Detalhe da pesquisa
1.
Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9.
Mol Ther
; 26(5): 1241-1254, 2018 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29599079
2.
Computationally designed liver-specific transcriptional modules and hyperactive factor IX improve hepatic gene therapy.
Blood
; 123(20): 3195-9, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24637359
3.
Genome-wide computational analysis reveals cardiomyocyte-specific transcriptional Cis-regulatory motifs that enable efficient cardiac gene therapy.
Mol Ther
; 23(1): 43-52, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25195597
4.
3D human induced pluripotent stem cell-derived bioengineered skeletal muscles for tissue, disease and therapy modeling.
Nat Protoc
; 18(4): 1337-1376, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36792780
5.
Modeling Skeletal Muscle Laminopathies Using Human Induced Pluripotent Stem Cells Carrying Pathogenic LMNA Mutations.
Front Physiol
; 9: 1332, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30405424
6.
Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering.
Cell Rep
; 23(3): 899-908, 2018 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-29669293
7.
Explant culture: a simple, reproducible, efficient and economic technique for isolation of mesenchymal stromal cells from human adipose tissue and lipoaspirate.
J Tissue Eng Regen Med
; 8(9): 706-16, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22837175