ライフサイエンスコーパス: ABC

1 ABC ATPases developed structural hallmarks that unambigu

2 ABC ATPases form one of the largest clades of P-loop NTP

3 ABC fractions remained high after transfer to device sub

4 ABC subfamily B member 1 (ABCB1) expression was reduced,

5 ABC subfamily B member 5 (ABCB5) has been identified as

6 ABC supports population expansion, possibly explained by

7 ABC transporters facilitate the movement of diverse mole

8 ABC transporters undergo substantial conformational chan

9 ABC treatment led to an inflammatory, prothrombotic endo

10 ABC-C6 represents a promising target for breeding or bio

11 ABC-DLBCL exhibits plasmablastic features and is charact

12 ABC-transporter copy number, expression and activity wer

13 ABC-treated cells and EMP had greater TF activity, while

14 ABC-treated endothelial cells had higher levels of ICAM

15 C) subfamily F member 3 (ABCF3) is a class 2 ABC protein that has previously been identified as a par

16 following a repeat structure (e.g., AB | AB, ABC | ABC), the latter requiring greater computational p

17 onths, and stable regimen with DTG/abacavir (ABC)/lamivudine (3TC) were 1:1 randomized to continue th

18 , tenofovir alafenamide (TAF)/FTC, abacavir (ABC)/lamivudine (3TC), and others were estimated through

19 this population after switching to abacavir (ABC)/lamivudine (3TC)/DTG over 6 months.

20 y] with emtricitabine [FTC]/TDF or abacavir [ABC]/3TC [n = 747]) compared with DRV+r (800/100 mg dail

21 ing a repeat structure (e.g., AB | AB, ABC | ABC), the latter requiring greater computational power t

22 We identified two ABCG1 (ABC subfamily G member 1) variants, which regulate cellu

23 lipoprotein PiuA from the piu Fe acquisition ABC transporter PiuBCDA, previously described as an Fe-h

24 An ABC transporter with a periplasmic metallo-aminopeptidas

25 for galactose, a galactose-PTS system and an ABC galactose transporter.

26 the potassium transporter operon kdp and an ABC transporter operon of uncharacterized function.

27 enes for a TonB-dependent transporter and an ABC-type transporter and demonstrate that both are essen

28 d as an operon and is predicted to encode an ABC importer for nutrient uptake (e.g., amino acids).

29 croscopy not only confirms that IrtAB has an ABC exporter fold, but also reveals structural peculiari

30 identified genes encode an MxaD homolog, an ABC-type transporter, an aminopeptidase, a putative homo

31 vation of a correlated Chern insulator in an ABC-TLG/hBN moire superlattice.

32 nd outer membrane integrity, and includes an ABC transporter, MlaFEDB.

33 ber of mutants with OM defects, including an ABC transporter system homologous to the Mla system in E

34 Multidrug resistance protein 1 (MRP1) is an ABC exporter that extrudes a variety of chemotherapeutic

35 ABCG2 is an ABC transporter that extrudes a variety of compounds fro

36 ABCB5 is an ABC transporter that was shown to confer low-level multi

37 Transforming P-gp or an ABC drug exporter from an efflux transporter into a drug

38 rulence, including an l,d-transpeptidase, an ABC transporter solute-binding protein, and a methionine

39 (BceRS) working in a sensory complex with an ABC-transporter (BceAB), together acting as a flux-senso

40 l design of strands that fold into A(2)B and ABC-type heterotrimers with only three salt bridges per

41 r genes in tomato cv. Moneymaker, ABC-C6 and ABC-G33, alters the composition of semi-volatile compoun

42 in magic-angle twisted-bilayer graphene and ABC trilayer graphene/boron nitride moire superlattices(

43 enger receptor class B member 1 (Scarb1) and ABC subfamily G member 8 (Abcg5/8), decreased hepatic an

44 ADME gene-centered network-including SLC and ABC "drug" transporters, "drug" metabolizing enzymes (DM

45 and signalling hypothesis identifies SLC and ABC transporter-mediated communication between organs an

