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1 traepidermal sensory innervation of adjacent epidermis.
2 ted DNA breakdown was not compromised in the epidermis.
3 ermates consistent with a hyperproliferative epidermis.
4 into mature melanocytes on their way to the epidermis.
5 tion of neuroendocrine cells that arise from epidermis.
6 control in the formation of an intact human epidermis.
7 ram wild-type keratinocytes into nipple-like epidermis.
8 tomatal closure in excised leaves and peeled epidermis.
9 occur given the tensile stresses across the epidermis.
10 atory and differentiation homeostasis in the epidermis.
11 re underexpressed in cSCC compared to normal epidermis.
12 illa, the secondary hair germ cells, and the epidermis.
13 at the site of fungal infection in the lower epidermis.
14 n, whose expression is largely restricted to epidermis.
15 ms that regulate wound healing in mouse tail epidermis.
16 to neural tube but also to neural crest and epidermis.
17 tains antigen-presenting cells in the dermis/epidermis.
18 tiny pulse changes arising on the surface of epidermis.
19 ound to be abundantly expressed in psoriatic epidermis.
20 for neural plate, neural crest, placodes and epidermis.
21 expressed in the root cortex or in the root epidermis.
22 nd up-regulates inflammatory pathways in the epidermis.
23 re dispensable for homeostasis of the murine epidermis.
24 are mediated by ssup-72 autonomously in the epidermis.
25 ools for targeting proteins to the seed coat epidermis.
26 microdisruptions in the papillary dermis and epidermis.
27 keratinocytes, the most abundant cell in the epidermis.
28 ils, glands, oral mucosa, and palmar-plantar epidermis.
29 esponses when antigen is concentrated in the epidermis.
30 and proper autoreactive T-cell homing to the epidermis.
31 is essential for all functions of the human epidermis.
32 of IAA-Glu (IAA-glutamate) in the hypocotyl epidermis.
33 atin filament network in the differentiating epidermis.
34 urine airway epithelia and in Xenopus laevis epidermis.
35 d mechanical support in keratinocytes of the epidermis.
36 d to identify the progenitors of regenerated epidermis.
37 ll functions, and it is highly active in the epidermis.
38 d maintenance of the barrier function of the epidermis.
39 pression pattern we had identified in keloid epidermis.
40 of autophagy marker expression in developing epidermis.
41 involved in maintaining the integrity of the epidermis.
42 vels in the proliferative basal layer of the epidermis.
43 stability of intercellular adhesions in the epidermis.
44 pes and their location within the dermis and epidermis.
45 nto preexisting ordered spatial units of the epidermis.
46 is highly expressed in the developing murine epidermis.
47 there are no specialized stem cells for the epidermis.
48 n EPI-/- skin and penetrated deeper into the epidermis.
49 retinoic acid synthesis deficiency in keloid epidermis.
50 tyl growth in shade, with a key role for the epidermis.
51 Root hairs are tubular extensions of the epidermis.
52 e and is required for the differentiation of epidermis.
53 ein kinase B (AKT) signaling pathways in the epidermis.
54 ls through changes in speciation at the root epidermis.
55 etime of individual cells in the ear and paw epidermis.
56 primary keratins expressed in differentiated epidermis.
57 so localized in trichomes covering the fruit epidermis.
58 proliferation in neonatal and wounded adult epidermis.
59 mpatible rhizobial exopolysaccharides at the epidermis.
60 the density of small nerve fibers within the epidermis.
61 (LCs) are the only DC subset in the healthy epidermis.
62 proliferation and differentiation within the epidermis.
63 tant for the terminal differentiation of the epidermis.
64 ithin the HF infundibulum and perifollicular epidermis.
65 p63-regulated gene expression program in the epidermis.
66 surface of both porcine and human cadaveric epidermis.
67 ncentrations of these elements than the root epidermis.
68 sequently promote cell-type diversity in the epidermis.
69 hat PFKFB3 was highly expressed in psoriatic epidermis.
70 ng of combinatorial integrin function in the epidermis.
71 the wound margins and/or in the regenerating epidermis.
