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1 tal intraepithelial neoplasias (eg, cervical intraepithelial neoplasia).
2 e without affecting hyperplasia or prostatic intraepithelial neoplasia.
3 yperplasia, or dysplastic lesions/pancreatic intraepithelial neoplasia.
4 fficient to induce hyperplasia and prostatic intraepithelial neoplasia.
5 ulation, leading to development of prostatic intraepithelial neoplasia.
6 arly as at the stage of high-grade prostatic intraepithelial neoplasia.
7 ve to surgery in female patients with vulval intraepithelial neoplasia.
8 results showed that 4 eyes had conjunctival intraepithelial neoplasia.
9 oliferation, hyperplasia, and early prostate intraepithelial neoplasia.
10 n Dist-Luminal-C cells resulted in prostatic intraepithelial neoplasia.
11 cifically overexpress ETV1 develop prostatic intraepithelial neoplasia.
12 pancreatic ducts, referred to as pancreatic intraepithelial neoplasias.
13 mice, but did not alter growth of pancreatic intraepithelial neoplasias.
14 grade dysplasia and some enlarged pancreatic intraepithelial neoplasias.
15 etaplasia, dysplasia, and ultimately gastric intraepithelial neoplasias.
16 papillary mucinous neoplasms and in multiple intraepithelial neoplasias.
17 and tolerable for treating usual-type vulvar intraepithelial neoplasia?
18 n of oncogenic KRAS, premalignant pancreatic intraepithelial neoplasia 1 (PanIN1) lesions rarely beco
19 ntial reduction of ADM as well as pancreatic intraepithelial neoplasia-1 (PanIN-1), PanIN-2, and PanI
20 Its expression is lost at the pancreatic intraepithelial neoplasia 1b (PanIN1b)/PanIN2 stage of p
21 ting premalignant cervical lesions (cervical intraepithelial neoplasia 2+ [CIN2+]) is an effective wa
22 e 70% of cervical cancer and 50% of cervical intraepithelial neoplasia 2/3 and adenocarcinoma in situ
24 ening algorithm found more disease (cervical intraepithelial neoplasia 3 or worse [CIN3+]) and also f
25 I, 1.67 to 3.31); grade 2 or higher cervical intraepithelial neoplasia, 6.9% vs. 3.4% (hazard ratio,
26 (2 benign papillomas, 2 grade 2 conjunctival intraepithelial neoplasias, 7 in situ squamous carcinoma
27 s to surgery for female patients with vulval intraepithelial neoplasia after exclusion of occult inva
28 amous intraepithelial lesions (ASIL) or anal intraepithelial neoplasia (AIN) are precancerous lesions
30 -related factors on anal HPV infection, anal intraepithelial neoplasia (AIN), and anal cancer among p
32 ients, including 11 low-grade, 14 high-grade intraepithelial neoplasia and 12 invasive carcinoma in 3
33 ped an earlier onset of high-grade prostatic intraepithelial neoplasia and accelerated prostate tumor
34 lly classified as benign prostate, prostatic intraepithelial neoplasia and adenocarcinoma, can be eva
35 normal mammary epithelium, developed ductal intraepithelial neoplasia and DCIS, and progressed to in
36 (Fl/Fl)) failed to progress beyond prostatic intraepithelial neoplasia and did not harbor genomic CNA
37 es local conservative treatment for cervical intraepithelial neoplasia and early invasive cervical ca
38 diminished SC chemoattraction to pancreatic intraepithelial neoplasia and increased abdominal hypers
39 ations showed that the severity of prostatic intraepithelial neoplasia and inflammation development g
40 levels of H3K27me3 are reduced in prostatic intraepithelial neoplasia and invasive adenocarcinoma le
41 low but increases significantly in cervical intraepithelial neoplasia and invasive squamous cervical
44 ls in culture and for Kras-driven pancreatic intraepithelial neoplasia and PDAC formation in vivo.
