ライフサイエンスコーパス: porcine

1 ), residual graft material (bovine = 20.47%, porcine = 19.52%, P = 0.82) and connective tissue/other

2 ge of vital bone formation (bovine = 36.21%, porcine = 31.27%, P = 0.49), residual graft material (bo

3 nd connective tissue/other (bovine = 43.32%, porcine = 49.21%, P = 0.19).

4 e saponification of triglycerides in ex vivo porcine adipose tissue.

5 y of patients who underwent AWR using either porcine ADM(PADM) or bovine ADM(BADM) from 2005 to 2019.

6 te a ready-to-use kit for rapid detection of porcine admixtures in processed meat products.

7 73 porcine adnexa and 9 patients (16 eyelids) who underwent

8 The present preclinical study used a porcine AF model to evaluate the antiarrhythmic efficacy

9 ion and associated inflammation processes in porcine airways, respiratory symptoms in humans were rar

10 the expressed TCR repertoire of conventional porcine alphabeta T cells, which identified 48 Valpha, 5

11 Interestingly, entry of the porcine alphaherpesvirus pseudorabies virus (PRV) was in

12 cterized the miRNA-targeted transcriptome of porcine alveolar macrophages (PAMs) at early times after

13 n of proteins which is able to differentiate porcine and bovine gelatins accurately, with distinctive

14 ess religious and cultural concerns, because porcine and bovine gelatins are prohibited in Halal, Kos

15 Generally, porcine and bovine gelatins are used in the food industr

16 The source of gelatins is usually from porcine and bovine, and less commonly from vegetable and

17 probe was developed to discriminate bovine, porcine and fish gelatin species in a single assay platf

18 ponses as a first reaction to NiV in primary porcine and human bronchial epithelial cells (PBEpC and

19 efficient integration at safe harbor loci in porcine and human cells.

20 veloped a novel ex vivo model using discs of porcine and human cornea and sclera (5 mm diameter) to a

21 and humans, indicating that the response of porcine and human iNKT cells to CD1d-restricted Ags may

22 ancreas morphology and function suggest that porcine and human pancreas developmental biology may hav

23 howed a characteristic change in crosslinked porcine and human specimens.

24 tarsal plate tissue and investigated this in porcine and human tarsal plate specimens.

25 Riboflavin-sensitized porcine and human tarsus samples were irradiated with ul

26 lin and imaged their spatial distribution in porcine and mouse xenograft tissue.

27 m response factor (SRF), is increased in DCM porcine and patient cardiac tissues and plays a crucial

28 s performed in eggs, poultry, bovine, ovine, porcine and rabbit tissue and exceptionally low LODs wer

29 Type I Interferon-primed ISG15-knockout porcine and rhesus cells demonstrate enhanced ISG expres

30 the therapeutic potential of ISG15-deficient porcine and rhesus models.

31 Canine, porcine, and rhesus macaque ISG15, such as human ISG15,

32 are typically derived from either bovine or porcine animals.

33 Treatment of GVHD was done with a new porcine antihuman lymphocyte serum active through comple

34 3-dimenstional-printed heart simulator with porcine aortic roots (n=5), the anticommissural plicatio

35 porcine pericardium were compared to native porcine aortic valve cusps in a rat subcutaneous model f

36 shown in the activation of mouse, human, and porcine APC, with increased expression of costimulatory

37 solution improved long-term cold storage of porcine arteries by limiting structural alterations, inc

38 d on S1 phylogeny and was closely related to porcine Asian strains.

39 Blastocyst complementation with wild-type porcine blastomeres generated viable chimeric embryos wh

40 Here, we demonstrate that small changes in porcine blood hemolysis can be detected through a simple

41 and cortisol on number and functionality of porcine blood immune cells.

42 andard diameter) were prepared in each of 36 porcine bone blocks.

43 We utilised a high TEER primary porcine brain microvascular endothelial cell (PBMEC) cul

44 vailable total cerebroside extracts from the porcine brain.

45 ulative insulin transport across the ex vivo porcine buccal tissue (~26% of loaded insulin) which was

46 elia in vitro and attenuating infection in a porcine burn model.

47 fects models of color images from a four day porcine burn study demonstrate that colorimetric changes

48 f this human cTnC variant into permeabilized porcine cardiac muscle preparations significantly decrea

49 was induced by immunizing rats (n = 18) with porcine cardiac myosin in complete Freund adjuvant.