72 another planar tissue, the Arabidopsis leaf epidermis [5], polarized, asymmetric divisions of stomat
73 outer (periclinal) cell wall of onion scale epidermis - a model system for relating wall structure t
74 ent to detoxify H2O2 that reaches the viable epidermis after exposure of skin to high concentrations
75 expression was predominantly located in the epidermis, although also evident in the papillary dermis
76 is also synthesized by keratinocytes in the epidermis, although its epidermal functions are not clea
78 eous nerves extend throughout the dermis and epidermis and control both the functional and reparative
79 howed differential expression of Epr3 in the epidermis and cortical primordia and identified key tran
80 ively proliferating cells of mouse and human epidermis and cSCC, and downregulated during terminal di
81 ure media and extracts from stratum corneum, epidermis and dermis after 24h, and the results were com
82 herapeutically relevant levels into both the epidermis and dermis and that the skin-penetrating aptam
83 ridization assay quantified aptamer from the epidermis and dermis, giving levels far exceeding the ce
86 rcade cell epithelium is generated after the epidermis and digestive tract epithelia have matured, en
87 meate through the stratum corneum and viable epidermis and efficiently deposit therapeutic levels of
91 ruits effector CD8(+) T cells that enter the epidermis and form populations of long-lived tissue-resi
92 where during homeostasis, stem cells of the epidermis and hair follicle fuel their respective tissue
93 rotein was found to be expressed in both the epidermis and hair follicle of normal skin, but its expr
95 l fate decisions in the embryo and the adult epidermis and immune systems, yet emerging evidence sugg
101 hemical transformations were observed on the epidermis and inside roots, even for Ag2S-NPs, leading t
103 cruitment of keratinocytes from the adjacent epidermis and make re-epithelialization independent of k
104 -related protein (PTHrP) in their developing epidermis and mammary glands] with those from wild type,
106 null mutant where rhizobial invasion of the epidermis and nodule organogenesis was unaffected but rh
107 re specifically localized to the presumptive epidermis and notochord, and play a critical and unexpec
108 t frequently occurring cell type in the leaf epidermis and play important roles in leaf growth and fu
110 rangements of altered gene expression in the epidermis and prominent clustering of the adjacent derma
111 or cells exist within the basal layer of the epidermis and serve to replenish the loss of differentia
112 ons and a dramatic depletion of mtDNA in the epidermis and showed macroscopic signs of severe skin in
113 e, we find that Sema-2b is secreted from the epidermis and signals through the Plexin B receptor in n
118 nges in DEK1 lead to cellular defects in the epidermis and the pathways through which DEK1 acts.
119 hairs are single-cell extensions of the root epidermis and the primary organs for water uptake and nu
122 s melted away by interstitial fluid from the epidermis and upper dermis, exposing the powder to epide
124 represent condensed remains of the cornified epidermis and, likely also, deeper anatomical features,
126 ortant controllers of gene expression in the epidermis, and altered AP1 factor function can perturb k
127 loss of the pigment-producing cells from the epidermis, and development of vitiligo-like lesions.
128 The outermost cell layer of plants, the epidermis, and its outer (lateral) membrane domain facin
129 ependent force anisotropy within the lateral epidermis, and stiffness anisotropy within the fiber-rei
131 ectomy produced nipples with abnormally thin epidermis, and we identified TGFbeta as a negatively reg
132 py within the fiber-reinforced dorso-ventral epidermis are critical in driving embryonic elongation.
133 ese data suggest that HA levels in the human epidermis are not directly correlated with keratinocyte
136 nockout mice a significant thickening of the epidermis associated with a decreased transepidermal wat
137 F infundibulum and adjoining interfollicular epidermis, associated with a switch from p63 transcripti
138 scriptome profiling of K14CreERT;DLX3(fl/fl) epidermis at 3 days identified activated STAT3 as a tran
139 ctions that most evaporation occurs from the epidermis at low light and moderate humidity but that th
141 ing melanocytes expanded clonally within the epidermis before losing their differentiated features th
143 AS40(T246A)) in basal keratinocytes of mouse epidermis (BK5.PRAS40(T246A) mice) has allowed further e
145 ontrol trichome initiation not only from the epidermis but also from the leaf layer underneath the ep
147 an epithelial bridge between the foregut and epidermis, but little is known about how development of
148 a and amyloid A mRNA levels increased in the epidermis, but not in the liver, in parallel with a sign
149 tion in cuticular ridges on the mature sepal epidermis, but only a moderate effect on petal cone cell
150 Staphylococcus aureus commonly colonizes the epidermis, but the mechanisms by which the host senses v
151 nk between GA and cytokinin signaling in the epidermis by negatively regulating downstream genes of b
154 saw puzzle-shaped pavement cells in the leaf epidermis collectively function as a load-bearing tissue
156 lysis and immunohistochemistry of the palmar epidermis demonstrated significantly increased expressio
158 es, which are involved either in the skin or epidermis development or in the collagen metabolism, and
163 qual to the distance from these veins to the epidermis (dy), expressed as dx:dy approximately 1.
