Structural and Functional Characterization of Runx1 Point Mutations Identified in Leukemia and Cleidocranial Dysplasia Patients.

doi 10.1349/ddlp.97
Full Text
Abstract

Available in full text

Date

Unknown

Authors
Publisher

Dartmouth College Library Press

Related search

Mediation Analysis Reveals Common Mechanisms of RUNX1 Point Mutations and RUNX1/RUNX1T1 Fusions Influencing Survival of Patients With Acute Myeloid Leukemia

Scientific Reports
Multidisciplinary
2018English

Molecular Characterization of Mutations in Galactosemia Genes: Structural and Functional Implications

Molecular Cytogenetics
BiochemistryMolecular MedicineGeneticsMolecular Biology
2014English

CBCT Findings in Cleidocranial Dysplasia

Scholars Journal of Dental Sciences
2020English

Molecular Characterization of Cleidocranial Dysplasia (CCD) in the Western Region in KSA

International Journal of Current Microbiology and Applied Sciences
2017English

Functional Effects of Mutations Identified in Patients With Multiminicore Disease

IUBMB Life
BiochemistryGeneticsClinical BiochemistryCell BiologyMolecular Biology
2007English

Mutation Analysis of Core Binding Factor A1 in Patients With Cleidocranial Dysplasia

American Journal of Human Genetics
Genetics
1999English

Diagnosis of Cleidocranial Dysplasia in Routine Chest Radiograph

Circulation
Cardiovascular MedicinePhysiologyCardiology
2007English

Coexistence of AML1/RUNX1 and BCR-ABL Point Mutations in an Imatinib-Resistant Form of CML

Leukemia
Cancer ResearchOncologyAnesthesiologyPain MedicineHematology
2005English

Functional Characterization of the Promoter Region of the Human EVI1 Gene in Acute Myeloid Leukemia: RUNX1 and ELK1 Directly Regulate Its Transcription

Oncogene
Cancer ResearchGeneticsMolecular Biology
2012English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy