|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Distinct residues of human p53 implicated in binding to DNA, simian virus 40 large T antigen, 53BP1, and 53BP2.
|
7969167 |
1994 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
EGFR-mutant lung adenocarcinoma in a patient with Li-Fraumeni syndrome.
|
17540308 |
2007 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.
|
1737852 |
1992 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms.
|
1565144 |
1992 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Mutants TP53 p.R273H and p.R273C but not p.R273G enhance cancer cell malignancy.
|
24677579 |
2014 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Gastric cancer in individuals with Li-Fraumeni syndrome.
|
21552135 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
High frequency of de novo mutations in Li-Fraumeni syndrome.
|
19556618 |
2009 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography.
|
17392385 |
2007 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms.
|
1978757 |
1990 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A germ line mutation in exon 5 of the p53 gene in an extended cancer family.
|
1933902 |
1991 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings.
|
8479749 |
1993 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
|
8825920 |
1995 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers.
|
24493721 |
2014 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Gastric cancer in individuals with Li-Fraumeni syndrome.
|
21552135 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
"Apparently ""BRCA-related"" breast and ovarian cancer patient with germline TP53 mutation."
|
21535297 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
"Apparently ""BRCA-related"" breast and ovarian cancer patient with germline TP53 mutation."
|
21535297 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis.
|
12826609 |
2003 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Sebaceous gland carcinoma of the eyelid masquerading as a cutaneous horn in Li--Fraumeni syndrome.
|
20693561 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Transcriptional functionality of germ line p53 mutants influences cancer phenotype.
|
17606709 |
2007 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
CausalMutation
|
CLINVAR |
Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation.
|
20128691 |
2010 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Gastric cancer in individuals with Li-Fraumeni syndrome.
|
21552135 |
2011 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.
|
10484981 |
1999 |
|
Li-Fraumeni Syndrome
|
|
0.800 |
GeneticVariation
|
CLINVAR |
Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings.
|
8479749 |
1993 |