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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;
18 ontrol restorations, 38 (42%) (p < 0.000001; NNT 3).
19 ontrol restorations, 60 (46%) (p < 0.000001; NNT 3).
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,
23 ears (RR, 0.84; 95% CI, 0.79-0.89; P < .001; NNT, 17).
24 ore (RR, 0.40 [95% CI, 0.25-0.73]; P < .001; NNT, 18 [95% CI, 12-34]).
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 = .
26 year (RR, 0.66; 95% CI, 0.43-0.99; P < .001; NNT, 26).
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
29  the RR was 0.19 (95% CI, 0.06-0.53; P=.002; NNT, 15).
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
33 ery (OR = 0.43; 95% CI: 0.20-0.93; P = 0.03; NNT = 9) specifically.
34 years (RR, 0.94; 95% CI, 0.89-1.00; P = .04; NNT, 593).
35 actions with severity (t451 = 1.97; P = .05; NNT, 5) and chronicity (chi2 = 7.46; P = .02; NNT, 6) su
36 83.7%; RR, 1.21; 95% CI, 1.00-1.46; P = .05; NNT, 6.9).
37 pregnated catheters (-1.98%, -3.90 to -0.06, NNT 51, 26-1667).
38 ssion at week 8 (RR, 4.5 [95% CI, 1.4-14.1]; NNT = 2.45; P = .01).
39 ized for a hospital threshold volume of 100 (NNT=50) and a surgeon threshold volume of 50 (NNT=118).
40 22-0.74; 1.17% [12/1024] vs 3.04% [31/1019]; NNT = 54).
41 54.8%; RR, 1.26; 95% CI, 0.95-1.68; P = .11; NNT, 6.9).
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
44  neurotrophin-1/B cell-stimulating factor-3 (NNT-1/BSF-3).
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%
48  RR=0.80, CI: 0.70-0.91, P=0.0007, I(2)=37%; NNT=17, CI: 10-50, P=0.003).
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
51 NT=50) and a surgeon threshold volume of 50 (NNT=118).
52 3.96; P = .001; HR, 2.34; 95% CI, 1.54-3.57; NNT, 3; 95% CI, 2-5).
53                                      At P-6, NNT treatment decreased 5-HT levels slightly compared wi
54 elopment of HE (RR = 0.47, 95% CI 0.33-0.68, NNT = 6), the risk of developing serious liver-related a
55 renal syndrome (RR = 0.42, 95% CI 0.26-0.69, NNT = 50).
56 39-0.80; treatment-control difference, 1.7%; NNT, 60).
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 (
60 40) or delayed antibiotics (0.61, 0.50-0.74; NNT 18).
61 nts (relative risk, 0.58; 95% CI, 0.44-0.77; NNT, 6; 95% CI, 4-13).
62 bation failure (RR, 0.70; 95% CI, 0.60-0.81; NNT, 8; 95% CI, 5-13).
63  physiotherapy (RR, 0.32; 95% CI, 0.13-0.82; NNT, 15; 95% CI, 7-50) both reduced extubation failure r
64 82.5%; RR, 1.01; 95% CI, 0.88-1.17; P = .84; NNT, 84).
65 nd risperidone (OR, 1.83, 95% CI, 1.16-2.88; NNT, 8).
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
67  vs 8/26 [30.8%]; RR, 2.1 [95% CI, 1.1-3.9]; NNT = 2.99; P = .01).
68  with overt HE (RR = 0.36, 95% CI 0.14-0.94, NNT = 20), although not in patients with minimal HE.
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
71 uced mortality (RR = 0.63, 95% CI 0.40-0.98, NNT = 20).
72 rescription of antibiotics (0.58, 0.34-0.98; NNT 174).
73  the middle predicted benefit subgroup had a NNT of 76 (ARR = 0.013, 95% CI: -0.0001, 0.026; P = 0.05
74  of 0.91 (95% CI, 0.84-0.98), resulting in a NNT of 12 (95% CI, 7-78).