46 Solute carriers (SLC) and ABC transporters represented an important subset of DEG,

47 age, biomarker, clinical history)-stroke and ABC-bleeding risk scores incorporate clinical variables

48 The ABC-stroke and ABC-bleeding scores evaluated in this anticoagulated cli

49 The ABC-stroke and ABC-bleeding scores were well calibrated and yielded hig

50 iverts crucial media (The New York Times and ABC News) from topics that are potentially harmful to hi

51 following a mirror structure (e.g., AB | BA, ABC | CBA) and a context-sensitive grammar generating se

52 FtsEX is a bacterial ABC transporter that regulates the activity of periplasm

53 Three distinct bacterial ABC import systems of sulfur-containing compounds have b

54 y to substrate-binding proteins in bacterial ABC transporters.

55 At the example of the bacterial ABC transporter TM287/288, we show that two gadolinium-l

56 This study exposes the link between ABC transporters, root exudate composition, and ex plant

57 Blocking ABC transporter, PLA2 or 12-Lox activity also inhibits h

58 ions in the digestive vacuole membrane-bound ABC transporter PfMDR1 (P. falciparum multidrug resistan

59 e structure determination of substrate-bound ABC exporters, the inherently dynamic mechanism of subst

60 understanding of sterol transport driven by ABC transporters, with an emphasis on these two extensiv

61 an autocrine signaling molecule exported by ABC transporters that enhances chemotaxis in GSCs migrat

62 dard rejection ABC or sequential Monte Carlo ABC or (ii) ABC with Gaussian process emulation.

63 ase II metabolism, and ATP binding cassette (ABC) membrane transporter expression and function were m

64 ticancer drugs through ATP-binding cassette (ABC) pumps.

65 Mammalian ATP-binding cassette (ABC) subfamily F member 3 (ABCF3) is a class 2 ABC prote

66 ession and activity of ATP-binding cassette (ABC) superfamily transporters.

67 /MRP4 gene encoding an ATP-binding cassette (ABC) transporter in PEL-negative individuals.

68 o the cytoplasm by the ATP binding cassette (ABC) transporter IrtAB(4), which features an additional

69 In this system, the ATP-binding cassette (ABC) transporter LptB(2) FGC extracts LPS from the inner

70 The ATP-binding cassette (ABC) transporter of mitochondria (Atm1) mediates iron ho

71 (BCRP) is a member of ATP-binding cassette (ABC) transporter proteins whose primary function is to e

72 BCG2) is a homodimeric ATP-binding cassette (ABC) transporter that not only has a key role in helping

73 e we show that both an ATP-binding cassette (ABC) transporter(s) and an H(+)-antiporter(s) are involv

74 lute carrier (SLC) and ATP-binding cassette (ABC) transporters and drug-metabolizing enzymes, many of

75 ATP-binding cassette (ABC) transporters are membrane proteins present in all k

76 ATP-binding cassette (ABC) transporters are molecular pumps ubiquitous across

77 ATP-binding cassette (ABC) transporters are the largest family of ATP-hydrolyz

78 ATP-binding cassette (ABC) transporters chemomechanically couple ATP binding a

79 ATP-binding cassette (ABC) transporters constitute one of the largest and most

80 ATP-binding cassette (ABC) transporters constitute the largest family of prima

81 enosine triphosphate (ATP)-binding cassette (ABC) transporters in the pyrethroid-resistant Puerto Ric

82 ATP-binding cassette (ABC) transporters play several critical roles in this pr

83 ATP-binding cassette (ABC) transporters represent a large group of efflux pump

84 yl-activating enzymes, ATP binding cassette (ABC) transporters, and central carbon metabolic proteins

85 uctural information on ATP binding cassette (ABC) transporters, which are expressed in the human live

86 xtrusion from cells by ATP-binding cassette (ABC) transporters.

87 v1819c has a bacterial ATP-binding cassette (ABC)-exporter fold(1).

