ライフサイエンスコーパス: be deficient in

1 inished when antigen-specific CD8(+) T cells were deficient in 2B4.

2 cultivar accumulates 3-methyl myricetin and is deficient in 3'-methyl myricetins, demonstrating vari

3 PDE5 and nNOS were deficient in 5 of 5 biopsies.

4 emia (AML) cells from most patients with AML are deficient in a critical enzyme required for arginine

5 and amplification of DVGs in A549 cells that are deficient in a variety of innate intracellular antiv

6 f SFTS in hamsters genetically engineered to be deficient in a protein that helps protect humans and

7 the activation of the NF-kappaB pathway and was deficient in a mutant K13 with three alanine substit

8 Treg cell function is deficient in active rheumatoid arthritis (RA), a loss

9 te that T2DM patients with beta cell failure are deficient in adipsin.

10 a circulating pro-regenerative mediator that is deficient in aging and mitigates fibrosis in distant

11 al observations of APECED/APS1 patients, who are deficient in AIRE, a major regulator of central T ce

12 Using knockin mice that are deficient in AKAP-anchoring of either PKA or the opp

13 The cngc19 mutants are deficient in aliphatic glucosinolate accumulation an

14 Root wax from the mutant was deficient in alkylhydroxycinnamate esters.

15 We report here that spt mutants are deficient in all the types of early blood, have fewe

16 se and the glycolytic enzyme pyruvate kinase were deficient in an mntH strain grown under manganese l

17 ckout mice, which had intact ROS production, were deficient in anticryptococcal activity.

18 Using mice whose DCs are deficient in antigen presentation, we find spontaneo

19 enome edited cells expressing only Syk-Y130E were deficient in antigen-stimulated calcium release, de

20 e polarity and basal protrusive activity but are deficient in apical neighbor exchange.

21 multipotential neural precursors (NPs) that are deficient in arylsulfatase A (ASA) activity.

22 In vivo, PI3Kbeta-knockdown ECs are deficient in assembly of microvessel-like structures

23 ells and in Med23 knockout (KO) cells, L-E1A was deficient in association with other mediator subunit

24 herefore, we investigated whether caveolin-1 is deficient in asthmatic patients and in a murine model

25 An additional PilB mutant variant, which is deficient in ATP hydrolysis and T4P assembly, support

26 Consequently, Irf8(-/-) macrophages are deficient in autophagic activity, and excessively ac

27 Osteoarthritic chondrocytes, which are deficient in autophagy, did not increase ACV number

28 lacking B cells or mice lacking CD19, which are deficient in B-1a cells, an innate-like B-cell popul

29 The NSIN mice were deficient in B, T, and NK cells and not only showed

30 weakly tumorigenic and tumors that did form were deficient in BCSCs, abolishing metastatic capacity.

31 The 3xAsp mutant is deficient in bipolar thick filament assembly, fails t

32 MAIT cells are deficient in blood and bronchial tissue in steroid-t

33 licase is essential for genome integrity and is deficient in Bloom syndrome (BS), a rare genetic dise

34 ages beyond the commitment point, cells that are deficient in both checkpoints because they lack Rad5

35 Mice that lack TLR9 are deficient in both exercise-induced activation of AMP

36 Accordingly, when cells are deficient in both polymerases there is synergistic i

37 In cells that are deficient in both PU.1 and ETV5 there is lower IL-9

38 lacked Meissner corpuscles and found them to be deficient in both perceiving the gentlest detectable

39 tion labeling paradigm because such labeling is deficient in both patient groups.

40 e2-CreNox2 knockout (KO) mice (in which Nox2 was deficient in both endothelial cells and myeloid cell

41 e DWARF (DWF), and in the bzr1 mutant, which is deficient in BR signaling regulator BRASSINAZOLE RESI

42 In contrast, those cell lines that were deficient in brain colonization were infrequently f

43 f these agents as treatments for tumors that are deficient in BRCA2 and PTEN, among other DSB repair

44 g to preferentially undifferentiated tumors, was deficient in BRG1 expression.

