Varaico: Literature-Extracted Genetic Variants

Gene:LMF1
Variant:p.Y439*
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LMF1

NM_022773.4:p.Y439*

Associated Papers

Genetic and biochemical analysis of severe hypertriglyceridemia complicated with acute pancreatitis or with low post-heparin lipoprotein lipase mass.

Suzuki T et al.

Endocrine Journal, 2024

Understanding Hypertriglyceridemia: Integrating Genetic Insights.

Alves M et al.

Genes, 2024

The role of lipase maturation factor 1 in hypertriglyceridaemia and atherosclerosis: An update.

Dabravolski SA et al.

Sage Open Medicine, 2024

Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency.

Rodríguez-Gutiérrez PG et al.

International Journal of Molecular Sciences, 2022

Genetics of Familial Combined Hyperlipidemia (FCHL) Disorder: An Update.

Taghizadeh E et al.

Biochemical Genetics, 2022

A Heterozygous LMF1 Gene Mutation (c.1523C>T), Combined With an LPL Gene Mutation (c.590G>A), Aggravates the Clinical Symptoms in Hypertriglyceridemia.

Guo D et al.

Frontiers in Genetics, 2022

Genetic and functional studies of the LMF1 gene in Thai patients with severe hypertriglyceridemia.

Plengpanich W et al.

Molecular Genetics and Metabolism Reports, 2020

Six years' experience with LipidSeq: clinical and research learnings from a hybrid, targeted sequencing panel for dyslipidemias.

Dron JS et al.

Bmc Medical Genomics, 2020

32041611 (PubMed )
Supplement: 12920_2020_669_MOESM1_ESM.xlsx › Supp_Table_4

Identification of a novel and heterozygous LMF1 nonsense mutation in an acute pancreatitis patient with severe hypertriglyceridemia, severe obesity and heavy smoking.

Chen WW et al.

Lipids in Health and Disease, 2019

A Compound Heterozygous Mutation of Lipase Maturation Factor 1 is Responsible for Hypertriglyceridemia of a Patient.

Liu Y et al.

Journal of Atherosclerosis and Thrombosis, 2019

Update on the molecular biology of dyslipidemias.

Ramasamy I

Clinica Chimica Acta; International Journal of Clinical Chemistry, 2016

Genetic predisposition of human plasma triglyceride concentrations.

Schwarzova L et al.

Physiological Research, 2015

Purification, cellular levels, and functional domains of lipase maturation factor 1.

Babilonia-Rosa MA et al.

Biochemical and Biophysical Research Communications, 2014

Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia.

Surendran RP et al.

Journal of Internal Medicine, 2012

Allelic and phenotypic spectrum of plasma triglycerides.

Johansen CT et al.

Biochimica Et Biophysica Acta, 2012

Lipase maturation factor 1: a lipase chaperone involved in lipid metabolism.

Péterfy M

Biochimica Et Biophysica Acta, 2012

Lipase maturation factor 1 is required for endothelial lipase activity.

Ben-Zeev O et al.

Journal of Lipid Research, 2011

Lipase maturation factor 1: structure and role in lipase folding and assembly.

Doolittle MH et al.

Current Opinion in Lipidology, 2010

A quantitative assay measuring the function of lipase maturation factor 1.

Yin F et al.

Journal of Lipid Research, 2009

Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia.

Cefalù AB et al.

The Journal of Clinical Endocrinology and Metabolism, 2009

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia.

Péterfy M et al.

Nature Genetics, 2007

JCL Roundtable: Hypertriglyceridemia due to defects in lipoprotein lipase function.

Brown WV et al.

Journal of Clinical Lipidology, 0

Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing.

Cefalù AB et al.

Journal of Clinical Lipidology, 0

A novel homozygous nonsense variant of LMF1 in pregnancy-induced hypertriglyceridemia with acute pancreatitis.

Tanaka M et al.

Journal of Clinical Lipidology, 0

Identification and functional analysis of novel homozygous LMF1 variants in severe hypertriglyceridemia.

Bedoya C et al.

Journal of Clinical Lipidology, 0

Comprehensive analysis of Chinese patients with non-LPL familial chylomicronemia syndrome: Genetic variants, dietary interventions, and clinical insights.

Gong Z et al.

Journal of Clinical Lipidology, 0

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