Hasil Pencarian - Benilde García-De Teresa

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  1. 1
    Estudio multidisciplinario del paciente con anemia de Fanconi

    Estudio multidisciplinario del paciente con anemia de Fanconi oleh Benilde García de Teresa, Alfredo Rodríguez, Sara Frías

    Diterbitkan 2016-02-01
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  2. 2
    General aspects and current view of the molecular study of Phenylketonuria (PKU) in Mexico

    General aspects and current view of the molecular study of Phenylketonuria (PKU) in Mexico oleh Miguel Ángel Alcántara-Ortigoza, Benilde García-de Teresa, Rehotbevely Barrientos- Ríos

    Diterbitkan 2014-07-01
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  3. 3
    Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells.

    Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells. oleh Benilde García-de Teresa, Cecilia Ayala-Zambrano, Mirna González-Suárez, Bertha Molina, Leda Torres, Alfredo Rodríguez, Sara Frías

    Diterbitkan 2024-01-01
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  4. 4
    FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México

    FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México oleh Benilde García‐de Teresa, Sara Frias, Bertha Molina, María Teresa Villarreal, Alfredo Rodriguez, Alessandra Carnevale, Gerardo López‐Hernández, Lilia Vollbrechtshausen, Alberto Olaya‐Vargas, Leda Torres

    Diterbitkan 2019-06-01
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  5. 5
    WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways

    WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways oleh Alfredo Rodríguez, J. Jesús Naveja, Leda Torres, Benilde García de Teresa, Ulises Juárez-Figueroa, Ulises Juárez-Figueroa, Cecilia Ayala-Zambrano, Eugenio Azpeitia, Luis Mendoza, Sara Frías, Sara Frías

    Diterbitkan 2019-05-01
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  6. 6
    Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability

    Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability oleh Moisés Ó. Fiesco-Roa, Moisés Ó. Fiesco-Roa, Benilde García-de Teresa, Paula Leal-Anaya, Renée van ‘t Hek, Talia Wegman-Ostrosky, Sara Frías, Sara Frías, Alfredo Rodríguez, Alfredo Rodríguez

    Diterbitkan 2022-08-01
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  7. 7
    Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics

    Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics oleh Emiy Yokoyama, Victoria Del Castillo, Silvia Sánchez, Sandra Ramos, Bertha Molina, Leda Torres, María José Navarro, Silvia Avila, José Luis Castrillo, Benilde García-De Teresa, Bárbara Asch, Sara Frías

    Diterbitkan 2018-05-01
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  8. 8
    P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants

    P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants oleh Leda Torres, Pedro Reyes, Benilde García-de Teresa, María Teresa Villarreal Molina, Ulises Juárez, Angélica Solis, Moises Fiesco-Roa, Fernando Pérez Villatoro, Bertha Molina, Alfredo Rodríguez, Alessandra Carnevale, Sara Frías

    Diterbitkan 2024-01-01
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  9. 9
    Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in <i>FANCG</i>

    Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in <i>FANCG</i> oleh Pedro Reyes, Benilde García-de Teresa, Ulises Juárez, Fernando Pérez-Villatoro, Moisés O. Fiesco-Roa, Alfredo Rodríguez, Bertha Molina, María Teresa Villarreal-Molina, Jorge Meléndez-Zajgla, Alessandra Carnevale, Leda Torres, Sara Frias

    Diterbitkan 2022-02-01
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  10. 10
    Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico

    Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico oleh Paula Leal-Anaya, Paula Leal-Anaya, Paula Leal-Anaya, Tamara N. Kimball, Ana Lucia Yanez-Felix, Moisés Ó. Fiesco-Roa, Moisés Ó. Fiesco-Roa, Benilde García-de Teresa, Benilde García-de Teresa, Angélica Monsiváis, Rocío Juárez-Velázquez, Esther Lieberman, Camilo Villarroel, Emiy Yokoyama, Liliana Fernández-Hernández, Anet Rivera-Osorio, David Sosa, Maria Magdalena Ortiz Sandoval, Norma López-Santiago, Sara Frías, Sara Frías, Victoria del Castillo, Alfredo Rodríguez, Alfredo Rodríguez

    Diterbitkan 2024-01-01
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  11. 11
    P191: Old school and new findings: Expansion and delineation of the dysmorphological phenotype of Fanconi anemia

    P191: Old school and new findings: Expansion and delineation of the dysmorphological phenotype of Fanconi anemia oleh Moises Fiesco-Roa, Andrea Venegas-Andrade, María del Mar Sáez de Ocariz Gutiérrez, Sonia Toussaint-Caire, Armando Hernández Rodas, Gilberto Gómez Garza, Magdalena Ortiz Sandoval, Elia Ixel Apodaca Chávez, Leda Torres, Pedro Reyes, Ulises Juárez, Angélica Solis, Bertha Molina, Alfredo Rodríguez, Sara Frías, Benilde García-de Teresa

    Diterbitkan 2024-01-01
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