ライフサイエンスコーパス: protect @2 from

1 IF-1alpha in normoxia, induce autophagy, and protect cells from a subsequent OGD insult.

2 Intravenous infusion of Ab1485 protected macaques from a high dose challenge with SHIVA

3 single intranasal prophylactic dose of decoy protected Syrian hamsters from a subsequent lethal SARS-

4 Mammalian telomeres protect chromosome ends from aberrant DNA repair(1).

5 nslation termination codons (PTCs) serves to protect cells from accumulating non-functional and poten

6 usts cochlear gain and frequency tuning, and protects the ear from acoustic trauma.

7 onal cytomegalovirus (CMV) immunity does not protect the fetus from acquiring congenital CMV infectio

8 brane lipids, repair cellular organelles and protect mutant cells from acute iron overload.

9 ureus infection in vivo We conclude that EPS protects hosts from acute bloodstream S. aureus infectio

10 d a lipid droplet (LD)-mediated mechanism of protecting retinal cells from age-related degeneration.

11 ationships can inform policy making aimed at protecting public health from air pollution in China.

12 Studies have suggested that estrogens may protect mice from AKI.

13 Multiple COBRA H2 HA vaccines protected mice from all three viral challenges and produ

14 Long-term neutralization of IL-6 or TGF-beta protected TNF(-/-) mice from an otherwise lethal infecti

15 Adjusting the protecting group strategy, from an alkyl ether to a bide

16 ESR serves two purposes in aneuploid cells: protecting cells from aneuploidy-induced cellular stress

17 Exogenous IL-4 and IL-13 protect mice from antibody-mediated joint inflammation,

18 We investigated whether gC protects HSV from antibody neutralization.

19 ion of Env is an important feature that both protects the virus from antibody responses and serves as

20 le delivery of either FOXM1 or FOXF1 did not protect endothelial cells from apoptosis caused by hyper

21 tially increased BCL2 protein expression and protected cancer cells from apoptosis induced by cellula

22 ed M/M to a proinflammatory M1 phenotype and protected them from apoptosis.

23 monocytes, suggesting that autophagy was not protecting cells from apoptosis.

24 Protecting ECs from apoptosis in this model did not prev

25 tes to mechanical stress and showed that SOC protects these cells from apoptosis caused by extensive

26 ts as a buffer in MYC amplified settings and protects these cells from apoptosis.

27 found that KSHV uses specific mechanisms to protect its transcripts from ARS2-mediated decay.

28 cated laryngeal sensory motor reflex circuit protects our airways from aspirated foods or liquids.

29 upon DNA damage, whereas S429A substitution protects MDM2 from auto-degradation.

30 ciliated epithelia cell beat coordinately to protect the epithelium from bacteria, viruses, and harmf

31 P7C3-A20 also protected mice from BBB degradation after acute TBI.

32 nd memory, we tested a hypothesis that sleep protects old memories from being forgotten after new lea

33 nerates a metabolic homeostatic circuit that protects cells from bioenergetic crisis and mitochondria

34 ncing approaches, we demonstrate that TOLLIP protects cells from bleomycin-induced apoptosis using pr

35 ve evolved elegant and redundant pathways to protect their genomes from both genotoxic stressors and

36 x43-copy number in mdx/WT-Cx43(+/-) chimeras protected them from both cardiac and skeletal muscle fib

37 0 signaling axis in intestinal CD11c(+) APCs protects mice from CAC by regulating the expression of t

38 In addition, HSGN-218 protected mice from CDI recurrence.

39 uding glutathione peroxidase 4 (GPX4), which protected cells from chemotherapy-induced oxidative stre

40 nourish hypoxic, nutrient-starved tumors and protects them from chemotherapy-induced death.

41 through the noncanonical NF-kappaB pathway, protected these cells from chronic inflammation as compa

42 cally, SIRT2, an NAD+-dependent deacetylase, protected neurons from cisplatin cytotoxicity by promoti

43 m12 protein, and suggest that these mAb may protect mice from CMV infection via passive immunity.

44 Moreover, administration of GAG protected mice from colitis induced by dextran sulfate s

45 denosine receptor-mediated immunosuppression protects tissues from collateral damage by antipathogen

46 n, and the sequestration of miR399 molecules protects PHO2 mRNA from complete degradation.

47 sures put in place to manage groundwater and protect it from contamination.

