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1 scribed, translated, and expressed by ocular surface epithelia.
2 1) and Muc5AC mRNA transcripts by the ocular surface epithelia.
3 re typically organized into large bundles in surface epithelia.
4 eir expected biosynthetic pathways in ocular surface epithelia.
5 y occurs in nonkeratinized stratified ocular surface epithelia.
6 r Pax6 in controlling dynamics of the ocular surface epithelia.
7 ecific mutations on expression in a range of surface epithelia.
8 e mechanism of regulation is similar in most surface epithelia.
9 oligosaccharides in the protection of ocular surface epithelia.
10 voided due to sequestration of microflora by surface epithelia.
11 rtant role in mucin regulation in the ocular surface epithelia.
12 n of several aspects of keratin filaments in surface epithelia.
13 tment of the epidermis and other stratifying surface epithelia.
14 to identify sialomucin complex RNA in ocular surface epithelia.
15 iation-appropriate expression in stratifying surface epithelia.
16 ll fate decisions and differentiation in wet-surfaced epithelia.
17 to preventing damage to and infection of wet-surfaced epithelia.
18 sal glands, increased anion secretion across surface epithelia and decreased Na(+) absorption.
19 ranscripts were detected in the human ocular surface epithelia and in corneal cell cultures.
20 membrane protein, is expressed by the ocular surface epithelia and localized on the tips of the surfa
21 all K14 expressing cells, such as the ocular surface epithelia and ocular adnexa.
22 nds on water and ion transport across ocular surface epithelia and on fluid secretion by lacrimal gla
23            In contrast, immortalized ovarian surface epithelia and ovarian cystadenoma cells showed m
24 including the lung, where it is found in the surface epithelia and serous cells of the submucosal gla
25 mucin MUC16 is expressed by the human ocular surface epithelia and that MUC16 carries the H185 carboh
26 stribution of GalNAc-Ts in the normal ocular surface epithelia and to compare their distribution with
27 iferation or differentiation in any of these surface epithelia are central in the pathogenesis of man
28  membrane mucin produced by the human ocular surface epithelia but is also found in the tear fluid, p
29 ansduced and expressed exclusively in airway surface epithelia but not SMGs.
30 e SEAM, cells within it that resemble ocular-surface epithelia can be isolated by pipetting and FACS
31 ell lines compared with normal cells-ovarian surface epithelia cells and fallopian tube secretory epi
32  tissues, including primary cancers, ovarian surface epithelia cells, and cystadenoma cells.
33                                   Human body-surface epithelia coexist in close association with comp
34                  To determine whether ocular surface epithelia express MUC16, the relative expression
35 atin proteins and the filaments they form in surface epithelia has long been appreciated.
36                         After replicating in surface epithelia, herpes simplex virus type-1 (HSV-1) e
37 unctional Pax6 in both the optic vesicle and surface epithelia in order to mediate the interactions b
38 tion of MUC16 mRNA and protein in the ocular surface epithelia, in situ hybridization and immunohisto
39 ral protein that is selectively expressed in surface epithelia, including corneal epithelial cells.
40 ferentiation-appropriate expression in other surface epithelia, including epidermis, cervix, and esop
41                                   The ocular surface epithelia, including the stratified but non-kera
42 tream regulatory region are not expressed in surface epithelia, indicating that loss of the DRR (nucl
43           However, homeostatic regulation of surface epithelia is poorly understood.
44 d by keratin intermediate filaments (IFs) in surface epithelia likely requires that they be organized
45  in combination with demonstrated defects in surface epithelia, may play a role in the vulnerability
46 mbrane-associated mucins expressed by ocular surface epithelia, MUC1 and MUC4, are multifunctional an
47 The membrane-associated mucins of the ocular surface epithelia, MUC1, -4, and -16, are differentially
48 cells, and identify mitosis and apoptosis in surface epithelia of Drosophila imaginal discs.
49                     VDR was localized to the surface epithelia of germ-free mice, but to crypt epithe
50                                       Ocular surface epithelia of Muc1 null mice of the C57BL/6 strai
51 ntly been shown to be produced by the ocular surface epithelia of rats.
52 n the embryo, Pax-6 is expressed strongly in surface epithelia of the adult cornea and conjunctiva.
53  the pattern of Pax-6 gene expression in the surface epithelia of the late embryonic and adult eye.
54 Pax6 continues to be expressed in the ocular surface epithelia of the postnatal eye.
55 n cancer cell lines derived from the ovarian surface epithelia (OSE) of mice with conditional mutatio
56 nditional deletion of Notch1 from the ocular surface epithelia partially recapitulated OS(dnMaml1) ph
57                                              Surface epithelia provide a critical barrier to the outs
58 nt animals in that pustules did not form and surface epithelia remained intact.
59 f keratinocytes in the epidermis and related surface epithelia remains an open question.
60 gative mastermind-like 1 (dnMaml1) in ocular surface epithelia resulted in complete suppression of go
61 on, and defense functions, along with intact surface epithelia, smooth muscle, and cartilage.
62 sure to desiccating stress stimulates ocular surface epithelia to produce cornified envelope precurso
63 dentify vitamin A-responsive genes in ocular surface epithelia using gene microarray analysis of cult
64                      Structure of the ocular surface epithelia was examined by light microscopy, scan
65 y the direct autoimmune insult to the ocular surface epithelia, whereas in MGD patients, with an epit