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Results: 1 to 20 of 104

Similar articles for PubMed (Select 23624100)

1.

Fosfomycin increases chromosome instability in lymphocytes from Fanconi Anemia patients.

Sousa R, Ponte F, Teixeira S, Andrade L, Gonçalves C, Barbot J, Coutinho J, Carvalho F, Porto B.

Mutat Res. 2013 Jun 14;754(1-2):58-62. doi: 10.1016/j.mrgentox.2013.04.005. Epub 2013 Apr 25.

PMID:
23624100
2.

Diagnosis of fanconi anemia by diepoxybutane analysis.

Auerbach AD.

Curr Protoc Hum Genet. 2015 Apr 1;85:8.7.1-8.7.17. doi: 10.1002/0471142905.hg0807s85.

PMID:
25827349
3.

Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.

Fargo JH, Rochowski A, Giri N, Savage SA, Olson SB, Alter BP.

Cytogenet Genome Res. 2014;144(1):15-27. doi: 10.1159/000366251. Epub 2014 Sep 11.

PMID:
25227706
4.

[Cytogenetics study of chromosomal instability in Fanconi anemia in Tunisia].

Chbili C, Bouraoui S, El Ghezal H, Saad A.

Ann Biol Clin (Paris). 2014 Jul-Aug;72(4):473-8. doi: 10.1684/abc.2014.0983. French.

PMID:
25119806
5.

Chromosomal instability and molecular mutations in multi spectrum disease of Fanconi anemia.

Vundinti BR.

Mol Cytogenet. 2014 Jan 21;7(Suppl 1 Proceedings of the International Conference on Human):I47. doi: 10.1186/1755-8166-7-S1-I47. eCollection 2014. No abstract available.

6.

Chromosomal instability in patients with Fanconi anemia from Serbia.

Cirković S, Guć-Sćekić M, Vujić D, Mićić D, Skorić D.

Vojnosanit Pregl. 2014 Apr;71(4):368-72.

PMID:
24783417
7.

Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia.

Cirkovic S, Guc-Scekic M, Vujic D, Ilic N, Micic D, Skoric D, Jovanovic A.

Balkan J Med Genet. 2011 Dec;14(2):65-70. doi: 10.2478/v10034-011-0048-6.

8.

Improvement of genetic stability in lymphocytes from Fanconi anemia patients through the combined effect of α-lipoic acid and N-acetylcysteine.

Ponte F, Sousa R, Fernandes AP, Gonçalves C, Barbot J, Carvalho F, Porto B.

Orphanet J Rare Dis. 2012 May 16;7:28. doi: 10.1186/1750-1172-7-28.

9.

Squamous cell carcinomas of the head and neck in Fanconi anemia: risk, prevention, therapy, and the need for guidelines.

Scheckenbach K, Wagenmann M, Freund M, Schipper J, Hanenberg H.

Klin Padiatr. 2012 Apr;224(3):132-8. doi: 10.1055/s-0032-1308989. Epub 2012 Apr 13. Review.

10.

[Fanconi anemia: cytogenetic diagnosis of 40 cases].

Porto B, Sousa R, Ponte F, Torgal A, Campilho F, Campos A, Gonçalves C, Barbot J.

Acta Med Port. 2011 May-Jun;24(3):405-12. Epub 2011 Aug 12. Portuguese.

11.

Protective effect of acetyl-l-carnitine and α-lipoic acid against the acute toxicity of diepoxybutane to human lymphocytes.

Ponte F, Carvalho F, Porto B.

Toxicology. 2011 Oct 28;289(1):52-8. doi: 10.1016/j.tox.2011.07.009. Epub 2011 Jul 22.

PMID:
21807063
12.

Gender-related differences in the oxidant state of cells in Fanconi anemia heterozygotes.

Petrovic S, Leskovac A, Kotur-Stevuljevic J, Joksic J, Guc-Scekic M, Vujic D, Joksic G.

Biol Chem. 2011 Jul;392(7):625-32. doi: 10.1515/BC.2011.064. Epub 2011 May 28.

PMID:
21619480
13.

Fanconi anemia: at the crossroads of DNA repair.

Deakyne JS, Mazin AV.

Biochemistry (Mosc). 2011 Jan;76(1):36-48. Review.

PMID:
21568838
14.

Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing.

Webb ML, Rosen H, Taghinia A, McCarty ER, Cerrato F, Upton J, Labow BI.

J Hand Surg Am. 2011 Jun;36(6):1052-7. doi: 10.1016/j.jhsa.2011.02.018. Epub 2011 Apr 22.

PMID:
21514743
15.

Snm1B/Apollo functions in the Fanconi anemia pathway in response to DNA interstrand crosslinks.

Mason JM, Sekiguchi JM.

Hum Mol Genet. 2011 Jul 1;20(13):2549-59. doi: 10.1093/hmg/ddr153. Epub 2011 Apr 8.

16.

Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact.

Castella M, Pujol R, Callén E, Ramírez MJ, Casado JA, Talavera M, Ferro T, Muñoz A, Sevilla J, Madero L, Cela E, Beléndez C, de Heredia CD, Olivé T, de Toledo JS, Badell I, Estella J, Dasí Á, Rodríguez-Villa A, Gómez P, Tapia M, Molinés A, Figuera Á, Bueren JA, Surrallés J.

J Med Genet. 2011 Apr;48(4):242-50. doi: 10.1136/jmg.2010.084210. Epub 2011 Jan 7.

PMID:
21217111
17.

Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.

Mehta PA, Harris RE, Davies SM, Kim MO, Mueller R, Lampkin B, Mo J, Myers K, Smolarek TA.

Cancer Genet Cytogenet. 2010 Dec;203(2):180-6. doi: 10.1016/j.cancergencyto.2010.07.127.

PMID:
21156231
18.

Normal red blood cells partially decrease diepoxybutane-induced chromosome breakage in cultured lymphocytes from Fanconi anaemia patients.

Porto B, Sousa R, Malheiro I, Gaspar J, Rueff J, Gonçalves C, Barbot J.

Cell Prolif. 2010 Dec;43(6):573-8. doi: 10.1111/j.1365-2184.2010.00706.x.

PMID:
21039995
19.

Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population.

Korgaonkar S, Ghosh K, Jijina F, Vundinti BR.

J Pediatr Hematol Oncol. 2010 Nov;32(8):606-10. doi: 10.1097/MPH.0b013e3181e8865f.

PMID:
20881871
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