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Items: 37

1.

The lysine-specific methyltransferase KMT2C/MLL3 regulates DNA repair components in cancer.

Rampias T, Karagiannis D, Avgeris M, Polyzos A, Kokkalis A, Kanaki Z, Kousidou E, Tzetis M, Kanavakis E, Stravodimos K, Manola KN, Pantelias GE, Scorilas A, Klinakis A.

EMBO Rep. 2019 Mar;20(3). pii: e46821. doi: 10.15252/embr.201846821. Epub 2019 Jan 21.

2.

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

Ioannidou A, Zachaki S, Karakosta M, Daraki A, Roussou P, Manola KN.

Cytogenet Genome Res. 2018;154(3):126-131. doi: 10.1159/000487868. Epub 2018 Mar 24.

PMID:
29587287
3.

ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics.

Kakosaiou K, Panitsas F, Daraki A, Pagoni M, Apostolou P, Ioannidou A, Vlachadami I, Marinakis T, Giatra C, Vasilatou D, Sambani C, Pappa V, Manola KN.

Leuk Lymphoma. 2018 Oct;59(10):2439-2446. doi: 10.1080/10428194.2018.1433298. Epub 2018 Feb 7.

PMID:
29411666
4.

Association of GSTP1 inactivating polymorphism with acute myeloid leukemia and its specific chromosomal abnormalities.

Daraki A, Zachaki S, Rosmaraki F, Kalomoiraki M, Aleporou-Marinou V, Sambani C, Kollia P, Manola KN.

Leuk Lymphoma. 2017 Oct;58(10):2505-2507. doi: 10.1080/10428194.2017.1295148. Epub 2017 Mar 2. No abstract available.

PMID:
28278696
5.

GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.

Zachaki S, Daraki A, Polycarpou E, Stavropoulou C, Manola KN, Gavrili S.

Am J Perinatol. 2017 Jul;34(8):729-734. doi: 10.1055/s-0036-1597994. Epub 2017 Jan 12.

PMID:
28081574
6.

Polymorphisms and haplotypes of the CYP2B6 detoxification gene in the predisposition of Acute Myeloid Leukemia (AML) and induction of its cytogenetic abnormalities.

Daraki A, Kakosaiou K, Zachaki S, Sambani C, Aleporou-Marinou V, Kollia P, Manola KN.

Cancer Genet. 2016 Nov;209(11):525-533. doi: 10.1016/j.cancergen.2016.10.004. Epub 2016 Oct 28.

PMID:
27865701
7.

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.

Hematology. 2016 Oct;21(9):526-35. doi: 10.1080/10245332.2015.1110948. Epub 2016 Mar 15.

PMID:
27077766
8.

A novel mechanism of NPM1 cytoplasmic localization in acute myeloid leukemia: the recurrent gene fusion NPM1-HAUS1.

Campregher PV, de Oliveira Pereira W, Lisboa B, Puga R, Deolinda ER, Helman R, Marti LC, Guerra JC, Manola KN, Petroni RC, Bezerra AM, Costa FF, Hamerschlak N, de Souza Santos FP.

Haematologica. 2016 Jul;101(7):e287-90. doi: 10.3324/haematol.2015.137364. Epub 2016 Apr 1. No abstract available.

9.

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

Karakosta M, Delicha EM, Kouraklis G, Manola KN.

Arch Environ Occup Health. 2016 Nov;71(6):317-329. Epub 2015 Nov 13.

PMID:
26566973
10.

The G⁵¹⁶T CYP2B6 germline polymorphism affects the risk of acute myeloid leukemia and is associated with specific chromosomal abnormalities.

Daraki A, Zachaki S, Koromila T, Diamantopoulou P, Pantelias GE, Sambani C, Aleporou V, Kollia P, Manola KN.

PLoS One. 2014 Feb 24;9(2):e88879. doi: 10.1371/journal.pone.0088879. eCollection 2014.

11.

Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A³¹³G germline polymorphism and chromosomal abnormalities.

Daraki A, Zachaki S, Stavropoulou C, Aleporou-Marinou V, Sambani C, Manola KN.

Leuk Lymphoma. 2014 Nov;55(11):2637-9. doi: 10.3109/10428194.2014.894192. Epub 2014 Mar 18. No abstract available.

