The Felsenstein Medical Research Center
TOPIC

Laboratory of Pediatric Molecular Hematology

Head of Laboratory: Hannah Tamary M.D.

Head of Research Group: Orly Dgani Ph.D.

 Tel: 972-3-9376738
E-mail: htamary@post.tau.ac.il; odgany@post.tau.ac.il
Fax: 972-3-9211478

Research Topics

  1. Cellular localization and function of codanin-1 (CDA1)

  2. Molecular basis of inherited bone marrow failure syndromes in Israel

Selected Publications

  1. Tamary H, Shalev H, Perez-Avraham G, Zoldan M, Levi I, Swinkels DW, Tanno T, Miller JL. Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I. Blood 112:5241-4, 2008. MEDLINE

  2. Noy-Lotan S, Dgany O, Lahmi R, Marcoux N, Krasnov T, Yissachar N, Ginsberg D, Motro B, Resnitzky P, Yaniv I, Kupfer GM, Tamary H Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated. Haematologica. 94(5):629-37, 2009. MEDLINE

  3. Tamary H, Nishri D, Yacobovich J, Zilber R, Dgany O, Krasnov T, Aviner S, Stepensky P, Ravel-Vilk S, Bitan M, Kaplinsky C, Ben Barak A, Elhasid R, Kapelusnik J, Koren A, Levin C, Attias D, Laor R, Yaniv I, Rosenberg PS, Alter BP. Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry. Haematologica. 95(8):1300-1307, 2010 MEDLINE

  4. Amir A, Dgany O, Krasnov T, Resnitzky P, Mor-Cohen R, Bennett M, Berrebi A, Tamary H. E109K Is a SEC23B Founder mutation among Israeli Moroccan Jewish patients with Congenital Dyserythropoietic Anemia Type II Acta Haematol.125(4):202-207, 2011.MEDLINE

  5. Shalev H, Landau D, Pissard S, Krasnov T, Kapelushnik J, Gilad O, Broides A, Dgany O, Tamary H. A novel εγδβ thalassemias presenting with maternal pregnancy complications and severe neonatal anemia. Eur J Haematol. 90(2):127-33, 2013 MEDLINE