ライフサイエンスコーパス: be expressed in

1 All costs are expressed in 2017 euros (euro ).

2 and LASP2, are more structurally diverse and are expressed in a broader array of tissues.

3 e human TNF/LT locus genes TNF, LTA, and LTB are expressed in a cell type-specific manner.

4 eceding studies confirm that PD-L1 and PD-L2 are expressed in a high percentage of OASCs.

5 Two isoforms of MyBP-C (fast- and slow-type) are expressed in a muscle type-specific manner.

6 red several novel interactors of MAFR-1 that are expressed in a sperm- and germline-enriched manner.

7 ysis revealed that only 13% of Wolffia genes are expressed in a time-of-day (TOD) fashion, which is l

8 e gamma subunit by three genes, all of which are expressed in a tissue-specific manner.

9 associated antigen family A (MAGEA) antigens are expressed in a wide variety of malignant tumors but

10 that human leukocyte antigen (HLA) genes may be expressed in a cell type-specific and allele-specific

11 onstrate that the chemokine receptor Cxcr3.2 is expressed in a distinct subset of macrophages in the

12 nlp-2 is expressed in a pair of olfactory AWA neurons and cycl

13 Foxp2 is expressed in a subset of Layer VI cortical neurons.

14 ll sequencing data, we demonstrate that ACE2 is expressed in a subset of secretory cells in the respi

15 PAR4 is expressed in a variety of tissues and cell types, inc

16 ASP1) is a unique actin-binding protein that is expressed in a wide range of cells including neurons,

17 Surprisingly, we found that Piga was expressed in a fairly restricted pattern in the earl

18 , 13 protein-coding EoE candidate risk genes were expressed in a genotype-dependent manner.

19 ly regulated genes involved in tumorigenesis were expressed in a highly coordinated manner across end

20 Instead, familiar representations were expressed in a subset of hippocampal areas, with an

21 involving axonal retraction given that KIFC1 is expressed in adult neurons as well as developing neur

22 In mice, we demonstrate that PI5P4Kalpha is expressed in adulthood, whereas PI5P4Kbeta is express

23 egulation in the SAE of smokers; and 5) ACE2 is expressed in airway epithelium differentiated in vitr

24 Although PIF4 is expressed in all aerial tissues including the epiderm

25 ; 4) there is a unique opsin transcript that is expressed in all eight of the photoreceptive units de

26 In adult rodents, Rbfox2 is expressed in all retinal ganglion cell (RGC) subtypes

27 und that 11 715 genes and 15 852 transcripts were expressed in all 11 tissues and that 849 house-keep

28 cells and found that alphaV-integrin (CD51) was expressed in almost all cardiac PW1(+) cells (93% +/

29 lly expressed in beta-cells, whereas JAGGED1 is expressed in alpha-cells.

30 We find that miR-181a is expressed in amacrine cells during development and in

31 We observed that Hes1 is expressed in an oscillatory manner in activated stem

32 The ETS-transcription factor pointed (pnt) is expressed in an overlapping domain to mid in the foll

33 lity and for genes that in later development are expressed in anatomical patterns that highly corresp

34 Nearly two-thirds of the transcripts that are expressed in anatomically similar tendons were diffe

35 The water channel protein aquaporin-4 (AQP4) is expressed in astrocytes and mediates water flux acros

36 interactions are important in HD and fl-mHTT is expressed in astrocytes, it has not been determined w

37 are produced when a TCP transcription factor is expressed in axillary meristems and binds to the prom

38 e membrane-distal ectodomain of murine BTNL2 was expressed in bacteria as inclusion bodies, refolded

39 r expression in the SAE; 2) in the SAE, ACE2 is expressed in basal, intermediate, club, mucus, and ci

40 hough ~50% of total cerebellar Lphn3 protein is expressed in Bergmann glia, Lphn3 deletion from Bergm

41 cluding Apolipoprotein E (APOE) are found to be expressed in blood-derived macrophages and thus may a

42 All Panxs are expressed in bone, but their role in bone cell biolo

43 show that over 74% of identifiable circRNAs are expressed in both conditions and over 40 circRNAs ar

44 of the human ClC-K chloride channels, which are expressed in both the kidney and inner ear.

