Apo A-I Deficiency Latest Advances
Find the Latest Research About Apo A-I Deficiency
Last Updated: 04/28/2026
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Found 192 publications
Increased atherosclerosis and expression of inflammarafts in macrophage foam cells in AIBP-deficient mice.
Journal: bioRxiv : the preprint server for biology
Published: August 20, 2025
A Gut-Restricted Liver X Receptor Agonist Ameliorates Liver Injury in Experimental Short Bowel Syndrome.
Journal: Gastroenterology
Published: February 10, 2025
Vitamin D deficiency is associated with apolipoprotein A1 levels in patients with young-onset type 2 diabetes mellitus.
Journal: World journal of diabetes
Published: January 27, 2025
Association of apolipoprotein A1 (rs 5069) genotyping with 25-hydroxyvitamin D deficiency and insulin resistance as a metabolic and genetic difference in obesity and type 2 diabetes mellitus.
Journal: European journal of nutrition
Published: October 21, 2024
AIBP Protects Müller Glial Cells Against Oxidative Stress-Induced Mitochondrial Dysfunction and Reduces Retinal Neuroinflammation.
Journal: Antioxidants (Basel, Switzerland)
Published: September 05, 2024
Apolipoprotein A1 deficiency increases macrophage apoptosis and necrotic core development in atherosclerotic plaques in a Bim-dependent manner.
Journal: Journal of lipid research
Published: May 26, 2024
A decreased level of high-density lipoprotein is a possible risk factor for type 2 diabetes mellitus: A review.
Journal: Health science reports
Published: September 11, 2023
A novel splicing variant in ABCA1 in the first reported Hong Kong Chinese patient with high-density lipoprotein deficiency.
Journal: Endocrinology, diabetes & metabolism case reports
Published: September 01, 2023
Association of Circulating Apolipoprotein AI Levels in Patients With Alzheimer's Disease: A Systematic Review and Meta-Analysis.
Journal: Frontiers in aging neuroscience
Published: March 18, 2022
ApoA1 Deficiency Reshapes the Phenotypic and Molecular Characteristics of Bone Marrow Adipocytes in Mice.
Journal: International journal of molecular sciences
Published: March 18, 2022
A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency.
Journal: Journal of clinical lipidology
Published: January 03, 2022
Last Updated: 04/28/2026