ライフサイエンスコーパス: overexpressed

1 nd this burden varies with the protein being overexpressed.

2 s of neuroblastoma cells, where MYC is often overexpressed.

3 es mitochondrial contacts with rough ER when overexpressed.

4 other B cell malignancies where PKCbetaII is overexpressed.

5 ssivity dramatically elongate telomeres when overexpressed.

6 eased progesterone sensitivity when PR-A was overexpressed.

7 moting adipogenesis in culture when they are overexpressed.

8 s known to block the formation of cilia when overexpressed.

9 erved in vitro unless both SOD1 and CCS were overexpressed.

10 actor and exhibits oncogenic activities when overexpressed.

11 ity of tumour cells specifically when MYC is overexpressed.

12 GJ formation is inhibited even when Cx43 is overexpressed.

13 growth factor-receptor 2 is not amplified or overexpressed.

14 D-associated kinase tethered to the AIS) was overexpressed.

15 at rescued yeast from alphaSyn toxicity when overexpressed.

16 3 antiviral activity when both proteins were overexpressed.

17 We then overexpressed a blw cDNA construct driven by either the

18 y abrogation of binding from molar excess of overexpressed AAV-delivered mAgrin.

19 flammatory signaling in vascular disease, is overexpressed aberrantly in some breast cancers.

20 We found that 18 miRNAs are overexpressed and 28 miRNAs are underexpressed in cSCC c

21 KRAS, VEGFA, and BRD4 Specifically, BRD4 was overexpressed and acquired 5-hmC at enhancer regions in

22 Pathologically, BET proteins are frequently overexpressed and are clinically linked to various types

23 5TMD4, a splice variant of the sst5 gene, is overexpressed and associated with aggressiveness in vari

24 JAGGED2 was also overexpressed and associated with gene amplification in

25 NOTCH ligand JAGGED1 was overexpressed and associated with loss of CpG methylatio

26 Here we show that SPHK1 is overexpressed and constitutively activated in primary AM

27 fin cells and neurons, we now find that both overexpressed and endogenous synuclein accelerate the ki

28 es analyzed, there were areas where Cx43 was overexpressed and found along the lateral membrane of th

29 miR-146a was ectopically overexpressed and inhibited in keratinocytes treated wit

30 group transcriptional repressor Bmi-1 often overexpressed and participated in stem cells self-renewa

31 nant beta-conglutin isoforms (rbeta) that we overexpressed and purified and to their natural counterp

32 We first overexpressed and purified HadA to homogeneity.

33 nzymatic behavior of individual isoforms, we overexpressed and purified the three full-length human i

34 of branch reactions out of the cycle must be overexpressed and the affinity of these enzymes to their

35 erase) in the pentose phosphate pathway were overexpressed, and a geranyl diphosphate synthase from t

36 ondrial perturbations in models where APP is overexpressed, and a potential role of sAPPalpha or othe

37 jor intracellular target of HopAI when it is overexpressed, and MAP kinase signalling is important fo

38 Survivin, an overexpressed anti-apoptotic protein in cancer, represen

39 , OAP formation was considerably enhanced by overexpressed AQP4e.

40 Interestingly, we found that overexpressed ASYN interacted with dynein and induced a

41 we identified a total of 97 genes that were overexpressed at least 1.5-fold in the more invasive tum

42 HIV MDSC overexpressed B7-H4 and silencing B7-H4 increased the pr

43 When overexpressed, BES1 target gene RD26 can inhibit BR-regu

44 y TFs modulate reprogramming efficiency when overexpressed by altering OSK targeting, somatic-enhance

45 otein involved in tissue repair, is markedly overexpressed by cyst epithelial cells.

46 Fibroblast activation protein (FAP) is overexpressed by fibroblastlike synoviocytes in arthriti

47 cell-surface protein CD276/B7-H3 is broadly overexpressed by multiple tumor types on both cancer cel

48 TCTP was knocked down by siRNA or overexpressed by plasmid transfection.

49 oma A2 receptor (EphA2) is a tyrosine kinase overexpressed by tumor stroma and cancer cells.

