Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Carmen Alaez Verson"'
Autor:
Carolina Molina Garay, Karol Carrillo Sánchez, Luis Leonardo Flores Lagunes, Marco Jiménez Olivares, Anallely Muñoz Rivas, Beatríz Eugenia Villegas Torres, Hilario Flores Aguilar, Juan Carlos Núñez Enríquez, Elva Jiménez Hernández, Vilma Carolina Bekker Méndez, José Refugio Torres Nava, Janet Flores Lujano, Jorge Alfonso Martín Trejo, Minerva Mata Rocha, Aurora Medina Sansón, Laura Eugenia Espinoza Hernández, José Gabriel Peñaloza Gonzalez, Rosa Martha Espinosa Elizondo, Luz Victoria Flores Villegas, Raquel Amador Sanchez, María Luisa Pérez Saldívar, Omar Alejandro Sepúlveda Robles, Haydeé Rosas Vargas, Silvia Jiménez Morales, Patricia Galindo Delgado, Juan Manuel Mejía Aranguré, Carmen Alaez Verson
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundIn Mexico, the incidence of acute myeloid leukemia (AML) has increased in the last few years. Mortality is higher than in developed countries, even though the same chemotherapy protocols are used. CCAAT Enhancer Binding Protein Alpha (CEBPA
Externí odkaz:
https://doaj.org/article/7fa1cb598cc94178b175a54b2716be87
Autor:
Minerva Mata-Rocha, Angelica Rangel-López, Elva Jimenez-Hernandez, Juan Carlos Nuñez-Enríquez, Blanca Angélica Morales-Castillo, Norberto Sánchez-Escobar, Omar Alejandro Sepúlveda-Robles, Juan Carlos Bravata-Alcántara, Alan Steve Nájera-Cortés, María Luisa Pérez-Saldivar, Janet Flores-Lujano, David Aldebarán Duarte-Rodríguez, Norma Angélica Oviedo de Anda, Maria de los Angeles Romero Tlalolini, Carmen Alaez Verson, Jorge Alfonso Martín-Trejo, Jose Esteban Muñoz Medina, Cesar Raul Gonzalez-Bonilla, Maria de los Angeles Hernandez Cueto, VC. Bekker-Méndez, Silvia Jiménez-Morales, Aurora Medina-Sansón, Raquel Amador-Sánchez, José Gabriel Peñaloza-González, José Refugio Torres-Nava, Rosa Martha Espinosa-Elizondo, Beatriz Cortés-Herrera, Luz Victoria Flores-Villegas, Laura Elizabeth Merino-Pasaye, Maria de Lourdes Gutierrez-Rivera, Martha Margarita Velazquez-Aviña, Jessica Denisse Santillan-Juarez, Alma Gurrola-Silva, Gabriela Alicia Hernández Echáurregui, Alfredo Hidalgo-Miranda, José Arellano Galindo, Haydeé Rosas-Vargas, Juan Manuel Mejía-Aranguré
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ETV6::RUNX1 is a genetic rearrangement of good prognosis in children with acute lymphoblastic leukemia (ALL). In Mexico, its prevalence is low in comparison with Caucasian populations. We developed a novel TaqMan one-step RT-qPCR approach to assess t
Externí odkaz:
https://doaj.org/article/00a901f63259496a808f2388ff248bba
Autor:
Carolina Molina Garay, Karol Carrillo Sánchez, Luis Leonardo Flores Lagunes, Marco Jiménez Olivares, Anallely Muñoz Rivas, Beatríz Eugenia Villegas Torres, Hilario Flores Aguilar, Juan Carlos Núñez Enríquez, Elva Jiménez Hernández, Vilma Carolina Bekker Méndez, José Refugio Torres Nava, Janet Flores Lujano, Jorge Alfonso Martín Trejo, Minerva Mata Rocha, Aurora Medina Sansón, Laura Eugenia Espinoza Hernández, José Gabriel Peñaloza Gonzalez, Rosa Martha Espinosa Elizondo, Luz Victoria Flores Villegas, Raquel Amador Sanchez, Maria Luisa Pérez Saldívar, Omar Alejandro Sepúlveda Robles, Haydeé Rosas Vargas, Angélica Rangel López, María Lilia Domínguez López, Ethel Awilda García Latorre, Elba Reyes Maldonado, Patricia Galindo Delgado, Juan Manuel Mejía Aranguré, Carmen Alaez Verson
