D'Andrea AD - Search Results

1

Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.

Hirsch B, Shimamura A, Moreau L, Baldinger S, Hag-alshiekh M, Bostrom B, Sencer S, D'Andrea AD. Hirsch B, et al. Blood. 2004 Apr 1;103(7):2554-9. doi: 10.1182/blood-2003-06-1970. Epub 2003 Dec 11. Blood. 2004. PMID: 14670928 Free article.

2

Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9.

Yang Y, Kuang Y, Montes De Oca R, Hays T, Moreau L, Lu N, Seed B, D'Andrea AD. Yang Y, et al. Blood. 2001 Dec 1;98(12):3435-40. doi: 10.1182/blood.v98.12.3435. Blood. 2001. PMID: 11719385 Free article.

3

A novel diagnostic screen for defects in the Fanconi anemia pathway.

Shimamura A, Montes de Oca R, Svenson JL, Haining N, Moreau LA, Nathan DG, D'Andrea AD. Shimamura A, et al. Blood. 2002 Dec 15;100(13):4649-54. doi: 10.1182/blood-2002-05-1399. Epub 2002 Aug 29. Blood. 2002. PMID: 12393398 Free article.

4

Marrow failure.

D'Andrea AD, Dahl N, Guinan EC, Shimamura A. D'Andrea AD, et al. Hematology Am Soc Hematol Educ Program. 2002:58-72. doi: 10.1182/asheducation-2002.1.58. Hematology Am Soc Hematol Educ Program. 2002. PMID: 12446419 Review.

5

Subtyping of Fanconi anemia patients: implications for clinical management.

Shimamura A, D'Andrea AD. Shimamura A, et al. Blood. 2003 Nov 1;102(9):3459. doi: 10.1182/blood-2003-04-1297. Blood. 2003. PMID: 14568911 Free article. No abstract available.

6

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.

7

Fanconi anemia pathway-deficient tumor cells are hypersensitive to inhibition of ataxia telangiectasia mutated.

Kennedy RD, Chen CC, Stuckert P, Archila EM, De la Vega MA, Moreau LA, Shimamura A, D'Andrea AD. Kennedy RD, et al. J Clin Invest. 2007 May;117(5):1440-9. doi: 10.1172/JCI31245. Epub 2007 Apr 12. J Clin Invest. 2007. PMID: 17431503 Free PMC article.

8

Human MutS and FANCM complexes function as redundant DNA damage sensors in the Fanconi Anemia pathway.

Huang M, Kennedy R, Ali AM, Moreau LA, Meetei AR, D'Andrea AD, Chen CC. Huang M, et al. DNA Repair (Amst). 2011 Dec 10;10(12):1203-12. doi: 10.1016/j.dnarep.2011.09.006. Epub 2011 Oct 4. DNA Repair (Amst). 2011. PMID: 21975120

9

Inactivation of Uaf1 causes defective homologous recombination and early embryonic lethality in mice.

Park E, Kim JM, Primack B, Weinstock DM, Moreau LA, Parmar K, D'Andrea AD. Park E, et al. Mol Cell Biol. 2013 Nov;33(22):4360-70. doi: 10.1128/MCB.00870-13. Epub 2013 Sep 3. Mol Cell Biol. 2013. PMID: 24001775 Free PMC article.

10

Fanconi-BRCA pathway mutations in childhood T-cell acute lymphoblastic leukemia.

Pouliot GP, Degar J, Hinze L, Kochupurakkal B, Vo CD, Burns MA, Moreau L, Ganesa C, Roderick J, Peirs S, Menten B, Loh ML, Hunger SP, Silverman LB, Harris MH, Stevenson KE, Weinstock DM, Weng AP, Van Vlierberghe P, D'Andrea AD, Gutierrez A. Pouliot GP, et al. PLoS One. 2019 Nov 13;14(11):e0221288. doi: 10.1371/journal.pone.0221288. eCollection 2019. PLoS One. 2019. PMID: 31721781 Free PMC article.

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