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1 inflammation and collection in the adjoining soft tissue.
2 lid pediatric malignant neoplasm of bone and soft tissue.
3 etween groups of thick and thin peri-implant soft tissue.
4  promote bone regeneration and maturation of soft tissue.
5 ions of (66)Zn assimilation into the snail's soft tissues.
6 Columbia, many of which preserve evidence of soft tissues.
7 d wings from Burmese amber, with vestiges of soft tissues.
8 at it also promotes post-surgical healing of soft tissues.
9  be sites of infection such as the lungs and soft tissues.
10 f 10-200 kPa, which is in the region of many soft tissues.
11 rs presented stable and healthy peri-implant soft tissues.
12  the volume of de novo HO present within the soft tissues (0.12 mm vs 0.02 mm).
13 seudo-CT with air (-1,000 HU for ZTE < 0.2), soft-tissue (42 HU for ZTE > 0.75), and bone (-2,000 x [
14  No statistically significant differences in soft-tissue absorbed doses were found between the two pr
15 with excellent repeatability in extracranial soft tissues across a wide range of tumor sites, sizes,
16 with increased precancerous colon polyps and soft tissue adenomas, whereas short-stature humans harbo
17 e regularly used by paleontologists to infer soft tissue anatomy and to reconstruct behaviors of exti
18 els mimic many of the physical properties of soft tissue and are widely used biomaterials for tissue
19 tegrate tumor response in the primary tumor, soft tissue and bone metastases, and bone marrow.
20 ermediate histologies include tumors of both soft tissue and bone origin and are locally aggressive a
21                                              Soft tissue and bone sarcomas are malignancies of mesenc
22 he mannose-binding domain interacts with the soft tissue and cell membranes.
23 ce imaging (MRI) is critical for visualizing soft tissue and organs, with over 60 million MRI procedu
24  similarities and possible unique aspects of soft tissue and uterine LMS.
25  plan interceptive periodontal augmentation (soft tissue and/or bone augmentation) therapies for pati
26 ications were seen - inflammatory changes in soft tissues and bones (12 patients, 7.7%), stump fractu
27 ined with FDBA were effective in maintaining soft tissues and minimizing ridge resorption in all dime
28 AC (-0.7% +/- 1.1) compared with Dixon-based soft-tissue and air segmentation (-5.8% +/- 3.1) and ana
29 0.971 +/- 0.005 for air, 0.936 +/- 0.011 for soft tissue, and 0.803 +/- 0.021 for bone.
30 etter NPS and image quality scores for lung, soft tissue, and bone and with fewer beam-hardening arti
31 MR in-phase was segmented to air, inner air, soft tissue, and continuous bone.
32 s factor VIII to prevent bleeding in joints, soft tissue, and the central nervous system.
33 ight, WB lean soft tissue, appendicular lean soft tissue, and WB and skeletal site-specific BMC acqui
34                         Scales are rooted in soft tissues, and are regenerated by specialized cells.
35 testinal tract, frequently invades the skin, soft tissues, and bloodstreams of humans.
36 s (respiratory tract, urinary tract, skin or soft tissue), antibiotic resistance, and clinical outcom
37 ne the mean trajectories for height, WB lean soft tissue, appendicular lean soft tissue, and WB and s
38 x, imaging techniques that are applicable to soft tissues are generally difficult or impossible to ap
39 ation to resolve in diseased musculoskeletal soft tissues are unknown.
40 ub-acromial space by removing bone spurs and soft tissue arthroscopically) is a common surgery for su
41 axial images were reconstructed for bone and soft tissue assessment, respectively.
42                                              Soft tissue attenuation via imaging studies was demonstr
43                                     However, soft-tissue attenuation is a common artifact that limits
44                                              Soft tissue augmentation procedures may modify the biolo
45 e composite tissue defect comprising loss of soft tissue, bone and tooth in the mandible of a rabbit.
46 ery; and analytical techniques for assessing soft tissue, bone and vessel regeneration by gross evalu
47 neration of discrete-valued pseudo CT scans (soft tissue, bone, and air) from a single high-spatial-r
48 some of the mechanical properties of natural soft tissues, but at the expense of water content.