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Background: Acute myeloid leukemia (AML) is the second most frequent leukemia in childhood. The FLT3 gene participates in hematopoietic stem cell proliferation. FLT3 mutations are recurrent in AML and influence prognosis. In Mexican pediatric AML pat
Externí odkaz:
https://doaj.org/article/d9c177f0b3884e2899f30ef6b2757a03
Autor:
Angélica Martínez-Hernández, Elvia C. Mendoza-Caamal, Namibia G. Mendiola-Vidal, Francisco Barajas-Olmos, José Rafael Villafan-Bernal, Juan Luis Jiménez-Ruiz, Tulia Monge-Cazares, Humberto García-Ortiz, Cecilia Contreras- Cubas, Federico Centeno-Cruz, Carmen Alaez-Verson, Soraya Ortega-Torres, Adriana del C. Luna-Castañeda, Vicente Baca, José Luis Lezana, Lorena Orozco
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28984- (2024)
Background: Molecular diagnosis of cystic fibrosis (CF) is challenging in Mexico due to the population's high genetic heterogeneity. To date, 46 pathogenic variants (PVs) have been reported, yielding a detection rate of 77%. We updated the spectrum a
Externí odkaz:
https://doaj.org/article/ce4c8142ceb54ebeaeeec00442c786a9
Autor:
Joaquin Garcia-Solorio, Juan Carlos Núñez-Enriquez, Marco Jiménez-Olivares, Janet Flores-Lujano, Fernanda Flores-Espino, Carolina Molina-Garay, Alejandra Cervera, Diana Casique-Aguirre, José Gabriel Peñaloza-Gonzalez, Ma. Del Rocío Baños-Lara, Ángel García-Soto, César Alejandro Galván-Díaz, Alberto Olaya-Vargas, Hilario Flores Aguilar, Minerva Mata-Rocha, Miguel Ángel Garrido-Hernández, Juan Carlos Solís-Poblano, Nuria Citlalli Luna-Silva, Lena Sarahi Cano-Cuapio, Pierre Mitchel Aristil-Chery, Fernando Herrera-Quezada, Karol Carrillo-Sanchez, Anallely Muñoz-Rivas, Luis Leonardo Flores-Lagunes, Elvia Cristina Mendoza-Caamal, Beatriz Eugenia Villegas-Torres, Vincent González-Osnaya, Elva Jiménez-Hernández, José Refugio Torres-Nava, Jorge Alfonso Martín-Trejo, María de Lourdes Gutiérrez-Rivera, Rosa Martha Espinosa-Elizondo, Laura Elizabeth Merino-Pasaye, María Luisa Pérez-Saldívar, Silvia Jiménez-Morales, Everardo Curiel-Quesada, Haydeé Rosas-Vargas, Juan Manuel Mejía-Arangure, Carmen Alaez-Verson
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
BackgroundRecurrent genetic alterations contributing to leukemogenesis have been identified in pediatric B-cell Acute Lymphoblastic Leukemia (B-ALL), and some are useful for refining classification, prognosis, and treatment selection. IKZF1plus is a
Externí odkaz:
https://doaj.org/article/957fbd226ef74958b32478db98abf26c
Autor:
Joaquín García-Solorio, Octavio Martínez-Villegas, Ulises Rodríguez-Corona, Carolina Molina-Garay, Marco Jiménez-Olivares, Karol Carrillo-Sanchez, Elvia C. Mendoza-Caamal, Anallely Muñoz-Rivas, Beatriz E. Villegas-Torres, Alejandra Cervera, Luis L. Flores-Lagunes, Carmen Alaez-Verson
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
