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Mostrando ítems 1-10 de 184
Concentración sérica de apolipoproteínas A-I y B en niños y adolescentes
(Sociedad Chilena de Pediatría, 1995)
Angiotensin-converting enzyme and apolipoproteins genes polymorphism in coronary artery disease
(Clinical Cardiology Publ CoMahwahEUA, 2000)
Learning from synthetic models: Differential binding of apolipoprotein A?I variants to components of the extracellular matrix.
(2016)
Specific interactions of apolipoproteins with components of the extracellular matrix,
particularly proteoglycans (PGs), have been postulated to play a key role regulating events
associated to atherosclerosis. Modification ...
Data regarding the sensibility to proteolysis of a natural apolipoprotein A-I mutant
(Elsevier Science, 2020-08)
The article shows dataset of the proteolysis of a natural variant of apolipoprotein A-I (apoA-I) with a substitution of a leucine by and arginine in position 60 (L60R), in comparison with the protein with the native sequence ...
Apolipoproteins AI, B, and E polymorphisms in severe aortic valve stenosis
(Munksgaard Int Publ LtdCopenhagenDinamarca, 2001)
Learning from Synthetic Models of Extracellular Matrix; Differential Binding of Wild Type and Amyloidogenic Human Apolipoprotein A-I to Hydrogels Formed from Molecules Having Charges Similar to Those Found in Natural GAGs
(Springer, 2017-08)
Among other components of the extracellular matrix (ECM), glycoproteins and glycosaminoglycans (GAGs) have been strongly associated to the retention or misfolding of different proteins inducing the formation of deposits ...
Amyloidogenic Propensity of a Natural Variant of Human Apolipoprotein A-I: Stability and Interaction with Ligands
(Public Library of Science, 2015-05)
A number of naturally occurring mutations of human apolipoprotein A-I (apoA-I) have been associated with hereditary amyloidoses. The molecular mechanisms involved in amyloid-associated pathology remain largely unknown. ...