88 role in the control of ATP-binding cassette (ABC)-transporter mRNA degradation and translation into p

89 ncy antigen, ABCC4 (an ATP-binding cassette [ABC]-transporter).

90 ransfer promoted by amidine-based catalysts (ABCs) and a racemic chain mechanism mediated by a thiola

91 utcome were age >18 years; activated B-cell (ABC) DLBCL profile, HGBCL, NOS, high genetic complexity,

92 Activated B-cell (ABC)-diffuse large B-cell lymphomas (DLBCLs) are clinica

93 (GCBs) and early and late activated B cells (ABCs).

94 pulation of B cells (age-associated B cells [ABCs]) is increased in mice and humans with infections o

95 CM in the LHAad using chondroitinase ABC (Ch-ABC) blocked the expression of cue-induced reinstatement

96 ated with lower Aberrant Behavior Checklist (ABC) scores.

97 dult visual cortex induced by chondroitinase ABC (chABC)-mediated PNN removal requires intact signali

98 We use a lentiviral chondroitinase ABC, capable of being secreted from mammalian cells (mCh

99 sustained lentiviral-mediated chondroitinase ABC (ChABC) enzyme expression.

100 extracellular matrix modifier chondroitinase ABC (chABC), tested here in glial scar models, and abili

101 ints following trauma through chondroitinase ABC induced neuroplasticity.

102 f PNNs/ECM in the LHAad using chondroitinase ABC (Ch-ABC) blocked the expression of cue-induced reins

103 does not cause accelerated blood clearance (ABC).

104 An approximate Bayesian computation (ABC) approach with microsatellite markers compared the s

105 Approximate Bayesian computation (ABC) has grown into a standard methodology that manages

106 Approximate Bayesian computation (ABC) is an important framework within which to infer the

107 ecko using Approximate Bayesian Computation (ABC) supports two possible scenarios but fails to tease

108 binding and hydrolysis, protease-containing ABC transporters (PCATs) export amphipathic and hydrophi

109 Controllable ABC yields ~59% were achieved by tailoring substrate cur

110 oxantrone-resistant cell lines demonstrating ABC-transporter upregulation.

111 How do ABC transporters evolve to carry such diverse molecules

112 ns synergistically (3-40 fold) downregulated ABC transporter expression, and inhibited P-glycoprotein

113 or (INSTI) class; 1 patient discontinued DTG/ABC/3TC due to an adverse event.

114 in the DTG arm and 77/80 (96.3%) in the DTG/ABC/3TC arm (difference, 2.7%; 95% confidence interval [

115 ) in the DTG arm compared with 0% in the DTG/ABC/3TC arm (P = .005 by the log-rank test).

116 logical proposal and compare it with earlier ABC methods on a Normal toy example and a population gen

117 When compared with earlier ABC solutions, this method offers significant gains in t

118 dly during transition from late GCB to early ABC phase, after LMP1 upregulation.

119 d survival, and that GRK2 knockdown enhances ABC-DLBCL tumor growth in vitro and in vivo.

120 a path to large-scale synthesis of epitaxial ABC-TLG and other vdW materials.

121 a compensatory mechanism by other erythroid ABC transporters.

122 N- and C-terminal halves in many eukaryotic ABC transporters, allowing all four consensus functional

123 access mechanism as it applies to eukaryotic ABC transporters, focusing on type I exporters.

124 nstrate that knockdown of two root-expressed ABC transporter genes in tomato cv. Moneymaker, ABC-C6 a

125 We present a unified mechanism for ABC ATPase function across disparate systems like RNA ed

126 Finally, EMP isolated from ABC-treated cells enhanced collagen-evoked platelet inte

127 transmembrane domains of a conserved fungal ABC transporter that exports a mating pheromone and sele

128 P-glycoprotein (ABC subfamily B member 1, ABCB1) plays an important role

129 rative study of the hearing function in an H-ABC patient and in this mutant model.

