ライフサイエンスコーパス: adult male

1 acting neurons in the mating circuits of the adult male.

2 promote a social bond with the group's lone adult male.

3 aticum or H. huttiense in an immunocompetent adult male.

4 ated from one thoracic CT image of a healthy adult male.

5 (0.5- to 3.2-fold) vitellogenin induction in adult males.

6 y lower in age-matched adult females than in adult males.

7 s highly prevalent, particularly among young adult males.

8 egulation of juvenile hormone (JH) levels in adult males.

9 ogenesis and ensure its prodigious output in adult males.

10 ion and food deprivation activates odr-10 in adult males [4-6].

11 Most of the dead were adult males (68%), but the highest case fatality (39%) w

12 We recorded behavioral data for 21 adult males across 9 social groups during the 2013 matin

13 commenced spermatogenesis earlier than young adult males (aged 1-3 years old), whilst juveniles that

14 ty-like behavior and activity levels in MSEW adult males, along with increased theta power and enhanc

15 To this end, we scanned 42 adult male amateur American football players and a contr

16 Captive adult male American kestrels (Falco sparverius) were fed

17 Adult male and female betaeIF4G1KO mice displayed glucos

18 ion, we selectively ablated these neurons in adult male and female C57BL/6 J mice undergoing a volunt

19 g a compressed air-driven shock tube system, adult male and female C57BL/6 mice were exposed to blast

20 Hence, we examined the MePD from adult male and female C57Bl/6(J) mice.

21 and microstructural changes in the spleen of adult male and female CD-1 mice exposed to 4 to 40,000 m

22 ses, Cyp26a1 was knocked out in juvenile and adult male and female Cyp26a1 floxed mice using standard

23 of histamine-responsive amygdala neurons in adult male and female Fos:CreER(T2);R26(Ai14) mice using

24 fMRI), and trait anxiety measures in healthy adult male and female humans.

25 exposure increased anxiety-like behaviors in adult male and female mice and decreased acoustic startl

26 We also exposed adult male and female mice to CUS for 12 days beginning

27 fects of cholinergic transmission in HMNs in adult male and female mice using patch-clamp recordings

28 that the estimated effective human doses for adult male and female mice were comparable to those of o

29 recording and two-photon calcium imaging in adult male and female mice, we show that direction-selec

30 iatal short-term plasticity, and learning in adult male and female mice.

31 lls (NSCs) in the brain subependymal zone of adult male and female mice.

32 alculate radiation doses using the reference adult male and female models and to estimate radiation d

33 Adult male and female mosquitoes consume sugar as floral

34 omy-guided single-cell RNA sequencing of the adult male and female mouse kidney with in situ expressi

35 differences in neutrophil phenotype between adult male and female neutrophils are hormonally driven

36 Adult male and female offspring (8 weeks old) were asses

37 Incision in adult male and female rats induced equivalent hyperalges

38 bal transcription in the whole hippocampi of adult male and female rats.

39 equent cognitive flexibility was examined in adult male and female rats.

40 Adult male and female Siberian hamsters were exposed to

41 netics and a combination of viral vectors in adult male and female Th-Cre rats to transduce selective

42 Additionally, adult male and female Zfpm1 mutants had reduced serotoni

43 In contrast, in perinatal and adult male and female Zfpm1 mutants, a lateral subpopula

44 antly over time, with a loss of 7.9% mass in adult males and 10.9% mass in adult females over 16 year

45 Whiskers were collected from 20 adult males and 20 adult females and stable isotope rati

46 In both D. jamesoni and D. polylepis, adult males and females were recorded together in Septem

47 parasite prevalence is not different between adult males and females, although Nematodes showed a sta

48 This variability was observed in both adult males and females; of 41 rats between 8 and 15 wee

49 om POMC neurons decreased Pomc expression in adult males and mildly increased their body weight and a

50 ked together at the same pace, with only two adult males and one juvenile accompanying them.

51 egions of the forebrain SBNN in juvenile and adult, male and female rats.

52 avioral and fMRI data from older and younger adults (male and female) performing two probabilistic le

53 estures and spoken words in 17 healthy human adults (male and female).

