ライフサイエンスコーパス: juvenile

1 ious inference that the specimen is not of a juvenile.

2 les showing significantly higher levels than juvenile.

3 y lower levels in Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles.

4 ea anemone eggs and in brooding and released juveniles.

5 ales is usually higher than that of males or juveniles.

6 protein (p), high carbohydrate (c) diets as juveniles.

7 ological alterations observed in Lake Apopka juveniles.

8 e aquatic environments inhabited by mosquito juveniles.

9 sex in 83-177 day-old (120-160 g) loggerhead juveniles.

10 uring maturity to adulthood, here we treated juvenile (2-week), young adult (8-week), and mature adul

11 of European seabass (Dicentrarchus labrax), juveniles (78 +/- 0.4 g).

12 d compromised survival between years in both juveniles (86% reduction in interannual survival) and ad

13 357K) is associated with the relatively mild juvenile absence epilepsy syndrome.

14 We found that juvenile abundance is negatively associated with female

15 same pace, with only two adult males and one juvenile accompanying them.

16 -term potentiation in hippocampal CA1 in the juvenile-adolescent ELE group.

17 LE, P35-41), or 4(th)-6(th) postnatal weeks (juvenile-adolescent ELE, P21-41).

18 ental genes during a critical time window of juvenile adult brain development when neuronal circuits

19 es the brain to later execute high levels of juvenile adult sleep.

20 colonization of additional nematode stages: juvenile, adult and pre-transmission infective juvenile

21 or mississippiensis), we find that adult and juvenile alligator skulls are topologically similar, whe

22 ductions in ovarian follicle density between juvenile alligators from Lake Apopka and the reference s

23 Overall, this study of wild-caught, juvenile American alligator tails identifies a distinct

24 ipid handling between species, and the human juvenile and adult cell populations.

25 posterior lateral spinneret present in late juvenile and adult females, and CY spigots of males neve

26 The different responses of juvenile and adult fishes according to habitat descripto

27 We quantified the functional responses of juvenile and adult geckos in single-predator experiments

28 Here, we find that juvenile and adult leaves in all three species photosynt

29 these hypotheses, Cyp26a1 was knocked out in juvenile and adult male and female Cyp26a1 floxed mice u

30 murine model of sepsis; survival studies in juvenile and adult mice, assessment of lipoprotein fract

31 ex leads to decreased social interactions in juvenile and adult mice.

32 cell (LEC) junctions in different organs of juvenile and adult mice.

33 The hurricanes depressed the densities of juvenile and adult octocoral colonies as much as 47%.

34 able flows were also associated with reduced juvenile and adult production, highlighting the importan

35 of coral assemblages affect the abundance of juvenile and adult reef fishes.

36 ischistosomal activity in mice infected with juvenile and adult Schistosoma mansoni by incorporating

37 The fact that juvenile and adult skulls in birds do share a similar an

38 effects of Ano1 antagonists on muscles from juvenile and adult small intestinal muscles suggests tha

39 g prefrontal cortex and leads to deficits in juvenile and adult social behavior, suggesting that alte

40 ripts that produce postnatal piRNAs in human juvenile and adult testes.

41 ut has no visible impact on muscle growth in juvenile and adult zebrafish that escape the larval leth

42 Both juvenile and mature auditory nerve synapses onto bushy c

43 function may be important during the feeding juvenile and the adult stages of the lamprey life cycle.

44 um D1-medium spiny neurons (D1-MSNs) in both juvenile and young-adult mice.

45 By comparing within the same framework, juveniles and adults for crown birds and alligator (Alli

46 an be recognized, historically considered as juveniles and adults of the same species [4].

47 is essential for larval pigmentation, but in juveniles and adults, loss of FMO3 activity resulted in

48 pocampus of infant rats and mice compared to juveniles and adults.

49 spite several-fold increases in size between juveniles and adults.

50 mass change and interannual survival in both juveniles and adults.

