Detalhe da pesquisa
1.
uPAR enhances malignant potential of triple-negative breast cancer by directly interacting with uPA and IGF1R.
BMC Cancer
; 16: 615, 2016 08 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27502396
2.
Understanding the role of the Q338H MUTYH variant in oxidative damage repair.
Nucleic Acids Res
; 41(7): 4093-103, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23460202
3.
Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.
Proc Natl Acad Sci U S A
; 107(43): 18493-8, 2010 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-20937862
4.
A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization.
Hum Mutat
; 31(11): E1825-35, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20824794
5.
MUTYH mutations associated with familial adenomatous polyposis: functional characterization by a mammalian cell-based assay.
Hum Mutat
; 31(2): 159-66, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19953527
6.
Characterization of a naturally-occurring p27 mutation predisposing to multiple endocrine tumors.
Mol Cancer
; 9: 116, 2010 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-20492666
7.
Constitutional high expression of an APC mRNA isoform in a subset of attenuated familial adenomatous polyposis patients.
J Mol Med (Berl)
; 85(3): 305-12, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17143620
8.
Characterization of neuroendocrine tumors in heterozygous mutant MENX rats: a novel model of invasive medullary thyroid carcinoma.
Endocr Relat Cancer
; 25(2): 145-162, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29142006
9.
Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.
Genet Med
; 9(12): 836-41, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18091433
10.
Functional analysis and case-control study of -160C/A polymorphism in the E-cadherin gene promoter: association with cancer risk.
Anticancer Res
; 26(6B): 4627-32, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-17201188
11.
p27 variant and corticotropinoma susceptibility: a genetic and in vitro study.
Endocr Relat Cancer
; 21(3): 395-404, 2014 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24532476
12.
Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations.
Eur J Endocrinol
; 171(3): 335-42, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24920291
13.
Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas.
J Clin Endocrinol Metab
; 96(4): E701-6, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21289244
14.
Functional Imaging of Pheochromocytoma with Ga-DOTATOC and C-HED in a Genetically Defined Rat Model of Multiple Endocrine Neoplasia.
Int J Mol Imaging
; 2011: 175352, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21755051
15.
The MENX syndrome and p27: relationships with multiple endocrine neoplasia.
Prog Brain Res
; 182: 295-320, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541671
16.
Role of MUTYH and MSH2 in the control of oxidative DNA damage, genetic instability, and tumorigenesis.
Cancer Res
; 69(10): 4372-9, 2009 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19435918
17.
High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis.
Gastroenterology
; 126(7): 1681-5, 2004 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15188161