54 Twenty-nine young adults (males and females) were scanned while they incid

55 duals more likely to go to the forest (i.e., adult males) and with seroprevalences of up to 18% in so

56 sure to low-level LAN alters brain function, adult male, and female mice were housed in either light

57 ll and a similar non-significant trend among adult males, and (3) spatial partitioning by size among

58 As this hyperexcitability was only seen in adult males, and not in adult females or adolescent anim

59 females with cubs approximately subadults > adult males approximately yearlings > cubs-of-the-year a

60 graphic burden of TB among the population of adult males as a whole.

61 xicity of 15 compounds was evaluated against adult male bed bugs.

62 reared species, sterols were not detected in adult male beetles, and overall levels were generally lo

63 Greater adult male body mass in exclosures resulted from: (1) a

64 Histologic analysis of adult male brains identified a significant reduction in

65 Adult male but not female offspring of DOSS-treated dams

66 Adult male C57BL/6 mice received diffuse TBI by midline

67 Adult male C57BL/6 mice were randomly assigned to four d

68 consolidation of associative fear memory in adult male C57BL/6 mice.

69 HT22 neuronal cell line and adult male C57BL/6 mice.

70 tivity (c-Fos expression) in the amygdala in adult male C57BL/6 mice.

71 nd 3D electron microscopy, we demonstrate in adult male C57BL/6 wild-type mice marked differences bet

72 cortical activity induced by TMT exposure in adult male C57BL/6J mice and the influence of the stress

73 r, Plexxikon (PLX) 5622, was administered to adult male C57BL/6J mice at 1 month after controlled cor

74 Adult, male C57Bl/6J mice were subjected to bilateral co

75 Adult male, C57BL/6J mice were anesthetized and exposed

76 Adult male C57Black 6 mice, adult patients with septic s

77 brain on distinct features of birdsong using adult male canaries (Serinus canaria), which show extens

78 We investigated this question in adult male canaries (Serinus canaria), which show extens

79 Prostate cancer (CaP) is the most common adult male cancer in the developed world.

80 ters in repeated cystometrograms across five adult male cats.

81 we used bone marrow macrophages derived from adult male CCR3-proficient and CCR3-deficient mice to st

82 Adult male CD-1 mice received an intraperitoneal injecti

83 20/150) of locally acquired infections among adult males, characterized by distinct periodic Shigella

84 rous parameters, including the proportion of adult males circumcised, the frequency of condom use dur

85 Universal adult male circumcision alone resulted in a 21% incidenc

86 h differing combinations of male condom use, adult male circumcision, HIV testing, and early antiretr

87 st migration probabilities for juveniles and adult males coincided with years of relatively high calv

88 Finding adult male cotton rats were 9% heavier with mesocarnivor

89 DNH 155 is a well-preserved adult male cranium that shares with DNH 7 a suite of pri

90 Adult male Cynomolgus macaques (n = 6) were surgically i

91 BMPCs were isolated from adult male db/db type 2 diabetic mice and their healthy

92 gene amplicons from microbiomes harbored in adult males directly after emerging from pupae revealed

93 Dominant and small sub-adult males displayed year-round residency in/near river

94 In sexually and socially experienced adult males, divergent and characteristic neural ensembl

95 e males had a CY spigot on each PMS, whereas adult males either had a CY spigot or, more often, a non

96 s into the environment ensuring only sterile adult males emerge.

97 Additionally, Crkl heterozygous adult males exhibit cryptorchidism, lower testis weight,

98 e profound differences in gene expression in adult males exposed to injury and treatment compared to

99 nt of MC-deficient Kit (W-sh/W-sh) mice with adult male, female, or perinatally androgenized female M

100 Adult male/female rhesus monkeys self-administered metha

101 Adult male fish deprived of maternal rest present with a

102 Daily treatment of adult male fmr1 C57Bl6 knock-out mice with BPN14770 for

103 In the song control nucleus, HVC of adult male Gambel's white-crowned sparrows (Zonotrichia

104 al stem and progenitor cells (SSCs) generate adult male gametes.