45 However, current DELs tend to be deficient in C(sp(3)) carbon counts.

46 individuals with hereditary angioedema (HAE) are deficient in C1-inhibitor and consequently exhibit e

47 ven under conditions where miR-21 expression was deficient in cancer cells.

48 The mutant p53-MDM2 complex is deficient in catalyzing ubiquitin release from the ac

49 (TCRalpha(-/-)) mice, which express CD1d but are deficient in CD1d-dependent NKT cells, exhibited as

50 Since DBA/2J mice are deficient in CD94, an important immune modulator tha

51 late in microscopic proteinopathies, and can be deficient in cells or cellular compartments.

52 ns demonstrate that mice lacking V2a neurons are deficient in central respiratory rhythm generation.

53 ells, which initiate excess origins and also are deficient in checkpoint activation, showed slower fo

54 The mutant in CheR2 was deficient in chemotaxis, whereas mutation of CheR1 a

55 Cells of a porV deletion mutant were deficient in chitin utilization and failed to secre

56 notype was partly recapitulated in mice that were deficient in cIAP2 alone.

57 (SLQ-->AAA) with mutations S478A/L480A/Q481A was deficient in clotting activity and unable to efficie

58 binds microtubules with normal affinity but is deficient in clustering along protofilaments.

59 topenia (NAIT) possess oligosaccharides that are deficient in "core fucose" residues and appear to be

60 r patterns, the activation of Erk1/2 and JNK was deficient in Cot/tpl2 KO macrophages compared with t

61 cal G protein coupled receptor, whereas C5L2 is deficient in coupling to G proteins because of variat

62 Importantly, Stat2(-/-) cDCs were deficient in cross-presenting to CD8(+) T cells in

63 Intestines lacking Gata4 and Cdx2 were deficient in crypt cell replication, whereas combin

64 SCCOHT patient tumors are deficient in cyclin D1 yet retain the retinoblastoma

65 and 20-hydroxy-LTB(4) formation was found to be deficient in Cyp1 triple-knockout mice.

66 anism for these drugs and suggest Greyhounds are deficient in CYP2B11.

67 wild-type Arabidopsis; cyp89a9 mutants that are deficient in CYP89A9 function were devoid of NDCCs b

68 urthermore, macrophages from MARCO(-/-) mice were deficient in cytokine and chemokine production, inc

69 tumor protection, as vaccines in these mice were deficient in cytotoxic T lymphocytes priming and IL

70 Mice that are deficient in Dab1, Reelin, or the Reelin receptors A

71 Using genetically modified human cells that are deficient in DC2 or KCP2 proteins, we show that loss

72 We show that the gastrointestinal tract is deficient in de novo generation of Treg cells in alle

73 However, health-care systems are deficient in different stages of the HIV continuum o

74 resected DNA As a result, srs2Delta mutants are deficient in DNA repair correlating with extensive D

75 de in subtelomeric regions of chromatin that are deficient in DNA repair mechanisms.

76 e of xeroderma pigmentosum (XP) cells, which are deficient in DNA repair, rendered this assay more se

77 The C to A mutants are deficient in DNA replication and repair in vivo, and

78 We hypothesized that HD cells would be deficient in DNA repair gene expression.

79 dies of exon alpha Pol beta revealed that it is deficient in DNA binding to gapped DNA, has strongly

80 is able to protect blunt-ended telomeres but is deficient in DNA repair.

81 -specificity phosphatase (msg5Delta) or that are deficient in docking to the MAPK-scaffold (Ste5(ND))

82 Tears cover the surface of the eye and are deficient in dry eye, the most common eye disease af

83 It is deficient in EC-SMC Bmpr2 double heterozygous mice in

84 Synaptically induced LTD was deficient in Eif4ebp2(-/-) mice, and this deficit wa

85 erated mice that express TGF-beta1(C33S) and are deficient in either integrin beta8 or TSP-1, known a

86 A catalytic mutant of CtIP that is deficient in endonuclease activity exhibits wild-type

87 We have used the beige (Bg) mouse, which is deficient in endosome biogenesis, to evaluate the eff

88 All mutants were deficient in episome persistence, and the deficienc

89 Furthermore, splicing of ATR transcripts is deficient in ERH-depleted cells.

90 g a cardiac-tissue-specific knockout of Ctr1 are deficient in Erk phosphorylation in cardiac tissue.

