Expanding etiology of progressive familial intrahepatic cholestasis

Keyphrases

• Etiology 100%
• Progressive Familial Intrahepatic Cholestasis 100%
• Cholestasis 60%
• Disease Pattern 40%
• Bile 40%
• Genetic Basis 40%
• Bile Acid Homeostasis 40%
• TJP2 40%
• MYO5B 40%
• Liver Disease 20%
• Autosomal Recessive 20%
• Gene mutation 20%
• Hepatocytes 20%
• Disease Management 20%
• Cholestatic Disease 20%
• Extracted Data 20%
• Anatomic 20%
• MEDLINE 20%
• Phenotypic Spectrum 20%
• Manual Search 20%
• Pattern Recognition 20%
• Jaundice 20%
• Knowledge Base 20%
• End-stage Liver Disease 20%
• Transport Mechanism 20%
• Scientific Advancement 20%
• PubMed Search 20%
• PRISMA Guidelines 20%
• Multidrug Resistance Protein 3 (MDR3) 20%
• Systemic Review 20%
• ATP8B1 20%
• ABCB11 20%
• NR1H4 20%
• English-only 20%
• FIC1 20%
• Bile Transport 20%
• ABCB4 20%

Medicine and Dentistry

• Progressive Familial Intrahepatic Cholestasis 100%
• Diseases 100%
• Cholestasis 50%
• Bile 50%
• Homeostasis 33%
• Bile Acid 33%
• Base 16%
• Liver Disease 16%
• Autosomal Recessive Disorder 16%
• Gene Mutation 16%
• Hepatocyte 16%
• Disease 16%
• Jaundice 16%
• End Stage Liver Disease 16%
• Pattern Recognition 16%

Pharmacology, Toxicology and Pharmaceutical Science

• Intrahepatic Cholestasis 100%
• Diseases 100%
• Cholestasis 50%
• Bile Acid 33%
• Liver Disease 16%
• Base 16%
• End Stage Liver Disease 16%
• Autosomal Recessive Disorder 16%
• Jaundice 16%