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1 tal intraepithelial neoplasias (eg, cervical intraepithelial neoplasia).
2 ulation, leading to development of prostatic intraepithelial neoplasia.
3 arly as at the stage of high-grade prostatic intraepithelial neoplasia.
4 ve to surgery in female patients with vulval intraepithelial neoplasia.
5 results showed that 4 eyes had conjunctival intraepithelial neoplasia.
6 oliferation, hyperplasia, and early prostate intraepithelial neoplasia.
7 acilitates the onset of high-grade prostatic intraepithelial neoplasia.
8 e of palpable tumor and high-grade prostatic intraepithelial neoplasia.
9 e without affecting hyperplasia or prostatic intraepithelial neoplasia.
10 yperplasia, or dysplastic lesions/pancreatic intraepithelial neoplasia.
11 fficient to induce hyperplasia and prostatic intraepithelial neoplasia.
12 etaplasia, dysplasia, and ultimately gastric intraepithelial neoplasias.
13 papillary mucinous neoplasms and in multiple intraepithelial neoplasias.
14 pancreatic ducts, referred to as pancreatic intraepithelial neoplasias.
15 mice, but did not alter growth of pancreatic intraepithelial neoplasias.
16 and tolerable for treating usual-type vulvar intraepithelial neoplasia?
17 n of oncogenic KRAS, premalignant pancreatic intraepithelial neoplasia 1 (PanIN1) lesions rarely beco
18 ntial reduction of ADM as well as pancreatic intraepithelial neoplasia-1 (PanIN-1), PanIN-2, and PanI
19 Its expression is lost at the pancreatic intraepithelial neoplasia 1b (PanIN1b)/PanIN2 stage of p
20 e 70% of cervical cancer and 50% of cervical intraepithelial neoplasia 2/3 and adenocarcinoma in situ
22 ening algorithm found more disease (cervical intraepithelial neoplasia 3 or worse [CIN3+]) and also f
23 I, 1.67 to 3.31); grade 2 or higher cervical intraepithelial neoplasia, 6.9% vs. 3.4% (hazard ratio,
24 (2 benign papillomas, 2 grade 2 conjunctival intraepithelial neoplasias, 7 in situ squamous carcinoma
25 ring developed intestinal lesions, including intraepithelial neoplasia, adenomas, and adenocarcinomas
26 s to surgery for female patients with vulval intraepithelial neoplasia after exclusion of occult inva
28 ients, including 11 low-grade, 14 high-grade intraepithelial neoplasia and 12 invasive carcinoma in 3
29 lly classified as benign prostate, prostatic intraepithelial neoplasia and adenocarcinoma, can be eva
30 normal mammary epithelium, developed ductal intraepithelial neoplasia and DCIS, and progressed to in
31 (Fl/Fl)) failed to progress beyond prostatic intraepithelial neoplasia and did not harbor genomic CNA
32 es local conservative treatment for cervical intraepithelial neoplasia and early invasive cervical ca
33 becomes highly expressed in human prostatic intraepithelial neoplasia and in PCa, and that the funct
34 diminished SC chemoattraction to pancreatic intraepithelial neoplasia and increased abdominal hypers
35 enic mice presented with high-grade prostate intraepithelial neoplasia and increased nuclear cyclin D
36 levels of H3K27me3 are reduced in prostatic intraepithelial neoplasia and invasive adenocarcinoma le
37 low but increases significantly in cervical intraepithelial neoplasia and invasive squamous cervical
40 ls in culture and for Kras-driven pancreatic intraepithelial neoplasia and PDAC formation in vivo.
42 that Olfm4-knockout mice developed prostatic intraepithelial neoplasia and prostatic adenocarcinoma.
43 the expression of AnxA2 is lost in prostate intraepithelial neoplasia and reappears in the high-grad
44 l, leading to early onset of mouse prostatic intraepithelial neoplasia and the progression of prostat
45 , safe, and feasible for treatment of vulval intraepithelial neoplasia and warrant further investigat
47 ho received RFA for BE containing high-grade intraepithelial neoplasia and/or early-stage cancer for
48 rrett's esophagus (BE) containing high-grade intraepithelial neoplasia and/or early-stage cancer.
