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Study of inherited thrombocytopenia resulting from mutations in ETV6 or RUNX1 using a human pluripotent stem cell model

Stem Cell Reports(2021)10.1016/j.stemcr.2021.04.013Source: DataRank Database

Study of inherited thrombocytopenia resulting from mutations in ETV6 or RUNX1 using a human pluripotent stem cell model is a research paper published in Stem Cell Reports (2021). On theSindex it has a DataRank of 0. It has been cited 24 times.

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Open Access24 citations

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Enrichment:Funding (17 grants)OA: goldTopics (36)IDs (PubMed, PMC)Annotations (2)SDGs (1)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (11)

Catriana C. Nations ORCID,Joshua G. Klein ORCID,Giulia Pavani ORCID,Jean Ann Maguire,Rodney M. Camire ORCID

Live enrichment

PubMed:34019812 PMC:PMC8190596

National Institutes of Health

Grant: F31-HL140774

National Institutes of Health

Grant: R01-HL130698

National Institutes of Health

Grant: T32-DK007780

National Institutes of Health

Grant: T32-GM007229

National Institutes of Health

Grant: U01-HL134696

NICHD NIH HHS

Grant: T32 HD083185

NHLBI NIH HHS

Grant: F31 HL140774

NHLBI NIH HHS

Grant: R01 HL130698

NIGMS NIH HHS

Grant: T32 GM007229

NIDDK NIH HHS

Grant: T32 DK007780

National Institutes of Health

Grant: 5T32DK007780-14

Hematopoiesis training grant

National Institutes of Health

Grant: 5U01HL134696-03

Improving transfusion therapy for patients with sickle cell disease with pluripotent stem cell-derived red cells

National Institutes of Health

Grant: 5F31HL140774-02

Investigating the mechanism of thrombocytopenia due to ETV6 or RUNX1 mutations

National Institutes of Health

Grant: 5T32GM007229-14

CELLULAR AND MOLECULAR BIOLOGY

National Institutes of Health

Grant: 5R01HL130698-03

Optimization of Ex Vivo- and In Vivo- Generated Platelets

Leukemia and Lymphoma Society

Alex's Lemonade Stand Foundation for Childhood Cancer

goldLicense: cc-by-nc-nd

publisherhttp://www.cell.com/article/S2213671121002083/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2213671121002083?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2213671121002083?httpAccept=text/plain

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8190596

Europe_PMChttps://europepmc.org/articles/PMC8190596

Fields of Study

0301 basic medicine03 medical and health sciences

MeSH Terms

MegakaryocytesCells, CulturedHumansThrombocytopeniaGenetic Predisposition to DiseaseRepressor ProteinsHematopoiesisPhenotypeMutationModels, BiologicalCore Binding Factor Alpha 2 SubunitProto-Oncogene Proteins c-etsInduced Pluripotent Stem CellsETS Translocation Variant 6 Protein

Keywords

Embryonic stem cellsHematopoiesismegakaryocyteRunx1Etv6IpscsProto-Oncogene Proteins c-etsInduced Pluripotent Stem CellsModels, BiologicalThrombocytopeniaETS Translocation Variant 6 ProteinRepressor ProteinsPhenotypeReportCore Binding Factor Alpha 2 SubunitMutationHumansGenetic Predisposition to DiseaseMegakaryocytesCells, Cultured

Sustainable Development Goals

SDG 3: 3. Good health

Study of inherited thrombocytopenia resulting from mutations in ETV6 or RUNX1 using a human pluripotent stem cell model

FAIR Checklist

Authors (11)

Funding (17 grants)

Open Access

Topics

Annotations (Europe PMC)