48 inum oxide that adheres to the metal surface protects it from corrosive atmospheres and carbon (carbu

49 Furthermore, we show that heme protects P. aeruginosa from CP-mediated inhibition of ir

50 imilarly to P. aeruginosa, we show that heme protects S. aureus from CP-mediated inhibition of iron u

51 713T and Y768R), we were able to selectively protect receptors from cross-links at both the diagonal

52 uggest that higher AADAC expression in VSMCs protects T2DM patients from CVD.

53 electromagnetic (EM) wakefields excitation, protect detectors from damage at a range of installation

54 tion to drive rapid behavioral responses and protect teeth from damage.

55 C-L plays a role in protecting intestinal tissue from damage, LPS-induced we

56 RNAs via nontemplated nucleotide addition to protect messenger RNAs from deadenylation.

57 e FBF-2 is deadenylase-independent and might protect the targets from deadenylation.

58 Toll-like receptor 4 (TLR4) on hair cells to protect them from death.

59 The lead agent protects neurons from death in vivo.

60 strand displacement reaction is designed to protect MIC from decoding and falsification.

61 re environmental conditions physiochemically protect carbon stores from decomposition for thousands o

62 found that inactivating rhodopsin signaling protected photoreceptors from degeneration suggesting th

63 ry binding to RetGC, a process essential for protecting photoreceptors from degeneration.

64 Retinal degeneration-3 (RD3) protein protects photoreceptors from degeneration by preventing

65 ing conditions, these proteins were found to protect each other from degradation.

66 instigates Aurora B deubiquitination and/or protect it from degradation in a non-catalytic manner.

67 rategy, allowing yeast cells to save energy, protect proteins from degradation, and inhibit protein f

68 nding complex, localize at stalled forks and protect stalled forks from degradation by the MRE11 nucl

69 To protect the SAM from degradation and achieve efficient d

70 rticles formed homogeneous sizes of ~200 nm, protected siRNA from degradation, and showed excellent b

71 t of PTPN22 R620W to the plasma membrane but protected this mutant from degradation.

72 nstability, yet the molecular mechanisms for protecting forks from degradation/collapse are not well

73 s von Willebrand factor (VWF) stabilizes and protects FVIII from degradation and clearance, but it al

74 ding with the same region of TaSnRKalpha and protects it from degradation.

75 d during oxygen and amino acid depletion and protects LRS from degradation.

76 While efficient translation protects mRNA from degradation, uORF translation trigger

77 ciation with poly(ADP-ribose) chains, ZBTB24 protects them from degradation by poly(ADP-ribose) glyco

78 triphosphate (NTP) ratios in Deltalon cells protects them from deletion of otherwise essential deoxy

79 terials has shown great promise, not only in protecting the enzymes from denaturation under nonbiolog

80 SERCA activation, presumably because 14-3-3 protected PLN pentamers from dephosphorylation.

81 s, Tmods bind actin-tropomyosin filaments to protect them from depolymerizing, not elongating.

82 olinergic responses in prefrontal cortex and protect these responses from desensitization.

83 eds must possess a core set of mechanisms to protect them from desiccation- and rehydration-induced d

84 flavonoids prior to light insult remarkably protected retina from deterioration and preserved its fu

85 emic and topical treatment, with tofacitinib protecting mice from developing severe cutaneous leishma

86 Ucp1) expression in white adipose tissue and protects mice from developing obesity and insulin resist

87 ntially recruited to the retinal vessels and protect vessels from diabetic damage.

88 -induced fat thermogenesis was sufficient to protect mice from diet-induced body-weight gain.

89 naling in muscle by overexpression of the IR protects mice from diet-induced obesity and its effects

90 that adipocyte-specific deletion of P2Y(6)R protects mice from diet-induced obesity, improving gluco

91 s are natural bacterial antibiotics that can protect crops from disease.

92 maize ear-has multiple functions, including protecting the ear from diseases infection and dehydrati

93 zed nucleic acid-protein complexes that help protect chromosome ends from DNA damage.

94 toskeletal and supracellular rearrangements, protects nuclei from DNA damage.

95 s crucial for normal ER lipid metabolism and protects the ER from dysfunction.