91 Rab27b double-knockout (Rab27DKO) mice that are deficient in exosome secretion have a chronic, low-g

92 rted that mouse embryonic stem cells (mESCs) are deficient in expressing type I interferons (IFNs) in

93 MCPT4-deficient mice was abolished when GBS was deficient in expression of the fibronectin-binding p

94 SV-1 entry in murine dermal fibroblasts that were deficient in expression of either nectin-1 or HVEM

95 he sperm cell and the pollen vegetative cell were deficient in expression of key RNAi components.

96 s, regenerating axons form growth cones, yet are deficient in extension.

97 The mutant mice are deficient in extracellular collagen VI microfibrils

98 OR-gammat in a MyD88-dependent manner, which was deficient in FA infants and mice and ineffectively i

99 mice, lysosomal enzymes were expressed that are deficient in Fabry and Gaucher diseases and in Hurle

100 FakB2)2 complexes except FakB2(R202A), which is deficient in FakA binding.

101 Here, we find that Trpm7-/- T cells are deficient in Fas-receptor-induced apoptosis and that

102 Rice xax1 mutant plants are deficient in ferulic and coumaric acid, aromatic com

103 affected daughters, chromosomal break repair was deficient in fibroblasts from the affected individua

104 GOT2 enzyme activity was deficient in fibroblasts with bi-allelic mutations.

105 ther endogenous IL1RA production or function is deficient in FIRES patients.

106 ted in all cell lines, the DNA adaptor STING was deficient in FL83B hepatocytes (down by nearly 3 log

107 etically interacts with FMRP, a protein that is deficient in fragile X syndrome and is known to regul

108 cution of supraspinal motor commands, it may be deficient in freezers during APAs.

109 As and Argonaute proteins in eukaryotes that are deficient in functional RNA interference could provi

110 Cardiac and skeletal muscle were deficient in Gaa mRNA and enzymatic activity and ac

111 ene, which encodes the lysosomal enzyme that is deficient in Gaucher's disease, are important and com

112 dies revealed that DC-beta-catenin(-/-) mice were deficient in generating CD8(+) T-cell immunity desp

113 TMEM16F-dependent lipid scrambling activity are deficient in generation of extracellular vesicles (E

114 TFH development is deficient in germ-free mice and can be restored by fe

115 Macrophages that were deficient in GGTase I or p110delta exhibited consti

116 One mutant BChE was found to be deficient in ghrelin hydrolysis.

117 Importantly, although mitochondrial (mt)ROS were deficient in gp91(phox-/-) phagocytes, their restor

118 Data from mice that overexpress or are deficient in growth hormone (GH) indicate that GH st

119 reduced extracellular nuclease activity and is deficient in growth when DNA is provided as the sole

120 2 cells, deleting a Drosophila E(z) homolog, were deficient in H3K27 di- and trimethylation, with no

121 me system and the autophagy-lysosome pathway are deficient in handling large tau aggregates.

122 In total, 8299 API were found to be deficient in HBsAg completion at baseline within our

123 RNA-seq, we demonstrated that affl-2 mutants are deficient in heat-shock-induced transcription.

124 Moreover, tumor cells that are deficient in Hh signaling are compromised in their a

125 unctionally complemented a yeast strain that is deficient in high affinity ammonium transport, both a

126 activated protein kinase (MAPK) pathway that is deficient in highly aggressive BLBCs treated with che

127 We find that melanocytes depleted of MEN1 are deficient in homologous recombination (HR)-directed

128 tors in the treatment of breast cancers that are deficient in homologous recombination exemplifies th

129 line deleterious mutations of BRCA1 or BRCA2 are deficient in homologous recombination repair and the

130 These mutant VRE strains were deficient in host colonization because of their ina

131 ential of EXT1(-/-) mouse ESCs (mESCs), that are deficient in HS, to differentiate into primary germ

132 eport that mice with a betaCys93Ala mutation are deficient in hypoxic vasodilation that governs blood

133 trating pDCs are the major APC in glioma and are deficient in IFN-alpha secretion (p < 0.05).

