ライフサイエンスコーパス: porcine

1 A non-cross-linked porcine acellular dermal mesh was sutured to the pelvic

2 sterol in human serum and epidermis, and the porcine adrenal gland.

3 Constructs seeded with porcine AF cells and human mesenchymal stem cells (hMSCs

4 The constructs seeded with porcine AF cells showed approximately 11-, approximately

5 Loss of CFTR alters porcine airway smooth muscle function and may contribute

6 inant Na,K-ATPase (human alpha1beta1FXYD1 or porcine alpha1D369Nbeta1FXYD1) and purified human Src ki

7 T, IPAM-CD163, C2+ and WSL, were compared to porcine alveolar macrophage (PAM) in terms of surface ma

8 In this study, we established the porcine alveolar macrophages (PAM) cells model co-infect

9 This study compared the interactions between porcine alveolar macrophages (PAMs) and wild-type A. ple

10 Immunophenotyping of porcine alveolar macrophages (PAMs) showed that pigs wit

11 shown that native phosphorylated full-length porcine amelogenin (P173) and its predominant cleavage p

12 raphy - fluorescence detection in commercial porcine and bovine meat.

13 noculated (infection) on the surface of both porcine and human cadaveric epidermis.

14 L) by laser capture microdissection (LCM) in porcine and human eye cryosections.

15 the non-tryptophan (non-Trp) fluorescence of porcine and human eye lens proteins was identified by Ma

16 in rats, and has been partially explored in porcine and human lungs.

17 ains showed close genetic relationship among porcine and human strains suggesting zoonotic origin of

18 -Myc (a biomarker of non-healing wounds), in porcine and human wound models.

19 ecific delivery in small (rodent) and large (porcine and human) lungs.

20 Our combinatorial approach using human, porcine and monkey in vivo and in vitro models provides

21 r sulfated N-glycans were identified in both porcine and mouse PNS myelin, demonstrating that the 6-O

22 novel cell binding thrombin inhibitor, using porcine and unused human kidneys in a series of ex vivo

23 novel cell binding thrombin-inhibitor, using porcine and unused human kidneys in a series of ex-vivo

24 n the porcine SK6 cell line, as well as both porcine and, for the first time, human DCs.

25 food ingredients including adulteration with porcine and/or its derivatives.

26 of all the studied gelatin sources (bovine, porcine, and fish) were achieved by hierarchical cluster

27 ajor IgE-binding proteins were identified as porcine angiotensin-I-converting enzyme (ACE I) and amin

28 rafts donated after cardiac death (DCD) in a porcine animal model of transplantation.

29 stocompatibility complex (MHC) barriers in a porcine animal model.

30 Vital signs of porcine animals were continuously monitored and recorded

31 ncreased outflow rates in perfused human and porcine anterior segments, whereas genipin reduced outfl

32 hat may promote the recruitment of huTreg to porcine aortic endothelial cells (PAEC) and their capaci

33 was to investigate HMGB1-mediated effects on porcine aortic endothelial cells (PAEC) from wild-type (

34 VSMC lysates and cGMP accumulation in intact porcine aortic endothelial cells infected with wild-type

35 Porcine aortic endothelial cells were cultured at conflu

36 Porcine aortic endothelial cells were treated with HMGB1

37 nd the Orsiro hybrid drug-eluting stent in a porcine arteriovenous shunt model.

38 ioresorbable vascular scaffold in an ex vivo porcine arteriovenous shunt model.

39 Recently, inactivation of the porcine ASGR1 gene has been shown to decrease this pheno

40 SK currents play a role in porcine atrial repolarization, and pharmacological inhib

41 reported technique of matrix production of a porcine auricular subunit graft has been translated to a

42 was selected for further investigation using porcine AV leaflets in an ex vivo shear system.

43 RNA was isolated from either side of healthy porcine AVs for microarray analysis.

44 binoxylan (AX) and bile salt (BS) or diluted porcine bile, were identified by (13)C NMR and small ang

45 xing and protecting RepRNA for delivery into porcine blood DCs.

46 To characterise cDC populations in porcine blood, DC were enriched from PBMC by CD14 deplet

47 s for bovine blood meal; and one peptide for porcine blood.

