ライフサイエンスコーパス: be expressed in

1 1 cellular target HLA antigen for the serum was expressed in 238 cases, 209 and 29 being heterozygou

2 Studies have shown that lncRNAs are expressed in a highly lineage-specific manner and co

3 linked to morphological structure formation are expressed in a highly phase-specific pattern, sugges

4 We conclude that Nogo-A and NgR are expressed in a mammalian-like pattern and are upregu

5 Here, we have identified several genes that are expressed in a region-specific manner in the develop

6 While HBEGF has been found to be expressed in a subset of malignant gliomas, its suffi

7 frontal cortical odor-evoked activity, which is expressed in a performance- and task-dependent manner

8 es, located on the long arm of chromosome 4, is expressed in a sharp peak during zygotic genome activ

9 unostaining of anemones, we show that Nv-TLR is expressed in a subset of cnidocytes and that many of

10 The K(+) channel pore-forming subunit Kv4.3 is expressed in a subset of nonpeptidergic nociceptors w

11 Bruton's tyrosine kinase (Btk) is expressed in a variety of hematopoietic cells.

12 The ApoL1 protein is expressed in a wide variety of cell tissues.

13 Additionally, agrp2 was expressed in a small group of neurons in the preopti

14 Recombinant N9 (recN9) proteins were expressed in a baculovirus system in insect cells a

15 mbrane sequence containing a flexible linker were expressed in a cell line derived from PrP knockout

16 rats and identified approximately 600 genes were expressed in a sexually dimorphic manner.

17 Here we show that FTO is expressed in adult neural stem cells and neurons and

18 ine-rich G protein-coupled receptor-5 (LGR5) is expressed in adult tissue stem cells of many epitheli

19 INTU is expressed in adult tissues but its role in tissue mai

20 CD47 isoforms 3 and 4 are expressed in all cell types tested except mature ery

21 Both variants are expressed in all organs with the expression of CvAOX

22 rant and ionotropic receptor genes seemed to be expressed in all libraries.

23 that HTLV-1 bZIP factor (HBZ) protein which is expressed in all ATL cases physically interacts with

24 luorescent reporter knockin lines that Fgfr1 is expressed in all cell populations of the blastocyst,

25 We find that ATML1 is expressed in all epidermal cells.

26 collagen cross-linking enzyme lysyl oxidase is expressed in all vascular cells and that in vivo inhi

27 The SsMT2 gene was expressed in all organs except the flower and its ex

28 1793P, R1845W, and E1883K MSM mutant myosins were expressed in an indirect flight (IFM) and jump musc

29 f the distal-less (Dlx) homeobox gene family are expressed in, and regulate the development of, the b

30 nNOS is expressed in approximately 1% of NAcore neurons.

31 hypoxia-inducible histone demethylase KDM4B is expressed in approximately 60% of EOC tumors assayed,

32 resent in cultured mCCDcl1 cells, and DHHC 3 was expressed in aquaporin 2-positive principal cells of

33 omoter was fused with gusA reporter gene and was expressed in Arabidopsis and rice systems.

34 ve a causative role in the development of PD are expressed in astrocytes and have important roles in

35 ression profiling revealed that 84% of genes are expressed in at least one of the 190 brain structure

36 tor known for mediating xenobiotic toxicity, is expressed in B cells, which are known targets for env

37 Here Loh et al. show that the Y1 receptor is expressed in beta- cells and inhibition of its signal

38 ; chromosome 17 open reading frame 99), that is expressed in bone marrow and fetal liver and whose ex

39 tified a cluster of splicing regulators that are expressed in both beta cells and brain.

40 es are active in only one of two parents but are expressed in both reciprocal hybrids.

41 We demonstrate that HIPK1 is expressed in both androgen-dependent and androgen-ind

42 In T cells, Blimp1 is expressed in both effector (Teff) and regulatory (Tre

43 Here we report that PKC-theta is expressed in both human and mouse ILC2s.

44 s laccase domain-containing 1 (LACC1); LACC1 is expressed in both the cytoplasm and mitochondria.

45 emokine, stromal cell-derived factor 1, that is expressed in cardiomyocytes and decreases calcium inf

46 e show that the full-length CHADL transcript is expressed in cartilage.

47 human 12/15-lipoxygenase orthologue, ALOX12, is expressed in cavitary tuberculosis lesions; the abund

48 ing quantitative RT-PCR, GIMAP6 was found to be expressed in CD3+ cells.

