ライフサイエンスコーパス: lost in

1 atients revealed that Retinoblastoma (RB) is lost in 100% of these SCLC transformed cases, but rarely

2 Blood vessels were lost in 142 of 404 observations of EVD images (35.1%).

3 n Larsen B's stabilizing frontal portion was lost in 1995, the unstable remaining shelf accelerated,

4 als younger than 55 years, and years of life lost in 2014.

5 rt-wave-sensitive genes, SWS1 and SWS2, were lost in 23 and 6 species, respectively.

6 f SP62-specific B cell compartments normally lost in 2F5 Ab knockin mice.

7 On EVD images, squames and crusts were lost in 56 of 404 observations (13.9%) and 43 of 404 obs

8 to cross-link to rRNA was almost completely lost in a DICER knock-out cell line.

9 It was independently lost in a few groups in which MR1 is present, like prima

10 n is more stable than that of Src, an effect lost in a Fyn mutant lacking the palmitoylation sites.

11 ibility to this pathogen at subjective night lost in a jaz6 mutant.

12 t no x-ray photons scattered by a sample are lost in a limited-efficiency imaging system.

13 method to estimate the percentage of species lost in a mass extinction.

14 ained in a small fraction of GC patients and lost in a minimum number.

15 Unexpectedly, this coupling was chronically lost in a mouse model of mesial temporal lobe epilepsy (

16 ed with cilia defects, and cilia motility is lost in a number of ciliated tissues along with a reduct

17 arginine 175 (R175) and this modification is lost in a PRMT5 and WDR77-dependent manner.

18 lular potential is reset, DNA methylation is lost in a series of "sequential waves." The mechanism un

19 s, we show that miR-424(322)/503 is commonly lost in a subset of aggressive breast cancers and descri

20 obial sensor SLAMF1 (also known as CD150) is lost in a subset of patients with an aggressive CLL that

21 n molecule for DNA viruses whose function is lost in a variety of cancers has coincided with the appr

22 cal regulator of autophagy and apoptosis, is lost in a wide variety of tumors, although the mechanism

23 ceae family through gene duplication and was lost in A. thaliana, contributing to leaf simplification

24 by blockade of spinal and supraspinal A3AR, lost in A3AR knock-out mice, and independent of opioid a

25 ortant immune-regulatory roles that would be lost in AATD, yet adaptive immune responses in the lung

26 c microglia in rodents, which was completely lost in active and slowly expanding lesions.

27 ntractile effects of the adipose tissue were lost in Adipo-MROE mice but not in control-MR mice.

28 hed as early as 1 week postnatal and remains lost in adulthood.

29 -dependent choroid plexus activity, which is lost in aging.

30 ngle-stranded RNA, whereas this activity was lost in all altered forms of the protein.

31 These lateral eyes are lost in all crown-group Phalangida, but are observed in

32 Genes are lost in all functional categories, but core genes for ce

33 hibernation as an overwintering strategy was lost in all other primates in mainland Africa, Asia, and

34 e selectively enhanced in the GR lineage and lost in all others.

35 he sweet, umami, and bitter tastes have been lost in all penguins, an order of aquatic flightless bir

36 d tocolytics, and this prevention is largely lost in alpha-gustducin-knockout mice.

37 n of the NMD process, both of which would be lost in an ensemble study.

38 ssociated protein HU, and we show that it is lost in an HU deletion strain.

39 Allostery persisted, but trans-allostery was lost in an oligomerization-deficient GLUT1 variant in wh

40 s for three trophozoite-expressed genes were lost in AN3661-treated trophozoites, which was not obser

41 cells of the polarizing region - an ability lost in ancestral theropod dinosaurs.

42 teria, mosses, and microalgae, but have been lost in angiosperms.

43 e response to the same MC4R agonist was only lost in animals lacking G(s)alpha specifically in the PV

44 ), the temperature at which motor control is lost in animals, has the potential to determine if speci

45 o follow-up in pre-ART stage and 2847 (2.2%) lost in ART stage.

46 yroglobulin, to which tolerance is typically lost in autoimmune thyroiditis leading to hypothyroidism

47 nd this extension of lifespan was completely lost in backgrounds containing a mutated DAF-16 gene.

48 1/beta2) genes but alpha2-tubulin genes were lost in basidiomycetes and beta2-tubulin genes were lost

49 This loci was commonly lost in BCa cell lines and we show the deletions extende

50 Thus, mitochondria are prematurely lost in bdh2-inactivated erythrocytes.

51 ive feedback loop that we find is completely lost in beta-cells from donors with T2D.

