DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease von Barallobre, M J, Perier, C, Bové, J, Laguna, A, Delabar, J M, Vila, M, Arbonés, M L

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Plasma DYRK1A as a novel risk factor for Alzheimer’s disease von Janel, N, Sarazin, M, Corlier, F, Corne, H, de Souza, L C, Hamelin, L, Aka, A, Lagarde, J, Blehaut, H, Hindié, V, Rain, J-C, Arbones, M L, Dubois, B, Potier, M C, Bottlaender, M, Delabar, J M

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Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/− mouse von Benavides-Piccione, R., Dierssen, M., Ballesteros-Yáñez, I., Martínez de Lagrán, M., Arbonés, M.L., Fotaki, V., DeFelipe, J., Elston, G.N.

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Dyrk1A Haploinsufficiency Affects Viability and Causes Developmental Delay and Abnormal Brain Morphology in Mice von Fotaki, Vassiliki, Dierssen, Mara, Alcántara, Soledad, Martínez, Salvador, Martí, Eulàlia, Casas, Caty, Visa, Joana, Soriano, Eduardo, Estivill, Xavier, Arbonés, Maria L.

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MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss von Melchionda, Salvatore, Ahituv, Nadav, Bisceglia, Luigi, Sobe, Tama, Glaser, Fabian, Rabionet, Raquel, Arbones, Maria Lourdes, Notarangelo, Angelo, Di Iorio, Enzo, Carella, Massimo, Zelante, Leopoldo, Estivill, Xavier, Avraham, Karen B., Gasparini, Paolo

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene von RABIONET, R, ZELANTE, L, LOPEZ-BIGAS, N, D'AGRUMA, L, MELCHIONDA, S, RESTAGNO, G, ARBONES, M. L, GASPARINI, P, ESTIVILL, X

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Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis von Feliubadaló, Lídia, Arbonés, María Lourdes, Mañas, Sandra, Chillarón, Josep, Visa, Joana, Rodés, Margot, Rousaud, Ferran, Zorzano, Antonio, Palacín, Manuel, Nunes, Virginia

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Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment von LOPEZ-BIGAS, Nuria, OLIVE, Montserrat, FERRER, Isidre, ARBONES, Maria Lourdes, ESTIVILL, Xavier, RABIONET, Raquel, BEN-DAVID, Orit, MARTINEZ-MATOS, Juan Antonio, BRAVO, Olga, BANCHS, Isabel, VOLPINI, Victor, GASPARINI, Paolo, AVRAHAM, Karen B

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Sequential contribution of L- and P-selectin to leukocyte rolling in vivo von Ley, K, Bullard, D C, Arbonés, M L, Bosse, R, Vestweber, D, Tedder, T F, Beaudet, A L

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Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice von Arbonés, Maria L., Ord, David C., Ley, Klaus, Ratech, Howard, Maynard-Curry, Catherine, Otten, Gib, Capon, Daniel J., Teddert, Thomas F.

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Connexin mutations in hearing loss, dermatological and neurological disorders von Rabionet, Raquel, López-Bigas, Núria, Arbonès, Maria Lourdes, Estivill, Xavier

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Dopaminergic deficiency in mice with reduced levels of the dual‐specificity tyrosine‐phosphorylated and regulated kinase 1A, Dyrk1A+ von Martinez de Lagran, M., Bortolozzi, A., Millan, O., Gispert, J. D., Gonzalez, J. R., Arbones, M. L., Artigas, F., Dierssen, M.

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Gene targeting in normal somatic cells: inactivation of the interferon–γ receptor in myoblasts von Arbonés, Maria L., Austin, Harry A., Capon, Daniel J., Greenburg, Gary

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Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome von Pucharcós, Carles, Fuentes, Juan-José, Casas, Caty, de la Luna, Susana, Alcántara, Soledad, Arbonés, Maria L, Soriano, Eduardo, Estivill, Xavier, Pritchard, Melanie

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Characteristics of nitric oxide synthase type I of rat cerebellar astrocytes von Arbonés, Maria Lourdes, Ribera, Joan, Agulló, Luis, Baltrons, Maria Antonia, Casanovas, Anna, Riveros-Moreno, Valentina, García, Agustina

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Expression of the Type VI Secretion System 1 Component Hcp1 Is Indirectly Repressed by OpaR in Vibrio parahaemolyticus von Ma, Lizhi, Zhang, Yiquan, Yan, Xiaojuan, Guo, Liping, Wang, Li, Qiu, Jingfu, Yang, Ruifu, Zhou, Dongsheng

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[P1.27]: Dyrk1A gene dosage controls developmental cell death of the mesencephalic dopaminergic neurons von Barallobre, M.J., Laguna, A., Ramirez‐Bautista, E., Arbones, M.L.

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Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S r... von López-Bigas, N., Rabionet, R., Martinez, E., Bravo, O., Girons, J., Borragan, A., Pellicer, M., Arbonés, M.L., Estivill, X.

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Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression von THÖNNISSEN, Eva, RABIONET, Raquel, ARBONES, Maria Lourdes, ESTIVILL, Xavier, WILLECKE, Klaus, OTT, Thomas

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Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patients von WATTENHOFER, Marie, DI IORIO, Mario Vincenzo, D'AMELIO, Marcello, ALWAN, Sura, ROSSIER, Colette, DAHL, Hans-Henrik M, PETERSEN, Michael B, ESTIVILL, Xavier, GASPARINI, Paolo, SCOTT, Hamish S, ANTONARAKIS, Stylianos E, RABIONET, Raquel, DOUGHERTY, Loretta, PAMPANOS, Andreas, SCHWEDE, Torsten, MONTSERRAT-SENTIS, Barbara, ARBONES, Maria Lourdes, ILIADES, Theofilos, PASQUADIBISCEGLIE, Annamaria

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