ライフサイエンスコーパス: prepubertal

1 he dorsal penile nerve were not different in prepubertal (1,620 +/- 165 fibers per penis) and adult (

2 ur)) and Cftr(+/+) littermate controls at 6 (prepubertal), 10 (pubertal), and 14 (young adult) weeks

3 kidney, thymus, heart, spleen, liver, or in prepubertal 14day old rat testis.

4 d length and thickness of the mouse penis in prepubertal (3-4 week old) and adult (8-10 week old) mic

5 /or sexual abuse and 11 without a history of prepubertal abuse-and 14 healthy nonabused female volunt

6 bsolute BMR/RMR and TDEE in pubertal than in prepubertal adolescents.

7 Prepubertal African American (AA) youth compared with th

8 Subjects were 61 prepubertal African-American and Caucasian children.

9 , this disorder is now diagnosed even in the prepubertal age group.

10 in an aggressive MPN with death at a murine prepubertal age of 20 to 35 days (equivalent to an early

11 Changes were predominantly present at prepubertal ages (postnatal days 20 and 30).

12 enzymes (ApaI, BsmI, and TaqI) in 100 normal prepubertal American girls of Mexican descent.

13 the density of femoral and vertebral bone in prepubertal American girls of Mexican descent.

14 icrog/kg) and how these effects vary between prepubertal and adult conspecifics.

15 Oocyte endowment dwindles away during prepubertal and adult life until menopause occurs, and a

16 Sexually nai;ve prepubertal and adult male hamsters were exposed to cott

17 ssed by stem and progenitor spermatogonia in prepubertal and adult mouse testes.

18 rations of leptotene/zygotene spermatocytes, prepubertal and adult pachytene spermatocytes, as well a

19 myocytes isolated from the apex and base of prepubertal and adult rabbit hearts.

20 c buds from the urogenital sinus, during the prepubertal and androgen-driven proliferative expansion

21 the need for child informants in research on prepubertal and early adolescent bipolar disorder in chi

22 actor (BDNF) Val66 allele in children with a prepubertal and early adolescent bipolar disorder phenot

23 The prepubertal and early adolescent bipolar disorder phenot

24 s of recovery and relapse in children with a prepubertal and early adolescent bipolar disorder phenot

25 for mania in subjects who met criteria for a prepubertal and early adolescent bipolar disorder phenot

26 The definition of the prepubertal and early adolescent bipolar disorder phenot

27 imilarity between the characteristics of the prepubertal and early adolescent bipolar disorder phenot

28 xhibit increased anxiety-like behaviors over prepubertal and early adult development, show significan

29 A key question is whether a prepubertal and early-adolescent bipolar I disorder phen

30 pants with KS had received TRT, and all were prepubertal and had nonmosaic 47,XXY karyotypes.

31 nduced luteinizing hormone (LH) secretion in prepubertal and peripubertal females.

32 medial amygdala was significantly smaller in prepubertal and photoinhibited males compared to photost

33 levels of reproductive behavior exhibited by prepubertal and photoinhibited males would be correlated

34 the deficits in sexual behavior exhibited by prepubertal and photoinhibited males.

35 As ERalpha levels are elevated during the prepubertal and postmenopausal stages, these may represe

36 te a long-lasting activation in neurons from prepubertal and postpubertal mice of both sexes.

37 Data were dichotomized into prepubertal and pubertal groups and compared through the

38 ew DXA SM prediction model was developed for prepubertal and pubertal subjects (Tanner stage </=4) ag

39 No differences were detected between prepubertal and pubertal/postpubertal children.

40 In children they often present as prepubertal and/or peripubertal gynecomastia.

41 immunoreactivity was assessed in perinatal, prepubertal, and adult female and male rats.

42 RBM is a nuclear protein expressed in fetal, prepubertal, and adult male germ cells.

43 rm of the human prolactin receptor in fetal, prepubertal, and adult prostate.

44 ange, < 0.5-31 mug/dL), most boys (86%) were prepubertal, and mean +/- SD height and BMI z-scores wer

45 in epithelial cells of the fetal, neonatal, prepubertal, and normal adult prostate.

46 d for the epithelial cells from the uteri of prepubertal animals treated with PMSG, cells previously

47 of their dopamine afferents in adult but not prepubertal animals with a neonatal lesion.