49 t the interface between stiff byssus and the soft tissue by immunochemical staining and confocal Rama
50 abled the MNs to mechanically interlock with soft tissues by selective distal swelling after skin ins
51                                              Soft tissue calcification occurs in several common acqui
52                                              Soft-tissue calcification is associated with aging, comm
53      Rhabdomyosarcoma (RMS) is an aggressive soft tissue cancer characterized by disturbed myogenic d
54      Liposarcomas (LPSs) are the most common soft-tissue cancer.
55 nces relevant for the assessment of hard and soft tissue changes around dental implants.
56 noses showed no statistical association with soft tissue changes at follow-up ( P = 0.11).
57  resonance imaging (MRI) exquisitely reveals soft tissue changes such as muscle edema and scapulothor
58 is a clinical diagnosis, exquisitely reveals soft tissue changes such as muscle edema and scapulothor
59 olecular information that allows noninvasive soft-tissue characterization.
60  type 2, one or more linear pleural tag with soft tissue component at the pleural end; and type 3, on
61 n X-ray computed tomographic data in 3D, the soft tissue comprising blood vessels that are putatively
62 tical porosity simultaneously along with the soft tissue comprising the vasculature.
63  at the pleural end; and type 3, one or more soft tissue cord-like pleural tag) and prioritized into
64 s was performed with ultrasonic debridement, soft tissue curettage (STC), glycine powder air polishin
65 s was performed with ultrasonic debridement, soft tissue curettage (STC), glycine powder air polishin
66                                      Carcass soft tissue decomposes in 2-10 wk, and these nutrients a
67 present and 7-24% via biofilm on bones after soft tissue decomposition.
68 n the prevalence of chronic wounds and other soft tissue defects, there is an urgent need to regenera
69 g tool able to provide direct information on soft tissue degeneration.
70     Progressive infiltration, expansion, and soft tissue destruction lead to bleeding, pain, debilita
71                         The body outline and soft tissue details suggest significant functional decou
72          Longitudinally, 76% of baseline TMJ soft tissue diagnoses and 71% of the baseline hard tissu
73 CI, 4.9% to 12.3%); results were similar for soft tissue diagnoses and the left TMJ.
74               Of 789 baseline joint-specific soft tissue diagnoses of DD, 598 (76%) joints showed no
75                          Concurrent baseline soft tissue diagnoses were associated with hard tissue d
76  coefficient (ADC) estimates in extracranial soft-tissue diffusion-weighted magnetic resonance imagin
77                                 Load-bearing soft tissues, e.g., cartilage, ligaments, and blood vess
78 ificant attenuation of 1) total new bone and soft tissue ectopic bone with 0.5 mg/kg (38.5% and 14.7%
79 onal development and occurs spontaneously in soft tissue environments.
80             Due to the absence of fossilized soft tissue evidence, the functional consequences of bas
81                   Unfortunately, the lack of soft-tissue evidence in the fossil record turns difficul
82 injury-driven blister formation, progressive soft-tissue fibrosis, and a highly elevated risk of earl
83                                         Such soft tissue findings of snapping scapula syndrome need t
84 inked with the de novo formation bone within soft tissues following trauma, and their presence may fa
85 uent postoperative complication that impairs soft tissue form, function, or movement.
86 comes of the immediate implant combined with soft tissue graft (IMITG).
87                                              Soft tissue graft placement combined with immediate impl
88             While the feasibility of AVFs in soft tissues has been reported there is no study on osse
89 laced with an initially thicker peri-implant soft tissue have less radiographic MBL in the short term
90        The PRF group also showed significant soft tissue healing and reduction in PD.
91 th, and global Arid1a disruption potentiates soft tissue healing in the ear.
92              There was a mean improvement in soft tissue height (0.36 +/- 0.64 mm, P = 0.03).
93                         Importantly, de novo soft-tissue HO was eliminated or significantly diminishe
94 ally decreased HO, and again lack of de novo soft-tissue HO.
95 twork was trained to identify air, bone, and soft tissue in volumetric head MR images coregistered to
96             Recognition of these specialized soft tissues in Confuciusornis is enabled by our combina
97  over 75 sponge species, many with preserved soft tissues, in pronounced contrast to normal survival
98                      Exceptionally preserved soft tissues include an extendable, gullwing-shaped, ten
99 istant Staphylococcus aureus (MRSA) skin and soft tissue infection (SSTI).
