Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease

Keyphrases

• Polycystic Liver Disease 100%
• Hepatology 100%
• Congenital Disorders of Glycosylation 100%
• Cyst 22%
• PRKCSH 22%
• Sec63 22%
• Cystogenesis 22%
• Molecular Mechanism 11%
• Autosomal Recessive 11%
• Genetic Features 11%
• Epithelium 11%
• Distinct Subtypes 11%
• Endoplasmic Reticulum 11%
• Protein Folding 11%
• Protein Binding 11%
• Molecular Pathways 11%
• Liver 11%
• Genetic Disease 11%
• Disease-specific 11%
• Multisystem Disease 11%
• Unfolded Proteins 11%
• N-glycan 11%
• N-glycosylation 11%
• Disease-causing mutations 11%
• Progressive Disease 11%
• Gene Products 11%
• Clinical Genetics 11%
• Biochemical Pathways 11%
• Cyst Formation 11%
• Protein Import 11%
• Liver Volume 11%
• Disease Pathology 11%
• Translocon 11%
• ER-associated Degradation 11%
• Unfolding Method 11%
• Fluid-filled 11%
• Calnexin 11%
• Disease Pathophysiology 11%
• Calreticulin 11%
• Glucosidase II 11%
• Two-hit Model 11%
• Product Function 11%

Medicine and Dentistry

• Liver Polycystic Disease 100%
• Congenital Disorder of Glycosylation 100%
• Hepatology 100%
• Disease 33%
• Symptom 11%
• Genetic Disorder 11%
• Autosomal Recessive Inheritance 11%
• Autosomal Dominant Inheritance 11%
• Protein Binding 11%
• Epileptic Absence 11%
• Pathophysiology 11%
• Endoplasmic reticulum 11%
• Gene Product 11%
• Clinical Genetics 11%
• Cleft 11%
• Systemic Disease 11%
• Guanine Nucleotide Binding Protein 11%
• Protein Folding 11%
• Glycan 11%
• Glycosylation 11%
• Calnexin 11%
• Translocon 11%
• Glucosidase 11%
• Calreticulin 11%

Biochemistry, Genetics and Molecular Biology

• Congenital Disorder of Glycosylation 100%
• Genetics 25%
• Genetic Disorder 25%
• Autosomal Recessive Inheritance 25%
• Autosomal Dominant Inheritance 25%
• Liquid 25%
• Binding Protein 25%
• Glycosylation 25%
• Gene Product 25%
• Liver Weight 25%
• Protein Folding 25%
• Calnexin 25%
• Glucosidase 25%
• Translocon 25%
• Calreticulin 25%