105 The antennae of adult male German cockroaches detect a contact sex phero

106 While adult male gorillas have a defensible resource (i.e. fem

107 Twelve adult male guinea pigs were used in this experiment.

108 Neutrophils from young adult males had significantly increased mitochondrial me

109 We hypothesised that poor adult male health was partially attributable to aberrant

110 Here we report that brief exposure of adult male hippocampal slices to 1 nM E2 increases the p

111 ssions of the imprinted Dio3 and Igf2 in the adult male hippocampus, while metformin restored FAE-cau

112 ere made of mPFC pyramidal neurons (PN) from adult male HIV-1 transgenic (Tg) F344 rats (which expres

113 using a controlled cortical impact model in adult male IFN-beta-deficient (IFN-beta(-/-)) mice and a

114 ci 1 and 2) includes the skeleton of a young adult male in a bear nest, rearranged by postdecompositi

115 ducing millions of spermatozoa per day in an adult male in rodents and humans.

116 identify these mechanisms in a population of adult male incarcerated offenders.

117 Kin-based?), the discovery of two adult males intentionally buried hand-in-hand may have p

118 lapping flight during their migrations; this adult male is carrying a satellite transmitter.

119 up to 4.23 years, while for the least frail adult males it was of 2.68 years.

120 Adult male Japanese quail were orally dosed with wheat s

121 In addition, adult male KO mice showed reduced ventral hippocampus-mP

122 d ultrasonic vocalizations) were examined in adult male Lister-hooded rats, using selective antagonis

123 or exposure model to characterize feeding in adult male Long Evans rats and aligned this behavioral r

124 This study was performed in adult male Long-Evans rats at 48-h withdrawal from chron

125 tral hippocampal (VH) terminals in the PL of adult male Long-Evans rats selectively during paired tri

126 d on a delayed-match-to-sample test of WM in adult male macaques (n = 7).

127 , in (M1) (n = 187), and F5 (n = 115) as two adult male macaques executed, observed, or withheld (NoG

128 During the dry season, large sub-adult males made significant (~15 km) upstream movements

129 However, in inexperienced adult males, male and female intruders activated overlap

130 ons with an estrous female were noted in the adult male MAR-ASD animals, as well as reduced vocalizat

131 cumbens (NAc), a key brain reward region, of adult male mice after cocaine administration.

132 Adult male mice and hippocampal brain slices.

133 er disruption of hepatic estrogens action in adult male mice could recapitulate aspects of the metabo

134 Previously, we found that adult male mice expressing the autism-associated SERT Al

135 or CA2/CA3a-restricted excitatory neurons in adult male mice impaired the persistence of long-term SR

136 Here, we trained adult male mice in a cortex-dependent auditory discrimin

137 wn in the medial prefrontal cortex (mPFC) of adult male mice induces depressive-like behaviors.

138 Mimicking this decrease in young adult male mice led to age-like memory deficits in hippo

139 We used adult male mice on the C57BL/6 or BALB/c backgrounds, in

140 In neurons of adult male mice pretreated with LPS, the number of actio

141 and activator of transcription-5 (pSTAT5) in adult male mice that received an intraperitoneal GH inje

142 We 1) exposed adult male mice to an odor, acetophenone (Ace) or Lyral

143 hat both authentic and transmitted stress in adult male mice trigger metaplastic facilitation of long

144 neurons of the aIC projecting to the BLA in adult male mice using a retro-AAV construct and assessed

145 ns in the anterior cingulate cortex (ACC) of adult male mice we found good coupling, particularly of

146 In this study adult male mice were randomized to receive TAC surgery w

147 social hierarchy on micturition patterns in adult male mice, confirming the existence of a micturiti

148 n the CA1 region of the hippocampus in young adult male mice, enhances neuronal excitability and impr

149 -resolution functional and structural MRI in adult male mice, here we show that loss of Shank3 (Shank

150 In the present study, we have found that in adult male mice, prefrontocortical PV+ cells surrounded

151 Overall these results indicate that, in adult male mice, the BDNF Val66Met polymorphism impairs

152 is associated with thinner cortical bone in adult male mice.