48 ation on LHRH and/or gonadotropin release in prepubertal animals, nothing is known about the receptor

49 of gonadotropin secretion similar to that of prepubertal animals.

50 ptic activity differs between hemispheres in prepubertal animals.

51 sults are affirmed, the early recognition of prepubertal bipolar disorder will be important, so that

52 hydroxyvitamin D [25(OH)D] concentrations in prepubertal black and white girls (n = 83) living in nor

53 atric pelvis, including ambiguous genitalia, prepubertal bleeding, primary amenorrhea, pelvic mass, a

54 of which show opposing correlations between prepubertal BMI and male puberty.

55 st inverse predictor of pubertal timing than prepubertal BMI in boys.

56 st inverse predictor of pubertal timing than prepubertal BMI in boys.

57 idemiological correlations between increased prepubertal body mass and earlier pubertal timing in gir

58 Inclusion of girls' prepubertal body mass index slightly attenuated these as

59 Men with information on prepubertal body weight and BMI at 8 y of age and age at

60 In conclusion, prepubertal body weight is a more robust inverse predict

61 the critical weight hypothesis and tested if prepubertal body weight is a more robust inverse predict

62 Gynecomastia in a prepubertal boy is rare and should prompt an immediate e

63 analyzed retrospectively in 24 testes in 12 prepubertal boys (mean age, 4 years) and 49 testes in 25

64 ith IGF-1 was stronger for mid-pubertal than prepubertal boys (p = 0.04).

65 airflow values are present by spirometry for prepubertal boys than for age-matched girls; however, gr

66 ted possible causes of gynecomastia in three prepubertal boys who were otherwise healthy and had norm

67 d thicknesses to predict body fat in African prepubertal boys, controlling for chronologic age, was t

68 For prepubertal boys, testicular biopsy cryopreservation is

69 re significantly greater in pubertal than in prepubertal boys.

70 The decrease is partially reversed by prepubertal but not postpubertal gonadectomy.

71 t the presence of severe hyperinsulinemia in prepubertal carriers of the proline-467-leucine (P467L)

72 IUGR and increase IGF bioavailability during prepubertal catch-up growth.

73 Prepubertal children >or=5 y of age with IE were eligibl

74 y infrequently collected specimen types from prepubertal children <13 years of age.

75 Forty-two prepubertal children (20 girls and 22 boys) aged 4-10 y

76 Forty-four prepubertal children (22 AA and 22 AW) with comparable b

77 blind, placebo-controlled trial of CLA in 62 prepubertal children aged 6-10 y who were overweight or

78 Immune function was measured in 472 prepubertal children aged 6.5-9.5 y from 28 villages in

79 d serotonergic function has been observed in prepubertal children and adults with an acute episode of

80 hildren with SCD had significantly lower FM (prepubertal children and pubertal males only) and FFM (a

81 erg equations to predict body fat in African prepubertal children and to compare the results with bod

82 ge fat to body mass index (BMI; in kg/m2) in prepubertal children are programmed during intrauterine

83 nding of the regulation of energy balance in prepubertal children by using the doubly labeled water m

84 cid amplification tests (NAATs), to evaluate prepubertal children for N. gonorrhoeae or C. trachomati

85 ulinemia is a risk factor for weight gain in prepubertal children in the Pima Indian population-a pop

86 gth to the suggestion that percentage fat in prepubertal children is programmed in utero (independent

87 ects of vitamin D supplementation in healthy prepubertal children on physiologic outcomes have not be

88 d with the use of inhaled glucocorticoids in prepubertal children persisted as a reduction in adult h

89 s report prevalence rates ranging from 1% in prepubertal children to 4% in adolescents.

90 uscle cell culture model derived from normal prepubertal children to investigate the effects of insul

91 Thirty-four prepubertal children with ADHD and chronic multiple tic

92 for evaluating systemic exposure to ICSs in prepubertal children with asthma.

93 Eighteen prepubertal children with JRA and growth retardation rec

94 an be used to determine testicular status in prepubertal children with nonpalpable gonads, thus diffe

95 Prepubertal children with SCD fail to compensate for the

96 Prepubertal children with SCD-SS may have zinc deficienc

97 The most pronounced effect was seen in prepubertal children with SDS of 0.28 (95% CI, 0.14-0.41

98 ese subjects, the identification of affected prepubertal children within one of the original families

99 menopausal and postmenopausal females), age (prepubertal children), and the presence of hypoxia are t

100 There are no standard options for prepubertal children, and women with hematologic maligna

101 Prepubertal children, pubertal males, and pubertal femal

102 Specific infections in prepubertal children, such as Neisseria gonorrhoeae or C

103 bias in MC-associated diseases is evident in prepubertal children, suggesting early-life origins of s

104 gative effect on bone mineralization even in prepubertal children, which can be demonstrated despite

105 ut the appropriateness of this threshold for prepubertal children.

