Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Irene Sanchez-Martin"'
The dengue virus 4 component of NIAID’s tetravalent TV003 vaccine drives its innate immune signature
Autor:
Jessica Pintado Silva, Rafael Fenutria, Dabeiba Bernal-Rubio, Irene Sanchez-Martin, Annika Hunziker, Eva Chebishev, Jeury Veloz, Geoffrey Kelly, Seunghee Kim-Schulze, Steve Whitehead, Anna Durbin, Irene Ramos, Ana Fernandez-Sesma
Publikováno v:
Exp Biol Med (Maywood)
Annually, roughly 2.5 billion people are at risk for dengue virus (DENV) infection, and the incidence of infection has increased 30-fold since its discovery in the 1900s. At present, there are no globally licensed antiviral treatments or vaccines tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10890aa72c3401006aa5efc5bdad269
https://doi.org/10.1177/15353702231151241
https://doi.org/10.1177/15353702231151241
Autor:
Laurent Fasano, Colette Denis, Guylène Feuillet, Andy Saurin, Ahmed Fatmi, Thien Phong Vu Manh, Petra Zürbig, Joost P. Schanstra, Irene Sanchez-Martin, Xavier Caubit, Fabrice Richard, Pedro Magalhães
Renal tract defects and autism spectrum disorder (ASD) deficits represent the phenotypic core of the 19q12 deletion syndrome caused by the loss of one copy of the TSHZ3 gene. While a proportion of Tshz3 heterozygous (Tshz3+/lacZ) mice display uretera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7fa07821ba7d49d9e9d4985e463b7f5
https://halshs.archives-ouvertes.fr/halshs-03410717
https://halshs.archives-ouvertes.fr/halshs-03410717
Autor:
Irene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad, Ahmed Fatmi, Fabrice Richard, Thien Phong Vu Manh, Andrew J Saurin, Guylène Feuillet, Colette Denis, Adrian S Woolf, Joost P Schanstra, Petra Zürbig, Xavier Caubit, Laurent Fasano
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, In press, ⟨10.1093/hmg/ddab362⟩
Human Molecular Genetics, In press, ⟨10.1093/hmg/ddab362⟩
Renal tract defects and autism spectrum disorder (ASD) deficits represent the phenotypic core of the 19q12 deletion syndrome caused by the loss of one copy of the TSHZ3 gene. Although a proportion of Tshz3 heterozygous (Tshz3+/lacZ) mice display uret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5da62227f52ef83a9d01003d53c964f
https://pubmed.ncbi.nlm.nih.gov/34919690
https://pubmed.ncbi.nlm.nih.gov/34919690
Autor:
Josep Quer, Qian Chen, Ana Isabel de Ávila, Irene Sanchez-Martin, Celia Perales, Isabel Gallego, Inés Palacios-Blanco, Jordi Gómez, María Eugenia Soria, Brenda Martínez-González, Damir Garcia-Cehic, Soumaya Khalfaoui, Josep Gregori, Patricia Martínez-Barragán, Carlos Briones, Esteban Domingo, Juan Ignacio Esteban, Carlos García-Crespo
Publikováno v:
DIGITAL.INTA Repositorio Digital del Instituto Nacional de Técnica Aeroespacial
instname
J Virol
Instituto Nacional de Técnica Aeroespacial (INTA)
Digital.CSIC. Repositorio Institucional del CSIC
instname
J Virol
Instituto Nacional de Técnica Aeroespacial (INTA)
Digital.CSIC. Repositorio Institucional del CSIC
Previous studies documented that long-term hepatitis C virus (HCV) replication in human hepatoma Huh-7.5 cells resulted in viral fitness gain, expansion of the mutant spectrum, and several phenotypic alterations. In the present work, we show that mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::365c1db20d15a1a051ce923950f2b9db
http://hdl.handle.net/20.500.12666/417
http://hdl.handle.net/20.500.12666/417
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1926
Microarrays and RNA-seq (RNA sequencing) are powerful techniques to assess transcript abundance in biological samples and to improve our understanding of the relationship between genotype and phenotype. Tshz3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bdba0ae19bd0f21c5d8fbbefb0847001
https://pubmed.ncbi.nlm.nih.gov/30742275
https://pubmed.ncbi.nlm.nih.gov/30742275
Publikováno v:
Kidney Organogenesis Methods and Protocols
Seppo Vainio. Kidney Organogenesis Methods and Protocols, 1926, Springer, pp.223-232, 2019, Methods in Molecular Biology, 978-1-4939-9020-7. ⟨10.1007/978-1-4939-9021-4_18⟩
Methods in Molecular Biology ISBN: 9781493990207
Seppo Vainio. Kidney Organogenesis Methods and Protocols, 1926, Springer, pp.223-232, 2019, Methods in Molecular Biology, 978-1-4939-9020-7. ⟨10.1007/978-1-4939-9021-4_18⟩
Methods in Molecular Biology ISBN: 9781493990207
International audience; Microarrays and RNA-seq (RNA sequencing) are powerful techniques to assess transcript abundance in biological samples and to improve our understanding of the relationship between genotype and phenotype. Tshz3+/- heterozygous m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::049a3c2c95df2a7a269222ccad2e935f
https://hal.archives-ouvertes.fr/hal-02048084
https://hal.archives-ouvertes.fr/hal-02048084