×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Relative frequency and morphology of cancers in STK11 mutation carriers.
15188174
2004
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
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.
23718779
2013
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome.
10623683
2000
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
An updated mutation spectrum in an Australian series of PJS patients provides further evidence for only one gene locus.
17026623
2006
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.
16707622
2006
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Novel and recurrent mutations of STK11 gene in six Chinese cases with Peutz-Jeghers syndrome.
24604241
2014
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
10408777
1999
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
23415580
2013
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients.
12372054
2002
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
9850045
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
STK11 domain XI mutations: candidate genetic drivers leading to the development of dysplastic polyps in Peutz-Jeghers syndrome.
24652667
2014
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
15121768
2004
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Morphology-dependent resonances in a large dielectric sphere: An asymptotic calculation using local coordinates.
9908348
1992
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
SIRT1 modulation of the acetylation status, cytosolic localization, and activity of LKB1. Possible role in AMP-activated protein kinase activation.
18687677
2008
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Novel mutations in the STK11 gene in Thai patients with Peutz-Jeghers syndrome.
19908348
2009
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Prevalence of germline PTEN, BMPR1A, SMAD4, STK11, and ENG mutations in patients with moderate-load colorectal polyps.
23399955
2013
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
9428765
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Clinical characteristics and STK11 gene mutations in Chinese children with Peutz-Jeghers syndrome.
26607058
2015
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.
9809980
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Functional analysis of LKB1/STK11 mutants and two aberrant isoforms found in Peutz-Jeghers Syndrome patients.
12552571
2003
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Insights into the phosphoryl transfer catalyzed by cAMP-dependent protein kinase: an X-ray crystallographic study of complexes with various metals and peptide substrate SP20.
23672593
2013
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma.
11389158
2001
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.
16582077
2006
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
CausalMutation
group
CLINVAR
High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients.
21118512
2010
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
0.120
GeneticVariation
group
CLINVAR
Genetic and Clinical Analyses of Southern Chinese Children with Peutz-Jeghers Syndrome.
26225618
2015