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1 unravel new molecular landscapes within the dermal papilla.
2 f specialized mesenchymal cells known as the dermal papilla.
3 talized DPCs have high resemblance to intact dermal papilla.
4 n interpreting a gradient emanating from the dermal papilla.
5 hought to be determined by the volume of its dermal papilla.
6 rea of the hair cortex and the volume of the dermal papilla.
7 s androgens must regulate is the size of the dermal papilla.
8 large abnormal follicles containing a small dermal papilla.
9 c staining of the nuclei of the cells of the dermal papilla.
10 ent hair buds also show abnormalities in the dermal papilla.
11 es, namely epithelial matrix and mesenchymal dermal papilla.
12 b expressed markers of the dermal sheath and dermal papilla.
13 the diffusible IGF antagonist Igfbp3 in the dermal papilla.
14 o detect genes specifically expressed in the dermal papilla.
15 populate a papillar ectoderm niche near the dermal papilla.
16 base of rete ridges or overlying the tip of dermal papilla.
18 thought to be controlled by signals from the dermal papilla, a specialized cluster of mesenchymal cel
19 mean 17-fold greater number of cells in the dermal papilla and a 2.4-fold greater volume associated
21 ession of IP-associated genes in cultured HF dermal papilla and dermal sheath cup cells (DSCCs) compa
23 licles exhibited pigment incontinence in the dermal papilla and in selected outer root sheath keratin
24 oughout the murine hair cycle, including the dermal papilla and lower epithelial strand of late-catag
25 trix expressed SUR1 and Kir6.2, whereas both dermal papilla and sheath exhibited SUR2B and Kir6.1.
26 olled by reciprocal interactions between the dermal papilla and the surrounding epidermal hair precur
27 o correlated with the number of cells in the dermal papilla and with the volume of dermal papilla per
28 d in the outer root sheath, sebaceous gland, dermal papilla, and connective tissue sheath of human an
29 romote the formation of a tightly aggregated dermal papilla, and/or protect the dermal papilla cells
30 interactions that lead to the formation of a dermal papilla anlage and ingrowth of the epidermis.
31 Further, IGF-I receptor expression by the dermal papilla appears to be switched off during the tra
33 Melanocyte stem cells more distant from the dermal papilla are unscathed, thereby preventing hair gr
34 estricted to the hair matrix surrounding the dermal papilla, are found in the precortex and hair shaf
35 stem cell homeostasis beneath the stem cell-dermal papilla-based epithelial-mesenchymal interaction
36 e located in the key follicle regulator, the dermal papilla, by analyzing individual follicular struc
42 that the comparison of the mRNA of cultured dermal papilla cells and fibroblasts can lead to the ide
43 d a previously unrecognised heterogeneity in dermal papilla cells and shown that Sox2-positive cells
45 in large quantities in cultured rat vibrissa dermal papilla cells but undetectable in cultured rat sk
46 this study was designed to determine whether dermal papilla cells cultured from human hair follicles
47 ptor and/or aromatase expression in cultured dermal papilla cells derived from human hair follicles.