PMID:
24547706
12.

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.

Acta Haematol. 2014;132(1):59-67. doi: 10.1159/000355714. Epub 2014 Jan 23.

PMID:
24458221
13.

Cytogenetic abnormalities in acute leukaemia of ambiguous lineage: an overview.

Manola KN.

Br J Haematol. 2013 Oct;163(1):24-39. doi: 10.1111/bjh.12484. Epub 2013 Jul 25. Review.

PMID:
23888868
14.

High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.

Zachaki S, Stavropoulou C, Koromila T, Manola KN, Kalomoiraki M, Daraki A, Koumbi D, Athanasiadou A, Kanavakis E, Kollia P, Sambani C.

Leuk Res. 2013 Jul;37(7):742-6. doi: 10.1016/j.leukres.2013.04.015. Epub 2013 May 1.

PMID:
23643325
15.

Translocation t(5;18)(q35;q21) as a rare nonrandom abnormality in acute myeloid leukemia.

Daraki A, Bourantas LK, Manola KN.

Cytogenet Genome Res. 2013;139(4):289-94. doi: 10.1159/000348786. Epub 2013 Mar 23.

PMID:
23548668
16.

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.

Cancer Genet. 2013 Mar;206(3):63-72. doi: 10.1016/j.cancergen.2013.01.001. Epub 2013 Feb 12.

PMID:
23411131
17.

Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome.

Zachaki S, Stavropoulou C, Kalomoiraki M, Koromila T, Daraki A, Manola KN, Mavrou A, Kanavakis E, Pantelias GE, Sambani C.

Leuk Lymphoma. 2013 Aug;54(8):1756-61. doi: 10.3109/10428194.2012.762647. Epub 2013 Jan 28.

PMID:
23278642
18.

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

Karakosta M, Tsakiridou A, Korantzis I, Manola KN.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):175-9. doi: 10.1016/j.cancergencyto.2010.04.002.

PMID:
20620603
19.

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

Karakosta M, Voulgarelis M, Vlachadami I, Manola KN.

Cancer Genet Cytogenet. 2010 Apr 1;198(1):66-70. doi: 10.1016/j.cancergencyto.2009.12.009.

PMID:
20303017
20.

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.

Acta Haematol. 2010;123(3):162-70. doi: 10.1159/000294959. Epub 2010 Mar 11. Review.

PMID:
20224268
21.

Plasmablastic crisis of Philadelphia chromosome-positive chronic myeloid leukemia.

Manola KN, Pantelidou D, Papaioannou M.

Ann Hematol. 2010 Jun;89(6):641-2. doi: 10.1007/s00277-009-0852-1. Epub 2009 Oct 21. No abstract available.

PMID:
19844710
22.

G2-checkpoint abrogation in irradiated lymphocytes: A new cytogenetic approach to assess individual radiosensitivity and predisposition to cancer.

Terzoudi GI, Hatzi VI, Barszczewska K, Manola KN, Stavropoulou C, Angelakis P, Pantelias GE.

Int J Oncol. 2009 Nov;35(5):1223-30.

PMID:
19787278
23.

Cytogenetics of pediatric acute myeloid leukemia.

Manola KN.

Eur J Haematol. 2009 Nov;83(5):391-405. doi: 10.1111/j.1600-0609.2009.01308.x. Epub 2009 Jun 25. Review.

PMID:
19563518
24.

Jumping translocations in hematological malignancies: a cytogenetic study of five cases.

Manola KN, Georgakakos VN, Stavropoulou C, Spyridonidis A, Angelopoulou MK, Vlachadami I, Katsigiannis A, Roussou P, Pantelias GE, Sambani C.

Cancer Genet Cytogenet. 2008 Dec;187(2):85-94. doi: 10.1016/j.cancergencyto.2008.07.010.

PMID:
19027489
25.

5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.

Stavropoulou C, Georgakakos VN, Manola KN, Pagoni M, Garofalaki M, Pantelias GE, Sambani C.

Cancer Genet Cytogenet. 2008 Apr 1;182(1):50-5. doi: 10.1016/j.cancergencyto.2007.12.011.

PMID:
18328952
26.

Low frequency of the glutathione-S-transferase T1-null genotype in patients with primary myelodysplastic syndrome and 5q deletion.