134 the Ifnar1(S526A) (SA) knock-in mice, which are deficient in IFNAR1 downregulation.

135 Patients who are deficient in IL-12Rbeta1 may have candidiasis, usual

136 urther demonstrate that beta-arr-1(-/-) mice are deficient in IL-6 expression in the colon, but have

137 ntly lower levels of inflammatory monocytes, were deficient in IL-18 production, and lacked NK cell-d

138 cohol use disorder presenting to the ICU may be deficient in important vitamins and electrolytes and

139 GEF-H1(-/-) leukocytes were deficient in in vivo crawling and TEM in the postca

140 S. pneumoniae strain JMG1 (DeltafakB3) was deficient in incorporation of linoleate from human s

141 Mice lacking IL-1beta were deficient in inducing CXCL1 secretion, suggesting t

142 TREX1 mutants related to AGS were deficient in inducing ORF1p depletion and could not

143 cts were significantly attenuated when MDSCs were deficient in iNOS.

144 Mouse models used to test dengue vaccine are deficient in interferon (IFN) type I signaling and s

145 AK4, and MYD88; however, the deletion clones are deficient in interleukin-10 (IL-10) production.

146 Globally, ~70% of adults are deficient in intestinal lactase, the enzyme required

147 e show that an E. faecalis epa mutant strain is deficient in intestinal colonization, cannot expand i

148 MAPKs, MNK1 and MSK1, whose phosphorylation is deficient in IRAK4(KDKI) macrophages stimulated throu

149 rate a SNAP25 extreme C-terminal mutant that is deficient in its ability to bind Gbetagamma while ret

150 lotting assays revealed that although fV(Q3) was deficient in its clotting activity, fV(DeltaB9/Q3) h

151 Arabidopsis mutants that are deficient in jasmonate perception (coronatine insens

152 Phosphorylation-defective histone H4 mutant is deficient in K20 methylation, leading to reduced DNA

153 s in a series of primary cells and mice that were deficient in key innate immune genes involved in pa

154 rotein markers and mRNA profiles in DCs that are deficient in known or candidate genes, we classified

155 o control cells, FH iPSC-derived hepatocytes are deficient in LDL-C uptake; (3) control but not FH iP

156 eight of ob/ob and db/db mice, both of which are deficient in leptin signaling.

157 Patients were deficient in lipoylation of mitochondrial proteins.

158 Furthermore, mice that are deficient in lung ILC2s by bone marrow transfer from

159 Of more importance, mice that were deficient in MCU were protected from pulmonary fibr

160 echanisms that mediate type I IFN expression are deficient in mESCs.

161 By using the human cell line K562, which is deficient in MHC class I/II and CD1 expression, we ge

162 plasmic streaming, we used a Khc mutant that is deficient in microtubule sliding but able to transpor

163 In vitro, placental endothelial cells were deficient in migration, cord formation and sproutin

164 tor-Tg mice to generate 2D2 CD4 T cells that are deficient in miR-146a and specific for myelin oligod

165 In the current study, mice that were deficient in miR-133a demonstrated low maximal exer

166 Interestingly, mutant CPCs are deficient in mitochondrial respiration and rely on g

167 Animals defective in ceramide biosynthesis are deficient in mitochondrial surveillance, and additio

168 howed extreme susceptibility to Yersinia and were deficient in monocyte and neutrophil-derived produc

169 y express human resistin (hRTN(+/-)(/-)) but are deficient in mouse resistin.

170 Analysis of NOD mice that were deficient in MR1, and therefore lacked MAIT cells,

171 It has been shown to be deficient in MSA brain tissue, thus implicating mitoc

172 roblasts had low SELENBP1 protein levels and were deficient in MTO enzymatic activity; these effects

173 We have studied Arabidopsis mutants that are deficient in multiple MTs to learn about the functio

174 demonstration that mitochondrial biogenesis is deficient in Multiple Sclerosis patients, which could

175 elets obtained from Unc13d(Jinx) mice, which are deficient in Munc13-4 and have an exocytosis defect.

