Search Results - "Faro, Rosário"

An atypical aspartic protease modulates lateral root development in Arabidopsis thaliana by Soares, André, Niedermaier, Stefan, Faro, Rosário, Loos, Andreas, Manadas, Bruno, Faro, Carlos, Huesgen, Pitter F, Cheung, Alice Y, Simões, Isaura

“…Aspartic protease ASPR1 modulates lateral root development and displays atypical enzymatic properties, including fungal-like specificity preferences,…”
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Extracellular vesicle-based delivery of silencing sequences for the treatment of Machado-Joseph disease/spinocerebellar ataxia type 3 by Rufino-Ramos, David, Albuquerque, Patrícia R., Leandro, Kevin, Carmona, Vitor, Martins, Inês M., Fernandes, Rita, Henriques, Carina, Lobo, Diana, Faro, Rosário, Perfeito, Rita, Mendonça, Liliana S., Pereira, Dina, Gomes, Célia M., Nobre, Rui Jorge, Pereira de Almeida, Luís

“…Machado-Joseph disease (MJD)/spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominantly inherited ataxia worldwide. It is caused by an…”
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ULK overexpression mitigates motor deficits and neuropathology in mouse models of Machado-Joseph disease by Vasconcelos-Ferreira, Ana, Martins, Inês Morgado, Lobo, Diana, Pereira, Dina, Lopes, Miguel M., Faro, Rosário, Lopes, Sara M., Verbeek, Dineke, Schmidt, Thorsten, Nóbrega, Clévio, Pereira de Almeida, Luís

“…Machado-Joseph disease (MJD) is a fatal neurodegenerative disorder clinically characterized by prominent ataxia. It is caused by an expansion of a CAG…”
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Protocol for the Characterization of the Cytosine-Adenine-Guanine Tract and Flanking Polymorphisms in Machado-Joseph Disease: Impact on Diagnosis and Development of Gene-Based Therapies by Lopes, Sara Monteiro, Faro, Rosário, Lopes, Miguel Monteiro, Onofre, Isabel, Mendonça, Nuno, Ribeiro, Joana, Januário, Cristina, Nobre, Rui Jorge, Pereira de Almeida, Luís

“…Polyglutamine spinocerebellar ataxias (SCAs) constitute a group of autosomal dominantly inherited neurodegenerative disorders with considerable phenotypic…”
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Molecular cloning and characterization of procirsin, an active aspartic protease precursor from Cirsium vulgare (Asteraceae) by Lufrano, Daniela, Faro, Rosário, Castanheira, Pedro, Parisi, Gustavo, Veríssimo, Paula, Vairo-Cavalli, Sandra, Simões, Isaura, Faro, Carlos

“…Recombinant procirsin displayed a high specificity towards κ-casein and milk-clotting activity suggesting its potential use as a new milk coagulant. [Display…”
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Enzymatic properties, evidence for in vivo expression, and intracellular localization of shewasin D, the pepsin homolog from Shewanella denitrificans by Leal, Ana Rita, Cruz, Rui, Bur, Daniel, Huesgen, Pitter F., Faro, Rosário, Manadas, Bruno, Wlodawer, Alexander, Faro, Carlos, Simões, Isaura

“…The widespread presence of pepsin-like enzymes in eukaryotes together with their relevance in the control of multiple biological processes is reflected in the…”
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Shewasin A, an active pepsin homolog from the bacterium Shewanella amazonensis by Simões, Isaura, Faro, Rosário, Bur, Daniel, Kay, John, Faro, Carlos

“…The view has been widely held that pepsin‐like aspartic proteinases are found only in eukaryotes, and not in bacteria. However, a recent bioinformatics search…”
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Characterization of Recombinant CDR1, an Arabidopsis Aspartic Proteinase Involved in Disease Resistance by Simões, Isaura, Faro, Rosário, Bur, Daniel, Faro, Carlos

“…The Arabidopsis thaliana constitutive disease resistance 1 (CDR1) gene product is an aspartic proteinase that has been implicated in disease resistance…”
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An atypical aspartic protease modulates lateral root development in Arabidopsis thaliana by Soares, André, Niedermaier, Stefan, Faro, Rosário, Loos, Andreas, Manadas, Bruno, Faro, Carlos, Huesgen, Pitter F, Cheung, Alice Y, Simões, Isaura

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Protocol for the Characterization of the Cytosine-Adenine-Guanine Tract and Flanking Polymorphisms in Machado-Joseph Disease by Lopes, Sara M., Faro, Rosário, Lopes, Miguel M., Onofre, Isabel, Mendonça, Nuno, Ribeiro, Joana, Januário, Cristina, Nobre, Rui Jorge, Pereira de Almeida, Luís

“…Polyglutamine spinocerebellar ataxias (SCAs) constitute a group of autosomal dominantly inherited neurodegenerative disorders with considerable phenotypic…”
Get full text