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1 f specialized mesenchymal cells known as the dermal papilla.
2 n interpreting a gradient emanating from the dermal papilla.
3 hought to be determined by the volume of its dermal papilla.
4 rea of the hair cortex and the volume of the dermal papilla.
5 s androgens must regulate is the size of the dermal papilla.
6  large abnormal follicles containing a small dermal papilla.
7 c staining of the nuclei of the cells of the dermal papilla.
8 eceptor was expressed in the hair matrix and dermal papilla.
9 label-retaining cells, descend to the apical dermal papilla.
10 WNT6 and WNT10B, and inhibiting SFRP1 in the dermal papilla.
11 s, including HFSCs, secondary hair germ, and dermal papilla.
12 talized DPCs have high resemblance to intact dermal papilla.
13 ent hair buds also show abnormalities in the dermal papilla.
14 es, namely epithelial matrix and mesenchymal dermal papilla.
15 ndrogenetic alopecia by interfering with the dermal papilla.
16 b expressed markers of the dermal sheath and dermal papilla.
17  the diffusible IGF antagonist Igfbp3 in the dermal papilla.
18 o detect genes specifically expressed in the dermal papilla.
19  unravel new molecular landscapes within the dermal papilla.
20  populate a papillar ectoderm niche near the dermal papilla.
21  base of rete ridges or overlying the tip of dermal papilla.
22 nitor cells that maintain and regenerate the dermal papilla, a key component for hair growth.
23 thought to be controlled by signals from the dermal papilla, a specialized cluster of mesenchymal cel
24 ired for hair cycle regulation and hair germ-dermal papilla anchoring.
25  mean 17-fold greater number of cells in the dermal papilla and a 2.4-fold greater volume associated
26 t the functional lineage restriction between dermal papilla and adipocyte fates is regulated by disti
27 he close reciprocal relationship between the dermal papilla and adjacent HF epithelial cells.
28 ession of IP-associated genes in cultured HF dermal papilla and dermal sheath cup cells (DSCCs) compa
29 trix metalloproteinase 1 was elevated in the dermal papilla and dermal sheath in situ.
30 tes in the basal layer of the IFE and in the dermal papilla and hair bulb.
31 licles exhibited pigment incontinence in the dermal papilla and in selected outer root sheath keratin
32 oughout the murine hair cycle, including the dermal papilla and lower epithelial strand of late-catag
33 hifts in noncoding regions also included the dermal papilla and matrix regions of the hair follicle t
34           Signaling interactions between the dermal papilla and neighboring stem cells (SCs) in the h
35  supported by reduced proliferation of human dermal papilla and predominantly epithelial keratinocyte
36 owth phase, lower dermal sheath can generate dermal papilla and pulp.
37 ic cartilage, connective tissue fibroblasts, dermal papilla and sheath cells, and adipocytes in the a
38 trix expressed SUR1 and Kir6.2, whereas both dermal papilla and sheath exhibited SUR2B and Kir6.1.
39 gest that onychodermis is the counterpart of dermal papilla and that BMP5 in onychofibroblasts plays
40 olled by reciprocal interactions between the dermal papilla and the surrounding epidermal hair precur
41 o correlated with the number of cells in the dermal papilla and with the volume of dermal papilla per
42 d in the outer root sheath, sebaceous gland, dermal papilla, and connective tissue sheath of human an
43 romote the formation of a tightly aggregated dermal papilla, and/or protect the dermal papilla cells
44 interactions that lead to the formation of a dermal papilla anlage and ingrowth of the epidermis.
45    Further, IGF-I receptor expression by the dermal papilla appears to be switched off during the tra
46                                 The follicle dermal papilla appears to be the site of androgen action
47  Melanocyte stem cells more distant from the dermal papilla are unscathed, thereby preventing hair gr
48 estricted to the hair matrix surrounding the dermal papilla, are found in the precortex and hair shaf
49 pled receptor kinase 2 deletion displace the dermal papilla away from the bulge and promote irreversi
50  stem cell homeostasis beneath the stem cell-dermal papilla-based epithelial-mesenchymal interaction
51                  Onychodermis and follicular dermal papilla both expressed Wnt and bone morphogenetic
52 0 years revealed many previously undescribed dermal papilla, bulge SC, and hair germ SC genes in mous
53 ll transcriptomics established signatures of dermal papilla, bulge SCs, and hair germ SCs, but low de
54 e located in the key follicle regulator, the dermal papilla, by analyzing individual follicular struc
55 s stimulated in both frontal scalp and beard dermal papilla cell cultures by dexamethasone.
