Hana Raslova

Villejuif, France

Last Updated: 09/26/2026

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Found 74 publications

Acquired Bernard-Soulier syndrome as the presenting feature of GATA2-related myeloid neoplasm in an adolescent: an insight into the mechanisms underlying the platelet defect.

Acquired Bernard-Soulier syndrome as the presenting feature of GATA2-related myeloid neoplasm in an adolescent: an insight into the mechanisms underlying the platelet defect.

Journal: Haematologica
Published: February 13, 2025

F-actin disassembly by the oxidoreductase MICAL1 promotes mechano-dependent VWF-GPIbα interaction in platelets.

F-actin disassembly by the oxidoreductase MICAL1 promotes mechano-dependent VWF-GPIbα interaction in platelets.

Journal: Nature communications
Published: February 06, 2025

Increased RhoA pathway activation downstream of αIIbβ3/SRC contributes to heterozygous Bernard Soulier syndrome.

Increased RhoA pathway activation downstream of αIIbβ3/SRC contributes to heterozygous Bernard Soulier syndrome.

Journal: Haematologica
Published: August 09, 2024

Dose-dependent effects of eltrombopag iron chelation on platelet formation.

Dose-dependent effects of eltrombopag iron chelation on platelet formation.

Journal: Blood vessels, thrombosis & hemostasis
Published: July 16, 2024

Monocytes generated by interleukin-6-treated human hematopoietic stem and progenitor cells secrete calprotectin that inhibits erythropoiesis.

Monocytes generated by interleukin-6-treated human hematopoietic stem and progenitor cells secrete calprotectin that inhibits erythropoiesis.

Journal: iScience
Published: June 20, 2024

Progressive chromatin rewiring by ETO2::GLIS2 revealed in a genome-edited human iPSC model of pediatric leukemia initiation.

Progressive chromatin rewiring by ETO2::GLIS2 revealed in a genome-edited human iPSC model of pediatric leukemia initiation.

Journal: Blood
Published: March 01, 2024

Deregulation of the p19/CDK4/CDK6 axis in Jak2V617F megakaryocytes accelerates the development of myelofibrosis.

Deregulation of the p19/CDK4/CDK6 axis in Jak2V617F megakaryocytes accelerates the development of myelofibrosis.

Journal: Leukemia
Published: June 30, 2023

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.

Journal: Blood advances
Published: February 23, 2023

DiPRO1 distinctly reprograms muscle and mesenchymal cancer cells.

DiPRO1 distinctly reprograms muscle and mesenchymal cancer cells.

Journal: EMBO molecular medicine
Published: January 10, 2023

ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopoiesis.

ANKRD26 is a new regulator of type I cytokine receptor signaling in normal and pathological hematopoiesis.

Journal: Haematologica
Published: September 05, 2022

A gain-of-function filamin A mutation in mouse platelets induces thrombus instability.

A gain-of-function filamin A mutation in mouse platelets induces thrombus instability.

Journal: Journal of thrombosis and haemostasis : JTH
Published: March 08, 2022

An inherited gain-of-function risk allele in EPOR predisposes to familial JAK2V617F myeloproliferative neoplasms.

An inherited gain-of-function risk allele in EPOR predisposes to familial JAK2V617F myeloproliferative neoplasms.

Journal: British journal of haematology
Published: January 06, 2022
Showing 1-12 of 74

Last Updated: 09/26/2026