106 e for predicting body fat in 9-y-old African prepubertal children.

107 ical growth and serum zinc concentrations of prepubertal children.

108 determine if similar relationships exist in prepubertal children.

109 safety and efficacy of bariatric surgery in prepubertal children.

110 years after transplantation, particularly in prepubertal children.

111 a temporary reduction in growth velocity in prepubertal children.

112 the form of the cranial base differs between prepubertal Class I and Class III subjects.

113 ed and control animals at juvenile (day 20), prepubertal (day 30), postpubertal (day 56), and adult (

114 ductive tracts were excised on days 5 or 10 (prepubertal), day 30 (pubertal), day 90 (young adult), o

115 gene; its expression is induced later during prepubertal development (between days 23 and 30 post par

116 To examine SC function during fetal and prepubertal development we generated two transgenic mous

117 ion differentially, and predominantly during prepubertal development.

118 ence of cognitive function, primarily during prepubertal development.SIGNIFICANCE STATEMENT Parvalbum

119 , significantly more of the subjects who had prepubertal diagnoses of major depressive disorder (N=24

120 Subjects who had prepubertal diagnoses of major depressive disorder also

121 subjects and included 72 subjects who had a prepubertal diagnosis of major depressive disorder and 2

122 miR-30 binding to Mkrn3 3' UTR, reversed the prepubertal down-regulation of hypothalamic Mkrn3 protei

123 (Eda) as a unique regulator of embryonic and prepubertal ductal morphogenesis.

124 Prepubertal EE also prevented hyperactivity in the ventr

125 Twenty-day prepubertal EE is sufficient to prevent DA hyperresponsi

126 Prepubertal EE prevented the increased population activi

127 ehaviors in MAM rats were not ameliorated by prepubertal exposure to EE.

128 dissociated from brain slices prepared from prepubertal female GnRH-EGFP mice.

129 Ca,L) were not significant in adult male and prepubertal female hearts.

130 Normal prepubertal female mice injected with leptin grew at a s

131 Consistent with this, treatment of prepubertal female mice with the mitotic germ-cell toxic

132 were implanted into the mammary fat pads of prepubertal female mice.

133 hat 17 beta-estradiol (E2) administration to prepubertal female rats leads to acquisition of the abil

134 mone-releasing hormone (LHRH) secretion from prepubertal female rats.

135 ubset of GnRH neurons in the hypothalamus of prepubertal female rats.

136 tic and environmental risk factors among 182 prepubertal female, 237 prepubertal male, 314 pubertal f

137 of the mammary glands approximated that of a prepubertal female.

138 es in the BL: in acute slices from juvenile (prepubertal) female rats, wash-in of letrozole virtually

139 Behavioral hyporesponsiveness in prepubertal females may be due, in part, to deficiencies

140 Estrogen treatment of prepubertal fish elicited increases in tac3a, kiss1, kis

141 es of an NMDA antagonist cause an adult or a prepubertal form of neurodegeneration, depending on the

142 tudies in mammary whole mounts revealed that prepubertal genistein exposure resulted in fewer termina

143 few years, large advances have been made in prepubertal germ cell storage aimed at subsequent transp

144 on, notably for self-renewal genes, in these prepubertal germline cells between two species that dive

145 ns raise the suspicion for sexual abuse in a prepubertal girl, but the findings do not independently

146 usted energy intake tended to be lower among prepubertal girls (905 +/- 140 kcal) than among females

147 um 25(OH)D concentration was assessed in 168 prepubertal girls aged 4-8 y living in the southeastern

148 reater degree of subclinical air trapping in prepubertal girls because residual volumes are not detec

149 lial resemblance of body composition between prepubertal girls of normal weight and body fatness and

150 The body composition of prepubertal girls of normal weight and body fatness is s

151 nce in EE between normal-weight, multiethnic prepubertal girls predisposed to obesity and those not p

152 al trauma from sexual abuse, the majority of prepubertal girls will not have a hymenal transection (s

153 red in normal-weight-for-height, multiethnic prepubertal girls with or without a familial predisposit

154 d physical fitness on weight and fat gain in prepubertal girls with or without a predisposition to ob

155 Intestinal carriage of Escherichia coli in prepubertal girls without a history of urinary tract inf

156 cluded were poor-quality studies; studies of prepubertal girls, men, women without the potential for

157 lly diverse population groups, as well as in prepubertal girls, young adult and postmenopausal women,

158 xual abuse as the cause of genital trauma in prepubertal girls.

