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1 n-Probe Aptima Combo 2 and BD ProbeTec using Viper.
2 ext of the envenomation caused by the Gaboon viper.
3 from the venom of the Vipera lebetina obtusa viper.
4 that play key roles in subduing prey in many vipers.
5 nits in venoms of related Asian and American vipers.
6  example is the thermal imaging organ of pit vipers.
7                       Here, we introduce Man-VIPER, a self-assembling (40-50 nm micelles), pH-sensiti
8  Regulator activities were inferred with the VIPER algorithm that integrates enrichment of expected e
9                             We leveraged the VIPER algorithm to quantitate single-cell protein activi
10                                              VIPER analysis revealed FOXO1 as a master regulator, inf
11  or current best freely available pipelines (VIPER and BioJupies), Searchlight can reduce the time an
12  greater automation than current best tools (VIPER and BioJupies).
13  with increasing body size in the rhinoceros viper and black mamba, and males were found in arboreal
14 s that are affected by both Indian Russell's viper and cobra venoms and offers insights into the pote
15 medically important Indian snakes (Russell's viper and cobra) affect human skeletal muscle using a cu
16               Envenoming by Echis saw scaled vipers and Bitis arietans puff adders is the leading cau
17 genetically broad sampling of nonsidewinding vipers and other snakes from diverse habitats and wide g
18 iption factor) activity imputation (DoRothEA-VIPER), and trajectory analyses (Monocle3 and Velocyto-s
19 es, only vampire bats, boas, pythons and pit vipers are capable of detecting infrared radiation.
20 es of 484 snakes of five species (rhinoceros vipers Bitis nasicornis, black mambas Dendroaspis polyle
21 cetin" from the venom of West African gaboon viper, Bitis gabonica rhinoceros.
22 in, BomoTx, from the Brazilian lancehead pit viper (Bothrops moojeni).
23  (ADET) of myotoxin II from the venomous pit viper, Bothrops asper, in a mouse model of envenoming th
24  those obtained using existing tools such as VIPER, but with the added benefit of being able to trace
25 wed their orthogonality in vivo using the ON VIPER CAR and OFF lenalidomide-CAR systems.
26               Finally, we engineered several VIPER CAR circuits by combining various CAR technologies
27                             Here, we present VIPER CARs (versatile protease regulatable CARs), a coll
28                  Furthermore, we benchmarked VIPER CARs against other drug-gated systems and demonstr
29 l Gerbillus pyramidum and the Saharan horned viper Cerastes cerastes.
30  leakeyi (Kenya), and from the sahara horned viper, Cerastes cerastes cerastes (Egypt) and the puff a
31                                          Pit vipers (Crotalinae) have a specific sensory system that
32 ding domain of the venom of the American pit viper, Crotalus molossus molossus as the targeting moiet
33  different from that of previously published viper CTLs.
34 rt the high-quality genome of the five-pacer viper, Deinagkistrodon acutus, and comparative analyses
35                                          The VIPER display was shown to effectively expose the range
36    This paper describes an evaluation of how VIPER displays the different scales and types of dataset
37  venom gland EST database for the saw-scaled viper, Echis ocellatus (Nigeria), using the gene ontolog
38 pressed in the venom gland of the saw scaled viper, Echis ocellatus.
39  fatal thrombotic complications in Russell's viper envenomation.
40               Importantly, in murine models, VIPER facilitates effective gene transfer to solid tumor
41 as to enhance the safety and tolerability of VIPER for frequent dosing.
