Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Leticia Olavarrieta"'
Autor:
Javier Martínez-Sanz, Manuel Ponce-Alonso, Laura Martínez-García, Víctor de la Cueva, Leticia Olavarrieta, Laura Montero, María Jesús Pérez-Elías, Juan Carlos Galán
Publikováno v:
International Journal of Infectious Diseases, Vol 137, Iss , Pp 111-113 (2023)
Several possible mpox reinfections have been reported, however, the debate on whether these are confirmed reinfections remains open.A 30-year-old male living with HIV and a history of single-dose mpox vaccination, first diagnosed with mpox in Septemb
Externí odkaz:
https://doaj.org/article/b81ec94238d547deba07535bcac42e38
Autor:
Jesús, García-Fernández, Susana, Vilches-Arroyo, Leticia, Olavarrieta, Julián, Pérez-Pérez, Santiago, Rodríguez de Córdoba
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2227
The regulators of complement activation (RCA) gene cluster in 1q31-1q32 includes most of the genes encoding complement regulatory proteins. Genetic variability in the RCA gene cluster frequently involve copy number variations (CNVs), a type of chromo
Autor:
Santiago Rodríguez de Córdoba, Julián Pérez-Pérez, Jesús García-Fernández, Leticia Olavarrieta, Susana Vilches-Arroyo
Publikováno v:
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
The Complement System ISBN: 9781071610152
Consejo Superior de Investigaciones Científicas (CSIC)
Digital.CSIC. Repositorio Institucional del CSIC
instname
The Complement System ISBN: 9781071610152
20 p.-6 fig.-3 tab.
The regulators of complement activation (RCA) gene cluster in 1q31-1q32 includes most of the genes encoding complement regulatory proteins. Genetic variability in the RCA gene cluster frequently involve copy number variations
The regulators of complement activation (RCA) gene cluster in 1q31-1q32 includes most of the genes encoding complement regulatory proteins. Genetic variability in the RCA gene cluster frequently involve copy number variations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d45f598d0e7c3daa32a6290b0946163
http://hdl.handle.net/10261/239514
http://hdl.handle.net/10261/239514
Autor:
Maximino Abraldes, Estefanía Cobos, Alicia Valverde, Luis Arias, Sergio Recalde, Jaouad Anter, Marta Suarez-Figueroa, Julián Pérez-Pérez, Leticia Olavarrieta, Carla Barreales, Maria Hernandez-Sanchez, Fernando Cruz, Patricia Fernandez-Robredo, Alfredo García-Layana
Publikováno v:
Acta Ophthalmologica. 96:e201-e212
Purpose We sought to determine if specific genetic single nucleotide polymorphisms (SNPs) influence vascular endothelial growth factor inhibition response to ranibizumab in neovascular age-related macular degeneration (AMD). Methods A total of 403 Ca
Autor:
Pablo E. Hernández, Leticia Olavarrieta, Jorge Bernardo Schvartzman, José Sogo, Andrzej Stasiak, Dora B. Krimer, María Luisa Martínez-Robles
Publikováno v:
Nucleic Acids Research, vol. 30, no. 3, pp. 656-666
Scopus-Elsevier
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scopus-Elsevier
Digital.CSIC. Repositorio Institucional del CSIC
instname
11 páginas, 8 figuras, -- PAGS nros.656-666
To study the structure of partially replicated plasmids, we cloned the Escherichia coli polar replication terminator TerE in its active orientation at different locations in the ColE1 vector pBR18. Th
To study the structure of partially replicated plasmids, we cloned the Escherichia coli polar replication terminator TerE in its active orientation at different locations in the ColE1 vector pBR18. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61a5e039b29f7894a1e677762d552b79
http://doc.rero.ch/record/293748/files/gkf150.pdf
http://doc.rero.ch/record/293748/files/gkf150.pdf
Autor:
Maria Paz Zafra, Leticia Olavarrieta, Roberto Zarrabeitia, Julián Pérez-Pérez, Virginia Albiñana, Lucía Recio-Poveda, Luisa María Botella, Jorge Colau
Publikováno v:
BMC Medical Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
[Background] Hereditary hemorrhagic telangiectasia (HHT) is a vascular multi-organ system disorder. Its diagnostic criteria include epistaxis, telangiectases in mucocutaneous sites, arteriovenous malformations (AVMs), and familial inheritance. HHT is
Autor:
Leticia Olavarrieta, Matías Morín, Tamas Dalmay, Nick Redshaw, Karen P. Steel, Ángeles Mencía, Ignacio del Castillo, Felipe Moreno, Fernando Mayo-Merino, Luis A. Aguirre, Silvia Modamio-Høybjør, M A Moreno-Pelayo
Publikováno v:
Nature Genetics. 41:609-613
Miguel Moreno-Pelayo and colleagues report mutations in the seed region of human miR-96 segregating with progressive hearing loss in two families. In an accompanying paper, Karen Steel and colleagues show that the mouse diminuendo mutant, which also
Autor:
Ángeles Mencía, Richard J. Goodyear, M A Moreno-Pelayo, Silvia Modamio-Høybjør, Leticia Olavarrieta, Felipe Moreno, P. Kevin Legan, Guy P. Richardson
Publikováno v:
Journal of the Association for Research in Otolaryngology. 9:202-214
The TECTA gene encodes alpha-tectorin (TECTA), a major noncollagenous component of the tectorial membrane (TM). In humans, mutations in TECTA lead to either dominant (DFNA8/A12) or recessive (DFNB21) forms of nonsyndromic hearing loss. All missense m
Autor:
Pablo E. Hernández, Leticia Olavarrieta, María Luisa Martínez-Robles, Dora B. Krimer, Jorge Bernardo Schvartzman
Publikováno v:
Molecular Microbiology. 46:699-707
The topology of plasmid DNA changes continuously as replication progresses. But the dynamics of the process remains to be fully understood. Knotted bubbles form when topo IV knots the daughter duplexes behind the fork in response to their degree of i
Autor:
Rubén, Martínez-Barricarte, Sergio, Recalde, Patricia, Fernández-Robredo, Isabel, Millán, Leticia, Olavarrieta, Antonio, Viñuela, Julián, Pérez-Pérez, Alfredo, García-Layana, Santiago, Rodríguez de Córdoba, Rosa, Sanabría
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
31 p.-4 fig.-4 tab.
Purpose. Age-related macular degeneration (AMD) has a strong genetic component with a major locus at 1q31, including the complement factor H (CFH) gene. Detailed analyses of this locus have demonstrated the existence of one S
Purpose. Age-related macular degeneration (AMD) has a strong genetic component with a major locus at 1q31, including the complement factor H (CFH) gene. Detailed analyses of this locus have demonstrated the existence of one S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::835b44f0f6ae1aca367ee8b2bcb859fe
http://hdl.handle.net/10261/60639
http://hdl.handle.net/10261/60639