PubMed (cited) for id: 607139

Year	Number of Results
1987	1
1991	1
1992	1
1995	1
1996	4
1997	5
1998	1
1999	6
2000	2
2001	5
2002	4
2003	3
2004	3
2005	4
2008	1
2009	1
2011	1
2018	1
2019	1
2024	0

1

From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia.

Krausz C, Riera-Escamilla A, Chianese C, Moreno-Mendoza D, Ars E, Rajmil O, Pujol R, Bogliolo M, Blanco I, Rodríguez I, Badell I, Ruiz-Castañé E, Surrallés J. Krausz C, et al. Genet Med. 2019 Jan;21(1):189-194. doi: 10.1038/s41436-018-0037-1. Epub 2018 Jun 14. Genet Med. 2019. PMID: 29904161 Free article.

2

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. 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.

3

Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.

Singh TR, Bakker ST, Agarwal S, Jansen M, Grassman E, Godthelp BC, Ali AM, Du CH, Rooimans MA, Fan Q, Wahengbam K, Steltenpool J, Andreassen PR, Williams DA, Joenje H, de Winter JP, Meetei AR. Singh TR, et al. Blood. 2009 Jul 2;114(1):174-80. doi: 10.1182/blood-2009-02-207811. Epub 2009 May 7. Blood. 2009. PMID: 19423727 Free PMC article.

4

HES1 is a novel interactor of the Fanconi anemia core complex.

Tremblay CS, Huang FF, Habi O, Huard CC, Godin C, Lévesque G, Carreau M. Tremblay CS, et al. Blood. 2008 Sep 1;112(5):2062-70. doi: 10.1182/blood-2008-04-152710. Epub 2008 Jun 11. Blood. 2008. PMID: 18550849 Free PMC article.

5

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

Meetei AR, Medhurst AL, Ling C, Xue Y, Singh TR, Bier P, Steltenpool J, Stone S, Dokal I, Mathew CG, Hoatlin M, Joenje H, de Winter JP, Wang W. Meetei AR, et al. Nat Genet. 2005 Sep;37(9):958-63. doi: 10.1038/ng1626. Epub 2005 Aug 21. Nat Genet. 2005. PMID: 16116422 Free PMC article.

6

Identification of multiple nuclear export sequences in Fanconi anemia group A protein that contribute to CRM1-dependent nuclear export.

Ferrer M, Rodríguez JA, Spierings EA, de Winter JP, Giaccone G, Kruyt FA. Ferrer M, et al. Hum Mol Genet. 2005 May 15;14(10):1271-81. doi: 10.1093/hmg/ddi138. Epub 2005 Mar 24. Hum Mol Genet. 2005. PMID: 15790592

7

Spectrum of sequence variations in the FANCA gene: an International Fanconi Anemia Registry (IFAR) study.

Levran O, Diotti R, Pujara K, Batish SD, Hanenberg H, Auerbach AD. Levran O, et al. Hum Mutat. 2005 Feb;25(2):142-9. doi: 10.1002/humu.20125. Hum Mutat. 2005. PMID: 15643609

8

Identification and characterization of novel mutations of the major Fanconi anemia gene FANCA in the Japanese population.

Yagasaki H, Hamanoue S, Oda T, Nakahata T, Asano S, Yamashita T. Yagasaki H, et al. Hum Mutat. 2004 Dec;24(6):481-90. doi: 10.1002/humu.20099. Hum Mutat. 2004. PMID: 15523645

9

Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway.

Soulier J, Leblanc T, Larghero J, Dastot H, Shimamura A, Guardiola P, Esperou H, Ferry C, Jubert C, Feugeas JP, Henri A, Toubert A, Socié G, Baruchel A, Sigaux F, D'Andrea AD, Gluckman E. Soulier J, et al. Blood. 2005 Feb 1;105(3):1329-36. doi: 10.1182/blood-2004-05-1852. Epub 2004 Sep 21. Blood. 2005. PMID: 15383454 Free article.

10

The Fanconi anemia proteins functionally interact with the protein kinase regulated by RNA (PKR).

Zhang X, Li J, Sejas DP, Rathbun KR, Bagby GC, Pang Q. Zhang X, et al. J Biol Chem. 2004 Oct 15;279(42):43910-9. doi: 10.1074/jbc.M403884200. Epub 2004 Aug 6. J Biol Chem. 2004. PMID: 15299030 Free article.

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