ライフサイエンスコーパス: lymphoblastoid

1 ithelial, blood, induced sputum, T cells and lymphoblastoids).

2 atency III proliferating B cells, on various lymphoblastoid and Burkitt lymphoma cell lines, some of

3 me and xeroderma pigmentosum patient-derived lymphoblastoid and fibroblast cells.

4 ased levels of CSF KYNA (P=0.03) and reduced lymphoblastoid and hippocampal KMO expression (P</=0.05)

5 of which were profiled in both the GM12878 (lymphoblastoid) and K562 (erythroleukemic) human hematop

6 covered that in human cancer cells (myeloma, lymphoblastoid, and breast cancer), when expression of h

7 of transcription start sites (TSSs) in human lymphoblastoid B cell (GM12878) and chronic myelogenous

8 aluated by site-directed mutagenesis using a lymphoblastoid B cell line (B-LCL) and U3A cells.

9 merase (PARP) on global gene expression in a lymphoblastoid B cell line.

10 EBV-transformed lymphoblastoid B cell lines (LCLs) derived from subjects

11 ow that Epstein-Barr virus (EBV) transformed lymphoblastoid B-cell lines (LCLs) not only express DEC-

12 *01:01 and HLA-G*01:01 were transfected into lymphoblastoid C1R cells expressing low endogenous HLA.

13 BV) super-enhancers (ESEs) are essential for lymphoblastoid cell (LCL) growth and survival.

14 uses NCL and RPL4 to establish persistent B-lymphoblastoid cell infection.

15 rom the exosome fractions derived from human lymphoblastoid cell line (LCL) culture media.

16 expression of most cell genes essential for lymphoblastoid cell line (LCL) growth and survival.

17 p16(INK4A) is essential for immortal human B-lymphoblastoid cell line (LCL) growth.

18 Perturbation of ESEs stops lymphoblastoid cell line (LCL) growth.

19 his study, integrative analyses of published lymphoblastoid cell line (LCL) Hi-C data and our 4C-seq

20 Lymphoblastoid cell line (LCL) is a common tool to study

21 n and subsequently almost completely ablated lymphoblastoid cell line (LCL) outgrowth.

22 (WES) are whole blood (WB) and immortalized lymphoblastoid cell line (LCL).

23 In this study, lymphoblastoid cell line cultures (LCLs) from women with

24 nome RNA-seq analysis between mouse vHpc and lymphoblastoid cell line cultures from control women and

25 Application of the methods to the human lymphoblastoid cell line data on chromosomes 14 and 22 f

26 in retroviral infection using the chicken B lymphoblastoid cell line DT40.

27 A lymphoblastoid cell line from one affected individual sh

28 Integration with ENCODE data from lymphoblastoid cell line GM12878, demonstrates that IRF4

29 cell RNA-seq protocol to study the reference lymphoblastoid cell line GM12878.

30 lic occupancy of 24 TFs and EP300 in a human lymphoblastoid cell line GM12878.

31 depletion and gene activation necessary for lymphoblastoid cell line growth and survival.

32 BNA-2 confers a type 1 growth phenotype in a lymphoblastoid cell line growth maintenance assay.

33 Moreover, NCL silencing impaired lymphoblastoid cell line growth.

34 Here, we show that growth of a human B lymphoblastoid cell line infected with Epstein-Barr viru

35 Infection of the JY lymphoblastoid cell line limited the accumulation of a m

36 miR-M4 from the MDV-induced lymphoma-derived lymphoblastoid cell line MDCC-HP8.

37 The BJAB lymphoblastoid cell line often serves as a model for B c

38 -infected B lymphocytes and are critical for lymphoblastoid cell line outgrowth.

39 Using whole-genome DNA and lymphoblastoid cell line RNA sequencing data from 360 Eu

40 C-seq by sequencing the methylome of a human lymphoblastoid cell line to approximately 8.6x high-qual

41 C data of chromosome 5 from GM12878 (a human lymphoblastoid cell line), (ii) 40-kb resolution whole-g

42 from GM06990, a near-normal EBV-transformed lymphoblastoid cell line, and have compared origin distr

43 Applied to high-resolution Hi-C data in a lymphoblastoid cell line, HiC-DC detects significant int

44 for PBL-to-atrium; and from 0.81 to 0.98 for lymphoblastoid cell line-to-PBL based on cross-validatio

45 RRP12 in LNCaP, USP14 in DU-145 and SMIN3 in lymphoblastoid cell line.

46 ed the genotype of an HPS1 patient-derived B-lymphoblastoid cell line.

