ライフサイエンスコーパス: male

1 nd Freedom from major adverse limb events (F-MALE).

2 in 533 households (median age 41 years; 43% male).

3 ipants (each group included both females and males).

4 g and assembling each type of female and the male.

5 uded, mean age was 60.9 years and 68.9% were male.

6 Approximately 73% of the patients were male.

7 ears (range, 39-92), and 30 of 50 (60%) were male.

8 V-2 infection than adolescents or adults and males.

9 way remodelling at a much earlier stage than males.

10 istant (p = 0.007) than those transmitted to males.

11 dial tip, and females had more dopamine than males.

12 ng fruitless reveals this latent behavior in males.

13 nterquartile range, 10-32); 423 (52.9%) were males.

14 taneously monitored for 30 min in 22 healthy males.

15 es and either AR is sufficient for attacking males.

16 cose intolerance in middle-aged females than males.

17 rger increase in CRFr1 and CRFr2 relative to males.

18 increase in GSC division frequency in mated males.

19 ed with FT(4) and FT(3) for both females and males.

20 und and enduring effects of MAS on memory in males.

21 ificantly more curved in females compared to males.

22 reporter genes in adult females, but not in males.

23 that HIV progress more rapid in females than males.

24 zygous Q175 mice, compared to age-matched WT males.

25 ed brain derived neurotrophic factor mRNA in males.

26 treated diabetic patients (median age: 68.6; males: 113 [58.2%]); 163 (84%) had acute kidney injury,

27 onfidence interval {CI} = 3.01 to 8.46]; for males, 16.5% versus 9.4% [OR = 1.91; 95% CI = 1.20 to 3.

28 rs in the kyphosis group and 36 subjects (11 males, 25 females) with a mean age of 81.00 +/- 5.5 year

29 In 11 healthy males (28 +/- 7 years; 23 +/- 2 kg m(-2) ), FMD (Duplex

30 There were 42 patients (14 males, 28 females) with a mean age of 81.10 +/- 6.3 year

31 One hundred twenty-three patients (85 male/38 female; mean age, 49.5 +/- 13.1 y old) were biop

32 ients (median age 69 years, (IQR 25) and 62% male), 381 (62%) had been discharged alive, 178 (29%) di

33 ars (range: 8-18 years); 46 of 62 (88%) were males; 57 of 62 cases (92%) had bilateral disease; 53 of

34 with mitral valve regurgitation (group 2; 32 males; 59+/-12 years).

35 tent/long-lasting persistent AF (group 1; 59 males; 60+/-11 years; 91 mitral disease-related AF, 30 n

36 Most participants were male (645 [84%] of 766) and white (560 [73%]), with a me

37 Of 98 included patients (males: 67%; mean +/- SD age: 59 +/- 16; and mean Simplif

38 60.6 +/- 18.7 yr; p < 0.0001), predominantly male (73.1% vs 53.9%; p < 0.0001), and more frequently t

39 The majority were male (73.4%) and had a mean age of 43.7 years.

40 s (median age of 58 years [range 38-73], 46% male, 95% white) were analysed in the UK Biobank; this l

41 omplications were more likely to be younger, male, African American, with a higher American Society o

42 sex dependent (95% adaptation in females and males after 114.9 +/- 81.1 vs 65.4 +/- 64.3 seconds, res

43 findings place the PA as a key node in both male aggression and reproduction circuits.

44 le exposure induces a persistent increase in male aggressiveness, an effect abrogated by interruption

45 Remarkably, fruitless males also gain strong attraction to a live human host,

46 those females previously housed with sterile males also showed enhanced late-life offspring productio

47 Methods: Six patients (5 male and 1 female; age range, 10-27 y) with CDCS were as

48 g cystometry and pressure flow studies in 16 male and 22 female rhesus macaques.

49 Twenty-four patients (30.4%) were male and 29 (36.7%) were splenectomized.

50 AO incidence was 4.4 (95% CI: 3.5-5.3) male and 3.8 (3.1-4.6) female cases/1,000/year.

51 s were included in this analysis, 3973 (53%) male and 3582 (47%) female patients.