50 Overexpressed C3G shows predominant cytoplasmic localiza

51 s, and a minor subpopulation (19%) with many overexpressed cancer genes.

52 Notably, patients with FEN1-overexpressed cancers were prone to have poor differenti

53 d cancer cell targeting via interaction with overexpressed CD44.

54 preclinical efficacy evoked by targeting the overexpressed cell-cycle checkpoint kinase CHK1 in SCLC.

55 TIFA protein was overexpressed concurrently with Aurora A and NF-kappaB s

56 celerated when IYO and RIMA are concurrently overexpressed, confirming their functional interaction.

57 ACA11 and MMSET are overexpressed cotranscriptionally as a result of the t(4

58 In addition, overexpressed COX-2 protein repressed the cleavage of ca

59 To test this hypothesis, we virally overexpressed CREB in CA1 of dorsal hippocampus.

60 Two of the overexpressed Cry toxin variants showed significant acti

61 that FL-infiltrating LN and BM stromal cells overexpressed CXCL12 in situ.

62 damage responses 1 (REDD1) is significantly overexpressed during FMF attacks.

63 identifies a suite of pollen-specific genes overexpressed during haploid induction, some of which ma

64 these NSCLC tissues (r = 0.485), suggesting overexpressed FEN1 conferred a proliferative advantage t

65 together, these findings have indicated that overexpressed FEN1 represents a prognostic biomarker and

66 cantly decreased the intracellular levels of overexpressed FLIL33, reversed by treatment with the 20S

67 prr2a transcription is directly repressed by overexpressed Foxc1 in keratinocytes.

68 ed down in HIMECs with small hairpin RNAs or overexpressed from a lentiviral vector.

69 se activity is driven by an N-terminal tumor overexpressed gene (TOG) domain array, proper cellular l

70 Crescerin use arrayed tubulin-binding tumor overexpressed gene (TOG) domains to modulate microtubule

71 rovide comprehensive information on mutated, overexpressed genes and aberrant splicing, which can be

72 When overexpressed, Gliotactin spreads away from the TCJs, re

73 BPP on cell extracts containing recombinant, overexpressed glycosidase as the easily accessible enzym

74 Importantly, when breast tumors overexpressed GRPR, high GRPR expression was also found

75 ompounds were effective in inhibiting the RA overexpressed hCA IX and XII, with KI values in the low

76 Although overexpressed hTACI A181E and mTACI A144E acted as domin

77 To accomplish this goal, we overexpressed human A53T-alpha- synuclein (hA53T-alpha-s

78 vulgare) ortholog and demonstrate that when overexpressed HvEPF1 limits entry to, and progression th

79 nity-variant CARs were constructed targeting overexpressed ICAM-1, a broad tumor biomarker, using its

80 These results demonstrate that overexpressed IGF-2 is the major tumorigenic driver in a

81 found that MYST3 was amplified in 11% and/or overexpressed in 15% of breast tumors, and overexpressio

82 the bone marrow (BM) microenvironment and is overexpressed in 25-30% of patients with acute myeloid l

83 s of breast cancer were considered, GRPR was overexpressed in 86.2% of luminal A-like tumors, 70.5% o

84 ally, binding to the folate receptor (FOLR1) overexpressed in a cancer cell line was measured by flow

85 apeutic target, the prolyl isomerase Pin1 is overexpressed in a majority of HCCs, whereas the mechani

86 We show that MICU1 is overexpressed in a panel of ovarian cancer cell lines an

87 nd NAD(+)-producing enzyme, is amplified and overexpressed in a subset of common types of cancer, inc

88 NEK6 was overexpressed in a subset of human prostate cancers.

89 However, FOXM1 is repeatedly overexpressed in a variety of human cancers, and it has

90 he steroid receptor coactivator 3 (SRC-3) is overexpressed in a wide range of cancers, driving tumor

91 that both FEN1 mRNA and protein were highly overexpressed in about 36% of 136 cancer tissues compare

92 p75(NTR) was overexpressed in anaplastic thyroid cancers compared wit

93 telomerase reverse transcriptase (hTERT), is overexpressed in approximately 90% of human cancers to m

94 ing agent in colorectal cancer, since CEA is overexpressed in approximately 95% of colorectal cancer.

