ライフサイエンスコーパス: lost in

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

2 Bom Jesus, a Portuguese nau (trading vessel) lost in 1533 while headed to India.(4-6) The cargo inclu

3 cases associated with 1,567 additional km(2) lost in 2008, the study midpoint, Amazon-wide).

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

7 d for enhancing both NUE and yield, has been lost in 90.3% of rice varieties due to the increased app

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

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

13 on, the anti-allodynic effects of SNC80 were lost in a model of opioid induced hyperalgesia/medicatio

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

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

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

17 dentified an immunoreactive antigen that was lost in a putative glycosyltransferase mutant, suggestin

18 sent across protostomes although it has been lost in a small number of taxa.

19 g the diversification of eukaryotes but were lost in a subgroup of Fungi.

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

21 n addition, SMARCA2, another SWI/SNF subunit lost in a subset of NSCLCs, also regulates cyclin D1 and

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

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

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

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

26 de, but why cardiac regenerative capacity is lost in adult humans remains an enigma.

27 photoreceptor loss occur, but cones are not lost in ageing primate although their function declines,

28 miRNAs of the miR-16 and miR-34 families is lost in aggressive OS.

29 conserved in cnidarians and vertebrates but lost in all other studied groups, is expressed in the ne

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

31 ained in place in SHAM and OVX ewes but were lost in all ZOL ewes.

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

33 with between 0.67 and 5.86 gigatonnes CO(2) lost in Amazon understory fires between 2001 and 2010.

34 ty, which suppresses NE gene expression, was lost in AMPC and SCNPC PDX models.

35 of the essential vitamin B1 (thiamine) were lost in an ancestor of a yeast lineage, the Wickerhamiel

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

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

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

39 by the reincorporation of the fixed carbons lost in anabolic and photorespiratory pathways in conjun

40 but what ID NOW gained in rapid results, it lost in analytical and clinical performance.

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 viremia was achieved-an observation that was lost in anti-TNF-alpha-treated IFNAR(-/-) animals.

46 Alternatively, this function may have been lost in Arabidopsis.

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

48 org) m(-2) year(-1) , respectively), but was lost in bare areas.

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 ctility and skeletal muscle hypertrophy were lost in beta-arrestin 1 knockout mice, implying that arr

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

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

54 higher levels of taxonomic uniqueness being lost in biodiversity coldspots compared to hotspots.

55 P-alpha-mediated regulation of claudin-5 was lost in blood vessels from tissue biopsies from patients

56 foraging advantage of bold colonies that is lost in bold neighbourhoods because prey become scarce,

57 This response was lost in bone marrow-derived macrophages from mice defici

58 tone, which is masked when COX1 activity is lost in both ECs and platelets.

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

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

61 s, but upon transformation this gradient was lost in both lesion types.

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

63 thelial cell membrane integrity, known to be lost in breast cancer progression.

64 in breast tissue, whose expression is often lost in breast cancers.

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

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

67 the catalytic sites of 17 enzymes frequently lost in cancer.

68 p27 is rarely fully lost in cancers because it can play both tumor suppressi

69 , the anti-proliferative activity of IRF1 is lost in cell lines expressing T181A mutant.

70 This requirement for PP1 is lost in cells expressing CDK1 phosphorylation-defective

71 Hypoxia-mediated induction of ATG9A was lost in cells lacking HIF-1.

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

73 iated protein) interacting protein, is often lost in cells using the alternative lengthening of telom

74 indle pole, and this increase in activity is lost in cenexin-depleted cells.

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

76 lic enzyme NAT2 at 8p22, which is frequently lost in colorectal cancers and has a common variant with

77 es more flexibly adapt to limited N, a trait lost in commercial potatoes.

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

79 ur without rhythmic feeding behavior and are lost in constant darkness.

80 oxygen sensitive (EOS) populations that were lost in conventional stool containers, and thus viabilit

81 We demonstrated that WTX frequently lost in CRC which was highly correlated with cell prolif

82 This adaptability is lost in cultured adult endothelial cells, which do not v

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

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

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

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

87 Similarly, lncRNAs are lost in diabetic humans.

88 ed for glomerular structure and function and lost in diabetic nephropathy.

89 The same quantity of habitat can be lost in different spatial patterns with varying habitat

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

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

92 onic nitroglycerin model, an effect that was lost in Dlx-DOR mice.

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

94 Pigment-binding capacity was completely lost in each of the OHPs when residues of the light-harv

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

96 formation that specifies cell types is often lost in EM reconstructions.