165 h transcriptional profiling of the hypocotyl epidermis from Brassica rapa, we show that auxin acts in
167 monstrate that Dnmt3a and Dnmt3b protect the epidermis from tumorigenesis and that squamous carcinoma
170 rcinomas (SCCs) derived from interfollicular epidermis (IFE) are generally well differentiated, while
171 ities in wild-type and CGI-58 overexpressing epidermis implicating that CGI-58 participates in omega-
172 uid, dissolved slowly, and diffused into the epidermis in a day against the interstitial fluid influx
173 attenuated freeze-dried BCG powder into the epidermis in a painless, lesion-free, and self-applicabl
175 lying hyperproliferation of the palmoplantar epidermis in both physiological and disease states, and
177 fected but rhizobia remain restricted to the epidermis in infection threads migrating parallel to the
178 rs in cortical cells before spreading to the epidermis in L. japonicus While mutant analysis identifi
179 rassica rapa, we show that auxin acts in the epidermis in part by inducing activity of the locally ac
180 ts and in long-term regenerated human mosaic epidermis in vivo, epidermal PRMT1 loss abolished progen
183 his approach works in multiple tissues - the epidermis, intestine, body wall muscle, ciliated sensory
185 oimmunity in vitiligo, and we found that the epidermis is a chemokine-high niche in both a mouse mode
186 that increased cis-to-trans UCA ratio in the epidermis is a distinct feature of CSU, which could enha
187 The major end product in human and porcine epidermis is a trihydroxy derivative, formed with a spec
188 ulse using a pressure sensor attached on the epidermis is an important technology for detecting the e
194 h is predominantly expressed in palmoplantar epidermis is implicated in AD may shed new light on the
195 , these results show that specialized nipple epidermis is maintained by estrogen-induced repression o
197 evelopment, recruitment and retention in the epidermis is orchestrated by interactions with keratinoc
198 hich the melanocyte-depleted interfollicular epidermis is repopulated by melanocyte precursors from h
199 a constitutively active DELLA protein in the epidermis is sufficient to promote ENOD11 expression in
201 ere we show that SAMHD1 is also expressed in epidermis-isolated Langerhans cells (LC), but degradatio
202 ogical analyses revealed the formation of an epidermis layer, neovascularization and cell proliferati
203 ting AP1 factor function in suprabasal adult epidermis leads to reduced filaggrin levels and to a phe
207 le biosensors that naturally comply with the epidermis, most designs measure only a small number of p
208 prostasin: a function in the interfollicular epidermis, not requiring activation site cleavage, that
209 s used to create a small cavity in the upper epidermis of A. tequilana leaves, where the fabricated e
211 eristem, mainly in the cytosol, and that the epidermis of adt3 cotyledons contains higher levels of R
213 ork (TGN) to the plasma membrane in the root epidermis of Arabidopsis (Arabidopsis thaliana) and that
214 he PIPs were not detected within the non-PIP epidermis of corresponding normal chronically exposed sk
215 integrin in controlling the secretion by the epidermis of factors that modulate the tissue microenvir
216 ) RNase 7 is constitutively expressed in the epidermis of healthy human skin and has been found to be
218 orbol-13-acetate restored TG activity in the epidermis of keratinocyte-specific Adam17(-/-) (AD17(Del
219 wed weaker intercellular connectivity in the epidermis of keratinocytes in AhR-knockout mice, and gen
220 Stomata are dispersed pores found in the epidermis of land plants that facilitate gas exchange fo
223 Stomatal guard cells surround pores in the epidermis of plant leaves, controlling the aperture of t
224 ession of glucocorticoid biosynthesis in the epidermis of psoriatic skin leading to localized deficie
225 expressions were significantly increased in epidermis of TC-PTP-deficient mice compared to control m
226 esses to close a discontinuity in the dorsal epidermis of the embryo, requires both cell-cell and cel
227 assessment of TRPV1-lineage afferents in the epidermis of the hind paws of the reporter mice showed t
228 ied NF (4 and 24 h of treatment) in the root epidermis of the model legume Medicago truncatula Tissue
231 We show that expression of COI1-YFP in the epidermis of the stamen filament and anther in coi1 muta
233 ely different, with iron bound mainly in the epidermis of the wild-type plants but confined to the co
235 of the small nerve fibers that innervate the epidermis, one hypothesis is that erythromelalgia could
236 ate that the elemental concentrations in the epidermis, outer endodermis and inner endodermis are sig
237 y required after wound closure, allowing the epidermis outside the wound to re-establish its normal t
238 tor function during development in embryonic epidermis produces marked phenotypic changes including r
239 ell migration, redox response, inflammation, epidermis re-epithelialization, granulation formation, a
240 vivo and in vitro evidence that SIRT1 in the epidermis regulates cell migration, redox response, infl
241 and the animals lacking BRAF and RAF1 in the epidermis represent a useful model for this disease.
