ライフサイエンスコーパス: carp

1 r of immobilized cyprinid fish (goldfish and carp).

2 that is highly pathogenic for koi and common carp.

3 event in the ancestor of goldfish and common carp.

4 uced gene expression compared with wild-type CARP.

5 of head kidney-derived macrophages of common carp.

6 protein (NSF), are specifically required for CARP.

7 be laterally mobilized into synapses during CARP.

8 pH-shift-based protein isolation from silver carp.

9 modulating immune cells of its natural host, carp.

10 -phosphorylated p53 is also ubiquitinated by CARPs.

11 CARP-1 also binds with anaphase-promoting complex/cyclos

12 oteome, regulation of NF-kappaB signaling by CARP-1 and the molecular mechanism(s) involved are uncle

13 Identification of CARP-1 as a key mediator of signaling by CD437 or adriam

14 Importantly, blockade of NEMO-CARP-1 binding diminished NF-kappaB activation, indicate

15 We conclude that inhibition of NEMO-CARP-1 binding enhances responses of cancer cells to che

16 mapping of the minimal epitopes involved in CARP-1 binding with APC-2, a fluorescence polarization a

17 CFM-4 prevents CARP-1 binding with APC-2, causes G(2)M cell cycle arres

18 Our yeast two-hybrid screen revealed CARP-1 binding with the anaphase-promoting complex/cyclo

19 y yielded a small molecule inhibitor of NEMO-CARP-1 binding, termed selective NF-kappaB inhibitor 1 (

20 n breast epithelial MCF-10A cells, elevating CARP-1 by CFM-4 and consequent apoptosis could in princi

21 adriamycin, whereas increased expression of CARP-1 causes elevated levels of cyclin-dependent kinase

22 ls, whereas antisense-dependent depletion of CARP-1 causes inhibition of apoptosis by ERRP.

23 CARP-1 contains multiple, nonoverlapping apoptosis-induc

24 Here, we report that CARP-1 directly binds the NF-kappaB-activating kinase Ik

25 , a lead compound, binds with and stimulates CARP-1 expression.

26 as serum deprivation of HBC cells, stimulate CARP-1 expression.

27 antagonists of CARP-1/APC-2 binding, termed CARP-1 functional mimetics.

28 CARP-1 interacts with 14-3-3 protein as well as causes r

29 Thus, apoptosis induction by CARP-1 involves sequestration of 14-3-3 and CARP-1-media

30 Although previous studies have reported that CARP-1 is a part of the NF-kappaB proteome, regulation o

31 Although CARP-1 is a regulator of chemotherapy-dependent apoptosi

32 ether, data demonstrate that tyrosine 192 of CARP-1 is a target of apoptosis signaling, and CARP-1, i

33 CARP-1 is a tyrosine-phosphorylated protein, and ERRP tr

34 rosine kinase inhibitor) results in elevated CARP-1 levels, whereas antisense-dependent depletion of

35 ll cycle and apoptosis regulatory protein 1 (CARP-1 or CCAR1) is a perinuclear phosphoprotein that re

36 Reduced levels of CARP-1 result in inhibition of apoptosis by CD437 or adr

37 ll cycle and apoptosis regulatory protein-1 (CARP-1), may function in the regulation of apoptosis.

38 130-kDa HBC cell perinuclear protein (termed CARP-1).

39 CARP-1, a novel apoptosis inducer, regulates apoptosis s

40 Depletion of CARP-1, however, interferes with CFM-4-dependent cell gr

41 RP-1 is a target of apoptosis signaling, and CARP-1, in turn, promotes apoptosis by activating p38 MA

42 ss of c-Myc sensitizes cells to apoptosis by CARP-1, whereas expression of c-Myc or 14-3-3 inhibits C

43 ated by wild type or CARP-1-(1-198), and not CARP-1-(1-198(Y192F)), results in activation of caspase-

44 Wild-type or CARP-1-(1-198) proteins that have substitution of tyrosi

45 addition, apoptosis mediated by wild type or CARP-1-(1-198), and not CARP-1-(1-198(Y192F)), results i

46 ereas expression of c-Myc or 14-3-3 inhibits CARP-1-dependent apoptosis.

47 CARP-1 involves sequestration of 14-3-3 and CARP-1-mediated altered expression of multiple cell cycl

48 s cause elevated tyrosine phosphorylation of CARP-1.

49 ielded several small molecule antagonists of CARP-1/APC-2 binding, termed CARP-1 functional mimetics.

50 a dissociation constant (K(d)) of 480 nm for CARP-1/APC-2 binding.

51 CARP-1/CCAR1, a perinuclear phosphoprotein, is a regulat

52 CARP-2 acts at the level of endocytic vesicles to limit

53 tue of its phospholipid-binding FYVE domain, CARP-2 localized to endocytic vesicles, where it interac

54 Knockdown of CARP-2 stabilized TNFR1-associated polyubiquitinated RIP

55 We report that CARP-2, a RING domain-containing ubiquitin protein ligas

56 CARP, a transcription coinhibitor, is a member of the ti

57 ndicating resistance strength increased with carp abundance.

58 ; median, 5th and 95th percentiles) of Asian carp access, while electric and acoustic-bubble-strobe b

59 Common carp accounts for a substantial proportion of global fre

60 on with a hypoallergenic mutant of the major carp allergen protect against allergic symptoms in sensi

61 The common carp alpha1-PI effectively reduced autolytic degradation

62 The common carp alpha1-PI showed high thermal stability with denatu

63 In addition, both CARP and ARPP are proposed to have regulatory functions,

64 l samples of Ikan pekasam made from Javanese carp and black tilapia, that had undergone either natura

65 Of the remaining clones, caveolin, CARP and CHAMP have been shown to inhibit remodelling of

66 Allosteric effectors were used to direct carp and chemically modified human hemoglobins into the

67 nduced differential distribution patterns of CARP and DARP: staining for both proteins was increased

68 s the causative agent of a lethal disease of carp and encodes for an Il10 homolog (ORF134).

69 owever, fish of the genus Carassius (crucian carp and goldfish) have evolved a specialized metabolic

70 5) against a fully conserved epitope between carp and human alpha-syn.

71 hanism that involves the regulatory proteins CarP and integration host factor.

72 summarizes the current state of knowledge of CARP and its regulation in biological systems.

73 sviruses 1 and 3 (CyHV1 and CyHV3) in common carp and koi and cyprinid herpesvirus 2 (CyHV2) in goldf

74 tion Hg(2+) ions from samples of tap waters, carp and saltwater fishes with satisfactory results.

75 elivery of GluR2-containing receptors during CARP and thus regulate the calcium permeability of AMPA

76 Divergence between grass carp and zebrafish is estimated to have occurred 49-54 m

77 candidate modifier genes to ITGA8, C10orf97 (CARP) and PTER.

78 tamination Assessment and Reduction Project (CARP) and were analyzed via Positive Matrix Factorizatio

79 New markers for black carp, grass carp, and a common carp/goldfish are reported and detail

80 diac hypertrophy (atrial natriuretic factor, CARP, and beta-myosin heavy chain), uncoupling protein 2

81 een zebrafish and medaka, common carp, grass carp, and goldfish to study the genome evolution events

82 n originally suspected such as bream, common carp, and roach.

83 CARP, ankrd-2/Arpp, and DARP, are three members of a con

84 Among these, cardiac ankyrin repeat protein (CARP, ankrd1) expression was markedly and persistently e

85 of the cardiac ankyrin repeat protein gene (Carp/Ankrd1) models CHD reported in humans with partial

86 ary members, cardiac ankyrin repeat protein (CARP), Ankyrin Repeat Domain 2 (ARPP), and diabetes-rela

87 ns (GEE) tested the association between anti-CarP antibodies and longitudinal HAQ and DAS28 scores.

88 Our results suggest that anti-CarP antibodies might provide additional prognostic info

89 ACPA and anti-CarP antibodies were measured on stored serum samples ob

90 Anti-CarP antibodies were positive in 460 patients (23%), and

91 ive and rheumatoid arthritis subgroups, anti-CarP antibodies were significantly associated with DAS28

92 to investigate the association between anti-CarP antibodies, disability, and disease activity in the

93 w set of antibodies, anti-carbamylated (anti-CarP) antibodies, have been identified in patients with

94 Patients who were anti-CarP antibody positive had significantly more disability

95 CARP appears to be the rat homolog of a previously repor

96 CARP appears to function as a negative regulator of card

97 ITGA8 and CARP are biologically plausible candidates as they are i

98 Because CARPs are overexpressed in cancer and their silencing re

99 Furthermore, CARPs are rapidly cleaved during apoptosis.

100 Caspase 8/10-associated RING proteins (CARPs) are a recently described family of protein ubiqui

101 c analysis suggests that at least one of the CARPs arose from a gene fusion.