50 After the 14-day follow-up period, porcine cardiomyocytes were isolated from right and left

51 Five ex vivo porcine carotid artery models (n = 6 each) were compared

52 reviously reported that treatment of ex vivo porcine cartilage with proteolytic enzymes resulted in d

53 Conversely, antibodies eluted from porcine cells are more commonly anti-HLA-A.

54 increased level of SLA-1 mRNA expression in porcine cells compared to that of the single copy haplot

55 ion of ISG15 and the ISGylation machinery in porcine cells resulted in moderate inhibition of FMDV re

56 viral RNA amounts as NiV-infected HBEpC, the porcine cells showed reduced IFN- and IFN-dependent anti

57 PGs sulfurylation, facilitate JEV entry into porcine cells.

58 y host factors facilitating JEV infection in porcine cells.

59 This receptor has been purified from porcine cerebral cortex mitochondria by a new Atx-affini

60 dressing (WED) was tested in an established porcine chronic wound polymicrobial biofilm infection mo

61 ta to phosphorylate lamin A/C and facilitate porcine circoviral nuclear egress, and they certainly he

62 rin.IMPORTANCE It has been demonstrated that porcine circovirus 2 (PCV2) attaches to cells via hepara

63 Upon porcine circovirus type 2 (PCV2) infection, p32 was recr

64 M structure and molecular model of assembled porcine clathrin, providing insights into interactions t

65 ups: Test: bovine bone graft associated with porcine collagen and collagen membrane was used; control

66 ; control: bovine bone graft associated with porcine collagen was used without association with colla

67 Experiments in ex vivo porcine cornea at different intraocular pressures reveal

68 senting lacrimal drainage) 0.071% penetrated porcine cornea by 60 min and 0.0002% penetrated human co

69 Our results suggest that porcine cornea has a higher relative suitability for cor

70 measure both as a function of IOP in ex vivo porcine cornea, obtaining values consistent with both te

71 ccurately measuring mechanical properties of porcine corneas based on volumetric deformation followin

72 and corneal surface displacement changes in porcine corneas under a range of IOPs, from 0-60 mmHg.

73 Porcine corneas were used, establishing two different gr

74 replication in vitro and ex vivo in cultured porcine corneas.

75 ging coronaviruses, including SARS-CoV-2 and porcine CoVs, can infect enterocytes, cause diarrhea, an

76 g ability were used to infect full-thickness porcine cutaneous wounds.

77 Porcine cysticercosis (PCC) age-prevalence data (from 15

78 ing oxygen during HMP on renal function in a porcine DCD model.

79 lude porcine epidemic diarrhea virus (PEDV), porcine deltacoronavirus (PDCoV), and swine enteric alph

80 The use of a porcine dermal matrix at time of implant placement is ef

81 cedure, patients were assigned into group A (porcine dermal matrix, n = 24) or B (healing abutment us

82 es C) blood perfusion in the preservation of porcine donation after circulatory death kidneys.

83 tor with a cytomegalovirus (CMV) promotor to porcine donor hearts prior to heterotopic implantation.

84 a similar peptide profile than that found in porcine duodenum.

85 nd somatic cell nuclear transfer to engineer porcine embryos deficient in ETV2, a master regulator of

86 umans as well as by the risk of transmitting porcine endogenous retroviruses (PERVs).

87 ANCE PEDV is the most economically important porcine enteric viral pathogen and has caused immense ec

88 res of dimeric ATP synthases in a tetrameric porcine enzyme have been seriously misinterpreted in the

89 Here, we asked if the EndoU activity of porcine epidemic diarrhea coronavirus (PEDV), which caus

90 Using an infectious clone of an enteric CoV, porcine epidemic diarrhea virus (icPEDV), we generated v

91 Porcine epidemic diarrhea virus (PEDV) causes high morta

92 Porcine epidemic diarrhea virus (PEDV) infection can ind

93 Porcine epidemic diarrhea virus (PEDV) is an alphacorona

94 l risk factors to identify the occurrence of porcine epidemic diarrhea virus (PEDV) outbreaks.

