Mostrando resultados 162 a 172 de 172
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| Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
| closedAccess |  | 2014 | The familial dementia gene revisited: a missense mutation revealed by whole exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family | Audo, Isabelle; Bhattacharya, Shom Shanker CSIC ORCID; Zeitz, Christina | artículo |
| closedAccess |  | 2019 | The Resveratrol Prodrug JC19 Delays Retinal Degeneration in rd10 Mice | Valdés-Sánchez, María Lourdes; García-Delgado, Ana B. CSIC; Montero-Sánchez, Adoración CSIC; Cerda, Berta de la CSIC ORCID; Lucas, Ricardo CSIC; Peñalver, Pablo CSIC ORCID; Morales, Juan C.; Bhattacharya, Shom Shanker CSIC ORCID; Díaz-Corrales, Francisco J. CSIC ORCID | capítulo de libro |
| openAccess |  | 2016 | TOPORS, a dual E3 ubiquitin and Sumo1 ligase, interacts with 26 S protease regulatory subunit 4, encoded by the PSMC1 gene | Czub, Barbara; Shah, Amna Z.; Alfano, Giovanna; Kruczek, P.M.; Chakarova, Christina; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess |  | 1-mar-2011 | TOPORS, implicated in retinal degeneration, is a cilia-centrosomal protein | Chakarova, Christina; Ríos, Rosa M. CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| openAccess |  | 2016 | Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosa | Rose, Anna M.; Shah, Amna Z.; Venturini, Giulia; Krishna, Abhay CSIC; Chakravarti, Aravinda; Rivolta, Carlo; Bhattacharya, Shom Shanker CSIC ORCID | artículo |
| closedAccess |  | sep-2010 | Transplanted Oligodendrocytes and Motoneuron Progenitors Generated from Human Embryonic Stem Cells Promote Locomotor Recovery After Spinal Cord Transection | Erceg, Slaven; Bhattacharya, Shom Shanker CSIC ORCID; Stojkovic, Miodrag | artículo |
| openAccess |  | 2011 | Triptico Cartera de Servicios de las Unidades de Apoyo de Cabimer | Aguilera, Andrés CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID; Soria Escoms, Bernat CSIC ORCID; Ríos, Rosa M. CSIC ORCID | presentación |
| openAccess |  | 2011 | Triptico divulgativo Unidad Genómica CABIMER | Aguilera, Andrés CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID; Ríos, Rosa M. CSIC ORCID; Soria Escoms, Bernat CSIC ORCID | presentación |
| openAccess |  | 2011 | Triptico divulgativo Unidad Producción Celular CABIMER | Soria Escoms, Bernat CSIC ORCID; Aguilera, Andrés CSIC ORCID; Ríos, Rosa M. CSIC ORCID; Bhattacharya, Shom Shanker CSIC ORCID | presentación |
| closedAccess |  | feb-2021 | WDR34, a candidate gene for non-syndromic rod-cone dystrophy | Solaguren-Beascoa, María; Bujakowska, Kinga; Méjécase, Cécile; Emmenegger, Lisa; Orhan, Elise; Neuillé, Marion; Mohand-Saïd, Saddek; Condroyer, Christel; Lancelot, Marie-Elise; Michiels, Christelle; Demontant, Vanessa; Antonio, Aline; Letexier, Mélanie; Saraiva, Jean-Paul; Lonjou, Christine; Carpentier, Wassila; Léveillard, Thierry; Pierce, Eric A.; Dollfus, Hélène; Sahel, José-Alain; Bhattacharya, Shom Shanker CSIC ORCID; Audo, Isabelle; Zeitz, Christina | artículo |
| closedAccess |  | 10-feb-2012 | Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness | Audo, Isabelle; Bhattacharya, Shom Shanker CSIC ORCID; Zeitz, Christina | artículo |
