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Autor: Alvarez-Baena, N., Carrera, R., Thompson, H., Balaguer-Nuñez, L., Bragaglia, A., Jordi, C., Silva-Villa, E., Vallenari, A.

Publikováno v: Astronomy & Astrophysics / Astronomie et Astrophysique; 7/15/2024, Vol. 687, p1-16, 16p

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Autor: Amer, N., Cabezón, M., Xicoy, B., Garrido, A., Baena, N., Canet, M., Arnan, M., Arenillas, L., Coll, R., Ortin, X., Diaz, M., Talarn, C., García-Caro, M., Zamora, L., Bargay, J.

Publikováno v: In Leukemia Research May 2023 128 Supplement

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Autor: García-Rodríguez, S., Alba-Baena, N., Rudolph, N.M., Wellekoetter, J., Li, X.C., Osswald, T.A.

Publikováno v: In Journal of Manufacturing Processes August 2012 14(3):388-392

Novel germline variants of CDKN1Band CDKN2Cidentified during screening for familial primary hyperparathyroidism

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X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

Autor: Xiol C, Vidal S, Pascual-Alonso A, Blasco L, Brandi N, Pacheco P, Gerotina E, O'Callaghan M, Pineda M, Armstrong J, Aguirre F, Aleu M, Alonso X, Alsius M, Amoros M, Antinolo G, Aquino L, Arellano C, Arriola G, Arteaga R, Baena N, Barcos M, Belzunces N, Boronat S, Camacho T, Campistol J, del Campo M, Campo A, Cancho R, Candau R, Canos I, Carrascosa M, Carratala-Marco F, Casano J, Castro P, Cobo A, Colomer J, Conejo D, Corrales M, Cortes R, Cruz G, Csanyi G, de Santos M, de Toledo M, Del Campo M, Del Toro M, Domingo R, Duat A, Duque R, Esparza A, Fernandez R, Fons M, Fontalba A, Galan E, Gallano P, Gamundi M, Garcia P, Garcia M, Garcia-Barcina M, Garcia-Catalan M, Garcia-Cazorla A, Garcia-Minaur S, Garcia-Penas J, Garcia-Silva M, Gassio R, Gean E, Gil B, Gokben S, Gonzalez L, Gonzalez V, Gonzalez J, Gonzalez G, Guillen E, Guitart M, Guitet M, Gutierrez J, Gutierrez E, Herranz J, Iglesias G, Karacic I, Lahoz C, Lao J, Lapunzina P, Lautre-Ecenarro M, Lluch M, Lopez L, Lopez-Ariztegui A, Macaya A, Marin R, Marquez C, Martin E, Martinez B, Martinez-Salcedo E, Mas M, Mateo G, Mendez P, Jimenez A, Moreno S, Mulas F, Narbona J, Nascimento A, Nieto M, Nunes T, Nunez N, Obon M, Onsurbe I, Ortez C, Orts E, Martinez F, Parrilla R, Pascual S, Patino A, Perez-Poyato M, Perez-Duenas B, Poo P, Puche E, Ramos F, Raspall M, Roche A, Roldan S, Rosell J, Ruiz C, Ruiz-Falco M, Russi M, Samarra J, San Antonio V, Sanchez I, Sanmartin X, Sans A, Santacana A, Scholl-Burgi S, Serrano N, Serrano M, Martin-Tamayo P, Tendero A, Torrents J, Tortosa D, Trivino E, Troncoso L, Turon E, Vazquez P, Vazquez C, Velazquez R, Ventura C, Verdu A, Vernet A, Vila M, Villar C, Rett Working Grp

Publikováno v: Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
SCIENTIFIC REPORTS
r-FISABIO. Repositorio Institucional de Producción Científica
Scientia
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
Consejo Superior de Investigaciones Científicas (CSIC)
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)

WOS: 000481590200024
PubMed ID: 31427717
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 chromosome inactivation (XCI) could play a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1a9ab94d2dcf8ad628e2e076112113f
http://zaguan.unizar.es/record/86210