95 further evidence that AURKA is significantly overexpressed in AR-positive CRPC samples carrying ampli

96 ot cause any change in hypocotyl length when overexpressed in Arabidopsis, the overexpression of full

97 ferred resistance to ionizing radiation when overexpressed in Ba/F3 cells under certain conditions.

98 Of them, 40 miRNAs commonly overexpressed in both PDAC and IPMN were selected for fu

99 When isoform 2 was overexpressed in BRAF mutant melanoma cell lines, melano

100 repressive complex 1 (PRC1) complex that is overexpressed in breast and other cancers, and promotes

101 Finally, we show that DPP3 is overexpressed in breast cancer and that elevated levels

102 ted to be a pharmacological target, as it is overexpressed in cancer cells as well as in inflammatory

103 Previously, we identified four proteins overexpressed in cancer-associated fibroblasts and linke

104 one S-transferase pi 1 (GSTP1) is frequently overexpressed in cancerous tumors and is a putative targ

105 MUC1-C is an oncoprotein that is similarly overexpressed in carcinomas and has been linked to epige

106 pharmacologically knocked out or genetically overexpressed in cardiomyocytes.

107 R-32 is an androgen receptor-regulated miRNA overexpressed in castration-resistant prostate cancer an

108 lear factor 1beta (HNF1beta) is ubiquitously overexpressed in CCC and is seen as an attractive therap

109 ates histone H3 lysine 27 trimethylation, is overexpressed in CD30+ anaplastic cells in primary cutan

110 RNF11 is overexpressed in certain tumors, and, importantly, we fo

111 Nlrp3 and its components were overexpressed in cholangiocytes of mice subjected to DDC

112 , a highly conserved molecular chaperone, is overexpressed in CLL compared with resting B cells.

113 eased tumor growth and upregulation of genes overexpressed in colon and lung cancers, respectively.

114 Ca(2+) protein alpha1D of CaV1.3 channel is overexpressed in colorectal cancer biopsies compared to

115 Tau is overexpressed in cytidine deaminase-deficient cells, and

116 Additionally, BCL-W was overexpressed in diffuse large B cell lymphoma and corre

117 Anterior gradient-2 (AGR2) is overexpressed in diverse human adenocarcinomas and it ex

118 We previously reported that Dyrk1A, which is overexpressed in Down syndrome brains, regulates alterna

119 Neurotensin receptor 1 (NTR1) is overexpressed in ductal pancreatic adenocarcinoma, which

120 We found that ADAR2 is overexpressed in EC and that the increase in expression

121 he mouse immunity-related GTPase (IRGM1) was overexpressed in embryonic fibroblasts from dynamin1 lik

122 IRGM1 was overexpressed in embryonic fibroblasts from receptor int

123 endothelial growth factor (VEGF) family are overexpressed in EOC and play key roles in its malignant

124 We found that activated STAT4 was overexpressed in epithelial cells of ovarian cancer and

125 Furthermore, STAiR18 was shown to be overexpressed in every tested tumor entity, indicating i

126 stent with a substrate relationship, Fxr1 is overexpressed in Fbxo4 knockout cells, tissues and in hu

127 microRNA-155 (miR-155) is specifically overexpressed in FLT3-ITD(+) AML compared with FLT3 wild

128 , we showed that lysine demethylase KDM1A is overexpressed in GBM.

