Dasoula A - Search Results

1

Mosaic trisomy r(14) associated with epilepsy and mental retardation.

Tzoufi M, Kanioglou C, Dasoula A, Asproudis I, Tsatsoulis A, Sismani C, Patsalis PC, Georgiou I, Syrrou M. Tzoufi M, et al. Among authors: dasoula a. J Child Neurol. 2007 Jul;22(7):869-73. doi: 10.1177/0883073807304196. J Child Neurol. 2007. PMID: 17715281

2

Promoter hypermethylation of the MEG3 (DLK1/MEG3) imprinted gene in multiple myeloma.

Benetatos L, Dasoula A, Hatzimichael E, Georgiou I, Syrrou M, Bourantas KL. Benetatos L, et al. Among authors: dasoula a. Clin Lymphoma Myeloma. 2008 Jun;8(3):171-5. doi: 10.3816/CLM.2008.n.021. Clin Lymphoma Myeloma. 2008. PMID: 18650181

3

Methylation status of the SNRPN and HUMARA genes in testicular biopsy samples.

Dasoula A, Georgiou I, Kontogianni E, Sofikitis N, Syrrou M. Dasoula A, et al. Fertil Steril. 2007 Apr;87(4):805-9. doi: 10.1016/j.fertnstert.2006.09.009. Epub 2007 Jan 4. Fertil Steril. 2007. PMID: 17207798 Free article.

4

CpG methylation analysis of the MEG3 and SNRPN imprinted genes in acute myeloid leukemia and myelodysplastic syndromes.

Benetatos L, Hatzimichael E, Dasoula A, Dranitsaris G, Tsiara S, Syrrou M, Georgiou I, Bourantas KL. Benetatos L, et al. Among authors: dasoula a. Leuk Res. 2010 Feb;34(2):148-53. doi: 10.1016/j.leukres.2009.06.019. Leuk Res. 2010. PMID: 19595458

5

Skewed X-chromosome inactivation in Greek women with idiopathic recurrent miscarriage.

Dasoula A, Kalantaridou S, Sotiriadis A, Pavlou M, Georgiou I, Paraskevaidis E, Makrigiannakis A, Syrrou M. Dasoula A, et al. Fetal Diagn Ther. 2008;23(3):198-203. doi: 10.1159/000116741. Epub 2008 Feb 20. Fetal Diagn Ther. 2008. PMID: 18417978

6

Absence of methylation-dependent transcriptional silencing in TP73 irrespective of the methylation status of the CDKN2A CpG island in plasma cell neoplasia.

Hatzimichael E, Benetatos L, Dasoula A, Dranitsaris G, Tsiara S, Georgiou I, Syrrou M, Stebbing J, Coley HM, Crook T, Bourantas KL. Hatzimichael E, et al. Among authors: dasoula a. Leuk Res. 2009 Sep;33(9):1272-5. doi: 10.1016/j.leukres.2009.04.009. Epub 2009 May 6. Leuk Res. 2009. PMID: 19423161

7

Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease.

Voutsinas GE, Stavrou EF, Karousos G, Dasoula A, Papachatzopoulou A, Syrrou M, Verkerk AJ, van der Spek P, Patrinos GP, Stöger R, Athanassiadou A. Voutsinas GE, et al. Among authors: dasoula a. Hum Mutat. 2010 Jun;31(6):685-91. doi: 10.1002/humu.21248. Hum Mutat. 2010. PMID: 20340137

8

The absence of CDKN1C (p57KIP2) promoter methylation in myeloid malignancies also characterizes plasma cell neoplasms.

Hatzimichael E, Dasoula A, Benetatos L, Makis A, Stebbing J, Crook T, Syrrou M, Bourantas KL. Hatzimichael E, et al. Among authors: dasoula a. Br J Haematol. 2008 May;141(4):557-8. doi: 10.1111/j.1365-2141.2008.07034.x. Epub 2008 Mar 26. Br J Haematol. 2008. PMID: 18371112 Free article. No abstract available.

9

Absence of mutations of the EPO-receptor gene in Greek patients with familial polycythemia.

Bourantas LK, Chatzikyriakidou A, Dasoula A, Syrrou M, Bournatas KL, Georgiou I. Bourantas LK, et al. Among authors: dasoula a. Eur J Haematol. 2006 Jun;76(6):537-8. doi: 10.1111/j.1600-0609.2006.00653.x. Epub 2006 Apr 11. Eur J Haematol. 2006. PMID: 16608505 No abstract available.

10

Study of specific genetic and epigenetic variables in multiple myeloma.

Hatzimichael E, Dasoula A, Benetatos L, Syed N, Dranitsaris G, Crook T, Bourantas K. Hatzimichael E, et al. Among authors: dasoula a. Leuk Lymphoma. 2010 Dec;51(12):2270-4. doi: 10.3109/10428194.2010.528095. Epub 2010 Nov 11. Leuk Lymphoma. 2010. PMID: 21067440

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