56               Spheroids, induced by printing dermal papilla cells (DPCs) and human umbilical vein cel
57                                              Dermal papilla cells (DPCs) located in the hair bulb are
58                                              Dermal papilla cells (DPCs) taken from male androgenetic
59 enes and promoted the proliferation of human dermal papilla cells (DPCs).
60                                        Human dermal papilla cells (HDPC) express mRNA for the key enz
61 alding occipital and frontal scalp and beard dermal papilla cells (n = 10) were established.
62  that the comparison of the mRNA of cultured dermal papilla cells and fibroblasts can lead to the ide
63 d a previously unrecognised heterogeneity in dermal papilla cells and shown that Sox2-positive cells
64                        Communication between dermal papilla cells and the overlying epithelium is ess
65 in large quantities in cultured rat vibrissa dermal papilla cells but undetectable in cultured rat sk
66 this study was designed to determine whether dermal papilla cells cultured from human hair follicles
67 ptor and/or aromatase expression in cultured dermal papilla cells derived from human hair follicles.
68 P-1 expression was absent from hair bulb and dermal papilla cells during early to mid-anagen but was
69 show that Blimp1 is dynamically regulated in dermal papilla cells during hair follicle (HF) morphogen
70  from neonatal foreskins and cultured murine dermal papilla cells from adult GFP transgenic mice and
71                         Low passage cultured dermal papilla cells from adult rats stimulate complete
72 ggregated dermal papilla, and/or protect the dermal papilla cells from apoptosis induced by cytokines
73                                         Once dermal papilla cells have lost hair-inducing properties
74 med global gene expression analysis of human dermal papilla cells in culture and discovered very rapi
75 apitulate this process in humans using human dermal papilla cells in human skin have failed, suggesti
76 and how to enrich for hair follicle-inducing dermal papilla cells in the dermal preparation.
77 imulated and androgen-treated cultured human dermal papilla cells isolated from beard (androgen-sensi
78 uman skin have failed, suggesting that human dermal papilla cells lose key inductive properties upon
79 ed that the osteopontin gene is expressed in dermal papilla cells of pelage follicles during catagen
80                                              Dermal papilla cells of the hair follicle can be maintai
81  addition, this study supports that cultured dermal papilla cells provide a cell-based model system t
82 n of these genes in cultured beard and scalp dermal papilla cells reflected similar differences in mi
83 ) was significantly upregulated in DSCCs and dermal papilla cells relative to FBs.
84 y skin keratinocytes and fibroblasts without dermal papilla cells served as positive and negative con
85        This implies that androgens stimulate dermal papilla cells to divide or to secrete autocrine m
86                         By inducing cultured dermal papilla cells to secrete Wnt themselves, we demon
87  this study, we define the transcriptomes of dermal papilla cells, bulge SCs, hair germ SCs, epiderma
88 ens do not stimulate mitogenesis in cultured dermal papilla cells, this study was designed to determi
89 inductive capability, and we show that human dermal papilla cells, when grown as spheroids, are capab
90 e, primary keratinocytes, preadipocytes, and dermal papilla cells.
91  in the inner root sheath, matrix cells, and dermal papilla cells.
92  in the inner root sheath, matrix cells, and dermal papilla cells.
93 s of the VDR status of the keratinocytes and dermal papilla cells.
94 nocytes of the outer root sheath, but not by dermal papilla cells.
95 eta-catenin and Hh pathways are activated in dermal papilla cells.
96 compared them with Sox2(-) (GFP(-)) CD133(+) dermal papilla cells.
97 duce potentially novel signaling pathways in dermal papilla cells.
98 ibulin-1d, was slightly upregulated in beard dermal papilla cells.
