Search Results - "Urata, Takayo"
-
1
Relapsed RUNX1-RUNX1T1-positive acute myeloid leukemia with pseudo-Chediak-Higashi granules
Published in International journal of hematology (01-05-2021)Get full text
Journal Article -
2
The Nup98::Nsd1 fusion gene induces CD123 expression in 32D cells
Published in International journal of hematology (01-08-2023)“…The NUP98::NSD1 fusion gene is associated with extremely poor prognosis in patients with acute myeloid leukemia (AML). NUP98::NSD1 induces self-renewal and…”
Get full text
Journal Article -
3
Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report
Published in Journal of pediatric hematology/oncology (01-03-2022)“…Fanconi anemia (FA) is a rare genetic disorder that manifests as congenital abnormalities and bone marrow failure (BMF). Most patients with FA present with BMF…”
Get full text
Journal Article -
4
Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report
Published in Journal of pediatric hematology/oncology (23-07-2021)“…Fanconi anemia (FA) is a rare genetic disorder that manifests as congenital abnormalities and bone marrow failure (BMF). Most patients with FA present with BMF…”
Get full text
Journal Article -
5
Allogeneic Hematopoietic Cell Transplantation for Dyskeratosis Congenita: A Report of 3 Cases
Published in Journal of pediatric hematology/oncology (01-10-2017)“…Although bone marrow failure in patients with dyskeratosis congenita (DKC) can be successfully treated with allogeneic hematopoietic cell transplantation…”
Get full text
Journal Article -
6
Relapsed RUNX1-RUNX1T1-positive acute myeloid leukemia with pseudo-Chediak-Higashi granules
Published in International journal of hematology (01-05-2021)Get full text
Report