153 a focal, lysolecithin-demyelinated lesion in adult male mice.

154 the rostral Re of brain slices prepared from adult male mice.

155 evelopment on indices of chronic diseases in adult male mice.

156 ocaine conditioned place preference (CPP) in adult male mice.

157 spiratory tract of an image-based whole-body adult male model (VIP-Man) to simulate radiation transpo

158 nted here was to assess fungal influences on adult male mosquito microbiomes to enable a more complet

159 ng with the entire somatodendritic domain of adult male mouse dopaminergic neurons, previously record

160 D1 and D2 medium spiny neurons (MSNs) in the adult male mouse NAc core.

161 mTOR in the ventral tegmental area (VTA) in adult male mTOR(loxP/loxP) mice, we investigated the rol

162 , odr-10 expression is high, but in well-fed adult males, odr-10 expression is low, promoting explora

163 and a reduced number of apoptotic cells, and adult male offspring exhibited higher fitness.

164 Adult male offspring of obese mice developed obesity, fa

165 increased body weight and adiposity index in adult male offspring that is paralleled by epigenomic al

166 increased body weight and adiposity index in adult male offspring that is paralleled by epigenomic al

167 ects manifesting as metabolic dysfunction in adult male offspring.

168 sistance, and organ weights were examined in adult male offspring.

169 ather than maternal relatives, and unrelated adult males often traveled together.

170 al long-term effects on reinjury response in adult males only, emphasizing the importance of evaluati

171 ns also declined by 15% per year considering adult males only, while a slower, nonsignificant decreas

172 eripherally-measured basal corticosterone in adult males only.

173 rity in annual dispersal of snail kites (all adults, males only, females only, and juveniles only) an

174 e anxiety or response to an acoustic tone in adult male or female mice as compared with nonstressed a

175 as evaluated using vitellogenin induction in adult male or larval fathead minnows.

176 ed in a human-animal conflict to those of 33 adult male orangutans of a similar developmental stage,

177 etitive operant aggression and reported that adult male outbred CD-1 mice lever-press for the opportu

178 % greater in ventricular myocytes from young adult males (P < 0.05).

179 Twelve healthy adult male participants who underwent nasogastric intuba

180 Adult male patients undergoing Lichtenstein hernioplasty

181 he study population comprised a total of 168 adult male patients who underwent cardiac ultrasound sca

182 e ratio was 2.52 when comparing MSM with the adult male population.

183 Only adult males presented marine sponges, typically doing so

184 We showed that adult male R59X mice recapitulated the behavioral outcom

185 Adult male rainbow darter (RBD) (Etheostoma caeruleum) w

186 (ION) transection on gene expression in the adult male rat barrel cortex were investigated using RNA

187 sponses to social affect are evident when an adult male rat is presented with a pair of unfamiliar ma

188 We investigated the adult male rat transcriptome using RNA-sequencing (RNA-s

189 Adult male rats (10/group) received a single dose of 0,

190 Retrograde tracing in adult male rats (Rattus norvegicus) revealed that the in

191 was recorded in anesthetized and ventilated adult male rats and a multielectrode array was used to r

192 to decrease mediodorsal thalamic activity in adult male rats and evaluated the consequences for E/I b

193 current circuits following motor training in adult male rats and find robust synaptic reorganization

194 Here, using hippocampal slices from young adult male rats and mice, we report that epileptiform ac

195 We randomly divided 24 adult male rats into 4 groups (n = 6 per group).

196 We trained adult male rats on a multistage decision-making task to

197 Chronic unpredictable stress (CUS) to adult male rats produced depression-like changes with co

198 Adult male rats received a 90-min right distal middle ce

199 Two weeks after GI, adult male rats received high-frequency EC DBS for 1 h,

200 M(1) receptor-selective agonist VU0364572 in adult male rats that self-administer cocaine in a cocain

201 nscribed mRNA (mtRNA) expression, we exposed adult male rats to both acute and chronic immobilization

202 We trained adolescent and adult male rats to self-administer nicotine (2 h/d for 1

203 rainer (LRT) and high-response trainer (HRT) adult male rats to various forms of physical exercise fo

204 Adult male rats underwent oral gavage with THC or vehicl

205 We assessed decision making in adult male rats using a probabilistic reversal learning

206 Stress-induced anhedonia was assessed in adult male rats using social defeat and intracranial sel

207 Finally, THC-exposed and control adult male rats were mated with THC-naive females.

208 Here we find that in adult male rats, presentation of a social stimulus (nove

209 tors in the prelimbic PFC (prPFC) and BLA of adult male rats.