49 ) glycoproteins from influenza A virus (IAV) are expressed in cells, ER stress is induced, resulting

50 of novel intronic circular RNAs (IcircRNAs) are expressed in cells.

51 MpWIP is expressed in cells of the developing air pore complex

52 In conclusion, GPBAR1 is expressed in circulating monocytes and colonic macrop

53 NOX5 was expressed in circulating myeloid DC, and at a lower

54 s mutant Kras but rather the mutant oncogene is expressed in CNS interstitial cells, including neuron

55 excitation and inhibition might develop and be expressed in cortical networks in association with sc

56 Full-length and truncated forms of SPDEF were expressed in CRC cells; cells were assayed for beta

57 -based calcium indicator (4mtD3cpv, MitoCam) was expressed in cultured adult rat cardiomyocytes and t

58 m the plants Mentha spicata and Citrus limon were expressed in cyanobacteria for limonene production.

59 These ZFPs were expressed in D1- vs D2-MSNs using Cre-dependent vir

60 scovered two novel target genes of SoxN that are expressed in denticle-producing cells and that are r

61 RSL class I genes in O. sativa and that each is expressed in developing root hair cells.

62 Many of these proteins are expressed in different tissues and have distinct tis

63 ed for calmodulin-regulated proteins, it may be expressed in different isoforms by alternative gene s

64 e, single cells, tandem copies of FASTmiR122 were expressed in different cell lines.

65 Both BamD and BamE are expressed in diverse gonococcal isolates, under host

66 Likewise, when tagged micro-opioid receptors were expressed in dopamine neurons they too were interna

67 r 40 000 unique human protein fragments have been expressed in E. coli.

68 We show that the CopA chaperone is expressed in E. coli from the same gene that encodes

69 sit peptides encoded a 64.9 kDa protein that was expressed in E. coli, and purified with Ni-NTA agaro

70 , the present study determined that LSD1 (1) is expressed in early dividing cells before OR expressio

71 R expression.IMPORTANCE The EBV protein LMP1 is expressed in EBV-associated epithelial cell diseases,

72 We find that UTF1 is expressed in embryonic and newborn gonocytes and in a

73 Here we report that Fgf20 is expressed in embryonic mammary glands and is regulate

74 0 million years ago became a human gene that is expressed in embryos and cancers, and can be detected

75 ia in 22q11DS, leading to 75% less claudin-5 being expressed in endothelial cells.

76 Claudin-5 is expressed in endothelial cells forming part of the bl

77 nostaining experiments indicated that HAT-L4 was expressed in epithelial cells and exocrine glands in

78 aining homotrimeric neck and lectin domains, was expressed in Escherichia coli BL21(lambdaDE3)pLysS c

79 in embryonic and adult tissues while TET1FL is expressed in ESCs, but repressed in adult tissues.

80 URONASE INVOLVED IN EXPANSION3 (PGX3), which is expressed in expanding tissues and guard cells.

81 GHRH and its receptors are expressed in experimental models of BPH, in which an

82 development by day E15.5, at which time EGR1 was expressed in eyelids of WT mice.

83 ROCK is expressed in fibroblastic, epithelial, endothelial, a

84 For example, cnrip1b is expressed in forming skeletal muscle.

85 RSL) class I basic helix-loop-helix proteins are expressed in future root hair cells (trichoblasts) o

86 Aminopeptidase A (APA) is expressed in glomerular podocytes and tubular epithel

87 We find that all three TET enzymes are expressed in gonadotrope-precursor cells, but Tet1 m

88 orphism encoding EGFR-K521 (K-allele), which is expressed in >40% of HNSCC cases.

89 or potential vanilloid 1 (TRPV1) ion channel was expressed in hADSC, and the TRPV1 ligand capsaicin (

90 This sensory transduction channel is expressed in hair cell stereocilia, and previous stud

91 In the present study, we found that CYGB is expressed in hCPCs.

92 the NCX1 large intracellular loop (YFP-NCX1) were expressed in HEK cells.

93 AGMO is expressed in hematopoietic cells, and is strongly exp

94 lopmentally, GATA-binding protein-2 (GATA-2) was expressed in hematopoietic stem cells, but not in NK

95 Edar (the receptor) is expressed in Hertwig's epithelial root sheath (HERS)

96 vel with human ABCD1, and during development is expressed in homologous regions including the central

97 Ca(2+) -activated K(+) channels (SK, KCa 2) are expressed in human atrial myocytes and are responsib

98 e regulated by Ca(2+) inside the cells; they are expressed in human atrial myocytes and responsible f

99 ort of infected humans and found these genes are expressed in human brain.

