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1 ctedly restricted to the dermal papillae and outer root sheath.
2 ocated in the bulge, a specialization of the outer root sheath.
3 f1, and increased proliferative cells in the outer root sheath.
4 root sheath, and the innermost layers of the outer root sheath.
5 r, proliferate, and appear to migrate up the outer root sheath.
6 t, bulb matrix cells, and basal layer of the outer root sheath.
7 vity was detected in the bulge region of the outer root sheath.
8 xpressed by a subset of keratinocytes in the outer root sheath.
9 the inner root sheath, and the third for the outer root sheath.
10 ow that the nestin-expressing cells form the outer-root sheath.
11 bulge are indeed progenitors of the follicle outer-root sheath.
12 sebaceous glands, hair shafts and inner and outer root sheaths.
13 a tractor mechanism involving the inner and outer root sheaths.
14 o the matrix, sebaceous gland, and inner and outer root sheaths.
15 lso exhibited increased proliferation in the outer root sheath, accelerated hair cycle, reduction of
16 Aldh1a2 expression was seen primarily in the outer root sheath and basal/spinous layer during all sta
18 t at high levels in a subset of cells in the outer root sheath and in precursor cells of the hair sha
19 -stripped hair showed separation between the outer root sheath and inner root sheath of the hair foll
20 detected in the differentiating cells of the outer root sheath and medulla of the follicle during the
21 ckouts, which showed defects in the follicle outer-root sheath and the hair growth cycle, respectivel
23 al basal cell layer and of the hair follicle outer root sheath, and ~50% reduction of cell numbers in
25 FP-expressing cells are located in the upper outer-root sheath as well as in the bulge area but not i
26 of normal human epidermis and the inner and outer root sheaths but not the matrix of the hair follic
30 Here, we hypothesized that hair follicle outer root sheath cells act as transducers of mechanical
31 in anagen follicles; and the single layer of outer root sheath cells directly abutting the club hair
32 h reveals a spiral-like downward movement of outer root sheath cells entering the lower bulb region.
33 ser capture microdissection, bulge cells and outer root sheath cells from other follicle regions were
34 K6(+) cells arise from Lgr5-expressing lower outer root sheath cells in anagen, our studies indicate
35 hair bulb cells were depleted, the surviving outer root sheath cells rapidly acquired an SC-like stat
36 arations in vitro, we were able to show that outer root sheath cells release ATP and the neurotransmi
37 combined with pharmacology in a coculture of outer root sheath cells with sensory neurons, we found t
39 colocalize in the hair follicle bulge cells, outer-root sheath cells, and basal cells of the sebaceou
40 model, where a pulling force induced by the outer root sheath contributes to hair fiber extrusion.
41 confirmed that c-Myc immunoreactivity in the outer root sheath correlates with the putative hair foll
43 tner keratin 6 in the companion layer of the outer root sheath during anagen and in the club hair she
48 that epithelial compartmentalization of the outer root sheath is more complex than interfollicular e
51 ably derived from pigment-carrying migrating outer root sheath keratinocytes from the proximal hair f
52 in basal cell carcinoma islands relative to outer root sheath keratinocytes is not simply a reflecti
55 Strong Gli1 immunostaining was seen in the outer root sheath keratinocytes of some hair follicles,
56 d ornithine decarboxylase (ODC) transgene in outer root sheath keratinocytes of the hair follicle wer
57 of foreskin keratinocytes, atopic dermatitis outer root sheath keratinocytes, and H4R-transfected HaC
58 mice that expressed high levels of TSP-1 in outer root sheath keratinocytes, associated with reduced
60 ed H4R mRNA on foreskin keratinocytes and on outer root sheath keratinocytes; H4R mRNA was more abund
61 Therefore, activation is the process whereby outer root sheath melanocytes acquire all of the structu
62 H-1 and alpha-PEP-8 antibodies revealed that outer root sheath melanocytes cannot be identified by an
67 sed in the interfollicular epidermis and the outer root sheath of hair follicles in normal skin as we
68 in the basal layer of the epidermis and the outer root sheath of hair follicles under the regulation
73 son, K14 expression was found throughout the outer root sheath of hair follicles; however, when both
75 ential microflora is harboured by the distal outer root sheath of the hair follicle and the hair cana
76 idermis, sebaceous glands, sweat glands, and outer root sheath of the hair follicle with weaker expre
77 prabasal layers of the epidermis, the distal outer root sheath of the hair follicle, and the piloseba
78 to the basal layer of the epidermis and the outer root sheath of the hair follicle, as well as other
79 iating keratinocytes of the epidermis in the outer root sheath of the hair follicle, in myoepithelial
83 lieved that DOPA-negative melanocytes in the outer root sheath of the human hair follicle are activat
85 olving the interfollicular epidermis and the outer root sheaths of 1 or more hair follicles down to t
87 repopulated by melanocytes arising from the outer root sheath or follicular papilla of early/mid-cat
88 he present study, hair follicle germinative, outer root sheath or skin basal epidermal cells were sep
90 ut off, and promote features of the follicle outer root sheath (ORS) and multipotent stem cells (bulg
93 ive expression in the innermost layer of the outer root sheath (ORS) of hair follicles and inducible
95 ure hair its expression is restricted to the outer root sheath (ORS), matrix cells and to the stem ce
96 ng hair follicles, specifically cells of the outer root sheath (ORS), were extensively infected by M-
99 Deletion of CCN2 in dermal papillae and the outer root sheath results in a shortened telogen-phase l
100 r-binding protein-alpha was expressed in the outer root sheath, sebaceous gland, and dermal papilla,
101 and -delta, and Gadd153 were observed in the outer root sheath, sebaceous gland, dermal papilla, and
102 ental and anatomical parallels with follicle outer root sheath, the epithelial component that contain
103 ng, nuclear PS2 staining was observed in the outer root sheath throughout the anagen growth phase.
104 bility of keratinocytes to migrate along the outer root sheath to receive hair inductive stimuli.
105 ss human Bcl-2 in basal epidermis and in the outer root sheath under the control of the human keratin
106 nt accompanied by increased apoptosis in the outer root sheath was significantly accelerated in downl
107 h (IRS), whereas the dermal papilla (DP) and outer root sheath were consistently hr mRNA-negative.
108 ubclass of cells expresses whn, while in the outer root sheath, whn promoter activity is induced as t