52 These patients were 61% male and 39% female, 89% White, 8% Black, and 3% other/r

53 A total of 7 patients (3 male and 4 female) were identified to have a clinically

54 participants who switched to INSTIs were 81% male and 50% nonwhite with a median age at switch of 50

55 icipants were a mean age of 43.80 years, 47% male and 53% female, 38.5% with a college degree, and 24

56 The mean age was 35.5 years, 79% were male and 82% were white.

57 Through single-cell recordings in behaving male and female C57BL/6 mice, we show here that an expli

58 esicle-based axonal transport of proteins in male and female flies (Drosophila melanogaster).

59 ed per experiment, with separate testing for male and female flies.

60 kage of factors with antagonistic effects on male and female function.

61 In conclusion, male and female human islets convert T into DHT and E2 v

62 coustics and electroencephalography (EEG) in male and female human listeners to examine potential eff

63 underlying this transformation, we presented male and female human listeners with tones embedded with

64 mporal expectations on brain and behavior in male and female human volunteers, using two matched visu

65 stream analyses were conducted separately in male and female individuals to identify genes associated

66 ummary estimates for >9 million variants for male and female individuals.

67 cal theta-gamma coupling was reduced in both male and female juvenile DS mice and persisted only if s

68 reproductive output and survival in dominant male and female meerkats, Suricata suricatta.

69 ild-type, D1-Cre, A2A-Cre, or vGluT2-Cre:Ai9 male and female mice in a cocaine conditioned place pref

70 Both male and female mice were used in the present study.

71 y and function under normal conditions (both male and female mice).

72 endothelial growth factor-A (VEGF-A) in both male and female mice, as well as increased VEGFR1 and in

73 g, Mogat1, Cd36, Acaab1, Fabp2, and Gdf15 in male and female mice.

74 encies in upright spinal cords prepared from male and female neonatal mice.

75 t and right amygdala of postnatal days 22-28 male and female offspring from normal bedding or LB moth

76 Male and female offspring were tested using a comprehens

77 mechanism of RLN3/RXFP3 signaling in PVN in male and female rats and characterized sex differences i

78 , a brain region linked to motor control, as male and female rats performed a novel variant of the st

79 Male and female rats were trained in the risky decision-

80 these markers to assess dispersal regimes in male and female T. longipes.

81 Further studies of male and female TDP-43(Q331K) knock-in mice may help to

82 nally, in our data set, for several regions, male and female volumetric measures were completely nono

83 s a predictor of worse primary patency and F-MALE and therefore close and long follow-up is advisable

84 2 months of spaceflight in 11 astronauts (10 males and 1 female, 46 +/- 7 years old at launch).

85 20 PBS-injected mice at three timepoints (10 males and 10 females per group).

86 Whiskers were collected from 20 adult males and 20 adult females and stable isotope ratios wer

87 s well as in 55.3% (84/152) of countries for males and 47.8% (76/159) of countries for females where

88 IR >=1.30), Chinese, Malay, and Asian-Indian males and females aged 35-69 y.

89 at microglial microRNA expression differs in males and females and that loss of microRNAs leads to se

90 The study population included 579,946 males and females between 16 and 19.9 years of age.

91 In both D. jamesoni and D. polylepis, adult males and females were recorded together in September-Oc

92 and associated PAC1R genotype in a cohort of males and females with a primary diagnosis of generalize

93 ion (CMEPs) on biceps and triceps brachii in males and females with and without chronic cervical inco

94 Crosses between H2A.B KO males and females yield embryos with lower viability and

95 ANCE Differences in HIV pathogenesis between males and females, including immunity postinfection, hav

96 genesis during prenatal development, in both males and females.

97 ess in two experiments in a group of healthy males and measured brain activity with positron emission

98 R) and sex-specific density explained 52.8% (males) and 91.0% (females) of variance in adult F/alpha

99 hort was 60.6 (16.2) years, 103 (52.3%) were male, and 156 (82.1%) were black.

