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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1992 1
1994 2
1995 3
1996 4
1997 7
1998 4
1999 5
2000 5
2001 1
2002 6
2003 5
2004 6
2005 3
2006 4
2007 8
2008 6
2009 2
2010 3
2011 6
2012 2
2013 3
2014 3
2015 7
2017 5
2018 9
2019 8
2020 7
2021 8
2022 6
2023 2
2024 0

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131 results

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Page 1
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.
Webster ALH, Sanders MA, Patel K, Dietrich R, Noonan RJ, Lach FP, White RR, Goldfarb A, Hadi K, Edwards MM, Donovan FX, Hoogenboezem RM, Jung M, Sridhar S, Wiley TF, Fedrigo O, Tian H, Rosiene J, Heineman T, Kennedy JA, Bean L, Rosti RO, Tryon R, Gonzalez AM, Rosenberg A, Luo JD, Carroll TS, Shroff S, Beaumont M, Velleuer E, Rastatter JC, Wells SI, Surrallés J, Bagby G, MacMillan ML, Wagner JE, Cancio M, Boulad F, Scognamiglio T, Vaughan R, Beaumont KG, Koren A, Imielinski M, Chandrasekharappa SC, Auerbach AD, Singh B, Kutler DI, Campbell PJ, Smogorzewska A. Webster ALH, et al. Among authors: surralles j. Nature. 2022 Dec;612(7940):495-502. doi: 10.1038/s41586-022-05253-4. Epub 2022 Nov 30. Nature. 2022. PMID: 36450981 Free PMC article.
Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations.
Castella M, Pujol R, Callén E, Trujillo JP, Casado JA, Gille H, Lach FP, Auerbach AD, Schindler D, Benítez J, Porto B, Ferro T, Muñoz A, Sevilla J, Madero L, Cela E, Beléndez C, de Heredia CD, Olivé T, de Toledo JS, Badell I, Torrent M, Estella J, Dasí A, Rodríguez-Villa A, Gómez P, Barbot J, Tapia M, Molinés A, Figuera A, Bueren JA, Surrallés J. Castella M, et al. Among authors: surralles j. Blood. 2011 Apr 7;117(14):3759-69. doi: 10.1182/blood-2010-08-299917. Epub 2011 Jan 27. Blood. 2011. PMID: 21273304 Free PMC article.
Gene therapy restores the transcriptional program of hematopoietic stem cells in Fanconi anemia.
Lasaga M, Río P, Vilas-Zornoza A, Planell N, Navarro S, Alignani D, Fernández-Varas B, Mouzo D, Zubicaray J, Pujol RM, Nicoletti E, Schwartz JD, Sevilla J, Ainciburi M, Ullate-Agote A, Surrallés J, Perona R, Sastre L, Prosper F, Gomez-Cabrero D, Bueren JA. Lasaga M, et al. Among authors: surralles j. Haematologica. 2023 Oct 1;108(10):2652-2663. doi: 10.3324/haematol.2022.282418. Haematologica. 2023. PMID: 37021532 Free PMC article.
In Memory of Professor Adayapalam T Natarajan.
Balajee AS, Palitti F, Surrallés J, Hande MP. Balajee AS, et al. Among authors: surralles j. Mutat Res Genet Toxicol Environ Mutagen. 2018 Dec;836(Pt A):1-2. doi: 10.1016/j.mrgentox.2018.04.008. Epub 2018 May 7. Mutat Res Genet Toxicol Environ Mutagen. 2018. PMID: 30389151 No abstract available.
Clinical consequences of BRCA2 hypomorphism.
Castells-Roca L, Gutiérrez-Enríquez S, Bonache S, Bogliolo M, Carrasco E, Aza-Carmona M, Montalban G, Muñoz-Subirana N, Pujol R, Cruz C, Llop-Guevara A, Ramírez MJ, Saura C, Lasa A, Serra V, Diez O, Balmaña J, Surrallés J. Castells-Roca L, et al. Among authors: surralles j. NPJ Breast Cancer. 2021 Sep 9;7(1):117. doi: 10.1038/s41523-021-00322-9. NPJ Breast Cancer. 2021. PMID: 34504103 Free PMC article.
Metformin for treatment of cytopenias in children and young adults with Fanconi anemia.
Pollard JA, Furutani E, Liu S, Esrick E, Cohen LE, Bledsoe J, Liu CW, Lu K, de Haro MJR, Surrallés J, Malsch M, Kuniholm A, Galvin A, Armant M, Kim AS, Ballotti K, Moreau L, Zhou Y, Babushok D, Boulad F, Carroll C, Hartung H, Hont A, Nakano T, Olson T, Sze SG, Thompson AA, Wlodarski MW, Gu X, Libermann TA, D'Andrea A, Grompe M, Weller E, Shimamura A. Pollard JA, et al. Among authors: surralles j. Blood Adv. 2022 Jun 28;6(12):3803-3811. doi: 10.1182/bloodadvances.2021006490. Blood Adv. 2022. PMID: 35500223 Free PMC article. Clinical Trial.
Therapeutic research in the crystal chromosome disease Fanconi anemia.
Minguillón J, Surrallés J. Minguillón J, et al. Among authors: surralles j. Mutat Res Genet Toxicol Environ Mutagen. 2018 Dec;836(Pt A):104-108. doi: 10.1016/j.mrgentox.2018.05.012. Epub 2018 May 7. Mutat Res Genet Toxicol Environ Mutagen. 2018. PMID: 30389152 Review.
Epidemiology of rare anaemias in Europe.
Gulbis B, Eleftheriou A, Angastiniotis M, Ball S, Surrallés J, Castella M, Heimpel H, Hill A, Corrons JL. Gulbis B, et al. Among authors: surralles j. Adv Exp Med Biol. 2010;686:375-96. doi: 10.1007/978-90-481-9485-8_22. Adv Exp Med Biol. 2010. PMID: 20824457 Review.
Telomere dysfunction in genome instability syndromes.
Callén E, Surrallés J. Callén E, et al. Among authors: surralles j. Mutat Res. 2004 Sep;567(1):85-104. doi: 10.1016/j.mrrev.2004.06.003. Mutat Res. 2004. PMID: 15341904 Review.
131 results