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 |
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 |
Entrez Id: |
6794 |
Gene Symbol: |
STK11 |
STK11
|
Neoplastic Syndromes, Hereditary
|
0.120 |
CausalMutation |
CLINVAR |
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome.
|
16287113 |
2005 |