51 ; elevated infection is commonly observed in juveniles and males, and, for females, with different re

52 e same allometric scaling laws as trees; (2) juveniles and mature individuals do not follow the same

53 expression analysis were performed on 3-wk- (juvenile) and 8-wk-old (adult) RSV-infected C57BL/6 mice

54 Examine the intracranial space of larval, juvenile, and adult zebrafish to determine whether and w

55 oss three developmental stages (metamorphic, juvenile, and adult) or as adults only, and compare thes

56 somatic expansion of Htt CAG repeats, in the juvenile- and the adult-onset HD ranges, whereas knock-o

57 Productivity and juvenile apparent survival at the largest colony appear

58 EHV) can cause lethal hemorrhagic disease in juvenile Asian elephants, both in captivity and in the w

59 o were positively affected by temperature as juvenile attack rates (a) increased as a function of inc

60 Single-unit recordings reveal that, during juvenile babbling, NIf neurons burst at syllable onsets,

61 fathers and sons by experimentally tutoring juvenile Bengalese finches with the songs of unrelated t

62 or skulls are topologically similar, whereas juvenile bird skulls have a morphological complexity and

63 When juvenile birds listen to their tutor, NIf neurons are al

64 illion year(-1), and relies upon a supply of juvenile bivalves produced by adult broodstock in hatche

65 In contrast, cycling juvenile BM HSCs preferentially located close to Cxcl12

66 ibution of phases of spermatogenesis between juvenile (born that season) and adult (born in previous

67 attracted more birds than other vessels, and juveniles both encountered fewer vessels and showed a lo

68 matrix fraction (tECM) by urea extraction of juvenile bovine tendons, which is capable of enhancing t

69 ial burden was increased in Il2rg (KO/)Tg(+) juveniles but returned to significantly lower levels in

70 ncreased following seawater (SW) exposure of juveniles, but expression of PRLR was not significantly

71 wn and bottom-up predictions, both adult and juvenile cheetahs experienced the lowest survival during

72 ort only for a density-dependent response in juvenile cheetahs, where they had a higher probability o

73 l to the results of a behavioural assay with juvenile Chinook salmon Oncorhynchus tshawytscha that va

74 Juvenile CLN3 disease, the most prevalent form of Batten

75 recent record-breaking drought on endangered juvenile Coho salmon.

76 icroplastics triggered premature moulting in juvenile copepods (Bernoulli GLM, P < 0.01).

77 er the dominant male, female and subordinate juvenile crested tit, respectively.

78 line of cortical plasticity after closure of juvenile critical period consolidates neural circuits an

79 nce-dependent plasticity observed during the juvenile critical period: to rapidly reduce the activity

80 nown hallmarks of cortical plasticity during juvenile critical periods.

81 Social isolation during the juvenile critical window is detrimental to proper functi

82 We further demonstrated that juvenile csf1r-deficient zebrafish exhibit systemic macr

83 ed to adults, and explained more than 20% of juvenile decline.

84 adult animals and at multiple stages during juvenile development.

85 8833, DK115824, DK116888, and DK116450); the Juvenile Diabetes Research Foundation (JDRF 3-SRA-2019-7

86 med maize during childhood (up to 70% of the juvenile diet), as shown by delta(13)C values, apatite-c

87 Juvenile diving behavior differed only modestly among ha

88 ent digestion leads to a lower BMF(lim) in a juvenile dog (approximately 35) compared to its older se

89 Juvenile dogs exhibited stunted postnatal growth, steato

90 We found that juveniles dominate the Coquimbo locality (Chile), wherea

91 coupling was reduced in both male and female juvenile DS mice and persisted only if spontaneous seizu

92 on European eel (Anguilla anguilla) in their juvenile, early life stage (glass eel), were conducted t

93 postnatal periods: the 4(th) postnatal week (juvenile ELE, P21-27), 6(th) postnatal week (adolescent

94 While most juveniles emigrated from the natal stream as fry or smol

95 explore the influence of regulated flows on juvenile emigration phenology, abundance, and recruitmen

96 Juvenile environment therefore shapes dispersal both dir

97 s previously reported, immunocompetent Tg(+) juveniles exhibited spontaneous neonatal bacterial infec

98 rg (KO)/Tg(+) and Il2rg (KO)/Rag1 (KO)/Tg(+) juveniles exhibited suppressed expression levels of Th2

99 ained into adulthood and present also within juvenile F2 offspring.

100 ise set of differentially expressed genes in juveniles fed the SBM-based diet, the majority of which

101 ed Se acquired through maternal transfer and juvenile feeding on contaminated prey.

