ライフサイエンスコーパス: feline

1 hat the lapping mechanism is conserved among felines.

2 HIVAN in mice, rats, nonhuman primates, and felines.

3 transmitted, protozoan parasite that infects felines.

4 argeted marker selection utilized the recent feline 1.9x genome assembly, concentrating on regions of

5 etic analyses have led to the inference that feline A3Z3 hap V emerged approximately 60,000 years ago

6 It is particularly noteworthy that feline A3Z3 hap V is resistant to FIV Vif-mediated degra

7 Taken together, these findings suggest that feline A3Z3 hap V may have been selected for escape from

8 We also revealed that codon 65 of feline A3Z3 is a positively selected site and that A3Z3

9 Interestingly, one feline A3Z3 variant is dominant, restrictive, and natura

10 In this study, we demonstrated that these feline A3Z3 variants suppress vif-defective FIV infectiv

11 Feline-adapted CWD (Fel(CWD)) was demonstrated in the br

12 eLV Env) protein for productive infection of feline AH927 cells.

13 ocytic cells (derived from normal marrow) in feline alpha-mannosidosis.

14 but still allowed efficient entry into both feline and canine cells without successful infection.

15 how differences in the interactions with the feline and canine TfRs that determine viral host range a

16 the ability of FIV to bind and utilize both feline and human CXCR4 makes the feline model an attract

17 us disease in cats for applicability to both feline and human disease.

18 The feline and human immunodeficiency viruses (FIV and HIV)

19 rfactant system in both NPC1 mutant mice and felines and in NPC2 mutant mice near the end of their ex

20 ina, consistent with MRI findings in rodent, feline, and baboon retinas.

21 tuted was recognized by a majority of human, feline, and canine myasthenia gravis sera.

22 s were highly conserved among human, simian, feline, and ungulate lentiviruses, which indicated that

23 In vivo, neural mapping experiments on feline animal models illustrate one mode of use for this

24 ion sites into the virus binding face of the feline apical domain reduced or eliminated both binding

25 opeptidase N (APN) of their natural host and feline APN (fAPN) as receptors.

26 Using mouse-feline APN chimeras, we identified three small, disconti

27 FIV Vif colocalized with feline APOBEC3 (fA3) proteins, targeted them for degrada

28 thermore, small interfering RNA knockdown of feline APOBEC3 genes resulted in equalization of replica

29 ability of 7 naturally occurring variants of feline APOBEC3, APOBEC3Z3 (A3Z3), to inhibit FIV replica

30 iminish these hallmark features in a chronic feline asthma model.

31 stered after development of chronic allergic feline asthma, MSCs failed to reduce airway inflammation

32 ntrating on regions of low marker density on feline autosomes and the X chromosome, in addition to re

33 cifically detect the DNA of these viruses in feline blood and found that the domestic cat and bobcat

34 e multiple dry samples of human, canine, and feline blood for the ultimate application to forensic sp

35 Of 101 FIV antibody-positive feline blood specimens submitted for FIV PCR diagnosis,

36 ew species, we studied feline CWD (fCWD) and feline BSE (i.e., feline spongiform encephalopathy [FSE]

37 Feline calicivirus (FCV) and murine norovirus (MNV) are

38 solution structures of the VPg proteins from feline calicivirus (FCV) and murine norovirus (MNV), whi

39 Open reading frame 2 (ORF2) of the feline calicivirus (FCV) genome encodes a capsid precurs

40 Here we show how longitudinal analysis of feline calicivirus (FCV) infection in an animal rescue s

41 Here, we examined the effect of feline calicivirus (FCV) infection on SG accumulation.

42 mid was engineered in which the LC region of feline calicivirus (FCV) was placed under the control of

43 Feline calicivirus (FCV), a member of the Vesivirus genu

44 qPCR) for feline herpesvirus type 1 (FHV-1), feline calicivirus (FCV), Mycoplasma felis, Chlamydophil

45 ause of infectious acute gastroenteritis and feline calicivirus (FCV), which causes respiratory illne

46 the attachment and infectious viral entry of feline calicivirus (FCV).

47 cule A (fJAM-A) is a functional receptor for feline calicivirus (FCV).

