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

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Year: 2007
Type: article
Source: The EMBO Journal
DOI: 10.1038/sj.emboj.7601568
Authors: Christina J Matheny, Maren E Speck, Patrick R Cushing, Yunpeng Zhou, Takeshi Corpora, Michael Regan, Miki Newman, Liya Roudaia, Caroline L Speck, Ting‐Lei Gu, Stephen M Griffey, John H Bushweller, Nancy A Speck
Institutions: Dartmouth College, Dartmouth Health, University of Virginia, University of California, Davis
Language: English

Topic: Acute Myeloid Leukemia Research
Subfield: Hematology
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: bronze

Funders: Norris Cotton Cancer Center, National Cancer Institute, National Institute of General Medical Sciences
Awards: MOUSE MODELS FOR FAMILIAL PLATELET DISORDER, G517873728, G518495827, Molecular and Cellular Biology at Dartmouth, Cancer Center Support Grant
OpenAlex ID: W2073608176
FWCI: 4.691
Cites: 50
Cited by: 119
Related to: 10
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