129 plore additional mechanisms by which ATP6V1A overexpressed in GCs, we investigated the relationship b

130 In this study, we report that miR-503 is overexpressed in glioblastoma tissue compared with norma

131 tudy, we initially demonstrated that CCR4 is overexpressed in HCC specimens, and its elevation in HCC

132 ctivated chloride channel that is frequently overexpressed in head and neck squamous cell carcinoma (

133 Moreover, we show that USP21 is overexpressed in hepatocellular carcinoma, where it prom

134 mes of the folic acid metabolic pathway were overexpressed in HGS ovarian cancer samples compared wit

135 EYA1 is known to be overexpressed in human breast cancer, in which the Myc p

136 a long noncoding RNA (lncRNA) that is widely overexpressed in human cancer.

137 Pin1 is prevalently overexpressed in human cancers including 70% of HCC, an

138 inactivating enzyme for vitamin D, is often overexpressed in human cancers, potentially neutralizing

139 oncogenic long noncoding RNA that is widely overexpressed in human cancers.

140 ort of many tumor suppressor proteins and is overexpressed in human cancers.

141 dentifying DANCR as a critical lncRNA widely overexpressed in human cancers.Significance: These findi

142 C1) C-terminal (MUC1-C) subunit is similarly overexpressed in human carcinoma cells and has been link

143 Human IRGM was overexpressed in human epithelial cell lines incubated w

144 L-13Ralpha2) is a cancer-associated receptor overexpressed in human glioblastoma multiforme (GBM).

145 More importantly, CDK20 is overexpressed in human lung cancer tissues, as determine

146 However, both proteins are frequently overexpressed in human malignancy.

147 h was present in mvT*s, was also found to be overexpressed in human MCs stimulated with these MVs.

148 Cullin4B-RING E3 ligase complex (CRL4B), is overexpressed in human osteosarcoma cells through an unk

149 Here we demonstrate that IL-35 is overexpressed in human pancreatic ductal adenocarcinoma

150 cally knocked down metabolic genes that were overexpressed in human PDAC tumor samples using short ha

151 Here, we report that TBX2 is overexpressed in human prostate cancer specimens and bon

152 eptide (GRP) receptors (GRPr) are frequently overexpressed in human prostate cancer, and radiolabeled

153 diac sodium channel in HEK293 cells and also overexpressed in induced pluripotent stem cells derived

154 sue, cathepsin K gene expression was 40-fold overexpressed in LAM compared with control lung tissue (

155 Here, we found CNTFRalpha was overexpressed in lower grade gliomas (LGG) compared with

156 The H3K4 demethylase KDM5B is amplified and overexpressed in luminal breast cancer, suggesting it mi

157 w cyclins evaluated, CNTD2 was significantly overexpressed in lung cancer compared to adjacent normal

158 We found that LINC00152 was highly overexpressed in lung tumors as compared to their adjace

159 d gene and open reading frame 2 (Amigo2) was overexpressed in LV12 cells.

160 gulators of cell survival and are frequently overexpressed in malignancies, leading to increased canc

161 oglein 2 (Dsg2), a desmosomal cadherin often overexpressed in malignancies.

162 a the large amino acid transporter, which is overexpressed in malignant cells, leading to tracer accu

163 1 (NRP1), a non-tyrosine kinase receptor, is overexpressed in many cancers including pancreatic and l

164 SETDB1 is overexpressed in many cancers, and loss of this gene in

165 sed of paralogous miRs-183, -96 and -182, is overexpressed in many cancers, including prostate adenoc

166 brane of most normal epithelial cells but is overexpressed in many epithelial cancers.

167 PIM1 is overexpressed in many human cancers and is a promising t

168 for cancer diagnosis and treatment, as it is overexpressed in many solid and hematologic cancers.

169 alpha1A/betaIII tubulin, a neuronal isotype overexpressed in many tumors, proportionally tunes the d

170 ave attracted much interest because they are overexpressed in many types of cancer.

