Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice

Keyphrases

• Docking Site 100%
• Adaptor 100%
• Organotypic 100%
• Neurocristopathies 100%
• Renal Malformations 100%
• Autonomic Nervous System 50%
• Urinary Tract 50%
• Genetic Renal Disease 50%
• Hirschsprung Disease 50%
• Enteric Nervous System 50%
• Genitourinary System 50%
• Grb2 50%
• Neural Crest 25%
• Signaling Pathway 25%
• Receptor Tyrosine Kinase 25%
• Nervous System 25%
• Adaptor Protein 25%
• Pleiotropic Effects 25%
• Multiple Organs 25%
• Oncogene 25%
• Aganglionosis 25%
• Redundancy 25%
• Developmental Defects 25%
• Tyrosine Residue 25%
• Distal Colon 25%
• RET Signaling 25%
• Minor Abnormalities 25%

Biochemistry, Genetics and Molecular Biology

• Isoform 100%
• Tyrosine 50%
• Neural Crest 50%
• Pleiotropy 50%
• Receptor Tyrosine Kinase 50%
• Colon 50%
• Proto Oncogene 50%

Neuroscience

• Autonomic Nervous System 100%
• Neural Crest 50%
• Adaptor Protein 50%
• Nervous System 50%
• Proto Oncogene 50%
• Protein Ret 50%