ライフサイエンスコーパス: squamous epithelium

1 e constitutively expressing BRAK in vivo was squamous epithelium.

2 ltrastructural characteristics of neoplastic squamous epithelium.

3 4 in early differentiation of the esophageal squamous epithelium.

4 n and autoantibodies to nuclei of stratified squamous epithelium.

5 rous connective tissue covered by stratified squamous epithelium.

6 actor in the normal maturation of stratified squamous epithelium.

7 from proliferation to differentiation in the squamous epithelium.

8 us and forestomach, all sharing a stratified squamous epithelium.

9 quamous markers was confined to the adjacent squamous epithelium.

10 highly expressed in differentiated layers of squamous epithelium.

11 biopsies showed a multilayered, keratinized, squamous epithelium.

12 (HPVs) amplify in differentiated strata of a squamous epithelium.

13 mechanism controlling the morphogenesis of a squamous epithelium.

14 estomach, which are composed of a stratified squamous epithelium.

15 d cyst lined by a non-keratinized stratified squamous epithelium.

16 esistant to apoptosis than normal esophageal squamous epithelium.

17 eloped DNA viruses with a strict tropism for squamous epithelium.

18 ic cells in the differentiated layers of the squamous epithelium.

19 A replicates as extrachromosomal plasmids in squamous epithelium.

20 iferate, stratify, and form a differentiated squamous epithelium.

21 tumors in vivo compared with adjacent normal squamous epithelium.

22 argeted to the basal layer of the stratified squamous epithelium.

23 ed to constitutive expression by normal oral squamous epithelium.

24 cepacia binding to and transmigration across squamous epithelium.

25 in a specific fashion to the oral-esophageal squamous epithelium.

26 lumnar cells to the basal layer cells of the squamous epithelium; (2) an overgrowth of columnar by sq

27 mi-1 expression significantly increased from squamous epithelium (7%), columnar cell metaplasia (22%)

28 generation of the oesophagus with stratified squamous epithelium, a normal five-layer wall, and peris

29 also found alpha v in the intact stratified squamous epithelium adjacent to ulcers.

30 ubset of dysplastic lesions of head and neck squamous epithelium and 2) present in approximately one-

31 CD44(-) cancer cells resemble differentiated squamous epithelium and express the differentiation mark

32 stinal--may be interposed between esophageal squamous epithelium and gastric oxyntic (acid secreting)

33 rs and differentiation markers of esophageal squamous epithelium and intestinal columnar epithelium.

34 us development that is expressed in immature squamous epithelium and reserve cells of the cervix.

35 different patterns of expression in normal (squamous epithelium and salivary glands) and diseased or

36 patterns are inversely correlated in normal squamous epithelium and squamous cell carcinomas.

37 ) absence of the layered structure of normal squamous epithelium and the vertical "pit and crypt" mor

38 ugh metaplasia of the most distal esophageal squamous epithelium and this process might predispose in

39 the formed human epicardium is not a simple squamous epithelium and we reveal evidence of more compl

40 apillae of the basal layer of the esophageal squamous epithelium, and in the neck/isthmus region of h

41 termine that KPRP is expressed in stratified squamous epithelium, and its approximately 2.8-kb cDNA e

42 -grade dysplasia, esophageal adenocarcinoma, squamous epithelium, and squamous cell carcinoma) were u

43 Human papillomavirus (HPV) infections of the squamous epithelium are associated with high-level expre

44 esions, the superficial layers of stratified squamous epithelium are disrupted, allowing easier acces

45 keratinocytes and fibroblasts in stratified squamous epithelium are not well-understood.