52 This MIF enrichment was lost in bevacizumab-resistant glioblastomas, driving a t

53 initiation, Nkx3.1 expression is frequently lost in both humans and mouse models.

54 um and lung, and its protective effects were lost in both Ifnar1(-/-) and germ-free mice, revealing e

55 udy, we demonstrate that PTF1A expression is lost in both mouse and human PanINs, and that this downr

56 that the remaining wild-type Bap1 allele was lost in both spontaneous ovarian tumors and mesothelioma

57 CRH2 was subsequently lost in both teleost fishes and eutherian mammals but re

58 is mediated by CTCF, and this regulation is lost in BWS, leading to aberrant overexpression of growt

59 Pase-activating protein and tumor suppressor lost in cancer by genomic deletion or epigenetic silenci

60 The chromatin-remodeler ATRX is frequently lost in cancer cells that use ALT (alternative lengtheni

61 ies of apoptosis-effector genes are commonly lost in cancer development, in comparison to proliferati

62 partite mechanism involving N-terminal exons lost in cancer.

63 t of PML nuclear bodies (PML NBs) frequently lost in cancer.

64 ed and its cell cycle-regulated abundance is lost in Cdc48-deficient cells.

65 t sites between transfected cells, which was lost in cells expressing cis- or predicted trans-dimeriz

66 Furthermore, the influences of butyrate are lost in cells lacking HIF, thus linking butyrate metabol

67 d lysine 20 at histone H4 (H4K20me1), a mark lost in cells lacking SMYD2.

68 g the epithelial state with their expression lost in cells undergoing EMT.

69 This diurnal radioprotective effect becomes lost in circadian mutants, consistent with asynchronous

70 The protective effects are lost in CMA-deficient cells, suggesting that they are me

71 sion of GABA neurotransmission in the VP was lost in cocaine-extinguished rats.

72 Accordingly, GM130 expression is frequently lost in colorectal and breast cancer patients.

73 ssentiality identified proteins conserved or lost in complexes of other species.

74 ravel demand explains the percentage of time lost in congestion.

75 ve of gene expression across the SCN that is lost in Cry1/2-deficient SCN.

76 as in real data, whereas fewer alleles were lost in D. odorata simulations than in the field.

77 tration, synaptic plasticity was selectively lost in D2, but not D1 inputs to the ventral pallidum.

78 -affinity rex sites and become diminished or lost in DCC-defective mutants, thereby converting the to

79 in compensating phase of RVH tissues but was lost in decompensation phase of RVH.

80 The restoration of dentine lost in deep caries lesions in teeth is a routine and co

81 Only the smallest spines are lost in deep layer 3 of the primary auditory cortex in s

82 and maintenance of outer segments, which are lost in degenerative diseases.

83 ction and biofilm formation ability that was lost in DeltaciaR, indicating that argB was essential fo

84 ether KIR4.1 immunoreactivity is retained or lost in demyelinating lesions.

85 ential for this adaptive change to occur was lost in developmentally mature chimeras.

86 l human genome, we identify megabases of DNA lost in different human lineages and pinpoint large dupl

87 Contact with the basement membrane is lost in differentiating daughter cells, where YAP and TA

88 urbed forests to recover and recapture the C lost in disturbances during 1993-2012.

89 ow here that meiotic crossover patterning is lost in Drosophila melanogaster mutants that lack the Bl

90 wed that some outer kinetochore proteins are lost in early meiosis.

91 Neither implants nor prostheses were lost in either group at the 5-year follow-up examination

92 Consequently, if the CB1 receptor is lost in either neuronal population, an allostatic shift

93 s of H3K9me3 at the Xist promoter region are lost in embryonic stem (ES) cells, and ES-cloned embryos

94 ndividual surface sites, information that is lost in ensemble-averaged techniques.

95 Pth4, an ancient parathyroid hormone lost in eutherian mammals, reveals a new brain-to-bone s

96 Nearly all SI stem cells were lost in fed mice, whereas fasting promoted sufficient SI

97 genesis in WAT and brown adipose tissue were lost in Fgf21(-/-) mice.

