Detalhe da pesquisa
1.
Contrasting somatic mutation patterns in aging human neurons and oligodendrocytes.
Cell;
187(8): 1955-1970.e23, 2024 Apr 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38503282
2.
Somatic genomic changes in single Alzheimer's disease neurons.
Nature;
604(7907): 714-722, 2022 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35444284
3.
Cerebral cavernous malformations arise from endothelial gain of MEKK3-KLF2/4 signalling.
Nature;
532(7597): 122-6, 2016 Apr 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27027284
4.
Corrigendum: Cerebral cavernous malformations arise from endothelial gain of MEKK3-KLF2/4 signalling.
Nature;
536(7617): 488, 2016 08 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27281211
5.
Stable isotope dilution liquid chromatography/mass spectrometry analysis of cellular and tissue medium- and long-chain acyl-coenzyme A thioesters.
Rapid Commun Mass Spectrom;
28(16): 1840-8, 2014 Aug 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25559454
6.
Sulfonated P-W modified nitrogen-containing carbon-based solid acid catalysts for one-pot conversion of cellulose to ethyl levulinate under water-ethanol medium.
Int J Biol Macromol;
260(Pt 1): 129472, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38262833
7.
Somatic cancer driver mutations are enriched and associated with inflammatory states in Alzheimer's disease microglia.
bioRxiv;
2024 Jan 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38260600
8.
Contrasting patterns of somatic mutations in neurons and glia reveal differential predisposition to disease in the aging human brain.
bioRxiv;
2023 Jan 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36711756
9.
Somatic Mosaicism in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Reveals Widespread Degeneration from Focal Mutations.
bioRxiv;
2023 Dec 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38077003
10.
Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicity.
Nat Aging;
2(8): 714-725, 2022 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36051457
11.
Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human Brain.
Cancer Discov;
12(1): 172-185, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34389641
12.
Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Nat Genet;
54(10): 1564-1571, 2022 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36163278
13.
A programmable qudit-based quantum processor.
Nat Commun;
13(1): 1166, 2022 Mar 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35246519
14.
Label-free fluorimetric detection of CEA using carbon dots derived from tomato juice.
Biosens Bioelectron;
86: 83-89, 2016 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27336615
15.
Micro-CT Imaging Reveals Mekk3 Heterozygosity Prevents Cerebral Cavernous Malformations in Ccm2-Deficient Mice.
PLoS One;
11(8): e0160833, 2016.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27513872
16.
Papain-templated Cu nanoclusters: assaying and exhibiting dramatic antibacterial activity cooperating with H2O2.
Nanoscale;
7(45): 19066-72, 2015 Dec 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26514845
17.
The cerebral cavernous malformation pathway controls cardiac development via regulation of endocardial MEKK3 signaling and KLF expression.
Dev Cell;
32(2): 168-80, 2015 Jan 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25625206
18.
Plk1-mediated phosphorylation of Topors regulates p53 stability.
J Biol Chem;
284(28): 18588-92, 2009 Jul 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19473992