戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 that TGX contributes to the formation of the cornified envelope.
2 n by covalent binding of acylceramide to the cornified envelope.
3 responsible for assembly of the keratinocyte cornified envelope.
4 and that FATP4 functions in establishing the cornified envelope.
5 ier structure on their periphery, termed the cornified envelope.
6 nocyte and critical for the formation of the cornified envelope.
7 ent proteins leading to the formation of the cornified envelope.
8 he late marker, loricrin, a component of the cornified envelope.
9 tuents of both keratohyalin granules and the cornified envelope.
10  junctions and terminally differentiate into cornified envelopes.
11 erentiation, as measured by the formation of cornified envelopes.
12 ced lower levels of cross-linked protein and cornified envelopes.
13 ycle, stratification, and even production of cornified envelopes.
14  reduced mechanical strength detected in the cornified envelopes.
15 inal differentiation markers and assembly of cornified envelopes.
16 in knockout mouse skin and confirm that late cornified envelope 1 genes are transcriptional targets o
17                We also demonstrate that late cornified envelope 1 genes are upregulated at the transc
18 we present evidence suggesting that the late cornified envelope 1 proteins are also compensatory comp
19 cross-linked keratin filaments enclosed in a cornified envelope [1].
20 gulating the expression of genes of the late cornified envelope-1 (Lce1) family involved in epidermal
21 n barrier, which is normally imparted by the cornified envelope, a composite of protein and lipid tha
22 res are selectively perturbed, including the cornified envelope, a likely scaffold for lipid organiza
23 amellar body, corneocyte lipid envelope, and cornified envelope abnormalities.
24 elope formation, evidenced by restoration of cornified envelopes after CLE rescue.
25 oteins are cross-linked together to form the cornified envelope, an essential and discrete unit of th
26 ly during fetal days E15.5 to E16.5, and the cornified envelope and desmosomes in the newborn mice we
27 eratinocytes reinforced by proteins of their cornified envelope and sequestered intercellular lipids.
28 NIKS keratinocytes produce similar levels of cornified envelopes and nucleosomal fragmentation in res
29 rkedly increased the number of cells forming cornified envelopes and the number of cells staining wit
30 y being structural protein precursors of the cornified envelope) and the other 13 belong to the S100
31 various protein and lipid components for the cornified envelope, and the controlled dissolution of ce
32  (LBs) and LB secretion, thinner lipid-bound cornified envelopes, and a defective permeability barrie
33 dermal differentiation, leading to thickened cornified envelopes; and (ii) enhanced epidermal lipid s
34                             However, because cornified envelopes are attenuated in these autosomal re
35    The third wave contains components of the cornified envelope, as keratinocytes enhance the epiderm
36 eability assays to show that final stages of cornified envelope assembly are coordinated with initial
37 d in CNBr extracts of purified keratinocytes cornified envelopes by western blot.
38 h loricrin is the predominant protein of the cornified envelope (CE) in keratinocytes, loss or gain o
39                                          The cornified envelope (CE) is an insoluble sheath of epsilo
40                                              Cornified envelope (CE) precursor protein expression and
41    Real-time PCR evaluated the expression of cornified envelope (CE) precursor proteins (involucrin a
42 t S100A11 is a component of the keratinocyte cornified envelope (CE) suggests that S100A11 is a trans
43 cross-linked in an orderly fashion to form a cornified envelope (CE).
44  epidermis, disturbed cornification, fragile cornified envelope (CE, a skin barrier structure), and i
45                    Comparative proteomics of cornified envelopes (CEs) from prenatal KtyI(-/-) and Kt
46 tain keratin filaments bound to a peripheral cornified envelope composed of cross-linked proteins.
47                 Sciellin, a precursor of the cornified envelope, contains a LIM domain that is known
48  than to corneocyte fragility or an abnormal cornified envelope/cornified-bound lipid envelope scaffo
49                        This directly affects cornified envelope cross-linking rather than corneodesmo
50 al proteins involved in the formation of the cornified envelope during squamous cell differentiation.
51 responsible for assembly of the keratinocyte cornified envelope during terminal keratinocyte differen
52                                              Cornified envelopes form but are ultrastructurally abnor
53 anced Oral Squamous Cell Carcinoma, with the cornified envelope formation and antigen processing cros
54 Ca2+-induced differentiation, as assessed by cornified envelope formation or transglutaminase activit
55 f the TIG3-positive cells and the effects on cornified envelope formation suggest that TIG3 is an act
56                                  The rate of cornified envelope formation was increased 3-fold in ker
57 t, corneocyte-bound lipid envelopes, whereas cornified envelope formation was unchanged.
58                                     Rates of cornified envelope formation, a marker of keratinocyte t
59                                     Rates of cornified envelope formation, an indicator of terminal d
60 LE may also provide a scaffold for subjacent cornified envelope formation, evidenced by restoration o
61 and mRNA levels of two proteins required for cornified envelope formation, involucrin (INV) and trans
62 ression of structural proteins necessary for cornified envelope formation, involucrin, loricrin, and
63 ed in SCC 12F cells, including inhibition of cornified envelope formation, reduction of involucrin mR
64 ikely to have a similar functional effect on cornified envelope formation, with disturbance of transg
65  inflammatory responses, keratinization, and cornified envelope formation.
