Search Results - "Sambani, Constantina" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Effect of lenalidomide therapy on hematopoiesis of patients with myelodysplastic syndrome associated with chromosome 5q deletion

Effect of lenalidomide therapy on hematopoiesis of patients with myelodysplastic syndrome associated with chromosome 5q deletion

by XIMERI, Maria, GALANOPOULOS, Athanasios, HATZIMICHAEL, Eleftheria, KOKORIS, Styliani, KORKOLOPOULOU, Penelope, SAMBANI, Constantina, PONTIKOGLOU, Charalampos, PAPADAKI, Helen A, KLAUS, Mirjam, PARCHARIDOU, Agapi, GIANNIKOU, Krinio, PSYLLAKI, Maria, SYMEONIDIS, Argyrios, PAPPA, Vasiliki, KARTASIS, Zafiris, LIAPI, Dimitra
Published in Haematologica (Roma) (01.03.2010)

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

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

by Daraki, Aggeliki, Zachaki, Sophia, Koromila, Theodora, Diamantopoulou, Paraskevi, Pantelias, Gabriel E, Sambani, Constantina, Aleporou, Vasiliki, Kollia, Panagoula, Manola, Kalliopi N
Published in PloS one (2014)

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NPM1 deletion is associated with gross chromosomal rearrangements in leukemia

NPM1 deletion is associated with gross chromosomal rearrangements in leukemia

by La Starza, Roberta, Matteucci, Caterina, Gorello, Paolo, Brandimarte, Lucia, Pierini, Valentina, Crescenzi, Barbara, Nofrini, Valeria, Rosati, Roberto, Gottardi, Enrico, Saglio, Giuseppe, Santucci, Antonella, Berchicci, Laura, Arcioni, Francesco, Falini, Brunangelo, Martelli, Massimo Fabrizio, Sambani, Constantina, Aventin, Anna, Mecucci, Cristina
Published in PloS one (21.09.2010)

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A novel t(X;21)(p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in myelodysplastic syndromes and acute myeloid leukemias

A novel t(X;21)(p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in myelodysplastic syndromes and acute myeloid leukemias

by Mavridou, Elena, Lema Fernandez, Anair Graciela, Nardelli, Carlotta, Pierini, Valentina, Quintini, Martina, Arniani, Silvia, Di Giacomo, Danika, Crescenzi, Barbara, Matteucci, Caterina, Sambani, Constantina, Mecucci, Cristina
Published in Genes chromosomes & cancer (01.04.2024)

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Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia

Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia

by Ioannidou, Agapi, Zachaki, Sophia, Daraki, Aggeliki, Margariti, Ioanna Maria, Pantelia, Domna, Diamantopoulou, Paraskevi, Sambani, Constantina, Roussou, Paraskevi, Manola, Kalliopi N
Published in Anticancer research (01.06.2019)

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

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

by Kakosaiou, Katerina, Panitsas, Fotios, Daraki, Aggeliki, Pagoni, Maria, Apostolou, Paraskevi, Ioannidou, Agapi, Vlachadami, Ioanna, Marinakis, Theodoros, Giatra, Chara, Vasilatou, Diamantina, Sambani, Constantina, Pappa, Vassiliki, Manola, Kalliopi N.
Published in Leukemia & lymphoma (03.10.2018)

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Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple Sclerosis

Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple Sclerosis

by Alexoudi, Athanasia, Zachaki, Sophia, Stavropoulou, Chrysa, Gavrili, Stavroula, Spiliopoulou, Chara, Papadodima, Stavroula, Karageorgiou, Clementine E, Sambani, Constantina
Published in Annals of clinical and laboratory science (01.12.2016)

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

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

by Daraki, Aggeliki, Zachaki, Sophia, Rosmaraki, Faidra, Kalomoiraki, Marina, Aleporou-Marinou, Vassiliki, Sambani, Constantina, Kollia, Panagoula, Manola, Kalliopi N.
Published in Leukemia & lymphoma (03.10.2017)

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Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates

Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates

by Gavrili, Stavroula, Zachaki, Sophia, Daraki, Aggeliki, Polycarpou, Elena, Manola, Kalliopi, Stavropoulou, Chryssa, Sambani, Constantina, Baroutis, George
Published in American journal of perinatology (01.05.2016)

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The G.sup.516T CYP2B6 Germline Polymorphism Affects the Risk of Acute Myeloid Leukemia and Is Associated with Specific Chromosomal Abnormalities

