rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
|
28349240 |
2017 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Germline TP53 Mutation and Clinical Characteristics of Korean Patients With Li-Fraumeni Syndrome.
|
27374712 |
2016 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Heterogeneity of Li-Fraumeni syndrome links to unequal gain-of-function effects of p53 mutations.
|
24573247 |
2014 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
p53 mutations in cancer.
|
23263379 |
2013 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
A common p53 mutation (R175H) activates c-Met receptor tyrosine kinase to enhance tumor cell invasion.
|
23792586 |
2013 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Early onset HER2-positive breast cancer is associated with germline TP53 mutations.
|
21761402 |
2012 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
|
22006311 |
2011 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Mutant p53(R175H) upregulates Twist1 expression and promotes epithelial-mesenchymal transition in immortalized prostate cells.
|
20689556 |
2011 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
The tumor suppressor p53: from structures to drug discovery.
|
20516128 |
2010 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
A common gain of function of p53 cancer mutants in inducing genetic instability.
|
19881536 |
2010 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Molecular basis of the Li-Fraumeni syndrome: an update from the French LFS families.
|
18511570 |
2008 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Prevalence of early onset colorectal cancer in 397 patients with classic Li-Fraumeni syndrome.
|
16401470 |
2006 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Mutant p53 gain of function in two mouse models of Li-Fraumeni syndrome.
|
15607980 |
2004 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Gain of function of a p53 hot spot mutation in a mouse model of Li-Fraumeni syndrome.
|
15607981 |
2004 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
The IARC TP53 database: new online mutation analysis and recommendations to users.
|
12007217 |
2002 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene.
|
9047394 |
1997 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
|
8825920 |
1995 |
rs28934578
|
|
T |
0.820 |
CausalMutation |
CLINVAR |
Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma.
|
8164043 |
1994 |