Guntram Busche

Carl Neuberg Str. 1
Hannover, NI 30625, Germany

Last Updated: 09/26/2026

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Found 53 publications

Author Correction: Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9.

Author Correction: Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9.

Journal: Nature medicine

Published: October 24, 2024

Sensitive and reliable detection of KIT p.D816V mutation in decalcified archival bone marrow trephines.

Sensitive and reliable detection of KIT p.D816V mutation in decalcified archival bone marrow trephines.

Journal: Virchows Archiv : an international journal of pathology

Published: August 08, 2024

XPO1-dependency of DEK::NUP214 leukemia.

XPO1-dependency of DEK::NUP214 leukemia.

Journal: Leukemia

Published: July 12, 2024

Evolution of severe (transfusion-dependent) anaemia in myelodysplastic syndromes with 5q deletion is characterized by a macrophage-associated failure of the eythropoietic niche.

Evolution of severe (transfusion-dependent) anaemia in myelodysplastic syndromes with 5q deletion is characterized by a macrophage-associated failure of the eythropoietic niche.

Journal: British journal of haematology

Published: December 04, 2021

A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutation.

A unique role of p53 haploinsufficiency or loss in the development of acute myeloid leukemia with FLT3-ITD mutation.

Journal: Leukemia

Published: January 19, 2021

Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q).

Genome-wide DNA methylation analysis pre- and post-lenalidomide treatment in patients with myelodysplastic syndrome with isolated deletion (5q).

Journal: Annals of hematology

Published: November 17, 2020

Combination of myeloproliferative neoplasm driver gene activation with mutations of splice factor or epigenetic modifier genes increases risk of rapid blastic progression.

Combination of myeloproliferative neoplasm driver gene activation with mutations of splice factor or epigenetic modifier genes increases risk of rapid blastic progression.

Journal: European journal of haematology

Published: November 06, 2020

Bone marrow fibrosis in primary myelofibrosis in relation to myelodysplasia- and age-related mutations of hematopoietic cells

Bone marrow fibrosis in primary myelofibrosis in relation to myelodysplasia- and age-related mutations of hematopoietic cells

Journal: Der Pathologe

Published: October 28, 2020

Genome-wide DNA methylation profiling is able to identify prefibrotic PMF cases at risk for progression to myelofibrosis.

Genome-wide DNA methylation profiling is able to identify prefibrotic PMF cases at risk for progression to myelofibrosis.

Journal: Clinical epigenetics

Published: September 25, 2020

3D culture conditions support Kaposi's sarcoma herpesvirus (KSHV) maintenance and viral spread in endothelial cells.

3D culture conditions support Kaposi's sarcoma herpesvirus (KSHV) maintenance and viral spread in endothelial cells.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: July 27, 2020

Exposure of Patient-Derived Mesenchymal Stromal Cells to TGFB1 Supports Fibrosis Induction in a Pediatric Acute Megakaryoblastic Leukemia Model.

Exposure of Patient-Derived Mesenchymal Stromal Cells to TGFB1 Supports Fibrosis Induction in a Pediatric Acute Megakaryoblastic Leukemia Model.

Journal: Molecular cancer research : MCR

Published: February 05, 2020

Heterogeneous bone-marrow stromal progenitors drive myelofibrosis via a druggable alarmin axis.

Heterogeneous bone-marrow stromal progenitors drive myelofibrosis via a druggable alarmin axis.

Journal: Cell stem cell

Published: November 15, 2019

Showing 1-12 of 53

Last Updated: 09/26/2026