48 death in young cats, and virulent, systemic feline calicivirus (vs-FCV) causes a highly fatal diseas

49 Previous studies on feline calicivirus and murine norovirus 1 (MNV1) demonst

50 We have shown for feline calicivirus and rabbit hemorrhagic disease virus

51 NV replication were derived from studies of feline calicivirus and rabbit hemorrhagic disease virus,

52 of the canonical start/stop site in huNV and feline calicivirus but not in rabbit hemorrhagic disease

53 el neutralizing B-cell epitope, derived from feline calicivirus capsid protein, and a well characteri

54 Feline calicivirus is a major causative agent of respira

55 we have been exploiting endemic infection of feline calicivirus within five geographically distinct h

56 As has been previously demonstrated for feline calicivirus, a member of the Vesivirus genus, PSa

57 Many viruses, including the related feline calicivirus, use terminal sialic acids (SA) as re

58 in types of feline coronaviruses (FCoVs) and feline caliciviruses (FCVs), respectively, and are impor

59 Adult feline cardiomyocytes in primary culture were treated wi

60 150-kb domestic cat BAC clone containing the feline CCR genes CCR1, CCR2, CCR3, and CCR5 to further a

61 ssion of CD134 in the cat using a novel anti-feline CD134 monoclonal antibody (MAb), 7D6, and showed

62 in the first cysteine-rich domain (CRD1) of feline CD134 to confer near-optimal receptor function, w

63 D134 expression on human and murine T cells, feline CD134 was abundant on mitogen-stimulated CD4+ T c

64 The feline cDNA identified by this method was approximately

65 The feline cDNA shares approximately 93% amino acid sequence

66 hDC-SIGN) and that infection of a permissive feline cell line (Crandall-Reese feline kidney) was mark

67 rrin receptors (TfR) on the surfaces of live feline cells and to monitor how these CPV-TfR complexes

68 bited FPV and CPV-2 binding and infection of feline cells but not CPV-2b, indicating that the recepto

69 urface with different kinetics in canine and feline cells but, unlike transferrin, most did not recyc

70 In FIV-infected feline cells, some intranuclear Gag was detected in the

71 tor binding, and relative in vitro growth in feline cells.

72 preading replication and passage of HIV-1 in feline cells.

73 achment, uptake, and infection in canine and feline cells.

74 e cells while they bound to the cell body of feline cells.

75 his budding mechanism is highly conserved in feline cells.

76 FIV) replication in lymphoid and nonlymphoid feline cells.

77 at and dog genomes, with an expansion of the feline chemosensory system for detecting pheromones at t

78 rming growth factor (TGF)-beta-dependence of feline corneal keratocyte differentiation into alpha-smo

79 Anti-TGFbeta treatment reduced feline corneal myofibroblast differentiation in vitro an

80 Feline coronavirus (FCoV), porcine transmissible gastroe

81 We showed that entry of the serotype II feline coronavirus strains feline infectious peritonitis

82 f felids caused by systemic infection with a feline coronavirus.

83 rus infection are caused by certain types of feline coronaviruses (FCoVs) and feline caliciviruses (F

84 irulent strains of serotype 1 and serotype 2 feline coronaviruses.

85 Hypercomplex cells found in feline cortex and small target motion detectors found in

86 n (GFP) in HIV-1 entry receptor-complemented feline (CrFK) cells enabled robust spreading HIV-1 repli

87 1 and hCRM1 and comparing those sequences to feline CRM1, we mapped the functional domain to HEAT (Hu

88 of transmission to a new species, we studied feline CWD (fCWD) and feline BSE (i.e., feline spongifor

89 Upon subpassage, feline CWD was transmitted to all i.c.-inoculated cats w

90 patterns consistent with the early stage of feline CWD.

91 croti infection in cats and suggest that the feline disease is a spillover from a disease maintained

92 cies, including non-human primates, canines, felines, equids, ovids, suids, bovins, salmonids and mur

93 The native recombinant feline erythropoietin (rfEPO) sequence was confirmed by

94 In this in vitro study, feline erythropoietin cDNA was cloned from feline renal

95 e in vitro production of biologically active feline erythropoietin.

96 phologically divergent trajectories early in feline evolution.

97 Excised feline eyeballs preserved in corneal storage medium and

98 hereas weaker cross-reactivity occurred with feline (feline infectious peritonitis virus) and canine

99 s indeed blocked by FeLV-A infection, and in feline fibroblasts that naturally express feTHTR1 and no

100 Feline fibroblasts, T-cell lines, and primary peripheral

101 of rotavirus in cats and the first report of feline G6P[9], which questions the previous belief that

102 tion (FIVDelta vifATGgamma) that coexpresses feline gamma interferon (IFN-gamma) was tested as a prov

103 Infection with a recombinant murine-feline gammaretrovirus, MoFe2, or with the parent virus,

104 sitions for 663,480 contigs, 20,285 putative feline gene orthologs, and 133,499 conserved sequence bl

105 and to aid in assembly of a higher coverage feline genome sequence.

