ライフサイエンスコーパス: femur

1 mparable SUV in the prominent lesions in the femur.

2 tric collectives were found in the lungs and femur.

3 T12, L5, sacrum, right iliac bone, and right femur.

4 process at the anteriodistal surface of the femur.

5 right iliac bone, and 3.90+/-1.57 for right femur.

6 th-like trunk, shoulder, pelvis and proximal femur.

7 cancer cells in the medullary channel of the femur.

8 sing geometrical deformities of the proximal femur.

9 ADSCs in an osteochondral defect of the left femur.

10 re associated with the shape of the proximal femur.

11 asal level at 4 wk in nonirradiated proximal femur.

12 , but no recovery was observed in the distal femur.

13 lytic and sclerotic lesions in vertebrae and femur.

14 tic MASIs in cartilage defects of the distal femur.

15 n of the pelvic girdle and retraction of the femur.

16 ity was observed in the P3 MSC sheet-grafted femur.

17 in pelvic girdles and small rudiments of the femur.

18 n several vertebras and in the proximal left femur.

19 lants were inserted in the distal end of the femurs.

20 bitors in bone tissues harvested from rabbit femurs.

21 ng was enhanced in Dmp1-Cre(+/-);Rosa(Notch) femurs.

22 95% CI, 0.90-0.91 g/cm2; P = .08) and total femur (0.94 g/cm2; 95% CI, 0.90-0.99 g/cm2 vs 0.99 g/cm2

23 0.71, P = .008, respectively), right medial femur (0.94 vs 0.72, P = .046), and right lateral tibia

24 teophyte detection in left and right lateral femur (0.96 vs 0.75, P = .025, and 1.00 vs 0.71, P = .00

25 curring in the subtrochanteric or diaphyseal femur, a combined rate of 2.3 per 10,000 patient-years.

26 n errors of -14% and -23% in bone marrow and femur-adjacent VOIs can affect PET quantification in the

27 4% +/- 5% and -23% +/- 6% in bone marrow and femur-adjacent VOIs with physiologic uptake for SEGbase,

28 s and reduced interpatient bias variation in femur-adjacent VOIs.

29 for segmentation were 0.97 +/- 0.09 for the femur and 0.96 +/- 0.11 for the tibia.

30 del was built from a CT scan of a real human femur and compared to the simplified femur model.

31 ranching in ways that differ in the proximal femur and distal tibia, based on motoneuronal birth orde

32 At the end of the study, BV/TV%, proximal femur and hemi-mandible bone mineral content and bone mi

33 om 21 to 27 wk was associated with increased femur and humerus lengths at 28 wk.Maternal weight gain

34 gnificantly positively associated with fetal femur and humerus z scores (P < 0.01).

35 Fetal femur and humerus z scores and neonatal birth length wer

36 , maternal 25(OH)D was associated with fetal femur and humerus z scores only when maternal calcium in

37 ed up to 3 times across gestation, and fetal femur and humerus z scores were generated.

38 ity and microarchitecture in weight bearing (femur and humerus) and non-weight bearing (2(nd) lumbar

39 abecular separation and trabecular number of femur and lumbar, serum osteocalcin, total calcium, inta

40 MD in total femur, and lower BV/TV in distal femur and LV in both genotypes.

41 st and ZOL the highest Ca and Pi contents in femur and maxilla (P < 0.05).

42 SCs) in an osteochondral defect of the right femur and mitomycin-pretreated apoptotic ADSCs in an ost

43 The femur and pelvis of Ardipithecus ramidus have characters

44 imaging (DTI) and tractography in the distal femur and proximal tibia related to age, sex, and height

45 iphery of the physis, and between the distal femur and proximal tibia.

46 tures with improved outcomes in the proximal femur and shaft.

47 level, parathyroid hormone (PTH) level, and femur and spine BMD T scores were compared before and 1

48 tic lesions, with the largest improvement in femur and spine lesions.

49 Exd are required for dAP-2 expression in the femur and that a conserved Exd/Hox binding site is essen

50 (CGRP) in both the peripheral cortex of the femur and the ipsilateral dorsal root ganglia (DRG).

51 bone mass phenotype (LBM) in both the distal femur and the vertebra of Krox20(+/-) mice.