47 that Olfm4-knockout mice developed prostatic intraepithelial neoplasia and prostatic adenocarcinoma.
48 l, leading to early onset of mouse prostatic intraepithelial neoplasia and the progression of prostat
49 , safe, and feasible for treatment of vulval intraepithelial neoplasia and warrant further investigat
50 ho received RFA for BE containing high-grade intraepithelial neoplasia and/or early-stage cancer for
51 rrett's esophagus (BE) containing high-grade intraepithelial neoplasia and/or early-stage cancer.
54 and RAC1 were increased in human pancreatic intraepithelial neoplasias and PDAs compared with health
55 rom the transgenic mice regenerated prostate intraepithelial neoplasias and prostatic adenocarcinoma
56 mation of precancerous lesions (endometrioid intraepithelial neoplasia) and well-differentiated endom
57 6% for PAM, 67% for conjunctival melanocytic intraepithelial neoplasia, and 81% for WHO classificatio
58 expression of Bmi1 in mice induced prostatic intraepithelial neoplasia, and elicited invasive adenoca
59 eads to the formation of kidney cysts, renal intraepithelial neoplasia, and invasive papillary renal
60 ation systems: PAM, conjunctival melanocytic intraepithelial neoplasia, and the WHO 4th edition class
61 decreased formation of high-grade pancreatic intraepithelial neoplasias, and accelerated development
62 y analyzed for formation of IPMN, pancreatic intraepithelial neoplasias, and PDAC, in addition to pro
63 for both pre- and postmenopausal women with intraepithelial neoplasia are discussed in the Clinical
65 that TopBP1 levels are increased in cervical intraepithelial neoplasias as well as cervical carcinoma
66 n; the corresponding efficacies against anal intraepithelial neoplasia associated with HPV of any typ
67 quadrivalent HPV vaccine (qHPV) against anal intraepithelial neoplasia associated with HPV-6, 11, 16,
68 Efficacy of the qHPV vaccine against anal intraepithelial neoplasia associated with HPV-6, 11, 16,
69 1 induced histological features of prostatic intraepithelial neoplasia at 7 months of age; these feat
71 PRKD1(KO)-KC mice developed more pancreatic intraepithelial neoplasia, at a faster rate, than KC mic
72 fective in preventing recurrence from breast intraepithelial neoplasia but have a lower toxicity than
73 sulted in development of high-grade cervical intraepithelial neoplasia, but not frank cervical carcin
74 ally accelerated the progression of prostate intraepithelial neoplasia, by promoting cell proliferati
75 t epithelial atypia (controls); conjunctival intraepithelial neoplasia, carcinoma in situ (CIS); and
76 bout test performance for detecting cervical intraepithelial neoplasia (CIN) and cancer and screening
77 t the long-term yield of high-grade cervical intraepithelial neoplasia (CIN) and the influence on bio
78 (LEEP) for histologically confirmed cervical intraepithelial neoplasia (CIN) grade 2 or higher regard
79 re defined as women classified with cervical intraepithelial neoplasia (CIN) grade 2+ (CIN2+) (n = 10
81 istory and histologically confirmed cervical intraepithelial neoplasia (CIN) in 2.5 years after the b
82 enic human papillomaviruses (HPVs), cervical intraepithelial neoplasia (CIN) is common, and current t
83 ous intraepithelial lesion (SIL) or cervical intraepithelial neoplasia (CIN) prevalence, incidence, p
84 To determine the population-based cervical intraepithelial neoplasia (CIN) trends when adjusting fo
86 rognostic test to ascertain whether cervical intraepithelial neoplasia (CIN) will regress or progress
87 specimens, including 38 normal, 52 cervical intraepithelial neoplasia (CIN), and 68 cervical cancer
88 hy, human papilloma virus (HPV) +/- cervical intraepithelial neoplasia (CIN), or cervical cancer.
