human RUNX1 protein

RefSeq NM_001001890

Also Known As:

RUNX1 protein, human; AML1 protein, human; CBFA2 protein, human; RUNX1b protein, human; RUNX1c protein, human; Runt related transcription factor isoform b, human; acute myeloid leukemia 1 protein, human; core binding factor alpha 2 subunit, human; runt-related transcription factor 1 protein, human

Networked: 1 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Transcription Factors: 38804
    - Core Binding Factors: 400
      - Core Binding Factor alpha Subunits: 36
        Core Binding Factor Alpha 2 Subunit: 128
        human RUNX1 protein: 1

Experts

1.	Gor, Rajvi: 1 article (05/2022)
2.	Hamid, Pousette: 1 article (05/2022)
3.	Illango, Janan: 1 article (05/2022)
4.	Malik, Mushrin: 1 article (05/2022)
5.	Siddiqui, Nabeel A: 1 article (05/2022)
6.	Sreekantan Nair, Archana: 1 article (05/2022)
7.	Wijeratne Fernando, Ransirini: 1 article (05/2022)

Related Diseases

1.	Hematologic Neoplasms (Hematological Malignancy) 05/01/2022 - "A PubMed database search was conducted using the following medical subject heading (MeSH) terms: "inherited bone marrow failure syndromes," "hematological neoplasms," "gene expression regulation, leukemic," "RUNX1 protein, human," "RUNX1 protein, mouse," and "Neutropenia, Severe Congenital, Autosomal recessive." Three studies published in 2020 were identified as meeting our inclusion and exclusion criteria. "
2.	Neutropenia 05/01/2022 - "A PubMed database search was conducted using the following medical subject heading (MeSH) terms: "inherited bone marrow failure syndromes," "hematological neoplasms," "gene expression regulation, leukemic," "RUNX1 protein, human," "RUNX1 protein, mouse," and "Neutropenia, Severe Congenital, Autosomal recessive." Three studies published in 2020 were identified as meeting our inclusion and exclusion criteria. "
3.	Congenital Bone Marrow Failure Syndromes 05/01/2022 - "A PubMed database search was conducted using the following medical subject heading (MeSH) terms: "inherited bone marrow failure syndromes," "hematological neoplasms," "gene expression regulation, leukemic," "RUNX1 protein, human," "RUNX1 protein, mouse," and "Neutropenia, Severe Congenital, Autosomal recessive." Three studies published in 2020 were identified as meeting our inclusion and exclusion criteria. "

Related Drugs and Biologics

1.	mouse Runx1 protein