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1 the skin layers and deposition at the upper dermis.
2 n skin, large amounts of HA are found in the dermis.
3 differentiation in the developing reticular dermis.
4 marrow-derived fibrocytes accumulate in the dermis.
5 on forces on and move directionally over the dermis.
6 clerosis, it can occur in all regions of the dermis.
7 ng of capillary thromboses (CT) in the upper dermis.
8 ansition between the papillary and reticular dermis.
9 ltration of skin homing lymphocytes into the dermis.
10 r matrix (ECM) remodelling in the underlying dermis.
11 d in the skin of mammals, most likely in the dermis.
12 monocyte-derived DCs were predominant in the dermis.
13 cells present in the papillary and reticular dermis.
14 , and a mixed inflammatory infiltrate in the dermis.
15 ae and associated muscle, tendons and dorsal dermis.
16 HSP70 can be found in both the epidermis and dermis.
17 ely generated around each microneedle in the dermis.
18 at the dermoepidermal junction and/or in the dermis.
19 opulation (gammadeltaT17 cells) in the mouse dermis.
20 nduces cutaneous fibers to die back into the dermis.
21 sal cell carcinoma stroma compared to normal dermis.
22 s inflammation surrounding tattoo ink in the dermis.
23 ifferentiation in developing and adult mouse dermis.
24 ed to regenerate HFs when combined with aged dermis.
25 but also within the papillary and reticular dermis.
26 onal collagen I gel, a representative of the dermis.
27 and increased numbers of fibroblasts in the dermis.
28 and 7.6+/-5.6 mum for the transition zone-to-dermis.
29 infected the epidermis and HCMV infected the dermis.
30 phils, macrophages, and T lymphocytes in the dermis.
31 t on other epithelial compartments or on the dermis.
32 ion by CD11c(+) dendritic cells (DCs) in the dermis.
33 with mononuclear cell infiltration into the dermis.
34 -Asp (RGD)-binding integrins in the inflamed dermis.
35 position and subsequent diffusion within the dermis.
36 tazarotene to the pilosebaceous unit of the dermis.
37 typic skin cultures comprising epidermis and dermis.
38 ratosis, and inflammatory infiltrates in the dermis.
39 nd other inflammation-related changes in the dermis.
40 mimicking the in vivo pathophysiology of the dermis.
41 ustered around the central arterioles of the dermis.
42 mechanoreceptors that remained deeper in the dermis.
43 or tunable penetration into the epidermis or dermis.
44 trastructure to possible changes in the skin dermis.
45 ominant gammadelta cell in the epidermis and dermis.
46 um granulosum (SG), stratum basale (SB), and dermis.
47 ced micro-vacuolization in the epidermis and dermis.
48 njection of ink and/or dye pigments into the dermis.
49 ient to estimate the volume deposited in the dermis.
50 al melanomas that invade into the underlying dermis.
51 are impaired in their maintenance within the dermis.
52 reach the blood vessels in the vascularized dermis.
53 on and denser neutrophil infiltration in the dermis.
54 ettings were not seen in the inflamed murine dermis.
55 Th1 and Th2 cell navigation of the inflamed dermis.
56 rmis, although also evident in the papillary dermis.
57 albicans in subepithelial layers such as the dermis.
58 al reprogramming and eventually invading the dermis.
59 esent in the underlying viable epidermis and dermis.
60 aration of the epidermis from the underlying dermis.
61 sebaceous glands relative to the surrounding dermis.
62 igmented melanocytes that extend through the dermis.
63 and deposit it at the lower epidermis/upper dermis.
65 CD200(+) cells in SCC stroma than in normal dermis (180.8 cells/mm(2) vs 24.6 cells/mm(2)) (P<.01).
66 elanosomes in the exterior-most layer of the dermis [7, 8] and that this layer lacks the unpigmented
68 s a rare mesenchymal neoplasm arising in the dermis, accounting for less than 0.1% of all cancers.
