Výsledky vyhledávání - "Proteínas Mutantes"

Construcción de proteína quimérica de proteína verde fluorescente y calpaína 10

Autor: Rojas Meza, Lucía Alana

Las calpaínas son proteasas dependientes de calcio de la familia de las cistein proteasas, cuya participación en enfermedades neurodegenerativas está siendo documentada y estudiada. En nuestro laboratorio se han encontrado evidencias de la interac

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3932::5fda3714285736b170ebd9a0cf9208d9
https://hdl.handle.net/20.500.12866/6616

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Changes in the hemagglutinin of H5N1 viruses during human infection - Influence on receptor binding

Publikováno v: RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
Virology, 447(1-2), 326-337. Academic Press Inc.
Virology

As avian influenza A(H5N1) viruses continue to circulate in Asia and Africa, global concerns of an imminent pandemic persist. Recent experimental studies suggest that efficient transmission between humans of current H5N1 viruses only requires a few g

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2606a1d216ab72da7642929cdfbc9b73
https://doi.org/10.1016/j.virol.2013.08.010

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Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis

Autor: Carmen Cenit, Maria, Marquez, Ana, Cordero-Coma, Miguel, Fonollosa, Alejandro, Llorenc, Victor, Artaraz, Joseba, Diaz Valle, David, Blanco, Ricardo, Canal, Joaquin, Salom, David, Garcia Serrano, Jose Luis, Ramon, Enrique, Jose Del Rio, Maria, Begona Gorrono-Echebarria, Marina, Manuel Martin-Villa, Jose, Molins, Blanca, Ortego-Centeno, Norberto, Javier Martin

Publikováno v: Europe PubMed Central
Scopus-Elsevier
MOLECULAR VISION
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Molecular Vision
ResearcherID

Journal Article; OBJECTIVE Endogenous uveitis is a major cause of visual loss mediated by the immune system. The protein tyrosine phosphatase non-receptor type 22 (PTPN22) gene encodes a lymphoid-specific phosphatase that plays a key role in T-cell r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::069944b4bf4e181dfe92c8b521f21ea5
https://hdl.handle.net/10668/1590

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Mutation analysis in breast cancer cases and study of P53 mutated protein; tumor fisiopathological aspects

Autor: Levy, Claudia Bustamante

Publikováno v: Biblioteca Digital de Teses e Dissertações da UERJ
Universidade do Estado do Rio de Janeiro (UERJ)
instacron:UERJ

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Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3056::589a2ac0fbe7af907d7bb6c2a04d5d8b
http://www.bdtd.uerj.br/handle/1/7888

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Human MAMLD1 gene variations seem not sufficient to explain a 46,XY DSD phenotype

Autor: Camats Tarruella, Núria, Fernández Cancio, Mónica, Audí, Laura, Mullis, Primus E., Moreno, Francisca, González Casado, Isabel, López-Siguero, Juan Pedro, Corripio, Raquel, Bermúdez de la Vega, José Antonio, Blanco, José Antonio, Flück, Christa E., Universitat Autònoma de Barcelona

Publikováno v: PLoS One
PLoS ONE
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Camats Tarruella, Núria; Fernández-Cancio, Mónica; Audí, Laura; Mullis, Primus-Eugen; Moreno, Francisca; González Casado, Isabel; López-Siguero, Juan Pedro; Corripio, Raquel; Bermúdez de la Vega, José Antonio; Blanco, José Antonio; Flück, Christa Emma (2015). Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype. PLoS ONE, 10(11), e0142831. Public Library of Science 10.1371/journal.pone.0142831
PLoS ONE, Vol 10, Iss 11, p e0142831 (2015)

Ajuts: Swiss National Science Foundation (320030-146127), the Instituto de Salud Carlos III CIBERER U-712, i the University and Research Management and Evaluation Agency (2009SGR31) MAMLD1 is thought to cause disordered sex development in 46,XY patie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7b69ae641bdf12c1daf404bc12df341
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0142831

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