95 Using porcine epidemic diarrhea virus (PEDV), an Alphacoronavi

96 Porcine epidemic diarrhea virus (PEDV), an alphacoronavi

97 a reverse genetic system for an enteric CoV, porcine epidemic diarrhea virus (PEDV), and outline an a

98 Examples of pig CoVs include porcine epidemic diarrhea virus (PEDV), porcine deltacor

99 solution structure of the spike protein from porcine epidemic diarrhea virus, a pathogenic alphacoron

100 Intestinal porcine epithelial cell 1 (IPEC-1) cells were cultured w

101 lication in Vero CCL-81 cells and intestinal porcine epithelial cells (IPEC-DQ).

102 propagation of icPEDV-EnUmt was impaired in porcine epithelial cells (LLC-PK1), where we detected an

103 role in antagonizing the innate response in porcine epithelial cells and macrophages, the sites of v

104 d alleviate DON-induced injury to intestinal porcine epithelial cells through modulation of the necro

105 Here, we report the derivation of porcine EPSCs, which express key pluripotency genes, are

106 lar and functional attributes reminiscent of porcine EPSCs.

107 In an in vivo porcine esophageal injury model, we compared the effects

108 Porcine experiments revealed that 1 L DSR solution remov

109 Porcine experiments were analyzed with gross photographs

110 Porcine experiments were conducted to investigate the op

111 In the porcine experiments, the superior mesenteric artery was

112 In de-epithelialized porcine eyes, a femtosecond-laser-generated tunnel was u

113 anatomical ex-vivo eye tissue segments from porcine eyes, yielding an accuracy >93% across 5 tissue

114 ecreased mitochondrial membrane potential in porcine fetal fibroblasts, the number and size of mitoch

115 ds were fabricated and used as 3D system for porcine follicles culture.

116 The use of porcine follicles implied many advantages respect to the

117 the IM- and LC-separation of O-glycans from porcine gastric and human salivary mucins.

118 Encapsulated crude extract in porcine gelatin presented the smallest size and polydisp

119 loupe melon carotenoids were encapsulated in porcine gelatin, whey protein isolate and concentrate by

120 Here, we design a porcine genome-scale CRISPR/Cas9 knockout (PigGeCKO) lib

121 er and highly purified lyophilized pituitary porcine GH treatment (0.6 mg/day); Group-3 (positive con

122 a robotically handled system that uses large porcine GI tissue explants that are functionally maintai

123 e inserted into the center of full-thickness porcine gingival explants (n = 31).

124 However, a higher number of patients in the porcine group had additional grafting at the time of imp

125 dy, 17 from the bovine group and 21 from the porcine group.

126 demonstrated that the antiviral role of the porcine HB (pHB) is mediated by promoting type I interfe

127 phy by augmenting carbohydrate metabolism in porcine heart failure.

128 stitute purified monomeric ATP synthase from porcine heart mitochondria into small unilamellar vesicl

129 USF imaging in porcine heart tissue and mouse breast tumor via local in

130 t gene delivery experiments to the explanted porcine heart utilized an autologous blood recovery appr

131 dentified four O-glycosites in proANP in the porcine heart, and surprisingly, two of these were locat

132 In this study, we isolated PV leaflets from porcine hearts in different age groups (~ 4-6 months, de

133 In 5 porcine hearts, bipolar ablation was compared between th

134 onavirus (BCoV)-its presumptive ancestor-and porcine hemagglutinating encephalomyelitis virus (PHEV).

135 We have previously reported that the porcine hemoglobin subunit beta (HB) exerts antiviral ac

136 aggregate propagation similarly to standard porcine heparin.

137 Studies with porcine herpesvirus demonstrated that primary enveloped

138 in the field of analytical methods used for porcine identification.

139 During dissolution, retention in porcine iliofemoral arteries is predicted to be dominate

140 cocorticoid and catecholamine actions on the porcine immune system in this level of detail and confir

141 sm for human physiology, knowledge about the porcine immune system under the influence of stress horm

142 constriction and pulmonary vasodilation in a porcine in vivo model of acute pulmonary embolism and va

143 lted in reduced deISGylation in vitro and in porcine-infected cells.

144 In this porcine ischemia-reperfusion autotransplant model, the l

145 ent long-term survival (>=6 months) of adult porcine islet grafts was achieved in five independent, d

146 Indeed, the porcine islets in the biopsied monkey liver samples were

147 as to examine ATP level and PG production of porcine IVD cells under prolonged exposure to hypoxia wi

148 PRV entry into several cell lines, including porcine kidney (PK15) cells and African green monkey kid

149 on (HAMP) and static cold storage (SCS) in a porcine kidney autotransplantation model.

