Detalhe da pesquisa
1.
Int22h1/Int22h2-mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features.
Hum Mutat;
41(7): 1238-1249, 2020 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32112660
2.
mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide.
PLoS Genet;
13(8): e1006974, 2017 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28827832
3.
Genome-wide uniparental disomy as a mechanism of immune escape in acquired aplastic anaemia.
Br J Haematol;
198(6): e78-e81, 2022 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35876645
4.
Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia.
Mol Genet Genomic Med;
10(4): e1888, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35119225
5.
Human MLH1/3 variants causing aneuploidy, pregnancy loss, and premature reproductive aging.
Nat Commun;
12(1): 5005, 2021 08 18.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34408140
6.
Incompatibilities in Mismatch Repair Genes MLH1-PMS1 Contribute to a Wide Range of Mutation Rates in Human Isolates of Baker's Yeast.
Genetics;
210(4): 1253-1266, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30348651
7.
Mismatch Repair Incompatibilities in Diverse Yeast Populations.
Genetics;
205(4): 1459-1471, 2017 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28193730
8.
Carboxypeptidase E promotes cancer cell survival, but inhibits migration and invasion.
Cancer Lett;
341(2): 204-13, 2013 Dec 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23941827