48 P-1 expression was absent from hair bulb and dermal papilla cells during early to mid-anagen but was
49 show that Blimp1 is dynamically regulated in dermal papilla cells during hair follicle (HF) morphogen
50 from neonatal foreskins and cultured murine dermal papilla cells from adult GFP transgenic mice and
52 ggregated dermal papilla, and/or protect the dermal papilla cells from apoptosis induced by cytokines
54 med global gene expression analysis of human dermal papilla cells in culture and discovered very rapi
55 apitulate this process in humans using human dermal papilla cells in human skin have failed, suggesti
57 imulated and androgen-treated cultured human dermal papilla cells isolated from beard (androgen-sensi
58 uman skin have failed, suggesting that human dermal papilla cells lose key inductive properties upon
59 ed that the osteopontin gene is expressed in dermal papilla cells of pelage follicles during catagen
61 addition, this study supports that cultured dermal papilla cells provide a cell-based model system t
62 n of these genes in cultured beard and scalp dermal papilla cells reflected similar differences in mi
64 y skin keratinocytes and fibroblasts without dermal papilla cells served as positive and negative con
67 ens do not stimulate mitogenesis in cultured dermal papilla cells, this study was designed to determi
68 inductive capability, and we show that human dermal papilla cells, when grown as spheroids, are capab
79 reased [3H] thymidine incorporation by other dermal papilla cells; trypsin treatment significantly re
83 in the inner root sheath (IRS), whereas the dermal papilla (DP) and outer root sheath were consisten
85 assembly strategies for the interactions of dermal papilla (DP) cells with adipose-derived stem cell
87 bridization to identify genes induced in the dermal papilla (DP) during anagen as a result of the int
91 ranscription factor Sox2 is expressed in the dermal papilla (DP) of guard/awl/auchene hair follicles
93 and gain of function of beta-catenin in the dermal papilla (DP) of the hair follicle results in yell
94 ranscription factor Tbx18 specifically marks dermal papilla (DP) precursor cells during embryonic hai
97 Systematic ablation of previously identified dermal papilla (DP) signature genes in embryonic DP prec
100 by a specialized mesenchymal population, the dermal papilla (DP), that is embedded in the hair bulb.
107 expression in the mesenchymal component, the dermal papilla, has hampered progress towards understand
109 imply that the increase in the volume of the dermal papilla in these follicles is due to an increase
110 sence of ectodermal placode and primodium of dermal papilla in these mice, yet the subsequent hair sh
111 e functional role of Blimp1 in promoting the dermal papilla inductive signaling cascade that initiate
112 limp1 is both a target and a mediator of key dermal papilla inductive signaling pathways including tr
114 d et al show that JAK/STAT5 signaling in the dermal papilla is required for anagen onset in the murin
115 lected similar differences in microdissected dermal papilla isolated from intact beard and scalp foll
116 o key compartments (matrix keratinocytes and dermal papilla) leads to dynamic instabilities in the po
117 uce hair growth independently of mesenchymal dermal papilla niche signals normally required for hair
118 he new follicles formed sebaceous glands and dermal papilla, normally established only in embryogenes
121 the epidermis (Lef-1, beta-catenin, Shh) and dermal papilla (p75 kDa neurotrophin receptor, alkaline
123 reas Aldh1a3 expression was primarily in the dermal papilla, pre-cortex, and hair shaft during mid-la
124 cate an estrogen receptor pathway within the dermal papilla regulates the telogen-anagen follicle tra
125 s, precursors of adult HF stem cells and the dermal papilla/sheath niche, along with lineage-related
127 Furthermore, we pinpoint KIT-ligand as a dermal papilla signal promoting melanocyte stem cell dif
129 oth BAB and BAN retained high proportions of dermal papilla signature gene and versican protein expre
130 these genes, sfrp-2 has been identified as a dermal papilla signature gene in mouse pelage follicles.
131 ctors may be involved in the key increase of dermal papilla size necessary for androgen-induced chang
132 ecause hair size has been clearly related to dermal papilla size, one of the key functions androgens
133 ytes, and BMP signaling positively regulates dermal papilla-specific enhancer of the Agouti gene in p
134 da-A1 expression is required until the early dermal papilla stage for guard hair germs to make follic
135 One forms the upper dermis, including the dermal papilla that regulates hair growth and the arrect
138 leads to endogenous EDN3 upregulation in the dermal papilla, the secondary hair germ cells, and the e
139 ndrogens are thought to act primarily on the dermal papilla, these changes may have a direct bearing
140 derived from human and rodent epidermis and dermal papilla to reconstitute hair-follicle mini-organs
142 n large male facial follicles the mean total dermal papilla volume was almost 40-fold higher than in
143 e expression of the estrogen receptor in the dermal papilla was hair cycle-dependent with the highest
144 the outer root sheath, sebaceous gland, and dermal papilla, whereas CCAAT/enhancer-binding protein-b
145 r matrix which forms the hair itself, or the dermal papilla which is responsible for induction of the
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