100  Cellulitis is a commonly occurring skin and soft tissue infection and one of the most frequently see
101                                      In vivo soft tissue infection in wild-type mice demonstrated tha
102 creased lesion size and severity in a murine soft tissue infection model when compared with parental
103 gnificantly attenuated in the bacteremia and soft tissue infection models, and the mutant strain lack
104 hil deployment protected mice against lethal soft tissue infection with Streptococcus pyogenes and pr
105                   The risk for MRSA skin and soft tissue infection within 3 months after documented c
106                 Ten cases (42%) had skin and soft tissue infection, and 2 cases had invasive disease.
107 crotizing myositis, bacteremia, and skin and soft tissue infection.
108 lococcus aureus is a major cause of skin and soft tissue infection.
109 t (ED) visit or hospitalization for skin and soft-tissue infection (SSTI), respiratory infection, int
110     (68)Ga-NOTA-UBI could diagnose bone- and soft-tissue infection in 3 of 3 patients.
111 l infection rates and rates of RTI, skin and soft-tissue infection, urinary tract infection, and bloo
112 ive infections, such as necrotizing skin and soft tissue infections (NSSTI).
113 ccus aureus is the leading cause of skin and soft tissue infections (SSTIs) and mounting antibiotic r
114  other nontuberculous mycobacterial skin and soft tissue infections (SSTIs) associated with handling
115  is causing an increasing number of skin and soft tissue infections (SSTIs) in Denmark and other Euro
116 illin-susceptible, has been causing skin and soft tissue infections (SSTIs) in epidemic proportions a
117 tive bacteria cause the majority of skin and soft tissue infections (SSTIs), resulting in the most co
118  aureus is the most common cause of skin and soft tissue infections (SSTIs), yet sex bias in suscepti
119                                     Skin and soft tissue infections are common reasons for medical ca
120  injection drug use who were readmitted with soft tissue infections at new sites (16.8% of readmissio
121 re pandemic consisting primarily of skin and soft tissue infections.
122 ossible, probable, or definite cellulitis or soft tissue infections.
123 014 primarily reflected declines in skin and soft tissue infections.
124 s aureus (MRSA) is a major cause of skin and soft tissue infections.
125 s invasive disease, most frequently skin and soft tissue infections.
126  aureus, a common cause for serious skin and soft tissues infections.
127 ave increased the overall number of skin and soft-tissue infections (SSTIs), increasing the overall d
128 tates and has caused an epidemic of skin and soft-tissue infections.
129 a-analysis for Staphylococcus aureus skin or soft-tissue infections.
130 l, predominantly for abdominal, urinary, and soft-tissue infections.
131 idence of infections, such as RTIs; skin and soft-tissue infections; chronic comorbid conditions, inc
132        Tobacco smoking enhances peri-implant soft tissue inflammation and CBL around IL and DL implan
133  shoulder to define the nature and extent of soft tissue injuries prior to physical therapy.
134 ulated contrast material-enhanced blood, and soft-tissue inserts with known elemental compositions wa
135 demonstrated by manufacturing a complex hard/soft tissue interface and demonstrating that cell phenot
136 eased in frequency, virulence, and degree of soft-tissue involvement.
137  (HO), the abnormal formation of bone within soft tissues, is a major complication after severe traum
138 68% for ZeDD PET) and by a factor of 1.5 for soft-tissue lesions (6.24% for Dixon PET and 4.07% for Z
139             In total, 30 bone lesions and 60 soft-tissue lesions were evaluated.
140                                     Bone and soft-tissue lesions were identified, and the SUVmax was
141                            Both skeletal and soft-tissue lesions were visualized with high contrast.
142 S) of small metastatic prostate cancer (PCa) soft-tissue lesions.
143     No significant differences were found in soft tissue level changes, technical and biologic compli
144 matic review is to examine marginal bone and soft tissue level changes, technical and biologic compli
145             Synovial sarcomas are aggressive soft-tissue malignancies that express chromosomal transl
146 th progression of synovial sarcoma, a deadly soft tissue malignancy initiated by a t(X;18) chromosoma
147                  Rhabdomyosarcoma is a rare, soft tissue malignancy, diagnosed particularly in adults
148       Synovial sarcoma (SS) is an aggressive soft-tissue malignancy characterized by expression of SS
149  test group showed a higher mean gain at the soft tissue margin, but not for the papilla.
150 metastases throughout the lumbar spine and a soft tissue mass in the lower sacral region.
151 ases were not evident on the CT scan and the soft tissue mass was out of the coverage area of the CT.