159 itamin D [25(OH)D] and bone were examined in prepubertal girls.

160 cantly lower among pubertal girls than among prepubertal girls.

161 These findings were strongest in prepubertal girls.

162 rine growth retardation (IUGR) and increased prepubertal growth rate in female lambs.

163 play of progesterone-facilitated lordosis in prepubertal guinea pigs following MPOA lesions is due to

164 igh systemic estrogen levels, short stature, prepubertal gynecomastia and testicular failure in males

165 Most cases of male prepubertal gynecomastia are classified as idiopathic.

166 o lavender and tea tree oils probably caused prepubertal gynecomastia in these boys.

167 ional dimensions were studied in 31 pairs of prepubertal healthy white girls and boys 5-10 years of a

168 ggests birth weight is a better predictor of prepubertal height than is self-reported midparental hei

169 B, Bcl6b) were more highly expressed in both prepubertal human spermatogonia and mouse gonocytes than

170 Essentially pure populations of prepubertal human spermatogonia and mouse gonocytes were

171 arche, a key endocrine event associated with prepubertal increases in the adrenal production of andro

172 onstrated that in a mildly to moderately ill prepubertal JRA population that had never been exposed t

173 We also show that female prepubertal Kiss1 neurons are under higher inhibitory in

174 tly at T2, T3, and T4, but decreases to near prepubertal levels at T5; and 3) while insulin resistanc

175 onset of puberty (T2), but returned to near prepubertal levels by the end of puberty (T5).

176 al laser microscopy revealed that subsets of prepubertal LHRH neurons are endowed with alpha 1, alpha

177 e NO, hence generating cGMP and resulting in prepubertal LHRH release.

178 notype of peritubular myoid cells (PTMCs) in prepubertal life; (2) to maintain the ALC progenitor pop

179 nal study, the mean age of the children with prepubertal major depressive disorder was 10.3 years (SD

180 ound in the one other adult outcome study of prepubertal major depressive disorder.

181 ear to be of physiologic significance, since prepubertal male mice (age 5 wk) displayed accelerated b

182 reased avoidance in both sexes of adults and prepubertal male partners.

183 ell patch-clamp recordings were performed on prepubertal male rat hypothalamic slices, where TIDA neu

184 sk factors among 182 prepubertal female, 237 prepubertal male, 314 pubertal female, and 171 pubertal

185 Half of the prepubertal males (P7-P14) received 200 micrograms of te

186 testosterone (500 microg/kg) pretreatment in prepubertal males administered LPS restored the expressi

187 display of reproductive behavior in adults, prepubertal males do not engage in these same behaviors.

188 POA DOPAC concentrations did not increase in prepubertal males exposed to pheromone.

189 Even a 2.5-fold higher load of LPS in prepubertal males failed to produce aversive odor cues,

190 We also found that prepubertal males have a larger anterior subdivision of

191 d that, specifically in the left hemisphere, prepubertal males have approximately 80% more excitatory

192 at the left MeApd is significantly larger in prepubertal males than females.

193 o puberty may contribute to the inability of prepubertal males to display reproductive behavior.

194 per se did not influence odor properties of prepubertal males, indicating that estrogen receptors ma

195 Because estradiol induced PR in prepubertal males, these data also suggest that ERa is f

196 nd if so, whether this response is absent in prepubertal males, which do not mate.

197 hen they were exposed to odor of LPS-treated prepubertal males.

198 activated behavior in postpubertal, but not prepubertal, males.

199 nical presentations and biologic behavior of prepubertal melanoma are discussed.

200 This is the largest known study of prepubertal melanoma patients.

201 1% (128 of 142) had diagnosed no more than 2 prepubertal melanomas in the past 5 years.

