×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
9428765
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
9428765
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome.
9760200
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.
9809980
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.
9850045
1998
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
9887330
1999
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.
9887330
1999
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
Morphology-dependent resonances in a large dielectric sphere: An asymptotic calculation using local coordinates.
9908348
1992
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families.
10408777
1999
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
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
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Two novel mutations and a new STK11/LKB1 gene isoform in Peutz-Jeghers patients.
12112668
2002
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
BEFREE
LKB1 is a serine-threonine protein kinase mutated in patients with an autosomal dominantly inherited cancer syndrome predisposing to multiple benign and malignant tumours, termed Peutz-Jeghers syndrome.
12829253
2003
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
12865922
2003
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.
12865922
2003
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Genotype-phenotype correlations in Peutz-Jeghers syndrome.
15121768
2004
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
Relative frequency and morphology of cancers in STK11 mutation carriers.
15188174
2004
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Relative frequency and morphology of cancers in STK11 mutation carriers.
15188174
2004
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
An LKB1 AT-AC intron mutation causes Peutz-Jeghers syndrome via splicing at noncanonical cryptic splice sites.
15608654
2005
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
GeneticVariation
CLINVAR
STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.
15863673
2005
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.
15863673
2005
×
Entrez Id:
6794
Gene Symbol:
STK11
STK11
Neoplastic Syndromes, Hereditary
0.120
CausalMutation
CLINVAR
Mutations in the human LKB1/STK11 gene.
16110486
2005