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1 SMR at 10 years was higher until age 75 year, predominat
2 SMR can increase or decrease in response to food availab
3 SMR devices are unique in their ability to provide mass-
4 SMR due to cancer was 0.89 (95% CI 0.83 to 0.97).
5 SMR facilities are often confidential.
6 SMR facilities by compiling and matching the facility-re
7 SMR for cardiovascular disease was significant only in P
8 SMR increased when individuals were switched to a high f
9 SMR was 9.4 at 5 years and 5.4 at 10 years.
10 SMR was inversely related to baseline FVC% and increased
11 SMRs and EARs differed substantially by cause of death a
12 SMRs demonstrate spatial clustering of alterations in mo
13 SMRs due to cardiovascular diseases, suicide, infection
14 SMRs for cancer and liver disease (recurrent or transpla
15 SMRs ranged from 3.1 (95% CI, 2.1-4.3) for trauma to 8.7
16 SMRs reveal recurrent alterations across a spectrum of c
17 SMRs were broadly similar in different ethnic groups wit
18 SMRs were extracted.
19 SMRs were increased for cardiovascular disease (2.39; 95
20 SMRs were stratified for sex, age, and calendar period.
21 ath were those for heart disease (EAR, 15.1; SMR, 2.1), infections (EAR, 10.6; SMR, 3.9), interstitia
23 ears in fast vs slow privatised towns: 1.13, SMR 0.83, 95% CI 0.77-0.88 vs 0.73, 0.69-0.77, respectiv
26 tly increased in subjects living after 1965 (SMR, 1.27; 95% CI, 1.04-1.53; P=0.009) and aged >=60 yea
27 (expected deaths, 209; observed deaths, 242; SMR, 1.16; 95% CI, 1.02 to 1.31), but it was reduced amo
30 AEs) related to medications/drugs (EAR, 7.4; SMR, 5.0) after advanced-stage cHL and heart disease (EA
31 EAR, 15.1; SMR, 2.1), infections (EAR, 10.6; SMR, 3.9), interstitial lung disease (ILD; EAR, 9.7; SMR
32 anced-stage cHL and heart disease (EAR, 6.6; SMR, 1.7), ILD (EAR, 3.7; SMR, 13.1), and infections (EA
33 disease (EAR, 6.6; SMR, 1.7), ILD (EAR, 3.7; SMR, 13.1), and infections (EAR, 3.1; SMR, 2.2) after ea
34 ), interstitial lung disease (ILD; EAR, 9.7; SMR, 22.1), and adverse events (AEs) related to medicati
35 ity, we solved X-ray crystal structures of a SMR transporter Gdx-Clo in complex with substrates to a
41 were expected and 383 were observed, for an SMR of 0.96 (95% confidence interval [CI], 0.87 to 1.06)
42 lore this proposition, we are using Hsmr, an SMR from Halobacter salinarum that dimerizes to extrude
43 gle conservative mutation introduced into an SMR dimer is sufficient to change the resting conformati
46 rst-cousin (SMR, 1.85; 95% CI, 1.70-2.00 and SMR, 1.50; 95% CI, 1.29-1.73, respectively) relatives of
47 ond-degree (SMR, 4.31; 95% CI, 3.98-4.65 and SMR, 2.70; 95% CI, 2.30-3.14, respectively) and first-co
49 ter high-quality colonoscopy did the SIR and SMR for 10.1 to 17.4 years of follow-up not differ compa
53 .5 (95% CI, 30.2 to 46.0), respectively, and SMRs of 2,301 (95% CI, 1,652 to 3,122) and 30.2 (95% CI,
55 y correlated with extent of lung fibrosis as SMR increased from 2.2 with no fibrosis to 8.0 with grea
60 In 26 of 36 studies reporting LV function by SMR grade, increasing SMR severity was associated with w
61 al understanding of substrate selectivity by SMR transporters is needed to identify the types of sele
63 10 000 person-years) and gallbladder cancer (SMR, 3.82 [95% CI, 3.31-4.39]; mortality, 341 per 10 000
64 icipants who did not have surgery, all-cause SMR was 2.15 (95% CI, 2.11-2.20), which remained stable
68 ophrenia were more than 3.5 times (all-cause SMR, 3.7; 95% CI, 3.7-3.7) as likely to die in the follo
