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1 within phylogroup D-that is associated with multidrug resistance.
2 ified harbinger mutations that often precede multidrug resistance.
3 ay help to reduce the use of antibiotics and multidrug resistance.
4 pecific therapeutics in the effort to combat multidrug resistance.
5 nfections that are difficult to treat due to multidrug resistance.
6 path leading to the emergence of high-level, multidrug resistance.
7 of tuberculosis incidence and prevalence of multidrug resistance.
8 ost critical mechanisms leading to bacterial multidrug resistance.
9 s, which may have important implications for multidrug resistance.
10 ibiotics for tackling the issue of bacterial multidrug resistance.
11 might be clinically relevant to the rise of multidrug resistance.
12 etics and contributing to the development of multidrug resistance.
13 pathway represents a linchpin in C. glabrata multidrug resistance.
14 valganciclovir, and a UL54 mutation confers multidrug resistance.
15 les in microbial pathogenesis, virulence and multidrug resistance.
16 ids as potential targets to fight pathogenic multidrug resistance.
17 ilome that were associated with plasmids and multidrug resistance.
18 ota makes it a potential reservoir of mobile multidrug resistance.
19 infections, with many strains demonstrating multidrug resistance.
20 association of baseline characteristics with multidrug resistance.
21 lthough all 3 epidemics were associated with multidrug resistance.
22 idence, and summarized clinical features and multidrug resistance.
23 idenced an ability to overcome cisplatin and multidrug resistance.
24 worldwide, with an increasing prevalence of multidrug resistance.
25 s resistant to TCS exhibited higher rates of multidrug resistance.
26 ddress the global health need and burgeoning multidrug resistance.
27 or roles in drug pharmacokinetics and cancer multidrug resistance.
28 ounds and have been implicated in conferring multidrug resistance.
29 gly rendered ineffective by rising bacterial multidrug resistance.
30 -negative bacterium with the highest rate of multidrug resistance.
31 nosocomial pathogen with a high incidence of multidrug resistance.
32 t options include minocycline in the case of multidrug resistance.
33 re mediated by increased copy numbers of the multidrug resistance 1 gene (pvmdr1) may select for mefl
34 und to be a poor substrate (>30 muM) for the multidrug resistance 1 protein, suggesting low likelihoo
37 c-finger nucleases to genetically modify the multidrug resistance-1 transporter PfMDR1 at amino acids
40 We have shown that partial hepatectomy in multidrug resistance 2 knockout (Mdr2(-/-) ) mice, a mod
43 antly reduces FBP levels in HCC cells and in multidrug resistance 2-deficient mice that develop HCC d
44 and a high prevalence of clinically relevant multidrug resistance (252 [52%] of 485 samples), which v
46 n genes involved in bile disposition: ABCB4 (multidrug resistance 3) rs2302387 and ABCB11 [bile salt
47 e niche-adaptive accessory traits, including multidrug resistance; 3) the accessory genome of the meg
52 inical success, followed by echinocandin and multidrug resistance among some Candida species, especia
54 st that the HpnN transporter is critical for multidrug resistance and cell wall remodeling in Burkhol
56 , respectively, and 18.3% displayed combined multidrug resistance and DCS; rates of azithromycin and
58 utic drugs, including temozolomide, reverses multidrug resistance and increases survival in glioblast
60 binding cassette (ABCC) transporters mediate multidrug resistance and ion conductance regulation.
