Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Wei-Xia Lin
Sodium Taurocholate Cotransporting Polypeptide (NTCP) Deficiency: Identification of a Novel SLC10A1 Mutation in Two Unrelated Infants Presenting With Neonatal Indirect Hyperbilirubinemia and Remarkable Hypercholanemia
Oncotarget
Oncology
SLC25A13 Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China
PLoS ONE
Multidisciplinary
Related publications
A Single Adaptive Mutation in Sodium Taurocholate Cotransporting Polypeptide Induced by Hepadnaviruses Determines Virus Species Specificity
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Blocking Sodium‐taurocholate Cotransporting Polypeptide Stimulates Biliary Cholesterol and Phospholipid Secretion
Hepatology
Medicine
Hepatology
Clinical and Molecular Characterization of Four Patients With NTCP Deficiency From Two Unrelated Families Harboring the Novel SLC10A1 Variant C.595A>C (p.Ser199Arg)
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Sodium Taurocholate Cotransporting Polypeptide Mediates Woolly Monkey Hepatitis B Virus Infection of Tupaia Hepatocytes
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Sodium Taurocholate Cotransporting Polypeptide Is the Limiting Host Factor of Hepatitis B Virus Infection in Macaque and Pig Hepatocytes
Hepatology
Medicine
Hepatology
Neonatal Hyperbilirubinemia in Infants With G6PD C.563C > T Variant
BMC Pediatrics
Child Health
Pediatrics
Perinatology
Identification of a Novel TTC19 Mutation in a Portuguese Family With Complex III Deficiency
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Phenotype and Genotype of FXIII Deficiency in Two Unrelated Probands: Identification of a Novel F13A1 Large Deletion Mediated by Complex Rearrangement
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Investigation of the Potential Risk Factors of Indirect Hyperbilirubinemia in Patients Admitted to the Neonatal Intensive Care Unit With Hyperbilirubinemia
Akdeniz Medical Journal