100 SDD, females tended to disperse farther than males, and distance was positively correlated with densi

101 ssociated with a TB diagnosis included being male (aOR 1.4; 95% CI: 1.03-2.0), residing in an urban s

102 Adolescent sexual minority males (ASMM) are among the highest risk groups for suici

103 The proportions of females and males at each academic rank (assistant 69.5% vs 41.8%; a

104 ose intravenous administration to female and male BALB/c mice (10 animal/sex/group) along with their

105 w that heavier angiosperm flowers tend to be male-biased and invest strongly in petals to promote pol

106 eptor (TLR) 7 and TLR8 reportedly results in male-biased litters by selectively disrupting the motili

107 were randomized (mean age = 62.8 years; 57% male; body-mass-index = 27.9).

108 om parental reports: both parents full-time, male-breadwinner, female-breadwinner, shared-part-time e

109 default mode (DMN) subsystems in adolescent males, but has no effect in females.

110 Ten weeks old male C57BL/6 mice (n = 9) underwent left anterior descen

111 We performed studies with male C57BL/6 mice that persistently replicate HBV (genot

112 or in established relationships, fathers or male caregivers aged 18 years or older were also eligibl

113 tiretroviral therapy (ART), and strengthened male circumcision services, and 15 received standard of

114 normoxic conditions, both healthy female and male diaphragms fatigue at a similar degree when matched

115 stly promoted USV(+) mounting, and converted male-directed attack to mounting with USVs.

116 Of the 1494 samples tested from first-time male donors, 9 (0.6%; 95% CI, 0.03% to 1.1%) had tenofov

117 m of IIS and links feeding to odr-10 only in males, due in part to the male-specific expression of da

118 ng the influence of dominant and subordinate males during normal social interactions and in a more co

119 Our results demonstrate that male elephants increased their daily mean speed and rang

120 We show that male elephants increased their energetic allocation into

121 Thus, adult C. elegans males employ a neuroendocrine feedback loop that integra

122 Males exhibited only late stage reductions in acylcarnit

123 years, 19/14 male/female PM carriers, 15/13 male/female controls).

124 amined in 61 children (age 8-12 years, 19/14 male/female PM carriers, 15/13 male/female controls).

125 ateral LT (n = 157; age +/- SD: 54 +/- 13 y, male:female = 91:66).

126 genesis, had no effect on spermatogenesis or male fertility under normal conditions.

127 erably more altered than the placenta with a male fetus in FOXA2 cKO dams.

128 singly mated in a fully reciprocal design to males from the same three genotypic backgrounds.

129 free testosterone on 461 outcomes in 161,268 males from the UK Biobank study.

130 als and plants, including important roles in male gamete physiology.

131 Despite being found diversely in male gametes (e.g., Plasmodium falciparum microgametocyt

132 nsities were frequently below 1 female and 1 male gametocyte/uL by qRT-PCR.

133 ults provide evidence that during Plasmodium male gametogony, this divergent cyclin/CDK pair fills th

134 40) is the main exocyst EXO70 isoform in the male gametophyte, governing the conventional secretory f

135 d extracellular cell-wall matrix surrounding male gametophytes and acts as a natural protector of pol

136 ctures evolved, which genes occur de novo in male gametophytes of angiosperms, and to which extent PT

137 4; 95% confidence interval [CI], 1.01-1.07), male gender (HR, 2.48; 95% CI, 1.21-5.05), history of pr

138 ultivariate stepwise analysis including age, male gender, paroxysmal atrial fibrillation, basal QTc v

139 Male germ cells are sensitive to heat stress and testes

140 Golgi glycoprotein MGAT4D as a protector of male germ cells from heat stress.

141 ptical and electron microscopy of HIPK4-null male germ cells reveals defects in the filamentous actin

142 echanism centers on the vulnerability of the male germline to oxidative stress and the induction of o

143 tion of NHR-23/NR1F1 within hermaphrodite or male germlines causes sterility due to an absence of fun

144 Male-to-male, male-to-female and female-to-male grooming strength decreased after simulated intrusi

145 Moreover, the trajectories of male groups contained diagnoses belonging to various cat

146 Compared with the trajectories of male groups, those of female groups included relatively

147 -19-related death was associated with: being male (hazard ratio (HR) 1.59 (95% confidence interval 1.

148 ology and the deficits stemming from them in male heterozygous Q175 mice, compared to age-matched WT

149 assess relationships between post-procedure MALE hospitalization and subsequent events.