106 tified viruses may have important effects on feline health and ecology.

107 , accessible species for advancing human and feline health.

108 Cardiac injury was induced in the adult feline heart by infusing isoproterenol (ISO) for 10 days

109 aMKII-CA infected NRVMs and in hypertrophied feline hearts.

110 r) CS/PCs were isolated from 11- and 22-week feline hearts.

111 for mammalian expression of a representative feline heavy (IGHG1a) together with a light (lambda or k

112 ced the variable and constant domains of the feline heavy chains of IgG1a (IGHG1a), IgG2 (IGHG2), and

113 um" strain Birmingham 1, a low-pathogenicity feline hemoplasma strain.

114 ted by quantitative real-time PCR (qPCR) for feline herpesvirus type 1 (FHV-1), feline calicivirus (F

115 We established a feline HFpEF model induced by slow-progressive pressure

116 Sequencing the feline HMB-synthase gene revealed different mutations in

117 The feline homologue of CD134 is the primary binding recepto

118 we report identification and analysis of the feline homologue to the human lectin DC-SIGN and show th

119 eceptor, albeit at lower efficiency than the feline homologue.

120 re two different viral species with distinct feline hosts and evolutionary histories.

121 Like its definitive feline hosts, T. gondii may have entered South America a

122 me sequence that target previous gaps in the feline-human comparative map.

123 between healthy and sick cats diagnosed with Feline Hyperthyroidism (FH).

124 ssociated virus serotype 8 vector expressing feline IDUA from a liver-specific promoter.

125 DNA or with both FIV-pPPRDelta vif DNA and a feline IFN-gamma expression plasmid (pCDNA-IFNgamma).

126 Here we report novel feline Ig sequences, a technique to express antigen-spec

127 GFAP-IL-1betaXAT mice were injected with the feline immunodeficiency virus (FIV) (Cre) vector in the

128 Feline immunodeficiency virus (FIV) and human immunodefi

129 an immunodeficiency virus type 2 (HIV-2) and feline immunodeficiency virus (FIV) but not HIV-1.

130 Infection with feline immunodeficiency virus (FIV) causes an immunosupp

131 Feline immunodeficiency virus (FIV) causes progressive i

132 tested the hypothesis that vectors based on feline immunodeficiency virus (FIV) could be used for co

133 combinant soluble CD134 (sCD134) facilitated feline immunodeficiency virus (FIV) entry into CXCR4-pos

134 We previously observed feline immunodeficiency virus (FIV) Gag accumulating at

135 In feline immunodeficiency virus (FIV) infected cats, daily

136 cells (Tregs) activated during the course of feline immunodeficiency virus (FIV) infection suppress C

137 Herein we demonstrate that in vitro feline immunodeficiency virus (FIV) infection, but not U

138 Feline immunodeficiency virus (FIV) infects many species

139 Feline immunodeficiency virus (FIV) is a lentivirus that

140 Feline immunodeficiency virus (FIV) is among the most co

141 Infection of domestic cats with feline immunodeficiency virus (FIV) is an important mode

142 Feline immunodeficiency virus (FIV) naturally infects mu

143 Feline immunodeficiency virus (FIV) OrfA is an accessory

144 were evaluated for their incorporation onto feline immunodeficiency virus (FIV) particles, transduct

145 A feline immunodeficiency virus (FIV) provirus with a vif

146 ron (IFN-alpha) induced tetherin and blocked feline immunodeficiency virus (FIV) replication in lymph

147 ily conserved on both HIV type 1 (HIV-1) and feline immunodeficiency virus (FIV) reverse transcriptas

148 Feline immunodeficiency virus (FIV) shares with T-cell t

149 The feline immunodeficiency virus (FIV) targets activated CD

150 an immunodeficiency virus type 1 (HIV-1) and feline immunodeficiency virus (FIV) the least.