49 promote progression of high-grade prostatic intraepithelial neoplasia and/or prostate cancers that e
52 and RAC1 were increased in human pancreatic intraepithelial neoplasias and PDAs compared with health
53 rom the transgenic mice regenerated prostate intraepithelial neoplasias and prostatic adenocarcinoma
54 expression of Bmi1 in mice induced prostatic intraepithelial neoplasia, and elicited invasive adenoca
55 eads to the formation of kidney cysts, renal intraepithelial neoplasia, and invasive papillary renal
56 decreased formation of high-grade pancreatic intraepithelial neoplasias, and accelerated development
57 y analyzed for formation of IPMN, pancreatic intraepithelial neoplasias, and PDAC, in addition to pro
58 Transgenic ETV1 mice developed prostatic intraepithelial neoplasia as well as hyperplasia/neoplas
59 n; the corresponding efficacies against anal intraepithelial neoplasia associated with HPV of any typ
60 quadrivalent HPV vaccine (qHPV) against anal intraepithelial neoplasia associated with HPV-6, 11, 16,
61 Efficacy of the qHPV vaccine against anal intraepithelial neoplasia associated with HPV-6, 11, 16,
62 1 induced histological features of prostatic intraepithelial neoplasia at 7 months of age; these feat
64 10 v 2.5 to 3.9 ng/mL), high-grade prostatic intraepithelial neoplasia/atypical glands (HR = 2.97), g
65 sulted in development of high-grade cervical intraepithelial neoplasia, but not frank cervical carcin
66 ally accelerated the progression of prostate intraepithelial neoplasia, by promoting cell proliferati
67 t epithelial atypia (controls); conjunctival intraepithelial neoplasia, carcinoma in situ (CIS); and
68 unlike normal prostate epithelium, prostatic intraepithelial neoplasia cells showed strong coexpressi
69 nterval [CI], 5.1% to 28.7%) and of cervical intraepithelial neoplasia (CIN) 1-3 or adenocarcinoma in
70 the risk of HPV-6/11/16/18-related cervical intraepithelial neoplasia (CIN) 1-3 or adenocarcinoma in
71 bout test performance for detecting cervical intraepithelial neoplasia (CIN) and cancer and screening
72 tly diagnosed with higher grades of cervical intraepithelial neoplasia (CIN) and cancer, as compared
73 t the long-term yield of high-grade cervical intraepithelial neoplasia (CIN) and the influence on bio
74 re defined as women classified with cervical intraepithelial neoplasia (CIN) grade 2+ (CIN2+) (n = 10
75 istory and histologically confirmed cervical intraepithelial neoplasia (CIN) in 2.5 years after the b
76 enic human papillomaviruses (HPVs), cervical intraepithelial neoplasia (CIN) is common, and current t
77 ous intraepithelial lesion (SIL) or cervical intraepithelial neoplasia (CIN) prevalence, incidence, p
78 To determine the population-based cervical intraepithelial neoplasia (CIN) trends when adjusting fo
80 specimens, including 38 normal, 52 cervical intraepithelial neoplasia (CIN), and 68 cervical cancer
85 iruses (HPV) results in precancers [cervical intraepithelial neoplasia (CIN)] and cancers near the ec
86 ly increased with disease severity (cervical intraepithelial neoplasia [CIN] 3, 17.9% [+/-7.2] vs CIN
87 ated STAT3 increased from low-grade cervical intraepithelial neoplasia (CIN1) to precancerous CIN3 le
88 nning normalcy, increasingly severe cervical intraepithelial neoplasia (CIN1- CIN3), and cervical can
89 HC2 for the detection of high-grade cervical intraepithelial neoplasia (CIN2+) in a total of 8,610 ce
90 span of progression from high-grade cervical intraepithelial neoplasia (CIN2/3) to invasive cervical
91 r the ability to predict high-grade cervical intraepithelial neoplasias (CIN2 or worse) in correspond
92 cidence rates (CIRs) of >/= grade 3 cervical intraepithelial neoplasia (CIN3+) or cancer for enrollme