102 ene encoding cardiac ankyrin repeat protein (CARP), as a novel candidate gene for dilated cardiomyopa

103 rticles were detected in diseased farmed koi carp, ayu, and Atlantic salmon, their genetic relationsh

104 ene, zebrafish ubiquitin promoter and common carp beta-actin promoter, harboring a 250-bp homologous

105 The M184I mutation results in loss of CARP binding with Talin 1 and FHL2, and the P105S mutati

106 pecies richness was halved in lakes in which carp biomass exceeded 190 kg ha(-1) .

107 cover and richness declined exponentially as carp biomass increased such that plant cover was reduced

108 editing tools, are employed to target common carp bone-related genes sp7, runx2, bmp2a, spp1, opg, an

109 laminergic and serotoninergic neurons in the carp brain.

110 oil-in-water emulsions fortified with common carp (C. carpio) roe protein hydrolysate (CRPH) were exa

111 Co-transfection assays indicate that CARP can negatively regulate an HF-1-TK minimal promoter

112 ntextually appropriate response perspective (CARP) can be judged, in part, by its potential to stimul

113 ct transgene expression under control of the CARP (cardiac ankyrin repeat protein) promoter, which is

114 ctin, titin, cardiac ankyrin repeat protein (CARP), cardiac-specific RNA-helicase activated by MEF2C

115 cyhv3Il10 exerts any biological activity on carp cells.

116 fold with 4.97% recovery from the viscera of carp Cirrhinus mrigala (mrigal) by ammonium sulfate prec

117 Four fish species were examined: pike, carp, cod, and herring.

118 We refer to this approach as CARP: Combined Analysis of RNA-seq and PRO-seq.

119 In this study, using purified carp cone membrane preparations, we first confirmed that

120 The lower effectiveness of PDE activation in carp cones is due partly to the fact that the activation

121 vated visual pigment (R*) is 5-fold lower in carp cones than in rods.

122 These findings indicate that CARP could play a unique role in therapeutic angiogenesi

123 ng black carp (Mylpharyngodon piceus), grass carp (Ctenopharyngodon idella), bighead carp (Hypophthal

124 highly invasive fish in Europe) by resident carp Cyprinus carpio was tested in experimental mesocosm

125 een quantitative PCR assay to observe Common Carp ( Cyprinus carpio ) eDNA degradation in laboratory

126 The common carp (Cyprinus carpio) as one of the most important aqua

127 ure and trophic state on the decay of Common Carp (Cyprinus carpio) eDNA was evaluated using lake wat

128 e we investigated the effects of exposure of carp (Cyprinus carpio) primary hepatocytes to the human

129 fication of proteinase inhibitor from common carp (Cyprinus carpio) sarcoplasmic proteins resulted in

130 a to show that managed aquaculture of common carp (Cyprinus carpio) was present at the Early Neolithi

131 Carp (Cyprinus carpio), although closely related to zebr

132 r carp (Hypophthalmichthys molitrix), common carp (Cyprinus carpio), and goldfish (Carassius auratus)

133 inbow trout (Oncorhynchus mykiss) and common carp (Cyprinus carpio).

134 muscle and gonad tissues of marketed common carp (Cyprinus carpio).

135 The common carp, Cyprinus carpio, is one of the most important cypr

136 e central nervous system (CNS) of the common carp, Cyprinus carpio, with the aim of comparing its ana

137 ewater, landfill leachate, and biosolids (NY CARP data set) to determine whether peri and peri/latera

138 q and ribosome profiling, demonstrating that CARP defines a comprehensive repertoire of targets.

139 rotein (MARP) genes (myoD, myogenin, MLP and CARP) depended both on peak muscle stress achieved durin

140 ce-dependent manner in cardiac myocytes, and CARP displays a transcriptional inhibitory activity when

141 In regions dominated by carp (e.g., Great Plains), carp had a stronger impact on

142 Common Carp eDNA concentration followed a pattern of exponentia

143 t tested the effect of temperature on Common Carp eDNA decay.

144 in laboratory mesocosms, our rate of Common Carp eDNA detection decreased over time.

145 In this experiment, Common Carp eDNA exhibited biphasic exponential decay, characte

146 Common Carp eDNA exhibited exponential decay that increased wit

147 strain adheres to epithelioma papillosum of carp (EPC) cells 3 to 5 times more extensively than the

148 tes amassed from 2000+ lakes, we showed that carp exceeded this biomass level in 70.6% of Great Plain

149 ansfer leads to a high vascular density, and CARP exerts effects on endothelial behavior.

