Detalhe da pesquisa
1.
Cas9-Mediated Nanopore Sequencing Enables Precise Characterization of Structural Variants in CCM Genes.
Int J Mol Sci
; 23(24)2022 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36555281
2.
Fibronectin rescues aberrant phenotype of endothelial cells lacking either CCM1, CCM2 or CCM3.
FASEB J
; 34(7): 9018-9033, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32515053
3.
Biallelic CCM3 mutations cause a clonogenic survival advantage and endothelial cell stiffening.
J Cell Mol Med
; 23(3): 1771-1783, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30549232
4.
Bringing CCM into a dish: cell culture models for cerebral cavernous malformations.
Med Genet
; 33(3): 251-259, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-38835694
5.
Inactivation of Cerebral Cavernous Malformation Genes Results in Accumulation of von Willebrand Factor and Redistribution of Weibel-Palade Bodies in Endothelial Cells.
Front Mol Biosci
; 8: 622547, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34307446
6.
CRISPR/Cas9-mediated Generation of Human Endothelial Cell Knockout Models of CCM Disease.
Methods Mol Biol
; 2152: 169-177, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32524552
7.
Precise CCM1 gene correction and inactivation in patient-derived endothelial cells: Modeling Knudson's two-hit hypothesis in vitro.
Mol Genet Genomic Med
; 7(7): e00755, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31124307
8.
Novel Pathogenic Variants in a Cassette Exon of CCM2 in Patients With Cerebral Cavernous Malformations.
Front Neurol
; 10: 1219, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31824402