99 ssed at significantly higher levels in beard dermal papilla cells.
100 ivity is a direct effect of Wnt signaling to dermal papilla cells.
101 reased [3H] thymidine incorporation by other dermal papilla cells; trypsin treatment significantly re
102 mary DPCs in hair-related studies often lack dermal papilla characteristics.
103                                          The dermal papilla comprises the specialised mesenchymal cel
104 nterior-posterior Wnt2b signaling within the dermal papilla controls barbule cell fates with spatiote
105                            The volume of the dermal papilla depends on the number of cells it contain
106 ) morphogenesis and cycling, the location of dermal papilla (DP) alternates between the dermis and hy
107  in the inner root sheath (IRS), whereas the dermal papilla (DP) and outer root sheath were consisten
108         In neonatal mouse skin, two types of dermal papilla (DP) are distinguished by Sox2 expression
109  assembly strategies for the interactions of dermal papilla (DP) cells with adipose-derived stem cell
110 ls receive cues from specialized mesenchymal dermal papilla (DP) cells.
111 bridization to identify genes induced in the dermal papilla (DP) during anagen as a result of the int
112                            The hair follicle dermal papilla (DP) expresses androgen receptors (AR) an
113                                              Dermal papilla (DP) from laminin-511 mutants showed deve
114                                          How dermal papilla (DP) niche cells regulate hair follicle p
115 ranscription factor Sox2 is expressed in the dermal papilla (DP) of guard/awl/auchene hair follicles
116 3 (Prom1) is expressed by fibroblasts in the dermal papilla (DP) of the hair follicle (HF).
117  and gain of function of beta-catenin in the dermal papilla (DP) of the hair follicle results in yell
118 ranscription factor Tbx18 specifically marks dermal papilla (DP) precursor cells during embryonic hai
119                                          The dermal papilla (DP) provide instructive signals required
120  cILC2s accumulated around the hair follicle dermal papilla (DP) region to facilitate the process.
121                        Functional testing of dermal papilla (DP) signaling inputs into hair follicle
122 Systematic ablation of previously identified dermal papilla (DP) signature genes in embryonic DP prec
123 eets target lung CSCs but not normal primary dermal papilla (DP) stem cells.
124                                          The dermal papilla (DP), a dense aggregate of specialized de
125            The dermal organizing center, the dermal papilla (DP), regulates development of the epider
126 by a specialized mesenchymal population, the dermal papilla (DP), that is embedded in the hair bulb.
127 in a unique niche at the HF base, called the dermal papilla (DP).
128 clusters of precursors for the hair follicle dermal papilla (DP).
129 ts at the base of the follicle, known as the dermal papilla (DP).
130 ls from a specialized mesenchymal niche, the dermal papilla (DP).
131 ion of the Wnt3a gradient is dictated by the dermal papilla (DP).
132                                    Moreover, dermal-papilla-enriched expression of SCUBE3 and its gro
133 n wound closure, we found that hair follicle dermal papilla fibroblasts could accelerate closure of i
134               On single-cell RNA sequencing, dermal papilla fibroblasts increase heterogeneity to inc
135  polarity, and loss of TGF-beta signaling in dermal papilla fibroblasts leads them to progressively l
136 rough mouse intravital imaging, we show that dermal papilla fibroblasts remodel individually and coll
137 e used a cytokine array to determine how the dermal papilla fibroblasts were eliciting this effect an
138                                              Dermal papilla fibroblasts were the most highly differen
139 uctive potential and premature senescence of dermal papilla fibroblasts, or by intraepithelial events
140    Hair follicle stem cells are regulated by dermal papilla fibroblasts, their principal signaling ni
141 n follicular melanocytes, keratinocytes, and dermal papilla fibroblasts.
142  that beta-catenin is required for Hh-driven dermal papilla formation.
143 sion of selected ones, namely PAPPA2 for the dermal papilla, FOXM1 for the germinative hair matrix, A
144 ompartment ablation and inhibition of mature dermal papilla functions, confirmed by additional single
145                    In addition to the 'core' dermal papilla gene signature, each subpopulation expres
146 expression in the mesenchymal component, the dermal papilla, has hampered progress towards understand
147 n tumours, but confined to the hair follicle dermal papilla in normal postnatal skin.
