TitleDateReferenceDOI
Zonation of Ribosomal DNA Transcription Defines a Stem Cell Hierarchy in Colorectal Cancer2020-06-04Morral, C; Stanisavljevic, J; Hernando-Momblona, X; Mereu, E; Alvarez-Varela, A; Cortina, C; Stork, D; Slebe, F; Turon, G; Whissell, G; Sevillano, M; (2020). Zonation of Ribosomal DNA Transcription Defines a Stem Cell Hierarchy in Colorectal Cancer. Cell Stem Cell, 26(6), 845-+. DOI: 10.1016/j.stem.2020.04.012https://doi.org/10.1016/j.stem.2020.04.012
Benchmarking single-cell RNA-sequencing protocols for cell atlas projects2020-06-01Mereu, E; Lafzi, A; Moutinho, C; Ziegenhain, C; McCarthy, DJ; Alvarez-Varela, A; Batlle, E; Sagar; Grün, D; Lau, JK; Boutet, SC; Sanada, C; Ooi, A; Jo (2020). Benchmarking single-cell RNA-sequencing protocols for cell atlas projects. Nature Biotechnology, 38(6), 747-+. DOI: 10.1038/s41587-020-0469-4https://doi.org/10.1038/s41587-020-0469-4
Metagenomic analysis of a blood stain from the French revolutionary Jean-Paul Marat (1743-1793)2020-06-01de-Dios, T; van Dorp, L; Charlier, P; Morfopoulou, S; Lizano, E; Bon, C; Le Bitouzé, C; Alvarez-Estape, M; Marquès-Bonet, T; Balloux, F; Lalueza-Fox, (2020). Metagenomic analysis of a blood stain from the French revolutionary Jean-Paul Marat (1743-1793). Infection Genetics And Evolution, 80(), 104209-. DOI: 10.1016/j.meegid.2020.104209https://doi.org/10.1016/j.meegid.2020.104209
Genomic adaptations to aquatic and aerial life in mayflies and the origin of insect wings2020-05-26Almudi, I; Vizueta, J; Wyatt, CDR; de Mendoza, A; Marlétaz, F; Firbas, PN; Feuda, R; Masiero, G; Medina, P; Alcaina-Caro, A; Cruz, F; Gómez-Garrido, J (2020). Genomic adaptations to aquatic and aerial life in mayflies and the origin of insect wings. Nature Communications, 11(1), 2631-. DOI: 10.1038/s41467-020-16284-8https://doi.org/10.1038/s41467-020-16284-8
Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples2020-05-25Esteller-Cucala, P; Maceda, I; Borglum, AD; Demontis, D; Faraone, SV; Cormand, B; Lao, O (2020). Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples. Scientific Reports, 10(1), 8622-. DOI: 10.1038/s41598-020-65322-4https://doi.org/10.1038/s41598-020-65322-4
Transcriptional activation during cell reprogramming correlates with the formation of 3D open chromatin hubs2020-05-22Di Stefano, M; Stadhouders, R; Farabella, I; Castillo, D; Serra, F; Graf, T; Marti-Renom, MA (2020). Transcriptional activation during cell reprogramming correlates with the formation of 3D open chromatin hubs. Nature Communications, 11(1), 2564-. DOI: 10.1038/s41467-020-16396-1https://doi.org/10.1038/s41467-020-16396-1
Extreme differences between human germline and tumor mutation densities are driven by ancestral human-specific deviations2020-05-19Heredia-Genestar, JM; Marquès-Bonet, T; Juan, D; Navarro, A (2020). Extreme differences between human germline and tumor mutation densities are driven by ancestral human-specific deviations. Nature Communications, 11(1), 2512-. DOI: 10.1038/s41467-020-16296-4https://doi.org/10.1038/s41467-020-16296-4
The evolutionary history of extinct and living lions2020-05-19de Manuel, M; Barnett, R; Sandoval-Velasco, M; Yamaguchi, N; Vieira, FG; Mendoza, MLZ; Liu, SP; Martin, MD; Sinding, MHS; Mak, SST; Caroe, C; Liu, SL; (2020). The evolutionary history of extinct and living lions. Proceedings Of The National Academy Of Sciences Of The United States Of America, 117(20), 10927-10934. DOI: 10.1073/pnas.1919423117https://doi.org/10.1073/pnas.1919423117
Sampling time-dependent artifacts in single-cell genomics studies2020-05-11Massoni-Badosa, R; Iacono, G; Moutinho, C; Kulis, M; Palau, N; Marchese, D; Rodríguez-Ubreva, J; Ballestar, E; Rodriguez-Esteban, G; Marsal, S; Aymeri (2020). Sampling time-dependent artifacts in single-cell genomics studies. Genome Biology, 21(1), 112-. DOI: 10.1186/s13059-020-02032-0https://doi.org/10.1186/s13059-020-02032-0
Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks2020-05-07Madrid-Mencía, M; Raineri, E; Cao, TBN; Pancaldi, V (2020). Using GARDEN-NET and ChAseR to explore human haematopoietic 3D chromatin interaction networks. Nucleic Acids Research, 48(8), 4066-4080. DOI: 10.1093/nar/gkaa159https://doi.org/10.1093/nar/gkaa159
