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1 trolled release to the proposed drug target (colon).
2 ulation was unique to the proximal or distal colon.
3 eption is the invagination of ileum into the colon.
4 ed by microbial fermentation of fiber in the colon.
5 ogy to identify biopsy-worthy lesions in the colon.
6 lity of primary afferents that innervate the colon.
7 anatomical alterations detected in the human colon.
8 gulatory T cells between lymphoid tissue and colon.
9 ith specialized cellular distribution in the colon.
10 d homeobox 1 (PROX1) in the developing chick colon.
11 ike structures, called diverticula, over the colon.
12 ounts in both the mesenteric lymph nodes and colon.
13 neration and suppressed tumorigenesis in the colon.
14 rences between the ileum and proximal/distal colon.
15  injury and pathological inflammation in the colon.
16 rger than 5 mm, both proximal to the sigmoid colon.
17 velopment of adenomas in small intestine and colon.
18 ses and peptidases can be upregulated in the colon.
19 ommunity residing in the small intestine and colon.
20 5- to 10-fold higher than that in uninfected colons.
21 mGy/MBq) in normal tissues were to the right colon (0.167 +/- 0.04) and small intestine (0.153 +/- 0.
22 co-2 cells at the concentrations seen in the colon (1.0 mug/mL).
23 art:mediastinum ratios (P < 10-5, ANOVA) and colon 11C-donepezil standard uptake values (P = 0.008, A
24     We report that opioids from the inflamed colon activate delta-opioid receptors (DOPr) in endosome
25  and 47 cancers from The Cancer Genome Atlas Colon Adenocarcinoma database.
26 man colon but significantly downregulated in colon adenocarcinoma.
27 d be used to identify functional clusters of colon afferents from thoracolumbar (TL), lumbosacral (LS
28           In addition, transcriptionally, NG colon afferents were almost completely segregated from c
29 n epithelial cells communicate directly with colon afferents.
30                         Reduced pathology in colon after DMOG treatment associates with intestinal ep
31 ceived a deceased-donor small intestinal and colon allograft with standard immunosuppressive treatmen
32 ukin-22 (IL-22) production in the tonsil and colon; an increase in the levels of CD107a, gamma interf
33 ion led to a 3-fold depletion of ILC3 in the colon and an increase in the levels of NK cells in tonsi
34                                 Furthermore, colon and bladder afferents expressed genes at similar l
35                       There were clusters of colon and bladder afferents, defined by mRNA profiling,
36 by which platelets promote the metastasis of colon and breast cancer cells and suggests that GPVI rep
37 well as human GPVI, had platelet adhesion to colon and breast cancer cells.
38 d experimental and spontaneous metastasis of colon and breast cancer cells.
39  cell line, but also cell lines derived from colon and breast tissues.
40  The major sensory nerve pathway between the colon and central nervous system (spinal cord and brain)
41  activation and migration profiles along the colon and characterize the transcriptional adaptation tr
42  patients afflicted with pancreatic, breast, colon and colorectal cancer show that our proposed metho
43    These findings were all restricted to the colon and correlated to circulating markers of enterocyt
44 ated with increased numbers of mast cells in colon and expression of the receptor for AGER in proxima
45 parison of monocyte differentiation into the colon and ileum-resident macrophages revealed the gradua
46 onal frequency from the cecum to the sigmoid colon and link this to the increasing number of reactive
47 how that human APOBEC3A expression in murine colon and liver tissues increases tumorigenesis.
48             Here we demonstrate that, within colon and pancreatic ductal adenocarcinoma tumors, effic
49 lation inhibited both contractions of distal colon and propulsive contractions represented by the col
50 r risk stratification for cancers of breast, colon and prostate, but less so for others because of mo
51 t scores were associated with risk of distal colon and rectal cancers, after adjusting for other risk
52 atures in gut mucosal specimens from sigmoid colon and terminal ileum of 19 INR and 20 IR in addition
53 selection mechanisms in the colitis-affected colon and that somatic mutations potentially play a caus
54 ising from DRG were identified in the distal colon and their morphological features and CGRP immunore
55                                              Colon and tumor tissues were analyzed by histology, quan
56               We next examined patient skin, colon, and blood during acute GVHD.
57 e removed, and colon contents (feces, distal colon, and tumor) were collected.