93 ied well" patients with high-grade prostatic intraepithelial neoplasia combined with issues of recurr
94 ical surgical prevention includes removal of intraepithelial neoplasia detected by screening (includi
95 established metaplastic lesions, and lost in intraepithelial neoplasia/dysplasia and carcinoma of var
96 anogenital warts, oral warts, and anogenital intraepithelial neoplasias (eg, cervical intraepithelial
99 ere dysplasia manifested as gastrointestinal intraepithelial neoplasia (GIN) after 28 weeks post-H. p
100 eous atrophic gastritis and gastrointestinal intraepithelial neoplasia (GIN) with 80% prevalence 6 mo
101 usly expressed in human high-grade prostatic intraepithelial neoplasia, Gleason grades 3 through 5 pr
102 diagnosed cytologically; 1198 with cervical intraepithelial neoplasia grade 1 (CIN1), 456 with CIN2,
103 nst 6-month persistent infection or cervical intraepithelial neoplasia grade 1 or greater (CIN1+) ass
105 nst 6-month persistent infection or cervical intraepithelial neoplasia grade 1 or higher (CIN1+) asso
106 h channel based on the detection of cervical intraepithelial neoplasia grade 2 (CIN2) or greater (>/=
107 , clinical performance in detecting cervical intraepithelial neoplasia grade 2 (CIN2) or more severe
108 ic diagnosis of controls (less than cervical intraepithelial neoplasia grade 2 [<CIN2]) or cases (cer
109 t viral load, which varied by type (cervical intraepithelial neoplasia grade 2 [CIN2] for HPV52, CIN3
110 f a high-grade precancerous lesion (cervical intraepithelial neoplasia grade 2 or 3) or cervical canc
111 nce of high-grade cervical disease (cervical intraepithelial neoplasia grade 2 or 3, adenocarcinoma i
112 dy, we selected women with incident cervical intraepithelial neoplasia grade 2 or grade 3 (CIN2/3; n
114 ainst 6-month persistent infection, cervical intraepithelial neoplasia grade 2 or greater (CIN2+) ass
115 the Xpert HPV for the detection of cervical intraepithelial neoplasia grade 2 or higher (CIN2+) and
116 eoplasia grade 2 [<CIN2]) or cases (cervical intraepithelial neoplasia grade 2 or higher [CIN2+]) for
117 des 2/3 and adenocarcinoma in situ (cervical intraepithelial neoplasia grade 2 or higher [CIN2+]) in
119 ing for the detection of underlying cervical intraepithelial neoplasia grade 2 or worse (CIN2+) in th
120 n have used the disease endpoint of cervical intraepithelial neoplasia grade 2 or worse (CIN2+).
121 women with histologically confirmed cervical-intraepithelial neoplasia grade 2 or worse [>or= CIN2])
122 ce in vaccine efficacy (VE) against cervical intraepithelial neoplasia grade 2 or worse in HPV-naive
123 ICIA criteria, VE estimates against cervical intraepithelial neoplasia grade 2 or worse, regardless o
124 nclarity assay for the detection of cervical intraepithelial neoplasia grade 2+ (CIN2+) and CIN3+ was
126 result, we identified 90 women with cervical intraepithelial neoplasia grade 2+ (CIN2+), including 43
127 lastic lesions and invasive cancer (cervical intraepithelial neoplasia grade 2+ [CIN2+]) compared to
128 low specificities for the detection of anal intraepithelial neoplasia grade 2/3 (AIN2/3) in this pop
129 We assessed if risk of developing cervical intraepithelial neoplasia grade 2/3 (CIN2/3) or adenocar
130 uamous intraepithelial lesions (ie, cervical intraepithelial neoplasia grade 2/3 [CIN 2/3]) and (2) i
131 s from patients with HPV-associated cervical intraepithelial neoplasia grade 2/3 and murine skin disp
132 vulvar cancer), and vaginal disease (vaginal intraepithelial neoplasia grade 2/3, vaginal cancer) rel
133 cervical carcinoma), vulvar disease (vulvar intraepithelial neoplasia grade 2/3, vulvar cancer), and
135 at high risk of cervical cancer or cervical intraepithelial neoplasia grade 3 (CIN3) or worse over 5