130 rophy of the basal ganglia and cerebellum (H-ABC) is a neurodegenerative disease due to mutations in

131 h Atrophy of Basal Ganglia and Cerebellum (H-ABC), a rare hypomyelinating leukodystrophy, often assoc

132 n with tremor, dystonia and ataxia seen in H-ABC.

133 nstrate the complex cellular physiology of H-ABC, likely due to independent effects on oligodendrocyt

134 f the clinical and radiological signs with H-ABC patients.

135 in a significant fraction of patients with H-ABC; therefore, screening for auditory function should b

136 ry of the current knowledge of hepatobiliary ABC transporters.

137 substrate translocation in the heterodimeric ABC exporter TM287/288 from the hyperthermophilic bacter

138 chanistic understanding of the heterodimeric ABC transporter TmrAB, a functional homolog of the trans

139 Many human ABC transporters are associated with disease; we highlig

140 n lung diseases, the goal was to find out if ABC-like cells were at elevated levels in such patients.

141 of other solute binding proteins of type II ABC transporters.

142 on ABC or sequential Monte Carlo ABC or (ii) ABC with Gaussian process emulation.

143 signaling pathways that are dysregulated in ABC-DLBCL are, however, not fully understood.

144 2 activity is constitutively dysregulated in ABC-DLBCL but not in GCB-DLBCL and BL.

145 n, the presence of altered 3'-UTR lengths in ABC transporters could lead to functional consequences r

146 ROCK2 also controls the expression of MYC in ABC-DLBCL by regulating MYC protein levels.

147 welve miRNAs were confirmed using RT-qPCR in ABC-DLBCL and GCB-DLBCL cells, respectively.

148 triggers potent cytotoxicity specifically in ABC DLBCL cells.

149 survival of ABC-DLBCL in vitro and inhibits ABC-DLBCL growth in xenograft models.

150 Instead, ABC transporters may be induced after insecticide exposu

151 d with BCL-2 and MCL-1 inhibitors in killing ABC DLBCL cells.

152 rate (FTC/TDF) in P007; abacavir/lamivudine (ABC/3TC) or FTC/TDF in DRIVE-FORWARD; and 3TC/TDF for DO

153 Within the larger ABC superfamily of ATPases, ABCF family members eEF3 in

154 Uup is a UvrA-like ABC family ATPase.

155 Deletions of uup (encoding the UvrA-like ABC system Uup), recO, or recF also suppress the Deltare

156 to tumor stasis in an activated B-cell-like (ABC) diffuse large B-cell lymphoma (DLBCL) xenograft mod

157 ke and the aggressive activated B-cell-like (ABC) DLBCL.

158 n associates with the activated B-cell-like (ABC) subtype and genetic alterations that drive constitu

159 e associated computational cost often limits ABC to models that are relatively quick to simulate in p

160 d B cell-type diffuse large B cell lymphoma (ABC-DLBCL) are associated with reduced survival, and tha

161 d B-cell-like diffuse large B-cell lymphoma (ABC-DLBCL) is an aggressive subtype of lymphoma usually

162 vels in such patients.Objectives: To measure ABC-like cell percentages in patients with lung granulom

163 The Znu system consists of an inner membrane ABC transporter and an outer membrane TonB-dependent rec

164 he cytoplasmic portion of the larger MlaFEDB ABC transporter complex, which drives phospholipid traff

165 transporter genes in tomato cv. Moneymaker, ABC-C6 and ABC-G33, alters the composition of semi-volat

166 the functionality of two different multidrug ABC transporters, the homodimer BmrA from Bacillus subti

167 em as some of the 50 most potent multitarget ABC transporter inhibitors.

168 d led to tumor regression in a CARD11 mutant ABC-DLBCL lymphoma xenograft model.

