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1 specific proliferative effects on intestinal crypt cells.
2 eth cell markers were maximally expressed in crypt cells.
3 ng bone marrow and differentiated intestinal crypt cells.
4 d staining along the basolateral membrane of crypt cells.
5 ed iron incorporation into immature duodenal crypt cells.
6 while Klf5 is primarily in the proliferating crypt cells.
7 plaques were formed within a subset of basal crypt cells.
8 alized on the lateral and basal membranes in crypt cells.
9 d 2-3 times higher uptake of ionic iron than crypt cells.
10 mature absorptive rather than proliferative crypt cells.
11 no immunoreactive enzyme was present in the crypt cells.
12 he mRNA encoding isoform II was found in the crypt cells.
13 cretion in a tissue culture model of colonic crypt cells.
14 contrast, Le(x) antigens were restricted to crypt cells.
15 ogene-induced senescence (OIS) of intestinal crypt cells.
16 either renew themselves or become committed crypt cells.
17 ent in villus cells but barely detectable in crypt cells.
18 otein restricted to proliferating intestinal crypt cells.
19 an colon tumor cells and "normal" intestinal crypt cells.
20 ly marks long-term BrdU-retaining intestinal crypt cells.
21 ated an increase in Wnt-activated intestinal crypt cells.
22 that annexin-II binds PG in situ in colonic crypt cells.
23 of 4E-BP1 in IEC-18 nontransformed rat ileal crypt cells.
24 onserved in T84 cells, models for intestinal crypt cells.
25 tracellular cAMP in villus cells, but not in crypt cells.
26 erved in the myenteric plexus and epithelial crypt cells.
30 ticipating in electrolyte transport, colonic crypt cells also synthesize and secrete a number of prot
31 NOS mRNA was up-regulated in both villus and crypt cells, although LPS-induced iNOS mRNA was more pro
32 turnover, with an increase in proliferating crypt cells and a decrease in their differentiated villo
34 tigens in both undifferentiated proliferated crypt cells and in differentiated postmitotic villus-ass
36 h the transferrin receptor (TfR) in duodenal crypt cells and proposed that mutations in HFE attenuate
37 With this input, HFE enables the intestinal crypt cells and reticuloendothelial system to interpret
38 system in 2 dpf larvae, suggesting that the crypt cells and sensory cells in the neuromasts have sim
39 nd shows that tamoxifen induces apoptosis in crypt cells and that suppressing apoptosis alters lineag
40 ppreciably alter radiation damage to jejunal crypt cells and tissue involved in the development of ra
41 esicles (BBMV) were prepared from villus and crypt cells and uptake studies were performed using rapi
42 nd EGF-induced migration of small intestinal crypt cells, and that Rho proteins are essential element
44 m in the extent of radiation-induced jejunal crypt cell apoptosis, with female mice having higher lev
49 ght to originate in the expansion of colonic crypt cells as a result of aberrant gene expression caus
51 amic, with proliferation of undifferentiated crypt cells balanced by terminal differentiation and cel
53 y normal mucosa, in contrast to targeting of crypt cells by inheritance of an Apc(1638N) allele or ho
54 t was demonstrated that both the surface and crypt cells can perform secretory and absorptive functio
55 lycytidylic acid challenge and expression by crypt cells clearly distinguish Clr-a from the likewise
56 gether with biochemical evidence of NeuGc in crypt cells, correlated exactly with the ability of the
57 n the normal intestine, localizing mainly in crypt cells; d) iNOS inhibitors attenuated PAF-induced i
58 activity in IEC-18 nontransformed intestinal crypt cells determined that PKCalpha suppresses Id1 mRNA
59 r capture microdissection to isolate colonic crypt cells, differentiated surface epithelium, adenomas
60 dine pulse-chase, we find that proliferating crypt cells dilute the (15)N label, consistent with rand
61 ell proliferation, we determined the rate of crypt cell DNA synthesis by detection of 5-bromo-2-deoxy
66 sis significantly more often than intestinal crypt cells found in B[c]PhDE-treated Msh2(-/-) or Mlh1(
69 V (rhR4) protein protected normal intestinal crypt cells from IR-induced apoptosis by increasing the
70 Importantly, cdk2 activity was unchanged in crypt cells from p21(-/-) mice, which do not develop int
72 is list of differentially expressed adapting crypt cell genes with a generalized mouse gene expressio
73 the small intestine and colon by stimulating crypt cell growth and mucosal regeneration in DSS-treate
74 of inflammatory bowel disease by stimulating crypt cell growth, accelerating mucosal regeneration, an
75 cells but produces a marked amplification of crypt cells having a morphology intermediate between Pan
78 gene alters the proteome of normal-appearing crypt cells in a gene-specific manner, consistent with a
79 e provided a time line of differentiation of crypt cells in development of the olfactory system and d
82 depth, ornithine decarboxylase activity, and crypt cells in S-phase occurred between enteral intakes
87 thdrawal in IEC-18 nontransformed intestinal crypt cells, involving rapid disappearance of cyclin D1,