69 s shelter during the study period (all-cause SMR: 1.35, 95% confidence interval (CI): 1.14, 1.59; dru
70 than the general population for all causes (SMR 5.7, 95% CI 5.5-5.8), particularly non-AIDS infectio
71 d CVD mortality occurred after chemotherapy (SMR, 1.36; 95% CI, 1.03 to 1.78; n=54) but not surgery (
72 rgan transplantation was higher in children (SMR, 84.61 [95% CI, 52.00-128.40]) and lower in patients
73 4-18.8), and primary sclerosing cholangitis (SMR 11.0-4.2), and deterioration in alcoholic liver dise
75 , 2.30-3.14, respectively) and first-cousin (SMR, 1.85; 95% CI, 1.70-2.00 and SMR, 1.50; 95% CI, 1.29
78 also found to be elevated in second-degree (SMR, 4.31; 95% CI, 3.98-4.65 and SMR, 2.70; 95% CI, 2.30
80 ricted to the first year after TC diagnosis (SMR, 5.31; AER, 13.90; n=11) and included cerebrovascula
83 n=11) and included cerebrovascular disease (SMR, 21.72; AER, 7.43; n=5) and heart disease (SMR, 3.45
85 infections (SMR 22-693) and kidney disease (SMR 13-45) across all indications, and from suicide in H
90 s using a shuttle-box, and then measured for SMR and AS at 10 degrees C, estimated by rates of oxygen
93 ree of SMR compared with patients not having SMR (21 studies, 21081 patients; RR, 1.96; 95% CI, 1.67-
94 e 23.1-9.2), hepatocellular carcinoma (HCC) (SMR 38.4-18.8), and primary sclerosing cholangitis (SMR
95 1985-1999 to 2000-2010 in hepatitis C (HCV) (SMR change 23.1-9.2), hepatocellular carcinoma (HCC) (SM
97 e processes and transplant expertise at high-SMR centers may improve short-term and overall survival
98 mone and corticosterone content, and highest SMR, and these trait values are least affected by pond d
102 ociated with 73% increased odds of improving SMR over time [odds ratio (OR) 1.73; 95% confidence inte
108 porting LV function by SMR grade, increasing SMR severity was associated with worse LV function.
109 There was no association between individual SMR, or the tendency to obtain oxygen from air when in i
110 levated premature mortality from infections (SMR 22-693) and kidney disease (SMR 13-45) across all in
111 interval: 0.55, 2.51; 8 deaths) and kidney (SMR = 1.44; 95% confidence interval: 0.69, 2.65; 10 deat
113 al: 0.69, 2.65; 10 deaths) and for leukemia (SMR = 1.48; 95% confidence interval: 0.77, 2.59; 12 deat
114 as increased risks for cancer of the liver (SMR = 1.27; 95% confidence interval: 0.55, 2.51; 8 death
115 olescent and young adult survivors had lower SMRs for death from health-related causes (ie, condition
117 ing for gains in fat-free mass and fat mass, SMR increased by 43 +/- 123 kcal/d more than expected (P
118 sed significantly in the total group of men (SMR, 1.27; 95% CI, 1.03-1.56) and in women 60 to 69 year
119 rved an excess of death due to mesothelioma (SMR = 2.24, 95% confidence interval (CI): 1.39, 3.42); n
120 SIR, 0.16 [CI, 0.13 to 0.20]) and mortality (SMR, 0.10 [CI, 0.06 to 0.14]) than low-quality examinati
121 ality ratios (SMRs) for all-cause mortality (SMR 1.14, 95% CI 0.65-1.85; p=0.67) or cancer-specific m
122 ng analysis showed overall excess mortality (SMR, 1.26; 95% CI, 1.07-1.48; P=0.003), driven by subjec
125 estimates for a 45 megawatts-electric (MWe) SMR range from $4,000 to $16,300/kWe and from $3,200 to
127 ity racial differences in the computation of SMR helps to clarify disparities in quality of health ca
128 y increased in patients having any degree of SMR compared with patients not having SMR (21 studies, 2
130 ary to quantify the environmental impacts of SMR hydrogen production alongside the use-phase of FCEVs
131 und considerable overlap with the results of SMR analyses performed with expression QTL (eQTL) data.
