Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.
Patients with Peutz-Jeghers' syndrome (PJS) develop hamartomatous gastrointestinal polyps and characteristic pigmentation, as a result of germline mutations in the LKB1 gene. The hamartomas in PJS were long considered to be without malignant potential. There is, however, accumulating epidemiolo...
Autori principali: | Wang, Z, Ellis, I, Zauber, P, Iwama, T, Marchese, C, Talbot, I, Xue, W, Yan, Z, Tomlinson, I |
---|---|
Natura: | Journal article |
Lingua: | English |
Pubblicazione: |
1999
|
Documenti analoghi
Documenti analoghi
-
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.
di: Wang, Z, et al.
Pubblicazione: (1999) -
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
di: Lim, W, et al.
Pubblicazione: (2003) -
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
di: Hearle, N, et al.
Pubblicazione: (2005) -
Allele loss and mutation screen at the Peutz-Jeghers (LKB1) locus (19p13.3) in sporadic ovarian tumours.
di: Wang, Z, et al.
Pubblicazione: (1999) -
Identification of a novel mRNA species of the LKB1/STK11 Peutz-Jeghers serine/threonine kinase.
di: Churchman, M, et al.
Pubblicazione: (1999)