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The renin-angiotensin system meets the hallmarks of cancer

Journal of the Renin-Angiotensin-Aldosterone System, 2015-06, Vol.16 (2), p.227-233

2015

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A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population

International journal of molecular sciences, 2022-09, Vol.23 (19), p.11549

2022

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Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Boletín médico del Hospital Infantil de México, 2021-07, Vol.78 (4), p.341-345

2021

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A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9–12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer

International journal of molecular sciences, 2024-06, Vol.25 (12), p.6773

2024

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Gastric cancer in Latin America

Scandinavian journal of gastroenterology, 2018-02, Vol.53 (2), p.124-129

2018

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Deep DNA sequencing of MGMT, TP53 and AGT in Mexican astrocytoma patients identifies an excess of genetic variants in women and a predictive biomarker

Journal of neuro-oncology, 2023, Vol.161 (1), p.165-174

2023

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Clinical prognostic factors in adults with astrocytoma: Historic cohort

Clinical neurology and neurosurgery, 2016-07, Vol.146, p.116-122

2016

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Association Between rs2981582 Polymorphism in the FGFR2 Gene and the Risk of Breast Cancer in Mexican Women

Archives of medical research, 2013-08, Vol.44 (6), p.459-466

2013

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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 (Basel), 2016, Vol.61 (6), p.313-318

2016

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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

Revista de investigacion clinica, 2016-05, Vol.68 (3), p.154-162

2016

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Identification of a novel germ-line mutation in the TP53 gene in a Mexican family with Li-Fraumeni syndrome

World journal of surgical oncology, 2009-12, Vol.7 (1), p.97-97, Article 97

2009

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Thiopurine S-methyltransferase Gene (TMPT) polymorphisms in a Mexican population of healthy individuals and leukemic patients

Medical oncology (Northwood, London, England), 2008-03, Vol.25 (1), p.56-62

2008

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Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Frontiers in oncology, 2024-01, Vol.13, p.1291286

2024

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Treatment experiences of testicular cancer in Hispanic patients with Down’s syndrome at the National Cancer Institute of Mexico

Clinical & translational oncology, 2008-11, Vol.10 (11), p.768-771

2008

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Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer

PloS one, 2012-05, Vol.7 (5), p.e37432-e37432

2012

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Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma

Cellular and molecular neurobiology, 2021-08, Vol.41 (6), p.1285-1297

2021

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Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Boletín médico del Hospital Infantil de México (Spanish edition), 2021-05, Vol.78 (4)

2021

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Polymorphisms of the thiopurine methyl transferase gene in healthy and acute lymphoblastic leukemia mestizos

BMC cancer, 2007-02, Vol.7 (S1), p.A39-A39, Article A39

2007

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Abstract 594: AGT mutations as a prognosis factor in patients with astrocytoma

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.594-594

2015

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Importancia del asesoramiento genético en familiascon alta susceptibilidad a cáncerque serán sometidas a pruebas moleculares

Cirugia y cirujanos, 2006, Vol.74 (2)

2006

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Expression levels of nucleoside transporter hENT1 and dCK enzyme, as prognostic factors in patients with AML treated with cytarabine

Journal of clinical oncology, 2012-05, Vol.30 (15_suppl), p.6599-6599

2012

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Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives

Anti-cancer drugs, 2005-10, Vol.16 (9), p.923-933

2005

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Importance of genetic counseling and molecular diagnosis testing in families at high risk for cancer

Cirugia y cirujanos, 2006-03, Vol.74 (2), p.137-142

2006

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The renin-angiotensin system meets the hallmarks of cancer

A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population

Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9–12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer

Gastric cancer in Latin America

Deep DNA sequencing of MGMT, TP53 and AGT in Mexican astrocytoma patients identifies an excess of genetic variants in women and a predictive biomarker

Angiotensinogen rs5050 germline genetic variant as potential biomarker of poor prognosis in astrocytoma

Clinical prognostic factors in adults with astrocytoma: Historic cohort

Association Between rs2981582 Polymorphism in the FGFR2 Gene and the Risk of Breast Cancer in Mexican Women

Expression Levels of Human Equilibrative Nucleoside Transporter 1 and Deoxycytidine Kinase Enzyme as Prognostic Factors in Patients with Acute Myeloid Leukemia Treated with Cytarabine

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

Identification of a novel germ-line mutation in the TP53 gene in a Mexican family with Li-Fraumeni syndrome

Thiopurine S-methyltransferase Gene (TMPT) polymorphisms in a Mexican population of healthy individuals and leukemic patients

Case report: Benign and malignant tumors in adult patients with neurofibromatosis type 1: a comprehensive case series from a large oncologic reference center

Treatment experiences of testicular cancer in Hispanic patients with Down’s syndrome at the National Cancer Institute of Mexico

Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer

Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients

Landscape of Germline Genetic Variants in AGT, MGMT, and TP53 in Mexican Adult Patients with Astrocytoma

Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

Polymorphisms of the thiopurine methyl transferase gene in healthy and acute lymphoblastic leukemia mestizos

Abstract 594: AGT mutations as a prognosis factor in patients with astrocytoma

Importancia del asesoramiento genético en familiascon alta susceptibilidad a cáncerque serán sometidas a pruebas moleculares

Expression levels of nucleoside transporter hENT1 and dCK enzyme, as prognostic factors in patients with AML treated with cytarabine

Genetic determinants of cancer drug efficacy and toxicity: practical considerations and perspectives

Importance of genetic counseling and molecular diagnosis testing in families at high risk for cancer

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