Associated Papers
Structures of Angptl3 and Angptl4, modulators of triglyceride levels and coronary artery disease.
Biterova E et al.
Scientific Reports, 2018
ANGPTL4 T266M variant is associated with reduced cancer invasiveness.
Tan ZW et al.
Biochimica Et Biophysica Acta. Molecular Cell Research, 2017
Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism.
Ionita-Laza I et al.
Plos Genetics, 2014
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
24448499 (PubMed )
Supplement: NIHMS551112-supplement-7.xlsx › S_Data_6
Phylogenetics applied to genotype/phenotype association and selection analyses with sequence data from angptl4 in humans.
Maxwell TJ et al.
International Journal of Molecular Sciences, 2010
Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.
Romeo S et al.
The Journal of Clinical Investigation, 2009
Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.
Romeo S et al.
Nature Genetics, 2007
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