58  according to the histologic layers of mouse colon, and we compared cellular properties between micro
59        In conclusion, CGRP+ baskets in mouse colon are formed by intrinsic enteric neurons with a neu
60      RORgamma+ and Helios+ Treg cells in the colon are phenotypically and functionally distinct, but
61                          The small bowel and colon are the sites most commonly involved.
62 that these mice exhibit Mn deficiency in the colon associated with impaired intestinal barrier functi
63 ied tumor-characteristics (primary T4, right colon), biological features (K/N-RAS status), and respon
64                                              Colon biopsies from patients with IBS-D had increased le
65 e patients using 16S rRNA gene sequencing of colon biopsies, coupled with metagenomic and metatranscr
66 colon length, and histopathology analysis of colon biopsies.
67 ir phosphorylation profile and truncation in colon biopsy specimens from 16 Crohn's disease (CD) and
68                                              Colon biopsy specimens from patients with IBD (30 with C
69 dataset to examine 12 tumor types (including colon, breast, prostate, pancreas, lung adenocarcinoma,
70 , 95% CI: 1.06, 1.36) of cancer of the right colon but not of the left colon (HR = 0.96, 95% CI: 0.80
71 of cancer of the left (distal or descending) colon but not of the right (proximal or ascending) colon
72 A1 is robustly expressed in the normal human colon but significantly downregulated in colon adenocarc
73 intains its long-lasting colonization in the colon by evading IFN-gamma from group 3-like ILCs.
74 tested in high-AQP1-expressing cancer lines, colon cancer (HT29) and AQP1-expressing breast cancer (M
75  they have a higher incidence of right-sided colon cancer (RCC).
76 t male smokers are at increased risk of left colon cancer and female smokers are at increased risk of
77             Furthermore, using PDX models of colon cancer and resected tumors from colon cancer patie
78 was reported in the secukinumab group due to colon cancer and was assessed as not related to the stud
79 of RSK1 and MSK2, can suppress the growth of colon cancer by attenuating RSK1 and MSK2 signaling.
80                                   Around 20% colon cancer cases are closely linked with colitis.
81  that 4-hydroxyacetophenone (4-HAP) inhibits colon cancer cell adhesion, invasion, and migration in v
82 ctangular geometries of bio-printed 3D human colon cancer cell constructs.
83        We performed Protect-seq on the human colon cancer cell line HCT-116 and observed overlap with
84                 In vivo, SHH interference in colon cancer cell lines decreased primary tumor growth a
85 as well as several Ras mutations in lung and colon cancer cell lines on fast 10 min gradient separati
86 iated mutations, we report that human HCT116 colon cancer cells also survive when ORC5 protein expres
87 ax as well as cleaved caspase-3 and -PARP in colon cancer cells by downregulating RSK1 and MSK2 downs
88                   Furthermore, GNL1 protects colon cancer cells from chemo-drug-induced apoptosis.
89 nst various human cancer cells, killing SW48 colon cancer cells in particular with a submicromolar ha
90 % of active MYC alleles at any given time in colon cancer cells.
91 on of talin1 inhibited 3D spheroid growth in colon cancer cells.
92 signal and redox state in human cervical and colon cancer cells.
93  and p120-catenin isoform switching in SW480 colon cancer cells: fl-APC increased the expression of g
94 re we find that cohesin depletion in a human colon cancer derived cell line results in endomitosis an
95 aluate the role of G6PD in lung, breast, and colon cancer driven by oncogenic K-Ras.
96  for pancreas, esophageal, lung, rectal, and colon cancer from 2014 to 2016 were identified.
97 omparatively evaluate CNNs on 170 breast and colon cancer images with pathologist-annotated nuclei, f
98 mption was associated with a reduced risk of colon cancer in age-adjusted analyses (P for trend < 0.0
99  mechanisms contributing to the promotion of colon cancer in obese individuals.
100  0.70-0.99; P trend = 0.04) for the proximal colon cancer incidence.
101 tor which allows stratification of stage III colon cancer into high- and low-risk recurrence groups,
102 nic inflammation leads to the development of colon cancer is lacking.
103 e need for adjuvant chemotherapy in stage II colon cancer is still debated.