48 Screening mixtures of lipids extracted from porcine brain and a human epithelial cell line against C

49 co-cultured BBB model consisting of primary porcine brain endothelial cells (PBEC) and primary rat a

50 In vitro autoradiographic studies on porcine brain sections indicated interaction of [(18)F]6

51 -MS/MS method is applied for the analysis of porcine brain, human kidney, lungs, plasma, and erythroc

52 oneedles and a high delivery efficiency into porcine cadaver skin.

53 rmance and value-based benefit compared with porcine cadaveric biologic mesh.

54 a consecutive contiguous group treated with porcine cadaveric mesh for complex abdominal wall recons

55 rniation (6.5% vs 23.8%; P < 0.049) than the porcine cadaveric mesh group (n = 42).

56 tivariate analysis for infection identified: porcine cadaveric mesh odds ratio 2.82, length of stay o

57 .11; complications: drinker odds ratio 6.52, porcine cadaveric mesh odds ratio 4.03, African American

58 stay odds ratio 1.11; and hernia recurrence: porcine cadaveric mesh odds ratio 5.18, drinker odds rat

59 esulting in $9570.07 per case advantage over porcine cadaveric mesh.

60 Silencing the porcine carbohydrate genes necessary to avoid antibody-m

61 opic imaging, as was demonstrated on ex vivo porcine cardiac tissue.

62 coated decellularized vessels obtained from porcine carotid arteries with poly (ethylmethacrylate-co

63 METHODS AND An ex vivo porcine carotid jugular arteriovenous shunt was establis

64 Two distinct porcine cDC subpopulations were FACSorted CD1(-) cDC (Li

65 nity inhibitors of human CELA3A, CELA3B, and porcine CELA1.

66 In the present study, four established porcine cell lines, IPAM-WT, IPAM-CD163, C2+ and WSL, we

67 cent probe to detect this epitope on primary porcine cells in vitro In summary, our biochemical and s

68 related to the human CF operon CS18 and the porcine CF operon 987P (F6).

69 Prolongation of transient porcine chimerism via transgenic expression of human CD4

70 Here, a novel porcine circovirus (PCV3) that is distantly related to k

71 Porcine circovirus 2 (PCV2) is an essential component of

72 While porcine circovirus 2 (PCV2) was first identified in spor

73 uses, such as chicken anemia virus (CAV) and porcine circovirus 2 (PCV2), as serious pathogens of euk

74 Here, a novel circovirus, designated porcine circovirus 3 (PCV3), was identified in sows that

75 ctive respiratory syndrome virus (PRRSV) and porcine circovirus type 2 (PCV2) is quite common in clin

76 l-free immunoassay for specific detection of porcine circovirus type 2 (PCV2), which is a minim anima

77 Porcine circovirus-associated disease (PCVAD) is clinica

78 of gelatin batches with regard to bovine and porcine constituents.

79 overall approach is demonstrated in ex-vivo porcine cornea.

80 infectivity was seen in ex vivo cultures of porcine corneas.

81 of cinaciguat was studied on vessel tone of porcine coronary arteries and rat thoracic aortas.

82 healing profile compared with BVS in normal porcine coronary arteries.

83 se activity, was induced by the passaging of porcine coronary artery ECs from passage P1 to P4, and w

84 and greater sensitivity to PGF2alpha in the porcine coronary artery from males.

85 Primary porcine coronary ECs were isolated from the left circumf

86 ively reduce neointimal proliferation in the porcine coronary model but differ considerably in retent

87 g formulations and doses were studied in the porcine coronary model to investigate sirolimus tissue l

88 owever, the potential cross-reactivity among porcine coronaviruses is a major concern for the develop

89 Importantly, treatment of porcine cultured cells with Ad5-poIRF7/3(5D) inhibited t

90 n activator inhibitor (PAI)-1), secretion of porcine cytokines and chemokines (HMGB1, TNFalpha, IL-8,

91 After infection of the porcine dam at about 90 days of gestation, porcine repro

92 The response of porcine DC subsets to TLR ligands revealed that pDCs are

93 , porcine respiratory coronavirus (PRCV), or porcine deltacoronavirus (PDCoV) pig antisera.

94 Porcine dendritic cells (DCs) are relatively well charac

95 lar dTBs; 2) recellularized dTBs seeded with porcine dental epithelial cells, human dental pulp cells

96 own circoviruses was identified in sows with porcine dermatitis and nephropathy syndrome (PDNS) and r

97 d enteric disease, reproductive failure, and porcine dermatitis and nephropathy syndrome (PDNS).

