Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of...
Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1
About this item
Full title
Author / Creator
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
More information
Scope and Contents
Contents
Dyskeratosis congenita (DC) is a rare telomere biology disorder, which results in different clinical manifestations, including severe bone marrow failure. To date, the only curative treatment for the bone marrow failure in DC patients is allogeneic hematopoietic stem cell transplantation. However, due to the toxicity associated to this treatment, i...
Alternative Titles
Full title
Generation of dyskeratosis congenita-like hematopoietic stem cells through the stable inhibition of DKC1
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_3e9b4086c5e84d35a41e8439e2fd5480
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3e9b4086c5e84d35a41e8439e2fd5480
Other Identifiers
ISSN
1757-6512
E-ISSN
1757-6512
DOI
10.1186/s13287-021-02145-8