104                                              Colon cancer is the most aggressive tumor in both men an
105  liver-metastasis resection for treatment of colon cancer may increase the risk of further metastasis
106 the metastatic burden in an in vivo model of colon cancer metastasis to the liver.
107 atively correlated with the survival rate of colon cancer patients and that depletion of talin1 inhib
108 els of colon cancer and resected tumors from colon cancer patients, our data demonstrated that HT-DBP
109 w toxicity, it could be potentially used for colon cancer prevention or therapy.
110 one in identifying subclones using stage III colon cancer primary tumor samples as well as simulated
111  they may in part explain how obesity drives colon cancer progression.
112 esenting a non-cell autonomous mechanism for colon cancer progression.
113 ecule adiponectin receptor agonist, suppress colon cancer risk in part by reducing the number of Lgr5
114 the adiponectin signaling pathway attenuates colon cancer risk remains to be addressed.
115 extent to which CRM involvement exists after colon cancer surgery is unknown.
116 enous n-3 PUFAs on inflammatory cytokines in colon cancer surgery.
117          RSK1 and MSK2 were overexpressed in colon cancer tissues confirmed by western blot and IHC.
118 se of tumor burden in an orthotopic model of colon cancer via luciferase-positive CT26 cells.
119 ant chemotherapy for patients with stage III colon cancer was not confirmed in terms of overall survi
120 oma and a patient-derived xenograft model of colon cancer with a favorable safety profile.
121  efficacy and bioavailability in ovarian and colon cancer xenograft models when evaluated for dose-ra
122 ancer cell lines (MCF-7 breast cancer, SW480 colon cancer, and PC3 prostate cancer), and one kind of
123  Tumor entities comprised esophageal cancer, colon cancer, rectal cancer and pancreatic cancer.
124 of long non-coding RNAs (lncRNAs) in primary colon cancer, their role in mCRC and treatment resistanc
125 s an alternative to animal studies or use of colon cancer-derived cell lines.
126 hlights the therapeutic potential of Gal2 in colon cancer.
127 l of a highly aggressive liver metastasis of colon cancer.
128 emale smokers are at increased risk of right colon cancer.
129 e the potential targets for the treatment of colon cancer.
130 ver injury following IRI in a mouse model of colon cancer.
131 al outcomes based on the presence of TILs in colon cancer.
132 ity in tumour-bearing mice and patients with colon cancer.
133 n to aid treatment planning during stage III colon cancer.
134 gen positive (ER(+ve)) breast cancer and for colon cancer.
135 to 76% for breast cancer, and 11% to 80% for colon cancer.
136 end = 0.03), and were restricted to proximal colon cancer.
137 tumor efficacy on mouse models of breast and colon cancers, with cure rates of 40% and 60%, respectiv
138 origenesis via the Wnt-Ras-p53 axis in human colon cancers.
139 has a potential to be used as an effector in colon carcinogenic transformation.
140 e series, HSGN-218, is nontoxic to mammalian colon cells and is gut-restrictive.
141                               Organoids from colon cells of CRT-knockout mice and control mice were a
142 than the ancestral form on human lung cells, colon cells, and on cells rendered permissive by ectopic
143 ffects by inducing different gene markers in colon cells.
144 icantly increased histological damage in the colon compared to control.
145 apoptotic factors (Aifm1 and Bcl2l10) in the colon compared to control.
146 pectively reviewed to identify patients with colon complications, including ischemia, perforation, fi
147  days later, distal colons were removed, and colon contents (feces, distal colon, and tumor) were col
148 ion, increased arginine concentration in the colon correlated with down-regulation of the host SLC7A2
149               In turn, O-glycans on proximal colon-derived Muc2 modulate the structure and function o
150 expression of alpha-1 adrenoceptors in human colon emphasize the translational relevance of our mouse
151         Here we review recent studies on how colon epithelial cells communicate directly with colon a
152 o colorectal cancer cells, but not to normal colon epithelial cells.
153 ression of the receptor for AGER in proximal colon epithelium.
