H. Rosas-Vargas

发表

Genotype-Environment Interaction Analysis of NQO1, CYP2E1, and NAT2 Polymorphisms and the Risk of Childhood Acute Lymphoblastic Leukemia: A Report From the Mexican Interinstitutional Group for the Identification of the Causes of Childhood Leukemia

A. Hidalgo-Miranda, J. Fernández-López, J. Mejía-Aranguré, 2020, Frontiers in Oncology.

Children’s perception on obesity and quality of life: a Mexican survey

M. Villasís-Keever, H. Rosas-Vargas, M. Rendón-Macías, 2014, BMC Pediatrics.

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

J. Mejía-Aranguré, J. C. Núñez-Enríquez, H. Rosas-Vargas, 2020, Current Oncology Reports.

Overweight and obesity as predictors of early mortality in Mexican children with acute lymphoblastic leukemia: a multicenter cohort study

J. Mejía-Aranguré, J. C. Núñez-Enríquez, D. A. Duarte-Rodríguez, 2019, BMC Cancer.

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

S. Encarnación-Guevara, H. Rosas-Vargas, L. Gómez-caudillo, 2020, Oncology reports.

Development of a novel protein identification approach to define mitochondrial proteomic signatures in glioblastoma oncogenesis: T98G vs U87MG cell lines model

S. Encarnación-Guevara, H. Rosas-Vargas, L. Gómez-caudillo, 2018, bioRxiv.

Glu298Asp endothelial nitric oxide synthase polymorphism is a risk factor for erectile dysfunction in the Mexican Mestizo population.

R. Coral-Vázquez, H. Rosas-Vargas, R. Tapia, 2004, Journal of andrology.

In vitro and molecular modeling analysis of two mutant desert hedgehog proteins associated with 46,XY gonadal dysgenesis.

M. Soriano-Ursúa, R. Coral-Vázquez, P. Canto, 2013, DNA and cell biology.

Human DNA AI Model to Predict COVID-19 Symptomatic or Asymptomatic Percentages

L. Gaggero-Sager, H. Rosas-Vargas, Peter Oropeza Martinez, 2021 .

Low Prevalence of ETV6::RUNX1 Fusion Gene in a Hispanic Population

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2022, Frontiers in Pediatrics.

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

J. Mejía-Aranguré, D. A. Duarte-Rodríguez, S. Jiménez-Morales, 2021, Archives of medical research.

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

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2022, Frontiers in Oncology.

Telomere shortening and frailty in Mexican older adults

H. Rosas-Vargas, E. Reyes-Maldonado, S. Sánchez-García, 2018, Geriatrics & gerontology international.

Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy.

A. Afenjar, J. Chelly, B. Girard, 2007, Pediatric neurology.

Key clinical features to identify girls with CDKL5 mutations.

N. Boddaert, A. Afenjar, C. Philippe, 2008, Brain : a journal of neurology.

Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy

C. Philippe, P. Jonveaux, J. Chelly, 2007, Journal of Medical Genetics.

Identification and Characterization of Novel Fusion Genes with Potential Clinical Applications in Mexican Children with Acute Lymphoblastic Leukemia

J. Mejía-Aranguré, D. A. Duarte-Rodríguez, A. Fajardo-Gutiérrez, 2019, International journal of molecular sciences.

Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia.

J. Mejía-Aranguré, V. Bekker-Méndez, E. Jiménez‐Hernández, 2016, Archives of medical research.

Expression Analysis of the SG-SSPN Complex in Smooth Muscle and Endothelial Cells of Human Umbilical Cord Vessels

R. Coral-Vázquez, G. Ceballos-Reyes, I. Ramírez-Sánchez, 2005, Journal of Vascular Research.

NK cells with decreased expression of multiple activating receptors is a dominant phenotype in pediatric patients with acute lymphoblastic leukemia

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2022, Frontiers in Oncology.

Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

J. Chelly, J. Nectoux, Y. Fichou, 2010, Journal of cellular and molecular medicine.

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

R. Coral-Vázquez, J. Granados, G. Vargas-Alarcón, 2003, Human biology.

Galectin-1 reduced the effect of LPS on the IL-6 production in decidual cells by inhibiting LPS on the stimulation of IκBζ.