171 ctor with ubiquitin (Ub) ligase activity, is overexpressed in MDS hematopoietic stem/progenitor cells

172 We found that Mps-1 is overexpressed in MM and that its expression correlates w

173 malian 2-Cys peroxiredoxin (Prx) enzymes are overexpressed in most cancer tissues, but their specific

174 ate for HCC targeted therapy because Pin1 is overexpressed in most HCC and activates numerous cancer-

175 hesion, migration, and proliferation and are overexpressed in most tumors, making them attractive the

176 Furthermore, PYCR1 is overexpressed in multiple cancers, and the PYCR1 knock-o

177 24 PCD stage-specific miRNAs are aberrantly overexpressed in multiple myeloma (MM) tumor plasma cell

178 nd CD79B, two clinically established targets overexpressed in multiple myeloma and non-Hodgkin lympho

179 D38) is a type II transmembrane glycoprotein overexpressed in myeloma cells and is implicated in MM c

180 a2b reduces the expression of many cytokines overexpressed in neurofibroma.

181 Mucin 1 (MUC1) is aberrantly overexpressed in NSCLC, activates the nuclear factor-kap

182 ed from the cell surface by metalloproteases overexpressed in numerous cancers.

183 26 is a member of the IL-10 cytokine family, overexpressed in numerous chronic inflammatory diseases,

184 miR-155 is one of the miRNAs overexpressed in obese ATM Exos, and earlier studies hav

185 PAK4 is also overexpressed in other types of cancer, making it a prom

186 that the cell adhesion molecule Nectin-4 is overexpressed in ovarian cancer tumors, and its cleaved

187 iquitin-conjugating enzyme, is significantly overexpressed in ovarian tumors and its expression incre

188 Myosin VI (MVI) has been found to be overexpressed in ovarian, breast and prostate cancers.

189 We found that CCAR2 is highly overexpressed in p53-deficient SCC cell lines compared w

190 model, flow-cytometry revealed that AGR2 was overexpressed in pancreatic cancer stem cells (CSC) comp

191 tein 1 (Sp1), a transcription factor that is overexpressed in pancreatic cancer, activates UPR and re

192 RNA HOX transcript antisense RNA (HOTAIR) is overexpressed in pancreatic cancer.

193 MAN2A1-FER was also overexpressed in PC3 or DU145 (prostate cancer), NIH3T3

194 Altogether, we demonstrate that sst5TMD4 is overexpressed in PCa, especially in those patients with

195 prostate-specific membrane antigen (PSMA) is overexpressed in PCa, it represents a promising target f

196 Kal9 was overexpressed in primary rat cortical neurons or human e

197 igen (PSMA), a transmembrane protein that is overexpressed in prostate cancer (PCa), and evaluated th

198 ETV1/4/5 factors are often overexpressed in prostate cancer and genome-wide studies

199 on of PACE4, a proprotein convertase that is overexpressed in prostate cancer, has been shown to bloc

200 factors ETV1, ETV4 and ETV5, which are often overexpressed in prostate cancer.

201 When overexpressed in rat hippocampal neurons, the hyperactiv

202 mutations in particular domains of Lyn were overexpressed in RAW264 macrophage-like cells or murine

203 GRP3, which is significantly and selectively overexpressed in response to GNAQ/11 mutation in UM.

204 ulating multiple pro-survival mechanisms and overexpressed in response to stress in cancer cells.

205 tokines and various toll-like receptors were overexpressed in SAH neutrophils compared to healthy neu

206 cle checkpoint kinase CHK1, is significantly overexpressed in SCLC, compared to lung adenocarcinoma.

207 ed amino acid transporters (PATs), which are overexpressed in selected tissues and solid tumors.

208 r to human EGF receptors 2 (HER2), which are overexpressed in several cancer cells.

209 Fanconi anemia DNA repair pathway and it is overexpressed in several cancers, representing an attrac

210 ly 7 member 11 (SLC7A11, also called xCT) is overexpressed in several cancers.