150 nt covariate adjusted models, post-procedure MALE hospitalization was associated with greater risk of

151 demonstrate this double dissociation in 129 male humans using eye-tracking, pupillometry and functio

152 Male immigration and female residency were favoured.

153 were enrolled (mean age 42 +/- 17 years, 97 males) in this multicenter prospective registry.

154 hile 1,5-anhydroglucitol levels decreased in males indicating susceptibility to insulin resistance.

155 inhibition (CBI) in young healthy female and male individuals.

156 In well-fed males, insulin-like (insulin/IGF-1 signaling [IIS]) and

157 Male intestine showed significantly higher levels of UPR

158 A majority of SIV adults were male (Iraqi 54.0%, Afghan 58.6%) and aged 18-44 (Iraqi 8

159 oproteins decreased and one increased versus male islets.

160 Here, we report that males lacking piRNAs from a conserved mouse pachytene pi

161 ng rates of CA3 neurons from young and aged, male, Long-Evans rats along the CA3 transverse axis.

162 In 678 post-pubertal adolescents (52% males, M(SD) age = 16.8 (0.2) years), height, weight, wa

163 mporal structure to humans of either sex and male macaque monkeys.

164 functional MRI adaptation paradigm in awake male macaques.

165 Male-to-male, male-to-female and female-to-male grooming strengt

166 imary factor affecting the trade-off between male mating and parenting effort suggests different poss

167 s: The cohort included 24 patients (20 [83%] male, mean age for all patients at death, 75.4 +/- 10.0

168 m 354 patients (mean age 55 +/- 14 yr, 28.5% male, median admission Glasgow Coma Scale 14 [10-15]) we

169 Here, we report the first evidence of male-mediated maturation in a wild primate, the gelada (

170 essary for recombination and synapsis during male meiosis at high ambient temperature.

171 nt of MSCI permits the timely progression of male meiosis.

172 ICH induction in male mice caused profound HN loss in the affected hemisp

173 Male mice lacking sperm-specific calcineurin (PP2B), a c

174 Macrophages from male mice maintained migratory capacity when cultured wi

175 beta4 knock-out (KO) male mice show increased novelty-induced locomotor activ

176 inding is corroborated in stress-susceptible male mice that have undergone chronic social defeat stre

177 SCN rhythmicity in these temporally chimeric male mice thus enabled us to determine the contribution

178 ve way, here we exposed 6-month-old C57BL/6J male mice to whole-body space radiation and subsequently

179 We have previously shown that in male mice transient blockade of NMDA receptors (NMDARs)

180 Cdkl5 knockout male mice treated with isoform 1 via intrajugular inject

181 these measures were observed when adolescent male mice were exposed to concomitant ketamine and socia

182 Non-diabetic and Akita/+ male mice with different duration of diabetes were subje

183 nje cells in cerebellar slices prepared from male mice ~48 h after they learned a delay eye-blink con

184 Here we show that male mice, pigs, goats, and cattle harboring knockout al

185 tight junction protein claudin-5 (cldn5) in male mice, promoting passage of circulating proinflammat

186 s along the dorsal CA1-DG axis from sleeping male mice, we detected and classified two types of LFP e

187 Using male mice, we tested whether Fragile X Mental Retardatio

188 osterior parietal cortex (PPC) in adolescent male mice.

189 ereas these drastic changes did not occur in male mice.

190 sociated with thinner cortical bone in adult male mice.

191 of monoaminergic axons in female, but not in male mice.

192 spectively, with no effect on sexually naive male mice.

193 and 3) manipulation increases aggression in male mice.

194 velopmental conditions (e.g., autism) affect males more frequently than females.

195 ld-type males never display, suggesting that male mosquitoes possess the central or peripheral neural

196 to repeated tones pyramidal (Pyr) neurons in male mouse auditory cortex (A1) exhibit facilitating and

197 rmaphrodites; rather, tra-1 also acts in the male nervous system to transiently suppress a sexual dim

198 In male neurons, the ED peptide enhanced neuritogenesis in

199 a live human host, a behavior that wild-type males never display, suggesting that male mosquitoes pos

200 higher mitochondrial respiration compared to male newborns.

201 Radiosensitive male NSCLC cell lines demonstrated a dose-dependent indu

202 on, which was not observed in radioresistant male NSCLC cell lines.

