Aspartic Acid

gelsolin ; Homo sapiens







8 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 11753432 Loss of a metal-binding site in gelsolin leads to familial amyloidosis-Finnish type. 2002 Feb 1
2 12124262 Steered molecular dynamics simulations on the "tail helix latch" hypothesis in the gelsolin activation process. 2002 Aug 2
3 10767822 Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type). 2000 Feb 2
4 10322122 The amyloidogenicity of gelsolin is controlled by proteolysis and pH. 1999 May 2
5 7881424 Toward understanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitro expression reveals an abnormal gelsolin fragment. 1994 Dec 1
6 8176895 Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides. 1994 Apr 1
7 1338910 Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187. 1992 Oct 1
8 1849145 Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin. 1991 Apr 1