69 extracts from stratum corneum, epidermis and dermis after 24h, and the results were compared to those
72 ccumulation of mast cells and CD3+T-cells in dermis, all of which were observed in mice in which the
74 axa, transmission electron microscopy of the dermis also showed pronounced changes in the structure a
75 -dose allergen inoculation directly into the dermis, an immunologically active area containing abunda
76 (HA) and versican are key components of the dermis and are responsive to ultraviolet (UV)B-induced r
78 eductions in CD1a(+) Langerhans cells in the dermis and CD11c(+) dermal dendritic cells were observed
79 , fibroblast density declined throughout the dermis and clones of fibroblasts became more dispersed.
85 higher recruitment of neutrophils to the ear dermis and ear draining lymph nodes (dLN) as early as 6-
89 Beyond anchoring of LTMRs to the surrounding dermis and epidermis, recent evidence suggests that the
93 roughout the inter-follicular regions of the dermis and form clusters with antigen presenting cells a
94 dings reveal adaptations of Y. pestis to the dermis and how these adaptations can define the progress
95 degranulation was equivalent for MCs in the dermis and hypodermis of all three strains, but only the
97 we defined a new role for fibroblasts in the dermis and identified a minimal set of cell types for sk
98 delta T cells establish residence within the dermis and identify a role for S1PR2 in restraining the
99 ncluding interstitial dendritic cells of the dermis and Langerhans cells of the epidermis, in a dose-
102 d composed of stratified epidermis, fat-rich dermis and pigmented hair follicles that are equipped wi
103 can introduce immunogenic particles into the dermis and potentiate local or systemic hypersensitivity
104 lter the balance of S. aureus entry into the dermis and provide an explanation for how such dermal dy
105 ight scattering from collagen fibrils in the dermis and refractive index mismatch owing to the presen
110 reatment quickly clears spirochetes from the dermis and that the rash appearance is not indicative of
111 relevant levels into both the epidermis and dermis and that the skin-penetrating aptamer retains its
113 in a process that bypasses the epidermis and dermis and their attendant innate and adaptive immune at
115 rmore, rVN bound to VG1Fs extracted from the dermis and to nondenatured versican but not to fibrillin
116 rich epidermis and extracellular matrix-rich dermis and to show that conventional histological and im
117 that involves dermatophytic infection of the dermis and/or lymph nodes and sometimes the central nerv
118 agen deposition leading to thickening of the dermis and/or subcutaneous tissues and may cause signifi
119 onstituents of human skin connective tissue (dermis) and are essential for maintaining mechanical str
120 top-view (skin wheal), underside (below the dermis), and cross-section (true skin bleb) perspectives
121 ological cues alone also migrate through the dermis, and break in lymphatics, indicating that the abi
124 cures the attachment of the epidermis to the dermis, and its mutations cause a human skin fragility d
127 nical problems in adipose tissue, cartilage, dermis, and tendon are discussed that inspire the need t
129 ic neutrophilic infiltrate in the epidermis, dermis, and/or hypodermis and are often associated with
132 haps even dendritic cells (DCs) in the outer dermis, as well as to lesion infiltrating activated T ly
134 ssion becomes more widespread throughout the dermis at later developmental stages, we use tamoxifen-i
135 e gene expression profiling of back and tail dermis at P1 and dorsal fibroblasts at P2 and P50 showed
137 Z normally localizes to the cytoplasm in the dermis but is distributed in both the nucleus and cytopl
139 er, Lgr5-expressing cells contribute to this dermis, but not the blastema, during digit tip regenerat
142 he immune response to P. acnes in the murine dermis by controlling neutrophil recruitment to the infl
143 s and infiltration of both the epidermis and dermis by neutrophils and eosinophils, resulting in form
144 The mild inflammatory milieu created in the dermis by skin laser microporation itself most likely fa
145 eneic fibroblasts injected directly into the dermis can mediate transient disease modulation, autolog
146 eneic fibroblasts injected directly into the dermis can mediate transient disease modulation, autolog
147 inherent structural instability of the RDEB dermis, combined with repeated injury, increased the bio
149 ion of cells in lesional epidermis (EPI) and dermis, compared with the corresponding non-lesional reg
150 melanocytes displayed invasion into adjacent dermis, consistent with loss of invasion-suppressing act
152 ic fibers in the synovial membrane and upper dermis contribute to the pain-related behavior associate
153 lieved that site-specific fibroblasts in the dermis control postnatal skin identity by modulating the
154 hibition of neutrophil infiltration into the dermis, demonstrating that DM keratinocytes produced les
155 between healthy and tumor skin surfaces and dermis, demonstrating that the change in microbiota comp
157 t dermal DCs unexpectedly accumulated in the dermis despite their actomyosin-dependent migratory capa
159 hen Hh signalling is inhibited the reticular dermis does not respond to epidermal beta-catenin activa
161 etrium, the natural trophoblast target, with dermis dramatically reduces trophoblast interstitial inv
162 amplifying Wnt activity throughout the wound dermis during a crucial phase of skin regeneration.
165 ed accumulation of infiltrating cells in the dermis, elevated expression of IFN-gamma, CCL5, CCL8, an
166 Conditional deficiency of Cyp26b1 in the dermis (En1Cre;Cyp26b1f/-) results in decreased hair fol
168 ignaling leads to the formation of thickened dermis, enlarged epidermal placodes and dermal condensat
171 irochete transmits from the tick to the host dermis, eventually colonizing and persisting within mult
173 m responsible for the action of TIP39 in the dermis, fibroblasts were cultured in three-dimensional c
175 ay quantified aptamer from the epidermis and dermis, giving levels far exceeding the cellular half ma
177 ermis and crossing between the epidermis and dermis have distinct roles and specific functions in ski
181 mic modification occurs in the epidermis and dermis in CD1 transgenic mice following either intraperi
182 This transition is limited to the upper dermis in several inflammatory skin diseases, yet in sys
184 s) have been identified in extracts from the dermis in which hyaluronan (HA)-versican-fibrillin compl
187 rrence of senescent fibroblasts in geriatric dermis, increase the dermal expression of IGF-1, and cor
190 n the host, sporozoites navigate through the dermis, into the bloodstream, and eventually invade hepa
192 The ability of cells to invade into the dermis is a critical event in the development of cutaneo
193 bers of DCs, including XCR1(+) DCs, the skin dermis is an attractive site for vaccine administration.
197 that active macrophages are cleared from the dermis is the principle determinant of rash morphology.
198 d human dermis: the skin is wrinkled and the dermis is thin and composed of loose, disorganized, and
200 hypodermis layer, were present in the upper dermis layer within proximity to in situ melanoma cells,
201 Vector-borne infections initiated in the dermis likely involve adaptations to this unique microen
202 a CD141(hi) DC present in human interstitial dermis, liver, and lung that was distinct from the major
203 e SPPs (SPACE peptide, TD-1, polyarginine, a dermis-localizing peptide and a skin penetrating linear
204 gulated proliferation of melanoblasts in the dermis may be critical for production of epidermally-bou
210 ; despite often being deeply embedded in the dermis, no other species has been reported as feeding on
211 liminary data on bacterial population of MCT dermis, obtained only on three dogs, demonstrated an int
215 he proportion of IL-22(+) GDL T cells in the dermis of CCR6 KO mice (vs WT mice), suggesting that eff
216 in fibroblasts from the palmar and nonpalmar dermis of Dupuytren's patients and palmar fibroblasts fr
217 3.4-fold and 2.7-fold, respectively, in the dermis of elderly (>80 years) versus young (21-30 years)
218 howed that>40% of drugs were retained in the dermis of excised neonatal porcine skin up to 24h post-M
220 y tissue-resident dendritic cell (DC) in the dermis of human skin that is characterized by surface ex
222 Cs creates an in vivo synthetic niche in the dermis of immunodeficient mice driving the differentiati
223 ype VI collagen was expressed throughout the dermis of intact human skin, at the expanding margins of
224 was performed to separate the epidermis and dermis of lesional and nonlesional skin from patients wi
226 atment on the aortic ultrastructure and skin dermis of MFS mice through immunohistochemical evaluatio
236 autonomic sympathetic fibers into the upper dermis of the skin, an area that is normally devoid of t
237 eous mechanoreceptor located deep within the dermis of the skin, detects high frequency vibrations th
238 neutrophil infiltration in the epidermis and dermis of the skin, leading to disease manifestations.
243 nin pathway is activated most notably in the dermis of the wound bed early (d 2) after injury and sub
246 microdialysis probes were inserted into the dermis on the dorsal aspect of the forearm in 15 young,
248 presence of pathogenic microorganisms in the dermis or lungs elicits a robust gammadelta17 response t
249 monstrate that nociceptive fibers within the dermis play a crucial role in antifungal defenses throug
250 eus penetrates the epidermis and reaches the dermis, polymorphonuclear leukocytes (PMLs) accumulate a
251 id infiltrate was observed in the underlying dermis, predominantly composed of CD3+ T cells, scattere
255 +) neonatal fibroblasts from upper and lower dermis, respectively, confirmed that Sca1(+) cells had a
259 ets including RORgamma(+) ILC3s into wounded dermis; RORgamma(+) ILC3s are potent sources of IL17F in
262 iltrating tumour cells extending through the dermis, subcutis, orbicularis muscle bundles and nerve f
264 ost immune cells while migrating through the dermis, suggesting the importance of B. burgdorferi moti
268 ype in COL1A2-CCN1 mice resembles aged human dermis: the skin is wrinkled and the dermis is thin and
269 the epidermis, but a minimal presence in the dermis, thereby reducing the likelihood of FLUO entering
270 sults show the microbiota extends within the dermis, therefore, enabling physical contact between bac
272 recruitment and maturation of MCs within the dermis through SCF production by LTA-stimulated keratino
273 arrange the collagenous fibre network of the dermis to form a collagen-free zone at the wound centre.
276 of odontogenic competence from the external dermis to internal epithelium soon after the origin of j
277 ting from the neural crest must traverse the dermis to reach the epidermis of the skin and hair folli
278 along the developing embryo and traverse the dermis to reach the epidermis, colonising the skin and e
282 at the transition from the epidermis to the dermis underneath, which determines the drug distributio
283 Delivery of vaccine formulations into the dermis using antigen-coated microneedle patches is a pro
284 the percentage of 5-MTHF of the total in the dermis was similar to that in other organs, it was espec
285 unt immunofluorescence staining of the human dermis, we demonstrated the three-dimensional distributi
286 ring in situ tensile testing of sea cucumber dermis, we investigate the ultrastructural mechanics of
289 lk tips are implanted in the epidermis/upper dermis where they release vaccine over a time period det
290 presence in large numbers in the superficial dermis, where Leishmania is encountered, suggests that t
291 was found to spread into the upper papillary dermis, whereas S100A9 was shown to induce fibroblast pr
292 ntrols adipogenic cell fate within the lower dermis, which potentially contributes to the pathogenesi
293 ) showed a few melan-A-positive cells in the dermis, which was insufficient for a diagnosis of invasi
294 paths for drug and vaccine delivery into the dermis while maintaining integrity of the skin by quick
295 Cs regenerated HFs when supported with young dermis, while young HFSCs failed to regenerate HFs when
296 studies showed marked edema of the papillary dermis with an inflammatory infiltrate consisting mainly
299 to deliver botulinum toxin A into the human dermis with the aim of reducing patient pain, improving
300 cargo distributed both in the epidermis and dermis, with acquisition by CD11c(+) dendritic cells (DC