45 ntrast agents is often limited by the target being expressed in both healthy and tumour tissues.

46 ort that, in human and mouse prostates, Klf5 is expressed in both basal and luminal cells, with basal

47 Therefore, RORgammat is expressed in both effector and regulatory subsets of

48 Although we report that Toll-like receptor 4 is expressed in both excitatory and inhibitory mouse hip

49 munofluorescence staining showed that CC2D1A is expressed in both excitatory and inhibitory neurons o

50 Direct effects are plausible because KLOTHO is expressed in both germ cells and spermatozoa and form

51 Pcdh-gammaC4 is expressed in both neurons and astrocytes.

52 ssed in the epithelium at E11.5 to E13.5 but was expressed in both dental epithelium and dental papil

53 P2Y14 was expressed in both human and rodent pancreatic beta-c

54 Inhibition of the JAK/STAT pathway, which was expressed in both malignant cells and cancer-associa

55 Moreover, while GnRH was expressed in both neuronal cell body and axons in th

56 ocalized to the nucleus and the OsCADT1 gene was expressed in both roots and shoots.

57 ension and in rats with PAH, Kv11.1 channels were expressed in both the large and small PAs.

58 We show that Pkm2 is expressed in cardiomyocytes during development and im

59 RNA-based BLAS can be expressed in cells and used for the intracellular mon

60 or core binding factor beta (CBFbeta), which is expressed in cells in limiting quantities.

61 we show escapes nonsense mediated decay and is expressed in CH patient nerves.

62 idence that orexin and its related receptors are expressed in chicken hepatocytes.

63 5HTR2A/2B/2C and MAO-A/TPH1 are expressed in cholangiocytes and HSCs from BDL rats a

64 g Xenopus tropicalis We discover that Dyrk1a is expressed in ciliated tissues, localizes to ciliary a

65 We determined that Basigin is expressed in close proximity to integrin at the glial

66 er, some EN subtype-specific genes from mice are expressed in completely distinct morphologically def

67 We find that NRCAM is expressed in cortical astrocytes, localizes to perisy

68 IL-17a receptor was expressed in cortical glutamatergic neurons under st

69 mRNA transcript variants of the AR gene are expressed in CRPC cells and can be translated to pro

70 Both GEP1 and GCalpha are expressed in cytoplasmic puncta of both male and fem

71 TaNRT2.5 is expressed in developing grain, particularly the embry

72 Genes of the Notch signaling pathway are expressed in different cell types and organs at diff

73 rent subsets of the tRNA pool in human cells are expressed in different cellular conditions.

74 hybridization, we showed that distinct NOSs are expressed in different subpopulations of cells, with

75 More recently, FPR1 has been shown to be expressed in different types of cancer and in this co

76 EoE risk genes were expressed in disease-relevant cell types, including

77 CCT is expressed in diverse cancers and could be an ideal th

78 We found that many neurotransmitter GPCRs are expressed in each neuron, that neurons also appear t

79 Hivep3 is expressed in early precursors and regulates the post-

80 related to the native strain than when they were expressed in either native or more distantly relate

81 TEX15 is expressed in embryonic germ cells and functions durin

82 Those proteins were expressed in embryonic mouse brain.

83 ycystin-2, TRPP1), a TRP polycystin channel, is expressed in endothelial cells (ECs), but its physiol

84 Two fetal markers were expressed in eosinophilic cells potentially derived

85 tumour suppressor in various solid tumours, is expressed in erythroid cells.