100 inding immunoglobulin-like-lectins (siglecs) are expressed in human pancreatic islets in a cell-type

101 scribing the main types of ion channels that are expressed in human synovial fibroblast preparations

102 nducible NK cell-selective transcripts would be expressed in human AMR biopsies and would offer evide

103 ium channel transmembrane regulatory subunit is expressed in human and mouse pancreatic beta cells.

104 DLX5 is expressed in human but not in murine trophoblast.

105 Each of the 852 mutants was expressed in human cells and screened for antigenici

106 We then found CX45 was expressed in human embryonic stem cells (hESCs) and

107 ranscripts encoding heavy metal transporters were expressed in hypnozoites and the copper chelator ne

108 Kcnq1 is expressed in hypothalamic GHRH neurons and pituitary

109 5-LO is expressed in immune cells but also found in cancer ce

110 s an intracellular innate immune sensor that is expressed in immune cells, including monocytes and ma

111 apoptosis pathways and was recently found to be expressed in islet beta-cells.

112 d in the pancreas only during embryogenesis, is expressed in islets of diabetic rodents and humans wi

113 me nonsense codon at an essential lysine can be expressed in its native state only upon genetic incor

114 histochemistry confirmed cathepsin K protein was expressed in LAM but not control lungs.

115 We found that burs alpha and burs beta are expressed in larvae, pupae and newly emerged adults.

116 When tagged D2 receptors were expressed in locus coeruleus neurons, a desensitizi

117 GEA1) is member of the MAGE gene family that is expressed in male germ line cells and placenta under

118 noma (PRAME) is a cancer-testis antigen that is expressed in many cancers and leukemias.

119 e enzyme isoform, glutaminase C (GAC), which is expressed in many cancers, was a late retrotransposit

120 The Tec tyrosine kinase is expressed in many cell types, including hematopoietic

121 dy due to its key role in biomineralization, is expressed in many species and tissues to play a range

122 It is expressed in many tissues where it contributes to org

123 Dipeptidyl peptidase 4 was found to be expressed in mast cells in normal, psoriasis, and mas

124 s is supported by evidence that both enzymes are expressed in mineralizing cells and data showing tha

125 in N-glycolylneuraminic acid (Neu5Gc), which are expressed in most other mammals (14) .

126 CD19 is an attractive CAR target, which is expressed in most B cell malignancies, as well as in

127 TGF-beta signaling components were expressed in most HCC cells, and activation of TGF-

128 Cannabinoid CB2 receptors (CB2Rs) are expressed in mouse brain dopamine (DA) neurons and a

129 isoforms and found that only SGLT1 and SMIT1 were expressed in mouse, rat and human hearts.

130 i.e., dose response), particularly when diet was expressed in mug.

131 Tcf1 is expressed in multiple isoforms, with all isoforms sha

132 SOX5 encodes a transcription factor that is expressed in multiple tissues including heart, lung a

133 We show that SREBF1 is expressed in murine and human osteoblasts, as well as

134 side-VI is expressed in muscle fibers targeted by the ISNb nerve

135 2, a member of the NOD-like receptor family, is expressed in myeloid and bone marrow cells and was im

136 Finally, PGC-1alpha was expressed in NAc D1-MSNs versus D2-MSNs using a Cre-

137 Mucin 4 (MUC4)-tethered mucin is expressed in nasal polyp (NP) epithelial cells and up

138 The maternal UBE3A allele is expressed in nearly all neurons of the brain and spin

139 Our studies reveal that in the embryo, disc1 is expressed in neural progenitor cells of the hypothala

140 CHD7 is expressed in neural stem and progenitor cells, but it

141 that the PCDH-alpha, -beta and -gamma genes are expressed in neurons in a highly organized manner.

142 Gfral is expressed in neurons of the area postrema and nucleus

143 n equivalent mutant Drosophila beta-spectrin is expressed in neurons that extend complex dendritic ar

144 The proteins were expressed in NIH-3T3 fibroblasts, and their activit

145 The OSMR is expressed in nonhematopoietic, nonepithelial intestin

146 cts, showing that Eda and Edar-related genes are expressed in normal palatal tissues and that the Eda

147 In contrast, TET2 is expressed in normal naive B cells and ABC type lympho

148 TET2 is expressed in normal prostate tissue and reduced in a

149 Because both proteins are expressed in normally aging non-HGPS individuals, an

150 CAs are expressed in numerous plant tissues and in different

151 , it is clear that amyloid precursor protein is expressed in numerous cell types and tissues.

