Detalhe da pesquisa
1.
Inflammatory profile in X-linked adrenoleukodystrophy patients: Understanding disease progression.
J Cell Biochem
; 119(1): 1223-1233, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28722826
2.
Metabolic dysfunction in a rat model of early-life scarcity-adversity: Modulatory role of cafeteria diet.
Exp Physiol
; 103(11): 1481-1493, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30211444
3.
Comparison of multiple genotyping methods for the identification of the cancer predisposing founder mutation p.R337H in TP53.
Genet Mol Biol
; 39(2): 203-9, 2016 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27275664
4.
Costs of genetic testing: Supporting Brazilian Public Policies for the incorporating of molecular diagnostic technologies.
Genet Mol Biol
; 38(3): 332-7, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26500437
5.
Frequency of the common germline MUTYH mutations p.G396D and p.Y179C in patients diagnosed with colorectal cancer in Southern Brazil.
Int J Colorectal Dis
; 26(7): 841-6, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21424714
6.
BDNF/TrkB content and interaction with gastrin-releasing peptide receptor blockade in colorectal cancer.
Oncology
; 79(5-6): 430-9, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21474968
7.
Cytopathological tests for early detection of oral carcinogenesis.
Eur J Cancer Prev
; 29(1): 73-79, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30913094
8.
Effect of Diacerein on Metabolic Control and Inflammatory Markers in Patients with Type 2 Diabetes Using Antidiabetic Agents: A Randomized Controlled Trial.
J Diabetes Res
; 2018: 4246521, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29805981
9.
Fc Gamma Receptor IIA (CD32A) R131 Polymorphism as a Marker of Genetic Susceptibility to Sepsis.
Inflammation
; 39(2): 518-25, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26490967
10.
Erratum: CHEK2 1100DELC germline mutation: a frequency study in hereditary breast and colon cancer Brazilian families.
Arq Gastroenterol
; 52(1): VIII, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26498296
11.
Prevalence of the TP53 p.R337H mutation in breast cancer patients in Brazil.
PLoS One
; 9(6): e99893, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24936644
12.
A TP53 founder mutation, p.R337H, is associated with phyllodes breast tumors in Brazil.
Virchows Arch
; 463(1): 17-22, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23794094
13.
CHEK2 1100DELC germline mutation: a frequency study in hereditary breast and colon cancer Brazilian families.
Arq Gastroenterol
; 49(4): 273-8, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23329222
14.
Identification of patients at-risk for Lynch syndrome in a hospital-based colorectal surgery clinic.
World J Gastroenterol
; 17(6): 766-73, 2011 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-21390147
15.
Prevalence of the BRCA1 founder mutation c.5266dupin Brazilian individuals at-risk for the hereditary breast and ovarian cancer syndrome.
Hered Cancer Clin Pract
; 9: 12, 2011 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22185575
16.
Clinical and histomolecular endometrial tumor characterization of patients at-risk for Lynch syndrome in South of Brazil.
Fam Cancer
; 9(2): 131-9, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19821155
17.
Pathogenesis-related proteins in Brazilian wheat genotypes: protein induction and partial gene sequencing
Ciênc. rural
; 33(3): 497-500, maio-jun. 2003. tab
Artigo
em Inglês
| LILACS | ID: lil-338909