98 ein ex vivo and in vitro hydrolysis by human/porcine digestive enzymes, respectively, was examined.

99 Porcine DNA was firstly amplified using loop-mediated is

100 luminescence (ECL) technique for Sus scrofa (Porcine) DNA detection.

101 study, we considered alternatives including porcine embryos that, as in humans, develop as bilaminar

102 y, the risk of cross-species transmission of porcine endogenous retroviruses (PERVs) has impeded the

103 ilar population of SA CMCs was isolated from porcine endomyocardial biopsy samples.

104 Recruitment of huTreg to porcine endothelium depends on particular chemokine rece

105 roteins were more resistant to hydrolysis by porcine enzymes than by human digestive juices.

106 ter than the myofibrillar ones by both human/porcine enzymes.

107 The development of porcine epidemic diarrhea virus (PEDV) antibody-based as

108 Porcine epidemic diarrhea virus (PEDV) causes severe dia

109 Porcine epidemic diarrhea virus (PEDV) is a devastating

110 We previously isolated a porcine epidemic diarrhea virus (PEDV) strain, PC177, by

111 confronted with the disruptive emergence of porcine epidemic diarrhoea (PED).

112 oate as the single major triol esterified in porcine epidermis and the same isomer with lesser amount

113 The major end product in human and porcine epidermis is a trihydroxy derivative, formed wit

114 quencing we identified and characterized the porcine equivalent of conventional DCs (cDC) 1 and cDC2

115 rformed well, with expansion rate (>100%) in porcine ex vivo model.

116 environments including static, dynamic, and porcine ex vivo models.

117 infrared (2D IR) spectra on tissue slices of porcine eye lenses.

118 PV under general anesthesia was performed on porcine eyes (Yorkshire species) at a University Surgica

119 Ex vivo trans-sclera drug delivery in porcine eyes is demonstrated by utilizing the biokinetic

120 From each of 6 porcine eyes, 4 regions were obtained: cornea, equatoria

121 ighly resorbable following implantation in a porcine femoral artery.

122 eptides of TG (five markers), and bovine and porcine fibrinogen (six markers each).

123 rom Streptomyces mobaraensis, and bovine and porcine fibrinogen/thrombin in restructured meat was dev

124 of antibody cross-reactivity with human and porcine fVIII leading to false-negative HSM results.

125 genesis (HSM) with single human domain human/porcine fVIII proteins and antibody binding to human A2,

126 . jejuni genes required for infection of the porcine gastrointestinal tract utilising a transposon (T

127 re bovine gelatin from mixture of bovine and porcine gelatins, which is very important for the food i

128 Disrupting the porcine GGTA1 and CMAH genes [double knockout (DKO)] tha

129 g a minilibrary of porcine ISGs, we identify porcine guanylate-binding protein 1 (GBP1) as a potent a

130 results showed that microbial shifts in the porcine gut in response to diets containing E. faecalis

131 The devices were implanted in 11 porcine hearts simulating FTR.

132 ntramyocardial delivery of CSCs to infarcted porcine hearts.

133 Rapid clearance of administered porcine hematopoietic stem cells by primate macrophages

134 Unlike USP porcine heparin, bovine intestinal heparin (BIH) has a l

135 es efficient cleavage of the hinge region of porcine IgG with a high degree of specificity.

136 d protease ofS. suisthat exclusively targets porcine IgG.

137 y protease ofS. suisthat exclusively cleaves porcine IgM and represents the first virulence factor de

138 However, addition of exogenous recombinant porcine IL-10 + IL-6 to mononuclear cells cocultured wit

139 itro wound healing assays, human ex vivo and porcine in vivo wound models, and DFU tissue.

140 generating skeletal muscle efficiently from porcine induced pluripotent stem cells (piPSC) in vitro

141 he most important bacterial pathogens in the porcine industry.

142 Here, we expressed and purified full-length porcine INSL3 (pINSL3) using a silkworm-based Bombyx mor

143 lcN residue in a recently purchased batch of porcine intestinal mucosal HS.

144 its isolation from animal sources (primarily porcine intestine) as well as its manufacturing processe

145 preparations obtained from bovine kidney and porcine intestine.