151 ssion in arthritic joints of mice, using the feline immunodeficiency virus (FIV) vector, which is cap

152 V), bovine immunodeficiency virus (BIV), and feline immunodeficiency virus (FIV) Vif appear specific

153 Stable expression of feline immunodeficiency virus (FIV) Vif-green fluorescen

154 d from the pathogenic GL8 molecular clone of feline immunodeficiency virus (FIV), a range of viral va

155 BIV), equine infectious anemia virus (EIAV), feline immunodeficiency virus (FIV), and Rous sarcoma vi

156 cells and cell lines did not restrict HIV-1, feline immunodeficiency virus (FIV), equine infectious a

157 of CD134 is the primary binding receptor for feline immunodeficiency virus (FIV), targeting the virus

158 pression following a single application of a feline immunodeficiency virus (FIV)-based lentivirus vec

159 epatoma cells following gene transfer with a feline immunodeficiency virus (FIV)-based lentivirus vec

160 We analyzed antibody responses in sera from feline immunodeficiency virus (FIV)-infected and uninfec

161 s were mucosally challenged with 10(2)-10(6) feline immunodeficiency virus (FIV)-infected T cells.

162 es in the production of infectious HIV-1 and feline immunodeficiency virus (FIV).

163 f many viruses, including strains of HIV and feline immunodeficiency virus (FIV).

164 suppresses the infectivity of vif-defective feline immunodeficiency virus (FIV).

165 An infectious chimeric feline immunodeficiency virus (FIV)/HIV strain carrying

166 transmission pathways for three subtypes of feline immunodeficiency virus (FIVPle ) in African lions

167 onprimate lentiviral genomic RNAs (HIV-1 and feline immunodeficiency virus [FIV]) vis-a-vis their Gag

168 s, we evaluated the molecular evolution of a feline immunodeficiency virus derived from a wild cougar

169 This investigation of feline immunodeficiency virus infection in bobcats and p

170 IDS, and their homologues may play a role in feline immunodeficiency virus infection.

171 The earliest experiments were in the cat/feline immunodeficiency virus model, followed a decade l

172 Lion lentivirus (LLV; also known as feline immunodeficiency virus of lion, Panthera leo [FIV

173 TRIMCyp transgenic cat lymphocytes resisted feline immunodeficiency virus replication.

174 eported previously for functional binding of feline immunodeficiency virus SU to its coreceptor CD134

175 , we demonstrate that a fast-evolving virus (feline immunodeficiency virus, FIV) can reveal details o

176 l cross-species transmission of a subtype of feline immunodeficiency virus, puma lentivirus A (PLVA),

177 tranasal insulin treatment of experimentally feline immunodeficiency virus-infected animals resulted

178 us, human immunodeficiency virus type 1, and feline immunodeficiency virus.

179 Although feline infections are typically asymptomatic, infection

180 lethal systemic granulomatous disease called feline infectious peritonitis (FIP), which is one of the

181 Feline infectious peritonitis and virulent, systemic cal

182 Feline infectious peritonitis is a lethal disease of fel

183 Feline infectious peritonitis virus (FIPV) belongs to th

184 Feline infectious peritonitis virus (FIPV) is the leadin

185 f the serotype II feline coronavirus strains feline infectious peritonitis virus (FIPV) WSU 79-1146 a

186 sm targeting CoV main protease (M(pro)) from feline infectious peritonitis virus (FIPV), which leads

187 eaker cross-reactivity occurred with feline (feline infectious peritonitis virus) and canine CoVs.

188 In the veterinary school database, 4.5% of feline intraocular and adnexal neoplasms (234/5153) were

189 of AGN 211334 were characterized in isolated feline iris preparations in organ culture and heterologo

190 Conversely, most (74%) of the feline isolates belonged to ST4, ST6, and ST7.

191 Feline junctional adhesion molecule 1 (fJAM-1) was recen

192 The feline junctional adhesion molecule A (fJAM-A) is a func

193 Feline junctional adhesion molecule A (fJAM-A) mediates

194 FCV attachment and entry is mediated by feline junctional adhesion molecule A (fJAM-A), which bi

195 ion of the capsid proteins alone in Crandell feline kidney (CrFK) cells reproduced the cleavage of th

196 nd monkey, using porcine kidney (PK 032495), feline kidney (NLFK), or baby hamster kidney (BHK-21) as

197 nfection of human 293H cells, Crandall Renal Feline Kidney cell line and primary feline peripheral bl

198 V with a characteristic cytopathic effect in feline kidney cells.

199 permissive feline cell line (Crandall-Reese feline kidney) was markedly enhanced by the overexpressi

200 composition among the study set and archived feline lentivirus sequences.