152                     Subsequent biopsy of the soft tissue mass was performed and histopathology conclu
153                   On imaging, a heterogenous soft tissue mass with internal calcific densities was no
154 p in mediating regeneration of lost bone and soft tissue maturation.
155 cal information, biomechanical properties of soft tissues may provide additional clues for disease di
156 that chronic inflammation in musculoskeletal soft tissues may result from dysregulated LM-SPM product
157 lopment of (225) Ac TAT for the treatment of soft-tissue metastases.
158 ecreased invasion and abrogation of bone and soft tissue metastasis.
159 ts with bone metastasis versus patients with soft-tissue metastasis (P < 0.0001).
160 ostatic, including all lymph nodes, bone, or soft-tissue metastasis), and subject level.
161 cial by a dual effect for preventing ectopic soft tissue mineralization while correcting decreased bo
162  but 2 months later developed a new left hip soft tissue nodule.
163 d fin spines, but the functional role of the soft tissues of the disc are poorly understood.
164 os designed to intimately interface with the soft tissues of the human body are of growing interest,
165             Beneath the feathers, carbonized soft tissues offer a glimpse of preservational potential
166 athologic development of ectopic bone within soft tissues often following severe trauma.
167 er suturing, EMD was injected underneath the soft tissues on one side, whereas the EMD vehicle was in
168 r export compound, in patients with advanced soft tissue or bone sarcoma with progressive disease.
169 ion with suturing and coverage with adjacent soft tissue or muscle, large defects >50% of the trachea
170 on, with both models avoiding involvement of soft tissue or teeth.
171 val for patients with bone metastasis versus soft-tissue or no metastasis for both (18)F-FDG (P = 0.0
172 aim of this study is to compare peri-implant soft tissue parameters (plaque index [PI], bleeding on p
173  evaluation of OMC anatomical variations and soft tissue pathology has increased..
174                       Buccal bone thickness, soft tissue peri-implant parameters, esthetic indices, a
175 cryogenically 3D printed CH structures, from soft tissue phantoms for surgical training and simulatio
176 to favor lamin-A,C accumulation and suppress soft tissue phenotypes.
177 hylococcus aureus infections of the skin and soft tissue pose a major concern to public health, large
178 derstanding of the mechanisms of exceptional soft tissue preservation frames all interpretations of t
179                           However, models of soft tissue preservation lack empirical support from act
180          The lack of internal characters and soft-tissue preservation in many arthropod fossils, howe
181     Here we analyse details of appendage and soft-tissue preservation in Yunnanolimulus luopingensis,
182 ell documented by fossils, but appendage and soft-tissue preservation is extremely rare.
183                                 Peri-implant soft tissue reactive lesions (I-RLs) may jeopardize impl
184 esis inducer with a therapeutic potential in soft tissue reconstruction and augmentation.
185 ch as surgery, skin rejuvenation, ocular and soft tissue recontouring, and antitumor and antimicrobia
186  as the essential surgical element (bone and soft tissue removal) was omitted.
187    Here we develop a 3D biomimetic model for soft tissue repair and demonstrate that fibroblasts ensc
188  and elasticity are also highly expected for soft tissue repair and soft electronics.
189 atform due to their current clinical use for soft tissue repair, off-the-shelf availability, and zero
190 els and prolonged hyperemia characterize the soft tissue response.
191                                        These soft tissue responses do not determine radiographic bone
192 nchiornis based on high-definition images of soft tissues revealed by laser-stimulated fluorescence.
193 ts were treated according to the Cooperative Soft Tissue Sarcoma (CWS) trial protocols.
194       Randomized controlled trials (RCTs) in soft tissue sarcoma (STS) have used varying end points.
195  Here, in a study of 18 canine patients with soft tissue sarcoma (STS), CIVO captured complex, patien
196 d trabectedin are considered active drugs in soft tissue sarcoma (STS).
197            Synovial sarcoma is an aggressive soft tissue sarcoma genetically defined by the fusion on
198  (LMS) is one of the most common subtypes of soft tissue sarcoma in adults and can occur in almost an
199 S/DDLS) account for approximately 13% of all soft tissue sarcoma in adults and cause substantial morb
200  Rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma in children that shares many feature
201    Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of skeletal muscle origin in childre
202     We applied this approach to 52 childhood soft tissue sarcoma specimens in an attempt to identify
203              In 2005, the European Pediatric Soft Tissue Sarcoma Study Group (EpSSG) proposed a conse
204  future studies of doxorubicin in metastatic soft tissue sarcoma.