176 oated by retromer and Mvp1, and cargo export is deficient in mvp1- and vps1-null cells, but with dist

177 Most inbred laboratory mouse strains are deficient in Mx1, but congenic B6-Mx1(r/r) mice that

178 otective effects were abrogated in mice that were deficient in MyD88 and Trif, molecules that are cri

179 ells) and LysM CreNox2KO mice (in which Nox2 was deficient in myeloid cells) had significantly lower

180 o form a biofilm in vitro and, additionally, were deficient in natural transformation.

181 nt of phosphorylated actin and LTP induction is deficient in neurons expressing mutant actin that mim

182 derscored by a growing number of persons who are deficient in NK cells and/or their functions.

183 ve an open neural tube, such as embryos that are deficient in Nodal signaling or the cell adhesion pr

184 Cells expressing the mutant Ku are deficient in nuclear accumulation of TLC1, as expect

185 osum complementation group A (XPA) mice that are deficient in nucleotide excision repair (NER).

186 d to develop complete convergence when Mecp2 is deficient in olfactory sensory neurons (OSNs) in an o

187 0E), Ply(W433G), Ply(W433E), and Ply(L460E)) were deficient in oligomer formation.

188 However, BIF are deficient in OM, which is postulated to be the resul

189 veloped the Deltap35KI transgenic mouse that is deficient in p25 generation and Cdk5 hyperactivation.

190 smic domain of TF (F3) (TF(DeltaCT)) or that are deficient in PAR2 (F2rl1), as well as by pharmacolog

191 brain states of attention and arousal and to be deficient in pathologies such as Alzheimer's disease,

192 asmacytoid dendritic cells (pDCs), which can be deficient in patients with allergic asthma.

193 al enzyme, alpha-l-iduronidase (IDUA), which is deficient in patients with mucopolysaccharidosis type

194 nal survival motor neuron (SMN) protein that is deficient in patients with spinal muscular atrophy.

195 samine-6-sulfatase and GalN6S; E.C. 3.1.6.4) is deficient in patients with the lysosomal storage dise

196 ivity against allogeneic CD4(+) T cells, but were deficient in patients with cGVHD.

197 Additionally, these mutants were deficient in Pel-dependent biofilm formation and wr

198 However, T(R)1-like cells were deficient in PGE(2) and 4-fold less potent than wer

199 ancisella pathogenicity island (FPI) mutant, is deficient in phagosomal escape and intracellular grow

200 yzed pheophorbide a oxygenase1 (pao1), which is deficient in pheophorbide catabolism and accumulates

201 The FN68 mutant is deficient in phytoene synthase, the first enzyme of t

202 Murine embryonic fibroblasts (MEFs) that are deficient in PICALM display several characteristics

203 nzyme hyaluronidase-2 (HYAL2) and that HYAL2 is deficient in platelets isolated from patients with in

204 of C. reinhardtii vtc1 mutant strains, which are deficient in polyphosphate synthesis, to accumulate

205 ion, and a subset of these was identified to be deficient in post-transcriptional steps of chloroplas

206 owing demands of the fetus - a process which is deficient in preeclampsia.

207 n at restriction enzyme-generated breaks but is deficient in processing topoisomerase adducts and rad

208 ith previous data demonstrating both enzymes were deficient in processive searching.

209 allele DCXG253D still binds microtubules but is deficient in promoting neurofascin endocytosis.

210 s assembled in the absence of VII (Ad5-VII-) are deficient in proteolytic maturation of protein VI an

211 studies in mouse and zebrafish embryos that are deficient in RA-generating enzymes or RARs have been

212 numbers correlated with disease activity and were deficient in regulatory T cells relative to healthy

213 ion and repair of UV-induced DNA damage, but is deficient in repair of mitomycin C (MMC)-induced DNA

214 failed to cluster in membrane microdomains, was deficient in restriction of particle release, and ex

215 rde-12 mutants are deficient in RNAi, including viral suppression, and

216 as found in the supernatant of a strain that was deficient in S-layer attachment.