133 e requirements, high precision, and speed of SMR measurements, the method may become a valuable new t
136 its correlation with outcomes, mixed data on SMR and primary mitral regurgitation, studies not clearl
137 te publication data, studies lacking data on SMR grade and its correlation with outcomes, mixed data
139 esults, our work suggests that SIM and other SMRs likely have a multivalent interaction with CYC/CDK
143 n women with NF1 age < 40 years; the overall SMR for breast cancer was 5.20 (95% CI, 2.38 to 9.88).
145 l similar to that of the general population (SMR 0.95, 95% CI 0.58-1.55) compared with those who were
147 o address this issue, we studied a maize PPR-SMR protein denoted PPR53 (GRMZM2G438524), which is orth
148 visit, those who had a lower-than-predicted SMR (basal EE) retained more of the fat gained during OF
149 ps, the small multidrug resistance proteins (SMRs), consists of proteins of about 110 residues that n
150 summary-data-based Mendelian randomization (SMR), a method developed to identify variants pleiotropi
151 ments for 8 wk, and sleeping metabolic rate (SMR) and 24-h sedentary energy expenditure (24h-EE) were
152 ch feeding history, standard metabolic rate (SMR) and aerobic scope (AS), interact to affect temperat
153 estimate individual standard metabolic rate (SMR) and the tendency to utilize aerial oxygen when alon
154 Flexibility in standard metabolic rate (SMR) may be particularly important since SMR reflects th
155 morphosis, increase standard metabolic rate (SMR), and elevate whole-body content of thyroid hormone
157 age 15 years (standardized mortality ratio (SMR) = 2.00, 95% confidence interval (CI): 1.09, 3.35),
158 atio (SIR) and standardized mortality ratio (SMR) compared with those expected in the general populat
159 calculated the standardized mortality ratio (SMR) for COVID-19 comparing HIV positive vs. negative ad
161 years, and the standardized mortality ratio (SMR) of fatal heart disease is 2.24 (95% CI: 2.23-2.25).
162 years, and the standardized mortality ratio (SMR) of fatal stroke was 2.17 (95% CI, 2.15, 2.19).
164 timates of the standardised mortality ratio (SMR) or hazard ratios associated with type 1 diabetes, e
165 A center-level standardized mortality ratio (SMR) was constructed (ratio of observed to expected deat
166 rtality rates, standardised mortality ratio (SMR), and hazard ratios (HR) for risk factors were estim
167 e ratio (SIR), standardized mortality ratio (SMR), or data on expected and observed cases of melanoma
171 eater for men (standardized mortality ratio [SMR], 1.32 [95% CI, 1.18-1.48]) than for women (SMR, 1.1
172 dertaken, and standardised morbidity ratios (SMR) calculated, assessing morbidity prevalence relative
173 We estimated standardized mortality ratios (SMR) and used competing risks models to identify risk fa
174 nd calculated standardized mortality ratios (SMR) for kidney transplant centers over five distinct er
175 by analyzing standardized mortality ratios (SMR) in multigenerational pedigrees and in close relativ
178 Comparative standardized mortality ratios (SMRs) and causes of death were obtained from the Office
181 dised and sex-standardised mortality ratios (SMRs) for all-cause mortality (SMR 1.14, 95% CI 0.65-1.8
182 We calculated standardised mortality ratios (SMRs) for all-cause, suicide-specific, and cancer-specif
184 s (CMRs), and standardised mortality ratios (SMRs) in MS, and estimated the rate of change of CMR and
185 , age-and-sex-standardised mortality ratios (SMRs) in people with severe mental illness were increase
186 os (SIRs) and standardized mortality ratios (SMRs) of CRC after high- and low-quality single negative
189 We calculated standardised mortality ratios (SMRs) to compare the mortality in the study populations
191 andardized incidence-based mortality ratios (SMRs) using rates for the Norwegian population at large
193 al status and standardized mortality ratios (SMRs) were estimated at study end (2018) in the 630 inci
197 record data, standardized mortality ratios (SMRs), relative SMRs (rSMRs), and proportional mortality
204 ey cancer (12.5); for transplant recipients, SMRs were highest for non-Hodgkin lymphoma (10.7), kidne
207 ic cracker (FCC) and steam methane reformer (SMR) units, and alternative hydrogen production technolo
