Detalhe da pesquisa
1.
Comparison of Eight Technologies to Determine Genotype at the UGT1A1 (TA)n Repeat Polymorphism: Potential Clinical Consequences of Genotyping Errors?
Int J Mol Sci
; 21(3)2020 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32019188
2.
Frameshift mutations in peripheral blood as a biomarker for surveillance of Lynch syndrome.
J Natl Cancer Inst
; 116(6): 957-965, 2024 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-38466935
3.
Organoids and metastatic orthotopic mouse model for mismatch repair-deficient colorectal cancer.
Front Oncol
; 13: 1223915, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37746286
4.
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair.
J Med Genet
; 48(3): 168-76, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21097776
5.
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing.
Cell Death Dis
; 12(9): 838, 2021 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34489406
6.
Pharmacogenomics Implementation at the National Institutes of Health Clinical Center.
J Clin Pharmacol
; 57 Suppl 10: S67-S77, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28921647