96 phagic flux may be a therapeutic strategy to protect endothelial function from dyslipidemia and diabe

97 ly acquired maternal GBS-specific antibodies protect newborns from early-onset disease, yet their imp

98 enes likely expanded in eutherian mammals to protect the germline from environmental stress and aid i

99 in several food and nutraceutical matrices, protecting the ingredients from environmental conditions

100 can be considered as a passive barrier that protects food from environmental factors such as ultravi

101 We conclude that MHCI binding protects peptides from ERAP1 degradation and that trimmi

102 the DNA damage response (DDR) and completely protected cells from ETO-induced genome instability, the

103 ated at the surface of KRAS-mutated CRC, and protects cells from excess copper-ion toxicity.

104 y to inhibitory neurons and is essential for protecting the brain from excessive activation in health

105 The additional three nucleotides may protect the inhibitor from excision by the viral 3'-5' e

106 though mask wearing is intended, in part, to protect others from exhaled, virus-containing particles,

107 Remarkably, existing antibodies could not protect cattle from experimental reinfection with IDV.

108 ed disruption of Paneth cell lysozyme (Lyz1) protected mice from experimental colitis.

109 ed in public health guidelines to adequately protect vulnerable patients from exposure to the virus.

110 r and the blood cerebrospinal fluid barrier, protect the CNS from external agents.

111 encouraging competition and choice may help protect populations from extinction; (b) by contrast, if

112 Additionally, noise can protect this allele from extinction, accelerate its spre

113 y for functional complementary mutations may protect individuals from FA.

114 of Ser(3) may be an additional mechanism to protect RGS2 from FBXO44-mediated proteasomal degradatio

115 ione peroxidase 4 (GPX4) uses glutathione to protect cells from ferroptosis by eliminating phospholip

116 rts that the unique composition of lymph may protect melanoma cells from ferroptosis-a form of iron-d

117 Oleic acid protected melanoma cells from ferroptosis in an Acsl3-de

118 This concurrent activation of autophagy protects cells from ferroptotic death and release of mit

119 ur study reveals that a fundamental strategy protecting human eggs from fertilization by multiple spe

120 In vitro, PLK-1 and SPD-2 directly protected centrosome scaffolds from force-induced disass

121 provides insights into bacteria that help to protect crops from fungal diseases by producing chemical

122 infection results in an immune response that protects individuals from future infections or illness f

123 ting an adaptive immune memory response that protects mice from future tumor recurrence and increases

124 We find that melanin does not protect E. dermatitidis from gamma-radiation.

125 tomy and loss of adipose triglyceride lipase protect mice from GDF15-induced weight loss.

126 Drugs and mechanisms that protect beta-cells from GLT stress could potentially imp

127 seeking low-molecular-weight compounds that protected beta-cells from GLT, we identified compound A

128 r by the corresponding nucleophilic suitable protected thioaldoses derived from glucuronic acid (GlcA

129 humans are particularly adept at learning to protect others from harm.

130 ppropriately forgo ablation effectiveness to protect patients from harm.

131 SAM long before germ cell differentiation to protect the genome from harmful TEs.

132 ows uptake of nutrients while simultaneously protecting the cell from harmful compounds.

133 metabolism with stomatal movement, and that protect CAM plants from harsh environmental conditions.

134 ST2 deficiency partially protected mice from HDM + DEP induced AHR in association

135 re two evolutionarily conserved systems that protect plants from heat stress.

136 t set of proteins upon heat stress, possibly protecting them from heat injuries.

137 on whether PGIPs also inhibit insect PGs and protect plants from herbivores.

138 Finally, overexpression of myeloid KLF2 protects mice from HFD-induced obesity and insulin resis

139 ficant increase in aorta-associated pMos and protected Ldlr(-/-) mice from high-fat diet-induced athe

140 development of obesity and dyslipidemia, it protected mice from high-fat diet-induced glucose intole

141 encoded mRNAs to mimic cellular mRNAs, thus protecting the virus from host innate immune restriction

142 ion of glycoprotein D, DeltagD-2, completely protected mice from HSV-1 and HSV-2 skin or vaginal dise

143 Further, protecting natural areas from human incursion should red

144 e renal function despite BP fluctuations and protects glomerular capillaries from hypertensive injury

145 In a screen for mutations protecting C. elegans from hypoxic stress, we isolated m

146 digenous peoples' original right to land and protect their territories from illegal deforestation.

147 Moreover, the gCM shell protects the MNs from immune clearance; and in turn, the

148 indings suggest that the persistent cohesion protects short telomeres from inappropriate recombinatio

149 Telomeres protect chromosome ends from inappropriately activating

150 ession of IFN-stimulated genes (ISGs), which protect hosts from infection.