52 e in anteroposterior bending strength of the femur and tibia occurs beginning in the Neolithic ( appr

53 BMSCs isolated from femur and tibia of Sprague-Dawley rats were seeded onto

54 Hdac3 deficiency reduced femur and tibia periosteal circumference and increased c

55 al neural network was trained to segment the femur and tibia versus manual segmentation.

56 ent on the ground, the bone mass of humerus, femur and tibia was measured using micro-computed tomogr

57 ns of tibiofemoral joint (medial and lateral femur and tibia) was recorded.

58 In the physis of the femur and tibia, a significant age-related decrease was

59 BMCs were harvested from femur and tibia, and the expression of surface markers o

60 in showed significant strengthening in their femur and tibia, as measured by maximum force sustained

61 s foot is exceptionally long relative to the femur and tibia, proportions never before documented in

62 ology analyses of bone showed destruction of femur and tibia.

63 ns and prevented mechanical weakening of the femur and tibia.

64 e prediction of failure load of the proximal femur and to identify the best densitometric or geometri

65 separation (Tb.Sp) in trabecular bone of the femur and vertebra.

66 res in childhood, including fractures of her femur and wrist; fractured her ankles several times in h

67 e sialoprotein (BSP) and osteonectin in both femurs and bone marrow osteoblastic cells of mice.

68 ll defects in the mid-diaphysis of E18 chick femurs and cultured organotypically for 10 d.

69 omputed tomography (microCT) analyses of the femurs and lumbar vertebrae revealed delayed or incomple

70 mineral density and bone mineral content in femurs and lumbar vertebrae when compared with the wild-

71 Despite microanatomical differences in femurs and sterna, their adult alpha-catulin-GFP+ HSCs h

72 2 was also expressed at higher levels in the femurs and tibias of Aldh1a1(-/-) mice with accompanying

73 mia lose cortical and trabecular bone in the femurs and vertebrae (bone mineral density was decreased

74 strength, and the loss of trabecular bone in femurs and vertebrae following Folfiri administration.

75 In the stylopod (humerus and femur) and sternum, bone marrow MSCs express other regio

76 t were placed in the physis of the tibia and femur, and in the epiphyseal and articular cartilage of

77 HU resulted in lower BMC and BMD in total femur, and lower BV/TV in distal femur and LV in both ge

78 (BMD) of the femoral neck, trochanter, total femur, and lumbar spine (L2-L4) were measured by using d

79 The whole joint (i.e., tibia, femur, and patella) 3-D bone shape vector had the strong

80 atherlike structures around the humerus, the femur, and the tibia.

81 d crossbite, straightening of the tibias and femurs, and correction of the growth-plate defect.

82 f the principal nutrient artery (PNA) of the femur are associated with changes in trabecular bone vol

83 tical irregularities at the posterior distal femur are common incidental findings in adolescents, but

84 their developmental time, size (length of a femur as a proxy) and resistance to starvation without a

85 Its proximal femur, BAR 1002'00, was originally described as being ve

86 owest decile of growth velocity of the fetal femur between 20 and 28 weeks was associated with increa

87 Following euthanasia, femur biomechanics were assessed by 3-point bending and

88 GH treatment increased femur BMD and lean body mass but decreased the % fat mea

89 Femur BMD improved in 18.8% of medically treated patient

90 Pelvic radiographs and proximal femur BMD measurements were obtained in 53 women aged 79

91 ed with significant improvement in spine and femur BMD, suggesting that the superior effects of surge

92 Femur bone density was unchanged in mice heterozygous fo

93 transfection following a single treatment of femur bone marrow isolated rat MSCs with efficiencies fo

94 CRB-15 also delayed loss of femur bone mineral density and trabecular microarchitect

95 was greater than 20% (FRAX), quantitative CT femur bone strength was less than 3000 N, or occurrence

96 sulted in lower cortical bone accrual in the femur but had no effect on cortical bone in the humerus

97 wing an increase in the irradiated BM of the femurs, but not the tibias, of HBS animals when compared

98 Later, the patella is separated from the femur by a joint formation process that is regulated by

99 dially reformatted MR images of the proximal femur by two independent readers.

100 nsity (BMD) of the lumbar spine and proximal femur (by DXA), liver function, and bone markers were me

101 at chondroitin sulfation across the proximal femur cartilage varied dramatically in dtd, but not in t

102 r changes in bone mineral composition in the femur compared to respective controls.