86 Moreover, recombinant CpCP3 was expressed in Escherichia coli.

87 s sharing >40% amino acid sequence identity, were expressed in Escherichia coli Functional characteri

88 enic compounds tested, arsH1 and arsH2 genes were expressed in Escherichia coli, which has an endogen

89 tified Yes1 as the top-ranked candidate that was expressed in Etv2-EYFP(+) cells at E7.75 and E8.25 u

90 47 miRNAs were expressed in EVs and 16 thereof were significantly

91 s) are a family of scaffolding proteins that are expressed in excitatory glutamatergic synapses.

92 representative family members, and variants were expressed in Expi293 cells and tested for binding t

93 t human brain to determine where these genes are expressed in fine detail.

94 e found that more mu opioid receptors (MORs) are expressed in GABA neurons in the neighboring SNr tha

95 s Ena and profilin, but not the formins that are expressed in gamma-neurons.

96 iption factor is for the first time found to be expressed in GI crypt cells, and SHP2 expression in t

97 We show that Opn5 is expressed in glutamatergic warm-sensing POA neurons t

98 Two variants, CAP256-VRC26 (08 and 09) were expressed in glycoengineered Nicotiana benthamiana

99 e demonstrate that the D(1)R-H(3)R heteromer is expressed in HD mice at early but not late stages of

100 X, RUNX2, BMP2, ALP, OCN, BSP and CX43 genes were expressed in hDFC cultured for 1, 7, 14 and 21 days

101 Lapronic was expressed in HEK 293 cells showing a homogeneous cyt

102 ive axis of the renin-angiotensin system and are expressed in HSPCs.

103 e 1 (NAT1) and N-acetyltransferase 2 (NAT2), are expressed in human hepatocytes.

104 Both receptors could be expressed in human T lymphocytes; Epo ligation induce

105 We show that Sox9 is expressed in human and ferret BPs and is required for

106 Given that TRPC4 is expressed in human DRGs and a specific inhibitor is i

107 COX6B2 is expressed in human lung adenocarcinoma (LUAD) and exp

108 Here, we show that FAT10 mRNA is expressed in human retina and identify rod PDE6 as a

109 We show that Mlc1 is expressed in human stem-like GBM cells (GSCs) and is

110 When the FRET probe was expressed in human cells, both FRET efficiency and f

111 This single nucleotide polymorphism was expressed in human embryonic kidney cells, and its e

112 oform 1 and to a lesser extent the isoform 2 were expressed in human brain, and both neuronal and gli

113 Here we observed that Mycl is expressed in immature cDC1s but repressed on maturati

114 tissue heterogeneity revealed that the MCT1 is expressed in inducible beige adipocytes as the emerge

115 SA-CD47 protein was expressed in insect cells and efficiently displayed

116 HNF4A and HNF4G were expressed in ISCs and throughout the intestinal epi

117 inic acetylcholine receptors (mAChRs), which were expressed in Ixodes SG.

118 We demonstrated that Mkrn3 is expressed in Kiss1 neurons of the mouse hypothalamic

119 s a viral homolog of human IL-6 (hIL-6) that is expressed in KSHV-associated malignancies.

120 We found that Drosophila Rh50A is expressed in larval muscles and enriched in the posts

121 n CBH mice.IMPORTANCE The EBV protein EBNA3A is expressed in latently infected B cells and is importa

122 Tgfbetar1 is identified as being expressed in lateral progenitor cells and a Tgfbet

123 l-related homeobox transcription factor CDX2 is expressed in leukemic cells but not during normal blo

124 Characterising how climatic events were expressed in local environments is crucial to under

125 Fatty acid-binding protein 5 (FABP5) is expressed in lung cells, such as alveolar epithelial

126 use lymphatic muscle by PCR, but only Kir6.1 was expressed in lymphatic endothelium.

127 Pez is expressed in macrophages and is critical for their ef

128 Here we report that AIF1L is expressed in major adipose depots and kidney but was

129 lpha-R type 1 isoform (SRD5A1) and aromatase are expressed in male and female beta-cells.