66 nced transglutaminase activity and excessive cornified envelope formation.
67  possible link between connexin function and cornified envelope formation.
68 cessation of cell proliferation and enhanced cornified envelope formation.
69 bstrates, the small proline-rich proteins of cornified envelopes found in stratified squamous epithel
70 mal skin barrier requires the formation of a cornified envelope from terminally differentiating kerat
71 e-rich (Sprr2) protein, a major component of cornified envelopes in keratinized epidermis, were subst
72                                          The cornified envelope is a layer of transglutaminase cross-
73                                          The cornified envelope is assembled from transglutaminase cr
74 art of the scaffold onto which the epidermal cornified envelope is assembled.
75 ins may provide a scaffolding onto which the cornified envelope is assembled.
76 ggested that SerpinB2 (cross-linked into the cornified envelope) is present in the stratum corneum an
77 own that cyanogen bromide (CNBr) cleavage of cornified envelopes isolated from cultured foreskin kera
78                                     The late cornified envelope (LCE) gene cluster within the epiderm
79                             Deletion of late cornified envelope (LCE) genes LCE3B and LCE3C (LCE3B/C-
80                                         Late cornified envelope (LCE) genes, located in the epidermal
81                Six SNPs associated with late cornified envelope (LCE3) genes were present at greater
82 uclear shrinkage, and increased formation of cornified envelope-like structures.
83 tase/MT-SP1 perturbs lipid matrix formation, cornified envelope morphogenesis, and stratum corneum de
84 n and infection is bacterial adhesion to the cornified envelope of corneocytes in the outer layer, th
85  proteins that becomes incorporated into the cornified envelope of cultured epidermal keratinocytes,
86  of periplakin, and is incorporated into the cornified envelope of cultured keratinocytes.
87    Involucrin is a protein that makes up the cornified envelope of keratinocytes and is expressed in
88         Involucrin is a major protein of the cornified envelope of keratinocytes that provides much o
89         Involucrin is a major protein of the cornified envelope of keratinocytes that provides much o
90               Sciellin is a precursor of the cornified envelope of mammalian stratified epithelia cha
91               Sciellin is a precursor of the cornified envelopes of mammalian keratinizing tissues.
92 on microscopy showed no defect in either the cornified envelope or the adjacent cornified-bound lipid
93 hornerin [hrn] and filaggrin 2 [flg-2]); the cornified envelope precursor (ie, SPRR3); mattrin, which
94 kers K1 and K10 and the cross-linking of the cornified envelope precursor protein involucrin.
95 ssion of ZNF750-dependent genes encoding key cornified envelope precursor proteins and lipid-processi
96 xamine the intracellular distribution of the cornified envelope precursor S100A11 (S100C) and the eff
97 affinity column made with an antibody to the cornified envelope precursor sciellin.
98                                Involucrin, a cornified envelope precursor, and the cross-linking enzy
99 ), functions as a transglutaminase substrate/cornified envelope precursor, signal transduction protei
100 imulates ocular surface epithelia to produce cornified envelope precursors and the tissue transglutam
101 ne repeat organization is unique among other cornified envelope precursors characterized by homologou
102                          Several cytoplasmic cornified envelope precursors have been described.
103 to evaluate the presence and distribution of cornified envelope precursors in human corneal epitheliu
104 cal epithelia expressing increased levels of cornified envelope precursors.
105                          Desquamation of and cornified envelope protein (involucrin and small proline
106 corneocytes in the stratum corneum where the cornified envelope protein loricrin is the main ligand f
107 ing insertional mutants of Loricrin, a major cornified envelope protein of the epidermis, suggest a p
108                                          The cornified envelope protein small proline-rich protein 1B
109 pidermal keratins was unchanged, whereas the cornified envelope proteins involucrin and loricrin were
110                                    Levels of cornified envelope proteins mRNA were measured by real-t
111                   Thus, combined loss of the cornified envelope proteins not only impairs the epiderm
112 on, we identified three transcripts encoding cornified envelope proteins with altered expression in t
113 eramides covalently linked by ester bonds to cornified envelope proteins, most abundantly to involucr
114 cal desquamation and increased expression of cornified envelope proteins.
115 uman SPRR1 gene and other genes encoding for cornified envelope proteins.
116 e loss of loricrin, a major component of the cornified envelope, results in a delay of epidermal barr
117 ation of the epidermis and the production of cornified envelopes, structures essential for barrier ac
118 ant structural component of the keratinocyte cornified envelope that is expressed early in the kerati
119 in (hINV) is a precursor of the keratinocyte cornified envelope that is specifically expressed in the
120 diate filaments and is cross-linked into the cornified envelope to form the epidermal barrier.
121   Involucrin is an integral component of the cornified envelope which is a characteristic feature of
122 s peptide from recombinant hINV and from the cornified envelopes yields the sequence G-Q-L-K-H-L-E-Q-

 
Page Top