98 s mammalian hair cells are not replaced when lost, in fish they constantly renew and regenerate after

99 Here, we show that AMACO deposition is lost in Fras1-deficient zebrafish and mice and that Fras

100 knocked down, polarization of active Rac1 is lost in FRET experiments and culminates in shunting migr

101 during early G1 phase of each cell cycle and lost in G2 phase, but it is not known when TAD structure

102 liferative response after cardiac injury was lost in G3 Terc(-/-) newborns but rescued in G3 Terc(-/-

103 eletions of key tumor suppressors frequently lost in GBM, namely Ink4a, Ink4b, Arf and/or PTEN.

104 coupled to RGCs via gap junctions that were lost in glaucoma, whereas uncoupled ACs were largely una

105 The protective effect was lost in Gpbar1(-/-) mice.

106 These actions were lost in GPR18-deficient mice.

107 by single-gene deletion events, some may be lost in groups of consecutive genes.

108 RASA2 expression was lost in >/=30% of human melanomas and was associated wit

109 ING4 expression is lost in >60% of human primary prostate tumors.

110 lian Ste20-like serine/threonine kinases, is lost in >95% pancreatic cancer through proteasome-mediat

111 The effects of linaclotide were lost in Gucy2c(-/-) mice and prevented by inhibiting cGM

112 (2) = 0.83), but this optimized phenotype is lost in heart failure, suggesting restoration of normal

113 The Y chromosome is frequently lost in hematopoietic cells, which represents the most c

114 d cAMP concentrations and activate PDE4B are lost in hepatocytes deleted for both catalytic subunits

115 In the sheep, atrial t-tubules were also lost in HF and AmpII levels decreased.

116 c acetyl CoA, PC activity, and lipolysis was lost in high-fat-fed rats, a phenomenon reversible by IL

117 Innervation of the gut is segmentally lost in Hirschsprung disease (HSCR), a consequence of ce

118 tible to HIV in vitro and are preferentially lost in HIV-infected individuals compared with CMV-speci

119 stribution of RvD1 biosynthetic machinery is lost in hMSG with SS; (3) RvD1 levels in mSMG cell cultu

120 populations of (225)Ac(3+) ions: one rapidly lost in human serum and one that remains bound to the US

121 DLX3 expression is lost in human skin cancers and is extinguished during pr

122 Expression of NORE1A is frequently lost in human tumors, and its mechanism of action remain

123 mologue (PTEN) gene is frequently mutated or lost in human tumours and syndromes that predispose indi

124 The beneficial effects of BAR501 were lost in Il-10(-/-) mice.

125 f eosinophils and protection against EAE was lost in IL-33(-/-) mice and upon neutralization of IL-5.

126 The protective effect of TSO was lost in immunosuppressed rabbits, where TSO exacerbated

127 n of pancreatic beta-cells that is partially lost in individuals affected by Type 2 diabetes.

128 from the bilaterian ancestor that have been lost in insects.

129 Protection was lost in instances when T-cell responses were high or whe

130 shund homolog 1 (DACH1), whose expression is lost in invasive breast cancer.

131 oring metal cofactors that are spontaneously lost in iron deficient cells.

132 n the third trimester of human pregnancy are lost in large-for-gestational age infants and may be reg

133 This response is lost in late-stage metastatic melanomas expressing high

134 remain in the acrosome and are progressively lost in later steps of differentiation.

135 onphosphorylated LXRalpha S198, and this was lost in LXR-deficient BMDMs.

136 ins an apparent duplication with one paralog lost in mammals, and a number of crustacean genomes (lik

137 owever, such sorting mechanisms appear to be lost in mammals.

138 an obligate requirement for survival that is lost in mature hematopoietic and in transformed epitheli

139 conclude that NF1 is a key tumor suppressor lost in melanomas, and that concurrent RASopathy gene mu

140 cillation in markers of mRNA translation was lost in memory-deficient transgenic mice lacking calmodu

141 tasis suppressor protein whose expression is lost in metastatic bladder and prostate carcinomas.

142 ins a DNA primase activity, this function is lost in metazoan mtDNA helicase.

143 ediated improvement in glucose tolerance was lost in mice coinjected with a GLP-1 receptor antagonist

144 licits an anti-contractile effect, which was lost in mice deficient in eosinophils, mimicking the obe

145 ght-reducing effect of increased loading was lost in mice depleted of osteocytes.

146 m-dependent vasorelaxation by antibiotics is lost in mice lacking endothelial Sirt1.

147 hat IgE-mediated tumor protection was mostly lost in mice lacking FcepsilonRI.