61 transporter (PfCRT) is a key contributor to multidrug resistance and is also essential for the survi
62 ia is the epicentre of Plasmodium falciparum multidrug resistance and is facing high rates of dihydro
63 belonging to the H58 haplotype often exhibit multidrug resistance and may have a fitness advantage re
65 addressed the causal association between HIV multidrug resistance and mortality, excluding factors on
66 mps like P-glycoprotein (P-gp, ABCB1) confer multidrug resistance and mutant ABC proteins are respons
67 ncrease in the number of plasmids conferring multidrug resistance and strain replacement by a resista
68 lic health problem owing to the emergence of multidrug resistance and the lack of broadly efficient v
70 ed stemness to nonstem cancer cells, induced multidrug resistance, and enhanced the migration potenti
71 resistance, second-line injectable-resistant multidrug resistance, and extensive multidrug resistance
72 ppropriate antibacterial use contributing to multidrug resistance, and increased morbidity and mortal
74 i) hypersensitivity sometimes converted into multidrug resistance; and (iii) resistance gains frequen
76 nofluorescence analyses confirmed that MRP3 (multidrug resistance associated protein 3), which was hi
79 ivered IgGs can inhibit the drug efflux pump multidrug resistance-associated protein 1 (MRP1) and the
80 cytometry and immunostaining have shown that multidrug resistance-associated protein 1 (MRP1) is prev
81 regulates the cell surface expression of the multidrug resistance-associated protein 1 (MRP1) transpo
82 on a known ATP-binding cassette transporter, multidrug resistance-associated protein 1 (MRP1), and fo
85 th respect to potency and selectivity toward multidrug resistance-associated protein 1 (MRP1, ABCC1).
86 breast cancer resistance protein (BCRP), and multidrug resistance-associated protein 2 (MRP2) at the
87 eval of the bile salt export pump (Bsep) and multidrug resistance-associated protein 2 (Mrp2) from th
88 1A1 (Oatp1a1), the hepatobiliary transporter multidrug resistance-associated protein 2 (Mrp2), and th
89 0 administration significantly induced renal multidrug resistance-associated protein 2 and 4, peroxis
90 malignant lesions, we aim to investigate the multidrug resistance-associated protein 4 (MRP4)-depende
95 at a member of the distinct Escherichia coli multidrug resistance B (EmrB) family is a primary export
97 erfamily make a considerable contribution to multidrug resistance by catalysing efflux of myriad stru
98 ruginosa, MexAB-OprM plays a central role in multidrug resistance by ejecting various drug compounds,
100 extrusion (MATE) transporters contribute to multidrug resistance by extruding different drugs across
102 pound extrusion (MATE) transporters underpin multidrug resistance by using the H(+) or Na(+) electroc
104 resistance (SMR) family drive the spread of multidrug resistance cassettes among bacterial populatio
105 sed on a lapatinib induced inhibition of the multidrug-resistance efflux transporter ABCB1, which is
107 earch demonstrates that TCC can select for a multidrug resistance encoding gene in mixed community an
108 drug resistance, involving a combination of multidrug resistance, extended spectrum beta-lactamase p
109 o studies were performed in BDL rats and the multidrug resistance gene 2 knockout (Mdr2(-/-) ) mouse
111 in administration on hepatic fibrosis in the multidrug resistance gene 2-knockout (Mdr2(-/-)) mouse m
113 e-spanning transporter PfMDR1 (P. falciparum multidrug resistance gene-1) as a determinant of parasit
116 ation and T-cell activation while repressing multidrug resistance genes and cancer-related genes, the
117 on of ssa and transposable elements encoding multidrug resistance genes triggered the expansion of sc
118 of resistance to single drug classes and now multidrug resistance greatly hampers patient management.
120 e infections worldwide, is rapidly acquiring multidrug resistance, hastening the need for selective n
123 misclassification and its ability to develop multidrug resistance in a single step, highlights the ch
126 cs and toxic metabolites, thereby conferring multidrug resistance in bacterial pathogens and cancer c
127 red a nanoparticle mimic that both overcomes multidrug resistance in cancer cells and increases tumou
129 s key position, ABC transporters can mediate multidrug resistance in cancer therapy and their dysfunc
132 specific ATP-dependent transporter linked to multidrug resistance in cancer; it plays important roles
134 s of several variants, efficacy in reversing multidrug resistance in cell culture, and biochemical as
135 Transcription factors MarR and MarA confer multidrug resistance in enteric bacteria by modulating e
137 infections are hampered by the evolution of multidrug resistance in pathogens as well as the lack of
138 stromal cells can promote tumorigenesis and multidrug resistance in prostate or breast cancer cells.
