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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2010, Volume 107, Issue 26, pp. 11841 - 11846
Journal Article
by Xiol, C and Vidal, S and Pascual-Alonso, A and Blasco, L and Brandi, N and Pacheco, P and Gerotina, E and O'Callaghan, M and Pineda, M and Armstrong, J and Aguirre, FJ and Aleu, M and Alonso, X and Alsius, M and Amoros, M and Antinolo, G and Aquino, L and Arellano, C and Arriola, G and Arteaga, R and Baena, N and Barcos, M and Belzunces, N and Boronat, S and Camacho, T and Campistol, J and del Campo, M and Campo, A and Cancho, R and Candau, R and Canos, I and Carrascosa, MD and Carratala-Marco, F and Casano, J and Castro, P and Cobo, A and Colomer, J and Conejo, D and Corrales, MJ and Cortes, R and Cruz, G and Csanyi, G and de Santos, MT and de Toledo, M and Del Campo, M and Del Toro, M and Domingo, R and Duat, A and Duque, R and Esparza, AM and Fernandez, R and Fons, MC and Fontalba, A and Galan, E and Gallano, P and Gamundi, MJ and Garcia, PL and Garcia, MD and Garcia-Barcina, M and Garcia-Catalan, MJ and Garcia-Cazorla, A and Garcia-Minaur, S and Garcia-Penas, JJ and Garcia-Silva, MT and Gassio, R and Gean, E and Gil, B and Gokben, S and Gonzalez, L and Gonzalez, V and Gonzalez, J and Gonzalez, G and Guillen, E and Guitart, M and Guitet, M and Gutierrez, JM and Gutierrez, E and Herranz, JL and Iglesias, G and Karacic, I and Lahoz, CH and Lao, JI and Lapunzina, P and Lautre-Ecenarro, MJ and Lluch, MD and Lopez, L and Lopez-Ariztegui, A and Macaya, A and Marin, R and Marquez, CML and Martin, E and Martinez, B and Martinez-Salcedo, E and Mas, MJ and Mateo, G and Mendez, P and Jimenez, AM and Moreno, S and Mulas, F and Narbona, J and ... and Rett Working Grp and Rett Working Group
SCIENTIFIC REPORTS, ISSN 2045-2322, 08/2019, Volume 9, Issue 1, pp. 11983 - 9
Rett syndrome (RTT) is a severe neurological disorder usually caused by mutations in the MECP2 gene. Since the MECP2 gene is located on the X chromosome, X... 
MECP2 MUTATIONS | PATTERNS | METHYLATION | GENE | MULTIDISCIPLINARY SCIENCES | BRAIN | Phenotypes | Transcription | Phenotypic variations | Blood | Neurological diseases | Methyl-CpG binding protein | MeCP2 protein | X Chromosomes | Rett syndrome | Alleles | Mutation | Methylation | Chromosomes
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Autoimmunity, ISSN 0891-6934, 02/2016, Volume 49, Issue 2, pp. 102 - 108
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Science, ISSN 0036-8075, 8/2012, Volume 337, Issue 6094, pp. 529 - 530
  Eukaryotic genomes are populated by invading mobile genetic elements called transposons that threaten genome stability as they may cause mutations and... 
Transposons | Messenger RNA | Germ cells | RNA | PERSPECTIVES | Genomes | Outsourcing | Binding sites | PIRNAS | GERMLINE | EPIGENETIC MEMORY | MULTIDISCIPLINARY SCIENCES | Proteins | Ribonucleic acid--RNA | Mutations | Stability | Ribonucleic acids | Genetics | Worms
Journal Article
Critical Care, ISSN 1364-8535, 02/2015, Volume 19, Issue 1, pp. 59 - 59
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Journal Article
Gastroenterologia y Hepatologia, ISSN 0210-5705, 11/2016, Volume 39, Issue 9, pp. 607 - 626
Cirrhotic patients often develop severe complications requiring ICU admission. Grade III-IV hepatic encephalopathy, septic shock, acute-on-chronic liver... 
Variceal bleeding | Acute-on-chronic liver failure | Prognosis | Severe sepsis | Acute kidney injury | Hepatic encephalopathy
Journal Article
GASTROENTEROLOGIA Y HEPATOLOGIA, ISSN 0210-5705, 11/2016, Volume 39, Issue 9, pp. 607 - 626
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 06/2010, Volume 107, Issue 26, p. 11841
  Piwi-interacting RNAs (piRNAs) are essential for silencing of transposable elements in the germline, but their biogenesis is poorly understood. Here we... 
Proteins | Rodents | Genetics | Biosynthesis | Mutation | Cells
Journal Article