B-cell acute lymphoblastic leukemia (B-ALL) is one of the most common childhood cancers worldwide. Although most cases are sporadic, some familial forms, inherited as autosomal dominant traits with incomplete penetrance, have been described over the
Externí odkaz:
https://doaj.org/article/351cceac3fb747fcb8beed1a2d2d5fcf
Autor:
Ekaterina Kazakova, José Alberto Téllez-Martínez, Leonardo Flores-Lagunes, Ana Luisa Sosa-Ortiz, Karol Carillo-Sánchez, Carolina Molina-Garay, Carlos Alberto González-Domínguez, Marco Jimenez-Olivares, Francisca Fernandez-Valverde, Edwin Steven Vargas-Cañas, Martha Elisa Vázquez-Memije, Ethel Awilda Garcia-Latorre, Iván Martínez-Duncker, Carmen Alaez-Verson
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectivesTo report the first Mexican case with two novel AARS2 mutations causing primary ovarian failure, uterus infantilis, and early-onset dementia secondary to leukoencephalopathy.MethodsDetailed clinical, clinimetric, neuroimaging features, musc
Externí odkaz:
https://doaj.org/article/b02bf00be7fb4cff8b05a4456c936262
Autor:
Martín Barbosa-Amezcua, Betzaida Cuevas-Córdoba, Cristóbal Fresno, Joshua I. Haase-Hernández, Karol Carrillo-Sánchez, Minerva Mata-Rocha, Marcela Muñoz-Torrico, Claudia Bäcker, Vanessa González-Covarrubias, Carmen Alaez-Verson, Xavier Soberón
Publikováno v:
Microbiology Spectrum, Vol 10, Iss 5 (2022)
ABSTRACT Tuberculosis (TB) remains one of the most important infectious diseases globally. Establishing a resistance profile from the initial TB diagnosis is a priority. Rapid molecular tests evaluate only the most common genetic variants responsible
Externí odkaz:
https://doaj.org/article/cd1b29f3e7e7445997c43f3be9ac01c3
Autor:
Carlos Alberto González-Domínguez, Moisés O. Fiesco-Roa, Samuel Gómez-Carmona, Anke Paula Ingrid Kleinert-Altamirano, Miao He, Earnest James Paul Daniel, Kimiyo M. Raymond, Melania Abreu-González, Sandra Manrique-Hernández, Ana González-Jaimes, Roberta Salinas-Marín, Carolina Molina-Garay, Karol Carrillo-Sánchez, Luis Leonardo Flores-Lagunes, Marco Jiménez-Olivares, Anallely Muñoz-Rivas, Mario E. Cruz-Muñoz, Matilde Ruíz-García, Hudson H. Freeze, Héctor M. Mora-Montes, Carmen Alaez-Verson, Iván Martínez-Duncker
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/16f9a7c36b8c4e668090bb6fa6040a84
Autor:
Carlos Alberto González-Domínguez, Moisés O. Fiesco-Roa, Samuel Gómez-Carmona, Anke Paula Ingrid Kleinert-Altamirano, Miao He, Earnest James Paul Daniel, Kimiyo M. Raymond, Melania Abreu-González, Sandra Manrique-Hernández, Ana González-Jaimes, Roberta Salinas-Marín, Carolina Molina-Garay, Karol Carrillo-Sánchez, Luis Leonardo Flores-Lagunes, Marco Jiménez-Olivares, Anallely Muñoz-Rivas, Mario E. Cruz-Muñoz, Matilde Ruíz-García, Hudson H. Freeze, Héctor M. Mora-Montes, Carmen Alaez-Verson, Iván Martínez-Duncker
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
This study reports on a Mexican mestizo patient with a multi-systemic syndrome including neurological involvement and a type I serum transferrin profile. Clinical exome sequencing revealed complex alleles in ALG1, the encoding gene for the chitobiosy
Externí odkaz:
https://doaj.org/article/31a570422e514fc1967b53252d47ed25