42 nce of Protein-activity by Enriched Regulon (VIPER) for the MRA to identify top up- and down-regulate
43 otein activity by enriched regulon analysis (VIPER), for accurate assessment of protein activity from
44 etwork-based algorithms, such as OptiCon and VIPER, in the selection of target combinations is attrib
45               In vitro assays confirmed that VIPER-inferred protein activity outperformed mutational
46 se errors are exposed and explored using the VIPER interface and we evaluate the utility and usabilit
47                                              VIPER is composed of a polycation block for condensation
48 emonstrate that the region of A46 from which VIPER is derived represents the TLR4-specific inhibitory
49 llomavirus (HPV) assay (Onclarity) on the BD Viper LT platform using both contrived and clinical spec
50                           When combined with VIPER, NPSTING generated more antigen-presenting DCs in
51                  These results highlight Man-VIPER-NR as a safe and powerful peptide cancer vaccine p
52 our candidate for a therapeutic vaccine, Man-VIPER-NR exerted superior efficacy in a B16F10-OVA tumor
53        Remarkably, antigen delivery with Man-VIPER-NR generated significantly more antigen-specific c
54 easable (Man-VIPER-R) or non-releasable (Man-VIPER-NR) d-melittin.
55 d by venom from the most medically-important vipers of Africa, South Asia and Central America.
56                                   Asian mock vipers of the genus Psammodynastes and African forest sn
57 tide purified from the venom of Wagler's pit viper on the whole cell current response (I(GABA)) to ga
58 ed the behavior of 33 individuals to a model viper placed on their projected travel path.
59                                 In vivo, Man-VIPER polymers demonstrated an adjuvanting effect, induc
60                                     Both Man-VIPER polymers exhibited superior endosomolysis and anti
61                         In conclusion, siRNA/VIPER polyplexes efficiently delivered siRNA to lung epi
62                                  Here, siRNA/VIPER polyplexes efficiently inhibited SARS-CoV-2 replic
63                                        siRNA/VIPER polyplexes reached the cell monolayer and penetrat
64   Finally, we verified the delivery of siRNA/VIPER polyplexes to lung epithelial cells in vivo, which
65                   After characterizing siRNA/VIPER polyplexes, the activity and safety profile were c
66   TRPA1 orthologues from pit-bearing snakes (vipers, pythons and boas) are the most heat-sensitive ve
67  antigen-specific cytotoxic T cells than Man-VIPER-R in vivo.
68 evaluated polymers with both releasable (Man-VIPER-R) or non-releasable (Man-VIPER-NR) d-melittin.
69 nstituent functionality of venoms from these vipers remains poorly understood.
70 h boid and crotaline snakes (pythons and pit vipers, respectively).
71 ur experimentally, with a description of how VIPER's display interface and functionality meet the cha
72 h improvements ranging from 0.05 to 0.2 over VIPER, scImpute, DCA, DeepImpute, SAVER, scMultiGAN and
73                                              VIPER shows superior efficiencies compared to commercial
74 both foraged less in the presence of the pit-viper (sidewinder).
75                                          The VIPER software package is one of the key components of t
76 luster sequence conservation across all four viper species which were significantly different from th
77 es isolated (by PCR) from another saw-scaled viper species, E. pyramidum leakeyi (Kenya), and from th
78 tions of two desert rodents to two different viper species, testing their ability to adjust to novel
79                                         Both VIPER-STING drugamer platforms demonstrated efficacy in
80 , which can be performed on the automated BD Viper system.
81 dynamic lineage-specific expansion, and many viper TEs show brain-specific gene expression along with
82 n of this important group of venom toxins in vipers that are distributed throughout Africa, the Middl
83 n structures of a few sidewinding specialist vipers that inhabit sandy deserts-an isotropic texture t
84                                      We used VIPER to evaluate the functional relevance of genetic al
85 rus-inspired polymers for endosomal release (VIPER) to address systemic and intracellular delivery ob
86 RET reporter called VIral ProteasE Reporter (VIPER) to investigate heterogeneity of protease activati
87 cobra (Ophiophagus hannah; OH) and green pit viper (Trimeresurus albolabris) showed the broadest anti
88  antigen can enhance defense against Russell viper venom (RVV) and determined whether such responses
89 e was then induced with the use of Russell's viper venom (RVV) and histamine.
