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1 NNT knockdown in a human adrenocortical cell line result
2 NNT makes a major contribution to peroxide metabolism du
3 NNT-1/BSF-3 cDNA was cloned from activated Jurkat human
4 NNT-1/BSF-3 induces tyrosine phosphorylation of glycopro
5 NNT-1/BSF-3 is a gp130 activator with B-cell stimulating
6 NNT-1/BSF-3 mRNA is found mainly in lymph nodes and sple
7 NNT-1/BSF-3 regulates immunity by stimulating B cell fun
8 NNT-1/BSF-3 shows activities typical of IL-6 family memb
9 NNT-1/BSF-3 stimulates B cell proliferation and Ig produ
10 NNT-1/BSF-3-transgenic mice also show non-amyloid mesang
11 NNT-1/BSF-3-transgenic mice produce high amounts of Ag-s
12 NNT-1/BSF-3-transgenic mice show high serum levels of Ig
13 NNT-1/BSF-3-transgenic mice, engineered to express NNT-1
14 NNTs were lower for tricyclic antidepressants, strong op
15 NNTs were lowest for MSM and transgender women self-repo
16 ity (RR, 0.64; 95% CI, 0.46 to 0.89; I2, 0%; NNT, 23) in patients receiving ventilation with lower ti
17 93), quetiapine (OR, 1.53, 95% CI, 1.17-2.0; NNT, 10), and risperidone (OR, 1.83, 95% CI, 1.16-2.88;
20 ontrol restorations, 22 (17%) (p = 0.000004; NNT 7); and 'Minor' failures, HT, 7 (5%); control restor
21 trol restorations, 15 (16.5%) (p = 0.000488; NNT 8); and 'Minor' failures (reversible pulpitis, resto
22 ors (RR, 0.63 [95% CI, 0.50-0.80]; P < .001; NNT, 105 [95% CI, 69-212]), 3 factors (RR, 0.54 [95% CI,
25 year (RR, 0.77; 95% CI, 0.71-0.84; P < .001; NNT, 21) and 2 years (RR, 0.94; 95% CI, 0.89-1.00; P = .
27 est (RR, 0.67 [95% CI, 0.57-0.79]; P < .001; NNT, 339 [95% CI, 240-582]), again limited to patients u
28 ors (RR, 0.54 [95% CI, 0.39-0.73]; P < .001; NNT, 41 [95% CI, 28-80]), or 4 factors or more (RR, 0.40
30 cardiac mortality (0.67, 0.51-0.89; p=0.006; NNT=347), with similar cardiac mortality (0.93, 0.73-1.1
31 ean (OR = 0.53; 95% CI: 0.33-0.87; P = 0.01; NNT = 30) and clean-contaminated surgery (OR = 0.43; 95%
32 NT, 5) and chronicity (chi2 = 7.46; P = .02; NNT, 6) such that the advantage for combined treatment w
35 actions with severity (t451 = 1.97; P = .05; NNT, 5) and chronicity (chi2 = 7.46; P = .02; NNT, 6) su
39 ized for a hospital threshold volume of 100 (NNT=50) and a surgeon threshold volume of 50 (NNT=118).
42 onths (RR, 0.72; 95% CI, 0.48-1.09; P = .12; NNT, 14) and 1 year (RR, 0.66; 95% CI, 0.43-0.99; P < .0
43 acebo/UC in terms of response rate (RR=0.22, NNT=2), delirium severity scales scores (SMD=-1.27), CGI
45 neurotrophin-1/B cell-stimulating factor-3 (NNT-1/BSF-3; also reported as cardiotrophin-like cytokin
46 on (RR, 0.45; 95% CI, 0.22 to 0.92; I2, 32%; NNT, 26), lower mean (SD) hospital length of stay (6.91
47 37.9%; RR, 1.21; 95% CI, 0.82-1.81; P = .35; NNT, 12.4) or at week 20 (69.3% vs 54.8%; RR, 1.26; 95%
49 ause (OR 0.69, 0.62-0.78; ARR 2.7%, 2.0-3.5; NNT 37, 29-52), implying that 145 self-harm episodes and
50 vs 3/26 [11.5%]; RR, 4.0 [95% CI, 1.2-12.5]; NNT = 2.86; P = .01; and 25% response, 18/28 [64.2%] vs
54 elopment of HE (RR = 0.47, 95% CI 0.33-0.68, NNT = 6), the risk of developing serious liver-related a
57 adverse events (RR = 0.48, 95% CI 0.33-0.70, NNT = 6), and reduced mortality (RR = 0.63, 95% CI 0.40-
58 bation failure (RR, 0.48; 95% CI, 0.32-0.71; NNT, 4; 95% CI, 2-7) compared with placebo or no treatme
59 : aripiprazole (OR, 2.07; 95% CI, 1.58-2.72; NNT, 7), OFC (OR, 1.30, 95% CI, 0.87-1.93), quetiapine (
63 physiotherapy (RR, 0.32; 95% CI, 0.13-0.82; NNT, 15; 95% CI, 7-50) both reduced extubation failure r
66 cide (OR 0.75, 0.60-0.94; ARR 0.5%, 0.1-0.9; NNT 188, 108-725), and death by any cause (OR 0.69, 0.62
69 also reduced by immediate (0.83, 0.73-0.94; NNT 40) or delayed antibiotics (0.61, 0.50-0.74; NNT 18)
70 orticosteroids (RR, 0.18; 95% CI, 0.04-0.97; NNT, 12; 95% CI, 6-100) and chest physiotherapy (RR, 0.3
