Mostrando resultados 60 a 75 de 75
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Derechos | Preview | Fecha Public. | Título | Autor(es) | Tipo |
closedAccess | | mar-2013 | Neurexin and neuroligin genes in Alzheimer's disease | Ruiz, Agustín; Martínez Mir, Amalia CSIC ORCID; González-Pérez, Antonio; Gayán, Javier; Antúnez, Carmen; Marín, Juan J. CSIC; Boada, Mercè; López-Arrieta, Jesús; Fernández, Evaristo; Ramírez Lorca, Reposo CSIC ORCID; Sáez, María Eugenia; Scholl, Francisco G.; Real, Luis Miguel CSIC ORCID | póster de congreso |
closedAccess | | 14-jul-2005 | Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions | Ashoor, G.; Greenstein, Robert M.; Lam, H.; Martínez Mir, Amalia CSIC ORCID; Zlotogorski, Abraham; Christiano, Angela M. | artículo |
closedAccess | | oct-2002 | Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa | Paloma, Eva; Martínez Mir, Amalia CSIC ORCID; García-Sandoval, Blanca; Ayuso, Carmen; Vilageliu, L.; González-Duarte, Roser; Balcells, Susana | artículo |
closedAccess | | nov-2015 | Nueva mutación del gen MYH7 causante de la miopatía distal de Laing en Andalucía | Carbonell-Corvillo, Pilar; Martínez Mir, Amalia CSIC ORCID; Paradas, Carmen CSIC ORCID | comunicación de congreso |
openAccess | | 2010 | Papel de la proteína de adhesión sináptica neurexina 1 en autismo | Camacho García, R. J. CSIC; Pecero López, M. L. CSIC; Servián Morilla, E. CSIC ORCID; Planelles Fernández, I.; Margalef Estivil, M.; Meléndez Cadenas, Ricardo CSIC; Vilella, Elisabet; Martínez Mir, Amalia CSIC ORCID; Gómez Scholl, F. CSIC ORCID | comunicación de congreso |
openAccess | | 1997 | Putative association of a mutant ROM1 allele with retinitis pigmentosa | Martínez Mir, Amalia CSIC ORCID; Vilela, Concha; Bayés, Mónica; Valverde, Diana; Dain, L.; Beneyto, Magdalena; Marco, Marina; Baiget, Montserrat; Grinberg, Daniel; Balcells, Susana; González-Duarte, Roser; Vilageliu, L. | artículo |
closedAccess | | dic-2013 | Rare variants analysis of neurexin-1β in autism reveals a novel start codon mutation affecting protein levels at synapses | Camacho García, R. J. CSIC; Hervás, Amaia; Toma, Claudio; Balmana, Noemí; Cormand, Bru; Martínez Mir, Amalia CSIC ORCID; Scholl, Francisco G. | artículo |
openAccess | | ene-1998 | Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR | Martínez Mir, Amalia CSIC ORCID; Paloma, Eva; Allikmets, Rando; Ayuso, Carmen; Río, Teresa del; Dean, Michael; Vilageliu, L.; González-Duarte, Roser; Balcells, Susana | artículo |
openAccess | | 2005 | Search for Susceptibility Genes in Alopecia Areata | Martínez Mir, Amalia CSIC ORCID; Zlotogorski, Abraham; Christiano, Angela M. | comunicación de congreso |
openAccess | | ene-2022 | Selective expression of the neurexin substrate for presenilin in the adult forebrain causes deficits in associative memory and presynaptic plasticity | Sánchez-Hidalgo, Ana C. CSIC; Arias-Aragón, Francisco; Romero-Barragán, M. Teresa; Martín-Cuevas, Celia CSIC ORCID CVN; Delgado-García, José M.; Martínez Mir, Amalia CSIC ORCID | artículo |
openAccess | | 5-jun-2008 | Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy | Carranza, Daniel; Martínez Mir, Amalia CSIC ORCID; Macaya Ruiz, A. | artículo |
closedAccess | | 25-may-2001 | Spectrum of ABCA4 (ABCR) gene mutations in Spanish patients with autosomal recessive macular dystrophies | Paloma, Eva; Martínez Mir, Amalia CSIC ORCID; Vilageliu, L.; González-Duarte, Roser; Balcells, Susana | artículo |
closedAccess | | 1997 | Strategies for the genetic analysis of autosomal recessive retinitis pigmentosa in Spanish families | González-Duarte, Roser; Bayés, Mónica; Martínez Mir, Amalia CSIC ORCID; Valverde, Diana; Balcells, Susana; Baiget, Montserrat; Vilageliu, L.; Grinberg, Daniel | capítulo de libro |
openAccess | | 16-jun-2023 | Supplemental information. A Neuroligin-1 mutation associated with Alzheimer’s disease produces memory and age-dependent impairments in hippocampal plasticity | Arias-Aragón, Francisco; Tristán Clavijo, E. CSIC; Martínez-Gallego, Irene; Robles Lanuza, Estefanía CSIC; Coatl-Cuaya, Heriberto; Martín-Cuevas, Celia CSIC ORCID CVN; Sánchez-Hidalgo, Ana C. CSIC; Rodríguez-Moreno, Antonio CSIC ORCID; Martínez Mir, Amalia CSIC ORCID; Scholl, Francisco G. | dataset |
closedAccess | | 2003 | The first non-LTR retrotransposon characterised in the cephalochordate amphioxus, BfCR1, shows similarities to CR1-like elements | Albalat, Ricard; Permanyer, J.; Cañestro, Cristian; Martínez Mir, Amalia CSIC ORCID; González-Angulo, O.; González-Duarte, Roser | artículo |
closedAccess | | oct-2013 | The inactivation of PS activity affects vesicle release at neurexinneuroligin synapsis by abnormal processing of neurexins | Servián Morilla, E. CSIC ORCID; Camacho García, R. J. CSIC; Robles Lanuza, Estefanía CSIC; Martínez Mir, Amalia CSIC ORCID; Gómez Scholl, F. CSIC ORCID | póster de congreso |