217 al tissues acclimated to the HL stress, they were deficient in SAA to HL stress.

218 lopment was observed when the tumor and host were deficient in Sb9.

219 promoted turnover of Aurora B at the midbody was deficient in SCCRO- and KLHL21-deficient cells, sugg

220 tigated whether Lhx6 and/or Sox6 mRNA levels are deficient in schizophrenia, which may contribute to

221 ediated neurotransmission, which is known to be deficient in schizophrenia.

222 Mice in which LRP1 is deficient in Schwann cells represent a model for stud

223 The porV mutant also appeared to be deficient in secretion of numerous other proteins tha

224 encoded by the I3 alleles I3-4, -5, and -7, were deficient in self-interaction and unable to support

225 However, autapses are deficient in several aspects of synaptic plasticity.

226 RA FLS that were deficient in SHP-2 exhibited decreased activation o

227 we generated Myd88/Trif/Mavs(-/-) mice that are deficient in signalling by all TLRs, RLRs and IL-1R,

228 Conventional peanut extracts are deficient in significant IgE-binding components.

229 In consequence, SnRK1 degradation is deficient in siz1-2 mutants, leading to its accumulat

230 We identify a mutant of the Ndc80 tail that is deficient in Ska recruitment to kinetochores and in o

231 w that Ca(2+) entry through CATSPER channels is deficient in Slo3 mutant sperm lacking hyperpolarizat

232 one marrow failure and demonstrate that they are deficient in small nucleolar RNA binding.

233 ell as the wild type on soluble alginate but was deficient in soluble secreted alginate lyase activit

234 2NLS(tm) mutant mice and wild type mice, but are deficient in splenic macrophages isolated from mutan

235 Disease-linked PQBP1 mutants were deficient in splicing factor associations and could

236 at show normal levels of basal autophagy but are deficient in stimulus (exercise- or starvation)-indu

237 protozoan parasite Trypanosoma cruzi, which is deficient in strong PAMPs, we demonstrate a requireme

238 served with mms21-11, a mutant of Mms21 that is deficient in SUMO ligase activity.

239 derived from mouse spinal cord of both sexes are deficient in supporting both WT and SMN-deficient mo

240 n cells but does not bind well to cells that are deficient in surface glycosaminoglycans.

241 ly develop corneal and lymphatic vessels and are deficient in sVEGFR-3.

242 Early life immune responses are deficient in Th1 lymphocytes that compromise neonata

243 trated that homodimeric p55 disease variants are deficient in the ability to stimulate p140; however,

244 In mice that are deficient in the circadian gene Clock, renal fibrosi

245 10 myopathy patients, mutant Drosophila that are deficient in the homologue of MEGF10 (Drpr) and megf

246 However, in the CCRF-CEM-AraC-8C cells that are deficient in the human equilibrative nucleoside tran

247 rosine hydroxylase, and dopamine transporter are deficient in the ileum of Cdnf (-/-) mice.

248 Reversa mice, which are deficient in the low-density lipoprotein receptor an

249 function similarly to appendicular HSCs but are deficient in the lymphoid lineage.

250 nistration of rapamycin to these mice, which are deficient in the mitochondrial respiratory chain sub

251 We determined whether nucleases are deficient in the tear fluid of dry eye disease (DED)

252 Runx1(P1N/P1N) mice are deficient in the transcription factor distal promote

253 genes in an spt16 mutant, which was found to be deficient in the assembly of normal nucleosomes on in

254 recent pathological studies show that TNFRII is deficient in the brains of Alzheimer's disease (AD).

255 to the prokaryotic pathway, and fad6, which is deficient in the chloroplast 16:1/18:1 fatty acyl des

256 omonas reinhardtii) mutant (bkdE1alpha) that is deficient in the E1alpha subunit of the branched-chai

257 Dephosphorylated Synj, on the other hand, is deficient in the endocytosis of the active recycling

258 c reticulum Ca(2+)-ATPase (SERCA2a) activity is deficient in the failing heart.