97 the aggregate number of lives and life-years lost in England for per-patient delays of 1-6 months in

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

99 ced thousands of ancestral alleles that were lost in Eurasian populations before introgression.

100 pic divergence and are frequently gained and lost in eutherian genomes.

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

102 ore than previously anticipated and are only lost in extreme old age, with implications for the repai

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

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

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

106 neuronal differentiation and simultaneously lost in gliomagenesis.

107 verexpressers compared with WT parasites was lost in gp91-phox (-/-) macrophages, underscoring the ro

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

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

110 al-derived histamine on BAL inflammation was lost in HDC-deficient mice.

111 This close correlation was lost in heart failure myocytes from both species.

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 (including DICER1 and AKT1) were recurrently lost in HPV-positive OSCCs, in contrast to their gains i

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

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

118 are present across eukaryotes but have been lost in humans.

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

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

121 urance, and beneficial glycemic effects were lost in Il13(-/-) mice.

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

123 of phage particles have been preferentially lost in incomplete prophages, while tail fiber, transpos

124 ntial heterogeneity in protein age, which is lost in iPSC-derived neurons lacking the lysosomal prote

125 The capacity to engage this checkpoint is lost in ISCs from aging flies, and we show that it can b

126 Glucose-dependent excitability is lost in islets from K(ATP)-knockout (K(ATP)-KO) mice, in

127 s and SA perception pathways, since they are lost in isochorismate synthase1/salicylic acid induction

128 the most proximal BPs, and BPs were entirely lost in Jag1; Dll1 double mutants.

129 ficking, and function, a feature that may be lost in JNCL.

130 eed dispersal of large seeded plants, can be lost in large continuous forests due to the rarity of la

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

132 fate maps provide spatial information, often lost in lineage reconstruction, that can offer fundament

133 Finally, rhythmic clock gene expression is lost in Liver-RE mice under constant darkness.

134 Such Treg activity lost in male epididymal white adipose tissue (eWAT) and

135 f the G-protein networks; however, these are lost in many monocots.

136 Topologically associating domains (TADs) are lost in meiotic prophase, suggesting that assembly of th

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

138 ein in yeast (Saccharomyces cerevisiae), but lost in Metazoa.

139 These bonds were lost in MGL(short) H259T, thus explaining its lower bind

140 -L1 and is highly conserved in hominids, but lost in mice and a few related species.

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

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

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

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

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

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

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

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

149 a(2+) entry and muscle force production were lost in mice with muscle-specific loss of Orai1 function

150 Notably, miR-223 expression was lost in microdissected ductal carcinoma in situ (DCIS) f

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

152 n of housekeeping reactions, which are often lost in models built using standard thresholding approac

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

154 One of these is FAM46C that is lost in more than 10% of patients with multiple myeloma.

155 and translocation, frequently rearranged and lost in most Mycena species, but conserved in the Armill

156 t share features with animals that have been lost in most other fungi.

157 Itch sensation to histamine injection was lost in most symptomatic patients.

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

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

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

161 agonists to suppress IL-1beta secretion was lost in Nlrp3-null macrophages.

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

163 Sec was then lost in numerous independent events in various fungal li

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

165 hus, tonic PVN NPY inhibition of LSNA may be lost in obese males as a result of a decrease in NPY inp

166 In contrast, this response was lost in offspring exposed in utero to UFPs.

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

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

169 looked for alleles that are beneficial when lost in order to determine how prevalent this mode of ad

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

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

172 15556, shown to target MTAP (a gene commonly lost in pancreatic cancer)-negative tumors, was validate

173 eness in gonochoristic species, but has been lost in parallel in androdioecious species.

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

175 rated by CCR2 cells, and VGLUT1 synapses are lost in parallel.

176 is ability to impart left-sided character is lost in parapineal cells lacking Sox1a function, despite

177 The salutary effects of the drug were lost in Parkin knockout mice, implicating Parkin-mediate

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

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

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

181 Surprisingly, such effects are lost in per (0) mutants, supporting a PER-dependent inhi

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

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

184 onsive growth and development are completely lost in plants lacking both genes, suggesting that ELF3

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

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

187 d srg-37), which were previously shown to be lost in population-dense laboratory cultures.

188 ed that almost all CTCF chromatin binding is lost in prometaphase.