138 igibility criteria were biopsy-proven vulval intraepithelial neoplasia grade 3 and at least one lesio
139 aseline specimens from 482 cases of cervical intraepithelial neoplasia grade 3 or cancer (CIN3+) and
140 Similar results were observed for cervical intraepithelial neoplasia grade 3 or higher (CIN3+) (n =
142 y outcome was the detection rate of cervical intraepithelial neoplasia grade 3 or worse (CIN3+) in th
143 e timing of diagnosis of histologic cervical intraepithelial neoplasia grade 3 or worse (CIN3+) using
145 om women with a diagnosis of CIN3+ (cervical intraepithelial neoplasia grade 3+ or cervical cancer) t
146 ancer, 6.68 (95% CI, 3.64 to 12.25) for anal intraepithelial neoplasia grade 3, 4.97 (95% CI, 3.26 to
147 er, 13.66 (93% CI, 9.69 to 19.25) for vulvar intraepithelial neoplasia grade 3, 86.08 (95% CI, 11.98
148 , 25.65 (95% CI, 10.50 to 62.69) for vaginal intraepithelial neoplasia grade 3, and 5.51 (95% CI, 1.2
149 was upregulated in patients with pancreatic intraepithelial neoplasias grade 3 and PDAC lesions rela
150 sts for hrHPV and HPV 16/18 to find cervical intraepithelial neoplasia (grade >/=2 [CIN2+] or grade >
151 sts for hrHPV and HPV 16/18 to find cervical intraepithelial neoplasia (grade >/=2 [CIN2+] or grade >
153 gnificance or greater (ASCUS+), and cervical intraepithelial neoplasia grades 1/2 or greater (CIN1+,
154 1 (HPV31) DNA loads and the risk of cervical intraepithelial neoplasia grades 2 and 3 (CIN2-3) was ev
155 % CI = 37.9 to 68.3) for diagnosing cervical intraepithelial neoplasia grades 2/3 (CIN2/3) on histolo
156 implemented mandatory reporting of cervical intraepithelial neoplasia grades 2/3 and adenocarcinoma
157 Methods used to diagnose and treat cervical intraepithelial neoplasia have important potential adver
158 We modeled fractions of high-grade anal intraepithelial neoplasia (HGAIN) attributable to indivi
159 precancerous anal lesions or high-grade anal intraepithelial neoplasia (HGAIN) have been vaccinated e
160 (MSM) who have a history of high-grade anal intraepithelial neoplasia (HGAIN) was associated with a
163 tion and progression of high-grade prostatic intraepithelial neoplasia (HGPIN) to prostatic adenocarc
166 e Etk/BMX in mouse prostate induces prostate intraepithelial neoplasia, implying a possible causal ro
167 Confocal laser endomicroscopy can localize intraepithelial neoplasia in chronic ulcerative colitis
168 D2A resulted in the development of prostatic intraepithelial neoplasia in mice, demonstrating that JM
169 g a significant increase in the frequency of intraepithelial neoplasia in patients who received a lip
171 f the qHPV vaccine reduced the rates of anal intraepithelial neoplasia, including of grade 2 or 3, am
172 cally attenuates the formation of pancreatic intraepithelial neoplasia induced by mutant Kras(G12D),
173 normal prostate glands, high-grade prostatic intraepithelial neoplasia, invasive adenocarcinoma, or p
176 standard treatment for patients with vulval intraepithelial neoplasia is surgery, but this approach
177 was decoded from five grade 2 or 3 cervical intraepithelial neoplasia lesion (CIN2/3) samples and fi
179 PI3K activation occurred early in prostate intraepithelial neoplasia lesion formation in these anim
181 ramatic hyperplasia and multifocal prostatic intraepithelial neoplasia lesions from adjacent naive ep
182 eficient mice exhibited widespread prostatic intraepithelial neoplasia lesions in all prostatic lobes
183 ce and the replicative activity of prostatic intraepithelial neoplasia lesions in the dorsal prostate
185 l metaplasia (ADM)-a precursor of pancreatic intraepithelial neoplasia lesions that can progress to P