208 ogen production via steam methane reforming (SMR) is energy intensive, coproduces carbon dioxide, and
214 ence interval (CI): 1.14, 1.59; drug-related SMR: 4.60, 95% CI: 3.17, 6.46; HIV-related SMR: 1.54, 95
215 d SMR: 4.60, 95% CI: 3.17, 6.46; HIV-related SMR: 1.54, 95% CI: 1.03, 2.21); all-cause and HIV-relate
216 vors had lower non-recurrent, health-related SMRs and relative risks of developing grade 3-5 chronic
217 % CI: 1.03, 2.21); all-cause and HIV-related SMRs in other patterns were not statistically significan
218 arbor a carboxy-terminal small-MutS-related (SMR) domain, but the functions of the SMR appendage are
220 andardized mortality ratios (SMRs), relative SMRs (rSMRs), and proportional mortality ratios were cal
222 , and used generalized spatial mark-resight (SMR) models to estimate puma population density across 1
223 porters from the small multidrug resistance (SMR) family drive the spread of multidrug resistance cas
225 e members of the small multidrug resistance (SMR) family that are composed of four transmembrane (TM)
226 , we use a suspended microchannel resonator (SMR) to measure single-cell density, volume, and passage
231 ostructured morphology completely over 10 SE-SMR cycles due to its intrinsic lack of a support compon
233 ts with HF with moderate-to-severe or severe SMR were randomized to TMVr with the MitraClip plus guid
235 members of the SIAMESE/SIAMESE-RELATED (SIM/SMR) class of cyclin-dependent kinase inhibitors were di
236 cific and strong activation of the three SIM/SMR genes in the meristems upon DNA stress, whereas over
238 te (SMR) may be particularly important since SMR reflects the minimal energetic cost of living and is
240 se variance weighting to obtain sex-specific SMRs and their pooled ratio (women to men) for all-cause
247 herapy) than did childhood cancer survivors (SMR 4.8 [95% CI 4.4-5.1] vs 6.8 [6.2-7.4]), which was pr
248 st meta-analysis to date to demonstrate that SMR, even when mild, correlates with adverse outcomes in
258 rvivors (median age 42 years, IQR 34-50) the SMR compared to the general population for all-cause mor
259 ctured linker is likely conserved across the SMR family to play an active role in mediating the confo
260 ath, using Kaplan-Meier methodology, and the SMR based on mortality data from the Social Security Dea
261 this period the MDA8 reached 83 ppbv and the SMR suggests a wildfire contribution of 19 ppbv to the M
265 ut is known in multidrug transporters of the SMR family, and is suggestive of an evolutionary anteced
267 -dependent transcriptional activation of the SMR genes was confirmed by different ROS-inducing condit
270 arried out a structure-function study on the SMR protein EmrE using solid-state NMR spectroscopy in l
274 onfidence interval: 1.27-1.53); however, the SMRs for ARMD, glaucoma, and cataract were not statistic
276 owth; those individuals that increased their SMR more in response to elevated food levels grew fastes
277 hybrid, large spin-Hall magne toresistance (SMR) along with a sizable conventional anisotropic magne
280 r more preceding years of increasing volume (SMR change -0.008; 95% CI -0.015, -0.002; P = 0.01).
283 95% CI, 1.47-2.18; P < .001, I2 = 85%); when SMR was qualitatively graded, the incidence of all-cause
287 as significantly higher in the patients with SMR (17 studies, 26359 patients; risk ratio [RR],1.79; 9
288 ar adjudicated outcomes of all patients with SMR undergoing the MitraClip procedure in the EVEREST II
290 efer temperatures that vary predictably with SMR and activity level, which are both plastic in respon
292 roke deaths than expected, especially women (SMR in females: 19.7 [95% confidence interval, 12.9-30.3
293 roke deaths than expected, especially women (SMR in females:19.7 [95%CI:12.9-30.3] and males: 9.1 [95
295 ed with 2-fold increase in odds of worsening SMR over time (OR 2.14; 95% CI 1.07-4.26, P = 0.03).
296 imilar for those diagnosed aged 15-44 years (SMR = 1.06, 95% CI: 0.86-1.28), and lower for those diag
298 ) and lower in patients older than 60 years (SMR, 1.88 [95% CI, 1.62-2.18]) but remained elevated com
300 72]; incidence, 336 per 10 000 person-years; SMR, 4.56 [95% CI, 4.11-5.06]; mortality, 268 per 10 000