150 that alpha(1)-adrenergic signaling regulates CARP expression in cardiac myocytes, in part through the

151 Throughout cardiac development, CARP expression is specific for the myocardium; endocard

152 Long-term inhibition of CARP expression results in suppression of cancer cell gr

153 During murine embryogenesis, endogenous carp expression was first clearly detected as early as E

154 In Nkx2-5(-/-)embryos, carp expression was found to be significantly and select

155 romoter, which suggests that Nkx2.5 controls CARP expression, at least in part, through GATA-4.

156 sitized with recombinant wildtype Cyp c 1 or carp extract by intragastric gavage.

157 Additionally, we show that CARP facilitates the dissection of complex changes in ge

158 tionally washed minces from kilka and silver carp fillets; either alone or after blending.

159 The CARP gene encodes a nuclear co-regulator for cardiac gen

160 alpha(1)-adrenergic signaling activates the CARP gene, a 660 bp fragment of the mouse CARP promoter

161 e cardiac-restricted ankyrin repeat protein (CARP) gene as a model system to study these mechanisms.

162 me, and open avenues for facilitating common carp genetic studies and breeding.

163 We believe that the grass carp genome could serve as an initial platform for breed

164 hly efficient tools for modifying the common carp genome, and open avenues for facilitating common ca

165 ers for black carp, grass carp, and a common carp/goldfish are reported and details of the marker tes

166 New markers for black carp, grass carp, and a common carp/goldfish are reporte

167 nalysis between zebrafish and medaka, common carp, grass carp, and goldfish to study the genome evolu

168 ions dominated by carp (e.g., Great Plains), carp had a stronger impact on plant richness than human

169 Since CARP has been reported to be a transcriptional co-repres

170 When fused to a GAL4 DNA-binding domain, CARP has transcriptional inhibitory properties in noncar

171 enome and long generation-time of the common carp have made its breeding and genetic studies extremel

172 Exposure of the primary carp hepatocytes to the pharmaceuticals ibuprofen (IBU),

173 Omnivorous fish species (carp, herring) contained more TGs than did predatory one

174 kilka (Clupeonella cultriventris) and silver carp (Hypophthalmichthys molitrix) affected dynamic rheo

175 ad carp (Hypophthalmichthys nobilis), silver carp (Hypophthalmichthys molitrix), common carp (Cyprinu

176 obin (Mb) and haemoglobin (Hb), from bighead carp (Hypophthalmichthys nobilis), during 9 days of iced

177 rass carp (Ctenopharyngodon idella), bighead carp (Hypophthalmichthys nobilis), silver carp (Hypophth

178 Similar to mammalian IL-10, carp Il10 acts through a signaling pathway involving pho

179 ecretome and is structurally very similar to carp Il10 and also human IL10.

180 urrent study, we investigated the effects of carp Il10 on phagocytes and lymphocytes.

181 Overall, carp Il10 shares several prototypical activities with ma

182 Carp Il10 shares several prototypical inhibitory activit

183 is suggests that, under these circumstances, carp Il10 stimulates a subset of CD8+ memory T cells whi

184 ddition to the regulatory effect on T cells, carp Il10 stimulates proliferation, differentiation, and

185 l10 is biologically active and, similarly to carp Il10, signals via a conserved Stat3 pathway modulat

186 s that cyhv3Il10 is a true viral ortholog of carp Il10.

187 In particular, Indian major carps (IMCs) are highly susceptible to this disease.

188 ed minces, respectively, of kilka and silver carp improved physico-mechanical properties of the resul

189 ere it is sequestered by the adaptor protein CARP in a multiprotein complex together with PLCbeta1.

190 ontrast to previous studies using the common carp, in which temperature-specific MyHC isoform genes w

191 ifestation of behavioral fever in the common carp infected by cyprinid herpesvirus 3, a native carp p

192 Four days after infection, CARP-infected sponges in rats showed a remarkable increa

193 e showed many more LacZ-positive cells in Ad-CARP-infected sponges than in virus controls.

194 tion experiments in HeLa cells indicate that CARP inhibits Nkx2.5 transactivation of atrial natriuret

195 y of 17 proposed strategies to prevent Asian carp invasion of the Laurentian Great Lakes via the hydr

196 Thus, CARP is a YB-1 associated factor and represents the firs

197 y cell types including vascular endothelium, CARP is also a structural component of the sarcomere.