146 Using a minilibrary of porcine ISGs, we identify porcine guanylate-binding prot

147 vestigate early immune responses to neonatal porcine islet (NPI) xenografts compared with rhesus isle

148 Porcine islet xenografts have the potential to provide a

149 rted to increase proliferation in rodent and porcine islets (5), strongly and selectively increases h

150 an bone marrow-derived MSCs have on neonatal porcine islets (NPIs) in vitro and determined islet engr

151 treated human endothelial cells and neonatal porcine islets prolonged time to clot formation.

152 eport successful and safe transplantation of porcine islets with a bioartificial pancreas device in d

153 slightly delayed growth kinetics in primary porcine kidney cells, and they were significantly attenu

154 om amniotic fluid and Caco-2 cells, DAO from porcine kidneys, and rhDAO produced in two different HEK

155 Formalin-soaked porcine lenses were divided into 2 mm cubes (tip diamete

156 Porcine lenses were hardened in formalin for 2 hours and

157 Porcine lesion histology revealed transmurality in 51 of

158 (CD18, CD49d) on huTreg, or their respective porcine ligands intercellular adhesion molecule 2 (CD102

159 ed the role of the adhesion molecules, their porcine ligands, and the chemoattractant factors that ma

160 minority strains, the repeated detection of porcine-like rotavirus strains in Taiwanese children ove

161 stable ether can be removed by the action of porcine liver esterase (PLE) to reveal the bright unmodi

162 geneic consumption of human platelets by the porcine liver.

163 Porcine livers also have shown the ability to phagocytos

164 Non-porcine livestock in the family Bovidae shared the most

165 r-level characterization of a clinical-grade porcine lung surfactant extract using a multitechnique a

166 Using precision-cut slices from the porcine lung to passage the parental virus, isolates fro

167 bronchoscopy procedures performed in vivo on porcine lungs showed significantly reduced fouling, resu

168 riod had sustained effects on the developing porcine microbiota and host-microbe interface.

169 y introduced a new dilemma: Why do human and porcine mitoribosomes integrate contrasting mt-tRNAs?

170 METHODS AND In a porcine model (n=8), neuronal activity was recorded from

171 A porcine model (PSV) was utilized to validate these metab

172 f the effect of (90)Y radioembolization in a porcine model at different absorbed-dose endpoints.

173 This in vivo porcine model confirms that during the FAE in PPV, press

174 rrhythmic effects in a vernakalant-resistant porcine model of AF.

175 ed delivery of endothelial cell therapy in a porcine model of cirrhosis for liver regeneration.

176 assium channels curtailed VF occurrence in a porcine model of commotio cordis, VF has been suggested

177 (NEVKP) with static cold storage (SCS) in a porcine model of DCD autotransplantation.

178 crease vascular hyperplasia development in a porcine model of hemodialysis arteriovenous graft stenos

179 r a wide range of cardiac output in an adult porcine model of hemorrhagic shock and resuscitation.

180 dial extracellular volume in an experimental porcine model of PH because of aorto-pulmonary shunt usi

181 In a porcine model of prolonged cardiac arrest, t-ECPR improv

182 In a porcine model of severe liver failure, damage was assure

183 Here we characterized a porcine model of spinal cord injury using a combined beh

184 A porcine model of synthetic graft placed between carotid

185 ine care would improve 24-hour survival in a porcine model of ventricular fibrillation cardiac arrest

186 A trans-human skull porcine model was designed for the preclinical testing.

187 In a porcine model, pharmacokinetics of PGZ from fat depots t

188 In a porcine model, PRP coacervate significantly accelerated

189 Conclusion With a trans-human skull porcine model, this study demonstrated BBB opening with

190 In this porcine model, TMB resulted in an insignificant (p > 0.0

191 e strength in mice, and was validated in the porcine model.

192 echnique for the treatment of cirrhosis in a porcine model.

193 PLGA-PEG nanoparticles was demonstrated in a porcine model.

194 livery vehicle to improve wound healing in a porcine model.