47 astoid cell lines, and EBV genome number per lymphoblastoid cell line.

48 Glycosylation of mAb-Ds from human B-lymphoblastoid cell lines (B) was similar to anti-D Ig a

49 ized endogenously presented targets on EBV B lymphoblastoid cell lines (BLCLs), but not peripheral bl

50 different HLA-typed, human EBV-transformed B lymphoblastoid cell lines (BLCLs).

51 a demonstration, Epstein-Barr virus-infected lymphoblastoid cell lines (EBV-LCL) were isolated based

52 addition, human LRRK2 G2019S patient-derived lymphoblastoid cell lines (LCL) demonstrated increased m

53 l transcriptomics data from a panel of human lymphoblastoid cell lines (LCL) to infer drug response n

54 tore iNKT recognition in EBV-infected cells, lymphoblastoid cell lines (LCL) were treated with AM580,

55 allowed the establishment of MDV-transformed lymphoblastoid cell lines (LCL).

56 latency II NPC C666-1 cells, and latency III lymphoblastoid cell lines (LCL).

57 ntly reported gene expression changes in 480 lymphoblastoid cell lines (LCLs) after in vitro simvasta

58 lysis of RNA stability in seven human HapMap lymphoblastoid cell lines (LCLs) and analyzed the effect

59 lomere repeat elements (SREs) in transformed lymphoblastoid cell lines (LCLs) and human embryonic ste

60 otein isoforms across 68 Yoruba (YRI) HapMap lymphoblastoid cell lines (LCLs) and identified 12 cis a

61 on measured via RNA-seq analysis in adipose, lymphoblastoid cell lines (LCLs) and skin.

62 Using EBV-immortalized lymphoblastoid cell lines (LCLs) as a model, we found th

63 Patient-derived cell lines such as lymphoblastoid cell lines (LCLs) could represent the ide

64 Using a data set of gene expression in lymphoblastoid cell lines (LCLs) derived from 210 HapMap

65 tosine modifications at 283,540 CpG sites in lymphoblastoid cell lines (LCLs) derived from independen

66 We developed an in vitro model of PMD with lymphoblastoid cell lines (LCLs) derived from participan

67 Here we report that RP-mutated lymphoblastoid cell lines (LCLs) established from DBA pa

68 Using lymphoblastoid cell lines (LCLs) established with EBV re

69 How lymphoblastoid cell lines (LCLs) evolve from the infecte

70 ene expression profiles using microarrays on lymphoblastoid cell lines (LCLs) from 413 cases and 446

71 romatin profiling for three histone marks in lymphoblastoid cell lines (LCLs) from 75 sequenced indiv

72 Previously we hypothesized that a subset of lymphoblastoid cell lines (LCLs) from children with auti

73 Here we analyze m(6)A mRNA modifications in lymphoblastoid cell lines (LCLs) from human, chimpanzee

74 enome-wide association studies involving 523 lymphoblastoid cell lines (LCLs) from individuals of Eur

75 A21 to assess trisomic protein expression in lymphoblastoid cell lines (LCLs) from patients with DS a

76 Lymphoblastoid cell lines (LCLs) from some children with

77 B cell lymphoma infected with HHV-6B, (iii) lymphoblastoid cell lines (LCLs) from subjects with inhe

78 Using RNA-sequence data from lymphoblastoid cell lines (LCLs) from the TwinsUK cohort

79 EBV to convert human B cells into long-lived lymphoblastoid cell lines (LCLs) in vitro requires the c

80 rther demonstrated that knockdown of H2AX in lymphoblastoid cell lines (LCLs) led to the upregulation

81 ion, elicited lytic EBV in latently infected lymphoblastoid cell lines (LCLs) partially via Toll-like

82 r Virus (EBV) conversion of B-lymphocytes to Lymphoblastoid Cell Lines (LCLs) requires four EBV nucle