210 One hundred ninety-eight adult male rats.

211 mCherry was injected into the VTA of TH::Cre adult male rats.

212 d no effect of resistance training on AHN in adult male rats.

213 e arterio-venous fistula model (AV-Shunt) in adult male rats.

214 ites of CA1 pyramidal neurons in slices from adult male rats.

215 estigated in pavlovian cued-fear conditioned adult male rats.

216 infection in an avian host-parasite system: adult male red-winged blackbirds (Agelaius phoeniceus) i

217 cy requirements are higher than the previous adult male requirement (9.1 mg . kg-1 . d-1; 95% CI: 4.6

218 ay in the juvenile-to-adult transition, with adult males retaining pointed, juvenile tail tips, and d

219 Dietary intervention experiments with 59 adult male rhesus macaques indicated low plasma adropin

220 Adult male rhesus monkeys (N = 11) self-administered coc

221 Experiments used two adult male rhesus monkeys trained on a reaching task.

222 The differential ontogenetic trends cause adult male ribcages to become deeper, shorter, and wider

223 e is limited by its exclusive application to adult male rodents.

224 r, using quantitative PCR, we also find that adult male S. parvus maintain a unique androgenic phenot

225 performed in mouse embryos of either sex and adult males showed that the NKX motifs present in nPE1 a

226 tion values were linked to age and sex, with adult males showing significantly higher levels than juv

227 significant when we matched pooled ORs with adult male smoking prevalence (z = 2.55, p = 0.01) in ea

228 d genetic data, we hypothesise that pairs of adult male Sousa form at least temporary coalitions or a

229 e electroencephalographic data gathered from adult male Sprague Dawley rats during the aforementioned

230 al role of GLP1R signaling within the alBST, adult male Sprague Dawley rats received bilateral alBST-

231 role of the RMTg in punished reward seeking, adult male Sprague Dawley rats were tested in several co

232 l common carotid artery occlusion (BCCAO) in adult male Sprague Dawley rats.

233 Adult male Sprague-Dawley rats and pulmonary epithelial

234 To test this hypothesis, adult male Sprague-Dawley rats received sham surgery or

235 Using adult male Sprague-Dawley rats trained to self-administe

236 Adult male Sprague-Dawley rats underwent diaphragm elect

237 Adult male Sprague-Dawley rats underwent UNx (n = 6) or

238 inic stimulation in sympathetic neurons from adult male Sprague-Dawley rats with electrophysiological

239 ne) of new adult-born hippocampal neurons in adult male Sprague-Dawley rats.

240 ed neuroadaptations of CeA 5-HT signaling in adult, male Sprague Dawley rats using an established mod

241 ic manipulation of OVLT neurons, was used in adult, male Sprague Dawley rats.

242 Adult, male Sprague-Dawley rats were exposed to nicotine

243 ily from the prelimbic region of the mPFC of adult, male, Sprague Dawley rats impaired the acquisitio

244 Studies were performed on adult, male, Sprague-Dawley rats exposed to either short

245 es NMDAR function in hippocampal slices from adult male SR-/- mice.

246 States is overwhelmingly a disorder of older adult male subjects with a cardiac-predominant phenotype

247 led, cross-over study of 19 high-functioning adult male subjects with DSM-IV Autistic Disorder (age 1

248 dent inhibition of hepatic DNL in overweight adult male subjects.

249 verweight and/or obese but otherwise healthy adult male subjects.

250 Both adult female and adult male survival showed low temporal variation, where

251 ts of breeding density on both fecundity and adult male survival.