202 In cultured ovarian explants from prepubertal mice containing preantral follicles, treatme

203 Prepubertal mice overexpressing adiponectin from adipose

204 Oral antibiotic treatment of prepubertal mice prevented this cognitive impairment, bu

205 With prepubertal mice, allogeneic SSCT resulted in attainment

206 rn3 mRNA were high in the arcuate nucleus of prepubertal mice, decreased immediately before puberty,

207 gradient analyses of testes from 21-day-old prepubertal mice, which contain early round spermatids a

208 ns minimally colocalize with Kiss1(hrGFP) in prepubertal mice, ~30% of GHRH neurons coexpressed both

209 ]hexane-4,6-dicarboxylate) in adult, but not prepubertal, mice born to stressed mothers during pregna

210 eurons was lower in postpubertal relative to prepubertal monkeys.

211 essential for early folliculogenesis in the prepubertal mouse ovary.

212 Northern analyses of prepubertal mouse testes revealed that the time course o

213 In contrast, DNA from prepubertal mouse testis and from purified spermatocytes

214 There is also evidence that prepubertal neglect in children causes abnormal metaboli

215 findings are indicative of a characteristic prepubertal neuroanatomical phenotype that may be associ

216 lated C-peptide-modeled insulin secretion in prepubertal normal-weight AA versus C peers during a 2-h

217 BMI) (weight (kg)/height (m)(2))) effects of prepubertal OCP tertiles and quintiles with biomarkers.

218 ibodies only to clustered AChRs had frequent prepubertal onset (62.5% [median age, 6 years; age range

219 17-year-old boy with severe gynecomastia of prepubertal onset and hypogonadotropic hypogonadism caus

220 Gynecomastia of prepubertal onset may result from increased estrogen owi

221 eafness, constant vestibular dysfunction and prepubertal onset of retinitis pigmentosa.

222 ects with bipolar disorder presenting with a prepubertal onset was significantly higher in the later

223 rbidity in clinically referred children with prepubertal-onset MDD and anxiety, but continuity and sp

224 selecting clinically referred children with prepubertal-onset MDD for inclusion in genetic studies u

225 The clinical outcome of children with prepubertal-onset MDD in adulthood includes a high risk

226 Children with prepubertal-onset MDD with a recurrence of MDD during fo

227 Prepubertal onsets were uncommon, but high-risk offsprin

228 NMDA failed to stimulate GnRH/LH release in prepubertal or gonadally intact mutant male mice.

229 ature, pregnant, and postweaning, but not in prepubertal or lactating mammary glands.

230 muscle and stromal cells taken from uteri of prepubertal or PMSG-treated rats (shown previously to ex

231 Prepubertal ovariectomy of Wnt-1 TG mice also extended t

232 In contrast, prepubertal ovariectomy, which arrested mammary epitheli

233 aging, pathology, and clinical management of prepubertal paratesticular and testicular tumours.

234 Prepubertal participants (n = 12) had lower average BMI

235 n the budesonide group occurred primarily in prepubertal participants.

236 Prepubertal patients appeared to have the greatest benef

237 rimental method to preserve the fertility of prepubertal patients before they initiate gonadotoxic th

238 Among 57 patients who had an SLNB, prepubertal patients had a higher percentage of sentinel

239 month 36 were comparable, whereas growth in prepubertal patients on EVR + rTAC was better (P = .050)

240 85 and 131 percent, respectively, in the six prepubertal patients.

241 Growth improved in 3/3 growth-delayed prepubertal patients.

242 n age, 14.9 years; age range, 2-18 years; 28 prepubertal patients; 286 postpubertal patients; 260 fem

243 The data also highlight the prepubertal period as a sensitive time for redox-related

244 t injections of genistein in rats during the prepubertal period resulted in a 50% reduction of chemic

245 the face of abnormal hormonal stimuli in the prepubertal period.

246 were immunodetectable in oocytes during the prepubertal period.

247 case history, eliminated the possibility of prepubertal periodontitis and suggested a diagnosis of s

248 This condition was previously classified as prepubertal periodontitis, a disease diagnosis that focu

249 ed to acute and repeated footshock stress at prepubertal, peripubteral, and adult ages.

