Detalhe da pesquisa
1.
Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells.
Hum Mol Genet
; 21(17): 3883-95, 2012 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22678061
2.
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
em Inglês
| MEDLINE | ID: mdl-38387169
3.
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
em Inglês
| MEDLINE | ID: mdl-37148821
4.
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
em Inglês
| MEDLINE | ID: mdl-36868038
5.
Engineering 3D micro-compartments for highly efficient and scale-independent expansion of human pluripotent stem cells in bioreactors.
Biomaterials
; 295: 122033, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36764194
6.
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
em Inglês
| MEDLINE | ID: mdl-35334405
7.
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
em Inglês
| MEDLINE | ID: mdl-35389978
8.
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
J Clin Invest
; 132(10)2022 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35575086
9.
Striatal progenitors derived from human ES cells mature into DARPP32 neurons in vitro and in quinolinic acid-lesioned rats.
Proc Natl Acad Sci U S A
; 105(43): 16707-12, 2008 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-18922775
10.
Generation of an induced pluripotent stem cell (iPSC) line (IMAGINi007) from a patient with steroid-resistant nephrotic syndrome carrying the homozygous p.R138Q mutation in the podocin-encoding NPHS2 gene.
Stem Cell Res
; 46: 101878, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32585588
11.
Generation of two induced pluripotent stem cell lines IMAGINi004-A and IMAGINi005-A from healthy donors.
Stem Cell Res
; 48: 101959, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32866896
12.
Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation.
Stem Cell Res
; 50: 102107, 2020 Dec 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33340797
13.
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
em Inglês
| MEDLINE | ID: mdl-32795927
14.
MINPP1 prevents intracellular accumulation of the chelator inositol hexakisphosphate and is mutated in Pontocerebellar Hypoplasia.
Nat Commun
; 11(1): 6087, 2020 11 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257696
15.
Involvement of mitochondrial complex II defects in neuronal death produced by N-terminus fragment of mutated huntingtin.
Mol Biol Cell
; 17(4): 1652-63, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16452635
16.
High N-glycan multiplicity is critical for neuronal adhesion and sensitizes the developing cerebellum to N-glycosylation defect.
Elife
; 72018 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30311906
17.
[Jumping translocations of chromosome 1q are recurring chromosomal -aberrations in neural derivatives of pluripotent stem cells]. / Les dérivés neuraux des cellules souches pluripotentes échappent à la sénescence en gagnant le 1q sauteur.
Med Sci (Paris)
; 28(2): 219-21, 2012 Feb.
Artigo
em Francês
| MEDLINE | ID: mdl-22377313
18.
Short exposure to Notch ligand Delta-4 is sufficient to induce T-cell differentiation program and to increase the T cell potential of primary human CD34+ cells.
Exp Hematol
; 34(12): 1720-9, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17157169
19.
Association of a common coding polymorphism (N453S) of the cytochrome P450 1B1 (CYP1B1) gene with optic disc cupping and visual field alteration in French patients with primary open-angle glaucoma.
Mol Vis
; 11: 1012-7, 2005 Nov 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-16319821
20.
[A recurrent hotspot of genomic instability identified in human ES cells]. / Les cellules souches embryonnaires humaines révèlent l'existence d'une région hautement instable du génome.
Med Sci (Paris)
; 25(1): 99-101, 2009 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-19154702