151 ophages are the professional phagocytes that protect the host from infection or injury.

152 well as in natural and greenhouse soils, and protect tomato plants from infection.

153 The skin protects animals from infection and physical damage.

154 teer in an RTS,S/AS01 clinical trial, and it protects mice from infection by malaria sporozoites.

155 tion yields the direct individual benefit of protecting recipients from infectious diseases and also

156 lementation enhances IL-22 production, which protects intestines from inflammation.

157 nezolid has immunomodulatory properties that protect human neutrophils from injury and provides insig

158 t time, to our knowledge, we show that TRPV4 protects the lung from injury upon intratracheal Pseudom

159 number of these compounds are documented to protect plants from insects, pathogens, or herbivores or

160 Farnesoid X receptor (FXR), or NR1H4, protects the liver from insults of various etiologies.

161 ystem with in-built fail-safe processes that protect the host from intracellular infections.

162 Importantly, FcRn, by protecting IgG from intracellular degradation, results i

163 SAMHD1 protects cells from invading viruses that depend on dNTP

164 on against group B streptococcus (GBS) could protect infants from invasive GBS disease.

165 in triggering or executing bleaching, or in protecting corals from it, we used RNAseq to analyze gen

166 ns to T cells, subsequent PD-L1 upregulation protects them from killing by cytotoxic T lymphocytes, y

167 We conclude that physical fitness may protect astronauts from latent viral reactivation during

168 r maintaining fitness during a mission would protect astronauts from latent viral reactivation.

169 colonization and systemic dissemination, and protect mice from lethal infection.

170 More importantly, these immunogens protected animals from lethal challenge with both the Af

171 la telomere-binding protein, cav/HOAP, which protects chromosomes from lethal end-to-end fusions.

172 r in myeloid cells using the Cre-loxP system protects mice from lethal sepsis (caecal ligation and pu

173 and interleukin 1 signaling were required to protect trained mice from listeriosis.

174 ptor signaling and specific arms of immunity protect mice from long-term C. auris skin colonization.

175 Significantly, this approach protected offspring from long-term behavioral morbidity.

176 ansient, size-dependent permeable barrier to protect the embryo from maternal circulating harmful age

177 olved multiple, diverse defence systems that protect them from MGE assault via different mechanisms.

178 OO) and virgin olive oil (VOO) is crucial to protect consumers from misleading information.

179 g antibodies against TNF-alpha and IFN-gamma protected mice from mortality during SARS-CoV-2 infectio

180 totoxic effects of chemotherapy, but also in protecting organisms from multiple xeno- and endobiotics

181 hat it serves as a proofreading mechanism to protect primer-ends from mutagenic extensions.

182 side chain, suggesting that 2'-O-methylation protects small RNAs from Nbr-mediated trimming.

183 supportive of a critical role for t-loops in protecting chromosome ends from NHEJ and ATM activation,

184 neuploidies per gamete; crossovers partially protected chromosomes from nondisjunction at the meiosis

185 (heterogeneous nuclear ribonucleoprotein L) protect mRNAs from nonsense-mediated decay (NMD) by prev

186 Although association with AGO typically protects miRNAs from nucleases, extensive pairing to som

187 cies depends on the ability of germ cells to protect their genome from numerous exogenous and endogen

188 in the hospital's management to effectively protect nurses from obesity, and the health risks associ

189 a controlled failure mechanism (melting) to protect a circuit from overcurrent.

190 low-molecular-weight (LMW) thiol mycothiol, protecting it from overoxidation.

191 es (nano-SOD/CAT) - at the lesion site would protect mitochondria from oxidative stress, and hence th

192 concentrated in the human macula, where they protect the eye from oxidative damage and improve visual

193 rmulations to be used in functional foods to protect the intestine from oxidative stress.

194 Inhibition of LncRNA MALAT1 has potential to protect the retina from oxidative damage and to prevent

195 The BTZ derivative 13 protected neuronal cells from oxidative stimuli and incr

196 d ANGPT2 augments metastatic colonization by protecting tumor cells from oxidative stress.

197 tor nuclear factor-erythroid 2-like 2 (NRF2) protects cells from oxidative, proteotoxic, and metaboli

198 zymatic scavenger of superoxide radicals and protects the bacterium from oxidative stress conditions.