198 The grass carp is an important farmed fish, accounting for approxi

199 Following observations that CARP is differentially expressed in the Spalax muscle in

200 and RNase protection assays, suggesting that carp is downstream of the homeobox gene Nkx2-5 in the ca

201 However, because CARP is in a group of fetal genes activated in the adult

202 In mouse and human models, CARP is induced during wound healing, denervation, neuro

203 Cardiac ankyrin repeat protein (CARP) is a nuclear transcription cofactor that is activa

204 rtain genes (such as myoD, myogenin, MLP and CARP) is sensitive to muscle stress while another (Arpp/

205 The malformations in Carp-Lbh transgenic mice reflect impaired pulmonary outf

206 sion were also observed in embryonic day 9.5 Carp-Lbh transgenic mice.

207 isms using the carp monocytic cell line CLC (carp leukocyte culture).

208 and a soluble beta-glucan were used to train carp macrophages, after which cells were rested for 6 d

209 Carp maintained at 24 degrees C died from the infection,

210 unusual cellular distribution and actions of CARP make it a novel candidate gene in tissue repair.

211 ant vertebrates, painted turtles and crucian carp, meet the challenge of variable oxygen in fundament

212 We conclude that the CARP model is an efficient method for predicting catastr

213 d truth data generated by simulations of the CARP model with known parameters.

214 of M. marinum virulence mechanisms using the carp monocytic cell line CLC (carp leukocyte culture).

215 that alpha(1)-adrenergic signaling activates CARP mRNA expression in rat cardiac myocytes.

216 The pattern and timing of CARP mRNA expression, including transient expression in

217 cyprinid fishes are present, including black carp (Mylpharyngodon piceus), grass carp (Ctenopharyngod

218 s demonstrate that coral acid-rich proteins (CARPs) not only bind Ca(2+) stoichiometrically but also

219 To examine the effects of CARP on wound healing, we developed an adenoviral CARP v

220 The carp osteocalcin antibodies, cross-reactive to other spe

221 Using an immunoassay for carp osteocalcin, we determined that the relative conten

222 We have characterized the Cyprinus carpio (carp) osteocalcin for mineral binding to hydroxyapatite,

223 CARP overexpression in wounds by adenoviral gene transfe

224 fatty acid binding protein (beta-barrel) and carp parvalbumin (alpha-helical).

225 We present here the study of a mutant of carp parvalbumin bearing a single tryptophan residue at

226 We investigated whether resistance of carp parvalbumin to digestion affects oral tolerance ind

227 infected by cyprinid herpesvirus 3, a native carp pathogen.

228 l antibody, but no correlation with the anti-carp PAV monoclonal antibody.

229 CARPs physically interact with and ubiquitinate p53, tar

230 alysis shows that the introduction of common carp played a key role in driving a severe reduction in

231 The carp primary hepatocyte model serves as a useful system

232 se mice demonstrate the novel utility of the CARP promoter as an inducible element responsive to path

233 (1)-adrenergic signaling, bound to the mouse CARP promoter at several sites as determined by gel mobi

234 actors is required for basal activity of the CARP promoter in cardiac myocytes.

235 ors could not potentiate the response of the CARP promoter to alpha(1)-adrenergic stimulation.

236 he CARP gene, a 660 bp fragment of the mouse CARP promoter was cloned.

237 Previous reports suggested that the mouse CARP promoter was dependent on the GATA4 transcription f

238 GATA4 transcription factor whereas the human CARP promoter was dependent on transcriptional enhancer

239 lines of transgenic mouse harboring various CARP promoter/lacZ reporters, we have identified distinc

240 Five antioxidant peptides were identified in carp protein ex vivo and in vitro hydrolysates: FIKK, HL

241 with antioxidant properties released during carp protein ex vivo and in vitro hydrolysis by human/po

242 When CH was added to a silver carp protein isolate prior to gelation, the gel behavior

243 Intracellular localization of mutant CARP proteins is not altered.

244 Carp proteins were more resistant to hydrolysis by porci

245 two cosmopolitan, invasive cyprinids (common carp, Prussian carp) were fed to captive mallards.

246 unidirectional Rb+ flux analysis in crucian carp red blood cells (RBCs).

