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Brain-Derived Neurotrophic Factor, Food Intake Regulation, and Obesity

Archives of medical research, 2011-08, Vol.42 (6), p.482-494

2011

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Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women

Hypertension research, 2008-05, Vol.31 (5), p.1015-1019

2008

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Principal component analysis on LC‑MS/MS and 2DE‑MALDI‑TOF in glioblastoma cell lines reveals that mitochondria act as organelle sensors of the metabolic state in glioblastoma

Oncology reports, 2020-08, Vol.44 (2), p.661-673

2020

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Functional characterization of NK cells in Mexican pediatric patients with acute lymphoblastic leukemia: Report from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia

PloS one, 2020-01, Vol.15 (1), p.e0227314-e0227314

2020

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Sociodemographic and Lifestyle Characteristics Associated with Maternal Dietary Patterns in Mexico

Nutrients, 2024-05, Vol.16 (10), p.1451

2024

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Telomere shortening and frailty in Mexican older adults

Geriatrics & gerontology international, 2018-08, Vol.18 (8), p.1286-1292

2018

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Cytogenomic description of a Mexican cohort with differences in sex development

Molecular cytogenetics, 2024-07, Vol.17 (1), p.16-9, Article 16

2024

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Association between genetic variants of membrane transporters and the risk of high-grade hematologic adverse events in a cohort of Mexican children with B-cell acute lymphoblastic leukemia

Frontiers in oncology, 2024-01, Vol.13, p.1276352

2024

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Evidence of spatial clustering of childhood acute lymphoblastic leukemia cases in Greater Mexico City: report from the Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia

Frontiers in oncology, 2024-02, Vol.14, p.1304633

2024

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Underexpression of LINC00173 in TCF3/PBX1-Positive Cases Is Associated With Poor Prognosis in Children With B-Cell Precursor Acute Lymphoblastic Leukemia

Frontiers in oncology, 2022-06, Vol.12, p.887766-887766

2022

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Hutchinson-Gilford Progeria Syndrome: Cellular Mechanisms and Therapeutic Perspectives

Archives of medical research, 2023-07, Vol.54 (5), p.102837-102837, Article 102837

2023

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Telomere Length is Associated with the Prevalence, Persistence, and Incidence of Sarcopenia

Archives of medical research, 2024-06, Vol.55 (4), p.103007, Article 103007

2024

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Genetics of Transposition of Great Arteries: Between Laterality Abnormality and Outflow Tract Defect

Journal of cardiovascular translational research, 2021-06, Vol.14 (3), p.390-399

2021

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Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis

The clinical respiratory journal, 2019-02, Vol.13 (2), p.105-113

2019

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A greater birthweight increases the risk of acute leukemias in Mexican children—experience from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia (MIGICCL)

Cancer medicine (Malden, MA), 2018-04, Vol.7 (4), p.1528-1536

2018

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Key clinical features to identify girls with CDKL5 mutations

Brain (London, England : 1878), 2008-10, Vol.131 (10), p.2647-2661

2008

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Immunodetection analysis of muscular dystrophies in Mexico

Muscle & nerve, 2012-03, Vol.45 (3), p.338-345

2012

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Glu298Asp Endothelial Nitric Oxide Synthase Polymorphism Is a Risk Factor for Erectile Dysfunction in the Mexican Mestizo Population

Journal of andrology, 2004-09, Vol.25 (5), p.728-732

2004

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Prognostic Impact of Somatic Copy Number Alterations in Childhood B-Lineage Acute Lymphoblastic Leukemia

Current oncology reports, 2021, Vol.23 (1), p.2-2, Article 2

2021

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Revisiting the Genomic and Transcriptomic Landscapes from Female Malignancies Could Provide Molecular Markers and Targets for Precision Medicine

Archives of medical research, 2019-10, Vol.50 (7), p.428-436

2019

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Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries

Genes, 2022-09, Vol.13 (9), p.1662

2022

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Endothelial Nitric Oxide Synthase Gene Polymorphism in the Indian and Mestizo Populations of Mexico

Human biology, 2003-02, Vol.75 (1), p.91-96

2003

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Copy Number Alterations are Associated with the Risk of Very Early Relapse in Pediatric B-lineage Acute Lymphoblastic Leukemia: A Nested Case-control MIGICCL Study

Archives of medical research, 2021-05, Vol.52 (4), p.414-422

2021

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Description of a utrophin associated protein complex in lipid raft domains of human artery smooth muscle cells

Biochimica et biophysica acta, 2014-03, Vol.1838 (3), p.1047-1054

2014

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Netrin G1 Mutations Are an Uncommon Cause of Atypical Rett Syndrome With or Without Epilepsy

Pediatric neurology, 2007-10, Vol.37 (4), p.270-274

2007

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Brain-Derived Neurotrophic Factor, Food Intake Regulation, and Obesity

Methylenetetrahydrofolate reductase C677T and glutathione S-transferase P1 A313G are associated with a reduced risk of preeclampsia in Maya-Mestizo women

Principal component analysis on LC‑MS/MS and 2DE‑MALDI‑TOF in glioblastoma cell lines reveals that mitochondria act as organelle sensors of the metabolic state in glioblastoma

Functional characterization of NK cells in Mexican pediatric patients with acute lymphoblastic leukemia: Report from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia

Sociodemographic and Lifestyle Characteristics Associated with Maternal Dietary Patterns in Mexico

Telomere shortening and frailty in Mexican older adults

Cytogenomic description of a Mexican cohort with differences in sex development

Association between genetic variants of membrane transporters and the risk of high-grade hematologic adverse events in a cohort of Mexican children with B-cell acute lymphoblastic leukemia

Evidence of spatial clustering of childhood acute lymphoblastic leukemia cases in Greater Mexico City: report from the Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia

Underexpression of LINC00173 in TCF3/PBX1-Positive Cases Is Associated With Poor Prognosis in Children With B-Cell Precursor Acute Lymphoblastic Leukemia

Hutchinson-Gilford Progeria Syndrome: Cellular Mechanisms and Therapeutic Perspectives

Telomere Length is Associated with the Prevalence, Persistence, and Incidence of Sarcopenia

Genetics of Transposition of Great Arteries: Between Laterality Abnormality and Outflow Tract Defect

Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis

A greater birthweight increases the risk of acute leukemias in Mexican children—experience from the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia (MIGICCL)

Key clinical features to identify girls with CDKL5 mutations

Immunodetection analysis of muscular dystrophies in Mexico

Glu298Asp Endothelial Nitric Oxide Synthase Polymorphism Is a Risk Factor for Erectile Dysfunction in the Mexican Mestizo Population

Prognostic Impact of Somatic Copy Number Alterations in Childhood B-Lineage Acute Lymphoblastic Leukemia

Revisiting the Genomic and Transcriptomic Landscapes from Female Malignancies Could Provide Molecular Markers and Targets for Precision Medicine

Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries

Endothelial Nitric Oxide Synthase Gene Polymorphism in the Indian and Mestizo Populations of Mexico

Copy Number Alterations are Associated with the Risk of Very Early Relapse in Pediatric B-lineage Acute Lymphoblastic Leukemia: A Nested Case-control MIGICCL Study

Description of a utrophin associated protein complex in lipid raft domains of human artery smooth muscle cells

Netrin G1 Mutations Are an Uncommon Cause of Atypical Rett Syndrome With or Without Epilepsy

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