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
80 d from 837 at year 10 to 503 at year 12, and NNT decreased from 29 to 18.
81 eptibility between NNT-deficient 6J mice and NNT-competent C57BL/6 substrains.
82  NNT 44 for PCI-related delay 60-90 min; and NNT 250 for PCI-related delay >90 min].
83 val study setting such as the ERSPC, NNS and NNT are time specific, and reporting values at one time
84                             Although NNS and NNT are useful statistics to assess the benefits and har
85          According to our model, the NNS and NNT at 9 years were 1,254 and 43, respectively.
86 effect of varying follow-up times on NNS and NNT using data extrapolated from the ERSPC report.
87                 Consideration of the PAF and NNT can aid in discussion of the benefits and risks of p
88 Poisson model, and we calculated the PAF and NNT for risk behaviour subgroups.
89             We aimed to estimate the PAF and NNT of participants in the iPrEx (Pre-Exposure Prophylax
90                    Of 359 eligible articles, NNT was reported in 8 articles.
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
95                   Importantly, knocking down NNT inhibits reductive carboxylation in SkMel5 and 786-O
96 epidemiological impact (PIA) and efficiency (NNT) at plausible scale-up levels.
97                                The estimated NNT for routine PPI use to prevent one disabling or fata
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
100 ; number needed to treat to prevent 1 event [NNT], 48).
101 BSF-3-transgenic mice, engineered to express NNT-1/BSF-3 in the liver under control of the apolipopro
102                                 The gene for NNT-1/BSF-3 is on chromosome 11q13.
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)
105 ve anal sex without a condom had the highest NNTs (100 and 77, respectively).
106 lementation studies showed that mutant human NNT failed to rescue nnt morpholino-induced heart dysfun
107 dentified, which shows 96% homology to human NNT-1/BSF-3.
108                                           In NNT-treated rats, the Di-I-labeled vibrissae-related pat
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
113  times daily (5x/day), with either 0.1 mg/kg NNT or vehicle from birth to postnatal day 6 (P-6).
114 be defective in C57BL/6J mice, and no mature NNT protein could be detected.
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
120                               This action of NNT could explain its putative protective role in MnSOD-
121 kedly influence the relative contribution of NNT (i.e. varies between nearly 0 and 100%) to NADPH-dep
122                          The contribution of NNT to peroxide metabolism is decreased during ADP phosp
123              Here, we show that knockdown of NNT inhibits the contribution of glutamine to the TCA cy
124                                  The lack of NNT activity in Nnt(-/-) mice impairs peroxide metabolis
125 variances in the 6J stain, including loss of NNT function, these findings suggest that the 6N substra
126                            Overexpression of NNT in a macrophage cell-line resulted in decreased leve
127                            Overexpression of NNT is sufficient to stimulate glutamine oxidation and r
128                      The forward reaction of NNT, a nuclear-encoded mitochondrial inner membrane prot
129                              Resequencing of NNT in additional LVNC families identified a second like
130          Our findings underscore the role of NNT in regulating central carbon metabolism via redox ba
131 authors expressed their findings in terms of NNT or ARR.
132                                  The overall NNT per year for the cohort was 62 (95% CI 44-147).
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
136                                The predicted NNT for the guidelines would be 25.
137 d a very low event rate and a high projected NNT.
138  reporting methods (relative risk reduction, NNT, and ARR).
139 ed through pyruvate carboxylase and rendered NNT knockdown cells more sensitive to glucose deprivatio
140 0.39), and 0.55 (0.43-0.71), with respective NNTs of 4.1, 6.7, and 5.3.