152 It is expressed in numerous cell types including T-cells, c

153 In addition, ephrinB1 was expressed in odontoblastic processes 2 wk following

154 Sox8 is known to be expressed in oligodendrocyte precursor cells (OPCs) t

155 pporting the hypothesis that Satb1 and Satb2 are expressed in ON-OFF direction-selective (DS) RGCs, c

156 Chdh transcripts and CHDH protein were expressed in oocytes.

157 We found that TRPV1 is expressed in oriens-lacunosum-moleculare (OLM) intern

158 Sclerostin was expressed in osteocytes from bones from naive and my

159 Whether IPSE homologs are expressed in other schistosome species has not been

160 In summary, CTSD is expressed in pancreatic acinar and inflammatory cells

161 idered "neuron-specific" KCC2 co-transporter is expressed in pancreatic islet beta-cells where it mod

162 em brain tissue demonstrated that pIRE1alpha is expressed in PD brains within neurons containing elev

163 th AS, it is currently unknown whether Ube3a is expressed in peripheral sensory neurons or whether ma

164 -1 receptors, shown by immunofluorescence to be expressed in peritoneal capillaries in mice.

165 cid is a substrate of elongase ELOVL4, which is expressed in photoreceptor cells and generates very l

166 Recombinant thaumatin was expressed in Pichia pastoris and through a co-expres

167 ated in the xylanase by PCR, and the mutants were expressed in Pichia pastoris.

168 duction of a lipid biosynthetic pathway that is expressed in plant cells accommodating fungal arbuscu

169 Utf1 is expressed in pluripotent embryonic stem (ES) cells an

170 The proteins encoded by these genes are expressed in podocytes, and malfunction of these pro

171 immunostaining analysis confirmed that ShcA is expressed in podocytes.

172 8 determines expression of hox5 genes, which are expressed in posterior, but not anterior, vagus moto

173 uring tooth development, ephrinB1, and EphB2 were expressed in preodontoblast and odontoblasts at pos

174 hat Actalpha, Actbeta, and Actgamma isoforms are expressed in primary mouse motoneurons and their tra

175 nt gene signatures of early lung development are expressed in primordial human lung progenitors and r

176 At least one VZV sncRNA was expressed in productive infection of neurons and fib

177 We show that DONSON is expressed in progenitor cells of embryonic human brai

178 Although several 3' Hox mRNAs are expressed in progenitors in a noisy manner, these Ho

179 use cerebellar tissue demonstrated ZNHIT3 to be expressed in proliferating granule cell precursors, i

180 tabolic enzyme myo-inositol oxygenase (MIOX) is expressed in proximal tubules and up-regulated in the

181 Few known malaria drug targets are expressed in quiescent parasites, but pathways invol

182 In conclusion, Nlrp3 is expressed in reactive cholangiocytes, in both murine

183 Plasmodium physiological pathways, while 91% are expressed in replicating schizonts.

184 Repression of GADD45B, which is expressed in response to DNA damage, benefited surviv

185 tide (NT-proBNP) is considered a marker that is expressed in response to myocardial strain and possib

186 We report here that let-7 family members are expressed in retinal and choroidal endothelial cells

187 ive regulator of Wnt/beta-catenin signaling, is expressed in retinal endothelial cells during angioge

188 We show that OsALMT4 is expressed in roots and shoots and that the OsALMT4 pr

189 The tyrosine kinase receptor EGFR is expressed in Schwann cell precursors (SCP), which hav

190 The former two IR genes are expressed in several neurons per sensillum, while IR

191 " K(+)Cl(-) co-transporter 2 (KCC2, Slc12a5) is expressed in several endocrine cells of the pancreati

192 urther analyses showed that the hGH minigene was expressed in several tissues, also leading to increa

193 oderate levels in both fly and human tend to be expressed in similar tissues.

194 Notably, this intron was expressed in solid tumors in a stage-dependent manne

195 and significant association with genes that are expressed in specific cortical layers.

196 Different neuropeptides are expressed in specific, non-overlapping cells in the

197 ount in situ hybridization showed that CrANT is expressed in sperm and fertilized eggs.

