Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Wanyun Tao
A Compound Heterozygous Mutation of Lipase Maturation Factor 1 Is Responsible for Hypertriglyceridemia of a Patient
Journal of Atherosclerosis and Thrombosis
Biochemistry
Internal Medicine
Cardiovascular Medicine
Cardiology
Related publications
Withdrawal: Lipase Maturation Factor 1 Is Required for Endothelial Lipase Activity
Journal of Lipid Research
Biochemistry
Endocrinology
Cell Biology
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Compound Heterozygous Hemophilia a in a Female Patient and the Identification of a Novel Missense Mutation, p.Met1093Ile
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Nateglinide Is Effective for Diabetes Mellitus With Reactive Hypoglycemia in a Child With a Compound Heterozygous ABCC8 Mutation
Clinical Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Lipase Maturation Factor 1: Structure and Role in Lipase Folding and Assembly
Current Opinion in Lipidology
Nutrition
Genetics
Cell Biology
Molecular Biology
Cardiology
Endocrinology
Cardiovascular Medicine
Dietetics
Metabolism
Diabetes
A Novel Compound Heterozygous Stxbp2 Mutation in a Case With Familial Hemophagocytic Lymphohistiocytosis
Turkish Journal of Pediatric Disease
Phenotypic Expression of Heterozygous Lipoprotein Lipase Deficiency in the Extended Pedigree of a Proband Homozygous for a Missense Mutation.
Journal of Clinical Investigation
Medicine
Lipase Maturation Factor 1 (Lmf1) Is Induced by Endoplasmic Reticulum Stress Through Activating Transcription Factor 6α (Atf6α) Signaling
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Novel Heterozygous C243Y A20/Tnfaip3 Gene Mutation Is Responsible for Chronic Inflammation in Autosomal-Dominant Behçet's Disease
RMD Open
Rheumatology
Allergy
Immunology