46 esults show that, in normal development, the squamous epithelium arises from the columnar epithelium

47 rential gene expression of normal esophageal squamous epithelium, Barrett's esophagus, and adenocarci

48 Despite previous claims of the squamous epithelium being an efficient barrier to virus

49 bryos allows the formation of a multilayered squamous epithelium but this fails to differentiate, as

50 was specifically activated in differentiated squamous epithelium, but not in basal progenitor cells,

51 As expected, both rat and human squamous epithelium, but not intestinal metaplasia, expr

52 ogenesis and architecture of this stratified squamous epithelium, but resulted in profound defects in

53 to the replacement of the normal esophageal squamous epithelium by a columnar epithelium through a m

54 n to be a sequela of chronic inflammation in squamous epithelium caused by gastroesophageal reflux di

55 ility to bind to and transmigrate across the squamous epithelium compared to the wild-type strain, al

56 The epidermis is a stratified squamous epithelium composed primarily of keratinocytes

57 The epidermis is a stratified squamous epithelium composed primarily of keratinocytes

58 he esophageal lumen is lined by a stratified squamous epithelium comprised of proliferative basal cel

59 The stratified squamous epithelium comprises actively proliferating bas

60 yed an organotypic model of human stratified squamous epithelium derived from primary keratinocytes t

61 normal looking intact nondysplastic surface squamous epithelium disguising as a submucosal tumor.

62 pithelium, embryonic ganglia, and stratified squamous epithelium (ectoderm).

63 to cytokeratin 13 (CK13) strongly and invade squamous epithelium efficiently.

64 sophageal epithelium, a prototype stratified squamous epithelium, EGFR overexpression is relevant in

65 IGF2 and H19 were imprinted in all normal squamous epithelium examined.

66 rat and human intestinal metaplasia, but not squamous epithelium, expressed intestinal transcription

67 require the environment of a differentiating squamous epithelium for their life cycle.

68 cells positioned at the boundary between the squamous epithelium (forestomach) and the proximal gland

69 The epidermis is a stratified squamous epithelium forming the barrier that excludes ha

70 eratinocytes and fibroblasts in a stratified squamous epithelium have yet to be elucidated.

71 hickened gingiva revealed surface stratified squamous epithelium having needle-like rete pegs charact

72 promoter targets cyclin D1 to the stratified squamous epithelium in a tissue-specific fashion to the

73 protein were, however, strongly expressed by squamous epithelium in areas of hyperplasia and near are

74 he differentiated cells of normal stratified squamous epithelium in culture.

75 Biopsies were obtained from the squamous epithelium in the proximal tubular esophagus, B

76 The epidermis is a multilayered squamous epithelium in which dividing basal cells withdr

77 e superficial layer of the normal stratified squamous epithelium, indicating an increase in metabolic

78 The stratified squamous epithelium is a model system in which to define

79 Ablation of BE to squamous epithelium is achievable by combining a re-inju

80 molecular pathways activated when esophageal squamous epithelium is exposed to reflux underlie the de

81 A fully stratified squamous epithelium is formed by the NIKS keratinocytes

82 at, when there is complete ablation, the neo-squamous epithelium is normal histologically and in biom

83 ning of the oesophagus, such that the normal squamous epithelium is replaced by specialised or intest

84 Reversion to squamous epithelium is the most common primary outcome.

85 Our results show that normal esophageal squamous epithelium is unmethylated at all four CpG isla

86 e development of the epidermis, a stratified squamous epithelium, is dependent on the regulated diffe

87 prise a columnar cell monolayer covered by a squamous epithelium known as the peripodial membrane.

88 Normal squamous epithelium lacked microsatellite instability.

89 of Sonic hedgehog (SHH) in mouse esophageal squamous epithelium leads to a columnar phenotype.

90 LF on two promoters active in the esophageal squamous epithelium, namely the Epstein-Barr virus ED-L2

91 es generated from mucosal biopsies of normal squamous epithelium (NSE), BE and EAC obtained from a pa

92 Complete reversion to squamous epithelium occurs in more than 90% of nondyspla

93 e lamina propria, taste buds, and stratified squamous epithelium of fungiform papillae in the tongue,

94 cells solely within the cervical and vaginal squamous epithelium of K14-HPV16 mice.

95 mate lentiviruses to traverse the stratified squamous epithelium of mucosal surfaces remains undefine

96 sa of patients with ERD, and the distal-most squamous epithelium of patients with BE.