91 papillomavirus (HPV) infection, and cervical intraepithelial neoplasia (CIN); however, causal inferen
92 iruses (HPV) results in precancers [cervical intraepithelial neoplasia (CIN)] and cancers near the ec
93 ly increased with disease severity (cervical intraepithelial neoplasia [CIN] 3, 17.9% [+/-7.2] vs CIN
94 ated STAT3 increased from low-grade cervical intraepithelial neoplasia (CIN1) to precancerous CIN3 le
95 nning normalcy, increasingly severe cervical intraepithelial neoplasia (CIN1- CIN3), and cervical can
96 asma viral load (PVL) on high-grade cervical intraepithelial neoplasia (CIN2+) detection at follow-up
97 HC2 for the detection of high-grade cervical intraepithelial neoplasia (CIN2+) in a total of 8,610 ce
98 span of progression from high-grade cervical intraepithelial neoplasia (CIN2/3) to invasive cervical
99 r the ability to predict high-grade cervical intraepithelial neoplasias (CIN2 or worse) in correspond
101 cidence rates (CIRs) of >/= grade 3 cervical intraepithelial neoplasia (CIN3+) or cancer for enrollme
102 Cervical dysplastic lesions called cervical intraepithelial neoplasias (CINs) need be treated to pre
103 rognostic test to ascertain whether cervical intraepithelial neoplasias (CINs) regress or progress.
105 anogenital warts, oral warts, and anogenital intraepithelial neoplasias (eg, cervical intraepithelial
106 diagnosed cytologically; 1198 with cervical intraepithelial neoplasia grade 1 (CIN1), 456 with CIN2,
107 nst 6-month persistent infection or cervical intraepithelial neoplasia grade 1 or greater (CIN1+) ass
109 nst 6-month persistent infection or cervical intraepithelial neoplasia grade 1 or higher (CIN1+) asso
110 h channel based on the detection of cervical intraepithelial neoplasia grade 2 (CIN2) or greater (>/=
111 , clinical performance in detecting cervical intraepithelial neoplasia grade 2 (CIN2) or more severe
112 ic diagnosis of controls (less than cervical intraepithelial neoplasia grade 2 [<CIN2]) or cases (cer
113 t viral load, which varied by type (cervical intraepithelial neoplasia grade 2 [CIN2] for HPV52, CIN3
114 f a high-grade precancerous lesion (cervical intraepithelial neoplasia grade 2 or 3) or cervical canc
115 nce of high-grade cervical disease (cervical intraepithelial neoplasia grade 2 or 3, adenocarcinoma i
116 dy, we selected women with incident cervical intraepithelial neoplasia grade 2 or grade 3 (CIN2/3; n
118 ainst 6-month persistent infection, cervical intraepithelial neoplasia grade 2 or greater (CIN2+) ass
121 the Xpert HPV for the detection of cervical intraepithelial neoplasia grade 2 or higher (CIN2+) and
122 aginal samples for the detection of cervical intraepithelial neoplasia grade 2 or higher (CIN2+).
123 eoplasia grade 2 [<CIN2]) or cases (cervical intraepithelial neoplasia grade 2 or higher [CIN2+]) for
124 des 2/3 and adenocarcinoma in situ (cervical intraepithelial neoplasia grade 2 or higher [CIN2+]) in
126 amous intraepithelial lesion (HSIL) and anal intraepithelial neoplasia grade 2 or more severe diagnos
127 of doses administered, diagnoses of cervical intraepithelial neoplasia grade 2 or worse (CIN2+) or gr
128 n have used the disease endpoint of cervical intraepithelial neoplasia grade 2 or worse (CIN2+).
129 for preventing HPV 16/18-associated cervical intraepithelial neoplasia grade 2 or worse (CIN2+).