M. Cancino-Diaz, S. Rodríguez-Martínez, G. Estrada-Gutiérrez, 2015, Journal of reproductive immunology.

Expression and function of utrophin associated protein complex in stretched endothelial cells: dissociation and activation of eNOS.

R. Coral-Vázquez, A. Zentella-Dehesa, I. Ramírez-Sánchez, 2007, Frontiers in bioscience : a journal and virtual library.

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

B. Cisneros, Lucelli Yáñez-Gutiérrez, C. Ramírez-Portillo, 2022, Genes.

Dystrophins in developing retina: Dp260 expression correlates with synaptic maturation

F. Rodius, T. Claudepierre, B. Cisneros, 1997, Neuroreport.

Analytical study of RUNX1-RUNXT1, PML-RARA, CBFB-MYH11, BCR-ABL1p210, and KMT2-MLLT3 in Mexican children with acute myeloid leukemia: A multicenter study of the Mexican interinstitutional group for the identification of the causes of childhood leukemia (MIGICCL)

J. Mejía-Aranguré, S. Jiménez-Morales, V. Bekker-Méndez, 2022, Frontiers in Pediatrics.

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

J. Mejía-Aranguré, D. A. Duarte-Rodríguez, I. Mancilla-Herrera, 2020, PloS one.

Immunodetection analysis of muscular dystrophies in Mexico

R. Coral-Vázquez, P. Canto, H. Rosas-Vargas, 2012, Muscle & nerve.

Dysferlin homozygous mutation G1418D causes limb-girdle type 2B in a Mexican family.

R. Coral-Vázquez, H. Rosas-Vargas, B. Gómez-Díaz, 2007, Genetic testing.

Persistently high incidence rates of childhood acute leukemias from 2010 to 2017 in Mexico City: A population study from the MIGICCL

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2022, Frontiers in Public Health.

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)

J. Mejía-Aranguré, A. Fajardo-Gutiérrez, C. González-Bonilla, 2018, Cancer medicine.

Development and Validation of a One-Step RT-qPCR Assay for Identifying Common Fusion Gene Transcripts Associated with the Prognosis of Mexican Children with B-Lineage Acute Lymphoblastic Leukemia

J. E. Muñoz-Medina, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2021 .

Association of PPARG2 Pro12Ala Variant with Larger Body Mass Index in Mestizo and Amerindian Populations of Mexico

C. Aguilar-Salinas, M. Tusié-Luna, A. Medeiros-Domingo, 2007, Human biology.

Brain-derived neurotrophic factor, food intake regulation, and obesity.

T. Bienvenu, H. Rosas-Vargas, J. Martínez-Ezquerro, 2011, Archives of medical research.

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

M. Salcedo, H. Rosas-Vargas, A. Valdivia, 2019, Archives of medical research.

Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis

Carmina Jiménez-Ramírez, H. Rosas-Vargas, Fernando Fernández-Ramírez, 2019, The clinical respiratory journal.

OXIDATIVE STRESS, TELOMERE LENGTH, AND FRAILTY IN AN OLD AGE POPULATION.

H. Rosas-Vargas, S. Sánchez-García, J. Martínez-Ezquerro, 2019, Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion.

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

B. Cisneros, H. Rosas-Vargas, M. De Ita, 2020, Journal of Cardiovascular Translational Research.

The first missense mutation causing Rett syndrome specifically affecting the MeCP2_e1 isoform

J. Chelly, B. Girard, J. Nectoux, 2009, neurogenetics.

Differential expression and subcellular distribution of dystrophin Dp71 isoforms during differentiation process

B. Cisneros, D. Mornet, C. Montañez, 2003, Neuroscience.

Transcriptome Analysis Identifies LINC00152 as a Biomarker of Early Relapse and Mortality in Acute Lymphoblastic Leukemia

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2020, Genes.

