ライフサイエンスコーパス: adult male

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

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

3 hifted to simulate either a large or a small adult male.

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

5 s highly prevalent, particularly among young adult males.

6 genes account for 10% of all transcripts in adult males.

7 rial evaluating single oral doses in healthy adult males.

8 protective against periodontal bone loss in adult males.

9 s, social dominance, and competition between adult males.

10 e quantified the courtship rate exhibited by adult males.

11 in contrast to the urine taken from control adult males.

12 ired for primary spermatogonial divisions in adult males.

13 anced by increasing neuroestrogens in NCM in adult males.

14 lear, but may be related to the behaviour of adult males.

15 lt females had lower parasite intensity than adult males.

16 could be a result of an increased risk from adult males.

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

18 ogenesis and ensure its prodigious output in adult males.

19 microM, and 70.98 microM, respectively; for adult males, 41.6 microM, 3.87 microM, and 68.22 microM,

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

21 Although adolescent and young adult males accounted for fewer overall melanoma cases (

22 tinib, nilotinib, and dasatinib on B. malayi adult males, adult females, L3 larvae, and microfilariae

23 site intensity and lower body condition than adult males after parturition and during early lactation

24 One epithelial cell type in the adult male AGs, the secondary cell (SC), grows selective

25 nut consumption, our data indicate that some adult males also derive a large amount of dietary protei

26 cific precopulatory behavior as performed by adult males, although it apparently can be performed in

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

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

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

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

31 Adult male and female G/G mice and 'wild-type' litter ma

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

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

34 Adult male and female mice with lifelong expression of m

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

36 alculate the internal doses for the standard adult male and female models.

37 Adult male and female offenders serving sentences of 2 o

38 erm potentiation (LTP) differed in slices 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 encing at approximately 140-fold coverage of adult male and female T. suis and approximately 80-Mb dr

42 Nine adult male and three adult female rhesus macaque were un

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

44 Although both adult males and females and juveniles derive their dieta

45 mparison, eggs, early copepodite stages, and adult males and females were not affected lethally until

46 the neuroanatomy of autism differed between adult males and females, evidenced by minimal spatial ov

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

48 tacts on MePD neurons of both hemispheres in adult males and in females along the estrous cycle.

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

50 e population with a breakdown into juvenile, adult male, and female subclasses ranged from 3600 to 14

51 reduced caput epidydimal sperm counts in F1 adult males, and increased incidences of thyroid follicu

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

53 In chimpanzees (Pan troglodytes), adult males are more gregarious than females and rely on

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

55 s of transgenically labeled GnRH1 neurons in adult male Astatotilapia burtoni cichlid fish.

56 Adult male BALB/c mice received a sham (n = 52) or midli

57 in immature male liver, where repression of adult male-biased genes and expression of adult female-b

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

59 eukin (IL)-1beta levels within the brains of adult males but not females, and maternal DEP and NR bot

60 Furthermore, adult male, but not female, offspring had higher mean ar

61 surrounding tissues, particularly within the adult male, but not female, robust nucleus of the arcopa

62 Here, we show that depletion of 20E from adult males by overexpressing a dominant negative form o

63 Conventionally housed, nonobese, adult male C57BL/6 mice maintained on a normal chow diet

64 Adult male C57BL/6 mice were subjected to middle cerebra

65 the relationship in polymicrobial sepsis (in adult male C57BL/6 mice) between heart dysfunction and t

66 In adult male C57BL/6 mouse hearts, Gstp1/2 was the most ab

67 7A and IL-23 during endotoxic shock in young adult male C57BL/6J mice and has similar effects on macr

68 Specifically, adult male C57BL/6J mice were exposed to either emotiona

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

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

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

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

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

74 tes, as these measures are demasculinized in adult males carrying the testicular feminization mutatio

75 20/150) of locally acquired infections among adult males, characterized by distinct periodic Shigella

76 ervations of frequent meat eating among wild adult male chimpanzees (Pan troglodytes verus) in Tai Na

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

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

79 Eastern Africa, calling for 80% coverage of adult male circumcision by 2016.

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

81 In adult male cowbirds the largest wing movements of the di

82 Smoking will cause about 20% of all adult male deaths in China during the 2010s.

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

84 Thirty-six adult male Dorset sheep underwent permanent ligation of

85 onsequence of a GH axis deficit, neuroDrd2KO adult males excreted low levels of major urinary protein

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

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

88 Adult male/female rhesus monkeys self-administered metha

89 Adult male fish deprived of maternal rest present with a

90 In the presence of mating partners, adult male flies exhibited elevated levels of aggression

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

92 Competition between adult males for limited resources such as food and recep

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

94 ence of female-like brain characteristics in adult male, GnRH receptor knock-out mice.