201 Feline leukemia virus (FeLV) is a naturally transmitted

202 Feline leukemia virus (FeLV) is still a major cause of m

203 The 11-aa targeting domain of the modified feline leukemia virus envelope consists of a constrained

204 is through active heme export by the group C feline leukemia virus receptor (FLVCR).

205 rary within the receptor-binding domain of a feline leukemia virus retroviral Envelope (FeLV Env) pro

206 bon ape leukemia virus, woolly monkey virus, feline leukemia virus subgroup B, feline leukemia virus

207 ed a single-nucleotide coding variant in the feline leukemia virus subgroup C cellular receptor 1 (FL

208 Feline leukemia virus subgroup C cellular receptor 1a (F

209 The feline leukemia virus subgroup C receptor (FLVCR) is a 1

210 The feline leukemia virus subgroup C receptor (FLVCR) is a h

211 abrando et al. reveal that an isoform of the feline leukemia virus subgroup C receptor (FLVCR1) expor

212 ated to mRNA expression of the heme exporter feline leukemia virus subgroup C receptor 1 (beta = -0.3

213 Feline leukemia virus subgroup C receptor 1 (FLVCR1) is

214 key virus, feline leukemia virus subgroup B, feline leukemia virus subgroup T, and 10A1 murine leukem

215 g calicivirus, coronavirus, herpesvirus, and feline leukemia virus, did not.

216 We previously demonstrated that the feline leukemia virus, subgroup C, receptor (FLVCR) expo

217 mestic exposure to gammaretroviruses such as feline leukemia viruses (FeLVs) occurs worldwide, but th

218 to viruses that infect human cells in vitro Feline leukemia viruses (FeLVs) rank high on this list,

219 t least some conservation between murine and feline leukemia viruses is crucial for activity.

220 , including murine leukemia viruses (MuLVs), feline leukemia viruses, and gibbon-ape leukemia virus,

221 After cloning cDNA-encoding feline MAP4 and obtaining its deduced amino acid sequenc

222 271 candidate feline miRNA precursors, encoding a total of 475 mature

223 As a result, there are no feline miRNAs present in the reference miRNA databases,

224 tilize both feline and human CXCR4 makes the feline model an attractive venue for development of broa

225 Using the naturally occurring feline model of MPS I, we tested liver-directed gene the

226 facilitate positional cloning studies in the feline model.

227 ith mannan considerably reduced infection of feline monocyte-derived cells expressing DC-SIGN, indica

228 erent from that of the previously identified feline mutation.

229 m normal and pressure overload-hypertrophied feline myocardium; volume-overloaded myocardium, which h

230 TRPC3/4/6 expression in adult feline myocytes increased rested state contractions and

231 TRPC3/4/6 overexpression in adult feline myocytes induced calcineurin (Cn)-nuclear factor

232 sion of TRPC3/4/6 channels in cultured adult feline myocytes to define mechanistic aspects of these T

233 exal neoplasms (234/5153) were designated as feline ocular posttraumatic sarcoma, a tumor previously

234 xoplasma infection converted the aversion to feline odors into attraction.

235 subtype of HPV76, originally isolated from a feline oral squamous cell carcinoma, was detected in 7 n

236 e oral SCC (OSCC) derived from an osteolytic feline OSCC.

237 revealed two major groups related to either feline panleukopenia virus ("FPV-like") or canine parvov

238 Canine parvovirus (CPV) and feline panleukopenia virus (FPV) are closely related par

239 Canine parvovirus (CPV) and its relative feline panleukopenia virus (FPV) bind the transferrin re

240 s a host-range variant of a virus related to feline panleukopenia virus (FPV).

241 ith canine parvovirus (CPV) or its ancestor, feline panleukopenia virus (FPV).

242 tional felinized monoclonal antibody against feline panleukopenia virus.

243 he structures of canine parvovirus (CPV) and feline parvovirus (FPV) complexed with antibody fragment

244 rus type 2 (CPV-2) emerged as a variant of a feline parvovirus when it acquired mutations that allowe

245 CPV, but not the related feline parvovirus, could use receptors containing a cani

246 he detection and characterization of diverse feline pathogen taxa.

247 address this barrier, we isolated mRNAs from feline peripheral blood mononuclear cells (PBMCs), and u

248 ll Renal Feline Kidney cell line and primary feline peripheral blood mononuclear cells, bioactive rfE

249 ete wet (n = 97) and dry (n = 80) canine and feline pet food sold in the UK was measured to assess co

250 framework for identifying genes controlling feline phenotypes of interest, and to aid in assembly of

251 ation of a recessively inherited early-onset feline PRA.

