(Q36234845)

12 August 2017

1 reference

title

Mutations in the human LKB1/STK11 gene (English)

1 reference

12 August 2017

Virpi Launonen

1

1 reference

12 August 2017

1 October 2005

1 reference

12 August 2017

1 reference

12 August 2017

26

1 reference

12 August 2017

291-297

1 reference

12 August 2017

4

1 reference

LKB1 somatic mutations in sporadic tumors

12 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Increased risk for cancer in patients with the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Frameshift mutation of the STK11 gene in a sporadic gastrointestinal cancer with microsatellite instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Mutational analysis of STK11 gene in ovarian carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

STK11/LKB1 Peutz-Jeghers gene inactivation in intraductal papillary-mucinous neoplasms of the pancreas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Correlation of Staining for LKB1 and COX-2 in Hamartomatous Polyps and Carcinomas from Patients with Peutz–Jeghers Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597(insertion mark)598insIVS4)

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Genotype-phenotype correlations in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Loss of the Lkb1 tumour suppressor provokes intestinal polyposis but resistance to transformation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Analysis of the LKB1-STRAD-MO25 complex

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Search for the second Peutz-Jeghers syndrome locus: exclusion of the STK13, PRKCG, KLK10, and PSCD2 genes on chromosome 19 and the STK11IP gene on chromosome 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Novel and natural knockout lung cancer cell lines for the LKB1/STK11 tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Epigenetic inactivation of LKB1 in primary tumors associated with the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Distinctive gene expression of human lung adenocarcinomas carrying LKB1 mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Increased risk of cancer in the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

The molecular basis and clinical aspects of Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

De novo germline mutation in the serine-threonine kinase STK11/LKB1 gene associated with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

The Peutz-Jegher gene product LKB1 is a mediator of p53-dependent cell death

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Genetic analysis of the LKB1/STK11 gene in hepatocellular carcinomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mutation analysis in 46 German families with familial hypercholesterolemia: identification of 8 new mutations. Mutations in brief no. 226. Online

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mutations in the STK11 gene characterize minimal deviation adenocarcinoma of the uterine cervix.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Relative frequency and morphology of cancers in STK11 mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

LKB1 associates with Brg1 and is necessary for Brg1-induced growth arrest

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

LKB1, the multitasking tumour suppressor kinase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Duodenal cancer in a patient with Peutz-Jeghers syndrome: molecular analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Somatic mutations in the Peutz-Jeghers (LKB1/STKII) gene in sporadic malignant melanomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

STK11 genotyping and cancer risk in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Cancer and the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Growth suppression by Lkb1 is mediated by a G(1) cell cycle arrest

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Growth arrest by the LKB1 tumor suppressor: induction of p21(WAF1/CIP1).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers syndrome: 78-year follow-up of the original family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Peutz-Jeghers syndrome: risks of a hereditary condition.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Vascular abnormalities and deregulation of VEGF in Lkb1-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

LKB1--a master tumour suppressor of the small intestine and beyond

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20222

7 January 2021

Identifiers

DOI

10.1002/HUMU.20222

1 reference

12 August 2017

1 reference

PubMed ID

16110486