Platelet transcriptome analysis in patients with germline RUNX1 mutations

Author:

Palma-Barqueros VerónicaORCID,Bastida José MaríaORCID,López Andreo María José,Zámora-Cánovas Ana,Zaninetti CarloORCID,Ruiz-Pividal Juan Francisco,Bohdan Natalia,Padilla José,Teruel-Montoya Raúl,Marín-Quilez Ana,Revilla Nuria,Sánchez-Fuentes Ana,Rodriguez-Alen Agustín,Benito Rocío,Vicente Vicente,Iturbe Teodoro,Greinacher AndreasORCID,Lozano María LuisaORCID,Rivera JoséORCID

Publisher

Elsevier BV

Subject

Hematology

Reference30 articles.

1. AML1/Runx1 as a versatile regulator of hematopoiesis: regulation of its function and a role in adult hematopoiesis;Kurokawa;Int J Hematol,2006

2. The clinical, molecular, and mechanistic basis of RUNX1 mutations identified in hematological malignancies;Yokota;Mol Cells,2020

3. Inherited thrombocytopenias: history, advances and perspectives;Nurden;Haematologica,2020

4. Inherited thrombocytopenias: an updated guide for clinicians;Pecci;Blood Rev,2021

5. Transcription factor defects causing platelet disorders;Daly;Blood Rev,2017

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