247 Model parameters showed that carp reduced species richness to a similar degree across

248 We identify a chromosome fusion in grass carp relative to zebrafish and report frequent crossover

249 es undergo near-suspended animation, whereas carp remain active and responsive in the absence of oxyg

250 Grass carp reovirus (GCRV) is a member of the aquareovirus gen

251 Grass carp reovirus (GCRV) is a member of the Aquareovirus gen

252 nstruct a backbone model of the entire grass carp reovirus capsid and provide valuable functional ins

253 ar-atomic-resolution cryoEM map of the grass carp reovirus virion, a member of the Aquareovirus genus

254 es 11-cis-retinal from 11-cis-retinol in the carp retina.

255 teady and flickering light adaptation in the carp retina.

256 he potential of converting the soft textured carp roe mass into stable fish roe powder with superior

257 thesis in liver is associated with the grass carp's adaptation from a carnivorous to an herbivorous d

258 zebrafish cytokines and for the isolation of carp serum, which are essential components of the medium

259 In this area, CARP sheds new light on some old problems.

260 -osteocalcin from 2 pufferfish compared with carp shows that there are many conserved features in tel

261 CARP silencing stimulates p53 expression and promotes do

262 With CRISPR-Cas9, the two common carp sp7 genes, sp7a and sp7b, were mutated individually

263 We also identified DNA from one Asian carp species invasive to the Great Lakes but that had no

264 microcosms and quantitative PCR for a Common Carp-specific genetic marker in two experiments.

265 Seven days after TAC, CARP-ssARKct hearts had elevations in left ventricular m

266 ugh ssARK1 was increased in the hypertrophic CARP-ssARKct mice, the in vivo loss of ssAR responsivene

267 Consistent with this, adult CARP-ssARKct transgenic mice have normal in vivo cardiac

268 ARPs is induced upon injury and hypertrophy (CARP), stretch or denervation (ankrd2/Arpp), and during

269 s (KHV), a highly virulent disease affecting carp that emerged in the late 1990s, is a serious threat

270 We showed previously in carp that more light (>100-fold) is required in cones th

271 aspases-8- and -10-associated RING proteins (CARPs)] that bind to and negatively regulate DED caspase

272 In mice deficient for both MLP and CARP the chronic PKCalpha signalling chain at the interc

273 mic status differences in behavior and apply CARP to broader, policy-relevant issues in criminology.

274 We apply CARP to multiple miRNAs and show that it robustly distin

275 ury-old invasion, the introduction of common carp to North America, to illustrate potential consequen

276 e the Cascading Alternating Renewal Process (CARP) to forecast interconnected global risks.

277 CARP transcripts are prominent in cardiogenesis and musc

278 Ad-CARP treatment also induced neovascularization and incre

279 on wound healing, we developed an adenoviral CARP vector to treat subcutaneously implanted sponges in

280 When overexpressed, CARPs, via an IAP-like RING domain, can contribute to th

281 ovirus (SHRV) (SHRV-G), or spring viremia of carp virus (SVCV) (SVCV-G), elicited protective immunity

282 viruses, chandipura virus and spring viremia carp virus.

283 ing model selection analysis, we showed that carp was a key driver of plant species richness along wi

284 subcellular) changes in the outer retina of carp was assessed.

285 stry and in situ hybridization revealed that CARP was expressed in skeletal muscle, vessel wall, hair

286 Quantitative RT-PCR showed that CARP was strongly induced during the first day after wou

287 69 BMFs from 19 species (primarily trout and carp) was developed from the literature.

288 , desmin and cardiac ankyrin repeat protein (CARP) was evident in rat cardiomyocytes expressing MYPN(

289 Cardiac ankyrin repeat protein (CARP) was identified by subtractive hybridization as one

290 calcium-permeable AMPA receptor plasticity (CARP), we examined whether AMPA receptor exchange was me

291 rates of consensus ankyrin repeat proteins (CARPs), we find a clear increase in folding rates with i

292 Using CARP, we also demonstrate estimation using a disparate d

293 location and reduced binding of Y20C-MYPN to CARP were demonstrated using in vitro and in vivo system

294 Carps were shown to acquire pOKR like goldfish while zeb

295 n, invasive cyprinids (common carp, Prussian carp) were fed to captive mallards.

296 markers were orthologous to genes in common carp, which had four rounds of WGD.

297 yprinid herpesvirus 3 infects common and koi carp, which have PKZ, and encodes the ORF112 protein tha

298 t of major economic losses in common and koi carp worldwide.

299 Given the robustness of the approach, CARP would be particularly suitable for dissecting miRNA

300 report frequent crossovers between the grass carp X and Y chromosomes.