103 wer DXA measurements of the lumbar spine and femur compared with nonusers.

104 atible plate surgically fixated to the mouse femur containing a gradient refractive index lens.

105 The highest increase was seen in BV in femurs containing the HUVEC and HBMSC monocell construct

106 3, increased approximately 50% at the distal femur cortical bone region but not at trabecular bone re

107 ginate hydrogel carrying PRP was tested on a femur defect model ex vivo.

108 used an ex vivo [embryonic day (E)18] chick femur defect model to examine the bone regenerative capa

109 Mechanical testing of the femurs demonstrated that loss of bone in the mice with h

110 monitored the differentiation of human fetal-femur derived skeletal cells into cartilage in three-dim

111 hominins) and reconstruct hominoid proximal femur evolution using squared-change parsimony.

112 association between stimulant use and total femur, femoral neck, and lumbar spine bone mineral conte

113 otion (ROM) using a novel computer navigated femur first approach to conventional THA.

114 Navigation guided femur first THA is able to improve alignment of ROM axis

115 s and underwent ultrasonography to determine femur (FLZ) and humerus (HLZ) length z scores.

116 verse sequences over the proximal and distal femur for antetorsion measurement.

117 g respective bone matrices in osteotomies on femurs for 14 and 28 days and evaluated by microcomputed

118 ne marrow neuropathy was studied by staining femurs for tyrosine hydroxylase (TH) and neurofilament 2

119 The risk of atypical femur fracture increased with longer duration of bisphos

120 from normal hip cartilage donated by neck of femur fracture patients.

121 The absolute risk of atypical femur fracture remained very low as compared with reduct

122 taining intramedullary nail that facilitates femur fracture repair in rats with ovariectomy-induced o

123 Series 1: femur fracture was induced in anesthetized rats, followe

124 although the early inflammatory reaction to femur fracture was marginally enhanced.

125 ur fracture, or laparotomy with cecetomy and femur fracture with muscle tissue damage (polytrauma).

126 onecrosis of the jaw, four (1%) had atypical femur fracture, and four (1%) had hypercalcaemia occurri

127 emorrhage and hemorrhage with laparotomy and femur fracture, induced a loss of circulating CD4(+) T c

128 -hemorrhage), hemorrhage with laparotomy and femur fracture, or laparotomy with cecetomy and femur fr

129 After femur fracture, the inflammatory response was altered an

130 bisphosphonate use: atypical subtrochanteric femur fracture.

131 The primary outcome was atypical femur fracture.

132 ,752 patients with incident diagnoses of hip/femur fractures (cases), 130,471 matched members without

133 We reviewed 284 records for hip or femur fractures among 14,195 women in these trials.

134 n regarding the association between atypical femur fractures and bisphosphonates and other risk facto

135 Osteonecrosis of the jaw and atypical femur fractures have been reported with treatment but ar

136 However, concerns about atypical femur fractures have contributed to substantially decrea

137 s other regionally restricted Hox genes, and femur fractures heal normally in Hox11 mutants.

138 Among 196,129 women, 277 atypical femur fractures occurred.

139 adiographs (when available) from all hip and femur fractures to identify those below the lesser troch

140 hyseal flare (subtrochanteric and diaphyseal femur fractures) and to assess atypical features.

141 ist fractures to 8 days (IQR, 5-12 days) for femur fractures.

142 were highest for vertebral, pelvis/hip, and femur fractures.

143 Pigs underwent polytrauma (femur fractures/lung contusion, P), hemorrhage (mean art

144 evolutionary transformations of the proximal femur from a similar ancestral morphology that is not se

145 nical testing, with random assignment of one femur from each pair to the single-limb stance configura

146 e we report the complete mtDNA of an archaic femur from the Hohlenstein-Stadel (HST) cave in southwes

147 Microcomputed tomography analyses of femurs from CCR3-deficient mice revealed a bone phenotyp

148 at the lumbar spine, femoral neck, and total femur (grams per square centimeters).

149 testing confirmed that P3 MSC sheet-grafted femurs had the highest biomechanical strength in the thr

150 Avascular necrosis of the femur head (AVNFH) is a debilitating disease caused due

151 lls (training: 6 [5.7%], control: 4 [3.8%]), femur/hip fracture (2 in each group), pneumonia (trainin

152 rter imaging in hematopoietic niches such as femurs, humeri, vertebrae, and the thymus.

