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1 ed somatic PTEN alterations in the stroma of juvenile polyps.
2 because of the shared features of intestinal juvenile polyps.
3 ed to 10q22-24 in both familial and sporadic juvenile polyps.
5 gene were demonstrated in 50% of dysplastic juvenile polyps (3 of 6) but not in any of 16 juvenile p
6 deletions at 10q22 were detected in 39 of 47 juvenile polyps (83%) from 16 unrelated patients with ei
7 ers develop upper and lower gastrointestinal juvenile polyps and are at increased risk for gastrointe
8 sis that the genetic defect in both sporadic juvenile polyps and hereditary juvenile polyposis involv
9 tal epithelium was lost in 79% of dysplastic juvenile polyps and in 8% of nondysplastic juvenile poly
11 s is not a prerequisite for the formation of juvenile polyps, and that colorectal juvenile polyps in
12 patients with either hereditary or sporadic juvenile polyps, and the minimum overlap localized juven
13 y acts as a "gatekeeper" tumor suppressor in juvenile polyps, and there is no need to invoke a "lands
18 ith juvenile polyps syndrome and 34 sporadic juvenile polyps for epithelial dysplasia and genetic cha
19 ormal DNA with tumor DNA from a series of 47 juvenile polyps from 16 patients using polymerase chain
21 tion of juvenile polyps, and that colorectal juvenile polyps in CS are bona fide neoplastic precursor
22 specific PTEN deletion to cause formation of juvenile polyps in the colorectum without stromal PTEN l
27 play a role in neoplastic transformation of juvenile polyps, predominantly in juvenile polyposis syn
28 characteristic histopathological features of juvenile polyps seen in patients with CS, including stro
29 tal juvenile polyposis from 12 patients with juvenile polyps syndrome and 34 sporadic juvenile polyps
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