Article

THPO gene variants in patients with acquired aplastic anemia

2018-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: cec108ad-c11f-51b3-8efd-c3857366267e
DOI: 10.1016/j.htct.2018.01.009
PMCID: PMC6738484

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

THPO gene variants in patients with acquired aplastic anemiaDOI 10.1016/j.htct.2018.01.009Read

Inherited THPO mutation, with morphology resembling chronic myeloid leukaemia.Semantic proximity Read

Defective binding of ETS1 and STAT4 due to a mutation in the promoter region of THPO as a novel mechanism of congenital amegakaryocytic thrombocytopenia.Semantic proximity Read

Relative impact of THPO mutation causing hereditary thrombocythemia.Semantic proximity Read

Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia.Semantic proximity Read

Hereditary thrombocythemia due to splicing donor site mutation of THPO in a Japanese family.Semantic proximity Read

A novel thrombopoietin (THPO) mutation altering mRNA splicing in a case of familial thrombocytosis.Semantic proximity Read

Germline variants in acquired aplastic anemia: current knowledge and future perspectives.Semantic proximity Read

A de novo splice donor mutation in the thrombopoietin gene causes hereditary thrombocythemia in a Polish family.Semantic proximity Read

Functional and structural profiling of the human thrombopoietin gene promoter.Semantic proximity Read

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.Semantic proximity Read

GATA1 gene variants associated with thrombocytopenia and anemia.Semantic proximity Read

Genetic variation in telomeric repeat binding factors 1 and 2 in aplastic anemia.Semantic proximity Read