Detalhe da pesquisa
1.
Deep DNA sequencing of MGMT, TP53 and AGT in Mexican astrocytoma patients identifies an excess of genetic variants in women and a predictive biomarker.
J Neurooncol
; 161(1): 165-174, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36525166
2.
A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population.
Int J Mol Sci
; 23(19)2022 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36232851
3.
Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma.
Cell Mol Neurobiol
; 41(6): 1285-1297, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32535722
4.
Gastric cancer in Latin America.
Scand J Gastroenterol
; 53(2): 124-129, 2018 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-29275643
5.
Expression Levels of Human Equilibrative Nucleoside Transporter 1 and Deoxycytidine Kinase Enzyme as Prognostic Factors in Patients with Acute Myeloid Leukemia Treated with Cytarabine.
Chemotherapy
; 61(6): 313-8, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27119162
6.
G80A Single Nucleotide Polymorphism in Reduced Folate Carrier-1 Gene in a Mexican Population and its Impact on Survival in Patients with Acute Lymphoblastic Leukemia.
Rev Invest Clin
; 68(3): 154-62, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27409003
7.
Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center.
Front Oncol
; 13: 1291286, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38260834
8.
Acetylator status and N-acetyltransferase 2 gene polymorphisms; phenotype-genotype correlation with the sulfamethazine test.
Pharmacogenet Genomics
; 21(12): 894-901, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21946899
9.
Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient.
Bol Med Hosp Infant Mex
; 78(4): 341-345, 2021 05 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33938902
10.
Identification of a novel germ-line mutation in the TP53 gene in a Mexican family with Li-Fraumeni syndrome.
World J Surg Oncol
; 7: 97, 2009 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20017945
11.
Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients.
PLoS One
; 14(9): e0222709, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31545835
12.
Thiopurine S-methyltransferase gene (TMPT) polymorphisms in a Mexican population of healthy individuals and leukemic patients.
Med Oncol
; 25(1): 56-62, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18188716
13.
Treatment experiences of testicular cancer in Hispanic patients with Down's syndrome at the National Cancer Institute of Mexico.
Clin Transl Oncol
; 10(11): 768-71, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19015076
14.
Angiotensinogen rs5050 germline genetic variant as potential biomarker of poor prognosis in astrocytoma.
PLoS One
; 13(11): e0206590, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30383794
15.
Search of the p.M918T Mutation in the RET Oncogene in Mexican Adult Patients with Medullary Thyroid Carcinoma.
Exp Clin Endocrinol Diabetes
; 125(4): 218-222, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28166591
16.
Clinical prognostic factors in adults with astrocytoma: Historic cohort.
Clin Neurol Neurosurg
; 146: 116-22, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27208871
17.
Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient / Eritrocitosis familiar 2 y enfermedad de von Hippel-Lindau en el mismo paciente
Bol. méd. Hosp. Infant. Méx
; 78(4): 341-345, Jul.-Aug. 2021. graf
Artigo
em Inglês
|
LILACS-Express
| ID: biblio-1345422
18.
The renin-angiotensin system meets the hallmarks of cancer.
J Renin Angiotensin Aldosterone Syst
; 16(2): 227-33, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23934336
19.
Association between rs2981582 polymorphism in the FGFR2 gene and the risk of breast cancer in Mexican women.
Arch Med Res
; 44(6): 459-66, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24054997
20.
Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer.
PLoS One
; 7(5): e37432, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22655046