130 ce in vaccine efficacy (VE) against cervical intraepithelial neoplasia grade 2 or worse in HPV-naive
131 ICIA criteria, VE estimates against cervical intraepithelial neoplasia grade 2 or worse, regardless o
132 nclarity assay for the detection of cervical intraepithelial neoplasia grade 2+ (CIN2+) and CIN3+ was
134 ons, anogenital wart diagnoses, and cervical intraepithelial neoplasia grade 2+ (CIN2+) to summarise
135 result, we identified 90 women with cervical intraepithelial neoplasia grade 2+ (CIN2+), including 43
136 lastic lesions and invasive cancer (cervical intraepithelial neoplasia grade 2+ [CIN2+]) compared to
137 low specificities for the detection of anal intraepithelial neoplasia grade 2/3 (AIN2/3) in this pop
138 We assessed if risk of developing cervical intraepithelial neoplasia grade 2/3 (CIN2/3) or adenocar
139 uamous intraepithelial lesions (ie, cervical intraepithelial neoplasia grade 2/3 [CIN 2/3]) and (2) i
140 s from patients with HPV-associated cervical intraepithelial neoplasia grade 2/3 and murine skin disp
141 vulvar cancer), and vaginal disease (vaginal intraepithelial neoplasia grade 2/3, vaginal cancer) rel
142 cervical carcinoma), vulvar disease (vulvar intraepithelial neoplasia grade 2/3, vulvar cancer), and
143 at high risk of cervical cancer or cervical intraepithelial neoplasia grade 3 (CIN3) or worse over 5
146 igibility criteria were biopsy-proven vulval intraepithelial neoplasia grade 3 and at least one lesio
147 aseline specimens from 482 cases of cervical intraepithelial neoplasia grade 3 or cancer (CIN3+) and
148 Similar results were observed for cervical intraepithelial neoplasia grade 3 or higher (CIN3+) (n =
150 topathologically confirmed CIN2+ or cervical intraepithelial neoplasia grade 3 or worse associated wi
151 ancer, 6.68 (95% CI, 3.64 to 12.25) for anal intraepithelial neoplasia grade 3, 4.97 (95% CI, 3.26 to
152 er, 13.66 (93% CI, 9.69 to 19.25) for vulvar intraepithelial neoplasia grade 3, 86.08 (95% CI, 11.98
153 , 25.65 (95% CI, 10.50 to 62.69) for vaginal intraepithelial neoplasia grade 3, and 5.51 (95% CI, 1.2
154 was upregulated in patients with pancreatic intraepithelial neoplasias grade 3 and PDAC lesions rela
155 sts for hrHPV and HPV 16/18 to find cervical intraepithelial neoplasia (grade >/=2 [CIN2+] or grade >
156 sts for hrHPV and HPV 16/18 to find cervical intraepithelial neoplasia (grade >/=2 [CIN2+] or grade >
158 gnificance or greater (ASCUS+), and cervical intraepithelial neoplasia grades 1/2 or greater (CIN1+,
159 1 (HPV31) DNA loads and the risk of cervical intraepithelial neoplasia grades 2 and 3 (CIN2-3) was ev
160 We describe changes in rates of cervical intraepithelial neoplasia grades 2, 3 and adenocarcinoma
162 % CI = 37.9 to 68.3) for diagnosing cervical intraepithelial neoplasia grades 2/3 (CIN2/3) on histolo
163 implemented mandatory reporting of cervical intraepithelial neoplasia grades 2/3 and adenocarcinoma
164 ble knockouts presented high-grade prostatic intraepithelial neoplasia (HG-PIN) and hyperproliferatio
165 We modeled fractions of high-grade anal intraepithelial neoplasia (HGAIN) attributable to indivi
166 precancerous anal lesions or high-grade anal intraepithelial neoplasia (HGAIN) have been vaccinated e
167 omavirus (HPV) genotypes-and high-grade anal intraepithelial neoplasia (HGAIN) in men who have sex wi
168 (MSM) who have a history of high-grade anal intraepithelial neoplasia (HGAIN) was associated with a
171 be differentiated from high-grade prostatic intraepithelial neoplasia (HGPIN), a pre-malignant intra
174 D2A resulted in the development of prostatic intraepithelial neoplasia in mice, demonstrating that JM
175 g a significant increase in the frequency of intraepithelial neoplasia in patients who received a lip
177 al activation entirely surrounded pancreatic intraepithelial neoplasias in KPC/Cdh11(+/+) mice and in
178 f the qHPV vaccine reduced the rates of anal intraepithelial neoplasia, including of grade 2 or 3, am
179 cally attenuates the formation of pancreatic intraepithelial neoplasia induced by mutant Kras(G12D),
180 normal prostate glands, high-grade prostatic intraepithelial neoplasia, invasive adenocarcinoma, or p
