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10/09/2021 Improved collection of hematopoietic stem cells and progenitors from Fanconi anemia patients for gene therapy purposes
Sevilla, J, Navarro, S, Rio, P, Sanchez-Dominguez, R, Zubicaray, J, Galvez, E, Merino, E, Sebastian, E, Azqueta, C, Casado, JA, Segovia, JC, Alberquilla, O, Bogliolo, M, Roman-Rodriguez, FJ, Gimenez, Y, Larcher, L, Salgado, R, Pujol, RM, Hladun, R, Castillo, A, Soulier, J, Querol, S, Fernandez, J, Schwartz, J, de Andoin, NG, Lopez, R, Catala, A, Surralles, J, Diaz-de-Heredia, C, Bueren, JA. Improved collection of hematopoietic stem cells and progenitors from Fanconi anemia patients for gene therapy purposes. Molecular Therapy-Methods & Clinical Development. 2021; 22DOI:10.1016/j.omtm.2021.06.001. PMID:34485595. IF:5.849(Q2/4D).
09/09/2021 Clinical consequences of BRCA2 hypomorphism
Castells-Roca, L, Gutierrez-Enriquez, S, Bonache, S, Bogliolo, M, Carrasco, E, Aza-Carmona, M, Montalban, G, Munoz-Subirana, N, Pujol, R, Cruz, C, Llop-Guevara, A, Ramirez, MJ, Saura, C, Lasa, A, Serra, V, Diez, O, Balmana, J, Surralles, J. Clinical consequences of BRCA2 hypomorphism. npj Breast Cancer. 2021; 7(1)DOI:10.1038/s41523-021-00322-9. PMID:34504103. IF:7.519(Q1/3D).
07/09/2021 The impact of the COVID-19 pandemic on Sexually Transmitted Infections surveillance data: incidence drop or artefact?
Sentis, A, Prats-Uribe, A, Lopez-Corbeto, E, Montoro-Fernandez, M, Nomah, DK, de Olalla, PG, Mercuriali, L, Borrell, N, Guadalupe-Fernandez, V, Reyes-Uruena, J, Casabona, J, Catalan HIV STI Surveillance Grp. The impact of the COVID-19 pandemic on Sexually Transmitted Infections surveillance data: incidence drop or artefact?. BMC PUBLIC HEALTH. 2021; 21(1)DOI:10.1186/s12889-021-11630-x. PMID:34493244. IF:4.135(Q2/4D).
07/09/2021 The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (vol 7, 12288, 2021)
Vidal, S, Brandi, N, Pacheco, P, Gerotina, E, Blasco, L, Trotta, JR, Derdak, S, O'Callaghan, MD, Garcia-Cazorla, A, Pineda, M, Armstrong, J, Cortes, R., Gallano P., Villar, Cristina. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome (vol 7, 12288, 2021). Scientific Reports. 2021; 11(1)DOI:10.1038/s41598-021-97262-y. PMID:34493777. IF:4.997(Q2/3D).