High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
about
Hamartomatous polyposis syndromes: a reviewHigh proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndromeLKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndromeHamartomatous Tumors in the Gastrointestinal TractUpdate on our investigation of malignant tumors associated with Peutz-Jeghers syndrome in Japan.Organ-sparing surgery of the bilateral testicular large cell calcifying sertoli cell tumor in patient with atypical Peutz-Jeghers syndrome.A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Indian patients.Population-based estimate of sibling risk for preterm birth, preterm premature rupture of membranes, placental abruption and pre-eclampsia.Mutations in STK11 gene in Czech Peutz-Jeghers patientsGenetic testing for hereditary colorectal cancer.High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delayGenetic predisposition to colorectal cancer: where we stand and future perspectivesA novel mutation in STK11 gene is associated with Peutz-Jeghers syndrome in Chinese patients.Gene expression of the tumour suppressor LKB1 is mediated by Sp1, NF-Y and FOXO transcription factorsTranslational advances regarding hereditary breast cancer syndromes.Hereditary pancreatic cancer.Juvenile polyposis syndrome.High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.Liver kinase B1 (LKB1) in the pathogenesis of epithelial cancersFindings from the Peutz-Jeghers syndrome registry of uruguay.Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23A case of Peutz-Jeghers syndrome associated with high-grade intramucosal neoplasiaSpecific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz-Jeghers syndrome.Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndrome.Diagnostic Approach to Hereditary Colorectal Cancer Syndromes.ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromesCharacterization of the STK11 splicing variant as a normal splicing isomer in a patient with Peutz-Jeghers syndrome harboring genomic deletion of the STK11 geneNovel serine/threonine kinase 11 gene mutations in Peutz-Jeghers syndrome patients and endoscopic managementBreaking the epithelial polarity barrier in cancer: the strange case of LKB1/PAR-4mTOR and HIF-1alpha-mediated tumor metabolism in an LKB1 mouse model of Peutz-Jeghers syndrome.Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidates.LKB1; linking cell structure and tumor suppression.Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome.The molecular mechanisms that underlie the tumor suppressor function of LKB1.Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.LKB1 and AMPK family signaling: the intimate link between cell polarity and energy metabolism.Recurrent ovarian Sertoli-Leydig cell tumor in a child with Peutz-Jeghers syndrome.LKB1 loss of function studied in vivo.
P2860
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P2860
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
description
2005 nî lūn-bûn
@nan
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@ast
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@en
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@nl
type
label
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@ast
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@en
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@nl
prefLabel
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@ast
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@en
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@nl
P2093
P356
P1433
P1476
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
@en
P2093
Constanze Pagenstecher
D Ross McLeod
Dietlinde Stienen
Elisabeth Mangold
Gail E Graham
René Santer
Siegfried Uhlhaas
Stefan Aretz
Steffan Loff
Walter Back
P304
P356
10.1002/HUMU.20253
P577
2005-12-01T00:00:00Z