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Bertha Molina Alvarez
Bertha Molina Alvarez
Investigador, Instituto Nacional de Pediatría
Verified email at ciencias.unam.mx
Title
Cited by
Cited by
Year
DEB test for Fanconi anemia detection in patients with atypical phenotypes
C Esmer, S Silvia Ramos, Bertha, F Sara, A Carnevale
American Journal of Medical Genetics Parte A 124 (1), 35-39, 2004
752004
Genotoxic studies of vanadium pentoxide (V2O5) in male mice. II. Effects in several mouse tissues
M Altamirano‐Lozano, M Valverde, L Alvarez‐Barrera, B Molina, E Rojas
Teratogenesis, Carcinogenesis, and mutagenesis 19 (4), 243-255, 1999
601999
A Boolean network model of the FA/BRCA pathway
A Rodríguez, D Sosa, L Torres, M Molina, S Frias, L Mendoza
Bioinformatics 28 (6), 858-66, 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, 1-15, 2021
382021
Metabolic activation of herbicide products by Vicia faba detected in human peripheral lymphocytes using alkaline single cell gel electrophoresis
ME Calderón-Segura, S Gómez-Arroyo, B Molina-Alvarez, ...
Toxicology In Vitro 21 (6), 1143-1154, 2007
372007
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 520, 25-37, 2002
312002
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, R Gatti, ...
Am J Med Genet 70 (1), 24-7, 1997
281997
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 (37), 2019
272019
Trisomy of the short arm of chromosome 5 due to a de novo inversión and duplication (5) (p15.3 p13.3).
M Cervera, S Sánchez, B Molina, MA Alcántara, V Del Castillo, ...
American Journal of Medical Genetics Parte A 136 (381-385), 2005
272005
Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors.
C Salas, A Niembro, V Lozano, E Gallardo, B Molina, S Sánchez, ...
Environ Mol Mutagen 53 (4), 271-80, 2012
252012
Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment
A Martinez, JM Hinz, L Gómez, B Molina, H Acuña, IM Jones, S Frias, ...
Mutat Res 656 (1-2), 1-7, 2008
182008
Detection of Short-term Chromosomal Damage Due to Therapeutic 131I Exposure in Patients with Thyroid Cancer.
A Hernández-Jardines, B Molina, V Del Castillo, M Papadakis, T Rivera, ...
Rev Inv Clin. 62 (1), 31-38, 2010
162010
Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy
S Ramos, P Navarrete-Meneses, B Molina, D Cervantes-Barragán, ...
Environmental and Molecular Mutagenesis 59 (8), 755-768, 2018
132018
Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart …
MA Alcántara-Ortigoza, J De Rubens-Figueroa, ME Reyna-Fabian, ...
Pediatric cardiology 36, 802-808, 2015
132015
Trisomy 9 mosaicism in a girl with multiple malformations.
L Díaz-Mares, M Bertha, A Carnevale
Ann Genét. 33, 165-168, 1990
131990
Effect of hydroxyurea and normal plasma on DNA synthesis in lymphocytes from Fanconi anemia patients.
S Frias, L Gómez, B Molina, E Rojas, P Ostrosky, A Carnevale
Mutation Research 357, 115-121, 1996
121996
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.
E Yokoyama, V Del Castillo, S Sánchez, S Ramos, B Molina, L Torres, ...
Molecular Cytogenetics 11 (30), 2018
102018
The clastogenic response of the 1q12 heterochromatic region to DNA cross-linking agents is independent of the Fanconi anaemia pathway
E Callén, MJ Ramírez, A Creus, R Marcos, S Frias, B Molina, I Badell, ...
Carcinogenesis 22 (8), 1267-71, 2002
102002
FANCC Dutch Founder Mutation in a Mennonite Family from Tamaulipas Mexico.
B García-de Teresa, S Frias, B Molina, T Villarreal, A Rodriguez, ...
Mol Genet Genomic Med. 7 (6), 2019
92019
Heterogeneous Diagnoses Underlying Radial Ray Anomalies
R Sevilla-Montoya, M Aguinaga, A Martínez, G Razo, B Molina, S Frías, ...
Indian J Pediatr. 84 (3), 200-205, 2017
92017
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