199 e human acute phase protein haptoglobin (Hp) protects the host from oxidative damage by clearing hemo

200 nsitization, reduced total IgE serum levels, protected mice from passive and active IgE sensitization

201 produce a vast array of defense compounds to protect themselves from pathogen attack or herbivore pre

202 present two strategies that hosts evolved to protect themselves from pathogens.

203 y cell walls provide a physical barrier that protects plants from pathogens, promotes tolerance to ab

204 enacted in 11 states in the United States to protect healthcare workers from patient handing injuries

205 CD47 acts as a "don't eat me" signal that protects cells from phagocytosis by binding and activati

206 de nanofibers; with the nanofiber morphology protecting the peptide from plasma degradation and impro

207 l cells, the antiplasmin activity of miropin protects envelope proteins from plasmin-mediated degrada

208 hospitals have taken various precautions to protect patients from potential exposure.

209 We propose that this activity would protect the cell from potential DNA re-replication cause

210 raises concerns among regulators tasked with protecting human health from potential PFAS-contaminated

211 er interface and the graphene oxide surface, protecting them from potential denaturation and renderin

212 rly folded proteins, cells can pre-emptively protect themselves from potentially toxic aberrant trans

213 Bivalves protect themselves from predators using both mechanical

214 Aortic elasticity creates a cushion that protects the heart from pressure injury, and a recoil th

215 Droplets protect bound proteins from proteases, and these interac

216 constitutive protein complex with FANCD2 and protects FANCD2 from proteasomal degradation.

217 20 by preventing its ubiquitination, thereby protecting it from proteasome-dependent FAAP20 degradati

218 es have evolved counterdefense mechanisms to protect their genomes from R-M cleavage by covalent modi

219 ATR protects the genome from R loops by suppressing transcri

220 ed mouse serum, implicating that IL-18BP may protect multiple organs from radiation-induced inflammat

221 is secreted by primary mouse adipocytes and protects fibroblasts from radiation-induced cell death,

222 s are able to trap nutrient transporters and protect them from rapid endocytosis.

223 conditions found in hyperthermophiles, thus protecting DNA from rapid thermodegradation, which rende

224 ill limited, and it is unclear how the virus protects this surface from recognition by antibodies.

225 les, kinase impairment with BI-2536 does not protect centrioles from removal in the bat star Patiria

226 TAD2 shifts the balance of H4 acetylation by protecting this mark from removal and that HDAC2 but not

227 Periostin overexpression protected mice from renal injury compared with controls,

228 AZD1775 induced phosphorylation of DNA-PK, protecting cells from replication-associated DNA damage

229 nd that MLL2 functions in gene expression by protecting developmental genes from repression via repel

230 , were potent inhibitors of RTA in vitro and protected Vero cells from ricin when expressed as intrac

231 ctic and therapeutic application of CV07-209 protected hamsters from SARS-CoV-2 infection, weight los

232 generates neutralizing immune responses and protects mice from SARS-CoV-2.

233 m VSV-eGFP-SARS-CoV-2-immunized animals also protects naive mice from SARS-CoV-2 challenge.

234 ion, also have anti-inflammatory properties, protect mice from sepsis, and prevent IL-1beta secretion

235 ty of S. aureus to secrete cytolytic toxins, protect itself from several aspects of the human innate

236 showed that pre-exposure to SARS-CoV-2 could protect mice from severe pneumonia.

237 suggest a novel mechanism by which metformin protects vascular endothelium from SFA-induced ectopic l

238 pecific NAIP-NLRC4 activity is sufficient to protect mice from shigellosis.

239 lizing antibodies (bNAbs) against HIV-1 that protect macaques from simian immunodeficiency HIV chimer

240 Ultimately, this strategy failed to protect macaques from SIV acquisition.

241 Although VFV protects patients from small muscle imbalances over the

242 ed cholestatic injury in DDC-fed WT mice and protected Mdr2(-/-) mice from spontaneous liver injury,

243 FAM111A, but not SPRTN, protects replication forks from stalling at poly(ADP-rib

244 nce induction, seems to play a large role in protecting tolerant cultivars from sting nematode feedin

245 To travel safely behind screens that can protect us from stones and hail, we must understand the

246 e proposed to act as molecular chaperones to protect other proteins from stress-induced damage.

247 ans gut, we reveal the local effect of CA in protecting intestinal mitochondria from stress-induced h

248 tantly, vHMM-HA partially attenuates p53 and protects cells from stress in a p53-dependent manner.

249 ally safeguards cellular differentiation and protects cells from stress.

