Constantina Sambani
Athens, ESYE31, Greece
Last Updated: 09/26/2026
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Found 14 publications
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.
Journal: Genes, chromosomes & cancer
Published: December 28, 2023
ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics.
Journal: Leukemia & lymphoma
Published: February 08, 2018
Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple Sclerosis.
Journal: Annals of clinical and laboratory science
Published: December 21, 2016
Polymorphisms and haplotypes of the CYP2B6 detoxification gene in the predisposition of Acute Myeloid Leukemia (AML) and induction of its cytogenetic abnormalities.
Journal: Cancer genetics
Published: June 28, 2016
Association of C609T-Inborn Polymorphism of NAD(P)H: Quinone Oxidoreductase 1 with the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.
Journal: American journal of perinatology
Published: December 20, 2015
Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis.
Journal: The International journal of neuroscience
Published: March 05, 2014
Glutathione S-transferase P1 promoter hypermethylation in acute myeloid leukemia: association with A³¹³G germline polymorphism and chromosomal abnormalities.
Journal: Leukemia & lymphoma
Published: February 20, 2014
The G⁵¹⁶T CYP2B6 germline polymorphism affects the risk of acute myeloid leukemia and is associated with specific chromosomal abnormalities.
Journal: PloS one
Published: September 04, 2013
Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome.
Journal: Leukemia & lymphoma
Published: January 03, 2013
Last Updated: 09/26/2026