83 hocytes (RBLs) leads to the establishment of lymphoblastoid cell lines (LCLs) that can grow indefinit

84 transformed into continuously proliferating lymphoblastoid cell lines (LCLs) that carry EBV DNA as e

85 Lymphoblastoid cell lines (LCLs) were cocultured with au

86 Populations of human-derived HapMap lymphoblastoid cell lines (LCLs) were infected with RSV.

87 between vitamin D receptor (VDR) binding in lymphoblastoid cell lines (LCLs), chromatin states in LC

88 In contrast to wild-type lymphoblastoid cell lines (LCLs), dividing LCLs establis

89 ChIP-seq performed on lymphoblastoid cell lines (LCLs), expressing epitope-tag

90 Human lymphoblastoid cell lines (LCLs), generated through Epst

91 In GS-derived lymphoblastoid cell lines (LCLs), the proportion of ITPR

92 amining Epstein-Barr virus (EBV)-transformed lymphoblastoid cell lines (LCLs), we identified four EBV

93 sforms B cells to continuously proliferating lymphoblastoid cell lines (LCLs), which represent an exp

94 n vitro, EBV transforms primary B cells into lymphoblastoid cell lines (LCLs).

95 conducted a pharmacogenomic study using 266 lymphoblastoid cell lines (LCLs).

96 lation from chromatin to proteins, in Yoruba lymphoblastoid cell lines (LCLs).

97 s, nasopharyngeal carcinoma (NPC) cells, and lymphoblastoid cell lines (LCLs).

98 ll proliferation leading to the outgrowth of lymphoblastoid cell lines (LCLs).

99 oth in newly infected primary B cells and in lymphoblastoid cell lines (LCLs).

100 A polymerase II (Pol II) occupancy in Yoruba lymphoblastoid cell lines (LCLs).

101 s drives their indefinite proliferation into lymphoblastoid cell lines (LCLs).

102 roliferation and through transformation into lymphoblastoid cell lines (LCLs).

103 loci and facilitate KLF14 gene expression in lymphoblastoid cell lines (LCLs).

104 and transformation of quiescent B cells into lymphoblastoid cell lines (LCLs).

105 ISPR/Cas9 loss-of-function screens in BL and lymphoblastoid cell lines (LCLs).

106 a panel of iPSCs from 58 well-studied Yoruba lymphoblastoid cell lines (LCLs); 14 of these lines were

107 vitro results in their immortalization into lymphoblastoid cell lines (LCLs); this latency program i

108 loci in genome-wide expression data sets of lymphoblastoid cell lines (n = 1,830) and were related t

109 CAMKK2 in human brains (P=1.1 x 10(-6)) and lymphoblastoid cell lines (the lowest P=8.4 x 10(-6)).

110 ranscription initiation across several human lymphoblastoid cell lines (Yoruba population) and detect

111 Using 1220 lymphoblastoid cell lines across platforms and independe

112 eQTLs each affect hundreds of transcripts in lymphoblastoid cell lines across three African populatio

113 ong chromosomes from primary lymphocytes and lymphoblastoid cell lines adapted to long-term growth in

114 edish patients, and to KMO expression in 717 lymphoblastoid cell lines and 138 hippocampal biopsies.

115 s from human, chimpanzee, and rhesus macaque lymphoblastoid cell lines and compared them to transcrip

116 stimulation with autologous EBV-transformed lymphoblastoid cell lines and correlated with EBV load i

117 rm that CYFIP1 is upregulated in transformed lymphoblastoid cell lines and demonstrate its upregulati

118 R-181c, were significantly down-regulated in lymphoblastoid cell lines and fresh peripheral blood cel

119 990620, that differentially recruits CTCF in lymphoblastoid cell lines and human brain to influence C

120 and association with TMEM106B expression in lymphoblastoid cell lines and human brain.

121 hromatin signature to infer MAE for genes in lymphoblastoid cell lines and human fetal brain tissue.

122 sociated with lower CTSH expression in human lymphoblastoid cell lines and pancreatic tissue.

