Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ana Quelle-Regaldie"'
Autor:
Ana Quelle-Regaldie, Nerea Gandoy-Fieiras, Paula Rodríguez-Villamayor, Sandra Maceiras, Ana Paula Losada, Mónica Folgueira, Pablo Cabezas-Sáinz, Antón Barreiro-Iglesias, María Villar-López, María Isabel Quiroga-Berdeal, Laura Sánchez, María Jesús Sobrido
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
Niemann Pick disease type C (NPC) is an autosomal recessive neurodegenerative lysosomal disorder characterized by an accumulation of lipids in different organs. Clinical manifestations can start at any age and include hepatosplenomegaly, intellectual
Externí odkaz:
https://doaj.org/article/404006b531494bb6951427f80b353822
Autor:
María Cascallar, Pablo Hurtado, Saínza Lores, Alba Pensado-López, Ana Quelle-Regaldie, Laura Sánchez, Roberto Piñeiro, María de la Fuente
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Gene therapy is a promising therapeutic approach that has experienced significant groth in recent decades, with gene nanomedicines reaching the clinics. However, it is still necessary to continue developing novel vectors able to carry, protect, and r
Externí odkaz:
https://doaj.org/article/e65a6b54df4a4838819891d2bebc0861
Publikováno v:
Pharmaceutics, Vol 15, Iss 4, p 1247 (2023)
The aim of this work was to develop niosomes for the ocular delivery of epalrestat, a drug that inhibits the polyol pathway and protects diabetic eyes from damage linked to sorbitol production and accumulation. Cationic niosomes were made using polys
Externí odkaz:
https://doaj.org/article/9eb6001a427e4a1fa8da5b7eb6f57987
Autor:
Ana Quelle-Regaldie, Mónica Folgueira, Julián Yáñez, Daniel Sobrido-Cameán, Anabel Alba-González, Antón Barreiro-Iglesias, María-Jesús Sobrido, Laura Sánchez
Publikováno v:
Biomedicines, Vol 10, Iss 8, p 1814 (2022)
NOP56 belongs to a C/D box small nucleolar ribonucleoprotein complex that is in charge of cleavage and modification of precursor ribosomal RNAs and assembly of the 60S ribosomal subunit. An intronic expansion in NOP56 gene causes Spinocerebellar Atax
Externí odkaz:
https://doaj.org/article/38becb75c315468aad98a62531318ebb
Autor:
Ana Quelle-Regaldie, Daniel Sobrido-Cameán, Antón Barreiro-Iglesias, María Jesús Sobrido, Laura Sánchez
Publikováno v:
Cells, Vol 10, Iss 4, p 836 (2021)
Autosomal recessive ataxias are much less well studied than autosomal dominant ataxias and there are no clearly defined systems to classify them. Autosomal recessive ataxias, which are characterized by neuronal and multisystemic features, have signif
Externí odkaz:
https://doaj.org/article/6393713a50534a869ad9a0bc1c5b7ae2
Autor:
Ana Quelle-Regaldie, Daniel Sobrido-Cameán, Antón Barreiro-Iglesias, María Jesús Sobrido, Laura Sánchez
Publikováno v:
Cells, Vol 10, Iss 2, p 421 (2021)
Hereditary dominant ataxias are a heterogeneous group of neurodegenerative conditions causing cerebellar dysfunction and characterized by progressive motor incoordination. Despite many efforts put into the study of these diseases, there are no effect
Externí odkaz:
https://doaj.org/article/45b96895f02f4f5e807912a5d880b9c3
Autor:
Ana Quelle-Regaldie, Nerea Gandoy-Fieiras, Paula Rodríguez-Villamayor, Sandra Maceiras, Ana Paula Losada, Mónica Folgueira, Pablo Cabezas-Sáinz, Antón Barreiro-Iglesias, María Villar-López, María Isabel Quiroga Berdeal, Laura Sánchez, María-Jesús Sobrido
Niemann Pick disease type C (NPC) is an autosomal recessive neurodegenerative lysosomal disorder characterized by an accumulation of lipids in different organs. Clinical manifestations can start at any age and include hepatosplenomegaly, intellectual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8bf9375de7f071db5bd18d6a6c6a987
https://doi.org/10.1101/2023.02.09.527822
https://doi.org/10.1101/2023.02.09.527822
Autor:
Ana, Quelle-Regaldie, Mónica, Folgueira, Julián, Yáñez, Daniel, Sobrido-Cameán, Anabel, Alba-González, Antón, Barreiro-Iglesias, María-Jesús, Sobrido, Laura, Sánchez
Publikováno v:
Biomedicines. 10(8)
NOP56 belongs to a C/D box small nucleolar ribonucleoprotein complex that is in charge of cleavage and modification of precursor ribosomal RNAs and assembly of the 60S ribosomal subunit. An intronic expansion in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2915bdde524994fb5fe4eb14d599f294
https://pubmed.ncbi.nlm.nih.gov/36009362
https://pubmed.ncbi.nlm.nih.gov/36009362
Autor:
Ismael Hernández-Núñez, Maria Vivero-Lopez, Ana Quelle-Regaldie, Willem J. DeGrip, Laura Sánchez, Angel Concheiro, Carmen Alvarez-Lorenzo, Eva Candal, Antón Barreiro-Iglesias
Publikováno v:
Histochemistry and Cell Biology, 158, 401-409
Histochemistry and Cell Biology, 158, 4, pp. 401-409
Histochemistry and Cell Biology, 158, 4, pp. 401-409
Diabetic retinopathy (DR) is one of the leading causes of blindness in the world. While there is a major focus on the study of juvenile/adult DR, the effects of hyperglycemia during early retinal development are less well studied. Recent works in emb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f82263816f79c22210eb587bdd6a6538
https://doi.org/10.21203/rs.3.rs-1621911/v1
https://doi.org/10.21203/rs.3.rs-1621911/v1
Autor:
Maria Vivero-Lopez, Chiara Sparacino, Ana Quelle-Regaldie, Laura Sánchez, Eva Candal, Antón Barreiro-Iglesias, Fernando Huete-Toral, Gonzalo Carracedo, Ana Otero, Angel Concheiro, Carmen Alvarez-Lorenzo
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
instname
Ocular health may strongly benefit from the supply of antioxidant agents that counteract free radicals and reactive oxygen species responsible for long-term eye diseases. Additionally, natural antioxidants like resveratrol can inhibit bacteria growth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d54bf352803e6e1bf7e12ac7f84c1b9d
https://hdl.handle.net/10347/29383
https://hdl.handle.net/10347/29383