153 Spoiled gradient-echo in vivo images of the femur, humerus, upper spine, and lower spine were acquir

154 Cancellous bone loss in femur in both genotypes was associated with increases in

155 nd microarchitecture in the lumbar spine and femur in F508del mice.

156 reased radial bone expansion of the midshaft femur in female N-ERalphaKO along with higher serum leve

157 g ultrapure magnesium into the intact distal femur in rats.

158 ations were seen at the trochanter and total femur in women.

159 behavior and bone structure in the proximal femur, indicating that more highly mobile human populati

160 ats declines were higher than pancreatic and femur intermuscular fats (1% to 2%) loss.

161 conclude, slow growth velocity of the fetal femur is associated with an increased risk of sPTB.

162 f 20 kV for the following examinations: hip (femur), knee, ankle, and computed tomographic (CT) angio

163 more evenly distributed among motions of the femur, knee, and ankle.

164 before week 12 showed reduced growth only in femur length (-5.5; 95% CI: -10.1, -0.9).

165 mference (AC), estimated fetal weight (EFW), femur length (FL), and biparietal diameter (BPD) during

166 vidual fetal parameters (head circumference, femur length [FL], and abdominal circumference [AC]) fro

167 er, humerus length, abdominal circumference, femur length and its ratio with head circumference and w

168 lume fraction (BV/TV) in distal femur, lower femur length and total bone area, mineral content (BMC)

169 cental VDR was a positive predictor of fetal femur length Z score (P=0.018; R(2)=0.06) and was positi

170 nfirm initially observed loci for one trait (femur length), and, when the two groups were merged, the

171 Biparietal diameter, femur length, abdominal circumference, and estimated fet

172 growth characteristics (head circumference, femur length, abdominal circumference, and weight) were

173 occlusion, 10% lower body weight, 3% reduced femur length, and 30% elevated serum alkaline phosphatas

174 head circumference, abdominal circumference, femur length, and biparietal diameter are negatively ass

175 Ultrasound measures of head circumference, femur length, and estimated fetal weight from middle and

176 The reduction was greatest in femur length, at -9.4% (95% confidence interval -13.4, -

177 ormal by radiography, with no differences in femur length, cortical/trabecular structure or mineral d

178 ontal diameter, abdominal circumference, and femur length--were obtained every 5 weeks (within 1 week

179 eatments resulted in significantly increased femur length.

180 (0.8), 0.03 mm (0.8), and -0.65 mm (0.8) for femur length.

181 ine) were linear for biparietal diameter and femur length.

182 llous bone volume fraction (BV/TV) in distal femur, lower femur length and total bone area, mineral c

183 A total of 40 pairs of excised cadaver femurs (mean patient age at time of death, 82 years +/-

184 ontrol animals in lumbar vertebra and distal femur metaphysis and epiphysis; significant differences

185 loss (compared to baseline controls) in the femur metaphysis was associated with lower trabecular nu

186 spatial-resolution 3-T MR images of proximal femur microarchitecture can allow detection of lower ela

187 Images of proximal femur microarchitecture were obtained by using a high-sp

188 show improvements in new bone quality in rat femur model.

189 l human femur and compared to the simplified femur model.

190 to obtain critical stresses within the human femur model.

191 Geometrically simplified human femur models with different curvatures were developed an

192 consistently show increased rates of humerus/femur morphological evolution.

193 Primary tumor locations included the femur (n = 17; 50%), tibia (n = 9; 26%), and humerus (n

194 or patients with fracture to the neck of the femur (NOF) was assessed using a low-density array.

195 Studies to repair a femur non-union fracture demonstrate only osteogenic pro

196 d structures observed around the humerus and femur of Kulindadromeus are support fibers associated wi

197 al endothelial cells respectively inside the femur of mice bearing early, middle and late stage metas

198 cise reduced progression of OA in the medial femur of obese mice.

199 vantage of the first well-preserved proximal femur of the early Oligocene stem catarrhine Aegyptopith

200 ay a portion of trichome-free cuticle on the femur of the second leg called the "naked valley." It wa

201 metres long), likely including the holotype femur of Timimus hermani, and a single cervical vertebra

202 ion of ephrinB1 and EphB1, as well as B3, in femurs of adult mice injected with alendronate (10 micro

203 lysis was performed using RNA extracted from femurs of COP, DA, F344 and LEW rats.

