Detalhe da pesquisa
1.
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
Cell
; 146(6): 889-903, 2011 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-21925314
2.
Development of a robotic cluster for automated and scalable cell therapy manufacturing.
Cytotherapy
; 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38647505
3.
Comprehensive analysis of right fascicular and right bundle branch blocks: A multi-center study.
J Electrocardiol
; 83: 95-105, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38387106
4.
Analysis of the pathogenic variants of BRCA1 and BRCA2 using next-generation sequencing in women with familial breast cancer: a case-control study.
BMC Cancer
; 19(1): 722, 2019 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31331294
5.
Heterogeneous Contributing Factors in MPM Disease Development and Progression: Biological Advances and Clinical Implications.
Int J Mol Sci
; 19(1)2018 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29342862
6.
Human immunodeficiency viruses appear compartmentalized to the female genital tract in cross-sectional analyses but genital lineages do not persist over time.
J Infect Dis
; 207(8): 1206-15, 2013 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23315326
7.
A novel phenotype characterized by digital abnormalities, intellectual disability, and short stature in a Mexican family maps to Xp11.4-p11.21.
Am J Med Genet A
; 161A(2): 237-43, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23307567
8.
Chromosomal Abnormalities of Interest in Turner Syndrome: An Update.
J Pediatr Genet
; 12(4): 263-272, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38162151
9.
Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene.
Ophthalmic Genet
; 44(5): 465-468, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37519288
10.
Quality of Life Scores Remained Different among the Genotypic Groups of Patients with Suspected Hemochromatosis, Even after Treatment Period.
Genes (Basel)
; 13(1)2022 01 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35052458
11.
Congenital Heart Diseases: Genetic Risk Variants and Their Methylation Status.
Genes (Basel)
; 13(11)2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36421790
12.
Polyclonal Regulatory T Cell Manufacturing Under cGMP: A Decade of Experience.
Front Immunol
; 12: 744763, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34867967
13.
Maternal Folic Acid Intake and Methylation Status of Genes Associated with Ventricular Septal Defects in Children: Case-Control Study.
Nutrients
; 13(6)2021 Jun 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34204335
14.
Molecular Characterization of Associated Pathogens in Febrile Patients during Inter-Epidemic Periods of Urban Arboviral Diseases in Tapachula Southern Mexico.
Pathogens
; 10(11)2021 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34832606
15.
A case series of infants with increased VAMP7 gene dosage at birth and virilization defects.
J Pediatr Urol
; 16(4): 423.e1-423.e6, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32622737
16.
Gene Copy Number Quantification of SHOX, VAMP7, and SRY for the Detection of Sex Chromosome Aneuploidies in Neonates.
Genet Test Mol Biomarkers
; 24(6): 352-358, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32423256
17.
Marital and job satisfaction among non-resident physicians at a Hispanic academic medical center, 2006-2007.
Bol Asoc Med P R
; 101(1): 36-41, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19954085
18.
A review of soft-tissue sarcomas: translation of biological advances into treatment measures.
Cancer Manag Res
; 10: 1089-1114, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29785138
19.
Preclinical characterization of therapeutic antibodies targeted at the carboxy-terminus of Sonic hedgehog.
Oncotarget
; 9(18): 14311-14323, 2018 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29581846
20.
Genome-scale ChIP-chip analysis using 10,000 human cells.
Biotechniques
; 43(6): 791-7, 2007 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18251256