148 imply that the increase in the volume of the dermal papilla in these follicles is due to an increase
149 sence of ectodermal placode and primodium of dermal papilla in these mice, yet the subsequent hair sh
150 e functional role of Blimp1 in promoting the dermal papilla inductive signaling cascade that initiate
151 limp1 is both a target and a mediator of key dermal papilla inductive signaling pathways including tr
152 lial-fibroblast interface, namely, hair germ-dermal papilla interface, makes asymmetrically organized
153                         Since the follicular dermal papilla is known to control hair growth, and ster
154 d et al show that JAK/STAT5 signaling in the dermal papilla is required for anagen onset in the murin
155 lected similar differences in microdissected dermal papilla isolated from intact beard and scalp foll
156 o key compartments (matrix keratinocytes and dermal papilla) leads to dynamic instabilities in the po
157              In the next cycle, these apical dermal papilla LRDCs are re-activated to become new pulp
158 uce hair growth independently of mesenchymal dermal papilla niche signals normally required for hair
159 he new follicles formed sebaceous glands and dermal papilla, normally established only in embryogenes
160                       It is expressed in the dermal papilla of all pelage hair follicle types from th
161 ception of the sonic hedgehog pathway in the dermal papilla of developing hair follicles.
162 ial compartment and androgen receptor in the dermal papilla of miniaturized hair.
163 the epidermis (Lef-1, beta-catenin, Shh) and dermal papilla (p75 kDa neurotrophin receptor, alkaline
164 in the dermal papilla and with the volume of dermal papilla per cell.
165                            The appearance of dermal papilla (PRDM1+) and hair follicle (SLC26A7+) fib
166 reas Aldh1a3 expression was primarily in the dermal papilla, pre-cortex, and hair shaft during mid-la
167  with their remodeling fibroblast niche, the dermal papilla, providing a powerful model to functional
168 cate an estrogen receptor pathway within the dermal papilla regulates the telogen-anagen follicle tra
169  association studies signals are enriched in dermal papilla regulatory regions, supporting the role o
170 s, precursors of adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related
171           Both the follicular epithelium and dermal papilla showed markedly decreased Wnt/beta-cateni
172     Furthermore, we pinpoint KIT-ligand as a dermal papilla signal promoting melanocyte stem cell dif
173 nd the epithelial stem cells that respond to dermal papilla signaling.
174 oth BAB and BAN retained high proportions of dermal papilla signature gene and versican protein expre
175 these genes, sfrp-2 has been identified as a dermal papilla signature gene in mouse pelage follicles.
176 ctors may be involved in the key increase of dermal papilla size necessary for androgen-induced chang
177 ecause hair size has been clearly related to dermal papilla size, one of the key functions androgens
178 ytes, and BMP signaling positively regulates dermal papilla-specific enhancer of the Agouti gene in p
179 da-A1 expression is required until the early dermal papilla stage for guard hair germs to make follic
180          alpha-SMA (ACTA2) compartmentalizes dermal papilla stem cells for feather renewal cycling.
181    One forms the upper dermis, including the dermal papilla that regulates hair growth and the arrect
182                       The mesenchyme-derived dermal papilla that regulates the hair follicle is consi
183                           At the core is the dermal papilla, the organizing center, and the epithelia
184 leads to endogenous EDN3 upregulation in the dermal papilla, the secondary hair germ cells, and the e
185 ndrogens are thought to act primarily on the dermal papilla, these changes may have a direct bearing
186  derived from human and rodent epidermis and dermal papilla to reconstitute hair-follicle mini-organs
187               We demonstrate that the intact dermal papilla transcriptional signature can be partiall
188 n large male facial follicles the mean total dermal papilla volume was almost 40-fold higher than in
189 e expression of the estrogen receptor in the dermal papilla was hair cycle-dependent with the highest
190  the outer root sheath, sebaceous gland, and dermal papilla, whereas CCAAT/enhancer-binding protein-b
191 r matrix which forms the hair itself, or the dermal papilla which is responsible for induction of the

 
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