183 standard treatment for patients with vulval intraepithelial neoplasia is surgery, but this approach
184 was decoded from five grade 2 or 3 cervical intraepithelial neoplasia lesion (CIN2/3) samples and fi
186 ramatic hyperplasia and multifocal prostatic intraepithelial neoplasia lesions from adjacent naive ep
187 eficient mice exhibited widespread prostatic intraepithelial neoplasia lesions in all prostatic lobes
188 ce and the replicative activity of prostatic intraepithelial neoplasia lesions in the dorsal prostate
189 l metaplasia (ADM)-a precursor of pancreatic intraepithelial neoplasia lesions that can progress to P
190 induction of NFATc2 in late-stage pancreatic intraepithelial neoplasia lesions with increased express
191 cumulate low-grade, pre-malignant pancreatic intraepithelial neoplasia lesions, but progression to hi
194 is coexpressed with MUC1 in mouse pancreatic intraepithelial neoplasia (mPanIN)-like lesions and in t
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 le transgenic mice displayed mouse prostatic intraepithelial neoplasia (mPIN) in the ventral and dors
198 tive stroma activation surrounding prostatic intraepithelial neoplasia (mPIN) lesions found both in i
201 psy-proved squamous cell carcinoma or vulvar intraepithelial neoplasia occurred during follow-up in 0
202 f diagnoses of anogenital warts and cervical intraepithelial neoplasia of grade 2 or 3 and cases of c
203 f diagnoses of anogenital warts and cervical intraepithelial neoplasia of grade 2 or 3 and cases of c
204 incident persistent qHPV infection, cervical intraepithelial neoplasia of grade 2 or higher [CIN2+],
205 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
214 ), and KC(iMist1) mouse models of pancreatic intraepithelial neoplasia (PanIN) and analyzed by confoc
215 hat underwent ADM can progress to pancreatic intraepithelial neoplasia (PanIN) and eventually pancrea
216 A) develops predominantly through pancreatic intraepithelial neoplasia (PanIN) and intraductal papill
217 velopment and is induced in mouse pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal
218 d might be viewed as a prelude to pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal
219 ce of oncogenic KRAS, accelerates pancreatic intraepithelial neoplasia (PanIN) formation and the deve
220 ates acinar-to-ductal metaplasia, pancreatic intraepithelial neoplasia (PanIN) formation, and PanIN p
221 We previously demonstrated that pancreatic intraepithelial neoplasia (PanIN) formation, which prece
223 he earliest stages of preinvasive pancreatic intraepithelial neoplasia (PanIN) in the KrasLSL-G12D/+
224 hages contribute to fibrogenesis, pancreatic intraepithelial neoplasia (PanIN) lesion growth, and gen
225 progressively develop high-grade pancreatic intraepithelial neoplasia (PanIN) lesions and neoplasia
226 transition from early to advanced pancreatic intraepithelial neoplasia (PanIN) lesions, we assessed w
228 ions then convert to precancerous pancreatic intraepithelial neoplasia (PanIN) that progresses to PDA
229 anc-28 cells and samples of human pancreatic intraepithelial neoplasia (PanIN), along with several bi
230 IS biomarkers in human and murine pancreatic intraepithelial neoplasia (PanIN), and found that only s
233 ), accelerated the progression of pancreatic intraepithelial neoplasia (PanIN), and resulted in the a
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
242 M proteins in normal pancreas and pancreatic intraepithelial neoplasia (PanIN)- and PDAC-bearing panc
250 olves visualisation of high-grade pancreatic intraepithelial neoplasias (PanIN-3), generally regarded
251 olves visualization of high-grade pancreatic intraepithelial neoplasias (PanIN-3s), generally regarde
252 the formation and maintenance of pancreatic intraepithelial neoplasia (PanINs) in p48Cre; TetO-KrasG
253 cancer and initiate precancerous pancreatic intraepithelial neoplasia (PanINs) when induced in mouse
254 iation and expansion of low-grade pancreatic intraepithelial neoplasia (PanINs), likely through diffe
255 titute hallmark features of human pancreatic intraepithelial neoplasia (PanINs), the precursor to pan
256 sufficient to induce formation of pancreatic intraepithelial neoplasia (PanINs)-a precursor of PDAC.