205 ved no prior systemic therapy for metastatic soft tissue sarcoma.
206 n effective treatment strategy for childhood soft tissue sarcoma.
207  18 (41%) had bone sarcoma, and 26 (59%) had soft tissue sarcoma.
208  nerve sheath tumor (MPNST) is an aggressive soft tissue sarcoma.
209 arcinoma were breast cancer (5 patients) and soft-tissue sarcoma (2 patients).
210 homa (hazard ratio [95% CI], 3.5 [1.7-7.1]); soft-tissue sarcoma (2.8 [2.1-3.9]); breast carcinoma (2
211 and number of previous regimens for advanced soft-tissue sarcoma and in blocks of six.
212 tandard of care for patients with metastatic soft-tissue sarcoma and median overall survival for thos
213           Approximately 30% of patients with soft-tissue sarcoma die from pulmonary metastases.
214 activated partial thromboplastin time in the soft-tissue sarcoma group (three [7%] each).
215 the bone sarcoma group and four [10%] in the soft-tissue sarcoma group) had treatment-emergent seriou
216              Seven (18%) of 40 patients with soft-tissue sarcoma had an objective response, including
217                                Patients with soft-tissue sarcoma had to be aged 18 years or older to
218 treatment for locally advanced or metastatic soft-tissue sarcoma has been doxorubicin.
219 ival and distant metastases in patients with soft-tissue sarcoma in their extremities.
220 b with doxorubicin in patients with advanced soft-tissue sarcoma met its predefined primary endpoint
221  diagnosis of locally advanced or metastatic soft-tissue sarcoma not previously treated with an anthr
222 ases in patients after surgical resection of soft-tissue sarcoma of the extremities.
223 lly confirmed locally advanced or metastatic soft-tissue sarcoma of Trojani grade 2 or 3, disease pro
224 el, phase 2 study, we enrolled patients with soft-tissue sarcoma or bone sarcoma from 12 academic cen
225 afety and activity in patients with advanced soft-tissue sarcoma or bone sarcoma.
226 o investigate the genetic basis for bone and soft-tissue sarcoma seen in routine clinical practice.
227       Synovial sarcoma (SS) is an aggressive soft-tissue sarcoma that is often discovered during adol
228 ival in patients with advanced or metastatic soft-tissue sarcoma who received eribulin with that in p
229 on-Hodgkin lymphoma, acute myeloid leukemia, soft-tissue sarcoma, and central nervous system cancer.
230 is of an advanced unresectable or metastatic soft-tissue sarcoma, of intermediate or high grade, for
231 st-line treatment for advanced or metastatic soft-tissue sarcoma.
232 peripheral nerve sheath tumor, an aggressive soft-tissue sarcoma.
233 ary thyroid carcinoma, and 13% for secondary soft-tissue sarcoma.
234 esting a potential shift in the treatment of soft-tissue sarcoma.
235 lin could be a treatment option for advanced soft-tissue sarcoma.
236 bility of eribulin in advanced or metastatic soft-tissue sarcoma.
237 rcoma metastasis in a primary mouse model of soft-tissue sarcoma.
238 icin in patients with advanced or metastatic soft-tissue sarcoma.
239 treatment for locally advanced or metastatic soft-tissue sarcoma.
240 ne treatment for most patients with advanced soft-tissue sarcoma.
241                                           In soft tissue sarcomas (STS), low intratumoural O2 (hypoxi
242 habdomyosarcoma, synovial sarcoma, and adult soft tissue sarcomas diagnosed in adolescents and young
243 can be used to generate multiple subtypes of soft tissue sarcomas in mice.
244 for adolescent and young adult patients with soft tissue sarcomas lag behind those of children diagno
245 chymally transformed breast cancer cells and soft tissue sarcomas of diverse histological subtypes.
246 ti-platform molecular landscape of 206 adult soft tissue sarcomas representing 6 major types.
247 trated to be more active compared with other soft tissue sarcomas.
248 on and metastasis of many cancers, including soft tissue sarcomas.
249 S FDA approved for the treatment of advanced soft tissue sarcomas.
250 curative for primary nonmetastatic extremity soft tissue sarcomas.
