Karakosta M - Search Results

1

Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia.

Ioannidou A, Zachaki S, Karakosta M, Daraki A, Roussou P, Manola KN. Ioannidou A, et al. Among authors: karakosta m. Cytogenet Genome Res. 2018;154(3):126-131. doi: 10.1159/000487868. Epub 2018 Mar 24. Cytogenet Genome Res. 2018. PMID: 29587287

2

Translocation (6;13)(p21;q14.1) as a rare nonrandom cytogenetic abnormality in chronic lymphocytic leukemia.

Karakosta M, Voulgarelis M, Vlachadami I, Manola KN. Karakosta M, et al. Cancer Genet Cytogenet. 2010 Apr 1;198(1):66-70. doi: 10.1016/j.cancergencyto.2009.12.009. Cancer Genet Cytogenet. 2010. PMID: 20303017

3

Deletion of 5q as a rare abnormality in chronic lymphocytic leukemia.

Karakosta M, Tsakiridou A, Korantzis I, Manola KN. Karakosta M, et al. Cancer Genet Cytogenet. 2010 Jul 15;200(2):175-9. doi: 10.1016/j.cancergencyto.2010.04.002. Cancer Genet Cytogenet. 2010. PMID: 20620603

4

Association of various risk factors with chronic lymphocytic leukemia and its cytogenetic characteristics.

Karakosta M, Delicha EM, Kouraklis G, Manola KN. Karakosta M, et al. Arch Environ Occup Health. 2016 Nov;71(6):317-329. doi: 10.1080/19338244.2015.1116429. Epub 2015 Nov 13. Arch Environ Occup Health. 2016. PMID: 26566973

5

The parallel application of karyotype interphase and metaphase FISH after DSP-30/IL-2 stimulation is necessary for the investigation of chronic lymphocytic leukemia.

Karakosta M, Manola KN. Karakosta M, et al. Hematology. 2016 Oct;21(9):526-35. doi: 10.1080/10245332.2015.1110948. Epub 2016 Mar 15. Hematology. 2016. PMID: 27077766 Free article.

6

UGT1A1*28 polymorphism in chronic lymphocytic leukemia: the first investigation of the polymorphism in disease susceptibility and its specific cytogenetic abnormalities.

Karakosta M, Kalotychou V, Kostakis A, Pantelias G, Rombos I, Kouraklis G, Manola KN. Karakosta M, et al. Acta Haematol. 2014;132(1):59-67. doi: 10.1159/000355714. Epub 2014 Jan 23. Acta Haematol. 2014. PMID: 24458221

7

Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome.

Manola KN, Panitsas F, Polychronopoulou S, Daraki A, Karakosta M, Stavropoulou C, Avgerinou G, Hatzipantelis E, Pantelias G, Sambani C, Pagoni M. Manola KN, et al. Among authors: karakosta m. Cancer Genet. 2013 Mar;206(3):63-72. doi: 10.1016/j.cancergen.2013.01.001. Epub 2013 Feb 12. Cancer Genet. 2013. PMID: 23411131

8

Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature.

Manola KN, Karakosta M, Sambani C, Terzoudi G, Pagoni M, Gatsa E, Papaioannou M. Manola KN, et al. Among authors: karakosta m. Acta Haematol. 2010;123(3):162-70. doi: 10.1159/000294959. Epub 2010 Mar 11. Acta Haematol. 2010. PMID: 20224268 Review.

9

Contribution of G71R mutation to Gilbert's syndrome phenotype in a Greek patient: A case report.

Kalotychou V, Karakosta M, Tzanetea R, Stamoulakatou A, Konstantopoulos K, Rombos Y. Kalotychou V, et al. Among authors: karakosta m. World J Gastrointest Pharmacol Ther. 2011 Oct 6;2(5):42-5. doi: 10.4292/wjgpt.v2.i5.42. World J Gastrointest Pharmacol Ther. 2011. PMID: 22046580 Free PMC article.

10

Low concentrations of caffeine induce asymmetric cell division as observed in vitro by means of the CBMN-assay and iFISH.

Hatzi VI, Karakosta M, Barszczewska K, Karachristou I, Pantelias G, Terzoudi GI. Hatzi VI, et al. Among authors: karakosta m. Mutat Res Genet Toxicol Environ Mutagen. 2015 Nov;793:71-8. doi: 10.1016/j.mrgentox.2015.08.002. Epub 2015 Aug 5. Mutat Res Genet Toxicol Environ Mutagen. 2015. PMID: 26520375

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