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

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

97 e, the weak expression of odr-10 in well-fed adult males has important adaptive value, allowing males

98 In this species, adult males have a very restricted repertoire of vocaliz

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

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

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

102 ze supraalveolar peri-implant defects in six adult male Hound Labrador mongrel dogs received CHO cell

103 Results from blubber biopsy sampling of adult, male humpback whales at two time points of the an

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

105 2009-2011 estimated that circumcising 80% of adult males in 14 priority countries in Eastern and Sout

106 ryos alters the germline DNA methylome of F1 adult males in a locus-specific manner.

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

108 ansiently favors feeding over exploration in adult males, increases male food attraction by activatin

109 we found that injection of RA into wild-type adult males induced, independently, precocious spermatog

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

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

112 Adult male Japanese medaka (Oryzias latipes) were expose

113 Adult male leptin receptor null, homozygous db/db, or wi

114 Surprisingly, compared to wild-type mice, adult male Liv-Ikk2ca mice had higher hepatic mRNA expre

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

116 mice, exerts a powerful inhibitory effect on adult male mating behaviour, which is abolished in knock

117 ssing traumatic events is a potent stress in adult male mice capable of inducing long-lasting neurobi

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

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

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

121 Adult male mice lacking the main T-type Ca(2+) channel s

122 irus-mediated deletion of Esr1 in the MeA of adult male mice produced a rapid body weight gain that w

123 gt1(F/F)), Ugt1(DeltaHep), and Ugt1(DeltaGI) adult male mice were treated with different concentratio

124 Additionally, adult male mice were treated with the Nrf2 activator olt

125 r both early intervention (7-month-old young-adult male mice with low pathology) and treatment (24-mo

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

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

128 ; 6 hours/day for >/=21 consecutive days) to adult male mice, several hippocampal characteristics wer

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

130 embrane GluN1 in dendrites of PVN neurons in adult male mice.

131 nteraction and a reduced learning ability in adult male mice.

132 itted by chronically deaf and normal hearing adult male mice.

133 y using a conditional, inducible mutation in adult male mice.

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

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

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

137 Adult, male mice underwent constriction of the pulmonary

138 We show that excess adult male mortality is clearly rooted in specific age g

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

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

141 In these studies, adult male NIH Swiss mice were trained to discriminate 0

142 es in the microbiome to confer protection to adult male NOD mice from type 1 diabetes.

143 Adult male offspring (3-6 months old) were used in the e

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

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

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

147 rozygous females and behaviorally tested the adult male offspring.

148 ects manifesting as metabolic dysfunction in adult male offspring.

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

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

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

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

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

154 % greater in ventricular myocytes from young adult males (P < 0.05).

155 Twelve healthy adult male participants who underwent nasogastric intuba

156 ular volume, semen quality, and fertility in adult male patients after renal transplantation (RTx) du

157 Adult male patients undergoing Lichtenstein hernioplasty

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

159 Thirty adult male patients with a diagnosis of advanced choroid

160 ting, randomized placebo-controlled trial in adult male patients with dengue with <48 hours of fever.

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

162 Adult male prairie voles received a sham surgery, were g

163 Reproductively naive, adult male prairie voles were implanted with radiotransm

164 Only adult males presented marine sponges, typically doing so

165 puted cortical thickness maps in a sample of adult male prison inmates selected on the basis of psych

166 Using fMRI in 142 adult male prison inmates, we computed resting-state fun

167 Adult males produce frontalin, an eight-carbon antiaggre

168 ause increased adiposity was also evident in adult male progeny when normal two-cell embryos were tra

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

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

171 manipulations of vlPAG glia and TLR4 in the adult male rat, we show that intra-vlPAG administration

172 ent paradox, we evaluated the hippocampus of adult male rats after gonadectomy (Gdx) or sham surgery.

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

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

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

176 Adult male rats implanted with cannulas to either the la

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

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

179 Adult male rats received bilateral microinjections of ve

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

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

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

183 testosterone replacements in gonadectomized adult male rats were investigated using the sucrose pref

184 Overnight fasted adult male rats were studied.

185 Adult male rats were subjected to 60 min of bilateral re

186 sing high-resolution phase-contrast MRI in 9 adult male rats with myocardial infarction (MI) and in 5

187 kg) or zinc-adequate (35 mg Zn/kg, pair-fed) adult male rats, and zinc levels were manipulated to dis

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

189 long-term experience-dependent plasticity in adult male rats.

190 viral tracing experiments were performed in adult male rats.