154 , CHI3L1, OR1D4, and LIPG in breast; IGF2 in colon; ETV1 in prostate; and IGF2BP3 and SIX2 in thyroid
155 te that the intrinsic neural networks of the colon exhibit unique transcriptional profiles that are c
156 nally, applying YIGSR to E13.5 EdnrB(NCC-/-) colon explants resulted in 80%-100% colonization of the
157                                              Colon expression of alpha-SMA was significantly lower in
158                                              Colon-extracted lipids revealed that DiNP exposure signi
159 cient Chlamydia sp. was able to colonize the colon following an intracolon inoculation, suggesting th
160 relatively little is known about its role in colon formation during embryogenesis.
161 oderm, is required for hindgut extension and colon formation.
162 e the extension of the hindgut that leads to colon formation.
163                                              Colon from 2 pediatric patients with Hirschsprung diseas
164 se obstruction was located in the descending colon had a better TTP compared with ES group (HR 0.44 (
165  gallbladder, displacement of the transverse colon, hepatic flexure and duodenum.
166 ferent types of organoids, including kidney, colon, hepatocyte, ovarian, and breast.
167 s demonstrate the essential role of Fam3D in colon homeostasis, protection against inflammation assoc
168 ancer of the right colon but not of the left colon (HR = 0.96, 95% CI: 0.80, 1.15).
169 but not of the right (proximal or ascending) colon (HR = 1.03, 95% CI: 0.89, 1.18), while female ever
170  0.96; P-trend < 0.001), particularly distal colon (HRQ5 vs. Q1: 0.84; 95% CI: 0.73, 0.96; P-trend =
171 the viscoelastic moduli and mass of adherent colon (HT-29) and breast cancer (MCF-7) cells from the i
172 proliferative effects on cervical (HeLa) and colon (HT-29) cancer cells.
173 n and Rac-1 activation in B16F10, metastatic colon [HT29(US)] and breast cancer (MDA-MB-231) cell lin
174 ficant decrease in alpha4beta7 expression in colon ILC3.
175                               Full-thickness colon images, viewed with a 10x objective lens, were as
176 gest that more undigested starch reaches the colon in individuals with low AMY1 CN, and that the fate
177                                              Colon inclusive grafts had higher complication rates (P
178 Here, we found that Ninjurin1 (Ninj1) limits colon inflammation by regulating macrophage polarization
179 showed increased morbidity, weight loss, and colon injury, with a concomitant increase in inflammator
180  and provides protection against DSS-induced colon injury.
181      We hypothesized that the development of colon involvement in necrotizing pancreatitis (NP) negat
182                                              Colon involvement in necrotizing pancreatitis is associa
183                                              Colon involvement in necrotizing pancreatitis is common;
184                            Gradient Boosting-Colon is an independent machine prognostic predictor whi
185                                          The colon is innervated by intrinsic and extrinsic neurons t
186  how it organizes to function throughout the colon is unclear.
187 estive enzyme expression in the duodenum and colon is upregulated in SBS patients.
188    Clostridioides difficile infection of the colon leads to severe inflammation and damage to the gas
189 IIa significantly attenuated the DSS-induced colon length shortening, rectal bleeding, bodyweight los
190 everity was determined based on body weight, colon length, and histopathology analysis of colon biops
191 se the body weight loss, macroscopic damage, colon length, histological alteration, and inflammation
192 duced experimental colitis, as judged by the colon length.
193 IgA2+ and IgA1-IgA2+ bacteria coexist in the colon lumen, where Bacteroidetes is preferentially targe
194 ficant increases in the expression of IL6 in colon macrophages from Ptpn2-LysMCre mice.
195 s mechanism relies on a population of distal colon macrophages that are equipped with "balloon-like"
196                                    Rarely, a colon malignancy is misdiagnosed as diverticulitis.
197                       Later, sNCCs enter the colon mesenchyme to colonize and contribute to the intri
198                                  The altered colon microbiome approximated clinical findings in PD pa
199 l CART(+) neurons, enriched in the ileum and colon, modulated feeding and glucose metabolism.
200 dicate that subacute exposure to DiNP alters colon morphology and physiology in adult female mice.
201            Mice given ampicillin had reduced colon motility compared with mice given only water, and
202 PCR expression was markedly decreased in the colon mucosa during colitis.
203 e microbiota as well as transcription in the colon mucosa.