148 t delivered to PVN to inhibit food intake is lost in mice lacking G(q/11)alpha in the PVN but not in

149 ortantly, the anxiolytic effect of ML297 was lost in mice lacking GIRK1.

150 how that the orexigenic effect of ghrelin is lost in mice lacking MRAP2.

151 ithrombotic effects of exenatide were partly lost in mice transplanted with bone marrow from Glp1r(-/

152 d Flox mice to 47% after NTS treatment), was lost in mice with hepatic deletion of Pcsk9 (5% in both

153 F. tularensis infection; this protection was lost in MIIG mice.

154 The in vivo lipid A pattern is lost in minimally passaged bacteria isolated from the ti

155 -directed DNA methylation activities and are lost in mop1 and mop3 mutants, but the nearby genes rare

156 specific variation is widespread but then is lost in more derived theropods.

157 basidiomycetes and beta2-tubulin genes were lost in most ascomycetes.

158 The transcription factor HIC2 is lost in most distal deletions, as well as in a minority

159 During adipogenesis, Thy1 expression is lost in mouse 3T3-L1 cells.

160 gamma/delta recombination in fetal thymus is lost in mTORC1KO thymus, leading to elevated gammadeltaT

161 3K36 trimethylation (H3K36me3) is frequently lost in multiple cancer types, identifying it as an impo

162 Importantly, OTUD1 is lost in multiple types of human cancers and loss of OTUD

163 We show that BAT phenotype is lost in murine pregnancy, while there is a gain of white

164 Silent locus identity is similarly lost in mutants for the cytosine maintenance methyltrans

165 d in left-shifted band-stage neutrophils but lost in neutrophils from steady-state PB.

166 ed the inactive enantiomer, l-MDP, an effect lost in Nod2(-/-) mice.

167 By the time VA has been lost in nonexudative AMD, proof-of-concept early-stage c

168 cantly diminished SOCE in NPCs, and SOCE was lost in NPCs from transgenic mice lacking Orai1 or STIM1

169 Unexpectedly, RORbeta2 expression was lost in Nrl(-/-) mice.

170 ) is a GC-specific miRNA whose expression is lost in numerous mature B-cell neoplasms.

171 vasoconstriction observed in Young MAs were lost in Old MAs along with impaired dilatation to calcit

172 A large portion of the VL MU pool is lost in older men and those recruited during moderate in

173 match, and how much information is gained or lost in one allele of the polymorphism or mutation relat

174 intained in one differentiated cell fate but lost in others.

175 present in some ferns and has possibly been lost in others.

176 istical significance of this association was lost in our multivariate analysis (P=0.44).

177 By contrast, 21% and 31% of OHCbl was lost in oven-baking steps in straight- and sponge-dough

178 gration and airway infiltration were all but lost in P1V1 and P1V3 mice during lipopolysaccharide (LP

179 ic apolipoprotein E and this proteoglycan is lost in P2-null mice.

180 s are anchored by CTCF, and its occupancy is lost in parallel with loop decommissioning during differ

181 early stages of synapse development and were lost in parallel with maturation of the network due to o

182 c nucleus on intracerebellar connectivity is lost in Parkinson's disease, which may contribute to pat

183 This reward sensitivity was lost in patients off medication (5.2 [3.2], p=0.117).

184 in AIH/AISC, though suppressive function is lost in patients upon proinflammatory challenge; protrac

185 he normal mammary gland and is progressively lost in patients with metastatic BC.

186 ur data indicate that the NDH complex can be lost in photoautotrophic plant species.

187 This growth phenotype was lost in plants expressing the phosphosite variant, sugge

188 bility of scFvSCE5-scuPA to lyse thrombi was lost in plasminogen-deficient mice, but could be restore

189 in was apparent when the effect of WISP1 was lost in PMo isolated from beta3(-/-) mice.

190 icals, occurring in gas phase, is completely lost in polar solvents as predicted by theoretical compu

191 llular and spatial heterogeneities otherwise lost in population-averaged measurements.

192 This response is lost in PPARalpha knockout (Ppara(-/-), also known as Nr

193 BAP1 expression was maintained, rather than lost, in primary melanomas compared with nevi and normal

194 PTEN activity is often lost in prostate cancer.

195 and (3) it can retrieve significant peptides lost in protein-centric quantification for further downs

196 to alleviate mechanical hypersensitivity is lost in PSNL alpha2delta-1(-/-) mice.

197 in the actin-detached conformation, which is lost in R759E but is restored in N509K/R759E.

