Varun Sudunagunta
0000-0002-8639-8907
The Children's Hospital of Philadelphia
6 papers found
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RUNX-1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cells
RUNX1 haploinsufficiency causes a marked deficiency of megakaryocyte-biased hematopoietic progenitor cells: Mechanistic studies and drug correction
The Inherited Platelet Disorder of RUNX1 Haploinsufficiency (Familial Platelet Disorder with Associated Myeloid Malignancy (FPDMM)) Has a Marked Deficiency of Megakaryocyte-Biased Hematopoietic Progenitor Cells: Mechanistic Studies and Drug Correction
New insights into hematopoiesis and megakaryopoiesis in familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML): Role of transforming growth factor beta (TGFB) 1
Modulating TGFβ1 levels in FPD/AML patient iPSC-derived megakaryocytes
Englacial layer mapping correlation and consistency techniques: an example from airborne ice penetrating radar profiles in West Antarctica
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