73 the middle predicted benefit subgroup had a NNT of 76 (ARR = 0.013, 95% CI: -0.0001, 0.026; P = 0.05
75 nt(-/-) exhibit approximately 50% and absent NNT activity, respectively, but the activities of concur
76 s with eGFR<30 ml/min per 1.73 m(2) Adjusted NNT (95% confidence interval) to avoid dialysis was 22.4
77 risk patients with LDL-C >/=70 mg/dl, and an NNT </=30 for very high-risk and high-risk patients with
78 isk patients with LDL-C >/=190 mg/dl, and an NNT </=30 for very high-risk patients with LDL-C >/=160
79 lower LDL-C by at least 50% would provide an NNT </=50 for very high-risk and high-risk patients with
83 val study setting such as the ERSPC, NNS and NNT are time specific, and reporting values at one time
91 red metabolic disease susceptibility between NNT-deficient 6J mice and NNT-competent C57BL/6 substrai
92 imary measure and assessed publication bias; NNT was calculated with the fixed-effects Mantel-Haensze
93 re generally modest: in particular, combined NNTs were 6.4 (95% CI 5.2-8.4) for serotonin-noradrenali
94 receptive anal intercourse without a condom (NNT 36), cocaine use (12), or a sexually transmitted inf
98 r were upper gastrointestinal, the estimated NNT for routine PPI use to prevent such bleeds is low, a
99 he seemingly simplistic nature of estimating NNT, there is widespread misunderstanding of its pitfall
101 BSF-3-transgenic mice, engineered to express NNT-1/BSF-3 in the liver under control of the apolipopro
103 Our results demonstrate a novel role for NNT as a regulator of macrophage-mediated inflammatory r
104 ratio (RR), the number-needed-to-treat/harm (NNT/NNH), 95% CIs and standardised mean difference (SMD)
106 lementation studies showed that mutant human NNT failed to rescue nnt morpholino-induced heart dysfun
109 7BL/6J phenotype but the parameters of CP in NNT-expressing transgenic mice generated on a C57BL6/J b
110 mily, we identified a frameshift mutation in NNT, a nuclear-encoded mitochondrial protein, not implic
111 exome sequencing, we identified mutations in NNT, an antioxidant defense gene, in individuals with fa
112 OR 0.36, 0.26-0.50) in myocardial ischaemia (NNT 16) at the expense of an increase (OR 2.01, 1.27-3.6
115 es included regulators of energy metabolism (NNT), trafficking and membrane fusion (SLCO2A1 and ANXA7
116 reat (NNT) 23 for PCI-related delay >60 min; NNT 44 for PCI-related delay 60-90 min; and NNT 250 for
117 iority of SGAs regarding relapse was modest (NNT=17), but confirmed in double-blind trials, first- an
118 ther administration of 5-nonyloxytriptamine (NNT), a selective 5-HT(1B) receptor agonist, affects TCA
119 results indicate that the agonist action of NNT at the 5-HT(1B) receptor causes TCA disorganization
121 kedly influence the relative contribution of NNT (i.e. varies between nearly 0 and 100%) to NADPH-dep
125 variances in the 6J stain, including loss of NNT function, these findings suggest that the 6N substra
133 t doses must be administered to 12 patients (NNT, 12.2; 95% CI, 7.5 to 33.4) not receiving dexamethas
134 = 0.16; responder rate, 60% DES vs. 47% PLA; NNT, 8.1) but did show a statistically significant benef
135 = 0.01; responder rate, 73% DES vs. 49% PLA; NNT, 5.2), especially when participants with nondetectab
139 ed through pyruvate carboxylase and rendered NNT knockdown cells more sensitive to glucose deprivatio
141 methods are the nearest neighbor technique (NNT) and Moran's IPOP technique, a variation of Moran's
142 sulin resistance, coupled with the fact that NNT regulates peroxide detoxification, it was hypothesiz
145 udy, we demonstrated for the first time that NNT has a significant effect in the modulation of the im
149 performance of the entropy technique and the NNT were independent of scale, that of Moran's IPOP was
153 mortality difference continues to grow, the NNT to save a life with PSA screening will decrease.