169 ly active microRNAs (miRNAs) in EBV-negative ABC-DLBCL and GCB-DLBCL cell lines and their EBV-infecte

170 However, nitrate ABC transporter genes were upregulated under UV and FR l

171 C-trilayer graphene/hexagonal boron nitride (ABC-TLG/hBN) moire superlattice provides an attractive p

172 led many gene clusters including three novel ABC-type sugar transport clusters to be upregulated in B

173 al cells in vitro, reducing the abundance of ABC transporter A1 (ABCA1) and thus cholesterol efflux a

174 These findings highlight the application of ABC approaches to infer the connectivity in mobile speci

175 east five and up to eight distinct clades of ABC ATPases are reconstructed as being present in the la

176 responded differently, but a contribution of ABC transporters to deltamethrin toxicity is suspected.

177 s and explaining the number and diversity of ABC transporters.

178 signaling as a crucial functional driver of ABC DLBCL and highlight calcineurin inhibition as a nove

179 Hence, the humanization of ABC transporters in mice has become a major focus in pha

180 Here, we find that inhibition of ABC transporter activity reduces migration of GSCs towar

181 cell lines was reversible upon inhibition of ABC-transporters.

182 Knockdown of ABC-C6 inhibits egg hatching of Meloidogyne and Globoder

183 Knockdown of ABC-G33 has no impact on egg hatching of Meloidogyne spp

184 ls in blood.Conclusions: Increased levels of ABC-like cells in patients with sarcoidosis may be usefu

185 ectric field switches the moire minibands of ABC-TLG/hBN between zero and finite Chern numbers, as re

186 Overexpression of ABC transporters like P-glycoprotein (P-gp) has been cor

187 The increase in percentage of ABC-like cells in patients with lung granulomatous disea

188 th sarcoidosis led to reduced percentages of ABC-like cells in blood.Conclusions: Increased levels of

189 ributes to the aberrant molecular program of ABC-DLBCL via its dual ability to modulate both IRF4- an

190 ype TGs and five triplets of regioisomers of ABC type TGs with acyl carbon number (ACN) ranging from

191 ABC transporter inhibitors and reversers of ABC transporters-mediated MDR.

192 x in macrophages have focused on the role of ABC transporters in moving cholesterol onto high-density

193 yields greatly enhanced fraction and size of ABC domains.

194 The recent availability of structures of ABC transporters containing linker regions has allowed u

195 Sphingolipids are substrates of ABC proteins in cell signaling, membrane biosynthesis, a

196 e particularly important for the survival of ABC DLBCL.

197 decreases the proliferation and survival of ABC-DLBCL in vitro and inhibits ABC-DLBCL growth in xeno

198 tive therapeutic target for the treatment of ABC-DLBCL.

199 r current regimen compared to 8.2% (4/49) on ABC/3TC/LPV/r.

200 All but 2 children on ABC/3TC/LPV/r were <3 years and all CLHIV on ABC/3TC/EFV

201 ABC/3TC/LPV/r were <3 years and all CLHIV on ABC/3TC/EFV were >=3 years.

202 More CLHIV on ABC/3TC/EFV, 47.8% (11/23), were found to have 0 or only

203 Biochemical and structural information on ABC sterol transporters is beginning to emerge, with pub

204 s on their current HIV regimen than those on ABC/3TC/EFV.

205 eveals that CLHIV with detectable viremia on ABC/3TC/LPV/r are more likely to have maintained at leas

206 ith DRV+r (800/100 mg daily) with FTC/TDF or ABC/3TC (n = 383) or EFV/FTC/TDF (600/200/300 mg daily;

207 ters are mechanistically distinct from other ABC transport systems.

208 rch provided evidence that, along with other ABC transporters (ABCA1 and ABCA7), they might be corner

209 Using simulated data, we show that our ABC method accurately infers the strength of coevolution

210 rican Breast Cancer-Disparities in Outcomes (ABC-DO) prospective cohort study was done at eight hospi

211 The peroxisomal ABC transporter, Comatose (CTS), a full length transport

212 sin gene) and piaB (permease gene of the pia ABC transporter) are currently used as the gold-standard

213 The human lysosomal polypeptide ABC transporter TAPL (ABC subfamily B member 9, ABCB9) t

214 d miRNAs) between EBV-negative and -positive ABC-DLBCL cells and 12 miRNAs with differential abundanc

215 MDR, making it one of the three most potent ABC transporter inhibitors and reversers of ABC transpor

216 However, the predicted ABC exporter fold of IrtAB is seemingly contradictory to

217 arrays revealed changes affecting primarily ABC pump expression.