145 fferent cancer treatments with synergism and multidrug resistance inhibition, which has great potenti
147 herapeutic antibiotics; however, the rise in multidrug resistance is a growing threat to the utility
156 interaction of these agonists with the human multidrug resistance-linked transporter P-glycoprotein (
157 treatment enriched for strains that acquired multidrug resistance loci, encoding enzymes that confer
158 their parent compounds (e.g., circumventing multidrug resistance), making the dimerization concept h
160 bacterial resistance in hospitals, including multidrug resistance (MDR) and its association with seri
162 air, electron transfer, and a component of a multidrug resistance (MDR) efflux pump were concluded to
164 he chemotherapeutic to overcome both BBB and multidrug resistance (MDR) glioma cells while providing
166 e amplification release of DOX and overcomes multidrug resistance (MDR) in cancer cells, producing a
168 expression of P-glycoprotein (Pgp) increases multidrug resistance (MDR) in cancer, which greatly impe
172 f the promising strategies to overcome tumor multidrug resistance (MDR) is to deliver anticancer drug
176 Among the mechanisms of treatment failure is multidrug resistance (MDR) mediated by the ABCB1, ABCC1,
180 The most common solid tumors show intrinsic multidrug resistance (MDR) or inevitably acquire such wh
182 ay of treatment; however, the development of multidrug resistance (MDR) restricts the efficacy of cur
183 vels of GRP78 protein in cancer cells confer multidrug resistance (MDR) to therapeutic treatment.
184 lied this approach to a cellular reaction of multidrug resistance (MDR) transport, which was followed
185 lococcus aureus (MRSA) infection was 24% and multidrug resistance (MDR) was observed in 87% of the is
187 ) plays a crucial role in the development of multidrug resistance (MDR), a major obstacle for success
188 Conversely it is one of the main causes of multidrug resistance (MDR), being capable of effluxing m
190 d monoresistance, rifampicin monoresistance, multidrug resistance (MDR), fluoroquinolone-resistant mu
191 r treatment approach, suffers seriously from multidrug resistance (MDR), generally caused by innate D
192 pe characterized by increased proliferation, multidrug resistance (MDR), invasion and metastasis.
193 molecule chemosensitizers can reverse cancer multidrug resistance (MDR), thus significantly improving
194 f RND-type efflux pumps is a major factor in multidrug resistance (MDR), which makes these pumps impo
195 Here, we analyzed the expression of 377 multidrug resistance (MDR)-associated genes in two indep
200 ic metabolism, including a decrease in ABCB1/multidrug resistance (MDR)1 p-glycoprotein (p-gp) expres
204 ce, we provide a framework for understanding multidrug resistance, mediated by analogous systems, acr
205 demic C difficile ribotypes characterised by multidrug resistance might depend on antibiotic selectio
207 ibiotic regulations to prevent selection for multidrug resistance, new antibiotic classes, typhoid's
208 protein (Pgp) is an efflux pump important in multidrug resistance of cancer cells and in determining
209 and eukaryotes, with examples implicated in multidrug resistance of pathogens and cancer cells, as w
212 established mutations could confer potential multidrug resistance on pH1N1 or HPAI H5N1 viruses.