130 we show that class 1 CRISPR-Cas systems can be expressed in mammalian cells and used for DNA targeti

131 first cytoplasmic intermediate filaments to be expressed in mammalian cells during embryogenesis, bu

132 Here we show that, when Ag85A is expressed in mammalian cells, it is glycosylated, doe

133 PKM2 is expressed in many human cancers and is regulated by c

134 Orai1 is expressed in many regions of the mammalian brain; how

135 S100A4 is expressed in many tissues, including smooth muscle (S

136 but not EGF, is upregulated upon damage and is expressed in mesenchymal stromal cells, macrophages,

137 1, the candidate gene for DiGeorge syndrome, is expressed in mesoderm-derived chondrocytes and plays

138 Arsenic respiratory genes were expressed in metatranscriptomic libraries from the

139 , rather than merely adapt to them; and this is expressed in methodological differences between disci

140 Estrogen receptor beta (ERbeta) is expressed in microglia, macrophages within the centra

141 n-coupled receptor class 5 member D (GPRC5D) is expressed in MM and smoldering MM patient plasma cell

142 CSF1R-FRed was expressed in monocytes and macrophages and absent fr

143 reviously unpublished allergens, of which 11 were expressed in more than one expression system, were

144 ER is expressed in most resistance settings; thus, bromodom

145 arge neutral amino acid transporter 1 (which is expressed in most tumours), selectively accumulate in

146 d levels of dopamine receptors (Drd1), which are expressed in motile cilia.

147 K(ATP) channel Kir6.1 and SUR2B subunits are expressed in mouse lymphatic smooth muscle (LSM) and

148 results suggest that, although T-type VGCCs are expressed in mouse lymphatic smooth muscle, they do

149 , phosphodiesterase 5A (PDE5A), was found to be expressed in mouse and human bone as well as in speci

150 replacement strategy in which exogenous SV2A was expressed in mouse neuronal cultures of either sex,

151 CYLD forms were expressed in mouse embryonic fibroblasts, primary T

152 K(ATP) channel subunits Kir6.1 and SUR2B were expressed in mouse lymphatic muscle by PCR, but onl

153 Sox9 was expressed in MTJ, tendon, and bone progenitor cells

154 e respiratory syndrome coronaviruses 1 and 2 being expressed in multiple tissues including the lumina

155 or for the causative coronavirus SARS-CoV-2, is expressed in multiple extrapulmonary tissues, direct

156 equencing analysis, we found here that OLFM4 was expressed in multiple stem/progenitor-like cell popu

157 In Arabidopsis, (AtPTPN was expressed in multiple tissues and upregulated by ABA

158 In patients, PD-1 is expressed in Mycobacterium tuberculosis (Mtb)-infecte

159 nate receptor, glucocorticoid receptor (GR), is expressed in nearly all immune cells.

160 at a low level in neurons, while PI5P4Kbeta is expressed in neuronal populations, especially hippoca

161 Trk-A is expressed in neurons and signals in response to two l

162 (EBNA) and latent membrane proteins (LMPs), is expressed in newly infected B lymphocytes and in post

163 stem-cell-expressed E3 ligases Rnf43/Znrf3, is expressed in nodose-petrosal and geniculate ganglion

164 Because it is expressed in normal and cancerous cells alike, attemp

165 cusing on breast cancer, we found that CD177 is expressed in normal breast epithelial cells and is si

166 Olfactomedin 4 (OLFM4) is expressed in normal prostate epithelial cells and imm

167 Sox9 is expressed in not only tendon and bone progenitor cell

168 In juvenile (L3) males, tra-1 is expressed in numerous neurons; this expression dimini

169 MAL is expressed in oligodendrocytes, in Schwann cells, wher

170 y a new network of zinc-finger proteins that are expressed in one class of preadipocytes and is poten

