Investigation of the atypical FBXW7 mutation spectrum in human tumours by conditional expression of a heterozygous propellor tip missense allele in the mouse intestines

समान संसाधन

• Investigation of the atypical FBXW7 mutation spectrum in human tumours by conditional expression of a heterozygous propellor tip missense allele in the mouse intestines.
  द्वारा: Davis, H, और अन्य
  प्रकाशित: (2014)
• FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development
  द्वारा: Davis, H, और अन्य
  प्रकाशित: (2011)
• FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung development.
  द्वारा: Davis, H, और अन्य
  प्रकाशित: (2011)
• FBXW7 influences murine intestinal homeostasis and cancer, targeting Notch, Jun, and DEK for degradation.
  द्वारा: Babaei-Jadidi, R, और अन्य
  प्रकाशित: (2011)
• Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?
  द्वारा: Giorgia Canali, और अन्य
  प्रकाशित: (2018-11-01)