195 In four porcine models, the deep inferior epigastric perforator

196 We have previously shown that porcine MSC-derived EVs transport mRNA and miRNA capable

197 hat contribute to the therapeutic effects of porcine MSC-derived EVs, we characterized their protein

198 Porcine MSCs were cultured from abdominal fat, and EVs c

199 Two hundred biceps femoris porcine muscle samples from Spanish dry-cured ham were f

200 Previous studies showed porcine muscle satellite cells (PSCs) are important for

201 To create EHTs, sections of porcine myocardium were laser-cut into ribbon-like shape

202 ation blockade-induced dominant tolerance to porcine neonatal islet cell cluster (NICC) xenografts in

203 Porcine-NICC were transplanted under the renal capsule o

204 Porcine-NICC xenograft tolerance was abrogated after dep

205 Porcine-NICC xenografts from treated mice expressed elev

206 exhibited more potent regulatory function to porcine-NICC xenografts that naive Treg cell.

207 ers of Foxp3Treg cell were identified in the porcine-NICC xenografts, draining lymph node, and spleen

208 transplant perfusion of genetically modified porcine organs with CHC may benefit post-transplant xeno

209 cid (5-CQA) on digestion of potato starch by porcine pancreatic alpha amylase (PPAA) was investigated

210 d to analyse digestion curves obtained using porcine pancreatic alpha-amylase for a range of particle

211 nd Mycoplasma pneumoniae (MpnEf-Tu), and the porcine pathogen Mycoplasma hyopneumoniae (MhpEf-Tu).

212 ecies conserved subset-specific transcripts, porcine pDCs differed from the species described so far

213 e proteins hen egg-white lysozyme (HEWL) and porcine pepsin.

214 TRIF/MyD88-NF-kappaB signaling pathway when porcine peripheral blood monocyte-derived dendritic cell

215 noantigens reduces human antibody binding to porcine peripheral blood mononuclear cells.

216 ical swine fever virus (CSFV), a devastating porcine pestivirus.

217 Here we show that porcine PGCs originate from the posterior pre-primitive-

218 mixture (Activa, Ajinomoto), and bovine and porcine plasmapowder FG (PPFG; Sonac B.V.).

219 yopreservation of various kinds of human and porcine pluripotent stem cells at -80 degrees C for peri

220 raw meat from three animal species (bovine, porcine, poultry).

221 at, using a concentration of 0.6% bovine and porcine PPFG.

222 R-Cas9, we inactivated all of the PERVs in a porcine primary cell line and generated PERV-inactivated

223 pigs were also bioassayed in mice expressing porcine prion protein.

224 d the number of uncharacterized/unverifiable porcine proteins may have contributed to this largely un

225 RRSV infection of MARC-145 cells and primary porcine pulmonary alveolar macrophages led to significan

226 d to make new measurements of 'k' (W/m.K) of porcine PV, esophagus, and phrenic nerve, all needed for

227 Porcine RDT demonstrated region- and strain-dependent va

228 relaxation experiments were performed on 20 porcine RDT specimens, with strain increments from 5% to

229 istics and regional fibrillar arrangement of porcine RDT.

230 ter-individual variation in host response to porcine reproductive and respiratory syndrome (PRRS) has

231 far-reaching financial losses caused by the porcine reproductive and respiratory syndrome (PRRS).

232 Porcine reproductive and respiratory syndrome virus (PRR

233 istant to infection with genotype 2 (type 2) porcine reproductive and respiratory syndrome virus (PRR

234 Porcine reproductive and respiratory syndrome virus (PRR

235 Porcine reproductive and respiratory syndrome virus (PRR

236 Porcine reproductive and respiratory syndrome virus (PRR

237 In a previous study, ribavirin-resistant porcine reproductive and respiratory syndrome virus (PRR

238 Porcine reproductive and respiratory syndrome virus (PRR

239 In cells infected with porcine reproductive and respiratory syndrome virus (PRR

240 Porcine reproductive and respiratory syndrome virus (PRR

241 the immunosensor was inspected by detecting porcine reproductive and respiratory syndrome virus (PRR

242 e porcine dam at about 90 days of gestation, porcine reproductive and respiratory syndrome virus (PRR

243 of this study was to determine the effect of porcine reproductive and respiratory syndrome virus (PRR

244 The nsp2 PRF signal of porcine reproductive and respiratory syndrome virus is d

245 The co-infection of porcine reproductive respiratory syndrome virus (PRRSV)

246 transmissible gastroenteritis virus (TGEV), porcine respiratory coronavirus (PRCV), or porcine delta

247 Analysis by qPCR of 271 porcine respiratory disease diagnostic submission sample

248 ging the virus three times in differentiated porcine respiratory epithelial cells.