171 re ubiquitously expressed in tissues, others are expressed in only germ cells with aberrant reactivat

172 Nearly 5000 genes are expressed in only one parent in at least one tissue

173 Here we report that Slit ligands are expressed in overlapping and distinct patterns in bo

174 These loci are expressed in ovules before fertilization and in the

175 Ahnak is expressed in p11-positive as well as p11-negative neu

176 Since it was shown that TGR5 is expressed in pancreatic tissue, a direct TGR5 activat

177 Protein expression analysis showed that ENO1 is expressed in pDC and MM cells; and importantly, that

178 lectron microscopy demonstrated that betaARs are expressed in PF boutons.

179 urotrophic tyrosine kinase receptor 3 (TrkC) is expressed in podocytes and the protein transmits sign

180 ROBO2 is expressed in podocytes, inhibits nephrin-induced acti

181 We report that HuR is expressed in postmitotic projection neurons during mo

182 ions of the Sim1 transcription factor, which is expressed in postmitotic V3 INs.

183 le mice lack C3aR1 receptors, both receptors are expressed in primary cultured microglia.

184 We found that ABCB5 is expressed in primary GBM tumors, in which its express

185 We found that Cx43 was expressed in punctate fashion on astroglia, surround

186 We report that LASP1 is expressed in rat hippocampus early in development, an

187 with variants in the C3, C6, and C10 domains was expressed in rat ventricular myocytes.

188 Rgs16::GFP is expressed in response to caerulein-induced acinar cel

189 ferator-activated receptor alpha (PPARalpha) is expressed in retinal Muller cells, endothelial cells,

190 Although NUCB2/nesfatin-1 is expressed in reward-related brain areas, its role in

191 MCAT is expressed in RGC that are rich in mitochondria.

192 l periodicity, as reported for nlp-22, which is expressed in RIA.

193 wth factor receptor (EGFR) signaling pathway are expressed in RIS.

194 merase, dihydroceramide desaturase-1 (DES1), is expressed in RPE and Muller cells.

195 The protein was found to be expressed in schizonts, be localized at the apical en

196 NG2 is expressed in Schwann cells already associated with th

197 YAP is expressed in self-renewing embryonic stem cells (ESCs

198 pain, including T-type Ca(2+) channels that are expressed in sensory neurons, where they play a role

199 Ringer is expressed in sensory neurons before and after injury,

200 Melatonin receptors are expressed in several cell types in the retina, inclu

201 rom C57BL/6J mice, we demonstrate that Sfxn3 is expressed in several bipolar cell subtypes, retinal g

202 In the skin, AhR is expressed in several cell types, including keratinocy

203 Outside the brain, Kiss1r is expressed in several metabolic tissues, including bro

204 In Arabidopsis they were expressed in similar tissues and double mutants rev

205 We demonstrate that type I IFNRs are expressed in small/medium DRG neurons and that their

206 NT5E was expressed in SMCs > PDGFRalpha(+) cells.

207 luorescence techniques, we showed that PROX1 is expressed in sNCCs localized in the NoR and in the pe

208 In vertebrate embryos, Hedgehog (Hh) is expressed in some anterior basal plate domains and by

209 ncy of transcription, rather than some genes being expressed in specialised cell types.

210 the 4 gnrh-like (gnrhl) preprohormone genes are expressed in specific and distinct neuronal clusters

211 urokinin-1 receptor (NK1R; encoded by Tacr1) is expressed in spinal dorsal horn neurons and has been

212 Intriguingly, homologous WOX gene products are expressed in stem cell-organizing centers and traffi

213 versity and yield were greater when the BGCs were expressed in strains closely related to the native

214 Many are expressed in striking cell class-, type-, or region-

215 We found that ITGA1 was expressed in T cells and that interactions between t

216 best classifier was ROPN1L, a gene known to be expressed in testis, coincidentally the typical locat

217 In contrast to IL-17A and IL-17F, which are expressed in Th17 cells, IL-17D is expressed broadly

218 (3R) and 4 (4R) microtubule-binding repeats are expressed in the adult human brain, the pathological

219 e identified susceptibility genes for asthma are expressed in the airway epithelium, supporting the n

220 oteins, including Hexokinase 1 and Ras, also are expressed in the blood of FXS model mice and pharmac

221 ies: broadly expressed regulatory genes that are expressed in the brain and other organs, and brain-s

222 ne response can be elicited to antigens that are expressed in the brain(1-3).