198 ive effects conferred by Parp1 deletion were lost in Rag2(-/-) x Parp1(-/-) mice, highlighting the ro

199 elopment wherein miR-200 expression was only lost in regions with high ZEB expression.

200 ystem to undergo repair and to replace cells lost in response to injury and disease.

201 5hmC was lost in response to PIT, with DNA hypomethylation of the

202 This effect is lost in S1928A knock-in mice.

203 hosphorylation, this positive modulation was lost in S940A neurons.

204 This effect was lost in SCN slices treated with TPQ and SCN slices from

205 alphaIIbbeta3 activation by ADP and 5-HT is lost in SERT(-/-) platelets.

206 Has2 expression in the limb bud is lost in Shh null and expanded anteriorly in Gli3 mutants

207 This dampening effect is lost in slices from GluA2 KO mice, indicating a requirem

208 the motif and the rest of domain 4 that are lost in SLO.

209 isms of limb development were not completely lost in snakes.

210 p21.3, which is hemizygously or homozygously lost in some breast cancer patients.

211 ility to establish this partnership has been lost in some plant lineages like the Brassicaceae, which

212 The benefit could be lost in some subgroups of patients if noninvasive ventil

213 nes and gene functions that were acquired or lost in specific lineages during vascular plant evolutio

214 long the metazoan stem lineage and were then lost in sponges and placozoans or evolved at least twice

215 kinases are activated and hippo signaling is lost in sporadic human malignancies remains unknown.

216 that the robust response to IFN-alphabeta is lost in Stat1-Stat2 double-knockout macrophages suggest

217 oximately 200 A, which was almost completely lost in state 2.

218 of these CG-DMPs are inherited, some can be lost in subsequent generations.

219 their integrity, and this functionality was lost in synthetic peptides harboring amino acid substitu

220 rrelates with activation of HSP1; looping is lost in tail-deleted TFAM.

221 strate that IL-9 production is progressively lost in Th9 cultures during several rounds of differenti

222 e classification and source apportionment is lost in that case.

223 haploinsufficiency of Egr1 and Apc, 2 genes lost in the 5q deletion, are key players in the progress

224 elial cells during lactation was selectively lost in the absence of AFAP1.

225 -Guerin (BCG) vaccine-induced protection was lost in the absence of ESAT-6-dependent cytosolic contac

226 n of CXCL5 secretion by P2X4 antagonists was lost in the absence of extracellular Ca(2+) Reciprocally

227 throughout the night, and this stability is lost in the absence of RpaA.

228 es but not cycling cells, and this effect is lost in the absence of SAMHD1.

229 ssociation between ER and ERGIC membranes is lost in the absence of TFG.

230 passaged in the presence of rifampin but was lost in the absence of the drug, suggesting that the dup

231 al period, but this regenerative capacity is lost in the adult cochlea.

232 possessed two pdf homologs, one of which was lost in the arthropod or arthropod/tardigrade lineage, f

233 s (mesDA) are the nerve cells preferentially lost in the brains of Parkinson's disease patients.

234 (HSPCs), whereas they are hyperactivated and lost in the circulation when wild-type HSPCs are absent,

235 Often lost in the discussion are the human rights elements tha

236 What should not be lost in the discussions regarding the diverse biology of

237 +) dynamics at the heminode and terminal was lost in the dysmyelinated axon from Long-Evans shaker ra

238 H3K27me3-dependent imprinting is largely lost in the embryonic cell lineage, but at least five ge

239 n the mouse ENS and their expression is also lost in the ENS of Ret-null embryos.

240 he ancestral cytoplasmic IF protein gene was lost in the entire panarthropod (onychophoran + tardigra

241 one (Pth)4 in zebrafish that was secondarily lost in the eutherian mammals' lineage, including humans

242 This novel p53 activity is lost in the exonuclease-deficient but transcriptionally

243 The yield advantage of the F1 is lost in the F2 and subsequent generations.

244 After one year, 12% of patients were lost in the first group and 35% in the control group (P

245 signal-regulated protein kinase 5 (Erk5) is lost in the hearts of obese/diabetic animal models and t

246 aryotic common ancestor (LECA) that has been lost in the highly studied yeast lineages.

247 Interestingly, we found that GAD3 was lost in the hominid lineage.

248 Cellular and nuclear details were lost in the infected explants, consistent with cell deat

249 nolic acids) of almond kernels substantially lost in the initial phase; afterward these components gr

250 nd dynamics at the heminode and terminal was lost in the LES rat.

