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Imamoto, Akira
One or more keywords matched the following items that are connected to
Imamoto, Akira
Item Type
Name
Concept
Chromosomes, Human, Pair 22
Academic Article
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.
Academic Article
Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome.
Academic Article
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
Academic Article
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Academic Article
Murine model indicates 22q11.2 signaling adaptor CRKL is a dosage-sensitive regulator of genitourinary development.
Search Criteria
Chromosomes Human Pair 22