252 We enrolled a convenience sample of 220 adult male survivors of EVD in Sierra Leone, at various

253 Asymptotic length of adult males (SW = 246 cm, SB = 201 cm) and females (SW =

254 Adult male Swiss Webster mice were provided with food du

255 al classes were detected in the blubber of 4 adult male T. truncatus.

256 pathways should be developed to allow young adult males to enter accommodation facilities and build

257 lt females, and the orientation responses of adult males to sex pheromone were also significantly inh

258 al study in a rat model of septic shock (128 adult males) to assess the effects of ELA and Apelin-13

259 progenitor cells (BMPCs) were isolated from adult male type 2 diabetic and their littermate control

260 ed for multiple years (up to 1101 days) that adult males undertake annually repeated, round-trip migr

261 from streptozotocin-treated type 1 diabetic adult male vervet monkeys receiving twice-daily exogenou

262 plicated in testicular and sperm function in adult males via interaction with relaxin/insulin-like fa

263 Tanzanian adult male volunteers were immunized by direct venous in

264 of Gibraltar to winter in West Africa; this adult male was photographed on migration near Gibraltar.

265 ancy occurring primarily in adolescent/young adult males, we used next-generation RNA sequencing to i

266 Adult males were at greatest risk for exposure to S. neu

267 Adult males were more likely than females to have aortic

268 Six healthy adult males were randomized to receive either single dai

269 ns expressed in a small number of neurons in adult males, where it likely has a permissive role in od

270 RA) with retrograde tracer injected in RA of adult male white-crowned sparrows (Zonotrichia leucophry

271 penetrating foreign body (wooden twig) in an adult male who presented with discharging sinus in the o

272 Isoflurane-anesthetized adult male wild-type C57B/6 or alpha-Syn mice were subje

273 istered VU0409551 systemically for 5 days to adult male wild-type C57BL/6 animals to determine the op

274 Adult male wild-type C57BL/6 mice, Foxp3-diphtheria toxi

275 Healthy adult male Wistar rats underwent irradiation with arrays

276 Adult male Wistar rats were anaesthetized and ABP was mo

277 Adult male Wistar rats were exposed to predator odor str

278 Eighty adult male Wistar rats were randomly assigned to one of

279 Twenty minutes after icv FGF1 injection in adult male Wistar rats, pERK1/2 staining was detected pr

280 We found that in adult male Wistar rats, silencing the medial septum duri

281 gical, optogenetic, and biochemical tools in adult male Wistar rats, we demonstrate that reactivation

282 ecognition memory trace stored over time, in adult male Wistar rats.

283 ted wild herring gull (Larus argentatus) and adult male Wister-Han rat liver microsomal assays.

284 adult female and 33.1+/-1.4 muSv/MBq for an adult male with a 1.5 hour urinary bladder voiding inter

285 We report a case of an adult male with EPP and liver failure who successfully u

286 We analysed data from 14 adult males with adult cerebral adrenoleukodystrophy tre

287 Millions of factory-reared adult males with an artificial triple-Wolbachia infectio

288 By comparing TSPO in 15 young adult males with ASD with 18 age- and sex-matched contro

289 we compared the white matter networks of 61 adult males with autism spectrum disorder and 61 neuroty

290 l administrations of oxytocin (48 IU/day) in adult males with autism spectrum disorder.

291 crossover trial including 20 high-functional adult males with autism spectrum disorder.

292 Nine adult males with high (sero-high) and 10 with low (sero-

293 Nine adult males with high (sero-high) and ten with low (sero

294 dult female and 33.1 +/- 1.4 muSv/MBq for an adult male, with a 1.5-h urinary bladder voiding interva

295 s in England are persistently most common in adult males without a reported travel history, consisten

296 cronym is name) encodes the learned songs of adult male zebra finches (Taeniopygia guttata).

297 y, we manipulated NR2B expression in LMAN of adult male zebra finches by increasing its protein level

298 d bilaterally from auditory neurons in awake adult male zebra finches with multiple microelectrodes d

299 In the present study, adult male zebrafish were exposed to TDCIPP and global h

300 cerebellar neurogenic niche of normal young adult male zebrafish, with cells quantified in 2D (secti