123 with a decline in CLDN14 expression in both lymphoblastoid cell lines and T cells (Padj = 0.003 and

124 ic variation in TF binding affinity in human lymphoblastoid cell lines and test their association wit

125 med histone acetylation ChIP-seq on 57 human lymphoblastoid cell lines and used the resulting reads t

126 e associated with lower FBXO33 expression in lymphoblastoid cell lines and with reduced frontal gray

127 als on whom both haplotypes and DH status in lymphoblastoid cell lines are publicly available.

128 ng Salmonella typhimurium infection of human lymphoblastoid cell lines as a means of dissecting the g

129 Patient-derived lymphoblastoid cell lines bearing a range of expanded al

130 nomic and transcriptomic data from 445 human lymphoblastoid cell lines by combining an RNA editing QT

131 ne expression levels generated for 373 human lymphoblastoid cell lines by the Geuvadis consortium and

132 virus (EBV) to transform human B cells into lymphoblastoid cell lines compared to that of type 2 EBV

133 us (EBV)-encoded RNAs (EBERs) were tested in lymphoblastoid cell lines containing EBER mutants of EBV

134 study the response to 23 treatments in three lymphoblastoid cell lines demonstrating that it should a

135 associations with gene expression levels in lymphoblastoid cell lines derived from 480 participants

136 onstructed by transferring mitochondria from lymphoblastoid cell lines derived from a Chinese family

137 generated by transferring mitochondria from lymphoblastoid cell lines derived from a Chinese family

138 icative impairments could be demonstrated in lymphoblastoid cell lines derived from affected individu

139 Lymphoblastoid cell lines derived from carriers of misse

140 iated (P = .01) with FPGS gene expression in lymphoblastoid cell lines derived from combined HapMap A

141 , cytosine modification levels in 133 HapMap lymphoblastoid cell lines derived from individuals of Eu

142 ne expression in response to high glucose in lymphoblastoid cell lines derived from matched individua

143 We performed functional assays by using lymphoblastoid cell lines derived from members of Chines

144 expression by affecting the binding to GR in lymphoblastoid cell lines derived from the same patients

145 In MDV-induced T-cell lymphomas and in lymphoblastoid cell lines derived from them, MDV-miR-M4

146 ar susceptibility to cisplatin in 176 HapMap lymphoblastoid cell lines derived from Yoruba individual

147 Nonleukemic EBV-transformed lymphoblastoid cell lines displayed highly stable replic

148 The B-lymphoblastoid cell lines exhibited a unimodal distribut

149 otein from V362I and R381Q variants in human lymphoblastoid cell lines exhibited lower expression lev

150 with reduced survival in a panel of 24 human lymphoblastoid cell lines exposed to the alkylating agen

151 Here, we show that EBV-immortalized FSHD lymphoblastoid cell lines express DUX4 and both early an

152 Thus, FSHD lymphoblastoid cell lines express DUX4 and early and lat

153 udies, we collected RNA-sequencing data from lymphoblastoid cell lines for 431 Hutterite individuals.

154 red the cytotoxicity of 156 compounds in 884 lymphoblastoid cell lines for which genotype and transcr

155 address these questions, we perform Hi-C on lymphoblastoid cell lines from 20 individuals.

156 ne relative protein levels of 5,953 genes in lymphoblastoid cell lines from 95 diverse individuals ge

157 ormed a genome-wide gene expression study in lymphoblastoid cell lines from 96 Hutterites.

158 rometry to perform an integrated analysis in lymphoblastoid cell lines from a diverse group of indivi

159 itation, we derived normal and DNMT3A mutant lymphoblastoid cell lines from a germline mosaic individ

160 Using immortalized lymphoblastoid cell lines from a healthy study populatio

161 OGT protein levels was observed in isolated lymphoblastoid cell lines from affected individuals, con

162 This miniATM variant was also highlighted in lymphoblastoid cell lines from AT patients and was shown

163 f NK cells to kill freshly established human lymphoblastoid cell lines from autologous or allogeneic

164 and extended in three human EBV-transformed lymphoblastoid cell lines from individuals with MSS, lea

165 Using simvastatin and sham incubated lymphoblastoid cell lines from participants of the Chole

166 tein (FMRP), its upregulation in transformed lymphoblastoid cell lines from patients with duplication

167 Lymphoblastoid cell lines from subjects with the p.V228F

168 We used 1,086 lymphoblastoid cell lines from the 1000 Genomes Project,

169 Lymphoblastoid cell lines from the index family in compa

170 Lymphoblastoid cell lines generated from affected childr

171 DNA methylation (DNAm) measured in lymphoblastoid cell lines has been repeatedly demonstrat

172 in nonsynonymous substitutions in all three lymphoblastoid cell lines in our study, unlike RNA editi

173 nd transform B lymphocytes into immortalized lymphoblastoid cell lines in vitro.