223 the HECT-domain E3 ligases NEDD4 and NEDD4L are expressed in the crypt stem cell regions and regulat

224 stinal Hh signaling is paracrine: Hh ligands are expressed in the endodermally derived epithelium, wh

225 Maize Rtn1 and Rtn2 are expressed in the endosperm, localize to the ER, and

226 origins, the regions of the enRep locus that are expressed in the enRep-M9l gene are conserved across

227 Of 67 genes mapped to the shared loci, 65 are expressed in the human brain and show cell type-spec

228 P binding cassette (ABC) transporters, which are expressed in the human liver.

229 These enzymes are expressed in the liver and play an important role in

230 CYP2A13 and CYP2A6 are expressed in the lung and may contribute to local pr

231 s 2-arachidonylglycerol (2-AG) or anandamide are expressed in the MHb and MSDB, and that cannabinoid

232 Here we report that multiple MYO7A isoforms are expressed in the mouse cochlea.

233 Six1, Six2, Six4 and Six5 are expressed in the muscle lineage.

234 ntial and sufficient for the fusion of cells-are expressed in the nervous system of different species

235 Cannabinoid type-1 receptors (Cb1R) are expressed in the presynaptic membrane of many synaps

236 Polycystins are expressed in the primary cilium, and disrupting cili

237 MCT1, MCT3, and MCT4 are expressed in the retina and require association with

238 onstitution of active Cre when all fragments are expressed in the same neuroblast.

239 fRNA-Seq, we first determined the genes that are expressed in the whole muscle, including in nonmyoge

240 indication that susceptibility genes tend to be expressed in the brain during periods preceding the t

241 d ATP1A3 and all of its interactors known to be expressed in the brain to establish if variants could

242 l/neonatal paralog of TnI, a gene thought to be expressed in the heart up to the first 24 months of l

243 sferase enzyme, either EHMT2 or SETDB1, must be expressed in the oocyte to specify the asymmetry of 5

244 eceptor (LDLR) and of keratin genes known to be expressed in the outer root sheath of hair follicles.

245 ses (lws, sws1, sws2, rh1, and rh2) known to be expressed in the retina.

246 is lower in the parenchyma of IPF lungs but is expressed in the atypical epithelial cells of the dis

247 Cerebral dopamine neurotrophic factor (CDNF) is expressed in the brain and is neuroprotective.

248 XVP is expressed in the cambium, localized on the plasma mem

249 We show that Wnt3a is expressed in the caudal embryo in a dorsal-ventral (D

250 caused by mutations in the PLP1 gene, which is expressed in the CNS by oligodendrocytes.

251 Fgfbp1 is expressed in the CNS endothelium and secreted into th

252 Here, we report that EPCR is expressed in the colon epithelial cells, CD11c(+), an

253 The otx2b gene is expressed in the developing hypothalamus, and otx2bhu

254 The +TIP Navigator-1 (NAV1) is expressed in the developing nervous system, yet its n

255 However, Nkx2-5 is expressed in the developing SAN junction, suggesting

256 its endogenous promoter revealed that HSP-17 is expressed in the digestive and excretory organs, wher

257 e show that adiponectin receptor 1 (AdipoR1) is expressed in the dorsal raphe nucleus (DRN) and coloc