204 The femurs of each animal were subdivided into test and cont

205 e distal and proximal ablations in the right femurs of eight pigs.

206 ortical thickness and sub-periosteal area in femurs of HMWKO.

207 anium Kirshner-wire was surgically placed in femurs of LysEGFP mice, which possess EGFP-fluorescent n

208 cations of megakaryocyte accumulation in the femurs of mice after injection of metastatic or non-meta

209 rentiation, were reduced dramatically in the femurs of Myoc-null mice compared with wild-type mice.

210 k, there were numerous tdTomato(+) OC in the femurs of TRAP tdTomato mice but almost none in WT mice.

211 lines, whereas RUNX2 levels were elevated in femurs of Wwox-deficient mice.

212 pQCT evaluation of femurs of young adult male progeny of three lines showed

213 %), with the primary lesion diagnosed in the femur on sPET that persisted on iPET.

214 cortical parameters, and resulted in shorter femurs on postnatal day 21.

215 s: trial group; location of tumour (proximal femur or proximal humerus vs other limb vs axial skeleto

216 years of age with isolated fractured neck of femur or pubic ramus fracture were excluded.

217 atric patients (</=18 years) the pattern was femur (OR, 20.6; 95% CI, 8.4-48.1), humerus, then verteb

218 nd to influence new bone formation in a 3 mm femur osteoporotic defect model in ovariectomized rats.

219 renoreceptor (AR) blocker propranolol before femur osteotomy prevented bone marrow mobilization of ne

220 In addition, the mice were subjected to a femur osteotomy.

221 aling, 12-week-old C57BL/6J mice underwent a femur osteotomy.

222 terns of tractography varied with age in the femur (P < .001) and tibia (P < .001).

223 aBMD at the femoral neck (P = .05) and total femur (P < .05) but no differences at other sites.

224 significantly larger than that of the right femur (P = .01 for reader 1, P = .02 for reader 2).

225 s associated with significant improvement in femur (P = 0.03) and spine BMD (P < 0.001).

226 icient (P < .001 for both), axial diffusion (femur, P = .001; tibia, P < .001), and transverse diffus

227 physes were longer than those in the center (femur, P = .005; tibia, P = .004).

228 s significantly lower than sham (P = 0.0001, femurs; P < 0.0001, tibias) and returned to sham levels

229 turned to sham levels by day 10 (P = 0.6344, femurs; P = 0.3962, tibias).

230 animals when compared with 1LS (P = 0.0310, femurs; P = 0.5832, tibias).

231 The femur preserves small amounts of probable medullary bone

232 The number of MSCs in the proximal femur quickly recovered, but no recovery was observed in

233 alyzed an enhancer specific for the proximal femur region which corresponds to the distal-most expres

234 us than did control subjects in all proximal femur regions (femoral head, 8.51-8.73 GPa vs 9.32-9.67

235 e mineral density z scores (lumbar spine and femur) remained stable and were maintained in the health

236 al ridge and below the proximal third of the femur, respectively.

237 e tail limits pelvic rotation, which reduces femur retraction and decreases step length.

238 Micro-computed tomography analysis of femurs revealed increased trabecular bone volume, thickn

239 Microcomputed tomography of infected femurs revealed that S. aureus triggers profound alterat

240 al terms: humerus, handplate, fibula, tibia, femur, ribs, petrous part, scapula and head mesenchyme.

241 to 3000 muepsilon) to fluorescently stained femur samples from normal and ovariectomized rats.

242 ible to provide a seven-day fracture neck of femur service with no variation in thirty-day mortality

243 We prospectively studied patients with femur shaft fracture with RLS evaluation, daily transcra

244 action between the rs288326 SNP and proximal femur shape (SSM mode 2) in predicting radiographic hip

245 SNP alters the relationship between proximal femur shape and incident radiographic hip OA.

246 Sexual dimorphism in proximal femur shape can be discerned in adolescence and early ad

247 Here, we explore sex differences in proximal femur shape in a cohort of adolescents.

248 iation with increasing quartiles of proximal femur shape mode 2 (for the fourth quartile of mode 2, o

249 Observed differences in proximal femur shape, particularly at age 14 were largely indepen

250 Micro-computed tomography of A(2A)KO mouse femurs showed a significantly decreased bone volume/trab

251 A(2A)KO femurs showed an increased TRAP-positive osteoclast.

252 , microcomputed tomography analysis of adult femurs showed lower bone density in A2BAR KO mice as com

253 Electron microscopy in A(2A)KO femurs showed marked osteoclast membrane folding and inc

254 In vivo assessment in rat femurs shows the screws to be self-tapping, remain fixed

255 men, similar associations were seen at the 3 femur sites.