4D Genome Rewiring during Oncogene-Induced and Replicative Senescence2020-05-07Sati, S; Bonev, B; Szabo, Q; Jost, D; Bensadoun, P; Serra, F; Loubiere, V; Papadopoulos, GL; Rivera-Mulia, JC; Fritsch, L; Bouret, P; Castillo, D; Gel (2020). 4D Genome Rewiring during Oncogene-Induced and Replicative Senescence. Molecular Cell, 78(3), 522-+. DOI: 10.1016/j.molcel.2020.03.007https://doi.org/10.1016/j.molcel.2020.03.007
Tetracycline resistance transmission in Campylobacter is promoted at temperatures resembling the avian reservoir2020-05-01Cuevas-Ferrando, E; Guirado, P; Miró, E; Iglesias-Torrens, Y; Navarro, F; Alioto, TS; Gómez-Garrido, J; Madrid, C; Balsalobre, C (2020). Tetracycline resistance transmission in Campylobacter is promoted at temperatures resembling the avian reservoir. Veterinary Microbiology, 244(), 108652-. DOI: 10.1016/j.vetmic.2020.108652https://doi.org/10.1016/j.vetmic.2020.108652
Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing2020-05-01Batlle-Masó, L; Mensa-Vilaró, A; Solís-Moruno, M; Marquès-Bonet, T; Arostegui, JI; Casals, F (2020). Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencing. European Journal Of Medical Genetics, 63(5), 103920-. DOI: 10.1016/j.ejmg.2020.103920https://doi.org/10.1016/j.ejmg.2020.103920
Identification of tipifarnib sensitivity biomarkers in T-cell acute lymphoblastic leukemia and T-cell lymphoma2020-04-21Alonso-Alonso, R; Mondéjar, R; Martínez, N; García-Diaz, N; Pérez, C; Merino, D; Rodríguez, M; Esteve-Codina, A; Fuste, B; Gut, M; Burrows, F; Scholz, (2020). Identification of tipifarnib sensitivity biomarkers in T-cell acute lymphoblastic leukemia and T-cell lymphoma. Scientific Reports, 10(1), 6721-. DOI: 10.1038/s41598-020-63434-5https://doi.org/10.1038/s41598-020-63434-5
Multiple acyl-coenzyme A dehydrogenase deficiency shows a possible founder effect and is the most frequent cause of lipid storage myopathy in Iran2020-04-15Nilipour, Y; Fatehi, F; Sanatinia, S; Bradshaw, A; Duff, J; Lochmüller, H; Horvath, R; Nafissi, S (2020). Multiple acyl-coenzyme A dehydrogenase deficiency shows a possible founder effect and is the most frequent cause of lipid storage myopathy in Iran. Journal Of The Neurological Sciences, 411(), 116707-. DOI: 10.1016/j.jns.2020.116707https://doi.org/10.1016/j.jns.2020.116707
A single nucleotide deletion resulting in a frameshift in exon 4 of TAB2 is associated with a polyvalular syndrome2020-04-01Permanyer, E; Laurie, S; Blasco-Lucas, A; Maldonado, G; Amador-Catalan, A; Ferrer-Curriu, G; Fuste, B; Perez, ML; Gonzalez-Alujas, T; Beltran, S; Coma (2020). A single nucleotide deletion resulting in a frameshift in exon 4 of TAB2 is associated with a polyvalular syndrome. European Journal Of Medical Genetics, 63(4), 103854-. DOI: 10.1016/j.ejmg.2020.103854https://doi.org/10.1016/j.ejmg.2020.103854
The dental proteome of Homo antecessor2020-04-01Welker, F; Ramos-Madrigal, J; Gutenbrunner, P; Mackie, M; Tiwary, S; Jersie-Christensen, RR; Chiva, C; Dickinson, MR; Kuhlwilm, M; de Manuel, M; Gelab (2020). The dental proteome of Homo antecessor. Nature, 580(7802), 235-+. DOI: 10.1038/s41586-020-2153-8https://doi.org/10.1038/s41586-020-2153-8
Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients2020-04-01Capitanio, D; Moriggi, M; Torretta, E; Barbacini, P; De Palma, S; Viganó, A; Lochmüller, H; Muntoni, F; Ferlini, A; Mora, M; Gelfi, C (2020). Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients. Journal Of Cachexia Sarcopenia And Muscle, 11(2), 547-563. DOI: 10.1002/jcsm.12527https://doi.org/10.1002/jcsm.12527
Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophy2020-04-01Signorelli, M; Ayoglu, B; Johansson, C; Lochmüller, H; Straub, V; Muntoni, F; Niks, E; Tsonaka, R; Persson, A; Aartsma-Rus, A; Nilsson, P; Al-Khalili (2020). Longitudinal serum biomarker screening identifies malate dehydrogenase 2 as candidate prognostic biomarker for Duchenne muscular dystrophy. Journal Of Cachexia Sarcopenia And Muscle, 11(2), 505-517. DOI: 10.1002/jcsm.12517https://doi.org/10.1002/jcsm.12517
Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene2020-04-01Bonanno, C; Rodolico, C; Töpf, A; Foti, FM; Liu, WW; Beeson, D; Toscano, A; Lochmuller, H (2020). Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene. Neuromuscular Disorders, 30(4), 336-339. DOI: 10.1016/j.nmd.2020.02.012https://doi.org/10.1016/j.nmd.2020.02.012