150 enable a further dose saturation study in a porcine kidney model.

151 The porcine kidney study identified an optimal dose of 80 mg

152 of this portable analysis system to monitor porcine kidneys for the first time from organ retrieval,

153 Porcine kidneys were exposed to 30 minutes of warm ische

154 g the inner surface of the renal arteries in porcine kidneys with a heparin conjugate during hypother

155 Perfusion of porcine kidneys with heparin conjugate during HMP reduce

156 d effective, direct delivery of this drug to porcine kidneys, although further efficacy needs to be p

157 om NMP circuit for the treatment of isolated porcine kidneys, ascertaining the impact of the drug on

158 In the porcine large animal kidney transplant model, we investi

159 sue as well as on a cohort of postinfarction porcine left ventricular models constructed from ex vivo

160 demonstrated ex vivo and in vivo in exposed porcine liver and small animals.

161 Statistical classifiers built to distinguish porcine liver and stomach tissues using the in vivo data

162 e (BChE), and a structurally related enzyme, porcine liver carboxylesterase (CaE).

163 luorescence can be restored by the action of porcine liver esterase both in vitro and on the surface

164 e nanoparticles-assisted laser ablation on a porcine liver phantom.

165 ing hydrogel phantom, a solution sample, and porcine liver tissue with exchanged parameters by perfus

166 Using ex vivo peeling experiments on porcine liver, we characterized the adhesion between mod

167 Here we show that decellularized whole porcine livers revascularized with human umbilical vein

168 er microwave ablation zone volumes in normal porcine lung tissue.

169 ll RNAs extracted from ASFV-infected primary porcine macrophages (PAMs) was undertaken.

170 y, but these mechanisms are not at play when porcine macrophages are infected with attenuated NH/P68

171 en tested in this work by redesigning common porcine meat products (chorizo sausages and cooked ham)

172 The objective of this study was to generate porcine meniscus-derived matrix (MDM) scaffolds and test

173 a show that proteolytically damaged areas in porcine metacarpophalangeal joints present a reduced AFL

174 changes in AFL of ex vivo mouse knee joints, porcine metacarpophalangeal joints, normal human metatar

175 tion cohort (n=449), and in a representative porcine MI model with cardiac magnetic resonance-based m

176 In the porcine MI model, whole-blood levels of QSOX1 and PLBD1

177 Target genes are the porcine mitochondrial ND2 and equine ATP 6-8 genes.

178 aneous CT-guided interventions in an in vivo porcine model and to compare radiation dose, spatial acc

179 dially on the right and left ventricles of a porcine model and were inductively powered at 13.56 MHz

180 Experiments in a porcine model demonstrated the sensor's ability to detec

181 In a porcine model of acute intermediate-risk pulmonary embol

182 constriction and pulmonary vasodilation in a porcine model of acute pulmonary embolism.

183 ellular electrophysiological remodeling in a porcine model of AF.

184 thway in vivo was suggested by findings in a porcine model of cardiac cell therapy post-MI, whereby d

185 entified rotor-like electrical patterns in a porcine model of chronic AF.

186 c pyruvate metabolism and contractility in a porcine model of chronic pulmonary insufficiency causing

187 Using a novel and clinically relevant porcine model of circulatory arrest and ECPR, we demonst

188 A2AR agonist will reduce multiorgan IRI in a porcine model of ECPR.

189 In this novel porcine model of esophageal injury, biphasic PFA induced

190 In a porcine model of healed infarction, the spatial distribu

191 We developed a porcine model of infant cardiopulmonary bypass (CPB) wit

192 compared to WB and Hextend in a preclinical porcine model of lethal HS, despite decreased OCC from s

193 Translational potential was explored in a porcine model of reperfused MI using serial contrast-enh

194 conduction with a biological pacemaker in a porcine model of RV PICM.

195 components of the skin immune system in our porcine model of VCA tolerance, and the kinetics of cuta

196 ty was studied in an established preclinical porcine model of wound biofilm infection.

197 We developed an acute in vivo porcine model to assess the application of kilohertz fre

198 Therefore, we aimed to establish a porcine model to study the effects of ultra-high radiosu

199 cterize the process of lesion formation in a porcine model using particle therapy.