97 as in control biopsy samples from esophageal squamous epithelium of patients with functional dyspepsi

98 to the location of the junction between the squamous epithelium of the ectocervix and vagina and the

99 trast, beta1C was undetectable in stratified squamous epithelium of the epidermis and/or in hepatocyt

100 cell carcinoma and adjacent non-transformed squamous epithelium of the esophagus, as well as in cont

101 gastrointestinal tract, particularly in the squamous epithelium of the esophagus.

102 itutively expressed only in placenta and the squamous epithelium of the esophagus.

103 (NHEKs) to model N-BP effects on stratified squamous epithelium of the esophagus.

104 the skin but can also involve the stratified squamous epithelium of the external auditory canals and

105 rophages, bone marrow myeloid cells, and the squamous epithelium of the forestomach and epithelium of

106 aining was also identified in the stratified squamous epithelium of the lingual mucosa.

107 ing shows expression in salivary glands, the squamous epithelium of the stomach, and the villi of the

108 model to target cyclin D1 to the stratified squamous epithelium of the tongue and esophagus.

109 The maturation of stratified squamous epithelium of the upper gastrointestinal tract

110 hether they are derived embryologically from squamous epithelium of the urogenital sinus or from mull

111 ocalized in the upper half of the stratified squamous epithelium of the vagina and ectocervix, with t

112 mannosylated receptor for type 1 pili on the squamous epithelium of vaginal mucosa is unknown.

113 lar mucosa with or without dysplasia than in squamous epithelium or squamous cell carcinoma.

114 ia, and adenocarcinoma but not in esophageal squamous epithelium or squamous cell carcinoma.

115 erstanding of the mechanisms by which normal squamous epithelium progresses to early-stage invasive c

116 airway was reconstituted with an attenuated squamous epithelium rather than a normal pseudostratifie

117 lls capable of long-term reconstitution of a squamous epithelium reside in the interfollicular epider

118 sia (CM), squamous cell carcinoma (SCC), and squamous epithelium (SE) cases.

119 enesis we analyzed DNA extracted from normal squamous epithelium, severe dysplasia, and corresponding

120 ons to the luminal surface of the stratified squamous epithelium, significantly reducing the number o

121 lasia in the form of keratinizing stratified squamous epithelium, similar to that occurring in the mo

122 geal epithelium is a prototypical stratified squamous epithelium that exhibits an exquisite equilibri

123 ected cells were not found in the stratified squamous epithelium that is adjacent to the pharynx.

124 The skin is a squamous epithelium that is continuously renewed by a po

125 le epithelium throughout the cortex, and the squamous epithelium that normally lines Bowman's capsule

126 egated to form cysts lined with a stratified squamous epithelium, the structure of which resembled th

127 We show that upon programmed damage to the squamous epithelium, these embryonic cells migrate towar

128 y, cuboidal precursor cells transform into a squamous epithelium through a process that involves late

129 ontribute to proliferative disease states in squamous epithelium through NF-kappaB activation.

130 h converts from a nonkeratinized, stratified squamous epithelium to a nonsecretory, keratinized epith

131 postmitotic, differentiated keratinocytes in squamous epithelium to facilitate vegetative viral DNA a

132 of the esophagus transitions from stratified squamous epithelium to metaplastic columnar epithelium t

133 astro-oesophageal junction, where stratified squamous epithelium transitions into simple columnar cel

134 sement membrane assembly of human stratified squamous epithelium, we have generated novel, three-dime

135 In the squamous epithelium, we identify virus entry occurring t

136 cells form a well differentiated stratified squamous epithelium, whereas the tracheal cells form a c

137 by replacement of reflux-damaged oesophageal squamous epithelium with a columnar intestinal-like epit

138 es accompanying the transformation of normal squamous epithelium with Barrett's esophagus and adenoca

139 ests and cords of uniform, benign-appearing, squamous epithelium with occasional vacuolization and ke

140 surface of the implant exhibited stratified squamous epithelium with sparse cilia.