Cansu Koyunlar

Rotterdam, ZH 3015CN, Netherlands

Last Updated: 09/26/2026

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Found 8 publications

Hematological phenotypes in GATA2 deficiency syndrome arise from aging, maladaptation to proliferation, and somatic events.

Hematological phenotypes in GATA2 deficiency syndrome arise from aging, maladaptation to proliferation, and somatic events.

Journal: Blood advances

Published: October 18, 2024

GATA2 heterozygosity causes an epigenetic feedback mechanism resulting in myeloid and erythroid dysplasia.

GATA2 heterozygosity causes an epigenetic feedback mechanism resulting in myeloid and erythroid dysplasia.

Journal: British journal of haematology

Published: April 03, 2024

Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition.

Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition.

Journal: Blood advances

Published: May 04, 2022

Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux.

Knockout of zebrafish desmin genes does not cause skeletal muscle degeneration but alters calcium flux.

Journal: Scientific reports

Published: October 18, 2020

From Basic Biology to Patient Mutational Spectra of GATA2 Haploinsufficiencies: What Are the Mechanisms, Hurdles, and Prospects of Genome Editing for Treatment.

From Basic Biology to Patient Mutational Spectra of GATA2 Haploinsufficiencies: What Are the Mechanisms, Hurdles, and Prospects of Genome Editing for Treatment.

Journal: Frontiers in genome editing

Published: September 02, 2020

Essential role for Gata2 in modulating lineage output from hematopoietic stem cells in zebrafish.

Essential role for Gata2 in modulating lineage output from hematopoietic stem cells in zebrafish.

Journal: Blood advances

Published: July 20, 2020

Deletion of a conserved Gata2 enhancer impairs haemogenic endothelium programming and adult Zebrafish haematopoiesis.

Deletion of a conserved Gata2 enhancer impairs haemogenic endothelium programming and adult Zebrafish haematopoiesis.

Journal: Communications biology

Published: April 25, 2019

Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.

Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.

Journal: Journal of the American Society of Nephrology : JASN

Published: March 11, 2014

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Last Updated: 09/26/2026