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2005 1
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Page 1
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative.
Luque J, Mendes I, Gómez B, Morte B, López de Heredia M, Herreras E, Corrochano V, Bueren J, Gallano P, Artuch R, Fillat C, Pérez-Jurado LA, Montoliu L, Carracedo Á, Millán JM, Webb SM, Palau F; CIBERER Network; Lapunzina P. Luque J, et al. Clin Genet. 2022 May;101(5-6):481-493. doi: 10.1111/cge.14113. Epub 2022 Feb 4. Clin Genet. 2022. PMID: 35060122 Free PMC article. Review.
Newer generations of multi-target CAR and STAb-T immunotherapeutics: NEXT CART Consortium as a cooperative effort to overcome current limitations.
Martín-Antonio B, Blanco B, González-Murillo Á, Hidalgo L, Minguillón J, Pérez-Chacón G; Next Generation CART MAD Consortium. Martín-Antonio B, et al. Among authors: minguillon j. Front Immunol. 2024 May 8;15:1386856. doi: 10.3389/fimmu.2024.1386856. eCollection 2024. Front Immunol. 2024. PMID: 38779672 Free PMC article. Review.
Development of a mouse model for spontaneous oral squamous cell carcinoma in Fanconi anemia.
Errazquin R, Page A, Suñol A, Segrelles C, Carrasco E, Peral J, Garrido-Aranda A, Del Marro S, Ortiz J, Lorz C, Minguillon J, Surralles J, Belendez C, Alvarez M, Balmaña J, Bravo A, Ramirez A, Garcia-Escudero R. Errazquin R, et al. Among authors: minguillon j. Oral Oncol. 2022 Nov;134:106184. doi: 10.1016/j.oraloncology.2022.106184. Epub 2022 Sep 30. Oral Oncol. 2022. PMID: 36191479 Free article.
Fanconi-like anemia related to a FANCM mutation.
Encarnación JA, Cerezuela P, Español I, García MR, Manso C, De la Fuente I, Garrigós N, Viney A, Minguillon J, Surrallés J. Encarnación JA, et al. Among authors: minguillon j. Eur J Med Genet. 2022 Jan;65(1):104399. doi: 10.1016/j.ejmg.2021.104399. Epub 2021 Nov 15. Eur J Med Genet. 2022. PMID: 34793962
Stress Assessment by Prefrontal Relative Gamma.
Minguillon J, Lopez-Gordo MA, Pelayo F. Minguillon J, et al. Front Comput Neurosci. 2016 Sep 22;10:101. doi: 10.3389/fncom.2016.00101. eCollection 2016. Front Comput Neurosci. 2016. PMID: 27713698 Free PMC article.
Prognostic significance of mutation type and chromosome fragility in Fanconi anemia.
Ramírez MJ, Pujol R, Minguillón J, Bogliolo M, Persico I, Cavero D, de la Cal A, Río P, Navarro S, Casado JA, Bailador A, de la Fuente AS, de Heredia ML, Almazán F, Antelo ML, Argilés B, Badell I, Baragaño M, Beléndez C, Bermúdez M, Bernués M, Buedo MI, Carrasco E, Català A, Costa D, Cuesta I, Fernandez-Delgado R, Fernández-Teijeiro A, Figuera Á, García M, Gondra A, González M, Muñiz SG, Hernández-Rodríguez I, Ibañez F, Kelleher NJ, Lendínez F, López M, López-Almaraz R, Marchante I, Mendoza C, Nieto J, Ojeda E, Payán-Pernía S, Peláez I, de Soto IP, Portugal R, Ramos-Arroyo MA, Regueiro A, Rodríguez A, Rosell J, Saez R, Sánchez J, Sánchez M, Senent M, Tapia M, Trujillo-Quintero JP, Vagace JM, Verdú-Amorós J, Verdugo V, Vidales I, Villarreal J, Díaz-de-Heredia C, Sevilla J, Bueren JA, Surrallés J. Ramírez MJ, et al. Among authors: minguillon j. Am J Hematol. 2025 Feb;100(2):272-284. doi: 10.1002/ajh.27520. Epub 2024 Nov 19. Am J Hematol. 2025. PMID: 39562502 Free PMC article.
39 results