Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Susana Teijeira Bautista"'
Autor:
Tiffany W. Todd, Zachary T. McEachin, Jeannie Chew, Alexander R. Burch, Karen Jansen-West, Jimei Tong, Mei Yue, Yuping Song, Monica Castanedes-Casey, Aishe Kurti, Judith H. Dunmore, John D. Fryer, Yong-Jie Zhang, Beatriz San Millan, Susana Teijeira Bautista, Manuel Arias, Dennis Dickson, Tania F. Gendron, María-Jesús Sobrido, Matthew D. Disney, Gary J. Bassell, Wilfried Rossoll, Leonard Petrucelli
Publikováno v:
Cell Reports, Vol 31, Iss 5, Pp - (2020)
Summary: A G4C2 hexanucleotide repeat expansion in an intron of C9orf72 is the most common cause of frontal temporal dementia and amyotrophic lateral sclerosis (c9FTD/ALS). A remarkably similar intronic TG3C2 repeat expansion is associated with spino
Externí odkaz:
https://doaj.org/article/a1385bc8f994442d9c1094bb8a16c0d4
Autor:
Maria Grazia Biferi, Mathilde Cohen-Tannoudji, Andrea García-Silva, Olga Souto-Rodríguez, Irene Viéitez-González, Beatriz San-Millán-Tejado, Andrea Fernández-Carrera, Tania Pérez-Márquez, Susana Teijeira-Bautista, Soraya Barrera, Vanesa Domínguez, Thibaut Marais, África González-Fernández, Martine Barkats, Saida Ortolano
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss , Pp 1-17 (2021)
Fabry disease is a rare X-linked disorder affecting α-galactosidase A, a rate-limiting enzyme in lysosomal catabolism of glycosphingolipids. Current treatments present important limitations, such as low half-life and limited distribution, which gene
Externí odkaz:
https://doaj.org/article/b2d13278a02c48deb45d598f9f6bd188
Autor:
Martine Barkats, Irene Viéitez-González, África González-Fernández, Mathilde Cohen-Tannoudji, Andrea Fernandez-Carrera, Beatriz San-Millán-Tejado, Maria Grazia Biferi, Vanesa Domínguez, Saida Ortolano, Susana Teijeira-Bautista, Olga Souto-Rodriguez, Tania Pérez-Márquez, Thibaut Marais, Soraya Barrera, Andrea Garcia-Silva
Publikováno v:
Investigo. Repositorio Institucional de la Universidade de Vigo
Universidade de Vigo (UVigo)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods and Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 20, pp.1-17. ⟨10.1016/j.omtm.2020.10.016⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 20, pp.1-17. ⟨10.1016/j.omtm.2020.10.016⟩
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 1-17 (2021)
Universidade de Vigo (UVigo)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy-Methods and Clinical Development
Molecular Therapy-Methods and Clinical Development, 2021, 20, pp.1-17. ⟨10.1016/j.omtm.2020.10.016⟩
Molecular Therapy-Methods and Clinical Development, Nature Publishing Group, 2021, 20, pp.1-17. ⟨10.1016/j.omtm.2020.10.016⟩
Molecular Therapy: Methods & Clinical Development, Vol 20, Iss, Pp 1-17 (2021)
Fabry disease is a rare X-linked disorder affecting α-galactosidase A, a rate-limiting enzyme in lysosomal catabolism of glycosphingolipids. Current treatments present important limitations, such as low half-life and limited distribution, which gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2885db2614f355e811d45393c2dc42a5
https://linkinghub.elsevier.com/retrieve/pii/S2329050120302205
https://linkinghub.elsevier.com/retrieve/pii/S2329050120302205
Autor:
Tiffany W. Todd, Yuping Song, Wilfried Rossoll, Susana Teijeira Bautista, María Jesús Sobrido, Yong Jie Zhang, Monica Castanedes-Casey, Gary J. Bassell, Alexander R. Burch, Matthew D. Disney, Karen Jansen-West, Beatriz San Millán, Jimei Tong, Manuel Arias, Jeannie Chew, John D. Fryer, Judith Dunmore, Leonard Petrucelli, Mei Yue, Tania F. Gendron, Aishe Kurti, Zachary T. McEachin, Dennis W. Dickson
Publikováno v:
Cell Rep
Cell Reports, Vol 31, Iss 5, Pp-(2020)
Cell Reports, Vol 31, Iss 5, Pp-(2020)
A G(4)C(2) hexanucleotide repeat expansion in an intron of C9orf72 is the most common cause of frontal temporal dementia and amyotrophic lateral sclerosis (c9FTD/ALS). A remarkably similar intronic TG(3)C(2) repeat expansion is associated with spinoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f315aa6ae3c41dccf4c15d47469833c4
https://pubmed.ncbi.nlm.nih.gov/32375043
https://pubmed.ncbi.nlm.nih.gov/32375043
Autor:
Manuel Seijo Martínez, Carmen Navarro Fernández-Balbuena, Beatriz San Millán Tejado, Beatriz San Millán, Susana Teijeira Bautista, Begoña Iglesias Rodríguez
Publikováno v:
Alzheimer. Realidades e investigación en demencia. :5-12
Background: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common inherited cause of stroke and vascular dementia in adults. Objective: to report the histopathological and ultrastructu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9325c9265d5bab1b580664ba959ac954
https://doi.org/10.5538/1137-1242.2011.48.5
https://doi.org/10.5538/1137-1242.2011.48.5