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Science and research

Professional Publications

Author
Title
Year of publication

Publications (2655)

[61]

Greenberg, P.L.; Tuechler, H.; Schanz, J.; Sanz, G.; Garcia-Manero, G.; Solé, F.; Bennet; J.M.; Bowen, D.; Fenaux, P.; Dreyfus, F.; Kantarjian, H.; Kuendgen, A.; Levis, A.; Malcovati, L.; Cazzola, M.; Cermak, J.; Fonatsch, C.; Le Beau, M.M.; Slovak, M.L.; Krieger, O.; Luebbert, M.; Maciejewski, J.; Magalhaes, S.M.M.; Miyazaki, Y.; Pfeilstöcker, M.; Sekeres, M.; Sperr, W.R.; Stauder, R.; Tauro, S.; Valent, P.; Vallespi, T.; Van De Loosdrecht, A.A.; Germing, U.; Haase, D.

Revised international prognostic scoring system for myelodysplastic syndromes

[year of publication 2012, impact factor 9.060 ]

[62]

Michallet, M.; Sobh, M.; Milligan, D.; Morisset, S.; Niederwieser, D.; Koza, V.; Ruutu, T.; Russell, N.H.; Verdonck, L.; Dhedin, N.; Vitek, A.; Boogaerts, M.; Vindelov, L.; Finke, J.; Dubois, V.; van Biezen, A.; Brand, R.; de Witte, T.; Dreger, P.

The impact of HLA matching on long-term transplant outcome after allogeneic hematopoietic stem cell transplantation for CLL : a retrospective study from the EBMT registry

[year of publication 2010, impact factor 8.966]

[63]

Reed, A.L.; Califano, J.; Cairns, P.; Westra, W.H.; Jones, R.M.; Koch, W.; Ahrendt, S.; Eby, Y.; Sewell, D.; Nawroz, H.; Bartek, J.; Sidransky, D.

High frequency of p16 (CDKN2/MTS-1/INK4A) inactivation in head and neck squamous cell carcinoma

[year of publication 2006, impact factor 8.958]

[64]

Bartkova, J.; Lukas, J.; Guldberg, P.; Alsner, J.; Kirkin, A.F.; Zeuthen, J.; Bartek, J.

The p16-cyclin D/Cdk4-pRb pathway as a functional unit frequently altered in melanoma pathogenesis

[year of publication 2006, impact factor 8.958]

[65]

Trka, J.; Zuna, J.; Hrušák, O.; Michalová, K.; Mužíková, K.; Kalinová, K.; Starý, J.

No evidence for MLL/AF4 expression in normal cord blood samples

[year of publication 2006, impact factor 8.782]

[66]

Moravcová, J.; Nádvorníková, S.; Lukášová, M.; Klamová, H.

Polymerase chain reaction analyses should be used as a basis for clinical decision making in patients with chronic myelogenous leukemia

[year of publication 2006, impact factor 8.782]

[67]

Schwarz, J.; Penka, M.; Indrák, K.; Pospíšilová, D.; Pytlík, R.; Dulíček, P.; Doubek, M.; Křen, L.; Campr, V.

The WHO 2008 classification of Ph-myeloproliferative disorders : statement of the Czech MPD Working Group

[year of publication 2008, impact factor 8.634]

[68]

De Boer, C.J.; Schuuring, E.; Dreef, E.; Peters, G.; Bartek, J.; Kluin, P.M.; Van Krieken, J.H.

Cyclin D1 protein analysis in the diagnosis of mantle cell lymphoma

[year of publication 2006, impact factor 8.569]

[69]

Jarolim, P.; Rubin, H.L.; Brabec, V.; Palek, J.

Comparison of the ankyrin (AC)n microsatellites in genomic DNA and mRNA reveals absence of one ankyrin mRNA allele in 20% of patients with hereditary spherocytosis

[year of publication 2006, impact factor 8.569]

[70]

Jarolim, P.; Rubin, H.L.; Brabec, V.; Chrobak, L.; Zolotarev, A.S.; Alper, S.L.; Brugnara, C.; Wichterle, H.; Palek, J.

Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis

[year of publication 2006, impact factor 8.569]

[71]

Jarolim, P.; Rubin, H.L.; Liu, S.C.; Cho, M.R.; Brabec, V.; Derick, L.H.; Yi, S.J.; Saad, S.T.; Alper, S.; Brugnara, C.

Duplication of 10 nucleotides in the erythroid band 3 (Ae1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)

[year of publication 2006, impact factor 8.467]

[72]

Jarolim, P.; Rubin, H.L.; Brabec, V.; Palek, J.

A nonsense mutation 1669Glu->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis

[year of publication 2006, impact factor 8.467]

[73]

Stopka, T.; Zivny, J.H.; Stopkova, P.; Prchal, J.F.; Prchal, J.T.

Human hematopoietic progenitors express erythropoietin

[year of publication 2006, impact factor 8.372]

[74]

Jarolim, P.; Rubin, H.L.; Zakova, D.; Storry, J.; Reid, M.

Characterization of seven low incidence blood group antigens carried by erythrocyte band 3 proteins

[year of publication 2006, impact factor 8.372]

[75]

Ullmannova-Benson, V.; Guan, M.; Zhou, X.; Tripathi, V.; Yang, X.-Y.; Zimonjic, D.B.; Popescu, N.C.

DLC1 tumor suppressor gene inhibits migration and invasion of multiple myeloma cells through RhoA GTPase pathway

[year of publication 2009, impact factor 8.296]

[76]

Lenzner, C.; Nürnberg, P.; Thiele, B.J.; Reis, A.; Brabec, V.; Sakalová, A.; Jacobasch, G.

Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia

[year of publication 2006, impact factor 8.279]

[77]

Liu, S.C.; Jarolim, P.; Rubin, H.L.; Palek, J.; Amato, D.; Hassan, K.; Zaik, M.; Sapak, P.

The homozygous state for the band 3 protein mutation in southeast Asian ovalocytosis may be lethal

[year of publication 2006, impact factor 8.279]

[78]

Nagarajan, L.; Zavadil, J.; Claxton, D.; Lu, X.; Fairman, J.; Warrington, J.A.; Wasmuth, J.J.; Chinault, A.C.; Sever, C.E.; Slovak, M.L.; Willman, C.L.; Deisseroth, A.B.

Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to Egr-1 in patients with 5q- chromosome

[year of publication 2006, impact factor 8.279]

[79]

Bartkova, J.; Lukas, J.; Muller, H.; Strauss, M.; Gusterson, B.; Bartek, J.

Abnormal patterns of D-type cyclin expression and G(1) regulation in human head and neck cancer

[year of publication 2006, impact factor 8.206]

[80]

Lukas, J.; Aagaard, L.; Strauss, M.; Bartek, J.

Oncogenic aberrations of p16(INK4/CDKN2) and cyclin D1 cooperate to deregulate G(1) control

[year of publication 2006, impact factor 8.206]


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