174 of 237 up-regulated genes derived from FSHD lymphoblastoid cell lines is elevated in FSHD muscle bio

175 gh-throughput sequencing data sets for human lymphoblastoid cell lines mapped to the EBV genome.

176 Lymphoblastoid cell lines obtained from a patient and fr

177 elationship between COMETs and haplotypes in lymphoblastoid cell lines of African and European origin

178 lls or NK-cell clones with HLA-C2(+) CCR7(+) lymphoblastoid cell lines resulted in increased CCR7 upt

179 s, which leads to continuously proliferating lymphoblastoid cell lines through examination of the exp

180 red heteroplasmies in mtRNA from 446 human B-lymphoblastoid cell lines to their corresponding mtDNA u

181 logous dendritic cells and EBV-transformed B-lymphoblastoid cell lines transduced with an adenoviral

182 cellular phenotypes in three patient-derived lymphoblastoid cell lines with three variants: p.Gly535A

183 r virus-transformed B-cell cultures (human B-lymphoblastoid cell lines) from 19 healthy donors.

184 using >300 expression microarrays (from 117 lymphoblastoid cell lines) in corticosteroid (dexamethas

185 od-related cell types (CD3 and CD4+ T cells, lymphoblastoid cell lines).

186 appear to regulate gene expression in human lymphoblastoid cell lines, a tightly controlled, largely

187 ells, HeLa cells, HEK293 cells, and 16 human lymphoblastoid cell lines, all genotyped for the 9p21.3

188 iP luciferase reporter, EBNA1 DNA binding in lymphoblastoid cell lines, and EBV genome number per lym

189 evel was performed using patient and control lymphoblastoid cell lines, and established experimental

190 ed BZLF1 expression in latently EBV-infected lymphoblastoid cell lines, and knockdown of BGLF2 reduce

191 n transcriptional response in fibroblast and lymphoblastoid cell lines, as well as circulating monocy

192 cific quantification assays to a panel of HD lymphoblastoid cell lines, each carrying the major Europ

193 measure chromatin accessibility in 70 Yoruba lymphoblastoid cell lines, for which genome-wide genotyp

194 h resulted in the generation of EBV-positive lymphoblastoid cell lines, indicating that the virus in

195 eral blood mononuclear cells, monocytes, and lymphoblastoid cell lines, leading to enhanced autophagi

196 nscription factor MEF2A in 32 distinct human lymphoblastoid cell lines, providing insights into the m

197 entified as eQTL in monocytes, liver tissue, lymphoblastoid cell lines, T cells, and fibroblasts are

198 Here we report that, in lymphoblastoid cell lines, the translocation additionall

199 nd drug sensitivity measurements in 24 human lymphoblastoid cell lines, was applied to a panel of 12

200 Using the HapMap lymphoblastoid cell lines, we combine 1000 Genomes genot

201 Applying riboHMM to human lymphoblastoid cell lines, we identified 7273 novel codi

202 Using metaphase spreads from human lymphoblastoid cell lines, we previously showed how immu

203 sed gene editing approach in MDV-transformed lymphoblastoid cell lines, we show that MDV-miR-M4, desp

204 to the establishment of permanently growing lymphoblastoid cell lines, whereas CD40L/IL-4 blasts hav

205 iation in genome-wide gene expression in 107 lymphoblastoid cell lines, with alleles ranging from 15

206 d in proband versus control EBV-immortalized lymphoblastoid cell lines.

207 and RP1-10D13.2 expression levels in the CAP lymphoblastoid cell lines.

208 oning patterns are observed in two different lymphoblastoid cell lines.

209 the expression level of both transcripts in lymphoblastoid cell lines.

210 es less stable or leakier in EBV-transformed lymphoblastoid cell lines.