186 rostate (TRAMP-FVB) mice harboring prostatic intraepithelial neoplasia lesions until 20 weeks of age
187 induction of NFATc2 in late-stage pancreatic intraepithelial neoplasia lesions with increased express
188 cumulate low-grade, pre-malignant pancreatic intraepithelial neoplasia lesions, but progression to hi
192 uctal metaplasia (ADM), malignant pancreatic intraepithelial neoplasia (mPanIN), and PDAC within a ye
193 is coexpressed with MUC1 in mouse pancreatic intraepithelial neoplasia (mPanIN)-like lesions and in t
194 Ras activity and in sparse murine pancreatic intraepithelial neoplasias (mPanINs) that did not sponta
195 c-MYC-initiated cells progress to prostatic intraepithelial neoplasia (mPIN) and adenocarcinoma lesi
196 l transgenic mice developed murine prostatic intraepithelial neoplasia (mPIN) and prostatic adenocarc
197 but Tsc1-deficient mice developed prostatic intraepithelial neoplasia (mPIN) in lateral and anterior
198 le transgenic mice displayed mouse prostatic intraepithelial neoplasia (mPIN) in the ventral and dors
199 tive stroma activation surrounding prostatic intraepithelial neoplasia (mPIN) lesions found both in i
203 psy-proved squamous cell carcinoma or vulvar intraepithelial neoplasia occurred during follow-up in 0
204 of residual or recurrent high-grade cervical intraepithelial neoplasia of grade two or worse (CIN2+)
206 ry efficacy objective was prevention of anal intraepithelial neoplasia or anal cancer related to infe
207 s and 86.1% in women with NLIM (negative for intraepithelial neoplasia or malignancy) cytology who we
208 evels are associated with a history of prior intraepithelial neoplasia or pT1mic/pT1a breast cancer a
210 at either noninvasive precursor (pancreatic intraepithelial neoplasia) or the PDAC stage led to inva
212 ificantly with the progression of pancreatic intraepithelial neoplasias (P = 0.001) and development o
215 ), and KC(iMist1) mouse models of pancreatic intraepithelial neoplasia (PanIN) and analyzed by confoc
216 hat underwent ADM can progress to pancreatic intraepithelial neoplasia (PanIN) and eventually pancrea
217 is overexpressed in premalignant pancreatic intraepithelial neoplasia (PanIN) and in the majority of
218 A) develops predominantly through pancreatic intraepithelial neoplasia (PanIN) and intraductal papill
219 d might be viewed as a prelude to pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal
220 velopment and is induced in mouse pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal
222 ce of oncogenic KRAS, accelerates pancreatic intraepithelial neoplasia (PanIN) formation and the deve
223 ates acinar-to-ductal metaplasia, pancreatic intraepithelial neoplasia (PanIN) formation, and PanIN p
224 We previously demonstrated that pancreatic intraepithelial neoplasia (PanIN) formation, which prece
226 progressively develop high-grade pancreatic intraepithelial neoplasia (PanIN) lesions and neoplasia
227 both pancreatic cancer cells and pancreatic intraepithelial neoplasia (PanIN) lesions in human pancr
228 transition from early to advanced pancreatic intraepithelial neoplasia (PanIN) lesions, we assessed w
230 ions then convert to precancerous pancreatic intraepithelial neoplasia (PanIN) that progresses to PDA
231 IS biomarkers in human and murine pancreatic intraepithelial neoplasia (PanIN), and found that only s
234 C and its preinvasive precursors, pancreatic intraepithelial neoplasia (PanIN), arise via reprogrammi
235 ithelium accelerated formation of pancreatic intraepithelial neoplasia (PanIN), increased the frequen
236 ys, methylation analysis of early pancreatic intraepithelial neoplasia (PanIN), mouse models for PDAC
237 scin deficiency on development of pancreatic intraepithelial neoplasia (PanIn), PDAC, and metastasis.