203 Males of both diurnal and nocturnal mosquito species sho

204 onogenic blow fly (females produce female or male offspring, exclusively) by separately sequencing an

205 creased dorsal hippocampus prostaglandins in males only.

206 id in the cerebellar interpositus nucleus in males only; (2) decreased 2-arachidonoyl glycerol in fem

207 rmacological treatment to prevent relapse in male opioid users.

208 atients had higher odds of death compared to males (OR = 1.26, 95% CI 1.21-1.30).

209 ales, OR = 1.53 [95% CI = 1.09 to 2.14]; for males, OR = 1.42 [95% CI = 1.02 to 1.99]).

210 = 0.029), with a non-significant increase in males (p = 0.092).

211 Thirty-one healthy male participants performed a restless four-armed bandit

212 DKI data were examined for 16 male participants with a diagnosis of ASD and IQ>80 and

213 Among 1,737 female and 1,563 male participants, the overall prevalence of M. genitali

214 l load (gVL) and sexual transmission risk to male partners.

215 ed likelihood of HSV-2 in women and HSV-2 in male partners.

216 e, we report pathogenic variants in VMA21 in male patients with abnormal protein glycosylation that r

217 Some patients, particularly older male patients, may be good candidates for OSA evaluation

218 y mediators in their MEE compared to that of male patients, which were unrelated to microbiota compos

219 0A), resulting in intellectual disability in male patients.

220 itive/inflexible behaviors, respectively, in male PC-Tsc1 mutant mice.

221 men's UBL intervention significantly reduced male perpetration of past-year sexual IPV (AOR: 0.73; 95

222 efish family (syngnathids) that have evolved male pregnancy across a gradient from external oviparity

223 A 71-year-old, previously healthy male presented 6 h post apparently uncomplicated colonos

224 1 years (range 18-71 years) with a female to male ratio of 1.8:1.

225 d 49 PH-NF1 cases, characterized by a female/male ratio of 3.9 and a median (minimum-maximum) age at

226 These data show that male rats exhibit less impulsive choice than females and

227 Long Evans male rats received a controlled cortical impact (CCI) ov

228 maging and cluster analysis, we show that in male rats SCI decreases opioid responsiveness in vitro w

229 Here, male rats were trained to exert effort for a high-value

230 alled the rostromedial tegmental nucleus) in male rats.

231 perinatal, prepubertal, and adult female and male rats.

232 modified, real-world TRAP in both female and male rats.

233 Again, this association was not seen with male recipients.

234 eviation]; range, 9-18 years; 27 of 48 [56%] male) referred for cardiac screening 1.5-T MRI between 2

235 esidents and surgical residents, compared to male residents and nonsurgical residents, respectively.

236 ons and corresponding testosterone-dependent male resilience to reduced sucrose preference after subc

237 diffusion-weighted MRI data before and after male rhesus macaque monkeys received extensive training

238 while recording cellular activity in PFC of male rhesus monkeys performing a delayed decision task r

239 ials show that single releases of gene-drive males robustly result in efficient population modificati

240 imited by its exclusive application to adult male rodents.

241 ed the experimentally-accessible locust ear (male, Schistocerca gregaria) to characterize a decrease

242 Male sex (hazard ratio [HR] 2.54, P = 0.02), diabetes (H

243 Male sex (hazard ratio, 1.89 [95% CI, 1.04-3.44]; P=0.04

244 Those associated with sICH were male sex (HR 2.68, 95% CI 1.06 to 6.83), history of hype

245 to testicular differentiation and female-to-male sex reversal in a manner that does not requireSry o

246 udy of veterans, we found increasing age and male sex to be significantly associated with increased r

247 osure prophylaxis (PrEP) use among cisgender male sex workers (MSWs), a high-risk subset of cisgender

248 Older age, male sex, and being black or African American (compared

249 ified several confounding factors, including male sex, NSAID coadministration, advanced age, and prio

250 ceptors and are activated by oxytocin during male sexual behavior.