102 Juvenile finches raised with tutors of either the same o

103 Juvenile fish were exposed to reduced food availability,

104 In choice assays, juvenile fishes from the Caribbean (Belize) and Indo-Pac

105 (2) Do juveniles follow the same allocation patterns as mature

106 In only 4 hours, this compound killed the juvenile form of F. hepatica with an IC(50) of 3 uM, bet

107 g extant kinorhynchs; and abundant larval or juvenile forms.

108 rn Mediterranean coast leaving behind a less juvenile fraction.

109 Juveniles from both sites were divided and treated with

110 saturating Type-II functional responses, but juvenile functional responses and the novel Functional R

111 ver, the small size and dispersive nature of juveniles generally make studying their survival more di

112 ere we examine interaction strengths between juvenile giant kelp (Macrocystis pyrifera) and four comm

113 dry conditions were associated with reduced juvenile growth, mass loss in adults and compromised sur

114 ensional reconstruction of the thorax of the juvenile H. erectus skeleton, KNM-WT 15000, from Narioko

115 ed upper limit of spatial resolving power in juvenile H. portusjacksoni was 3.14 cycles deg(-1) , whi

116 L. sceleratus juveniles had been considered as non-toxic and, to our k

117 n both species males that reached puberty as juveniles had higher body mass, on average, than immatur

118 Cross-generational GS validation of juvenile height in Douglas-fir produced predictive accur

119 e neuronal CoREST corepressor and changes in juvenile hormone (JH) and ecdysone signaling during the

120 Here, the complex crosstalk between juvenile hormone (JH) and the two nutrient sensors insul

121 relatively little is known about the role of juvenile hormone (JH) in the control of female reproduct

122 In fruit flies, juvenile hormone (JH) induces intestinal stem cell (ISC)

123 nsects, increasing evidence has demonstrated juvenile hormone (JH) is involved in regulating adult re

124 nsect hormones, 20-hydroxyecdysone (20E) and juvenile hormone (JH) to elicit an important physiologic

125 represses expression of enzymes that degrade juvenile hormone (JH), a hormone elevated upon reprogram

126 ging), but not affected by dominance rank or juvenile hormone known to influence physiology and behav

127 tegrating reproductive maturity, signaled by juvenile hormone, and population density, signaled by CB

128 Juvenile hormones (JHs) are sesquiterpenoids synthesized

129 Euprymna scolopes and Vibrio fischeri As the juvenile host matures, it develops complex daily rhythms

130 n reduced hepatic bacterial clearance in the juvenile host with septic shock.

131 ype 9 loss-of-function is detrimental to the juvenile host with septic shock.

132 A protein also is weakly produced within the juvenile human islet beta-cell population and that MafB

133 The social positions occupied by juvenile hyenas did predict their fitness, but the effec

134 a in multiple autoimmune diseases, including juvenile idiopathic arthritis (JIA) has earned substanti

135 oved prospective study, 45 participants with juvenile idiopathic arthritis (JIA) or suspected of havi

136 ing arthritis in pediatric participants with juvenile idiopathic arthritis (JIA) or suspected of havi

137 of cataract development among patients with juvenile idiopathic arthritis (JIA)-associated uveitis t

138 identified: Crohn's disease (n = 8; 42%) and juvenile idiopathic arthritis (n = 6; 32%) were the comm

139 are often observed in children with systemic juvenile idiopathic arthritis (sJIA) and cytokine storm

140 tes and synechiae, and systemic diagnoses of juvenile idiopathic arthritis and spondyloarthropathy pr

141 Systemic diagnosis with juvenile idiopathic arthritis and spondyloarthropathy we

142 The aims of treating juvenile idiopathic arthritis are to elicit treatment re

143 atic diseases, such as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset Still's disea

144 ammatory diseases such as sepsis or systemic juvenile idiopathic arthritis.

145 id arthritis, spondyloarthritis and systemic juvenile idiopathic arthritis.

146 al nephritis with uveitis (6/52, 11.5%), and juvenile idiopathic uveitis (4/52, 7.7%).

147 nattereri (12.85%) became sexually mature as juveniles, (ii) the proportion of juveniles in reproduct

148 opathogenic nematodes (EPNs) drive infective juvenile (IJ) emergence from consumed cadavers and dispe

149 and colonization initiation in the infective juvenile (IJ) stage nematode that carries X. nematophila

150 venile, adult and pre-transmission infective juvenile (IJ).

151 larval mortality rate (80%) at 50 infective juveniles (IJs) cm(-2).

