using combined clinical scores and measures of right
94 gested that aggressive surgical treatment of RVF, including early use of temporary stoma and major pr
95 This review highlights recent research on RVF, focusing on vectors and their ecology, transmission
96 outbreak also was found, indicating ongoing RVF virus activity and evolution during the interepizoot
98 We report here the establishment of a pan-RVF virus quantitative real-time reverse transcription-P
100 lop a nonhuman primate (NHP) model of severe RVF in humans to better understand the pathogenesis of R
101 nt enhanced green fluorescent protein-tagged RVF viruses containing either the full-length, complete
102 n (EF) had both improved (P < 0.001) and the RVF had decreased (P < 0.001), at the expense of venous
103 notic infectious viral disease caused by the RVF virus (RVFV) (Bunyaviridae: Phlebovirus), presents s
104 ory effect was found only for targets in the RVF (LH), whereas for toddlers learning the color terms,
105 roposed approach for accurately modeling the RVF spreading process in additional regions of the world
107 G(N) chimeric proteins demonstrated that the RVF virus Golgi localization signal mapped to a 48-amino
108 s laboratory confirmation, a high-throughput RVF diagnostic facility was established at the Kenyan Ce
112 ulmonary hypertension or PVR or uncontrolled RVF after aggressive management with all standard curren
113 e disease, and the only available veterinary RVF vaccine in the United States is a live-attenuated MP
114 en challenged with 1 x 10(5) pfu of virulent RVF virus delivered by a small particle aerosol at 56 da
115 ntly challenged with a high dose of virulent RVF virus survived infection and could be serologically
121 ngle-dose subcutaneous immunization with VRP(RVF), although it is highly attenuated, completely prote
124 of human and animal illness consistent with RVF virus infection emerged across semiarid regions of t
126 picardial mapping of the LV in patients with RVF after chronic thromboembolic pulmonary hypertension
127 dies indicate that the coupling of SERS with RVF technology shows enormous potential for next-generat
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