251 mating and are necessary and sufficient for male sexual behaviors, while VMHvl-projecting PA(Esr1+)

252 The median lifetime number of male sexual partners was 17 (IQR: 6, 50) and 246 (19%) w

253 Here we show that only females and not males show a highly significant correlation between an i

254 This revealed that males showed statistically significant expansion of a re

255 The evolution of male signals and female preferences remains a central qu

256 Additional PB-projecting neurons regulated male sleep, suggesting several groups of PB-projecting n

257 efore, we tested this hypothesis in juvenile male songbirds using a comprehensive assessment of neuro

258 to odr-10 only in males, due in part to the male-specific expression of daf-7 in ASJ.

259 ntly lower in males than females, indicating males spent more time foraging south of the Polar Front

260 Adult, male Sprague-Dawley rats were exposed to nicotine (0.2 o

261 Here, 24 male Sprague-Dawley rats were randomly divided into four

262 lateral preoptic nucleus (VLPO) is lesioned (male Sprague-Dawley rats).

263 uropean ancestry, including 34 nonirradiated male survivors treated with 0 < CED < 4,000 mg/m(2) (P =

264 ED < 4,000 mg/m(2) (P = 3.1 x 10(-4)) and 24 male survivors treated with CED >=4,000 mg/m(2) and radi

265 odifications and RNA methylation in adult F1 male testes.

266 elta(13)C values were significantly lower in males than females, indicating males spent more time for

267 Primarily affecting males, the main manifestations of SRS include osteoporos

268 aviors were collected from six tapirs (three males, three females), from different breeding centers i

269 studies have cohorts that are predominately male, thus limiting knowledge of cerebral growth in fema

270 ut remains localized to the sciatic nerve in males (tier 3).

271 ian age of the patients was 30 years and the male to female ratio was 1.4:1.0.

272 line cells also eliminated the capability of males to increase the numbers of dividing GSCs in respon

273 Male-to-male, male-to-female and female-to-male grooming strength decr

274 nd untreated 299 patients (age, 31.3+/-16.0; male-to-female ratio, 144;155).

275 8;35) and 89 adults (age, 38.9+/-12.5 years; male-to-female ratio, 34;55) treated with Cidarcure((R))

276 cs under 15 yeas old (age, 10.8+/-2.6 years; male-to-female ratio, 68;35) and 89 adults (age, 38.9+/-

277 We found a 3:1 male-to-female ratio.

278 Male-to-male, male-to-female and female-to-male grooming

279 the behavioural response of 131 A. oculatus males towards relevant and controlled conspecific versus

280 of ASD and IQ>80 and 17 age- and IQ-matched male typically developing (TD) young adults 18-25 years

281 While greater male variability was found in morphological traits, fema

282 testosterone-dependent lower excitability in male versus female vHPC-NAc neurons and corresponding te

283 entially expressed in the proximal tubule of males versus females.

284 Here, we examine in male volunteers how sharpened visual processing is affec

285 t short (3.4 s) tVNS pulses in naive healthy male volunteers induced transient pupil dilation and att

286 Seventeen healthy male volunteers received [(11)C]CIMBI-36 PET scans befor

287 The mean age (% male) was 44.1 (45%) for patients with Fabry disease and

288 ccurring primarily in adolescent/young adult males, we used next-generation RNA sequencing to investi

289 non-response were least likely, while white males were most likely to report feeling very welcomed.

290 epartment, 181 subjects (mean age, 43.0; 44% male) were diagnosed with anaphylaxis.

291 ase) group, 21 (mean age, 14 years +/- 5; 11 male) were in the control group, and nine (mean age, 12

292 +/- standard deviation, 13 years +/- 5; nine male) were in the ferumoxytol-exposed (case) group, 21 (

293 up, and nine (mean age, 12 years +/- 6; four male) were in the subgroup.

294 ients with definite ARVC (40+/-16 years; 53% male) were included.

295 m acute hippocampal and cortical slices from male wild-type and amyloid precursor protein (APP) knock

296 A 37-year-old male with no relevant history presented to the Emergency

297 aternally inherited X chromosome variants in males with neurocognitive phenotypes continues to presen

298 e patients (63 +/- 11 years of age, 53% were male) with suspected CAD were assessed by stress CMR and

299 A total of 266 patients, 78.2% males, with a mean age of 60.8+/-11.3 years, were enroll

300 P RS was found in stage IV Appalachian white males within a subset of states.