211 or each of the four genes in the region in B lymphoblastoid cell lines.

212 rase reporter, and EBV genome maintenance in lymphoblastoid cell lines.

213 n human adipose tissue, skeletal muscle, and lymphoblastoid cell lines.

214 igene assays and, when available, in patient lymphoblastoid cell lines.

215 f virus gene expression and the outgrowth of lymphoblastoid cell lines.

216 available RNA-seq expression data sets from lymphoblastoid cell lines.

217 ed IRF7 is detected in latently infected EBV lymphoblastoid cell lines.

218 ype and reduced BAK1 expression was shown in lymphoblastoid cell lines.

219 phase arrest and apoptosis in leukemic and B-lymphoblastoid cell lines.

220 normal tissue pairs and 17 matched SCLC and lymphoblastoid cell lines.

221 tal mRNA fractions of 52 HapMap Yoruba human lymphoblastoid cell lines.

222 antly higher proliferation in DS than non-DS lymphoblastoid cell lines.

223 oci (QTLs) of m(6)A peaks in 60 Yoruba (YRI) lymphoblastoid cell lines.

224 ession in human aortic endothelial cells and lymphoblastoid cell lines.

225 (ChIP-exo) genome-wide analysis of 27 HapMap lymphoblastoid cell lines.

226 the TwinsUK microarray and RNA-Seq cohort in lymphoblastoid cell lines.

227 with daunorubicin IC50 values in a panel of lymphoblastoid cell lines.

228 ed in HL, diffuse large B-cell lymphoma, and lymphoblastoid cell lines.

229 uencing in ATAC-seq libraries generated from lymphoblastoid cell lines: targeted cleavage of mitochon

230 n both peripheral blood leukocytes (PBL) and lymphoblastoid cell lines; and a study of postoperative

231 e method was first applied to RNA-Seq from a lymphoblastoid cell-line, achieving 99.7% precision and

232 Whole-genome sequencing reads were from a lymphoblastoid cell-line.

233 gkm-SVM models of chromatin accessibility in lymphoblastoid cell-lines.

234 ys were performed on patient and control EBV lymphoblastoids cell lines.

235 hese cells do not resemble the proliferating lymphoblastoid cells (LCLs) (latency III) that are gener

236 ls with type I latency and reactivation from lymphoblastoid cells (LCLs) with type III latency.

237 acteristics of MMR-deficient tumor cells) in lymphoblastoid cells (LCs) from 3 patients with CMMRD an

238 strongly associated with CREB1 expression in lymphoblastoid cells (P<0.005) and the prefrontal cortex

239 in transfected murine macrophages and human lymphoblastoid cells affected anthrax toxin binding, int

240 Levels of coenzyme Q10 in lymphoblastoid cells and brain tissue were measured on h

241 Analysis of lymphoblastoid cells and fibroblasts from patients homoz

242 Gene expression profiling was performed on lymphoblastoid cells and levels of CXCL10 were measured

243 F8 mRNA and intracellular FVIII protein in B lymphoblastoid cells and liver biopsies from individuals

244 ntagonizes the growth inhibitory effect in B lymphoblastoid cells and might be used to modulate the f

245 lular fusion transcripts in transduced human lymphoblastoid cells and primary hematopoietic stem/prog

246 We also analyze data from individual lymphoblastoid cells and show that desirable properties

247 cently demonstrated that SRS patient-derived lymphoblastoid cells are capable of transporting exogeno

248 We apply 3D-EMISH to human lymphoblastoid cells at a 1.7 Mb segment of the genome a

249 NA from affected individuals' fibroblasts or lymphoblastoid cells confirmed mutant transcripts with p

250 Analysis of cDNA from lymphoblastoid cells demonstrated partial splice site ab

251 Lymphoblastoid cells derived from a HapMap Project cohor

252 Similar results were found in lymphoblastoid cells derived from a SMS patient carrying

253 Using B-lymphoblastoid cells derived from the HapMap Project coh

254 and associated with PRPF6 mRNA expression in lymphoblastoid cells from 373 Europeans in the 1000 Geno

255 Importantly, lymphoblastoid cells from an individual heterozygous for

256 Lymphoblastoid cells from individuals with BRCA1 pathoge

257 ce (MECP2-TG), and corrected MECP2 levels in lymphoblastoid cells from MECP2 duplication patients in

