M. Priwitzerova

protein expression and iron uptake Functional consequences of the human DMT1 (SLC11A2) mutation on

V. Divoky, D. Pospíšilová, A. Sheftel, 2013 .

the iron transport pathway in erythroid cells Severe hypochromic microcytic anemia caused by a congenital defect of

V. Divoky, J. Prchal, D. Pospíšilová, 2011 .

Functional consequences of the human DMT1 (SLC11A2) mutation on protein expression and iron uptake.

V. Divoky, D. Pospíšilová, Guangjun Nie, 2005, Blood.

Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells.

V. Divoky, J. Prchal, V. Mihál, 2004, Blood.

Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.

J. Prchal, D. Pospíšilová, K. Indrák, 2005, Blood.

Cryptic MLL-AF10 fusion caused by insertion of duplicated 5' part of MLL into 10p12 in acute leukemia: a case report.

M. Jarošová, V. Mihál, K. Indrák, 2005, Cancer genetics and cytogenetics.

Short communication Cryptic MLL-AF10 fusion caused by insertion of duplicated 5# part of MLL into 10p12 in acute leukemia: a case report

M. Jarošová, V. Mihál, K. Indrák, 2005 .