213 ted with HIV-infected patients (P = .03) and multidrug resistance (OR, 6.6; 95% CI, 2.5-17.2; P < .00
214 of transcription factors is associated with multidrug resistance, our aim was to evaluate whether th
215 zoyl]benzoic acid, an inhibitor of the ABC-B/multidrug resistance/P-glycoprotein subfamily of transpo
216 nd the ATP-binding cassette subfamily (ABC-B/multidrug resistance/P-glycoprotein) transporters from l
217 morphisms that occur before the emergence of multidrug resistance, particularly katG p.Ser315Thr, int
218 orthologues, which are key regulators of the multidrug resistance pathway in Saccharomyces cerevisiae
223 or (PXR) was observed together with ApoE and multidrug resistance protein 1 (MDR1) membrane transport
224 histochemical expression of bronchopulmonary multidrug resistance protein 1 (MRP1) and permeability g
226 eans to overcome resistance by silencing the multidrug resistance protein 1 (MRP1), before chemothera
227 ned against P-glycoprotein (P-gp, ABCB1) and multidrug resistance protein 1 (MRP1, ABCC1) to confirm
228 The ATP-binding cassette (ABC) transporter multidrug resistance protein 1 (MRP1/ABCC1) is responsib
230 mpicin-induced gene expression of CYP3A4 and multidrug resistance protein 1, as well as their respect
231 vity of two other major efflux transporters, multidrug resistance protein 2 and breast cancer resista
232 apical membrane to subapical puncta, whereas multidrug resistance protein 2 distributions were not ch
234 harmacological inhibition with JZL184 in the multidrug resistance protein 2 knockout (Mdr2(-/-) ) mou
235 ngiocyte proliferation and liver fibrosis in multidrug resistance protein 2 knockout (Mdr2KO) mice as
236 10 (apicoplast ribosomal protein S10), mdr2 (multidrug resistance protein 2) and crt (chloroquine res
237 information on the interaction of drugs with multidrug resistance protein 3 (MDR3) exists and its rol
238 hydroxysteroid sulfotransferase enzyme 2A1, multidrug resistance protein 3, and apical sodium-depend
239 drugs are either substrates or inhibitors of multidrug resistance protein 4 (MRP4), such as the anti-
240 In this study, we evaluated the role of multidrug resistance protein 4 (MRP4, or ABCC4), a nucle
241 signaling cascade (phospholipase A2, COX-2, multidrug resistance protein 4, and G-protein-coupled pr
243 y substrates for p-glycoprotein (ABCB1), the multidrug resistance protein known to facilitate transde
246 thiol/disulfide balance, greater extents of multidrug resistance protein-1 (MRP1) expression, and gr
247 ferase and the biliary phospholipid floppase multidrug-resistance protein 2 (Mdr2/Abcb4), resulting i
248 subfamily includes pumps, the long and short multidrug resistance proteins (MRPs), and an ATP-gated a
250 ucture of heterodimeric Thermus thermophilus multidrug resistance proteins A and B (TmrAB), which not
251 on antiparallel homo- or heterodimeric small multidrug resistance proteins and examine whether the in
252 n-regulation of miRNA downstream targets and multidrug resistance proteins and extent of apoptosis we
256 s of healthcare-associated infections (HAI); multidrug resistance reduces available options for antib
259 tuberculosis in the past 6 months or to the multidrug-resistance risk group if drugs for tuberculosi
260 in all analyses, whereas participants in the multidrug-resistance risk group were only included in an
262 resistance (MDR), fluoroquinolone-resistant multidrug resistance, second-line injectable-resistant m
263 mental biocides, transporters from the small multidrug resistance (SMR) family drive the spread of mu
265 transport proteins are members of the small multidrug resistance (SMR) family that are composed of f
267 cell response in melanoma cells resulting in multidrug resistance, termed induced drug-tolerant cells
268 Previously identified as a key mediator of multidrug resistance, the drug efflux behavior of P-glyc
270 e of such polymer-drug conjugates to reverse multidrug resistance through P-gp inhibition and to miti
277 esistance is uncommon, increasing reports of multidrug resistance to the azoles, echinocandins, and p
278 reened a known mutation(s) that could confer multidrug resistance to the currently approved NAIs osel
279 This study aimed to evaluate the prevalence, multidrug-resistance traits, PCR-detection of virulence,
280 loroquine resistance transporter (PfCRT) and multidrug resistance transporter (PfMDR1) can modulate t
281 , we sought to identify mutants of the small multidrug resistance transporter EmrE with reduced rates
284 and was a highly sensitive substrate of the multidrug resistance transporter P-glycoprotein (P-gp).
285 Inhibition of A(2B) AR signaling decreased multidrug resistance transporter protein expression, inc
290 progesterone as a modulator of P-gp-mediated multidrug resistance was established by esterification o
292 eptible to most antibiotics, indicating that multidrug resistance was not the dominant reason for pre
296 micking the ability of Salmonella to reverse multidrug resistance, we constructed a gold nanoparticle
298 n very young children and the development of multidrug resistance, which threatens efficacy of antimi
300 esistant multidrug resistance, and extensive multidrug resistance with resistance to both a fluoroqui