252 is of these data, which strongly suggest the feline protein is the orthologue of human THTR1, we have

253 The central pathways subserving the feline pupillary light reflex were examined by defining

254 orthologue of human THTR1, we have named the feline receptor feTHTR1.

255 rt arenavirus entry found that the human and feline receptors were able to enhance entry of the patho

256 Pulmonary features of NPC1 mutant felines reflected the disease described in NPC1 mutant m

257 , feline erythropoietin cDNA was cloned from feline renal tissue and utilized in the construction of

258 , a significant association between clinical feline respiratory disease and influenza virus infection

259 ation and oxygen consumption in the detached feline retina.

260 tor, CD134, whereas cats infected with other feline RNA viruses, including calicivirus, coronavirus,

261 est; (ii) fCWD was a more efficient seed for feline rPrP than for white-tailed deer rPrP; (iii) conve

262 , FSE more efficiently converted bovine than feline rPrP; (iv) and CWD, fCWD, BSE, and FSE all conver

263 McDonough feline sarcoma viral (v-fms) oncogene homolog (FMS) and

264 ne homolog (FMS) and v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog (KIT) are two hema

265 ent up-regulation of v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog (KIT) receptor tyr

266 MET through the nonreceptor tyrosine kinase feline sarcoma-related (FER).

267 Expression of the feline SLC35F2 cDNA in nonpermissive cells renders the c

268 Nonetheless, a LIX1-associated etiology in feline SMA implicates a previously undetected mechanism

269 ts of a whole-genome scan for linkage in the feline SMA pedigree using recently developed species-spe

270 To characterize the progression of feline SMA, we assessed pathological changes in muscle a

271 on of the tissue restriction of pathology in feline SMA.

272 tent, if any, muscle fascicles of denervated feline soleus (SO) change length during stance of walkin

273 ree new viruses that are widespread in three feline species, indicates risk factors for infection tha

274 first GHVs identified to be native to these feline species.

275 d push-pull in the motor output stage of the feline spinal cord, a system that allows independent con

276 Feline spinal muscular atrophy (SMA) is a fully penetran

277 ic cats have been shown to be susceptible to feline spongiform encephalopathy (FSE), almost certainly

278 died feline CWD (fCWD) and feline BSE (i.e., feline spongiform encephalopathy [FSE]).

279 uses in human cells and proved beneficial in feline stomatitis patients.

280 sing an in vitro coculture approach to model feline T. foetus infection of the intestinal epithelium,

281 y were to determine the pathogenic effect of feline T. foetus on porcine intestinal epithelial cells,

282 The purified feline TfR inhibited FPV and CPV-2 binding and infection

283 Replacement of critical feline TfR residue 221 with every amino acid had effects

284 Testing feline TfR variants for their binding and uptake pattern

285 reveal that the low affinity of capsids for feline TfRs limits the residence time of capsids on the

286 usive of mammalian species, such as domestic felines, that are not commonly considered intermediate h

287 sporters in mammals, THTR2, and we show that feline THTR1 (feTHTR1) and feTHTR2 both mediate thiamine

288 and characterize the cat miRNAome in normal feline tissues.

289 y used a controlled experimental paradigm in felines to examine whether relearning of motion discrimi

290 gue of the oncoproteins encoded by avian and feline transforming retroviruses, c-Fes has recently bee

291 hus raising the issue of potential cervid-to-feline transmission in nature.

292 carrying eukaryotic expression plasmids for feline tumor necrosis factor (TNF)- alpha , interleukin

293 Forced expression of STIM1 in cultured adult feline ventricular myocytes increased diastolic spark ra

294 In cultured adult feline ventricular myocytes, PKA inhibition protected my

295 l rat ventricular myocytes (NRVMs) and adult feline ventricular myocytes.

296 ST5, and ST8 (zoonosis associated) and ST6 (feline) was statistically significant (P < 0.05), indica

297 hanisms to extraclassical suppression in the feline, we made simultaneous single-unit recordings from

298 Sixteen corneas from healthy felines were obtained immediately after death.

299 Using chimeric feline x human CD134 receptors, the primary determinant

300 Transcriptional analysis revealed that most feline X-degenerate genes have retained housekeeping fun