251 ard to the management of these patients with soft tissue sarcomas: delays in diagnosis, trial availab
252                                        Human soft-tissue sarcomas (STS) are rare mesenchymal tumors w
253 ally engineered autochthonous mouse model of soft-tissue sarcomas (STSs) to determine NG2/CSPG4's rol
254 ocally advanced, unresectable, or metastatic soft-tissue sarcomas and so this combination cannot be r
255 therapy options for patients with metastatic soft-tissue sarcomas in the United States, after a gap o
256  MR imaging examinations in 23 patients with soft-tissue sarcomas who had undergone neoadjuvant thera
257 fficient details to encompass the variety of soft-tissue sarcomas, and available prognostic methods n
258 xorubicin as first-line therapy for advanced soft-tissue sarcomas.
259 maging for determining treatment response in soft-tissue sarcomas.
260 g from mesenchymal tissues, such as bone and soft-tissues sarcomas, is still largely unclear.
261 llagen and elastin fibers of periosteum, the soft tissue sheath bounding all nonarticular bone surfac
262                       Primary and metastatic soft tissue sites will be assessed using Response Evalua
263               For example, the periosteum, a soft tissue sleeve that envelops all nonarticular bony s
264 8 to -32; p < 0.001), fever, urinary or skin/soft-tissue source of infection.
265 tmental volumes were calculated: total body, soft tissue (ST), fat, lung, and intermediate tissue (IT
266  significant effect on peri-implant hard and soft tissue status in healthy smokers and non-smokers.
267             Data on the relationship between soft tissue structures and syringeal three-dimensional g
268                      The capacity to explore soft tissue structures in detail is important in underst
269  for recapitulating mechanical properties of soft tissues, suggesting its potential impact on a wide
270 f skeletal progenitors within periosteal and soft tissues surrounding bone, while bone marrow stromal
271 sult in irrigant extrusion into the bone and soft tissues surrounding the tooth.
272 d fatty cyst-like structure and inflammatory soft-tissue swelling.
273       Moreover, the infrapatellar fat pad, a soft tissue that becomes highly fibrotic in the post-TKA
274 alities of the hip joint and the surrounding soft tissues that can occur in athletes: intraarticular
275 an interfacial linker between the byssus and soft tissue, that is, the DOPA-containing domain interac
276   We identified the mineral locations in the soft tissues, the relative distributions of the minerals
277 ister, for articles up to May 2015 reporting soft tissue thickness at time of implant placement and M
278                                    Recently, soft tissue thickness has also been investigated as a po
279                                              Soft tissue thickness increased immediately after this e
280 dy aims to further evaluate the influence of soft tissue thickness on early MBL around dental implant
281 sing a wide range of diseases, from skin and soft tissue to life-threatening infections.
282 rior to push off, which tightens the plantar soft tissues to convert the foot into a stiff propulsive
283  MHM-K2 also preserves, with great fidelity, soft tissue traces visible as a sharply delineated carbo
284 anscription factor critical for the bone and soft tissue tumor Ewing sarcoma.
285 omyosarcoma (RMS) is an aggressive childhood soft tissue tumor, which exists in oncoprotein PAX-FOXO1
286                  Ewing sarcoma is a bone and soft-tissue tumor that depends on the activity of the EW
287                                     Bone and soft tissue tumors (BSTT) are relatively poorly understo
288 s therapeutics for the treatment of bone and soft tissue tumors along with other neoplasms driven by
289  Endothelial cell tumors are the most common soft tissue tumors in infants.
290                         All participants had soft tissue ultrasound performed at the time of enrollme
291 d in the measured values and a shift towards soft tissue values was observed with decreasing window p
292 (MTVt, TLGt) and from the manually contoured soft-tissue volumes.
293      The percentage residual viable tumor in soft tissue was significantly less with IRE (P = .005) a
294 e multidimensional fiber patterns of natural soft tissue weaves for rapid prototyping of advanced fun
295                               Bones and most soft tissues were segmented from images, and the generic
296                                 The adjacent soft tissues were thickened and irregular, suggestive of
297 essive vascular neoplasm, found in bones and soft tissue, whose cause is currently unknown, but may i
298  adapt itself under stress, enabling abiotic soft tissue with multiscale self-organization for effect
299  by FDM and cast with silica gel to simulate soft tissues, with contrast enhancement pigments added t
300 ng have made it increasingly common to study soft tissues without first embedding them in plastic or

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