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
143                                We found that NNT mRNA is enriched in immune system-related tissues an
144                     Our results suggest that NNT may have a role in ROS detoxification in human adren
145 udy, we demonstrated for the first time that NNT has a significant effect in the modulation of the im
146                                          The NNT to prevent return to any drinking for acamprosate wa
147                                          The NNT to prevent return to heavy drinking was 12 (95% CI,
148                                          The NNT was 14 (95% CI 8-50), suggesting that approximately
149 performance of the entropy technique and the NNT were independent of scale, that of Moran's IPOP was
150           For partial (>/=75%) clearance the NNT was 1.8 (1.7-2.0).
151  health investment in PrEP by decreasing the NNT.
152              For cardiovascular disease, the NNT was 124, 54, and 19.
153  mortality difference continues to grow, the NNT to save a life with PSA screening will decrease.
154 jointly raise the PIA, but reductions to the NNT were associated with better adherence only.
155  for the first three cutoff levels using the NNT.
156                       A murine equivalent to NNT-1/BSF-3 also was identified, which shows 96% homolog
157 tes highly expressed genes are biased toward NNT instead of NNC.
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
165 .33-0.77; P = 0.001; number needed to treat (NNT) = 21; I = 75%].
166 alculated the 5-year number needed to treat (NNT) after stratification based on the CAC score.
167                  The number needed to treat (NNT) analysis indicated that 562 (95% CI 366-1,210) indu
168 cit reporting of the number needed to treat (NNT) and the absolute risk reduction (ARR) in RCTs.
169                  The number needed to treat (NNT) at higher-volume providers to avoid a death was min
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
172              We used number needed to treat (NNT) for 50% pain relief as a primary measure and assess
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
178                  The number needed to treat (NNT) to benefit was 41 women/babies to prevent 1 baby fr
179 sed to determine the number needed to treat (NNT) to prevent 1 ASCVD event over 5 years for each pati
180 F]) and for whom the number needed to treat (NNT) to prevent infection is lowest.
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
184                  The number needed to treat (NNT) was 19 for OFC and nine for each other drug.
185                  The number needed to treat (NNT) was calculated by taking the inverse of the pooled
186                  The number needed to treat (NNT) with FB-CBT vs FB-RT was estimated as 3.2 (95% CI,
187                  The number needed to treat (NNT) with restrictive strategies to prevent serious infe
188 effects model, with numbers-needed-to-treat (NNT) calculations where appropriate.
189            Adjusted numbers needed to treat (NNTs; 95% confidence interval) to avoid composite primar
190 0.43-0.91, estimated number needed to treat [NNT 193) as was delayed prescription of antibiotics (0.5
191 70% CBT vs. 37% EDU; number needed to treat [NNT ], 3.1).
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
194 CI 1.1-3.7], p=0.03; number needed to treat [NNT] 6.6 [95% CI 3.5-81.8]).
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
198 ; 95% CI, 1.06-1.68; number needed to treat [NNT], 10; 95% CI, 5-72).
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
200 ; 95% CI, 0.81-0.98; number needed to treat [NNT], 11; 95% CI, 6-54).
201 ol difference, 6.5%; number needed to treat [NNT], 15), but there was no significant reduction among
202  1.2-12.5]; P = .01; number needed to treat [NNT], 2.86).
203 , 0.65-0.83; P < .001; number need to treat [NNT], 241; 95% CI, 173-397).
204 1.16-1.95; P = .002; number needed to treat [NNT], 3.6) suggested the efficacy of CGT, and the additi
205 ; 95% CI, 0.48-0.72; number needed to treat [NNT], 6; 95% CI, 3-9).
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
208  A total of 5 patients needed to be treated (NNT-value) to prevent 1 IAP.
209 95% CI 0.53 to 0.87, 3,988 babies, 4 trials, NNT to benefit 42).
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-
212 dL, the RR was 0.82 (95% CI, 0.70-0.97) with NNT of 20 (95% CI, 12-133).
213                     Normal mice treated with NNT-1/BSF-3 also produce high amounts of Ag-specific IgE
214 -density LDL-C by 20% would provide a 5-year NNT </=50 for very high-risk patients with LDL-C >/=130
215                         The estimated 5-year NNT to prevent 1 CVD event ranged from 81-130 for patien
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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