Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Marina Riera"'
Publikováno v:
Migraciones, Iss 52, Pp 31-57 (2021)
In this research we review academic publications on media and political discourse about migration published in Spain between 2014 and 2019. The review has been carried out following the principles of the Rapid Review and Rapid Evidence Assessment of
Externí odkaz:
https://doaj.org/article/92a4f93e07424b28869a4fcc93fbb1cc
Autor:
Marina Riera-Retamero, Fernando Hernández-Hernández, Silvia de Riba-Mayoral, Paula Lozano-Mulet, Paula Estalayo-Bielsa
Publikováno v:
Antípoda: Revista de Antropología y Arqueología, Vol 43, Pp 164-192 (2021)
This article is part of the European Migrant Children and Communities in a Transforming Europe (MiCreate) project. The text is intended to a) explore and describe how young migrants describe their experiences and life trajectories through artistic me
Externí odkaz:
https://doaj.org/article/16539a25d2624656adfa8d3e271284ca
Autor:
Judit Domingo-Prim, Víctor Abad-Morales, Marina Riera, Rafael Navarro, Borja Corcostegui, Esther Pomares
Publikováno v:
Stem Cell Research, Vol 40, Iss , Pp - (2019)
Incomplete achromatopsia (ACHM) is a disorder in which there is function defect of cone photoreceptors in the retina and individuals with such disease retain residual color vision. Here, we have generated an induced pluripotent stem cell (iPSC) line
Externí odkaz:
https://doaj.org/article/8ed68ca01604433783380fdba10d5920
Autor:
Judit Domingo-Prim, Marina Riera, Víctor Abad-Morales, Sheila Ruiz-Nogales, Borja Corcostegui, Esther Pomares
Publikováno v:
Stem Cell Research, Vol 40, Iss , Pp - (2019)
Best disease, also known as Best vitelliform macular dystrophy, is an autosomal dominant form of macular degeneration. Here, we have generated an induced pluripotent stem cell (iPSC) line derived from a Best disease patient carrying a new dominant mu
Externí odkaz:
https://doaj.org/article/8b3b5105d92048eba75d69621c8ddd4b
Publikováno v:
Stem Cell Research, Vol 38, Iss , Pp - (2019)
Retinitis pigmentosa (RP) is an inherited retinal dystrophy characterized by the progressive degeneration of photoreceptors. In the present study, we have generated an induced pluripotent stem cell (iPSC) line derived from a RP patient with a dominan
Externí odkaz:
https://doaj.org/article/94863a7ae28b4c099f5d4638c26dc42e
Autor:
Marina Riera, Achchhe Patel, Anniken Burés-Jelstrup, Borja Corcostegui, Stanley Chang, Esther Pomares, Barbara Corneo, Janet R. Sparrow
Publikováno v:
Stem Cell Research, Vol 36, Iss , Pp - (2019)
Recessive Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy, caused by mutations in the retina-specific ATP-binding cassette transporter (ABCA4) gene, which plays a role as a retinaldehyde flippase in the photoreceptor outer segme
Externí odkaz:
https://doaj.org/article/5a942f5ff53041a7bee35e65747b6434
Autor:
Marina Riera, Achchhe Patel, Borja Corcostegui, Stanley Chang, Barbara Corneo, Janet R. Sparrow, Esther Pomares
Publikováno v:
Stem Cell Research, Vol 35, Iss , Pp - (2019)
A human induced pluripotent stem cell (iPSC) line was generated from a female patient affected by autosomal recessive retinitis pigmentosa with two mutations in the USH2A gene: c.2209C > T (p.Arg737Ter) and c.8693A > C (p.Tyr2898Ser). Skin fibroblast
Externí odkaz:
https://doaj.org/article/3422b5ba16d44af79ef31d9c5adc7ab5
Autor:
Marina Riera, Achchhe Patel, Borja Corcostegui, Stanley Chang, Janet R. Sparrow, Esther Pomares, Barbara Corneo
Publikováno v:
Stem Cell Research, Vol 35, Iss , Pp - (2019)
Retinitis pigmentosa (RP) refers to a clinical and genetic heterogeneous group of inherited retinal degenerations characterized by photoreceptor cell death. In this work, we have generated an induced pluripotent stem cell (iPSC) line derived from a R
Externí odkaz:
https://doaj.org/article/ed4229bf45944482a62aff926f15ee70
Autor:
Marina Riera, Laura Fontrodona, Silvia Albert, Diana Mora Ramirez, Anna Seriola, Anna Salas, Yolanda Muoz, David Ramos, Maria Paz Villegas-Perez, Miguel Angel Zapata, Angel Raya, Jesus Ruberte, Anna Veiga, Jose Garcia-Arumi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 3, Iss C (2016)
Retinal dystrophies (RD) are major causes of familial blindness and are characterized by progressive dysfunction of photoreceptor and/or retinal pigment epithelium (RPE) cells. In this study, we aimed to evaluate and compare the therapeutic effects o
Externí odkaz:
https://doaj.org/article/3000da71943b4821abf456a575ba5838
Autor:
Alihamze Fathinajafabadi, Eva Pérez-Jiménez, Marina Riera, Erwin Knecht, Roser Gonzàlez-Duarte
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e87898 (2014)
The function of CERKL (CERamide Kinase Like), a causative gene of retinitis pigmentosa and cone-rod dystrophy, still awaits characterization. To approach its cellular role we have investigated the subcellular localization and interaction partners of
Externí odkaz:
https://doaj.org/article/137b022134104c63822854c025b0a0c2