88 ch HFE mutations lead to inappropriately low crypt cell iron, with resultant stabilization of DMT1(IR
93 ansferrin-bound iron from plasma by duodenal crypt cells, leading to up-regulation of transporters fo
95 thways were studied using a human intestinal crypt cell line (T84) grown in noncontact coculture with
98 udy, T84 cell monolayers, a human intestinal crypt cell line, and isolated human PMN were used to exa
100 the survivin/ABK cascade can explain delayed crypt cell maturation, expansion of proliferative cell p
103 are the result of a stimulus that increases crypt cell mitosis and augments cellular progression alo
108 oliferation, is highly expressed in dividing crypt cells of the gastrointestinal epithelium, and is i
109 is expressed predominantly in the epithelial crypt cells of the gastrointestinal tract and is a membe
112 ression of hensin in the less differentiated crypt cells of the intestine and the basal cells of the
113 renal proximal convoluted tubular cells, and crypt cells of the small intestine as well as in cerebra
114 aled that LTA4 hydrolase is localized in the crypt cells of the small intestine, white pulp of the sp
115 at recipients showed apoptosis of epithelial crypt cells on day 3 posttransplant as determined by ter
119 plain the shifts in pattern of proliferative crypt cell populations in early colon tumorigenesis, and
120 Lgr5 and Bmi1 are two molecular markers of crypt-cell populations that replenish all lineages over
121 methylhydrazine had no significant effect on crypt cell production rate nor on crypt area in the dist
122 venously infused EGF significantly increased crypt cell production rate, but the magnitude of the eff
123 E-cadherin or a secondary effect of reduced crypt cell production, another Fabp promoter was used to
124 e killed at 25 weeks and rates of intestinal crypt cell production, crypt size, and crypt fission wer
125 eased in epimorphin-/- mice due to augmented crypt cell proliferation and crypt fission during the ne
127 adaptive response characterized by increased crypt cell proliferation and enhanced villus height and
128 of Lgr5(+) stem cells and greater amounts of crypt cell proliferation and expression of Myc (a target
129 In the intestinal epithelium, Notch promotes crypt cell proliferation and inhibits goblet cell differ
130 88-signaling pathway and result in increased crypt cell proliferation and intestinal stem cell number
131 leum, deletion of Gata6 caused a decrease in crypt cell proliferation and numbers of enteroendocrine
134 r study shows that Klf5 is a key mediator of crypt cell proliferation in the colon in response to pat
135 nto mice, the protein induced rapid onset of crypt cell proliferation involving beta-catenin stabiliz
136 modulate crypt stem cell number and promote crypt cell proliferation to help maintain gut homeostasi
138 k between monocyte recruitment and increased crypt cell proliferation was further confirmed using a c
140 ement that regulates bacterial colonization, crypt cell proliferation, and epithelial cell regenerati
142 hydrazine, which are both known to stimulate crypt cell proliferation, on crypt fission in the rat in
143 GATA transcription factors are required for crypt cell proliferation, secretory cell differentiation
152 rly and on basolateral membranes of proximal crypt cells, providing evidence that annexin-II binds PG
154 section from either the villus epithelial or crypt cell regions of healthy human small intestinal muc
156 nes lacking Gata4 and Cdx2 were deficient in crypt cell replication, whereas combined loss of Hnf4a a
160 n S100 antibody that specifically recognizes crypt cells showed that S100-positive cells appear in ol
162 em for the clonal growth of a single colonic crypt cell suspension could facilitate the identificatio
163 oportion (proliferative fraction) of colonic crypt cells that can proliferate; the other is a cell cy
164 type mice exposed to B[c]PhDE had intestinal crypt cells that underwent apoptosis significantly more
165 ansporters, B0AT1 in villus cells and SN2 in crypts cells that are uniquely altered in the chronicall
166 s of aberrant differentiation of uncommitted crypt cells-these differentiated toward the secretory ce
169 tal dynamics of one of the neuron types, the crypt cells, to determine whether they are differentiate
171 C mutation carriers, indicating that a colon crypt cell under the one-hit state is already abnormal.
173 ecretion has been associated with changes in crypt cell volume, we hypothesized that CFTR-mediated ce
174 BBM, whereas the stimulation of SN2/SNAT5 in crypts cells was reversed secondary to restoration of af
183 effect of the HFE-beta2M complex in duodenal crypt cells, where the HFE-beta2M complex appears to fac
184 that this transcript is expressed in colonic crypt cells, whereas Northern blot analysis established
185 xpressed by liver macrophages and intestinal crypt cells, which behave as though they are relatively
186 r, treatment of non-transformed IEC-18 ileal crypt cells with PKC agonists has a biphasic effect on c
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