200 In a porcine model, carbon monoxide was added using a novel e

201 rapeutic potential of agrin in a preclinical porcine model, we performed ischemia-reperfusion injurie

202 ty compared to that of wild-type FMDV in the porcine model.

203 y of FUS-LBx in the normal brain tissue of a porcine model.

204 emodeling and heart failure in a nondiabetic porcine model.

205 FMS) for measurement of renal perfusion in a porcine model.

206 to assess acute ischemic kidney tissue in a porcine model.

207 o be partially rescuing the DCM phenotype in porcine model.

208 (PJ) anastomotic stricture in both a rat and porcine model.

209 Hydrogel implantation in mouse and porcine models of hindlimb ischemia rescues severely dam

210 In vitro mouse, in vivo rat and ex vivo porcine models show that the DST can achieve strong adhe

211 Testing with acute rabbit and porcine models, the device is proven to have robust and

212 ith triggerable benign detachment in ex vivo porcine models.

213 The interaction between stomach porcine mucin and 3 oenological tannins (extract of ella

214 ental scanning electron microscopy, and with porcine mucin as the model mucin system, this is the fir

215 Porcine mucin has been commonly used to enhance the infe

216 It is composed of porcine myeloperoxidase (pMPO), glucose oxidase (GO), gl

217 h4) is an indicator of hypertrophy, and both porcine MYH4-promoter activity and endogenous Myh4 mRNA

218 cted from bone and skin of mainly bovine and porcine origins.

219 e mapped the composition of the matrisome of porcine ovaries through the cortical compartment, where

220 ipase, and more selectivity is observed with Porcine Pancreas lipase type II.

221 with Human Salivary alpha-amylase (HSA) and Porcine Pancreatic alpha-amylase (PPA).

222 g the infrarenal, intraluminal aorta to PPE (porcine pancreatic elastase) under pressure to induce an

223 The antioxidant effect of porcine pancreatic phospholipase A2 (PLA2) was previousl

224 icroscopy, showed similarities to rodent and porcine parvovirus capsids.

225 d serotonin transporter (SERT)-by the use of porcine pepsin and three alternative aspartic proteases

226 ino acid residues) digested with immobilized porcine pepsin or NepII under conditions compatible with

227 s were observed with CD3 biomarker in native porcine pericardial tissue throughout the study.

228 transcatheter valve scaffolds (1) acellular porcine pericardium and (2) mesenchymal stem cell-seeded

229 Porcine Pericardium Collagen Membranes (PPCM) served as

230 d (2) mesenchymal stem cell-seeded acellular porcine pericardium were compared to native porcine aort

231 ials and Methods A calibration phantom and a porcine phantom with lumbar vertebrae were imaged with a

232 In the porcine PJ model, the mean luminal diameter and area of

233 niae (App) is the etiological agent of acute porcine pneumonia and responsible for severe economic lo

234 We previously reported an activated porcine Pol II elongation complex, EC*, encompassing the

235 Transfection of polarized RPE (porcine primary cells, iPSC-RPE) that endogenously expre

236 in vitro and in vivo using a native purified porcine PS combined with the hydrophobic anti-inflammato

237 nchitis, Newcastle disease, avian influenza, porcine reproductive and respiratory syndrome (PRRS) and

238 al investigations among countries.IMPORTANCE Porcine reproductive and respiratory syndrome (PRRS) is

239 Porcine reproductive and respiratory syndrome virus (PRR

240 Porcine reproductive and respiratory syndrome virus (PRR

241 he development of antiviral drugs.IMPORTANCE Porcine reproductive and respiratory syndrome virus (PRR

242 ntly, an effective therapeutic treatment for porcine reproductive and respiratory syndrome virus (PRR

243 Porcine reproductive and respiratory syndrome virus (PRR

244 nced replication during infection.IMPORTANCE Porcine reproductive and respiratory syndrome virus (PRR

245 Equine arteritis virus (EAV) and porcine reproductive and respiratory syndrome virus (PRR

246 Porcine reproductive and respiratory syndrome virus (PRR

247 somal frameshifting (-2/-1 PRF) mechanism in porcine reproductive and respiratory syndrome virus (PRR

248 Porcine reproductive and respiratory syndrome virus (PRR

249 F) is a mechanism used by arteriviruses like porcine reproductive and respiratory syndrome virus (PRR

250 nfection with a subtype 1.1 strain of PRRSV (Porcine Reproductive and Respiratory Syndrome Virus).