211 MMB target genes are overexpressed in several different cancer types and thei

212 GRPr proteins are highly overexpressed in several human tumors, including prostat

213 KDM1A is overexpressed in several tumor types, thus representing

214 Although EGFL7 is aberrantly overexpressed in solid tumors, its role in leukemia has

215 up approximately 8% of the human genome, are overexpressed in some breast cancer cells and tissues bu

216 et al. report that UBE2O, a ubiquitin ligase overexpressed in some human cancers, specifically trigge

217 RNA, the predicted TrkC-premir2 sequence was overexpressed in SW480 cells, which led to the detection

218 S AND Here, we demonstrate that miR-181b was overexpressed in symptomatic human atherosclerotic plaqu

219 f transitional B cells in the spleen and was overexpressed in T1 B cells from BXD2 lupus-prone mice.

220 bedded microRNAs, miR-100 and miR-125b, were overexpressed in the absence of known genetic events lin

221 culum homeostasis and PI3K/AKT signaling, is overexpressed in the acini and PDAC of Pdx1-Cre;Kras(G12

222 D, the translocator protein 18 kDa (TSPO) is overexpressed in the activated microglia that surround t

223 incipal structural component of caveolae, is overexpressed in the cancers noted above that respond to

224 The truncated AaIPPI1 was overexpressed in the cytosol of the SP A. annua variety.

225 GRK2 and GRK5 are overexpressed in the failing heart and thus have become

226 Similarly, MCPIP1 was overexpressed in the imiquimod (IMQ)-driven mouse model

227 modifier of multiple signalling pathways, is overexpressed in the majority of cancers and its activit

228 e LIN9 gene lacks an SE but was amplified or overexpressed in the majority of TNBCs.

229 CCN5 was overexpressed in the NSP but downregulated in the SP.

230 Here, we found PLD4 to be overexpressed in the proximal and distal tubular epithel

231 ansect, with CYP6P9a and CYP6P9b more highly overexpressed in the southern resistance front and CYP6M

232 turase (crtI) from Pantoea ananatis has been overexpressed in the tangerine mutant of tomato (Solanum

233 een miR-29b and BRD4, the latter of which is overexpressed in these cells.

234 ormation-specific proto-oncogene 1 (ETS1) is overexpressed in these FLI1-deficient iMegs, suggesting

235 Sortilin was overexpressed in thyroid cancers compared with benign th

236 ion factor has been shown to be specifically overexpressed in TNBC and associated with poor clinical

237 AT35.1, was found to trigger cell death when overexpressed in tobacco (Nicotiana benthamiana) leaves

238 is a protein involved in oncogenesis and is overexpressed in triple-negative breast cancer (TNBC).

239 targeting of an endothelial antigen that is overexpressed in triple-negative breast cancer and the a

240 LIF was overexpressed in tumor tissue compared with healthy panc

241 he top dysregulated lncRNAs, was found to be overexpressed in tumors relative to normal lung and sign

242 Mdm2 is often overexpressed in tumors that retain wild-type TP53 but m

243 iring its ability to inhibit exocytosis when overexpressed, indicating a selective defect in normal f

244 eath pathways, pharmacological activation of overexpressed ion channels has not been extensively eval

245 een a focus on pharmacological inhibition of overexpressed ion channels in specific cancer subtypes a

246 and Eg5 are partially redundant motors, and overexpressed Kif15 can drive spindle formation in the a

247 In CCA, ErbB receptors are frequently overexpressed, leading to tumor progression and low prog

248 Using a PDE4B overexpressed lentivirus transfection system, we suggest

249 In human tumours separase is overexpressed, making it a potential target for drug dis

250 Reactive oxygen species (ROS) produced by overexpressed MAOA plays an essential role in inhibiting

251 ansplanted endothelial progenitor cells that overexpressed MFSD2A not only localized to the inflamed

252 iorated the depressive-like phenotype of TG2-overexpressed mice.

253 genic expression of DNAJB5 in CCA cells that overexpressed MIR21 re-sensitized them to HSP90 inhibito

254 15a showed the highest fold change among the overexpressed miRNAs.