The G.sup.516T CYP2B6 Germline Polymorphism Affects the Risk of Acute Myeloid Leukemia and Is Associated with Specific Chromosomal Abnormalities

by Daraki, Aggeliki, Zachaki, Sophia, Koromila, Theodora, Diamantopoulou, Paraskevi, Pantelias, Gabriel E, Sambani, Constantina, Aleporou, Vasiliki, Kollia, Panagoula, Manola, Kalliopi N
Published in PloS one (24.02.2014)

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Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A 313 G germline polymorphism and chromosomal abnormalities

Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A 313 G germline polymorphism and chromosomal abnormalities

by Daraki, Aggeliki, Zachaki, Sophia, Stavropoulou, Chrysa, Aleporou-Marinou, Vassiliki, Sambani, Constantina, Manola, Kalliopi N.
Published in Leukemia & lymphoma (02.11.2014)

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Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis

Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis

by Alexoudi, Athanasia, Zachaki, Sophia, Stavropoulou, Chrysa, Chatzi, Ioanna, Koumbi, Daphne, Stavropoulou, Kalliopi, Kollia, Panagoula, Karageorgiou, Clementine E., Sambani, Constantina
Published in International journal of neuroscience (02.01.2015)

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

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

by Daraki, Aggeliki, Zachaki, Sophia, Stavropoulou, Chrysa, Aleporou-Marinou, Vassiliki, Sambani, Constantina, Manola, Kalliopi N.
Published in Leukemia & lymphoma (01.11.2014)

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Association of A313g Glutathione S-Transferase P1 (GSTP1) Inborn Polymorphism with Susceptibility to De Novo MDS

Association of A313g Glutathione S-Transferase P1 (GSTP1) Inborn Polymorphism with Susceptibility to De Novo MDS

by Zachaki, Sophia, Stavropoulou, Chryssa, Daraki, Aggeliki, Kalomoiraki, Marina, Kollia, Panagoula, Aleporou, Vassiliki, Pantelias, Gabriel, Kanavakis, Emmanuel, Sambani, Constantina
Published in Blood (16.11.2012)

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the G516 Polymorphism of Cytochrome P450 2B6 Gene in the Susceptibility of De Novo Acute Myeloid Leukemia

the G516 Polymorphism of Cytochrome P450 2B6 Gene in the Susceptibility of De Novo Acute Myeloid Leukemia

by Daraki, Aggeliki, Zachaki, Sophia, Koromila, Theodora, Karakosta, Maria, Pantelias, Gabriel, Aleporou, Vasiliki, Sambani, Constantina, Kollia, Panagoula, Manola, Kalliopi
Published in Blood (16.11.2012)

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

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

by Manola, Kalliopi N, Panitsas, Fotios, Polychronopoulou, Sophia, Daraki, Aggeliki, Karakosta, Maria, Stavropoulou, Cryssa, Avgerinou, Georgia, Hatzipantelis, Emmanuel, Pantelias, Gabriel, Sambani, Constantina, Pagoni, Maria
Published in Cancer genetics (01.03.2013)

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

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

by Daraki, Aggeliki, Kakosaiou, Katerina, Zachaki, Sophia, Sambani, Constantina, Aleporou-Marinou, Vassiliki, Kollia, Panagoula, Manola, Kalliopi
Published in Cancer genetics (01.11.2016)

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

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

by Zachaki, Sophia, Stavropoulou, Chrysa, Kalomoiraki, Marina, Koromila, Theodora, Daraki, Aggeliki, Manola, Kalliopi N, Mavrou, Ariadni, Kanavakis, Emmanuel, Pantelias, Gabriel E, Sambani, Constantina
Published in Leukemia & lymphoma (01.08.2013)

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Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome

Totipotent stem cells bearing del(20q) maintain multipotential differentiation in Shwachman Diamond syndrome

by Crescenzi, Barbara, La Starza, Roberta, Sambani, Constantina, Parcharidou, Agapi, Pierini, Valentina, Nofrini, Valeria, Brandimarte, Lucia, Matteucci, Caterina, Aversa, Franco, Martelli, Massimo Fabrizio, Mecucci, Cristina
Published in British journal of haematology (01.01.2009)

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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

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

by Manola, Kalliopi N, Karakosta, Maria, Sambani, Constantina, Terzoudi, Georgia, Pagoni, Maria, Gatsa, Eleni, Papaioannou, Maria
Published in Acta haematologica (01.01.2010)

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