Stavropoulou C, Sambani C, Rigana H, Georgakakos VN, Voutsinas G, Manola KN, Pantelias GE, Makropoulos V; Hellenic MDS Study Group.

Leukemia. 2008 Aug;22(8):1643-6. doi: 10.1038/leu.2008.35. Epub 2008 Feb 28. No abstract available.

PMID:
18305556
27.

Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.

Manola KN, Georgakakos VN, Margaritis D, Stavropoulou C, Panos C, Kotsianidis I, Pantelias GE, Sambani C.

Cancer Genet Cytogenet. 2008 Jan 1;180(1):37-42.

PMID:
18068531
28.

Leukemias associated with Turner syndrome: report of three cases and review of the literature.

Manola KN, Sambani C, Karakasis D, Kalliakosta G, Harhalakis N, Papaioannou M.

Leuk Res. 2008 Mar;32(3):481-6. Epub 2007 Jul 31. Review.

PMID:
17669490
29.

Glutathione-S-transferase T1 and M1 gene polymorphisms in Greek patients with multiple sclerosis: a pilot study.

Stavropoulou C, Korakaki D, Rigana H, Voutsinas G, Polyzoi M, Georgakakos VN, Manola KN, Karageorgiou CE, Sambani C.

Eur J Neurol. 2007 May;14(5):572-4.

PMID:
17437619
30.

Translocation (X;12)(p11;p13) as a sole abnormality in biphenotypic acute leukemia.

Manola KN, Georgakakos VN, Marinakis T, Stavropoulou C, Paterakis G, Anagnostopoulos NI, Pantelias GE, Sambani C.

Cancer Genet Cytogenet. 2007 Mar;173(2):159-63.

PMID:
17321333
31.

Switch in X-inactivation in a JAK2 V617F-negative case of polycythemia vera with two acquired X-autosome translocations.

Manola KN, Stavropoulou C, Georgakakos VN, Zoi K, Fisfis M, Evmorfiadis I, Zoi C, Pantelias GE, Stefanoudaki K, Sambani C.

Leuk Res. 2007 Jul;31(7):1009-14. Epub 2007 Jan 3.

PMID:
17204324
32.

Allogeneic stem cell transplantation from donors with mosaic Turner syndrome.

Manola KN, Sambani C, Karakasis D, Baltathakis I, Zoumbos N, Symeonidis A.

Bone Marrow Transplant. 2006 Sep;38(5):385-6. No abstract available.

PMID:
16915227
33.

Constitutional pericentric inversion of chromosome 9 and hematopoietic recovery after allogeneic stem cell transplantation.

Manola KN, Harhalakis N, Symeonidis A, Rigana H, Stavropoulou C, Karakasis D, Tiniakou M, Baltathakis I, Stamouli MI, Zoumbos N, Pantelias GE, Sambani C.

Ann Hematol. 2006 Sep;85(9):611-5. Epub 2006 Jun 7.

PMID:
16758191
34.

Checkpoint abrogation in G2 compromises repair of chromosomal breaks in ataxia telangiectasia cells.

Terzoudi GI, Manola KN, Pantelias GE, Iliakis G.

Cancer Res. 2005 Dec 15;65(24):11292-6.

35.

Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).

Sambani C, La Starza R, Pierini V, Vandenberghe P, Gonzales-Aguilera JJ, Rigana H, Koumbi D, Manola KN, Stavropoulou C, Georgakakos VN, Pagoni M, Wlodarska I, Mecucci C.

Cancer Genet Cytogenet. 2005 Oct 1;162(1):45-9.

PMID:
16157199
36.

Radioprotective effect of amifostine on cells from cancer prone patients and healthy individuals studied by the G2 and PCC assays.

Manola KN, Terzoudi GI, Dardoufas CE, Malik SI, Pantelias GE.

Int J Radiat Biol. 2003 Oct;79(10):831-8.

PMID:
14630542
37.

A novel dic(1;10) in a patient with myelodysplastic syndrome.

Sambani C, La Starza R, Stavropoulou C, Manola KN, Harhalakis N, Mecucci C.

Cancer Genet Cytogenet. 2002 Feb;133(1):87-9.

PMID:
11890996

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