259 retardation protein (FMRP), the protein that is deficient in the most common inherited form of mental

260 density protein 95 (PSD-95), a process that is deficient in the mouse model of Fragile X Syndrome, F

261 NEU1 is deficient in the neurodegenerative lysosomal storage

262 th non-NLRC4-triggering P. aeruginosa, which is deficient in the T3SS needle complex, did not alter t

263 For example, class I mutant rhodopsin is deficient in the VxPx trafficking signal, mislocalize

264 hemical analyses showed that the tla2 strain was deficient in the Chl a-b light-harvesting complex, a

265 rn-blot analyses showed that the tla3 strain was deficient in the Chl a/b light-harvesting complex.

266 Lactobacillus johnsonii, which was deficient in the more cancer-prone mouse colony, was

267 The synergism between light and heat shocks was deficient in the prr7 prr9, lhy cca1, pif4 pif5, cop

268 nt in the model system M. marinum background was deficient in the secretion of some members of the PE

269 cells rendered hyporesponsive in this manner were deficient in the ability of these cross-tolerized r

270 In vivo, mice that received FK506 or were deficient in the calcineurin isoform Abeta (CnAbeta

271 istent with these findings, I-A(b) mice that were deficient in the p47(phox) or gp91(phox) subunits o

272 une responses in primary cells and mice that were deficient in the RIG-I-like receptor signaling path

273 Mitochondria lacking Mgr2 were deficient in the Tim21-containing sorting form of t

274 Moreover, P. syringae mutants that were deficient in the uptake of choline compounds exhibi

275 S100A9 knockout (KO) mice, which are deficient in their ability to accumulate MDSC in tum

276 oimmune diseases, including type 1 diabetes, are deficient in their ability to control autologous pro

277 Ts and other components of HAT complexes but are deficient in their ability to restore ADA3-dependent

278 ng disulfide bonds that constrain the C-term are deficient in their ability to trigger fusion followi

279 to infants and the elderly, age cohorts that are deficient in their adaptive immune responses to such

280 is (Arabidopsis thaliana) mutant plants that are deficient in their endogenous BEs and therefore, can

281 monstrated that asthmatic airway fibroblasts are deficient in their packaging of fibrillar collagen-I

282 d functional recovery, whereas the aged rats were deficient in their regenerative capacity.

283 e CHGA-derived peptide catestatin (CST) that is deficient in these mice.

284 nvolved in the final step of heme synthesis, is deficient in these patients.

285 ading and restriction, KS-WNK1 knockout mice were deficient in these structures under identical condi

286 CD2 protein, and cells from most FA patients are deficient in this step.

287 er, a double site1/2 mutant (OSBP-S381A/S3D) was deficient in this activity and was constitutively co

288 did not accelerate tumor growth when ERalpha was deficient in Tie2-positive cells, even in mice graft

289 cells lacking the POLD3 subunit of Poldelta are deficient in TLS.

290 The raa7 mutant (RNA maturation of psaA 7) is deficient in trans-splicing of the second intron of p

291 mmation, we examined scurfy (Sf) mice, which are deficient in Tregs and succumb to severe multiorgan

292 n crwn1 crwn2 and crwn1 crwn4 mutants, which are deficient in two of the four CRWN paralogs.

293 The nrt2 mutant (which is deficient in two genes, NRT2.1 and NRT2.2) displays r

294 n an IL-12p35(-/-) dnTGFbetaRII strain which is deficient in two members of the IL-12 family, IL-12 a

295 We conclude that mESCs are deficient in type I IFN expression, but they can res

296 ocesses will be enhanced in individuals that are deficient in vitamin D.

297 sfunction of cholinergic metabolism when CHT is deficient in vivo.

298 s VSV-LUJV infection, and cells lacking NRP2 are deficient in wild-type LUJV infection.

299 requires the copper transporter Atp7b, which is deficient in Wilson disease.

300 he t-test showed that CLas-infected D. citri were deficients in zinc, iron, copper, magnesium, calciu