Detalhe da pesquisa
1.
Generation of IPi001-A/B/C human induced pluripotent stem cell lines from healthy amniotic fluid cells.
Stem Cell Res
; 76: 103350, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38387169
2.
Generation and characterization of induced pluripotent stem cell lines from two patients with recessive dystrophic epidermolysis Bullosa.
Stem Cell Res
; 69: 103104, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37148821
3.
Generation of induced pluripotent stem cells (iPSCs) from a microvillus inclusion disease patient with a homozygous missense mutation in UNC45A.
Stem Cell Res
; 68: 103057, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36868038
4.
Engineering 3D micro-compartments for highly efficient and scale-independent expansion of human pluripotent stem cells in bioreactors.
Biomaterials
; 295: 122033, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36764194
5.
Generation and characterization of IMAGINi013-A, an induced pluripotent stem cell line generated from a healthy donor.
Stem Cell Res
; 61: 102755, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35334405
6.
2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development.
J Vis Exp
; (181)2022 03 25.
Artigo
Inglês
| MEDLINE | ID: mdl-35389978
7.
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
J Clin Invest
; 132(10)2022 05 16.
Artigo
Inglês
| MEDLINE | ID: mdl-35575086
8.
Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors.
Stem Cell Res
; 48: 101959, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32866896
9.
Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation.
Stem Cell Res
; 50: 102107, 2020 Dec 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33340797
10.
Generation of an iPSC line (IMAGINi022-A) from a patient carrying a SOX10 missense mutation and presenting with deafness, depigmentation and progressive neurological impairment.
Stem Cell Res
; 48: 101936, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32795927
11.
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.
Nat Commun
; 11(1): 6087, 2020 11 30.
Artigo
Inglês
| MEDLINE | ID: mdl-33257696