258 miR-294 is expressed in the heart during development, prenatal s

259 e gene encoding the receptor for SARS-CoV-2, is expressed in the human airway epithelium, with variat

260 TGR5 is expressed in the intestinal epithelium, but it is not

261 feron-alpha (IFNalpha), a type I interferon, is expressed in the islets of type 1 diabetic individual

262 In this context, CD20 which is expressed in the membrane of B cells has received sig

263 MSDB, and that cannabinoid receptor 1 (CB1) is expressed in the MSDB.

264 brates but lost in all other studied groups, is expressed in the nervous system in the sea anemone Ne

265 Here we show that Xenopus sprouty2 is expressed in the optic vesicle at late neurula stage

266 The ClC-2 chloride channel is expressed in the plasma membrane of almost all mammal

267 oss mouse branchial arches, and HOXA2, which is expressed in the second and more posterior branchial

268 n clathrin-mediated endocytic processes, and is expressed in the syncytiotrophoblast (SynT), an epith

269 Here we show that GATA6, which is expressed in the upper pilosebaceous unit of normal h

270 evels occurred when the Pennycress FAE1 gene was expressed in the fae1-1 mutant, with high levels of

271 MYRF was expressed in the well-differentiated secretory cance

272 i.e., MiRALF1 and MiRALF3) from M. incognita were expressed in the esophageal gland with high express

273 oposed marker genes for cortical Sst neurons were expressed in the VTA Sst neurons.

274 earing protein DAP12, which was not known to be expressed in these cells.

275 When A3A is expressed in these cells, UdgX tends to form foci.

276 Here, we show that complement genes are expressed in tissue from patients with cSCC, and C3

277 Although, GPR27 is known to be expressed in tissues that regulate metabolism includi

278 The LTBentero protein was expressed in tobacco plants at up to 5.29 ug g(-1) f

279 visualize T95 dynamics, fluorescent chimeras were expressed in triadin knockout myotubes, and their m

280 coding D27, CCD7 and CCD8 and show that they are expressed in tubercles.

281 PD-L1 is expressed in tumor cells and its interaction with PD-

282 TREM2 was expressed in tumor macrophages in over 200 human can

283 related transcription factor (DMRT), dmd-4, is expressed in two classes of sex-shared phasmid neuron

284 In the rat BNC CCK is expressed in two separate IN subpopulations, termed l

285 ycerol and hydrogen peroxide (H(2)O(2)) that is expressed in various epithelial cells and in macropha

286 ologous to the human CBX7 gene (hCBX7v1) and is expressed in various mouse organs.

287 erase chain reaction, we showed that Tmprss9 is expressed in various mouse tissues, including the bra

288 DUOX1 is expressed in various tissues, including the thyroid a

289 We found that miR-128 was expressed in various tissues, primary murine cells,

290 rmone]/PTHrP [PTH-related protein] receptor) is expressed in vascular smooth muscle (VSM) and increas

291 ng II), Ang-(1-7), and receptors AT1 and Mas-are expressed in vasculogenic progenitor cells derived f

292 The giant protein titin is expressed in vertebrate striated muscle where it span

293 c PAH.Methods: Missense BMP9 mutant proteins were expressed in vitro and the impact on BMP9 protein p

294 e daf-2b genomic locus confirmed that DAF-2B is expressed in vivo and is likely secreted.

295 to ASP in HIV-1 patients indicates that ASP is expressed in vivo, but its role in HIV-1 replication

296 PKCdelta was expressed in VSMCs, and selective PKCdelta inhibitor

297 Here, we found that all NHE isoforms were expressed in wild-type (WT) mouse cochlea.

298 ilament subunits NF-L (NFEL) and NF-M (NFEM) were expressed in wild-type cells but were virtually abs

299 c of HLC allowing the recombinant protein to be expressed in Yeast (such as Pichia pastoris GS115) an

300 nAChR subunit transcripts were expressed in young excitatory and inhibitory neuron