Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome
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STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreasA role for LKB1 gene in human cancer beyond the Peutz-Jeghers syndromeDifferent pattern of loss of heterozygosity among endocervical-type adenocarcinoma, endometrioid-type adenocarcinoma and adenoma malignum of the uterine cervix.Somatic LKB1 mutations promote cervical cancer progression.Induction of ovarian leiomyosarcomas in mice by conditional inactivation of Brca1 and p53.Homozygous deletion of the STK11/LKB1 locus and the generation of novel fusion transcripts in cervical cancer cells.LKB1, the multitasking tumour suppressor kinaseNasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entityLiver kinase B1 (LKB1) in the pathogenesis of epithelial cancersDo hereditary syndrome-related gynecologic cancers have any specific features?Mutations in the human LKB1/STK11 gene.Virilizing leydig-sertoli cell ovarian tumor associated with endometrioid carcinoma of the endometrium in a postmenopausal patient: case report and general considerations.Ovarian Sex-cord Tumour with Peutz-Jeghers Polyp and Giant Keratoacanthoma.Hereditary gynecological tumors associated with Peutz-Jeghers syndrome (Review)Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.Clinical outcome of treatment with serine-threonine kinase inhibitors in recurrent epithelial ovarian cancer: a systematic review of literature.AMPK and Cancer.A tumor of the uterine cervix with a complex histology in a Peutz-Jeghers syndrome patient with genomic deletion of the STK11 exon 1 region.Gynecological tumors in Mulibrey nanism and role for RING finger protein TRIM37 in the pathogenesis of ovarian fibrothecomas.Polymorphisms of the apoptosis-associated gene DP1L1 (deleted in polyposis 1-like 1) in colon cancer and inflammatory bowel disease.
P2860
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P2860
Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome
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2000 nî lūn-bûn
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2000 թուականի Յունուարին հրատարակուած գիտական յօդուած
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2000 թվականի հունվարին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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name
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@ast
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@en
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@nl
type
label
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@ast
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@en
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@nl
prefLabel
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@ast
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@en
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@nl
P2093
P2860
P1476
Somatic mutations in the STK11 ...... d with Peutz-Jegher's syndrome
@en
P2093
D C Connolly
H Katabuchi
P2860
P304
P356
10.1016/S0002-9440(10)64735-9
P407
P50
P577
2000-01-01T00:00:00Z