Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles-Reference-Cited by-同舟云学术

Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles

Published:2007-02-08 Issue:4 Volume:26 Page:1163-1175
ISSN:0261-4189
Container-title:The EMBO Journal
language:
Short-container-title:EMBO J

Author:

Matheny Christina J,Speck Maren E,Cushing Patrick R,Zhou Yunpeng,Corpora Takeshi,Regan Michael,Newman Miki,Roudaia Liya,Speck Caroline L,Gu Ting-Lei,Griffey Stephen M,Bushweller John H,Speck Nancy A

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Reference49 articles.

1. The Ig fold of the core binding factor α Runt domain is a member of a family of structurally and functionally related Ig-fold DNA-binding domains

2. A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies

3. Rescuing the function of mutant p53

4. Properties of Some Variants of Human β2-Microglobulin and Amyloidogenesis

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