Hasil Pencarian - Sara Frías

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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
    Mitosis and its regulation

    Mitosis and its regulation oleh Alfredo de Jesús Rodríguez-Gómez, Sara Frías-Vázquez

    Diterbitkan 2014-07-01
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  3. 3
    Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas

    Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas oleh Emiy Yokoyama-Rebollar, Sara Frías, Victoria del Castillo-Ruiz

    Diterbitkan 2017-11-01
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  4. 4
    Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues

    Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues oleh Leda Torres, Ulises Juárez, Laura García, Juan Miranda-Ríos, Sara Frias

    Diterbitkan 2016-09-01
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  5. 5
    Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma.

    Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma. oleh Sara Frias, Paul Van Hummelen, Marvin L Meistrich, Andrew J Wyrobek

    Diterbitkan 2020-01-01
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  6. 6
    Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples

    Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples oleh Sandra Ramos, Rebeca Rodríguez, Oscar Castro, Patricia Grether, Bertha Molina, Sara Frias

    Diterbitkan 2019-10-01
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  7. 7
    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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  8. 8
    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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  9. 9
    Microtia-atresia: aspectos clínicos, genéticos y genómicos

    Microtia-atresia: aspectos clínicos, genéticos y genómicos oleh Mónica Aguinaga-Ríos, Sara Frías, Diego J. Arenas-Aranda, Verónica Fabiola Morán-Barroso

    Diterbitkan 2014-11-01
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  10. 10
    Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide

    Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide oleh Sandra Ramos, Bertha Molina, Patricia Grether, Dora Gilda Mayén, Oscar Castro, Marta Ángeles, Rebeca Rodríguez, Sara Frías

    Diterbitkan 2015-10-01
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  11. 11
    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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  12. 12
    Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells

    Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells oleh Rosalba Sevilla-Montoya, Maria de Jesus Zavaleta-Abreu, Gloria Queipo, Silvia Sanchez, Sara Frias, Alberto Hidalgo-Bravo, Patricia Grether-González

    Diterbitkan 2021-05-01
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  13. 13
    Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review

    Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review oleh Emiy Yokoyama, Camilo E. Villarroel, Sinhué Diaz, Victoria Del Castillo, Patricia Pérez-Vera, Consuelo Salas, Samuel Gómez, Reneé Barreda, Bertha Molina, Sara Frias

    Diterbitkan 2020-09-01
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  14. 14
    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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  15. 15
    7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype

    7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype oleh Emiy Yokoyama, Dennise Lesley Smith-Pellegrin, Silvia Sánchez, Bertha Molina, Alfredo Rodríguez, Rocío Juárez, Esther Lieberman, Silvia Avila, José Luis Castrillo, Victoria del Castillo, Sara Frías

    Diterbitkan 2017-11-01
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  16. 16
    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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  17. 17
    Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits

    Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits oleh Cristóbal Flores-Castillo, María Luna-Luna, Elizabeth Carreón-Torres, Victoria López-Olmos, Sara Frías, Marco Antonio Juárez-Oropeza, Martha Franco, José Manuel Fragoso, Gilberto Vargas-Alarcón, Óscar Pérez-Méndez

    Diterbitkan 2019-05-01
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  18. 18
    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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  19. 19
    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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  20. 20
    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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