242 barrier in multi-layered epithelia like the epidermis requires restricted positioning of functional
244 process that produces breathing pores in the epidermis, requires asymmetric cell division to differen
247 nistration deposits the DNA primarily on the epidermis resulting in a rapid loss of the DNA as well a
248 ntification of TIP39 and its receptor in the epidermis reveals an additional PTH family member that i
249 ng inhibition in crude preparations of mouse epidermis robustly increases proliferative capacity of p
252 native power was more than 90% in the viable epidermis skin layer; whereas for BRAF inhibitors, discr
253 ed in the switch from 'early' stages; normal epidermis, solar elastosis and early actinic keratosis t
254 lution of keratinocytes towards cSCC: Normal epidermis, solar elastosis, actinic keratosis KIN1-2, ad
255 l cell migration and survival, and wounds of epidermis-specific alpha3 knockout mice displayed impair
256 mulation of endothelial cells, and wounds of epidermis-specific alpha9 knockout mice displayed delaye
260 essential regulator in skin morphogenesis by epidermis-specific deletion of Mtor in mice (mTOR(EKO)).
263 ntiation and maintenance, acting upstream of epidermis-specific transcription factors, and is require
266 yme AKR1B10 as highly up-regulated in keloid epidermis suggested that an imbalance of retinoic acid m
267 nel of preterm transgenic mice, we show that epidermis-targeted coexpression of sT and the cell fate-
268 stingly, LmCYP4G102 was not expressed in the epidermis that produces the cuticle but in the sub-epdie
271 itochondrial helicase (K320E-TWINKLE) in the epidermis to accelerate the accumulation of mtDNA deleti
272 e hypothesized that transformation of normal epidermis to cutaneous squamous cell carcinoma (cSCC) is
273 nsiently divided clusters of Shha-expressing epidermis to escort pObs into similarly split groups.
275 non-autonomous signal produced in the anther epidermis to synchronize both anther dehiscence and poll
276 ee-energy barrier at the transition from the epidermis to the dermis underneath, which determines the
278 cross-tissue signaling from the hypodermis (epidermis) to the intestine to promote reproductive succ
279 l to this function, and demonstrates how the epidermis triggers unwanted skin inflammation under dise
280 io to explain pavement cell shapes within an epidermis under tension must involve mechanical wall het
282 Epidermal keratinocytes migrate through the epidermis up to the granular layer where, on terminal di
283 sit therapeutic levels of siRNA to the basal epidermis/upper dermis where melanoma cells reside.
285 we performed acute deletion of DLX3 in adult epidermis using a tamoxifen-inducible Krt14-cre/ERT syst
288 How DETC become uniquely associated with the epidermis was in large part solved by the identification
290 Since most PGPB colonize the plant root epidermis, we hypothesized that PGPB confer tolerance to
291 Hs) regulate mitochondrial function in human epidermis, we treated organ-cultured human skin, or isol
292 ponent of cornified envelopes in keratinized epidermis, were substantially up-regulated inMsx1(d/d)/M
295 rs in proliferative basal cells of mammalian epidermis whereupon cell division, transmembrane planar
296 imulators of mitochondrial function in human epidermis, which down-regulates rather than enhance the
298 early postnatal lethality, due to a thinned epidermis with decreased desmosomal protein expression a
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