Artikel dengan mandat akses publik - Patricia MacielPelajari lebih lanjut
Tidak tersedia di mana pun: 6
Leading the way in the nervous system: Lipid Droplets as new players in health and disease
V Teixeira, P Maciel, V Costa
Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2021
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Unravelling the anticancer potential of functionalized chromeno [2, 3-b] pyridines for breast cancer treatment
S Oliveira-Pinto, O Pontes, D Lopes, B Sampaio-Marques, MD Costa, ...
Bioorganic Chemistry 100, 103942, 2020
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
IP3R2 null mice display a normal acquisition of somatic and neurological development milestones
S Guerra‐Gomes, D Cunha‐Garcia, DS Marques Nascimento, ...
European Journal of Neuroscience 54 (5), 5673-5686, 2021
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Polyglutamine spinocerebellar ataxias: emerging therapeutic targets
A Neves-Carvalho, S Duarte-Silva, A Teixeira-Castro, P Maciel
Expert Opinion on Therapeutic Targets 24 (11), 1099-1119, 2020
Mandat: US Department of Defense, Fundação para a Ciência e a Tecnologia, Portugal
Loss of egli-1, the Caenorhabditis elegans Orthologue of a Downstream Target of SMN, Leads to Abnormalities in Sensorimotor Integration
JD Da Silva, S Oliveira, J Pereira-Sousa, A Teixeira-Castro, MD Costa, ...
Molecular Neurobiology 57, 1553-1569, 2020
Mandat: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
Computational Approaches for the Automatic Quantification of Cells from Brain Images
D Lopes, AB Campos, P Maciel, P Novais, B Fernandes
World Conference on Information Systems and Technologies, 570-580, 2023
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Tersedia di suatu tempat: 74
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Mandat: US National Science Foundation, US National Institutes of Health, Autism …
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
Mandat: US National Science Foundation, US National Institutes of Health, Autism …
Identification of novel genetic causes of Rett syndrome-like phenotypes
F Lopes, M Barbosa, A Ameur, G Soares, J de Sá, AI Dias, G Oliveira, ...
Journal of medical genetics 53 (3), 190-199, 2016
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Neuron-specific proteotoxicity of mutant ataxin-3 in C. elegans : rescue by the DAF-16 and HSF-1 pathways
A Teixeira-Castro, M Ailion, A Jalles, HR Brignull, JL Vilaça, N Dias, ...
Human molecular genetics 20 (15), 2996-3009, 2011
Mandat: US National Institutes of Health
The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3’-phosphatase in spinocerebellar ataxia type 3 pathogenesis
A Chatterjee, S Saha, A Chakraborty, A Silva-Fernandes, SM Mandal, ...
PLoS genetics 11 (1), e1004749, 2015
Mandat: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications
F Torres, M Barbosa, P Maciel
Journal of medical genetics 53 (2), 73-90, 2016
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Functional genomics and biochemical characterization of the C. elegans orthologue of the Machado‐Joseph disease protein ataxin‐3
AJ Rodrigues, G Coppola, C Santos, MC Costa, M Ailion, J Sequeiros, ...
The FASEB Journal 21 (4), 1126-1136, 2007
Mandat: Genome Canada
Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3
R Gao, Y Liu, A Silva-Fernandes, X Fang, A Paulucci-Holthauzen, ...
PLoS genetics 11 (1), e1004834, 2015
Mandat: US National Institutes of Health
Identification of rare de novo epigenetic variations in congenital disorders
M Barbosa, RS Joshi, P Garg, A Martin-Trujillo, N Patel, B Jadhav, ...
Nature communications 9 (1), 2064, 2018
Mandat: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
Serotonergic signalling suppresses ataxin 3 aggregation and neurotoxicity in animal models of Machado-Joseph disease
A Teixeira-Castro, A Jalles, S Esteves, S Kang, L da Silva Santos, ...
Brain 138 (11), 3221-3237, 2015
Mandat: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
Redefining the MED13L syndrome
A Adegbola, L Musante, B Callewaert, P Maciel, H Hu, B Isidor, ...
European Journal of Human Genetics 23 (10), 1308-1317, 2015
Mandat: German Research Foundation, Fundação para a Ciência e a Tecnologia, Portugal
Tauroursodeoxycholic acid improves motor symptoms in a mouse model of Parkinson’s disease
AI Rosa, S Duarte-Silva, A Silva-Fernandes, MJ Nunes, AN Carvalho, ...
Molecular neurobiology 55, 9139-9155, 2018
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
Positive allosteric modulation of indoleamine 2, 3-dioxygenase 1 restrains neuroinflammation
G Mondanelli, A Coletti, FA Greco, MT Pallotta, C Orabona, A Iacono, ...
Proceedings of the National Academy of Sciences 117 (7), 3848-3857, 2020
Mandat: US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
From pathogenesis to novel therapeutics for spinocerebellar ataxia type 3: evading potholes on the way to translation
JD Da Silva, A Teixeira-Castro, P Maciel
Neurotherapeutics 16 (4), 1009-1031, 2019
Mandat: Fundação para a Ciência e a Tecnologia, Portugal
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