Dysregulation of mitochondrial function and biogenesis modulators in adipose tissue of obese children

E. Lara-Padilla, M. Ramos-Cervantes, F. Villarreal, 2018, International Journal of Obesity.

Methylenetetrahydrofolate Reductase C677T and Glutathione S−Transferase P1 A313G Are Associated with a Reduced Risk of Preeclampsia in Maya-Mestizo Women

H. Rangel-Villalobos, S. Canizales-Quinteros, R. Coral-Vázquez, 2008, Hypertension Research.

Association between the brain-derived neurotrophic factor Val66Met polymorphism and overweight/obesity in Mexican pediatric population

M. Rodríguez-Cruz, M. López-Alarcón, H. Rosas-Vargas, 2017, bioRxiv.

Association Between the Brain-derived Neurotrophic Factor Val66Met Polymorphism and Overweight/Obesity in Pediatric Population.

M. Rodríguez-Cruz, M. López-Alarcón, H. Rosas-Vargas, 2017, Archives of medical research.

Breast cancer cell line MDA-MB-231 miRNA profile expression after BIK interference: BIK involvement in autophagy

M. Velázquez-Flores, F. Salamanca-Gómez, H. Rosas-Vargas, 2016, Tumor Biology.

A novel isoform of delta-sarcoglycan is localized at the sarcoplasmic reticulum of mouse skeletal muscle.

R. Coral-Vázquez, D. Mornet, H. Rosas-Vargas, 2006, Biochemical and biophysical research communications.

Partial characterization of the mouse α-sarcoglycan promoter and its responsiveness to MyoD

R. Coral-Vázquez, F. Recillas-Targa, P. Delgado-Olguín, 2006 .

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

R. Coral-Vázquez, P. Canto, I. Ramírez-Sánchez, 2014, Biochimica et biophysica acta.

NFI-C2 negatively regulates α-sarcoglycan promoter activity in C2C12 myoblasts

R. Coral-Vázquez, B. Cisneros, F. Recillas-Targa, 2004 .

Genomic insights of Leclercia adecarboxylata strains linked to an outbreak in public hospitals in Mexico

C. González-Bonilla, Margot González-León, M. Camorlinga-Ponce, 2023, Genes & Genomics.

Association Analysis Between the Functional Single Nucleotide Variants in miR-146a, miR-196a-2, miR-499a, and miR-612 With Acute Lymphoblastic Leukemia

A. Hidalgo-Miranda, J. Mejía-Aranguré, D. A. Duarte-Rodríguez, 2021, Frontiers in Oncology.

Analysis of Polymorphisms in Genes (AGT, MTHFR, GPIIIa, and GSTP1) Associated with Hypertension, Thrombophilia and Oxidative Stress in Mestizo and Amerindian Populations of México

H. Rangel-Villalobos, S. Canizales-Quinteros, R. Coral-Vázquez, 2010, Disease markers.

Maternal and paternal ages at conception of index child and risk of childhood acute leukaemia: A multicentre case-control study in Greater Mexico City.

J. Mejía-Aranguré, D. A. Duarte-Rodríguez, S. Jiménez-Morales, 2020, Cancer epidemiology.

Bibliometric analysis of the BDNF Val66Met polymorphism based on Web of Science, Pubmed, and Scopus databases

L. Michán, H. Rosas-Vargas, J. Martínez-Ezquerro, 2016 .

Hutchinson-Gilford Progeria Syndrome: Cellular Mechanisms and Therapeutic Perspectives.

B. Cisneros, H. Rosas-Vargas, I. Arrieta-Cruz, 2023, Archives of medical research.

Expression and localization of utrophin in differentiating PC12 cells

B. Cisneros, D. Mornet, C. Montañez, 2000, Neuroreport.

IKZF1plus is a frequent biomarker of adverse prognosis in Mexican pediatric patients with B-acute lymphoblastic leukemia

J. Mejía-Aranguré, E. Mendoza-Caamal, S. Jiménez-Morales, 2024, Frontiers in oncology.

Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin α-2 gene

R. Coral-Vázquez, H. Rosas-Vargas, F. Salamanca, 2003, Journal of Human Genetics.

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

J. Mejía-Aranguré, S. Jiménez-Morales, E. Jiménez‐Hernández, 2024, Frontiers in oncology.