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Results:
1-7
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Results: 7
Authors:
Brodmann, S
Passweg, JR
Gratwohl, A
Tichelli, A
Skoda, RC
Citation: S. Brodmann et al., Myeloproliferative disorders: complications, survival and causes of death, ANN HEMATOL, 79(6), 2000, pp. 312-318
Authors:
Wiestner, A
Padosch, SA
Ghilardi, N
Cesar, JM
Odriozola, J
Shapiro, A
Skoda, RC
Citation: A. Wiestner et al., Hereditary thrombocythaemia is a genetically heterogenous disorder: exclusion of TPO and MPL in two families with hereditary thrombocythaemia, BR J HAEM, 110(1), 2000, pp. 104-109
Authors:
Cazzola, M
Skoda, RC
Citation: M. Cazzola et Rc. Skoda, Translational pathophysiology: a novel molecular mechanism of human disease, BLOOD, 95(11), 2000, pp. 3280-3288
Authors:
Skoda, RC
Citation: Rc. Skoda, Specificity of signaling by hematopoietic cytokine receptors: Instructive versus permissive effects, J RECEPT SI, 19(1-4), 1999, pp. 741-772
Authors:
Stoffel, R
Ziegler, S
Ghilardi, N
Ledermann, B
De Sauvage, FJ
Skoda, RC
Citation: R. Stoffel et al., Permissive role of thrombopoietin and granulocyte colony-stimulating factor receptors in hematopoietic cell fate decisions in vivo, P NAS US, 96(2), 1999, pp. 698-702
Authors:
Ghilardi, N
Wiestner, A
Kikuchi, M
Ohsaka, A
Skoda, RC
Citation: N. Ghilardi et al., Hereditary thrombocythaemia in a Japanese family is caused by a novel point mutation in the thrombopoietin gene, BR J HAEM, 107(2), 1999, pp. 310-316
Authors:
Ghilardi, N
Skoda, RC
Citation: N. Ghilardi et Rc. Skoda, A single-base deletion in the thrombopoietin (TPO) gene causes familial essential thrombocythemia through a mechanism of more efficient translation of TPO mRNA, BLOOD, 94(4), 1999, pp. 1480-1482
Risultati:
1-7
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