218 mponents, including the NADPH oxidase RBOHD, ABC-transporter PEN3, calcium-ATPase ACA8, noncanonical

219 ssfully genotyped CLHIV, 49 (68.1%) received ABC/3TC/LPV/r, and 23 (31.9%) received ABC/3TC/EFV.

220 eived ABC/3TC/LPV/r, and 23 (31.9%) received ABC/3TC/EFV.

221 of NNRTI and NRTI DRMs among CLHIV receiving ABC/3TC/LPV/r suggests a lasting impact of failed PMTCT

222 3.4 (CI, 17.2 to 31.1) among those receiving ABC/3TC, and 20.0 (CI, 14.2 to 27.3) for those receiving

223 (compared with WT apoA-I) exhibited reduced ABC subfamily A member 1 (ABCA1)-dependent cholesterol a

224 ng Kir6.2 potassium channel and a regulatory ABC transporter sulfonylurea receptor 1 (SUR1) regulate

225 ochastic models using (i) standard rejection ABC or sequential Monte Carlo ABC or (ii) ABC with Gauss

226 t to and translocation by WzmWzt and related ABC transporters.

227 e architecture of several medically relevant ABC transporters and their supramolecular assemblies, in

228 cases, T-bet.Measurements and Main Results: ABC-like cells in blood were at low percentages in healt

229 ither a semimetallic ABA or a semiconducting ABC configuration with a gate-tunable band gap, but the

230 Silencing ABC-G33 induces a statistically significant reduction in

231 iffer from previous observations for similar ABC transporters, highlighting the extent of mechanistic

232 investigated the expression patterns of six ABC transporters previously characterized as differentia

233 Why do some ABC transporters have connectors and others not?

234 dscapes identified MCD/C5 tumors as specific ABC-DLBCLs with unfavorable clinical outcome, activating

235 eductase aor and represses tungsten-specific ABC-type transporter tupABC genes under tungsten-replete

236 ht is that substrate curvature can stabilize ABC domains.

237 g step appears to be unique to streptococcal ABC transporter-dependent RhaPS biosynthesis, whereas th

238 KES, and the ATP-binding cassette subfamily (ABC-B/multidrug resistance/P-glycoprotein) transporters

239 with the antiretrovirals abacavir sulphate (ABC), tenofovir disoproxil fumarate, or tenofovir alafen

240 serted within the central cavity of the SUR1 ABC core, adjacent the drug binding pocket.

241 on-based Active Bacterial Core surveillance (ABCs) at 10 US sites from 2010 to 2017.

242 lysosomal polypeptide ABC transporter TAPL (ABC subfamily B member 9, ABCB9) transports 6-59-amino-a

243 erization domain inserted into an N-terminal ABC ATPase fold and a C-terminal Toprim domain.

244 Our study shows that ABC-TLG/hBN heterostructures offer attractive model syst

245 The ABC (age, biomarker, clinical history)-stroke and ABC-bl

246 The ABC bundle was implemented from June 1, 2015 to May 31,

247 The ABC galactose transport system is regulated by a three-c

248 The ABC transporter Rv1747, which is important for Mycobacte

249 The ABC-stroke and ABC-bleeding scores evaluated in this ant

250 The ABC-stroke and ABC-bleeding scores were well calibrated

251 The ABC-trilayer graphene/hexagonal boron nitride (ABC-TLG/h

252 mechanisms may exist more broadly across the ABC transporter family.

253 MlaB, a STAS domain protein, binds the ABC nucleotide binding domain, MlaF, and is required for

254 btained based on a known model so-called the ABC model.