191 One hundred ninety-eight adult male rats.

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

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

194 Adult, male rats (n=10) underwent unilateral intrastriat

195 Seventy-two adult (male) rats were randomly assigned to one of three

196 Adult males received dietary exposures of BDE-209 at a l

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

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

199 Ten adult male rhesus macaques were studied at baseline and

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

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

202 ontrast, neonatal RU-486 treatment increased adult male sexual behavior and AR-ir in several brain ar

203 Adult males showed increased depression-like responses i

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

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

206 uid-percussion brain injury or sham surgery, adult male Sprague Dawley rats received vehicle or rolip

207 Young, adult male Sprague Dawley rats were implanted with bilat

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

209 uperior cervical ganglion (SCG) neurons from adult male Sprague Dawley rats with or without added NGF

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

211 Adult male Sprague-Dawley rats and pulmonary epithelial

212 r, serum, liver, and fat were collected from adult male Sprague-Dawley rats exposed to increasing dos

213 Adult male Sprague-Dawley rats INTERVENTIONS: Anesthetiz

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

215 Adult male Sprague-Dawley rats underwent diaphragm elect

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

217 Adult male Sprague-Dawley rats were implanted with elect

218 One week after MI, adult male Sprague-Dawley rats were randomized to treatm

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

220 Adult male Sprague-Dawley rats with hyperglycemia were d

221 y labelled neurons from the glabrous skin of adult male Sprague-Dawley rats, NCX activity, as assesse

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

223 l volume (VT ) were recorded in 28 conscious adult male Sprague-Dawley rats.

224 Thirty-two adult male Sprague-Dawley rats.

225 Adult, male Sprague-Dawley rats were given either lipopo

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

227 ohistochemical techniques, we demonstrate in adult, male, Sprague Dawley rats that EPO and its recept

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

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

230 ed to white matter structural properties, in adult male subjects diagnosed with ADHD in childhood (pr

231 Twelve healthy adult male subjects received 1-L intravenous infusions o

232 Twelve healthy adult male subjects received 2-L intravenous infusions o

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

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

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

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

237 cles and of glucose in Lev+Dep than those of adult males suggests that there may be a metabolic dimor

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

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

240 We did semen analysis on 214 adult male survivors of childhood cancer (median age 7.7

241 ls of FSH and inhibin B were measured in 275 adult male survivors of childhood cancer who had receive

242 decreased sperm concentration in a cohort of adult male survivors of childhood cancer who were not ex

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

244 on of the left anterior descending artery in adult male swine.

245 Adult male Swiss Webster mice were provided with food du

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

247 ely cover the scalp of a well-characterized, adult male template brain (Colin27).

248 However in the adult males, the muscle's sarcomere is reorganized to fa

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

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

251 patient characteristics by sex, compare the adult male-to-female mortality rate with data from the g

252 ion results in increased sexual behaviour of adult males towards juveniles, and sexual responses towa

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

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

255 e impact of BPA in primate brain by exposing adult male vervet monkeys for 4 weeks continuously to ci

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

257 ar pharmacological assessments in a group of adult male vervet monkeys.

258 d from genitourinary tract specimens from an adult male veteran patient population and, in particular

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

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

261 ke is associated with periodontal disease in adult males was explored.

262 nel cohort study of aging and oral health in adult males was used.

263 Adolescent and young adult males were 55% more likely to die of melanoma than

264 Adult males were more likely than females to have aortic

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

266 gSe), and less Hg in the muscles compared to adult males, which may be explained by accelerated metab

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

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

269 emophilia B to mild or moderate disease in 6 adult males who underwent intravenous infusion of an ade

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

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

272 Adult male wild-type or RAG C57B6-6J mice were fed a hig

273 Adult male Wistar rats (n=26) underwent either carotid c

274 Finally, adult male Wistar rats (n=33) underwent permanent ligati

275 s were implanted in the mPFC of anesthetized adult male Wistar rats for in vivo evaluation.

276 In adult male Wistar rats or wild-type mice subjected to un

277 To address this question, adult male Wistar rats received either streptozotocin (S

278 Healthy adult male Wistar rats underwent irradiation with arrays

279 Adult male Wistar rats were anaesthetized and ABP was mo

280 Adult male Wistar rats were exposed to predator odor str

281 Adult male Wistar rats were injured with controlled cort

282 ith alcohol withdrawal and KOR activation in adult male wistar rats.

283 (ARCN) was studied in urethane-anesthetized adult male Wistar rats.

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

285 mino acid within two residues of Arg51 in an adult male with bilateral colobomata.

286 presumed de novo mutant DAT-Asp421Asn, in an adult male with early-onset parkinsonism and ADHD.

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

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

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

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

291 erritory size is determined by the number of adult males, with the presence of subordinate females an

292 olbachia is restricted to somatic tissues in adult male worms, whereas females also harbor bacteria i

293 The songs of adult male zebra finches (Taeniopygia guttata), produced

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

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

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

297 4 mRNA and protein in brains of juvenile and adult male zebra finches.

298 epidermal tubercles (ETs) on the surfaces of adult male zebrafish pectoral fins.

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

300 city were not significantly altered in young-adult male Zucker diabetic fatty rats compare to their l