258 s the development of premalignant pancreatic intraepithelial neoplasias (PanINs) and cystic lesions i
259 ancreatic ductal adenocarcinomas, pancreatic intraepithelial neoplasias (PanINs) and normal pancreas
260 cinar-to-ductal metaplasia (ADM), pancreatic intraepithelial neoplasias (PanINs) and ultimately pancr
264 infection is sufficient to enhance prostate intraepithelial neoplasia (PIN) and microinvasive carcin
265 ostate cancer model, as well as in prostatic intraepithelial neoplasia (PIN) before histological or a
266 s in wild-type mice rarely induced prostatic intraepithelial neoplasia (PIN) in dorsal prostates (one
268 ed with development of premalignant prostate intraepithelial neoplasia (PIN) lesions and invasive ade
270 d loss of Akap12 and Rb results in prostatic intraepithelial neoplasia (PIN) that fails to progress t
271 sed the prevalence and severity of prostatic intraepithelial neoplasia (PIN), a premalignant lesion.
272 sses: epithelium, stroma, atrophy, prostatic intraepithelial neoplasia (PIN), and prostate cancer Gle
275 en of early-stage prostate cancer [prostatic intraepithelial neoplasia (PIN)] and well-differentiated
276 enign prostatic hyperplasia [BPH], prostatic intraepithelial neoplasia [PIN], inflammation, and atrop
277 d densely methylated in high-grade prostatic intraepithelial neoplasia, primary prostate carcinoma, a
278 SL-KrasG12D model by exacerbating pancreatic intraepithelial neoplasias, promoting facial papillomas,
280 of the mucin family during early pancreatic intraepithelial neoplasia stage I (PanIN-I) of pancreati
281 nactivation of this GTPase at the pancreatic intraepithelial neoplasia stage promotes pancreatic tiss
282 that survivin interference at the prostatic intraepithelial neoplasia stages may be a potential ther
283 reater number and higher grade of pancreatic intraepithelial neoplasias than KC mice, and 1 mouse dev
285 human pancreatic cancer cells and pancreatic intraepithelial neoplasia, the early lesion of pancreati
286 nic KRAS in both the formation of pancreatic intraepithelial neoplasias, the most common precursor le
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 is an essential component of the pancreatic intraepithelial neoplasias-to-PDAC route in Kras(G12D)-d
293 d cancer is not suspected, usual-type vulvar intraepithelial neoplasia treatment, including medical a
294 n paraffin-embedded VSCC and adjacent vulvar intraepithelial neoplasia (VIN) and VLS specimens, in ca
296 syndrome, clonal hematopoiesis, and cervical intraepithelial neoplasia which also serve as models for
297 o early pancreatic lesions called pancreatic intraepithelial neoplasias, which are challenging to det
298 d acinar-to-ductal metaplasia and pancreatic intraepithelial neoplasias, which rapidly progressed to
299 r 3 years can halve the recurrence of breast intraepithelial neoplasia with a limited toxicity, which
300 rly neoplastic lesions (high-grade prostatic intraepithelial neoplasia) with striking nuclear atypia