251 in response to maternal infection with live porcine reproductive and respiratory syndrome virus.

252 mercial sows following immune challenge with porcine respiratory and reproductive syndrome (PRRS) vac

253 complete TGEV genomes and a single strain of porcine respiratory coronavirus (PRCV) from the US were

254 For measurements, porcine respiratory coronavirus (PRCV) was nebulized in

255 of livestock: bovine coronavirus (BCoV) and porcine respiratory coronavirus (PRCV).

256 ion of apolipoproteins secreted from primary porcine RPE cells.

257 we reveal the regulatory mechanism by which porcine RyR2 is modulated by human CaM through the struc

258 S-PAGE at 140 kDa and 110 kDa for bovine and porcine samples, respectively.

259 of the eye and lacrimal glands, primarily in porcine samples.

260 Using porcine second-degree burn wounds infected with P. aerug

261 rst time in both open-chest and closed-chest porcine settings.

262 s were performed to extract Li(+) from under porcine skin by applying a current density of 0.4 mA cm(

263 In vitro studies in porcine skin confirmed the synergistic effect of these s

264 Porcine skin coupons were used to estimate the PSL swabb

265 dermal detection of potassium in chicken and porcine skin demonstrate that the microneedle patch is s

266 delivery of LNG from earring patches across porcine skin ex vivo achieved a steady state flux of 1.7

267 After gentle topical application for 10 s to porcine skin ex vivo, delivery of dermatological drugs a

268 meation studies using 350 mum thick neonatal porcine skin in modified Franz cell apparatus.

269 d collagen conformational changes in ex vivo porcine skin tissue.

270 ification of four burn conditions in ex vivo porcine skin tissue: (i) 200 degrees F for 10 s, (ii) 20

271 e retained in the dermis of excised neonatal porcine skin up to 24h post-MN application, indicating t

272 was assessed by DPV measurements in ex vivo porcine skin.

273 After 30 minutes of warm ischemia, porcine slaughterhouse kidneys were preserved for 24 hou

274 This work validates the use of porcine small intestinal mucus collected from fully-grow

275 he permeability characteristics of human and porcine small intestinal mucus secretions to sub-micron

276 edded the corrected UABCs on an FDA-approved porcine small intestinal submucosal membrane (pSIS), and

277 Gels from decellularized porcine small intestine (SI) mucosa/submucosa enable for

278 spectroscopy for determination of bovine and porcine source in gummy candies was examined and validat

279 d discriminated in relation to the bovine or porcine source of gelatin with 100% success without any

280 ples, only two were found to be positive for porcine species.

281 hed 78-99% when incubated ex vivo in ligated porcine stomachs.

282 n vivo tissue analysis in a robotic-assisted porcine surgery.

283 ar-thinning ECM-based hydrogel is shown in a porcine survival model of embolization in the iliac arte

284 Using porcine swine mesenteric arteries, the effects of up to

285 AS-OCT imaging in porcine tissue showed a distinct hyperreflective band in

286 arying from 0.004 mug kg(-1) (decoquinate in porcine tissue) to 0.560 mug kg(-1) (halofuginone in egg

287 When embedded in ex vivo porcine tissue, the integrated circuit efficiently harve

288 reater stiffness was observed in crosslinked porcine tissue.

289 consumption and lactate production rates of porcine TMJ discs were measured under varying tissue cul

290 Porcine tricuspid valve (TV) (n = 3) was extracted and i

291 the digestion of milk micellar casein in the porcine upper intestinal tract and to match the outcome

292 We also show, by using ex vivo porcine ureter segments and sedated pigs that, with resp

293 first two weeks after birth support that the porcine vagina continues to develop postnatal.

294 I(NaL) and I(Kr) during the AP in rabbit and porcine ventricular cardiomyocytes to test our hypothesi

295 Improved patency in a porcine vessel for 18 d is demonstrated while occlusive

296 ve ridge preservation using either bovine or porcine xenograft material.

297 indings suggest that ridge preservation with porcine xenograft results in comparable histomorphometri

298 tion is accomplished using a bovine versus a porcine xenograft.

299 The clinical applicability of porcine xenotransplantation-a long-investigated alternat

300 tem may eventually enable safe and effective porcine xenotransplantation.