258 RNA and protein abundance in patient-derived lymphoblastoid cells from one NUDT21 deletion and three

259 We quantified PIK3CD transcripts in B-lymphoblastoid cells from patients with SZ and examined

260 of plasmid replication (oriP) as a "bait" in lymphoblastoid cells further confirmed contacts with act

261 ter irradiation are cell type-specific, with lymphoblastoid cells generally showing more contact chan

262 Patient-derived SDH(var+) lymphoblastoid cells had elevated cellular reactive oxyg

263 omatin conformation capture (Hi-C) assays in lymphoblastoid cells have become available, enabling us

264 we utilized gene expression association from lymphoblastoid cells lines from 754 p.Phe508del CF-affec

265 Lymphoblastoid cells obtained from an affected individua

266 Lymphoblastoid cells of a mutant gene carrier had, in ad

267 In addition, the mutant gene carrier lymphoblastoid cells proliferated faster and were less r

268 roarray analysis performed on FRDA patient's lymphoblastoid cells stably reconstituted with frataxin,

269 cleus cytome (CBMN-Cyt) assay with WIL2-NS B lymphoblastoid cells to test the potential genotoxicity,

270 peptide profile of human EC and syngeneic B lymphoblastoid cells was biochemically analyzed and comp

271 Blood and lymphoblastoid cells were collected from patients and co

272 alleles in cells, irrelevant sera binding to lymphoblastoid cells were minimized by CRISPR/Cas9 elimi

273 EBV attachment sites in lymphoblastoid cells with different latency type show di

274 ere readily detected in DNA from the treated lymphoblastoid cells, and both were largely eliminated f

275 MK) enzyme activity was analyzed in cultured lymphoblastoid cells, and mevalonic acid levels were mea

276 The densest, in human lymphoblastoid cells, contains 4.9 billion contacts, ach

277 To date, only patient-derived lymphoblastoid cells, fibroblasts and SETX knockdown cel

278 2-depleted motor neurons, in patient-derived lymphoblastoid cells, induced pluripotent stem cell-deri

279 ction studies in EBV-positive B lymphoma and lymphoblastoid cells, we found that the levels of functi

280 tructures (at the macrodomain resolution) of lymphoblastoid cells, we identify an atlas of stable int

281 In cultured human CEM lymphoblastoid cells, which possess a single hNT type (h

282 NA and transcription factor targets in human lymphoblastoid cells, while being nearly a million times

283 tact map of chromosome 10 from human GM12878 lymphoblastoid cells.

284 res for mouse embryonic stem cells and human lymphoblastoid cells.

285 on HLA-A2(+) melanoma, breast carcinoma, and lymphoblastoid cells.

286 st and attenuated FBXL2-induced apoptosis of lymphoblastoid cells.

287 ed normal CEP290 splicing in patient-derived lymphoblastoid cells.

288 s) and active regions of the human genome in lymphoblastoid cells.IMPORTANCE EBV is associated with ~

289 ochondrial and redox abnormalities in autism lymphoblastoid cells: a sibling control study.

290 Global transcriptome analysis of L254F-OGT lymphoblastoids compared with controls revealed a small

291 Surprisingly, lymphoblastoids from affected individuals displayed a ma

292 ised myelogenous leukemia (K562) and healthy lymphoblastoid (GM12878) cell lines to train the learnin

293 Lymphoblastoid haQTLs were highly predictive of autoimmu

294 t fuses to other genes associated with acute lymphoblastoid leukemia (ALL).

295 reast cancer cell line (HCC1395) and matched lymphoblastoid line (HCC1395BL).

296 histone modifications, cohesin, and CTCF in lymphoblastoid lines from 19 individuals of diverse ance

297 We apply it to a collection of lymphoblastoid RNA-seq data from the 1000 Genomes Projec

298 ng data for various cell nucleus geometries (lymphoblastoid, skin fibroblast, and breast epithelial c

299 virus-driven luciferase expression, or A3R5 lymphoblastoid target cells, in which infectivity was ev

300 obtain such transcriptomes, we sequenced the lymphoblastoid transcriptomes of three family members (G