251 ancestral amniote hippocampus was gradually lost in the lineage leading to birds, and birds expanded

252 Lindau (VHL) is a tumour suppressor that is lost in the majority of clear cell RCC (ccRCC) cases.

253 sion is dependent on Myc and Pten, and it is lost in the majority of human prostate cancers.

254 t, the capacity for IBC/IPhC regeneration is lost in the mature organ of Corti, and consequently IHC

255 Switching was subsequently lost in the Metschnikowiaceae, including Candida albican

256 plex in true toads (Bufonidae), where it was lost in the most recent common ancestor, preceding a rad

257 ing the incidence of extra teeth, which were lost in the mouse lineage 45 million years ago (Ma).

258 s detected in the wild type, although it was lost in the mutant.

259 totopic representation present in the ELL is lost in the nucleus lateralis (NL) of the TS, while a ro

260 ips between the adipokines and body fat were lost in the patients with pNTM, a novel finding.

261 ake of carotenoids but that this function is lost in the predominant mutant isoform in white recessiv

262 protective effect of arginase inhibition was lost in the presence of a NOS inhibitor.

263 ion of multiple late viral protein mRNAs was lost in the presence of either drug, consistent with the

264 ), and CATAC-mediated expression rhythms are lost in the presence of null mutations in either cyc or

265 ol only accounted for 30%-60% of the benzene lost in the presence of O2.

266 This regulation is lost in the presence of polyglutamine, which mislocalize

267 agonist-stimulated receptor activity that is lost in the R6G;E42G mutant.

268 ato and found only in Rosids (but apparently lost in the Rosid A. thaliana) for which we propose the

269 f a single transcription factor binding site lost in the snake lineage reinstated full in vivo functi

270 in light-regulated histidine kinase activity lost in the streptophyte phytochrome lineage.

271 of TLE, parvalbumin neurons are selectively lost in the subiculum, the major output area of the hipp

272 ing that 3.2 Mbp with population support was lost in the transition from GRCh37 with 13.7 Mbp added t

273 patients, and these variants were routinely lost in the tumor cells by chromosomal deletions (e.g.,

274 This makes it easy to get lost in the vast amount of literature and forget about t

275 (absenteeism and presenteeism [productivity lost in the workplace]) were also calculated.

276 that is typical for pericyclic reactions is lost in their mechanistic cousins, cycloaromatization re

277 h other in central neurons, and that this is lost in their transformed counterparts.

278 One set of motifs frequently lost in these cancer-associated truncations is the SAMP

279 e growing polyketide chain and the enzyme is lost in these cases, which would limit efficient chain e

280 functional cp-ndh genes have been completely lost in these orchids or whether they have been transfer

281 PEDF was lost in thicker melanomas (P = 0.003), and correlated wi

282 er, remains TLR9-dependent, as inhibition is lost in TLR9 deficient mice.

283 We found that miR-34a was lost in TNBC, specifically within mesenchymal and mesenc

284 This response to exercise is lost in transgenic mice with constitutive expression of

285 ort: From cancer patient to cancer survivor: lost in transition, in 2005, there has been a national c

286 port From Cancer Patient to Cancer Survivor: Lost in Transition.

287 This clinical effect was lost in Treg-depleted mice, demonstrating the major cont

288 obes to genetic regions frequently gained or lost in tumor development.

289 el mechanism of Nrf2 regulation that may get lost in tumors and by which IER3 exerts its stress-adapt

290 cellularity and unicellularity processes was lost in tumors.

291 rs, one or more future drug options had been lost in two participants (Kaplan-Meier estimate 0.7%) in

292 lopment that lead to beta cell formation are lost in two-dimensional systems.

293 GP by central KATP channel activation may be lost in type 2 diabetes.

294 udied to date, suggesting they are symbionts lost in urban-industrialized societies.

295 enzyme in gluconeogenesis and is frequently lost in various types of cancer.

296 l cells was ectopically induced by Vegfa and lost in Vegfa signaling mutants.

297 rtebrates, suggesting that this receptor was lost in vertebrates during evolution.

298 tream, whereas the 5448 Deltasda1(M-) strain lost in vivo selection of CovRS mutations and was sensit

299 More subtle intergroup differences are lost in WO samples because of reduced statistical power.

300 ast, a subset of "ERAAP-edited" peptides was lost in WT cells, and ERAAP-deficient cells presented a