249 Porcine RMEC expressed gal-alpha(1,3)-gal, N-glycolylneu

250 Porcine RMEC will be a useful reagent for the further st

251 Primary cultures of porcine RPE cells were differentiated into polarized RPE

252 The porcine sapelovirus (PSV) is known to cause enteritis, p

253 The receptor(s) for porcine sapelovirus (PSV), which causes diarrhea, pneumo

254 In this study, infection with porcine sapovirus (PSaV) strain Cowden, the only cultiva

255 Here, using only cultivable porcine sapovirus (PSaV) strain Cowden, we demonstrate t

256 ical immunosensor for sensitive detection of porcine serum albumin (PSA) is reported in this work.

257 This was noted in the porcine SK6 cell line, as well as both porcine and, for

258 gelatins are often produced from bovine and porcine skin and bone and consist mainly of partially hy

259 An ex vivo evaluation using porcine skin displayed efficient and steady state flux o

260 A porcine skin ex vivo screening was performed for assessi

261 Neonatal porcine skin from the abdominal and back regions was use

262 Ex vivo intradermal neonatal porcine skin penetration of VD3 NMP from bilayer MN was

263 es into the skin, while the histology of the porcine skin revealed enhanced penetration potential of

264 l-thickness ex vivo human as well as ex vivo porcine skin samples.

265 Biocompatibility of two newly developed porcine skin scaffolds was assessed after 3, 14, 21 and

266 s (into a skin simulant and excised neonatal porcine skin) were confirmed by texture analysis and opt

267 e a full thickness (>10 mm) wound closure of porcine skin, which represents approximately 10-fold ext

268 e, Ovalbumin (OVA), to depths of 500mum into porcine skin.

269 y from bone and hide, mainly from bovine and porcine sources.

270 The purpose of this study was to identify porcine-specific peptide markers from thermally processe

271 on of LC-QTOF-MS data showed that only seven porcine-specific peptides were consistently detected.

272 after ablation in the epidural space of the porcine spine.

273 in stimulated gastric environment and fresh porcine stomach to validate the effectiveness and reliab

274 We found that porcine submucosal glands produce MUC5B, whereas goblet

275 nstituted from the hydrophobic fraction of a porcine surfactant made it more resistant to inhibition

276 the theoretical justification for bovine and porcine target selection.

277 Porcine TBs were harvested from discarded 6-mo-old pig j

278 Here, 39 porcine teeth (12 teeth with artificially deeper pockets

279 modified NS segment were split by using the porcine teschovirus 1 (PTV-1) 2A autoproteolytic cleavag

280 An in vivo porcine thigh model was used to study systemically deliv

281 ded localization of FeO nanoparticles within porcine thigh preps was demonstrated by magnetic resonan

282 e used to visualize the alpha-Gal epitope on porcine tissues.

283 ever, the paradigm is now switching from the porcine to the human model.

284 ed coupling in vitro retention using ex vivo porcine tongue, sensory perception with a trained panel

285 zed tooth buds (dTBs) created from unerupted porcine tooth buds (TBs) can be used to guide reseeded d

286 e gene expression was analyzed using Agilent porcine transcriptome microarrays and clusters of genes

287 We established the decellularization of porcine urethras to produce acellular urethra bioscaffol

288 ular imaging agent into the submucosa of the porcine urinary bladder.

289 to integrate mt-tRNA(Val) compared with the porcine use of mt-tRNA(Phe) We have explored this observ

290 METHODS AND In cultured porcine valve interstitial cells, CNP inhibited patholog

291 cGMP-dependent protein kinase 1) in cultured porcine valve interstitial cells.

292 ectable hydrogel derived from decellularized porcine ventricular myocardium has been shown to halt th

293 Five porcine vertebral bodies in one pig underwent interventi

294 toxic to the RPE cells, chemically stable in porcine vitreous and delivered cargo prototypes (hydroph

295 scle tissue remodeling was interrogated in a porcine VML injury model using unbiased assessments of m

296 During porcine whole blood coagulation, changes in the elastic

297 te the elastic properties of the recalcified porcine whole blood, blood added with kaolin as an activ

298 re and induces miR-15b-5p in acute human and porcine wound models and in chronic DFUs.

299 ex and short stretches of DNA sequences into porcine zygotes.

300 with a single-stranded repair template into porcine zygotes.