Detalhe da pesquisa
1.
Small-molecule-directed, efficient generation of retinal pigment epithelium from human pluripotent stem cells.
Proc Natl Acad Sci U S A
; 112(35): 10950-5, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26269569
2.
Stage-specific signaling through TGFß family members and WNT regulates patterning and pancreatic specification of human pluripotent stem cells.
Development
; 138(5): 861-71, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21270052
3.
Rag mutations reveal robust alternative end joining.
Nature
; 449(7161): 483-6, 2007 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-17898768
4.
Simple, Fast, and Efficient Method for Derivation of Dermal Fibroblasts From Skin Biopsies.
Curr Protoc
; 3(3): e714, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36912580
5.
iPSC-based modeling of helicase deficiency reveals impaired cell proliferation and increased apoptosis after NK cell lineage commitment.
bioRxiv
; 2023 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37808662
6.
Derivation and characterization of the induced pluripotent stem cell line CUIMCi004-A from a patient with a novel frameshift variant in exon 18a of OCRL.
Stem Cell Res
; 59: 102635, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35074682
7.
Efficient Cas9-based Genome Editing Using CRISPR Analysis Webtools in Severe Early-onset-obesity Patient-derived iPSCs.
Curr Protoc
; 2(8): e519, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35950852
8.
Establishment of the iPSC line CUIMCi005-A from a patient with Stargardt disease for retinal organoid culture.
Stem Cell Res
; 65: 102973, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36455383
9.
CRISPR-AsCas12a Efficiently Corrects a GPR143 Intronic Mutation in Induced Pluripotent Stem Cells from an Ocular Albinism Patient.
CRISPR J
; 5(3): 457-471, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35686978
10.
Fibroblast growth factor homologous factors serve as a molecular rheostat in tuning arrhythmogenic cardiac late sodium current.
Nat Cardiovasc Res
; 1(5): 1-13, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35662881
11.
Generation of the iPSC line CUIMCi003-A derived from a patient with severe early onset obesity.
Stem Cell Res
; 54: 102432, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34214899
12.
Depression patient-derived cortical neurons reveal potential biomarkers for antidepressant response.
Transl Psychiatry
; 11(1): 201, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33795631
13.
Molecular Features of the Measles Virus Viral Fusion Complex That Favor Infection and Spread in the Brain.
mBio
; 12(3): e0079921, 2021 06 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-34061592
14.
Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder.
Nat Commun
; 12(1): 4087, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34471112
15.
Establishment and characterization of two iPSC lines derived from healthy controls.
Stem Cell Res
; 47: 101926, 2020 Jul 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32738631
16.
Standardized Reporter Systems for Purification and Imaging of Human Pluripotent Stem Cell-derived Motor Neurons and Other Cholinergic Cells.
Neuroscience
; 450: 48-56, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32615233
17.
Small Molecules Restore Bestrophin 1 Expression and Function of Both Dominant and Recessive Bestrophinopathies in Patient-Derived Retinal Pigment Epithelium.
Invest Ophthalmol Vis Sci
; 61(5): 28, 2020 05 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32421148
18.
Generation of two iPS cell lines (FRIMOi003-A and FRIMOi004-A) derived from Stargardt patients carrying ABCA4 compound heterozygous mutations.
Stem Cell Res
; 36: 101389, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30798147
19.
Establishment and characterization of an iPSC line (FRIMOi001-A) derived from a retinitis pigmentosa patient carrying PDE6A mutations.
Stem Cell Res
; 35: 101385, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30685614
20.
Generation of an induced pluripotent stem cell line (FRIMOi002-A) from a retinitis pigmentosa patient carrying compound heterozygous mutations in USH2A gene.
Stem Cell Res
; 35: 101386, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30685615