198 These sequences are expressed in stigmas and anthers, respectively, and

199 ARPP-16 is expressed in striatal neurons where basal phosphoryla

200 IL-34, TGF-beta1, and BMP-2 were expressed in synovial fluids from RA patients.

201 Matrix metalloproteinase 9 (MMP9) is expressed in teeth from early embryonic to adult stag

202 Environmental impacts are expressed in terms of climate change and biodiversit

203 The seawater chemistry effects can be expressed in terms of the transfer efficiency of basa

204 Association strength (risk) was expressed in terms of odds ratios (ORs) with and wit

205 around one incisional tooth, and color data were expressed in terms of L*, a*, and b* values in acco

206 ember of the relaxin/insulin superfamily and is expressed in testicular Leydig cells.

207 (ERV), account for most novel insertions and are expressed in the absence of histone H3 lysine 9 trim

208 p of two muscle Troponin C (TpnC) genes that are expressed in the adult fruit fly, Drosophila melanog

209 re expressed in the embryonic heart, and 730 are expressed in the adult heart, including 2 novel linc

210 T) genes; two of which, TbSTT3A and TbSTT3B, are expressed in the bloodstream form of the parasite.

211 Moreover, three highly related AKT isoforms are expressed in the brain, but their individual roles a

212 ugh three major Foxp1 isoforms (A, C, and D) are expressed in the brain, only isoform-A has been stud

213 ture, and many genes associated with obesity are expressed in the central nervous system.

214 e show that Fgfr1/2/3 and Fgf7/9/10/22 mRNAs are expressed in the developing primary somatosensory (S

215 The implicated genes are expressed in the developmental and adult human brain

216 Among these lincRNAs, 564 are expressed in the embryonic heart, and 730 are expres

217 Two isoforms of each subunit are expressed in the heart, but the isoform-specific fun

218 itional analyses identified that these genes are expressed in the human superior frontal cortex, that

219 how here that high levels of EVI and MDS/EVI are expressed in the intestine at the climax of metamorp

220 The major clinical phenotypes are expressed in the kidney with dilatation of the colle

221 Both are expressed in the late distal nephron; however, no ev

222 Although Fgfr3 and Fgfr4 are expressed in the mesenchyme and epithelium, inactiva

223 TAS2Rs are expressed in the mouth and in several extraoral site

224 0 antimicrobial peptides and proteins (AMPs) are expressed in the oral cavity.

225 to the calpain family (SmCalp1 and SmCalp2) are expressed in the Schistosoma mansoni tegument.

226 loyl CoA 6'-hydroxylase genes, four of which are expressed in the storage root and, of these, three w

227 lcium binding protein calretinin is known to be expressed in the inner nuclear and the ganglion cell

228 amily member that was recently identified to be expressed in the skin, can induce decorin expression

229 himera studies show that aberrant Pkhd1 must be expressed in the target tissue (cholangiocytes) and t

230 In addition to being expressed in the distal aspects of the nephron, wh

231 PITX2 is expressed in the adult left atrium, but much less so

232 We showed that AKAP13 is expressed in the alveolar epithelium and lymphoid fol

233 e neuropeptide agouti-related protein (AgRP) is expressed in the arcuate nucleus of the mammalian hyp

234 Here, we report that Kv3.4 is expressed in the axonal growth cones of embryonic spi

235 We show that AROM is expressed in the BLA, particularly in the basolateral

236 ceptor for the abundant neuropeptide BigLEN, is expressed in the BLA, we investigated its role in fea

237 Here, we report that tenascin C is expressed in the bone endosteum and is associated wit

238 RT-PCR and confocal imaging that mouse Abcg4 is expressed in the brain capillary endothelial cells.

239 ) and in situ hybridization to test if GPR30 is expressed in the brain regions that might mediate vis

240 One sms-1 isoform is expressed in the C. elegans pharynx, and its transgen

241 We demonstrate that a second TH gene (TH2) is expressed in the CSF-c cells of all the three species

242 in mediating tyrosine kinase signaling, and is expressed in the developing GU-tract in mice and huma

243 und that genetic inactivation of Wise, which is expressed in the developing palatal shelves and encod

244 limb bud, for instance, Sonic hedgehog (Shh) is expressed in the distal posterior mesenchyme, where i

245 Intriguingly, the ligand pdgfaa is expressed in the endoderm medial to the pdgfra-expres

246 Lynx1 is expressed in the habenulopeduncular tract, where alph

247 a monoclonal antibody targeting CD33, which is expressed in the majority of acute myeloid leukemia (

