Detalhe da pesquisa
1.
Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function.
Hum Genet
; 142(4): 577-593, 2023 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-36964785
2.
Development and validation of a machine learning model to predict prognosis in HIV-negative cryptococcal meningitis patients: a multicenter study.
Eur J Clin Microbiol Infect Dis
; 42(10): 1183-1194, 2023 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-37606868
3.
Tankyrase inhibition promotes a stable human naïve pluripotent state with improved functionality.
Development
; 143(23): 4368-4380, 2016 12 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27660325
4.
An Optimized System for Effective Derivation of Three-Dimensional Retinal Tissue via Wnt Signaling Regulation.
Stem Cells
; 36(11): 1709-1722, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-29999566
5.
A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
BMC Pediatr
; 18(1): 116, 2018 03 17.
Artigo
Inglês
| MEDLINE | ID: mdl-29549887
6.
Distinct serum apolipoprotein A-I levels in neuromyelitis optica and acute transverse myelitis.
Lipids Health Dis
; 12: 150, 2013 Oct 23.
Artigo
Inglês
| MEDLINE | ID: mdl-24148653
7.
Generation and characterization of two induced pluripotent stem cell lines from conjunctiva of a retinoblastoma patient.
Stem Cell Res
; 72: 103200, 2023 10.
Artigo
Inglês
| MEDLINE | ID: mdl-37708614
8.
Generation and characterization of two iPSC lines carrying heterozygous or homozygous nonsense mutation in PROM1 gene from a single family.
Stem Cell Res
; 64: 102913, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36191543
9.
Generation of an RCVRN-eGFP Reporter hiPSC Line by CRISPR/Cas9 to Monitor Photoreceptor Cell Development and Facilitate the Cell Enrichment for Transplantation.
Front Cell Dev Biol
; 10: 870441, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35573687
10.
Spatial and Temporal Development of Müller Glial Cells in hiPSC-Derived Retinal Organoids Facilitates the Cell Enrichment and Transcriptome Analysis.
Front Cell Neurosci
; 16: 820396, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35663427
11.
Generation of a X-linked juvenile retinoschisis patient-derived induced pluripotent stem cell line ZOCi004-A.
Stem Cell Res
; 65: 102937, 2022 12.
Artigo
Inglês
| MEDLINE | ID: mdl-36270067
12.
Amniotic Membrane Enhances the Characteristics and Function of Stem Cell-Derived Retinal Pigment Epithelium Sheets by Inhibiting the Epithelial-Mesenchymal Transition.
Acta Biomater
; 151: 183-196, 2022 10 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35933105
13.
Vascular endothelial growth factor-B gene transfer exacerbates retinal and choroidal neovascularization and vasopermeability without promoting inflammation.
Mol Vis
; 17: 492-507, 2011 Feb 17.
Artigo
Inglês
| MEDLINE | ID: mdl-21364963
14.
E13.5 retinal progenitors induce mouse bone marrow mesenchymal stromal cells to differentiate into retinal progenitor-like cells.
Cytotherapy
; 13(3): 294-303, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-20979443
15.
Retinal Organoid Induction System for Derivation of 3D Retinal Tissues from Human Pluripotent Stem Cells.
J Vis Exp
; (170)2021 04 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33900292
16.
Human retinal organoids release extracellular vesicles that regulate gene expression in target human retinal progenitor cells.
Sci Rep
; 11(1): 21128, 2021 10 26.
Artigo
Inglês
| MEDLINE | ID: mdl-34702879
17.
Establishment of a Rapid Lesion-Controllable Retinal Degeneration Monkey Model for Preclinical Stem Cell Therapy.
Cells
; 9(11)2020 11 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33202702
18.
Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy.
Stem Cell Res
; 45: 101769, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32278302
19.
Role of MEF feeder cells in direct reprogramming of mousetail-tip fibroblasts.
Cell Biol Int
; 33(12): 1268-73, 2009 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-19524692
20.
Generation and Characterization of Induced Pluripotent Stem Cells and Retinal Organoids From a Leber's Congenital Amaurosis Patient With Novel RPE65 Mutations.
Front Mol Neurosci
; 12: 212, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31572124