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Danyllo Oliveira
Danyllo Oliveira
Postdoctoral researcher, University of São Paulo
Email confirmado em ib.usp.br
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Ano
Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells
LC Caires-Júnior, E Goulart, US Melo, BHS Araujo, L Alvizi, ...
Nature communications 9 (1), 1-11, 2018
1312018
3D bioprinting of liver spheroids derived from human induced pluripotent stem cells sustain liver function and viability in vitro
E Goulart, LC de Caires-Junior, KA Telles-Silva, BHS Araujo, SA Rocco, ...
Biofabrication 12 (1), 015010, 2019
1302019
Adult and iPS-derived non-parenchymal cells regulate liver organoid development through differential modulation of Wnt and TGF-β
E Goulart, LC de Caires-Junior, KA Telles-Silva, BHS Araujo, ...
Stem cell research & therapy 10 (1), 1-11, 2019
552019
Population and computational analysis of the MGEA6 P521A variation as a risk factor for familial idiopathic basal ganglia calcification (Fahr’s disease)
RR Lemos, DF Oliveira, M Zatz, JRM Oliveira
Journal of molecular neuroscience 43 (3), 333-336, 2011
382011
Exaggerated blood pressure response during the exercise treadmill test as a risk factor for hypertension
SG Lima, M Albuquerque, JRM Oliveira, CFJ Ayres, JEG Cunha, ...
Brazilian Journal of Medical and Biological Research 46, 368-347, 2013
212013
MS‐driven metabolic alterations are recapitulated in iPSC‐derived astrocytes
B Ghirotto, DF Oliveira, M Cipelli, PJ Basso, J de Lima, CNS Breda, ...
Annals of Neurology, 2021
202021
Pre-coating decellularized liver with HepG2-conditioned medium improves hepatic recellularization
LC Caires-Júnior, E Goulart, KA Telles-Silva, BHS Araujo, CM Musso, ...
Materials Science and Engineering: C 121, 111862, 2021
202021
Mechanistic Insights of Astrocyte-Mediated Hyperactive Autophagy and Loss of Motor Neuron Function in SOD1 L39R Linked Amyotrophic Lateral Sclerosis
CS Rajpurohit, V Kumar, A Cheffer, D Oliveira, H Ulrich, OK Okamoto, ...
Molecular Neurobiology 57 (10), 4117-4133, 2020
202020
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration
D Oliveira, DA Morales-Vicente, MS Amaral, L Luz, AL Sertié, FS Leite, ...
Human Molecular Genetics 29 (9), 1465-1475, 2020
162020
Mutations at the SLC20A2 gene and brain resilience in families with idiopathic basal ganglia calcification (“Fahr's disease”)
DF de Oliveira, RR de Lemos, JRM Oliveira
Frontiers in human neuroscience 7, 420, 2013
162013
DNA methylation fingerprint of monozygotic twins and their singleton sibling with intellectual disability carrying a novel KDM5C mutation
JVS Guerra, J Oliveira-Santos, DF Oliveira, GF Leal, JRM Oliveira, ...
European Journal of Medical Genetics 63 (3), 103737, 2020
142020
Inositol monophosphatase 1 (IMPA1) mutation in intellectual disability patients impairs neurogenesis but not gliogenesis
T Figueiredo, APD Mendes, DP Moreira, E Goulart, D Oliveira, ...
Molecular Psychiatry, 1-14, 2020
112020
Chromoanagenesis Event Underlies a de novo Pericentric and Multiple Paracentric Inversions in a Single Chromosome Causing Coffin–Siris Syndrome
CM Grochowski, ACV Krepischi, J Eisfeldt, H Du, DR Bertola, D Oliveira, ...
Frontiers in Genetics 12, 2021
102021
10q23. 31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly
D Oliveira, GF Leal, AL Sertié, LC Caires Jr, E Goulart, CM Musso, ...
Journal of medical genetics 56 (8), 543-547, 2019
102019
Exaggerated blood pressure response during exercise treadmill testing: functional and hemodynamic features, and risk factors
SG de Lima, MFPM de Albuquerque, JRM de Oliveira, CFJ Ayres, ...
Hypertension Research 35 (7), 733-738, 2012
102012
IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS‐associated amyotrophic lateral sclerosis
AF Assoni, EN Guerrero, R Wardenaar, D Oliveira, PL Bakker, LM Alves, ...
Brain Pathology 34 (1), e13206, 2024
82024
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delay
US Melo, D Bonner, KCK Lloyd, A Moshiri, B Willis, L Lanoue, L Bower, ...
Genetics in Medicine 23 (4), 661-668, 2021
62021
Revising the M235T polymorphism position for the AGT gene and reporting a modifying variant in the Brazilian population with potential cardiac and neural impact
RR Lemos, SG De Lima, JEG da Cunha, DF Oliveira, MBR de Souza, ...
Journal of Molecular Neuroscience 48 (1), 253-256, 2012
52012
Neuro-imaging genetics studies in basal ganglia calcification as a model to understand brain resilience
JRM Oliveira, MF Oliveira, R Kuhni, RR Lemos, D Oliveira
JOURNAL OF MOLECULAR NEUROSCIENCE 45 (SUPPL 1), S87-S88, 2011
42011
Report of a young patient with brain calcifications with a novel homozygous MYORG variant
SH Sadok, RL Borges-Medeiros, DF de Oliveira, M Zatz, JRM de Oliveira
Gene 859, 147213, 2023
22023
O sistema não pode efectuar a operação agora. Tente mais tarde.
Artigos 1–20