Detalhe da pesquisa
1.
Chromosome analysis of 303 pregnancy losses in Mexico.
Gac Med Mex
; 160(1): 76-85, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38753554
2.
A Boolean network model of the double-strand break repair pathway choice.
J Theor Biol
; 573: 111608, 2023 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37595867
3.
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.
Int J Mol Sci
; 23(4)2022 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216452
4.
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Gynecol Endocrinol
; 35(9): 772-776, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30887870
5.
A Boolean network model of human gonadal sex determination.
Theor Biol Med Model
; 12: 26, 2015 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26573569
6.
Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process.
Theor Biol Med Model
; 12: 19, 2015 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26385365
7.
Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells.
PLoS One
; 19(5): e0298032, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38820384
8.
A Boolean network model of the FA/BRCA pathway.
Bioinformatics
; 28(6): 858-66, 2012 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22267503
9.
Frequent copy number variants in a cohort of Mexican-Mestizo individuals.
Mol Cytogenet
; 16(1): 2, 2023 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36631885
10.
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.
Cell Stem Cell
; 28(1): 33-47.e8, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32997960
11.
Interstitial deletion of 2q24.2: further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction.
Am J Med Genet A
; 164A(3): 824-7, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24357343
12.
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.
Front Genet
; 10: 411, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31130988
13.
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
Mol Genet Genomic Med
; 7(6): e710, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31044565
14.
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.
Mol Cytogenet
; 11: 30, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29760780
15.
Paraptosis in human glioblastoma cell line induced by curcumin.
Toxicol In Vitro
; 51: 63-73, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29723631
16.
Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues.
Genom Data
; 9: 70-7, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-27408816
17.
External ear microRNA expression profiles during mouse development.
Int J Dev Biol
; 59(10-12): 497-503, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26864490
18.
Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells.
Environ Mol Mutagen
; 56(5): 457-67, 2015 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-25663157