90                     An enzyme from Russell's viper venom (RVV) cleaves human factor V at Arg1018 and
91                                    Russell's viper venom (RVV) contains protein(s) that destabilize A
92  of coagulation factors V and X by Russell's viper venom (RVV) has been implicated in the development
93  showed that factor X activator of Russell's viper venom (RVV-X) contains six N-linked oligosaccharid
94      The X-activating protein from Russell's viper venom activates fXSt. Louis II completely but at a
95  Plaque rupture was triggered with Russell's viper venom and histamine.
96 aque disruption was triggered with Russell's viper venom and histamine.
97 ger) inducing plaque disruption with Russell viper venom and histamine.
98  markedly procoagulant in a modified Russell viper venom assay.
99 GDFX and was also activated by the Russell's viper venom at similar rate, but it cleaved the chromoge
100 are capable of broadly neutralizing distinct viper venom bioactivities in vitro by inhibiting differe
101 peptide, was isolated from the Azemiops feae viper venom by combination of gel filtration and reverse
102 phospholipid-initiated and diluted Russell's viper venom clotting time, which could be partly rescued
103                                      Because viper venom CTLs exhibit a high degree of sequence simil
104  degrees of sequence similarity to published viper venom CTLs.
105                              Echistatin is a viper venom disintegrin containing RGD loop maintained b
106                                    Russell's viper venom factor X activator (RVV-X) triggers the casc
107 oresceinated antibody, and enzyme (Russell's viper venom factor X activator)-labeled antibody is allo
108        Factor X was activated with Russell's viper venom factor X activator, and single-chain unactiv
109                                              Viper venom induced haemorrhagic, coagulant and anticoag
110            We characterized HUVEC GPIb using viper venom proteins: alboaggregins A and B, echicetin,
111                                    Russell's viper venom reduced the total number of cells, their mig
112 coagulable state, we have used the Russell's viper venom test (RVV) to show that red blood cells (RBC
113 rogram/mL) did not prolong a modified Russel viper venom time, suggesting no significant inhibition o
114 re and 48 hours after injection of Russell's viper venom, an endothelial toxin.
115 s, such as cyclic RGD peptides isolated from viper venom, may prove to be useful as anti-inflammatory
116 f three of the four largest gene families in viper venom, showing that complexity evolution is a conc
117 ation by the factor X activator from Russell viper venom, the mutants were characterized with respect
118       In conclusion, we report a new, potent viper venom-derived inhibitor of alpha2beta1 integrin, w
119 olecules rescued the myotubes from Russell's viper venom-induced atrophy.
120 the ApoE(-/-) (-22.22+/-7.95%) and Russell's viper venom-injected (-10.37+/-17.60%) mice compared wit
121 0.54, R(12 weeks) 3.83+/-0.52) and Russell's viper venom-injected wild-type mice (R(1)=4.57+/-0.86).
122  the lethal effects of honeybee or Russell's viper venom.
123 factor, factors IXa and VIIIa, and Russell's viper venom.
124 ex or by a purified activator from Russell's viper venom.
125  are small non-enzymatic proteins present in viper venoms reported to modulate hemostasis of victims
126           Disintegrins are peptides found in viper venoms which bind to platelets through the glycopr
127                                The cobra and viper venoms-induced sterile inflammatory molecules (IL-
128 e beta-ntx from the venom of the nose-horned viper (Vipera a.
129 d a peptide fragment derived from A46 termed VIPER (Viral Inhibitory Peptide of TLR4), which specific
130                                          The VIPER (virus-inspired polymer for endosomal release) blo
131 to mimic viral mechanisms of delivery called VIPER (virus-inspired polymer for endosomal release).
132 der to assist this process we are developing VIPER (Visual Pedigree Explorer), a software tool that i
133  community, and the virus particle explorer (VIPER) was developed to enable users to easily generate
134 om gland of the snake Bitis gabonica (Gaboon viper) was used for the first time to construct a unidir
135 ARHgamma), from the venom of the Malayan pit viper, was used to selectively cleave human factor X in
136 irus-inspired polymer for endosomal release (VIPER), which employs pH-sensitive triggered display of
137 n), a cathelicidin from a South American pit viper, yielded fragments Ctn[1-14] and Ctn[15-34], which

 
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