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Sara Frias
Sara Frias
Instituto Nacional de Pediatria/Instituto de Investigaciones Biomedicas UNAM
在 biomedicas.unam.mx 的电子邮件经过验证
标题
引用次数
引用次数
年份
Delayed repair of DNA damage by ionizing radiation in cells from patients with juvenile systemic lupus erythematosus and rheumatoid arthritis
D McCurdy, LQ Tai, S Frias, Z Wang
Radiation research 147 (1), 48-54, 1997
971997
NOVP chemotherapy for Hodgkin’s disease transiently induces sperm aneuploidies associated with the major clinical aneuploidy syndromes involving chromosomes X, Y, 18, and 21
S Frias, P Van Hummelen, ML Meistrich, XR Lowe, FB Hagemeister, ...
Cancer research 63 (1), 44-51, 2003
902003
DEB test for Fanconi anemia detection in patients with atypical phenotypes
C Esmer, S Sanchez, S Ramos, B Molina, S Frias, A Carnevale
American Journal of Medical Genetics Part A 124 (1), 35-39, 2004
762004
Chromosome instability in Fanconi anemia: from breaks to phenotypic consequences
B García-de-Teresa, A Rodríguez, S Frias
Genes 11 (12), 1528, 2020
592020
A Boolean network model of human gonadal sex determination
O Ríos, S Frias, A Rodríguez, S Kofman, H Merchant, L Torres, ...
Theoretical Biology and Medical Modelling 12, 1-18, 2015
552015
A Boolean network model of the FA/BRCA pathway
A Rodriguez, D Sosa, L Torres, B Molina, S Frias, L Mendoza
Bioinformatics 28 (6), 858-866, 2012
552012
MYC promotes bone marrow stem cell dysfunction in Fanconi anemia
A Rodríguez, K Zhang, A Färkkilä, J Filiatrault, C Yang, M Velázquez, ...
Cell stem cell 28 (1), 33-47. e8, 2021
402021
An assessment of immediate DNA damage to occupationally exposed workers to low dose ionizing radiation by using the comet assay
A Martínez, M Coleman, CA Romero-Talamás, S Frías
Rev Invest Clin 62 (1), 23-30, 2010
372010
Cytogenetics in acute lymphoblastic leukemia in Mexican children: an institutional experience
P Pérez-Vera, M Mújica-Sánchez, A Carnevale, R Rivera-Luna, ...
Archives of Medical Research 32 (3), 202-207, 2001
342001
Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp (7; 14)(p11; p11)
A Carnevale, S Frías, V Castillo
Clinical Genetics 14 (4), 202-206, 1978
341978
Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring
S Frias, S Ramos, B Molina, V del Castillo, DG Mayén
Mutation Research/Genetic Toxicology and Environmental Mutagenesis 520 (1-2 …, 2002
312002
Nonclonal chromosome aberrations and genome chaos in somatic and germ cells from patients and survivors of hodgkin lymphoma
S Frias, S Ramos, C Salas, B Molina, S Sánchez, R Rivera-Luna
Genes 10 (1), 37, 2019
302019
A clinical syndrome associated with dup (5p)
A Carnevale, M Hernández, I Limón‐Toledo, S Frías, J Castillo, ...
American journal of medical genetics 13 (3), 277-283, 1982
301982
Local and circulating microchimerism is associated with hypersensitivity pneumonitis
ML Bustos, S Frías, S Ramos, A Estrada, JL Arreola, F Mendoza, ...
American journal of respiratory and critical care medicine 176 (1), 90-95, 2007
282007
Chromosome instability with bleomycin and x‐ray hypersensitivity in a boy with Nijmegen breakage syndrome
P Pérez‐Vera, A González‐del Angel, B Molina, L Gómez, S Frías, ...
American journal of medical genetics 70 (1), 24-27, 1997
281997
RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy
A Flores-Pérez, LE Rafaelli, N Ramírez-Torres, E Aréchaga-Ocampo, ...
Cancer Biology & Therapy 15 (6), 777-788, 2014
272014
Persistent genomic instability in peripheral blood lymphocytes from Hodgkin lymphoma survivors
C Salas, A Niembro, V Lozano, E Gallardo, B Molina, S Sanchez, ...
Environmental and molecular mutagenesis 53 (4), 271-280, 2012
252012
Partial trisomy 16q resulting from maternal translocation 11p/16q.
P Calva, S Frias, A Carnevale, P Reyes
Annales de Génétique 27 (2), 122-125, 1984
251984
Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in TP53- and BRCA1-Deficient Cells
A Färkkilä, A Rodríguez, J Oikkonen, DC Gulhan, H Nguyen, ...
Cancer research 81 (10), 2774-2787, 2021
232021
Analysis of gene rearrangements using a fluorescence in situ hybridization method in Mexican patients with acute lymphoblastic leukemia: experience at a single institution
P Pérez-Vera, C Salas, O Montero-Ruiz, S Frías, G Dehesa, B Jarquín, ...
Cancer Genetics and Cytogenetics 184 (2), 94-98, 2008
232008
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