238 n is expressed in human and mouse pancreatic intraepithelial neoplasia (PanIN), suggesting that N-cad
239 creatic acinar cells give rise to pancreatic intraepithelial neoplasia (PanIN), the most common precu
240 of PDA and its precursor lesion, pancreatic intraepithelial neoplasia (PanIN), we examined the effec
249 the formation and maintenance of pancreatic intraepithelial neoplasia (PanINs) in p48Cre; TetO-KrasG
250 iation and expansion of low-grade pancreatic intraepithelial neoplasia (PanINs), likely through diffe
251 titute hallmark features of human pancreatic intraepithelial neoplasia (PanINs), the precursor to pan
252 sufficient to induce formation of pancreatic intraepithelial neoplasia (PanINs)-a precursor of PDAC.
254 s the development of premalignant pancreatic intraepithelial neoplasias (PanINs) and cystic lesions i
255 ancreatic ductal adenocarcinomas, pancreatic intraepithelial neoplasias (PanINs) and normal pancreas
256 cinar-to-ductal metaplasia (ADM), pancreatic intraepithelial neoplasias (PanINs) and ultimately pancr
260 infection is sufficient to enhance prostate intraepithelial neoplasia (PIN) and microinvasive carcin
261 the Sirt1 gene in mice resulted in prostatic intraepithelial neoplasia (PIN) associated with reduced
262 ostate cancer model, as well as in prostatic intraepithelial neoplasia (PIN) before histological or a
263 s in wild-type mice rarely induced prostatic intraepithelial neoplasia (PIN) in dorsal prostates (one
265 ed with development of premalignant prostate intraepithelial neoplasia (PIN) lesions and invasive ade
266 ighly expressed in prostatic hyperplasia and intraepithelial neoplasia (PIN) lesions that also lack N
267 f epithelial hyperplasia and focal prostatic intraepithelial neoplasia (PIN) lesions, but not progres
269 d loss of Akap12 and Rb results in prostatic intraepithelial neoplasia (PIN) that fails to progress t
270 sed the prevalence and severity of prostatic intraepithelial neoplasia (PIN), a premalignant lesion.
271 sses: epithelium, stroma, atrophy, prostatic intraepithelial neoplasia (PIN), and prostate cancer Gle
272 rostate cancers, is less common in prostatic intraepithelial neoplasia (PIN), raising questions about
273 (AR) is essential for initiation of prostate intraepithelial neoplasia (PIN), the response of AR-null
276 en of early-stage prostate cancer [prostatic intraepithelial neoplasia (PIN)] and well-differentiated
277 enign prostatic hyperplasia [BPH], prostatic intraepithelial neoplasia [PIN], inflammation, and atrop
278 SL-KrasG12D model by exacerbating pancreatic intraepithelial neoplasias, promoting facial papillomas,
280 nactivation of this GTPase at the pancreatic intraepithelial neoplasia stage promotes pancreatic tiss
281 that survivin interference at the prostatic intraepithelial neoplasia stages may be a potential ther
282 reater number and higher grade of pancreatic intraepithelial neoplasias than KC mice, and 1 mouse dev
284 human pancreatic cancer cells and pancreatic intraepithelial neoplasia, the early lesion of pancreati
285 nic KRAS in both the formation of pancreatic intraepithelial neoplasias, the most common precursor le
286 state cancer (CaP) progresses from prostatic intraepithelial neoplasia through locally invasive adeno
287 PDAC tissues and in premalignant pancreatic intraepithelial neoplasia tissues isolated from Pdx-1-Cr
288 participates in the progression of prostatic intraepithelial neoplasia to adenocarcinoma, and that su
292 ntification and treatment of high-grade anal intraepithelial neoplasia to prevent anal cancer are war
293 is an essential component of the pancreatic intraepithelial neoplasias-to-PDAC route in Kras(G12D)-d
294 to document the efficacy of high-grade anal intraepithelial neoplasia treatment to reduce the incide
295 d cancer is not suspected, usual-type vulvar intraepithelial neoplasia treatment, including medical a
296 n paraffin-embedded VSCC and adjacent vulvar intraepithelial neoplasia (VIN) and VLS specimens, in ca
298 syndrome, clonal hematopoiesis, and cervical intraepithelial neoplasia which also serve as models for
299 d acinar-to-ductal metaplasia and pancreatic intraepithelial neoplasias, which rapidly progressed to
300 rly neoplastic lesions (high-grade prostatic intraepithelial neoplasia) with striking nuclear atypia
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