ライフサイエンスコーパス: columnar cell

1 ectious centers comprised of many contiguous columnar cells.

2 of simple cuboidal cells rather than of tall columnar cells.

3 squamous epithelium transitions into simple columnar cells.

4 chiefly or entirely of glands lined by tall columnar cells.

5 e for active amino acid uptake into adjacent columnar cells.

6 he proportion of undifferentiated crypt base columnar cells.

7 serve chondrocytes to actively proliferating columnar cells.

8 ore of a regulatory network in early foregut columnar cells.

9 x and is based on cytoplasm transfer between columnar cells.

10 required for survival of Lgr5(+) crypt-based columnar cells.

11 AVPTC included tall cell/columnar cell (89.5%) and diffuse sclerosing (10.5%) var

12 multiple cell lineages, including crypt base columnar cells, a proposed stem cell.

13 olve FC movements, that there is no role for columnar cell apical constriction in FC morphogenesis, a

14 bryonic lethality at the time that the first columnar cells appear.

15 view describes the rediscovery of crypt base columnar cells as LGR5(+) adult stem cells and summarize

16 the dynamic appearance and disappearance of columnar cells at the egg cylinder stage of the embryo.

17 pansion of PDGs with mucinous metaplasia and columnar cell atypia resembling low-grade PanIN in rats.

18 ay surfaces lost by evaporation, and (b) the columnar cell basolateral membrane and tight junctions l

19 hirdly, there is no preferential loss of the columnar cells by apoptosis.

20 ell populations identified as the crypt base columnar cell (CBCC) and at cell position 4 (cp4) are re

21 of epithelial stem cells: active crypt base columnar cells (CBCs) and quiescent +4 cells.

22 Cycling crypt base columnar cells (CBCs) at crypt positions +1-3 recently w

23 Lgr5-expressing crypt base columnar cells (CBCs) reside deep in the crypt, mingled

24 A subset of CD166-positive, crypt-based columnar cells coexpressed the stem cell markers Lgr5, M

25 tegrity, and spared cell death in crypt base columnar cells compared to TAI-CONV irradiation.

26 and up-regulated expression of the canonical columnar cell cytokeratin KRT8.

27 basal cells shrank, whereas the lumen-facing columnar cells did not.

28 thelia that, like the native tissue, contain columnar cells facing the lumen and basal cells that fac

29 t Brain Tumors 1, the human homologue of the columnar cell factor Hensin, occurs in Barrett's epithel

30 ling activity is required to maintain simple columnar cell fate in adult uterine epithelium.

31 The columnar cells had multiple morphological characteristic

32 Although crypt-based columnar cells have been recently shown to display self-

33 Columnar cell hyperplasia (CCH) is the earliest histolog

34 ial as well as stromal miRNA signatures from columnar cell hyperplasia lesions compared to normal ter

35 T1A and 5-HT2A to nerve terminals in lobular columnar cells in the visual system suggest new hypothes

36 rved in an extracellular gradient within the columnar cell layer of the disc, but also uniformly in t

37 umenal cavity between apposed peripodial and columnar cell layers of both wing and eye discs.

38 primordia comprising apposed peripodial and columnar cell layers.

39 mmendations for patients with a diagnosis of columnar cell lesions (CCLs) in a breast core needle bio

40 ivation caused endoplasmic reticulum stress, columnar cell lesions, and dedifferentiation of CD cells

41 Atypical cuboidal or columnar cells lined the lung periphery of SP-C/HFH-4 tr

42 r cell lineage specification and crypt-based columnar cell maintenance.

43 heir differentiation, thereby regulating the columnar cell mass independently of PTHrP.

44 tly increased from squamous epithelium (7%), columnar cell metaplasia (22%), Barrett's esophagus (22%

45 e dysplasia (LGD), Barrett's esophagus (BE), columnar cell metaplasia (CM), squamous cell carcinoma (

46 in 2.3% of squamous mucosa tissues, 3.7% in columnar cell metaplasia, 5.8% in Barrett's esophagus, 1

47 ays consisting of samples of 7 tissue types (columnar cell metaplasia, Barrett esophagus, low- and hi

48 een human esophageal squamous epithelial and columnar cells mimicking the esophageal squamous-columna

49 Anatomically, however, discs comprise a columnar cell monolayer covered by a squamous epithelium

50 he skin, vagina, bladder, urethra, and basal columnar cells of the caudal uterus in p63+/+ and +/- an

51 ocalization of apextrin is maintained in the columnar cells of the larval ectoderm until their intern

52 KAAT1 is expressed in absorptive columnar cells of the midgut and in labial glands.

53 r of systems, several of which show signs of columnar cell packing akin to that described here.

54 o results in the expansion of the crypt base columnar cell pool and a decrease in secretory enteroend

55 rker of ciliated cells, stained the atypical columnar cells produced by expression of high levels of

56 sed Paneth cells and intervening crypt-based columnar cells (putative stem cells).

57 (-) epithelial cells fail to elongate into a columnar cell shape and cannot maintain a monolayered ep

58 eam pathways, regulating cell proliferation, columnar cell shape and cell junctions.

59 AKT signalling, and is sufficient to promote columnar cell shape in primary tip progenitors.

60 , Bazooka, and aPKC, but not Canoe, regulate columnar cell shape.

61 alone is not sufficient to maintain organoid columnar cell shape.

62 types infected by RSV revealed that lumenal columnar cells, specifically ciliated epithelial cells,

63 alisade mesophyll consists of tightly packed columnar cells, the structure of spongy mesophyll is not

64 or the change are (1) a direct conversion of columnar cells to the basal layer cells of the squamous

65 development, peripodial cells signal to disc columnar cells via microtubule-based apical extensions.