158 Nicotinamide nucleotide transhydrogenase (NNT) is a mitochondrial enzyme that transfers reducing e
159 Nicotinamide nucleotide transhydrogenase (NNT) is a mitochondrial redox-driven proton pump that co
160 of nicotinamide nucleotide transhydrogenase (NNT) protein in C57BL/6J is responsible for the more sev
161 of nicotinamide nucleotide transhydrogenase (NNT) reduces NADP(+) at the expense of NADH oxidation an
162 gh nicotinamide nucleotide transhydrogenase (NNT)-deficient C57BL/6J (6J) mice are known to be highly
163 nd nicotinamide nucleotide transhydrogenase (NNT)], we selectively impaired mitochondrial respiratory
164 ty benefit of X-PCI [number needed to treat (NNT) 23 for PCI-related delay >60 min; NNT 44 for PCI-re
168 cit reporting of the number needed to treat (NNT) and the absolute risk reduction (ARR) in RCTs.
170 We calculated 5-year number needed to treat (NNT) by applying the benefit recorded in JUPITER to the
171 eductions (ARR) and numbers needed to treat (NNT) for 5-HT(3) antagonists, as monotherapy or as adjun
173 lative risks and the number needed to treat (NNT) for first variceal bleed, bleed-related mortality,
174 ith vehicle, and the number needed to treat (NNT) for one patient to have their keratosis completely
175 , corresponding to a number needed to treat (NNT) of 10 (95% CI, 7 to 15), 6 (4 to 8), and 3 (2 to 5)
176 nefit subgroup had a number needed to treat (NNT) of 24 to prevent 1 CVD event/death over 5 years (ab
177 (NNS) of 1,410 and a number needed to treat (NNT) of 48 to prevent one prostate cancer death at 9 yea
179 sed to determine the number needed to treat (NNT) to prevent 1 ASCVD event over 5 years for each pati
181 imated age-specific numbers needed to treat (NNT) to prevent upper gastrointestinal bleeding with rou
182 verted (PIA) and the number needed to treat (NNT) under behavioral indications of the CDC's PrEP guid
183 risk difference, the number needed to treat (NNT) was 15 (95% CI, 8-53), or equivalently 15 patients
190 0.43-0.91, estimated number needed to treat [NNT 193) as was delayed prescription of antibiotics (0.5
192 ARR] 2.6%, 1.5-3.7; numbers needed to treat [NNT] 39, 95% CI 27-69), deaths by suicide (OR 0.75, 0.60
193 % CI -4.09 to -0.20; number needed to treat [NNT] 47, 95% CI 25-500) and antibiotic-impregnated cathe
195 ocardial infarction (number needed to treat [NNT] 63) and decrease (OR 0.36, 0.26-0.50) in myocardial
196 rval [CI] 0.53-0.74, number needed to treat [NNT] = 4) and serious liver-related adverse events such
197 with anticoagulants; number needed to treat [NNT] = 59) and greater risks of major bleeding (OR, 2.73
199 .23 to 0.47; I2, 0%; number needed to treat [NNT], 11), and mortality (RR, 0.64; 95% CI, 0.46 to 0.89
201 ol difference, 6.5%; number needed to treat [NNT], 15), but there was no significant reduction among
204 1.16-1.95; P = .002; number needed to treat [NNT], 3.6) suggested the efficacy of CGT, and the additi
206 0.56-0.69; P < .001; number needed to treat [NNT], 9) and 2 years (RR, 0.84; 95% CI, 0.79-0.89; P < .
207 I 0.69-0.98; p=0.02; number needed to treat [NNT]=325), with no significant heterogeneity apparent ac
210 95% CI 0.54 to 0.87, 4,601 babies, 5 trials, NNT to benefit 46) and the neuroprotective intent analys
211 st variceal bleed was 0.48 (0.24-0.96), with NNT of 13; however, there was no effect on either bleed-
214 -density LDL-C by 20% would provide a 5-year NNT </=50 for very high-risk patients with LDL-C >/=130
216 coronary heart disease, the predicted 5-year NNT was 549 for CAC score 0, 94 for scores 1-100, and 24
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