152 ation and flower buds appeared 30-40 days on juvenile immature scions grafted onto transgenic rootsto

153 mature as juveniles, (ii) the proportion of juveniles in reproductive condition per annum was influe

154 the study period, with large proportions of juveniles in the years 1970 and 1985, and made a substan

155 ndition, muscle, primary moult, breeding and juveniles) in forest and coffee, and generated hypothese

156 by males is at least largely limited to late juvenile instars and is not involved with egg sac constr

157 clear number were differentially affected by juvenile irradiation and/or vincristine treatment.

158 Juvenile isolation led to both reduced excitability of m

159 C-PVI activity in the adult animal mitigates juvenile isolation-induced social deficits.

160 ld rescue the sociability deficits caused by juvenile isolation.

161 higher body mass, on average, than immature juveniles, (iv) older males (aged >=4 years old) commenc

162 ing is a significant source of mortality for juvenile kelp and, using field abundances, estimate graz

163 This study highlights potentially high juvenile kelp mortality from grazing.

164 of grazing threefold, from 15.4% to 4.0% of juvenile kelp removed, on average, per m(2) per day.

165 term behavioral consequences associated with juvenile ketamine exposure.

166 Thus, we examined if juvenile ketamine treatment results in long-lasting chan

167 We found that juvenile ketamine-pretreatment increased preference for

168 In juvenile (L3) males, tra-1 is expressed in numerous neur

169 es are maintained dynamically: HVC(X) within juveniles learning to sing show variable properties, whe

170 Further, we found juvenile leaves with high SLA were associated with bette

171 al meristem and an increase in the number of juvenile leaves.

172 -taking in the wild in two subpopulations of juvenile lemon sharks Negaprion brevirostris known to di

173 c survival may trade-off and interact across juvenile life stages to shape animal life histories.

174 d the embryonic period but perished in early juvenile life.

175 n the process of domestication for increased juvenile-like behavior in the adult domestic ferret, suc

176 Thus, juvenile-like plasticity induced by both chondroitinase

177 tro and in vivo in male and female mice, and juvenile-like plasticity is retained in the visual corte

178 ult sponge can reorganize and develop into a juvenile-like sponge, a remarkable phenomenon of regener

179 Diets were fed to juvenile LMB (initial weight, 25.87 +/- 0.08 g) to near

180 ce and neuro-ophthalmology.(1-5) Humans with juvenile macular degeneration (JMD) show significant blo

181 oil-exposed (24 h, 14.5 mug/L Sigma(50)PAH) juvenile mahi-mahi (27-85 mm) could detect crude oil as

182 We exposed acoustically naive juvenile male and female cowbirds to songs paired with c

183 In juvenile male mice, NMDAR ablation results in several pa

184 Therefore, we tested this hypothesis in juvenile male songbirds using a comprehensive assessment

185 etic Resonance Imaging with song analyses in juvenile male zebra finches during song learning and bey

186 uppress this sex difference in two contexts: juvenile males exhibit high odr-10 expression and food d

187 Late juvenile males had a CY spigot on each PMS, whereas adul

188 hese complexes consist of, at least by half, juvenile material forming some 5 million km(2) new conti

189 avorable environmental conditions flightless juveniles may aggregate into coherent, aligned swarms re

190 eterious effects of reducing EphA4 levels in juvenile mice and do not provide support for the hypothe

191 oth endogenous production of anti-GBS IgG in juvenile mice and vertical transfer of antibodies to off

192 ific IgG production in exposed offspring and juvenile mice at age 12 and 14 days, respectively.

193 inister fractionated hindlimb irradiation to juvenile mice bearing implanted rhabdomyosarcoma (RMS) t

194 Juvenile mice demonstrated alphaSma expression (indicati

195 elated differences in immunologic responses; juvenile mice displayed a sustained myeloid infiltrate (

196 ined influx of myeloid cells in the lungs of juvenile mice during acute RSV infection could potentiat

197 ccumulated in the calyx of Held terminals of juvenile mice of either sex during high-frequency spikin

198 Juvenile mice were given partial brain irradiation of 10

199 Slow waves in intestinal muscles of juvenile mice were more sensitive to anoctamin-1 antagon

200 ns and levels of BDNF protein are highest in juvenile mice when adult motor patterns are shaped, whil

201 at Schaffer-collateral synapses monitored in juvenile mice, but again decreased NMDA-receptor mediate

202 ype 9 loss-of-function decreased survival in juvenile mice, but increased survival in adult mice with

203 ial defeat stress in males or females and in juvenile mice, which typically are excluded from classic

204 ns and decreased hepatic bacterial burden in juvenile mice.

205 tions, bacterial burden, and inflammation in juvenile mice.

206 The snake caught the juvenile monkey on the ground during a terrestrial play

207 lcium imaging to characterize the effects of juvenile monocular deprivation (MD) on the responses of

208 ries between monotremes and marsupials, with juvenile monotremes retaining a double articulation, sim

209 hPSC-PCs most closely matched those of late juvenile mouse PCs (P21).

210 ation in children with septic shock and in a juvenile murine model of sepsis.

211 easured ex vivo in fetal (n = 5-8/group) and juvenile (n = 8/group) offspring.

212 up FhKT1) are secreted by the newly excysted juveniles (NEJs), the stage responsible for host infecti

213 n in patients from seven families presenting juvenile neuromuscular disease.

214 atients were also assessed using the Hamburg Juvenile Neuronal Ceroid Lipofuscinosis (JNCL) scoring s

215 hich is modified because of gene mutation in juvenile neuronal ceroid lipofuscinosis (JNCL).

216 Groups of juvenile New Zealand White rabbits were administered 3 s

217 cquisition influenced the winter survival of juvenile North American red squirrels Tamiasciurus hudso

218 of this effect varied by fish body size with juveniles of small-bodied species showing higher vulnera

219 Male juvenile offenders (N=1,215) from three regions of the U

220 In juvenile offspring, insulin-stimulated glucose uptake wa

221 hows repetitive rotations and head tics with juvenile onset.

222 ortem tissues from seven adult-onset and one juvenile-onset HD individual.

223 tic cholestasis type 3 (PFIC3), an inherited juvenile-onset, cholestatic liver disease caused by homo

224 ed primary congenital glaucoma (PCG n = 22), juvenile open angle glaucoma (JOAG n = 16), glaucoma fol

225 We report a case of advanced juvenile open-angle glaucoma (JOAG) in which peripapilla

226 cause of childhood glaucoma after CYP1B1 and juvenile open-angle glaucoma after MYOC.

227 d in the investigation of both childhood and juvenile open-angle glaucoma, particularly when associat

228 f biallelic CPAMD8 variants to childhood and juvenile open-angle glaucoma.

229 od glaucoma and 2.1% (2/96) of probands with juvenile open-angle glaucoma.

230 ns during postnatal life (P2-14), but not in juvenile or adult windows, increased anxiety-, despair-,

231 15 and 11 years old) with diagnosed stage II juvenile osteochondritis dissecans (JOCD).

232 to a significant shift in the microbiomes of juvenile oysters that reduces fitness and impedes natura

233 Very few LDs were found in normal human juvenile pancreatic acinar and islet cells, with numbers

234 e on average 15.4% and a maximum of 73.9% of juveniles per m(2) per day.

235 ticle-dependent leaf permeability during the juvenile phase of plant development are controlled by th

236 y led to competitive release for established juvenile pinyons, changes in EMF community composition w

237 Compared with controls, juvenile PiZ/Chop (-/-) mice showed reduced hepatic ATZ

238 idenced by dampened long-term likelihoods of juvenile ponderosa pine presence in areas that experienc

239 from a 96 h in vivo exposure experiment with juvenile rainbow trout.

240 ally validated the simulated SE in slices of juvenile rat brain (both sexes) by pairing two-photon un

241 density, population structure (e.g. adult to juvenile ratio) and the strength of intraspecific compet

242 arterially perfused in situ preparations of juvenile rats, we recorded the activity of expiratory ne

243 ased with above-average precipitation during juvenile rearing.

244 Juvenile recruitment (<75.0 cm straight carapace length;

245 his climatic dipole with short-term postfire juvenile recruitment.

246 Juvenile red squirrel survival was lower in the years of

247 data on the survival of individually marked juvenile red squirrels, we tested how the timing of terr

248 r reef rugosity, disproportionately affected juvenile reef fishes when compared to adults, and explai

249 onnectivity, exploit > 500 species with high juvenile removal, and directly damage seagrass ecosystem

250 ing temperatures in excised leaf segments of juvenile rice plants.