250 jor depressive disorder-21 with a history of prepubertal physical and/or sexual abuse and 11 without

251 he long-term electrophysiological effects of prepubertal (postnatal day 21-40) EE on DA neurons, pyra

252 In ovariectomized prepubertal PR-A transgenic mice, end buds with unusual

253 cantly reduced after AP-1 blockade in adult, prepubertal, pubertal, and hormone-stimulated mammary gl

254 ion under a constitutive active WAPCre(c) in prepubertal/pubertal mice, but not under MMTVCre in adul

255 In prepubertal rabbits (and children), the arrhythmia pheno

256 fore, we cultured testicular germ cells from prepubertal rabbits in the presence of GDNF and FGF2 and

257 In prepubertal rabbits, peak I(Ca,L) at the base was 22% hi

258 ommon to all organs, including the adult and prepubertal rat testis.

259 ABP(II) expression] was also observed if the prepubertal rat was treated with estrogen before cell co

260 s that double-labeled with NMDA-R1 was 2% in prepubertal rats and 3% in pubertal rats; this increased

261 evels of retinoic acid than did the uteri of prepubertal rats treated with the control vehicle.

262 ine surface epithelial cells by treatment of prepubertal rats with pregnant mare serum gonadotropin (

263 e expression of aversive odor in LPS-treated prepubertal rats.

264 The MeApd is also sexually dimorphic in prepubertal rats.

265 lantations into the testes of 18 adult and 5 prepubertal recipient macaques that were rendered infert

266 n the ejaculated sperm of 9/12 adult and 3/5 prepubertal recipients after they reached maturity.

267 renal (HPA) axis function of male and female prepubertal rhesus monkeys.

268 te an essential role of UPF2-mediated NMD in prepubertal SC development and male fertility.

269 Higher prepubertal serum HCB and betaHCH concentrations were as

270 rocytes as wild-type males at this age, this prepubertal sexual dimorphism is independent of ARs.

271 Collectively, our findings indicate that prepubertal skin is colonized by diverse fungi, whereas

272 aches in vivo to show that during the first, prepubertal, spermatogenic cycle (i) RALDH-dependent syn

273 ed in conscious female rhesus monkeys at the prepubertal stage using a push-pull perfusion method.

274 etarded with reduced ductal branching in the prepubertal stages, and fewer Cap cells in the terminal

275 pathological lesions more rapidly than their prepubertal standard-diet counterparts.

276 with inactivity (e.g., at age 50 years) were prepubertal stature (5% lower odds per 1-standard deviat

277 .41); P = 0.06), and significantly better in prepubertal subjects (0.50 (0.16, 0.84); P = 0.004).

278 in trabecular vBMD z scores were greater in prepubertal subjects.

279 occipital pole that was most significant in prepubertal subjects.

280 eria: presence of OCD and/or a tic disorder, prepubertal symptom onset, episodic course of symptom se

281 een for pubertal (Tanner stages 2-4) but not prepubertal (Tanner stage 1) white children over the ran

282 All patients were prepubertal (Tanner stage I or II) and had never taken c

283 is tightly regulated in fetal, neonatal, and prepubertal testes and adult ovaries and is well conserv

284 Color Doppler US depicted flow in 20 prepubertal testes and in all 49 postpubertal testes.

285 ng substance, produced constitutively by the prepubertal testes, promotes involution of the mullerian

286 essels, but flow cannot be identified in all prepubertal testes.

287 Prepubertal testicular and paratesticular tumours are a

288 depletion of both SCs and germ cells during prepubertal testicular development.

289 de the proof of principle that cryopreserved prepubertal testicular tissues can be autologously graft

290 SCR transcripts were undetectable in the prepubertal testis but were readily identified in sperma

291 ly from SC, germ cell or PTMC support in the prepubertal testis.

292 We further showed that in prepubertal Tg glands, signaling was mediated by formati

293 ctivated the PI3K/Akt pathway in glands from prepubertal Tg mice, resulting in increased cyclin D1 ex

294 gestation, at birth, approximately 5 months (prepubertal, the catch-up growth period), and approximat

295 tantly, pharmacological deprivation of NO in prepubertal to pubertal animals stiffens the extracellul

296 Mammary glands from prepubertal transgenic mice had significantly increased

297 oduced by cultured epithelial cells from the prepubertal uteri [shown previously to be negative for C

298 Normal-weight, prepubertal white (n = 52), African American (n = 30), a

299 In the prepubertal years, exercise results in periosteal gains,

300 In conclusion, AA and C prepubertal youth both demonstrated a decline in beta-ce