189 PTEN activity is often lost in prostate cancer.

190 otein levels are reduced, but never entirely lost, in prostate adenocarcinoma, enhancement of NKX3.1

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

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

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

194 Shh signaling is lost in reactive astrocytes at the lesion site, but pers

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

196 levels, with accompanying cAMP accumulation lost in sAC-/- cells.

197 -aza treatment, whereas OHCs were completely lost in saline-treated mice.

198 as a main component of floral scent has been lost in selfing C. rubella by mutation of cinnamate-CoA

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

200 All or majority of the key ATG genes were lost in several fungal groups with unique lifestyles and

201 an ancestral eukaryotic trait that has been lost in several lineages like flowering plants.

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

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

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

205 e families is highly lineage-specific, being lost in some descendant lineages, but undergoing extensi

206 ovide key insights into how cell identity is lost in some germ cell tumors.

207 FNDC3A was lost in some multiple myeloma cell lines.

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

209 While caspase-8 expression is lost in some tumors, it is increased in others, indicati

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

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

212 of fragmented DNA, information traditionally lost in standard NGS library preparation methods.

213 r effect induced by anti-MerTK treatment was lost in Sting(gt/gt) mice, but not in Cgas(-/-) mice.

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

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

216 ry scores) was found in the controls but was lost in TBI patients.

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

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

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

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

221 rical gaits are ancestral for Crocodylia and lost in the alligator lineage, or that asymmetrical gait

222 ar plant groups but is believed to have been lost in the ancestor of leptosporangiate ferns.

223 a medusa life stage, which was subsequently lost in the anthozoans.

224 This control is lost in the Asian haplotype, which may have evolved to b

225 however, the tracking of neurites is easily lost in the automated process due to the intrinsic varia

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

227 We show that Cdc14 was lost in the common ancestor of angiosperm plants but is

228 allograft loss was reported, whereas 3 were lost in the control group.

229 ified several proteins whose acetylation was lost in the Deltakatms strain, and whose transcript leve

230 lar Mg(2+) concentrations seen previously is lost in the DeltapitA mutant, we suggest that MgtS binds

231 equence, and the expression of this gene was lost in the developing gut of mice that lacked the ICR.

232 oliferation, and that this regulation can be lost in the development or progression of breast cancer.

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

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

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

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

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

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

239 In mice, this ability is lost in the first postnatal week, a period physiological

240 recise arrangement of feather primordia, are lost in the flightless emu and ostrich, though via diffe

241 freshwater fish diversity is not inevitably lost in the future.

242 This effect was completely lost in the HCAR2-null mice after a 2-d starvation proto

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

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

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

246 mmal and bird species on the brink have been lost in the last century.

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

248 ies, including PA, observed in wild type was lost in the LHY and CCA1 double knockout mutant.

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

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

251 able elements in Brassica oleracea, but were lost in the majority of the Bot1 elements in Brassica ra

252 ice, and the majority of male germ cells are lost in the meiotic defect of first wave spermatogenesis

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

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

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

256 A subset of medial and intermediate eCN are lost in the mutants, with an associated cell non-autonom

257 e heart during development, prenatal stages, lost in the neonate, and adult heart confirmed by qRT-PC

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

259 f a sample is directly related to the energy lost in the oscillating cantilever, which is a direct co

260 placebo; P = .03), but the significance was lost in the pooled analyses (P = .058).

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

262 Synergy was lost in the presence of an inhibitor of the p38 MAP kina

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 ight predict that that HSR function would be lost in the reproductive queens.

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

269 wever, this proreparative effect of MSCs was lost in the setting of HCA.

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

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

272 creases after approximately 10% of weight is lost in the surgical group and approximately 20% in the

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

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

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

276 activity was severely downregulated but not lost in the ventral forebrain and in regions adjacent to

277 onic hedgehog (Shh) expression was virtually lost in the ventral forebrain but maintained in the zona

278 ing of how and where stimulus information is lost in the visual system under crowding.

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

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

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

282 imaging and the crucial phase information is lost in these methods.

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

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

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

286 ce designs that can capture energy typically lost in traditional solar cells.

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

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

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

290 ife-history theory, but appears to have been lost in translation in recent developments of life-histo

291 ough NAFLD genomics sometimes appears to be "lost in translation," we envision clinical utility in tr

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

293 cellularity and unicellularity processes was lost in tumors.

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

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

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

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

298 Up to 84 000 tons of dye can be lost in water, and 90 million tons of water are attribut

299 The glucoregulatory effects of GB-IL were lost in whole-body Glp-1r(-/-) mice.

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