Akira Imamoto to Phenotype
This is a "connection" page, showing publications Akira Imamoto has written about Phenotype.
Connection Strength
0.121
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Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes. Dev Cell. 2006 Jan; 10(1):71-80.
Score: 0.043
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Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome. Nat Genet. 2001 Mar; 27(3):293-8.
Score: 0.031
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Specific and redundant roles of Src and Fyn in organizing the cytoskeleton. Nature. 1995 Jul 20; 376(6537):267-71.
Score: 0.021
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Disruption of the csk gene, encoding a negative regulator of Src family tyrosine kinases, leads to neural tube defects and embryonic lethality in mice. Cell. 1993 Jun 18; 73(6):1117-24.
Score: 0.018
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The adaptor protein paxillin is essential for normal development in the mouse and is a critical transducer of fibronectin signaling. Mol Cell Biol. 2002 Feb; 22(3):901-15.
Score: 0.008