250 ed antioxidation, resulting in deficiency in protecting cells from stresses.

251 ta2 as a potential pharmacological target to protect the brain from stroke injury.

252 ified in ANA+ healthy European Americans may protect them from T-cell expansion, heightened activatio

253 asis by inducing secretion of TGF-beta while protecting infected HPCs from TGF-beta-mediated effects

254 and disulfide-bonded OSTM1, which serves to protect CLC-7 from the degradative environment of the ly

255 Strategies should be designed to protect patients from the morbidity of recurrent infecti

256 properties of the choroid plexus (ChP) help protect the brain from the external world.

257 Microencapsulation of these cancer cells can protect the core from the harmful effects of the neighbo

258 ical, functional, and immunologic barrier to protect the host from the potential harming effects of i

259 lementation of conservation measures fail to protect the species from the impacts of bycatch and decl

260 Animals have evolved multiple mechanisms to protect themselves from the cumulative effects of age-re

261 at exert immunosuppression within the tumor, protecting cancer cells from the host's immune system an

262 during the COVID-19 outbreak is effective in protecting frontline staff from the infection.

263 a novel efficacious experimental ASF vaccine protecting pigs from the epidemiologically relevant ASFV

264 nerally understood to play critical roles in protecting societies from the adverse impacts of natural

265 f mitochondrial respiration, thus ultimately protecting the fetus from the potentially dire consequen

266 O-Acetylation of peptidoglycan protects bacteria from the lytic activity of lysozyme, a

267 pportunistic fungal pathogen whose cell wall protects it from the extracellular environment including

268 ereby a protein binds to the drug target and protects it from the inhibitory effects of the antibioti

269 of oil within the large wheat bran particles protects RP from the action of water and pro-oxidants du

270 ae resists penetration by antimicrobials and protects the bacteria from the innate immune system.

271 bacteriophage Ocr, a DNA mimic protein that protects the phage from the defensive action of type I r

272 Here we show that neuronal uPA protects the synapse from the harmful effects of soluble

273 stitute the most crucial defense system that protects cells from therapeutic agents.

274 s employ a variety of DNA repair pathways to protect themselves from these pro-mutagenic modification

275 due to an inadequate preventive strategy to protect the lens from this protist.

276 ation of COVID-19, and inhibiting PANoptosis protected mice from this pathology and death.

277 ed HOIP-dependent linear ubiquitylation, and protected cells from TNF-induced apoptosis.

278 me-associated quality control (RQC) pathways protect cells from toxicity caused by incomplete protein

279 upon exposure to mitochondrial toxins, which protect mitochondria from toxin-induced damage.

280 upon exposure to mitochondrial toxins, which protects mitochondria from toxin-induced damage.

281 so harbor several signaling alterations that protect them from traditional therapies that rely on apo

282 ng structure confines chromatin mobility and protects the genome from transcription-induced DNA damag

283 This could help protect chromosome attachments from transient forces whi

284 The mechanism may protect the eye from translaminar pressure swings and ma

285 duction of a typhoid conjugate vaccine would protect children from typhoid and avert typhoid hospital

286 that TMC6 and TMC8 regulated CIB1 levels by protecting CIB1 from ubiquitination and proteasomal degr

287 tion from CD4(+) T cell, and both treatments protected Il1rl2 (-/-) mice from uncontained infection.

288 ation of MLKL, suggesting that autophagy was protecting infected monocytes from undergoing necroptosi

289 es to diverse sHSPs and what processes sHSPs protect are far from understood.

290 verall, our studies show that the CA lattice protects the vRNP from untimely degradation in target ce

291 trate, but still dilution may be required to protect sensitive species from urban-use pesticides with

292 f UV-absorbing pigmentation on petals, which protects pollen from UV-damage.

293 ients can no longer rely on herd immunity to protect them from vaccine-preventable infections.

294 xpression of antiviral effectors that safely protect them from various viruses.

295 This work shows that GCNA protects germ cells from various sources of damage, prov

296 ainst the SIV envelope protein and failed to protect macaques from viral infection.

297 Envelope (E) domain I/III linker region and protects mice from viremia and viral dissemination follo

298 a murine model of SARS-CoV-2 infection, 2B04 protected challenged animals from weight loss, reduced l

299 or a combination of both of these antibodies protected mice from weight loss and reduced the viral bu

300 The BBB protects the brain from xenobiotic neurotoxicants and ha