Detalhe da pesquisa
1.
Characterization of genetic variants in the EGLN1/PHD2 gene identified in a European collection of patients with erythrocytosis.
Haematologica
; 108(11): 3068-3085, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37317877
2.
TET3 controls the expression of the H3K27me3 demethylase Kdm6b during neural commitment.
Cell Mol Life Sci
; 78(2): 757-768, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32405722
3.
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Eur Heart J
; 40(37): 3081-3094, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31114854
4.
Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line.
Stem Cell Res
; 77: 103396, 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38522388
5.
In vitro and in vivo models define a molecular signature reference for human embryonic notochordal cells.
iScience
; 27(2): 109018, 2024 Feb 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38357665
6.
Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background.
Stem Cell Res
; 59: 102647, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34999420
7.
Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.
Cardiovasc Res
; 117(9): 2092-2107, 2021 07 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32898233
8.
NOTO Transcription Factor Directs Human Induced Pluripotent Stem Cell-Derived Mesendoderm Progenitors to a Notochordal Fate.
Cells
; 9(2)2020 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-32102328
9.
A dominant vimentin variant causes a rare syndrome with premature aging.
Eur J Hum Genet
; 28(9): 1218-1230, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32066935
10.
Induction of Human Trophoblast Stem Cells from Somatic Cells and Pluripotent Stem Cells.
Cell Rep
; 33(8): 108419, 2020 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33238118
11.
Parallel derivation of isogenic human primed and naive induced pluripotent stem cells.
Nat Commun
; 9(1): 360, 2018 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-29367672
12.
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype.
Clin Transl Med
; 11(6): e413, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34185406