204                       In mice, we found that colon mucus consists of two distinct O-glycosylated enti
205                                              Colon mucus segregates the intestinal microbiota from ho
206 is is generally considered a risk factor for colon neoplasia.
207 ction, with increased expression of CD103 in colon NK cells and curtailment of CXCR3, and a significa
208                     While SBTS in neoplastic colon obstruction may reduce morbidity and need for a st
209           We determined that the jejunum and colon of black bears do not harbor significantly differe
210 were performed in full thickness segments of colon of five CD and five control subjects, in primary c
211  in the bacterial composition of the sigmoid colon of IBS patients were linked to symptoms and immune
212                                 The proximal colon of T. suis-infected pigs exhibited general inflamm
213 ime of peak disease severity in the ceca and colons of all mice infected with a high-virulence strain
214 anoids (colonoids) generated from the distal colons of mice.
215  3-year average annual IRs increased in both colon-only (+13% [12.21 to 13.85 per 100 000]; P < 0.050
216 injected into proximal and distal regions of colon or bladder, followed by single-cell qRT-PCR and an
217  patients age 18 years or older with breast, colon, or lung cancer who were prescribed cancer drug re
218 intestinal sphingolipid, both in mice and in colon organoids (colonoids) generated from the distal co
219 L1 insertions, we studied adenocarcinomas of colon, pancreas, and stomach, and found a variable numbe
220         Eighty percent, 64%, and 8% of human colon, pancreatic, and lung cancer cells, respectively,
221 ned unchanged, autocrine SHH interference in colon, pancreatic, and lung cell lines triggered cell de
222 ally significant risk factors for developing colon pathology include tobacco use (odds ratio (OR), 2.
223 he increased sensitivity of NIR readouts for colon permeability is shown using dextran sulfate sodium
224                                              Colon polyp surveillance now accounts for 25% of all col
225 ogic diagnoses (including different types of colon polypoid lesions), ablation, piecemeal resection.
226 a associated with high-grade dysplasia (HGD) colon polyps at baseline colonoscopy remains unclear.
227 In this pilot study we found that low-volume colon preparation may be preferred in the inpatient sett
228                     Data collection included colon preparation quality, based on the Boston Bowel Pre
229        The selected model (Gradient Boosting-Colon) provided a hazard ratio (HR) for high- vs. low-ri
230 itories for 11 cancers (oesophagus, stomach, colon, rectum, anus, liver, pancreas, lung, breast, cerv
231 iculosis (the presence of diverticula in the colon; referred to as diverticulosis) remains asymptomat
232 ither pancreas, esophageal, lung, rectal, or colon resection for cancer at a hospital within the high
233 ,557 Medicare patients underwent an elective colon resection for diverticulitis at 2462 hospitals ove
234      Forty-four patients undergoing elective colon resection for nonmetastasized cancer were randomly
235 variation (excess of 3-fold) in standardized colon resection ratios for recurrent diverticulitis.
236                                 Standardized colon resection ratios ranged from 0 in the Tuscaloosa H
237                    Individuals who underwent colon resection, coronary artery bypass graft (CABG), lu
238 re associated with higher predicted rates of colon resection.
239 me sequence reported in the present study in colon resections with primary anastomosis.
240 samples; in contrast, the majority of normal colon samples displayed no detectable expression.
241 emical profiles of human small intestine and colon scaffolds, indicating that they can be used interc
242  innate lymphoid cells (ILCs) located in the colon secondary to simian immunodeficiency virus (SIV) i
243                  Evidence for any dysplasia, colon segment resection, aneuploidy, male sex, and age w
244 sults in reduced peristaltic activity of the colon, similar to that observed in microbiota-depleted m
245                           After entering the colon, single axons ramified rostrally or caudally along
246                       The development of the colon starts with the formation and extension of the hin
247 ccludin and E-cadherin genes in DRA-KO mouse colon, suggesting that posttranscriptional mechanisms pl
248                  The use of robotic-assisted colon surgery is increasing.
249 se in the use of Pickering emulsions for the colon-targeted delivery of SCFAs.
250 developed a 3-dimensional imaging method for colon that provides more information about ENS structure
251 atty acids limits oxygen availability in the colon, thereby maintaining a balanced microbial communit
252                                      For the colon, this overlapping innervation is proposed to facil
253 s in stress distribution engendered over the colon tissue by the presence of a pouch-like structure.