251 lts not only suggest that many pools sustain juvenile salmon in non-drought years transition into eco

252 The abundance of parasitic, juvenile sea lampreys in the lakes is calculated by surv

253 We assessed juvenile sea lice abundance after 38 EMB treatments on s

254 there was, on average, an abundance of 0.12 juvenile sea lice per fish during the time period when t

255 6 emerging and legacy PFAS in livers from 31 juvenile seabirds from Massachusetts Bay, Narragansett B

256 Shifts in the return locations of juvenile seabirds migrating from the Irish Sea to Argent

257 for normal skoto- and photomorphogenesis in juvenile seedlings as well as long-term adult plant deve

258 Assessment of retinal topography in juvenile sharks indicated the presence of a distinct spe

259 surements of retinal spectral sensitivity in juvenile sharks, made using single flash and heterochrom

260 The effect of such treatments on juvenile skeletal muscle growth has yet to be investigat

261 hibition of the sleep center, abolishing the juvenile sleep state.

262 sociability that are profoundly affected by juvenile social experience.

263 Juvenile social isolation decouples dmPFC-PVI activation

264 Juvenile social isolation reduces sociability in adultho

265 temic estrogen synthesis blockade suppressed juvenile song production, neither systemic nor unilatera

266 daptive significance of wing development for juvenile songbirds under Arnold's (Integrative and Compa

267 labrum associated with the mouth opening in juvenile specimens of the megacheiran Leanchoilia illece

268 ify potent agents capable of blocking severe juvenile spine deformity.

269 mutant embryos develop normally into the mid-juvenile stage but demonstrate complete mortality by 2 m

270 e variation than their hosts, with a shorter juvenile stage duration than in constant temperatures an

271 Shortening the juvenile stage in citrus and inducing early flowering ha

272 small nub-like papillae during the parasitic juvenile stage, but SCCs were abundant on prominent papi

273 Juvenile survival to first breeding is a key life-histor

274 All of these function are critical to juvenile survival.

275 food resources become available would reduce juvenile susceptibility to predation and climatic factor

276 ung adult males (aged 1-3 years old), whilst juveniles that commenced spermatogenesis did so later in

277 In a 24.5 mm long juvenile the adult electric organ (EO) was not yet funct

278 he immunocompetent Tg(+) and Rag1 (KO)/Tg(+) juveniles, the Il2rg (KO)/Tg(+) and Il2rg (KO)/Rag1 (KO)

279 l after the transition of P. monophylla from juvenile to adult foliage.

280 ings reveal that coordinated transition from juvenile to adult involves branching of a linear pathway

281 copic morphology as the fish mature from the juvenile to the adult form.

282 e animal, lengthening during maturation from juvenile to the male phase and then gradually shortening

283 reous shell production and composition, from juveniles to large adults, mediates geographical pattern

284 the heterochronic pathway controls a timely juvenile-to-adult (J/A) transition.

285 maturation process of dmPFC-PVIs during the juvenile-to-adult transition.

286 it provides a temporal cue to facilitate the juvenile-to-adult transition.

287 Whole-plant harvests of mature and juvenile tropical deciduous trees, evergreen trees, and

288 in response to SBM-based diets, yellow perch juveniles up-regulate the cholesterol biosynthesis pathw

289 E13-13.5) corrected pre-mRNA splicing in the juvenile Usher syndrome type 1c (Ush1c) mouse mutant.

290 In contrast, the EOD of a 79 mm long juvenile was triphasic.

291 Recruitment of juveniles was dependent on the timing of breeding, being

292 males, expression fully stopped at stage 4 (juvenile), when male differentiation begins.

293 A 40 mm long juvenile, which produced a short biphasic EOD of 1.3 ms

294 mpt by an adult Boa constrictor (~ 2 m) on a juvenile white-faced capuchin (Cebus imitator) in the Se

295 Both juvenile wild-type mice and adult mice lacking ngr1 in L

296 s platform is suitable for gene insertion in juveniles with inherited disease, suggesting this approa

297 . lapponica, the unexpected finding of fewer juveniles with larger females suggests an increase in de

298 nscriptional differences in the intestine of juvenile yellow perch through RNA-sequencing (RNA-seq),

299 s have very few regenerating A. selaginoides juveniles yet tree-establishment reconstruction of fire-

300 ial deprivation reduced social preference in juvenile zebrafish.