255 emia (AML), we probed the AML surfaceome for overexpressed molecules with tolerable systemic expressi

256 Furthermore, transgenic mice that overexpressed monomeric sP-selectin did not exhibit incr

257 Isolates from PP overexpressed more ompA than those from colonized patien

258 Results demonstrated that sst5TMD4 is overexpressed (mRNA/protein) in PCa samples, and this is

259 ver, in contrast with previous studies using overexpressed mutant protein in cell lines, FPN1 could s

260 When overexpressed, mutant MDA5 failed to drive luciferase ac

261 This effect is abolished when we overexpressed mutants lacking part of N-terminal domains

262 We found miR-34c is decreased in PSCs overexpressed N1ICD.

263 ates from PP, those from bacteremic patients overexpressed nonsignificantly more ompA than those from

264 Overexpressed NPRL2 accumulates in the nucleus, together

265 n targeted drug delivery to tumor cells with overexpressed nuclear hormone receptors.

266 broadly expressed on normal cells and often overexpressed on cancer cells, and its counter-receptor,

267 nition between aptamer and MUC1 protein that overexpressed on the surface of MCF-7 cells, the aptamer

268 ect ECL imaging of a labeled plasma receptor overexpressed on tumor cells.

269 When C9ORF72 was overexpressed or antisense oligonucleotides were targete

270 wth deposition were observed when miR156 was overexpressed or its activity suppressed by target mimic

271 The EGFR is frequently overexpressed or mutated in various cancers leading to a

272 ituation in T2D islets, candidate genes were overexpressed or silenced in cultured beta-cells.

273 The 90 genes overexpressed (or UP genes) in MDD were significantly en

274 Moreover, endogenous ORAI1 and overexpressed ORAI1-GFP co-immunoprecipitated with endog

275 We overexpressed PDR1 (PDR1 OE) to investigate whether incr

276 The cellular distribution of an overexpressed phospho-null mutant, TH1-S31A, was restric

277 nock-out mice suggested that the cleavage of overexpressed proprotein C is predominantly performed by

278 chronic lymphocytic leukaemia (CLL) cells is overexpressed protein kinase CbetaII (PKCbetaII), an S/T

279 metry approach for rapid characterization of overexpressed proteins directly in crude cell lysates.

280 rkers are found in different forms including overexpressed proteins/surface antigens, metabolites, mi

281 responding to the binding specificity of the overexpressed SH2 domain.

282 cells in which plasminogen receptor (KT) was overexpressed, showing for the first time the role of a

283 uclear in primary neurons and, unexpectedly, overexpressed SK2 is neurotoxic in a dose-dependent mann

284 nduced behavioral plasticity, we selectively overexpressed Sox10 and BRG1 in the PFC.

285 lizing the Emu-myc mouse model, where Myc is overexpressed specifically in B cells, both basal and st

286 Cav) organize progrowth receptors, and, when overexpressed specifically in neurons, Cav-1 augments ne

287 We have previously reported that overexpressed SPL displays anti-influenza viral activity

288 udies of other tumor types in which cIAP1 is overexpressed suggest that multi-regimen treatments incl

289 , such enhancement is diminished when Gag is overexpressed, suggesting that the effects of viral RNA

290 We overexpressed the mutant constructs in HEK 293T cells an

291 , through immunoblotting, we found that AHAs overexpressed the NMDAR GluN2D subunit in the prefrontal

292 Here, we overexpressed the PtdSer receptor BAI1 in mice lacking M

293 When overexpressed, the SRCR repeats from other LOX family me

294 Radial patterning is disrupted when Wnt9a is overexpressed throughout the prosensory domain beginning

295 Wee1 was overexpressed to study antiapoptosis and the cell cycle.

296 To test this hypothesis, we overexpressed Trx-1 (cytosolic form of Trx) in the VMH o

297 Finally, we overexpressed ts-46 and ts-47 in two lung cancer cell li

298 gene CIRCADIAN CLOCK ASSOCIATED1 (CCA1) was overexpressed under the control of the guard-cell-specif

299 Consistent with its function, overexpressed Wdr34 is occasionally localized to cilia,

300 IL-33 protein was markedly overexpressed within the nuclei of a subpopulation of ba