254 rophil infiltration into the Il10(-/-) mouse colon tissue compared to Cj-P0, which was attenuated wit
255 iltration, and inflammatory cytokines in the colon tissue.
256 tients without IBD (control individuals) and colon tissues from mice (with and without disruption of
257                                              Colon tissues from patients with IBD had reduced levels
258 al biomarkers that differentiate the healthy colon tissues from the diseased tissues were identified
259 ative spectra of the hydrated and dehydrated colon tissues further revealed significant peak shifts a
260                                              Colon tissues were analyzed by histology for the presenc
261                                              Colon tissues were collected from some mice and analyzed
262 (46 CRCs, 74 advanced adenomas and 32 normal colon tissues).
263 rents were almost completely segregated from colon TL and LS neurons.
264 cognised prebiotic carbohydrate, reaches the colon to be fermented by the intestinal microbiota.
265 low cytometry and cell stimulation assays in colon, tonsil, and oral lymph node samples.
266 bes a case of intramural gas gangrene of the colon, treated conservatively with antibiotic therapy in
267 ression decreased the proliferation of human colon tumor epithelial cells and blunted H(2)O(2)-induce
268 e to its ability to induce colitis and cause colon tumor formation in mice through the production of
269 strate that Gal2 plays a suppressive role in colon tumor growth and highlights the therapeutic potent
270 jury-induced cell proliferation and promotes colon tumorigenesis in a preclinical colitis-associated
271                       Loss of FFAR2 promotes colon tumorigenesis in mice by reducing gut barrier inte
272 , the genetic factors regulating colitis and colon tumorigenesis remain elusive.
273 al data indicate that adiponectin suppresses colon tumorigenesis.
274             Metabolomics analysis of patient colon tumors (n = 197) and normal tissues (n = 39) revea
275      Here we integrated topological maps for colon tumors and normal colons with epigenetic, transcri
276                                              Colon tumors from Apc(Min/+)Ffar2(-/-) mice had a higher
277                                              Colon tumors from IL-17RD-deficient mice are characteriz
278 ice developed significantly more spontaneous colon tumors than Apc(Min/+) mice and had increased gut
279 ointestinal tract and downregulated in human colon tumors.
280  on CT from 22 right-sided and 64 left-sided colon tumours.
281  Although inflammation of the mid-descending colon typically resolved, a subset showed characteristic
282 r groups, the PDRBD+ group also had enlarged colon volumes (P < 0.001, ANOVA) and delayed colonic tra
283 ry bowel disease (IBD), and normal thickened colon wall (NTC) on computed tomography (CT) and assess
284                         MRC showed increased colon wall thickness in TNBS group compared to controls
285 eces, and mucosa of the duodenum and sigmoid colon was determined by 16S rRNA-amplicon-sequencing.
286                                    The whole colon was then removed and stained to visualize single a
287  percentage of IFN-gamma(+) ILCs in infected colons was 5- to 10-fold higher than that in uninfected
288 as associated with growth failure, increased colon weight/length ratio (p < 0.01), but did not affect
289                  Conversely, the stomach and colon were associated with structurally and functionally
290                Twenty-one days later, distal colons were removed, and colon contents (feces, distal c
291                    In contrast to the normal colon, where clonal expansions outside the confines of t
292  Some BAs (approximately 5%) escape into the colon, where gut commensal bacteria convert them into va
293 enesis is believed to occur in the ileum and colon, where the bacteria adhere and form a robust aggre
294 d differences in environmental milieu of the colon which vary between the sexes.
295 ta, and a minor form derived from the distal colon, which adheres to the major form.
296  Muc2: a major form produced by the proximal colon, which encapsulates the fecal material including t
297 a abrogated expression of SYNPO in the mouse colon, which was rescued with butyrate repletion.
298 topological maps for colon tumors and normal colons with epigenetic, transcriptional, and imaging dat
299 immune cells across the healthy, adult human colon, with paired characterization of immune cells in t
300 l ganglion innervated the proximal or distal colon, with processes closely opposed to multiple cell t
301 Hirschsprung disease was used to show distal colon without enteric ganglia, as well as a transition z

 
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