255 rly parenting intervention (in this case the ABC intervention) can enhance brain regions supporting c

256 reveal that the protein indeed contains the ABC-exporter fold, as well as a large water-filled cavit

257 were randomly assigned to receive either the ABC intervention (N=22) or a control intervention (N=24)

258 vesicles isolated from yeast expressing the ABC protein AtABCC2 are capable of MgATP-dependent uptak

259 hat under a vertical displacement field, the ABC-TLG/hBN heterostructure features an isolated flat va

260 e first time that calibration curves for the ABC type TGs are reported.

261 Children in the ABC condition showed greater maternal cue-related activa

262 Beta power in the ABC did not differ from that of the low-risk comparison

263 In the ABC transporter-dependent biosynthesis pathway, O antige

264 s six Mla proteins, MlaFEDBCA, including the ABC transporter MlaFEDB, which functions via an unknown

265 apamil, which were initially docked into the ABC transporter, get translocated through the exporter b

266 take systems, predominant among which is the ABC transporter family.

267 rovide a comprehensive classification of the ABC ATPase superfamily.

268 Implementation of the ABC care bundle was significantly associated with lower

269 es corroborated the specific assembly of the ABC heterotrimer.

270 s, evoking the classic A-C antagonism of the ABC model for floral organ development.

271 orming and membrane binding A subunit of the ABC toxin YenTc, produced by the insect pathogen Yersini

272 ansporters (PCATs) are unique members of the ABC transporter family that proteolytically process and

273 analogous to the multidrug exporters of the ABC transporter family, which pump out structurally dive

274 In Escherichia coli, FtsEX, a member of the ABC transporter superfamily, is involved in regulating t

275 oxybenzoyl]benzoic acid, an inhibitor of the ABC-B/multidrug resistance/P-glycoprotein subfamily of t

276 gainst closely related Bacillus strains, the ABC transporter exported the toxic Bacillunoic acids upo

277 ividual maturation factors, we find that the ABC transporter NosFY and the accessory NosD protein are

278 ugh both of these transporters belong to the ABC family and mediate the efflux of a sterol substrate,

279 , and we show that MetQ association with the ABC transporter MetNI depends on its N-terminal lipid an

280 ocycles with one (AAA), two (AAB), or three (ABC) different carbazole units, we needed to subvert the

281 Children assigned to ABC showed relatively greater high-frequency power (beta

282 increased NF-kappaB activation contribute to ABC DLBCL survival.

283 Similarities to ABC exporters suggest that ATG9A could be a transporter

284 es in susceptibility of ICEC0942 and THZ1 to ABC-transporters, may help guide their future clinical u

285 We corroborated previous reports that a TonB-ABC transport system is required for lanthanide incorpor

286 issue-specific clusters of SLC transporters, ABC transporters, and DMEs.

287 e pairs (AB, BC) drawn from distinct triads (ABC) that shared the same internal structure and were th

288 measurements revealing the expected tunable ABC band gap.

289 Our study provides insights into an unusual ABC exporter that evolved as highly specialized sideroph

290 , the Attachment and Biobehavioral Catch-up (ABC), delivered to parents and infants monitored for mal

291 tion (Attachment and Biobehavioral Catch-Up; ABC) on children's neural processing of parent cues and

292 yzed for the percentage of B cells that were ABC-like, defined by expression of CD11c, low levels of

293 s as a possible neural pathway through which ABC may prevent future behavior problems among high-risk

294 Patients with ABC-bleeding scores predicting a high 1-year risk of ble

295 osquitoes with deltamethrin, with or without ABC transporter modulators, showed that Rock and PR resp

296 lasmic leaflet by the channel-forming WzmWzt ABC transporter for ligation to the core lipopolysacchar

297 ated across the inner membrane by the WzmWzt ABC transporter for ligation to the lipopolysaccharide c

298 22) and Wzt(Mx) (MXAN_4623) form the Wzm/Wzt ABC transporter.

299 We describe a mutation, A666G, in the yeast ABC transporter Pdr5 that shows greater resistance to mo

300 ed synthesis of misfolded forms of the yeast ABC transporter Yor1.