248 Mkx is expressed in the mouse PDL at the age of 10 weeks and

249 Although alpha-syn is expressed in the neuroretina, absence of prominent ag

250 We observed that FTO is expressed in the nuclei, dendrites and near dendritic

251 PRRX1 could be a strong candidate gene as it is expressed in the pulmonary veins, a source of AF in m

252 Our results show that GPR30 is expressed in the retina and in many brain regions tha

253 AQP3 is the AQP that is expressed in the skin where it facilitates cell migra

254 Angptl4 is expressed in the Spemann organizer of Xenopus embryos

255 Here, we show that LRE is expressed in the synergid, egg, and central cells of

256 Troy is expressed in the ureteric bud during embryonic develo

257 During the period of CA growth, Ntn1 is expressed in the ventral two-thirds of the VZ, in add

258 tailed biochemical/biophysical studies, Myo2 was expressed in the baculovirus/Sf9 insect cell system

259 injury without pulp exposure, whereas EphB2 was expressed in the center of pulp niches but not odont

260 The Dp140 isoform was expressed in the cerebral cortex only in foetal life

261 plasts of photosynthetic tissues, while PGK2 was expressed in the chloroplast/plastid of photosynthet

262 ith ALS, but not Con, AD or CJD cases, CHIT1 was expressed in the corticospinal tract and CHIT1 stain

263 This gene was expressed in the dermis, skeletal muscles, periocula

264 Podoplanin was expressed in the IVC wall, where it was localized in

265 The agrp2 gene was expressed in the pineal gland in a previously unchar

266 This direction information was expressed in the right retrosplenial cortex and post

267 further showed that AMOTL2 mRNA and protein was expressed in the trophectoderm of human and mouse bl

268 PfUIS3 was expressed in the viral vectors chimpanzee adenovirus

269 nthesis under anaerobiosis, even though they were expressed in the absence of oxygen.

270 All these genes except for Tph1 were expressed in the brain above the array median, and

271 mmon forms of islet dysfunction and diabetes were expressed in the delta and PP/gamma cell types.

272 High levels of HEL were expressed in the eye compared to low expression thr

273 2 proteoglycans, biglycan and decorin, that were expressed in the palatal shelves prior to adhesion.

274 s and the integrin alpha4 Several chemokines were expressed in the salivary glands of infected and un

275 ts of these genes indicated that these genes were expressed in the skin, with little to no expression

276 The higher symmetry of the ACI perovskites is expressed in their physical properties, which show a

277 h), which encodes a secreted protein signal, is expressed in these sensory neurons, and that experime

278 gulatory transcription factors MYOD and MYF5 being expressed in this disease.

279 During development, slincR was expressed in tissues with sox9 essential functions,

280 These cDNAs were expressed in transgenic plants of a PORB-deficient

281 The MED25 gene is shown to be expressed in trichomes.

282 The MED25 gene is expressed in trichomes.

283 We found that the prevalent patterns are expressed in two opposing gradients.

284 to activate methylated viral promoters that are expressed in type III (but not type I) latency.

285 PD-1 and its ligands are expressed in urothelial cancer, and findings have sh

286 CCAAT/enhancer binding proteins (C/EBPs) are expressed in various tissues, including the CNS.

287 SIGLEC5 is expressed in various myeloid immune cells and classif

288 Pcdh19 was expressed in various brain regions including the cer

289 PRX17 was expressed in various tissues, including vascular tis

290 KATP channels are also thought to be expressed in vascular endothelial cells, but their pr

291 Tissue factor (TF) is expressed in vascular and nonvascular tissues and fun

292 However, CaMYB31 also was expressed in vegetative tissues (leaves, roots, and

293 ere may well be large numbers of miRNAs that are expressed in very particular cell types and remain e

294 ctivator of transcription (Tat) continues to be expressed in virally suppressed patients on cART.

295 Gal-1 is expressed in vivo at concentrations that favor the mo

296 ic activity, aids in intracellular survival, is expressed in vivo, elicits production of antibodies d

297 Both GluD receptors are expressed in wider brain regions than originally tho

298 The mutants were expressed in Xenopus laevis oocytes and tagged with

299 aled AMPA-, Kainate-, and NMDA-type subunits are expressed in zebrafish hair cells.

300 Here we show that RL-TGR is expressed in zebrafish in both i) apical microvilli o