256 re associated with the shape of the proximal femur (SSM mode 2).

257 ter- and intraoperator analyses for proximal femur stiffness, yield strain, yield load, ultimate stra

258 MR assessment of proximal femur strength may provide information about bone qualit

259 The trabecular structure of a proximal femur (StW 522) attributed to Australopithecus africanus

260 Meanwhile, CLA significantly reduced femur tartrate resistant acid phosphatase (TRAP) activit

261 centration and bone mineral density at total femur (TFBMD), femoral neck (FNBMD), lumbar spine (LSBMD

262 ozygous mutants were smaller and had shorter femurs than controls; and at 1 month of age they exhibit

263 affecting sites such as the subtrochanteric femur that are infrequently affected by osteoporotic fra

264 mineral density and geometry of the proximal femur, the amount of adipose tissue of the upper thigh a

265 ing a spring between the patella and lateral femur, the CNS would reduce the ratio between VL and VM

266 dicals diffuse ipsilaterally to the proximal femur through bone medullary canal.

267 ned the weight, length, and strength of egg, femur, tibia, and keel.

268 performed active appearance modeling of the femur, tibia, and patella and linear discriminant analys

269 e mice, infectious virus was detected in the femur, tibia, patella, and foot, together with reduced b

270 igated this issue in stick insect middle leg femur-tibia (FT) joint.

271 13Balpha neurons encode femur-tibia joint angle and mediate postural changes in

272 passes different joints (coxa-trochanter and femur-tibia), and in this species we also show that nub

273 profiling of osteoblasts from mandibular and femur/tibia bone marrow revealed deficiencies in several

274 ed them with donor-matched, mesoderm-derived femur/tibia HSCs, including clonogenic assay and long-te

275 istent with the hip morphology, allowing the femur to be fully adducted to position the feet beneath

276 irradiated the distal half of the mouse left femur to study the mechanism of irradiation-induced bone

277 configuration) and assignment of the paired femur to the sideways fall configuration (hereafter, sid

278 Proximal femur trabecular bone structure was quantified from micr

279 erformed to assess the shape of the proximal femur, using 10 independent modes of shape variation gen

280 I) transiently induced bone formation in the femur via the cannabinoid-1 (CB1) receptor.

281 the greater trochanter of the left proximal femur was exposed and the intraosseous space was cannula

282 r both readers), and antetorsion of the left femur was significantly larger than that of the right fe

283 ction matching ecogeographic hypotheses, the femur was subject to little or no directional selection

284 racture of the subtrochanteric or diaphyseal femur was very rare, even among women who had been treat

285 , prostate cancer cell trafficking to murine femurs was dependent on E-selectin ligand, beta1 integri

286 Contrast-enhanced uCT imaging of mouse femurs was performed to measure glycosaminoglycan conten

287 mplantation of mammary MRMT-1 cells in a rat femur, we performed minimally invasive imaging procedure

288 located muscles that retract and rotate the femur, we show with path analysis that locomotion is alt

289 e location: scaphoid, tibia plus fibula, and femur were most likely to be nonunion.

290 Femurs were evaluated using micro-computed tomography, h

291 The 80 femurs were fractured via mechanical testing, with rando

292 In this study femurs were isolated from genetically double-labeled mBS

293 images, the outer bone volume of the distal femurs were measured using a semi-automated contour base

294 In this study, mature mouse femurs were plastic-embedded and longitudinal sections w

295 d osteolytic tumors when injected into mouse femurs, whereas KLF4 re-expression immediately after the

296 The short, robust femur with hypertrophied flexor attachment and the low,

297 assess the compressive failure load of human femur with simulated lytic defects.

298 est the proposed method, ten human cadaveric femurs with and without simulated defects were mechanica

299 ium micro-implants were inserted into murine femurs with low and high IT using torque values that wer

300 Calcium intake was associated with fetal femur z scores and birth length only when maternal 25(OH