Detalhe da pesquisa
1.
Blood and immune development in human fetal bone marrow and Down syndrome.
Nature
; 598(7880): 327-331, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34588693
2.
Single-cell RNA sequencing reveals transcriptional changes of human choroidal and retinal pigment epithelium cells during fetal development, in healthy adult and intermediate age-related macular degeneration.
Hum Mol Genet
; 32(10): 1698-1710, 2023 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36645183
3.
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
PLoS Genet
; 18(4): e1010068, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35363781
4.
Single-cell DNA sequencing identifies risk-associated clonal complexity and evolutionary trajectories in childhood medulloblastoma development.
Acta Neuropathol
; 144(3): 565-578, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35831448
5.
Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.
BMC Dev Biol
; 21(1): 14, 2021 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34615475
6.
Deconstructing Retinal Organoids: Single Cell RNA-Seq Reveals the Cellular Components of Human Pluripotent Stem Cell-Derived Retina.
Stem Cells
; 37(5): 593-598, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30548510
7.
CRX Expression in Pluripotent Stem Cell-Derived Photoreceptors Marks a Transplantable Subpopulation of Early Cones.
Stem Cells
; 37(5): 609-622, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30681766
8.
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease.
Mov Disord
; 35(12): 2134-2136, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33070335
9.
Deciphering the spatiotemporal transcriptional and chromatin accessibility of human retinal organoid development at the single-cell level.
iScience
; 27(4): 109397, 2024 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38510120
10.
Single-cell insights into immune dysregulation in rheumatoid arthritis flare versus drug-free remission.
Nat Commun
; 15(1): 1063, 2024 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38316770
11.
Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina.
Nat Commun
; 15(1): 3567, 2024 Apr 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38670973
12.
Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).
Ann Rheum Dis
; 77(5): 783-786, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28659290
13.
Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.
Blood
; 118(10): 2656-8, 2011 Sep 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21765025
14.
pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation.
Stem Cells Transl Med
; 11(4): 415-433, 2022 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35325233
15.
Conjunctival epithelial cells resist productive SARS-CoV-2 infection.
Stem Cell Reports
; 17(7): 1699-1713, 2022 07 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35750043
16.
Co-expression of SARS-CoV-2 entry genes in the superficial adult human conjunctival, limbal and corneal epithelium suggests an additional route of entry via the ocular surface.
Ocul Surf
; 19: 190-200, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32502616
17.
A single cell atlas of human cornea that defines its development, limbal progenitor cells and their interactions with the immune cells.
Ocul Surf
; 21: 279-298, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33865984
18.
Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2.
Nat Commun
; 12(1): 7092, 2021 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34876592
19.
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2.
Sci Immunol
; 4(42)2019 12 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31836668
20.
Somatic mtDNA variation is an important component of Parkinson's disease.
Neurobiol Aging
; 38: 217.e1-217.e6, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26639157