Sequence-based prediction of pathological mutations by Ferrer-Costa, C., Orozco, M., de la Cruz, X.

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An Atomistic View to the Gas Phase Proteome by Meyer, Tim, de la Cruz, Xavier, Orozco, Modesto

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First international workshop of the ATM and cancer risk group (4-5 December 2019) by Lesueur, Fabienne, Easton, Douglas F., Renault, Anne-Laure, Tavtigian, Sean V., Bernstein, Jonine L., Kote-Jarai, Zsofia, Eeles, Rosalind A., Plaseska-Karanfia, Dijana, Feliubadaló, Lidia, Arun, Banu, Herold, Natalie, Versmold, Beatrix, Schmutzler, Rita Katharina, Nguyen-Dumont, Tú, Southey, Melissa C., Dorling, Leila, Dunning, Alison M., Ghiorzo, Paola, Dalmasso, Bruna Samia, Cavaciuti, Eve, Le Gal, Dorothée, Roberts, Nicholas J., Dominguez-Valentin, Mev, Rookus, Matti, Taylor, Alexander M. R., Goldstein, Alisa M., Goldgar, David E., Stoppa-Lyonnet, Dominique, Andrieu, Nadine

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Prediction of pathological mutations in proteins: the challenge of integrating sequence conservation and structure stability principles by Riera, Casandra, Lois, Sergio, de la Cruz, Xavier

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hSos1 Contains a New Amino-terminal Regulatory Motif with Specific Binding Affinity for Its Pleckstrin Homology Domain by Jorge, Rocío, Zarich, Natasha, Oliva, José Luis, Azañedo, Marta, Martínez, Natalia, de la Cruz, Xavier, Rojas, José M

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Loss of microRNA-135b Enhances Bone Metastasis in Prostate Cancer and Predicts Aggressiveness in Human Prostate Samples by Olivan, Mireia, Garcia, Marta, Suárez, Leticia, Guiu, Marc, Gros, Laura, Méndez, Olga, Rigau, Marina, Reventós, Jaume, Segura, Miguel F, de Torres, Inés, Planas, Jacques, de la Cruz, Xavier, Gomis, Roger R, Morote, Juan, Rodríguez-Barrueco, Ruth, Santamaria, Anna

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hSos1 contains a new amino-terminal regulatory motif with specific binding affinity for its pleckstrin homology domain by Jorge, Rocío, Zarich, Natasha, Oliva, José Luis, Azañedo, Marta, Martínez, Natalia, de la Cruz, Xavier, Rojas, José M

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Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Consequences Illustrated in Two Families with Novel Homozygous CFI Mutations by Franco-Jarava, Clara, Álvarez de la Campa, Elena, Solanich, Xavier, Morandeira-Rego, Francisco, Mas-Bosch, Virgínia, García-Prat, Marina, de la Cruz, Xavier, Martín-Nalda, Andrea, Soler-Palacín, Pere, Hernández-González, Manuel, Colobran, Roger

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Molecular damage in Fabry disease: Characterization and prediction of alpha-galactosidase A pathological mutations by Riera, Casandra, Lois, Sergio, Domínguez, Carmen, Fernandez-Cadenas, Israel, Montaner, Joan, Rodríguez-Sureda, Victor, de la Cruz, Xavier

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Do protein motifs read the histone code? by de la Cruz, Xavier, Lois, Sergio, Sánchez-Molina, Sara, Martínez-Balbás, Marian A.

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Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties by Ferrer-Costa, Carles, Orozco, Modesto, de la Cruz, Xavier

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Clinical and structural impact of mutations affecting the residue Phe367 of FOXP3 in patients with IPEX syndrome by Colobran, Roger, Álvarez de la Campa, Elena, Soler-Palacín, Pere, Martín-Nalda, Andrea, Pujol-Borrell, Ricardo, de la Cruz, Xavier, Martínez-Gallo, Mónica

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CORRELATION ANALYSIS OF miRNA AND mRNA EXPRESSION PROFILES IN PERIPHERAL BLOOD MONONUCLEAR CELLS FROM ADHD PATIENTS AND CONTROLS by Sanchez-Mora, Cristina, Garcia-Martínez, Iris, Pagerols, Mireia, Soler, María, Rovira, Paula, Calvo, Eva, Padilla, Natalia, Richarte, Vanessa, Corrales, Montse, Franke, Barbara, de la Cruz, Xavier, Casas, Miguel, Cormand, Bru, Ramos-Quiroga, JA, Arias-Vásquez, Alejandro, Ribases, Marta

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SU2 - CORRELATION ANALYSIS OF miRNA AND mRNA EXPRESSION PROFILES IN PERIPHERAL BLOOD MONONUCLEAR CELLS FROM ADHD PATIENTS AND CONTROLS by Sanchez-Mora, Cristina, Garcia-Martínez, Iris, Pagerols, Mireia, Soler, María, Rovira, Paula, Calvo, Eva, Padilla, Natalia, Richarte, Vanessa, Corrales, Montse, Franke, Barbara, de la Cruz, Xavier, Casas, Miguel, Cormand, Bru, Ramos-Quiroga, JA, Arias-Vásquez, Alejandro, Ribases, Marta

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F5EPIGENETIC SIGNATURE FOR ATTENTION DEFICIT HYPERACTIVITY DISORDER: IDENTIFICATION OF MIR-23A-5P, MIR-26B-5P, MIR-185-5P AND MIR-191-5P AS A POTENTIAL BIOMARKER IN PERIPHERAL BLOO... by Sanchez-Mora, Cristina, Artigas, Maria Soler, Garcia-Martínez, Iris, Pagerols, Mireia, Rovira, Paula, Corrales, Montse, Fadeuilhe, Christian, Padilla, Natalia, de la Cruz, Xavier, Frankex, Barbara, Arias-Vásquez, Alejandro, Casas, Miguel, Ramos-Quiroga, Josep-Antoni, Ribasés, Marta

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Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome by Carreño-Gago, Lidia, Gamez, Josep, Cámara, Yolanda, Alvarez de la Campa, Elena, Aller-Alvarez, Juan Sebastian, Moncho, Dulce, Salvado, Maria, Galan, Alicia, de la Cruz, Xavier, Pinós, Tomàs, García-Arumí, Elena

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Triplex‐forming oligonucleotide target sequences in the human genome by Goñi, J. Ramon, de la Cruz, Xavier, Orozco, Modesto

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Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema by Colobran, Roger, Lois, Sergio, de la Cruz, Xavier, Pujol-Borrell, Ricardo, Hernández-González, Manuel, Guilarte, Mar

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Molecular damage in F abry disease: Characterization and prediction of alpha‐galactosidase A pathological mutations by Riera, Casandra, Lois, Sergio, Domínguez, Carmen, Fernandez‐Cadenas, Israel, Montaner, Joan, Rodríguez‐Sureda, Victor, de la Cruz, Xavier

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Molecular dynamics study of natural existing cavity couplings in proteins by Barbany, Montserrat, Meyer, Tim, Hospital Gasch, Adam, Faustino Pló, Ignacio, D´Abramo, Marco, Morata Chirivella, Jordi, Orozco López, Modesto, Cruz, Xavier de la

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