197 related articles for article (PubMed ID: 8383491)
1. Demonstration of a circulating 65K gelsolin variant specific for familial amyloidosis, Finnish type.
Maury CP; Rossi H
Biochem Biophys Res Commun; 1993 Feb; 191(1):41-4. PubMed ID: 8383491
[TBL] [Abstract][Full Text] [Related]
2. Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.
de la Chapelle A; Tolvanen R; Boysen G; Santavy J; Bleeker-Wagemakers L; Maury CP; Kere J
Nat Genet; 1992 Oct; 2(2):157-60. PubMed ID: 1338910
[TBL] [Abstract][Full Text] [Related]
3. Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assay.
Haltia M; Levy E; Meretoja J; Fernandez-Madrid I; Koivunen O; Frangione B
Am J Med Genet; 1992 Feb; 42(3):357-9. PubMed ID: 1311149
[TBL] [Abstract][Full Text] [Related]
4. Gelsolin-related amyloidosis. Identification of the amyloid protein in Finnish hereditary amyloidosis as a fragment of variant gelsolin.
Maury CP
J Clin Invest; 1991 Apr; 87(4):1195-9. PubMed ID: 1849145
[TBL] [Abstract][Full Text] [Related]
5. Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications.
Maury CP; Sletten K; Totty N; Kangas H; Liljeström M
Lab Invest; 1997 Oct; 77(4):299-304. PubMed ID: 9354764
[TBL] [Abstract][Full Text] [Related]
6. Homozygous familial amyloidosis, Finnish type: demonstration of glomerular gelsolin-derived amyloid and non-amyloid tubular gelsolin.
Maury CP
Clin Nephrol; 1993 Jul; 40(1):53-6. PubMed ID: 8395367
[TBL] [Abstract][Full Text] [Related]
7. Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.
Ghiso J; Haltia M; Prelli F; Novello J; Frangione B
Biochem J; 1990 Dec; 272(3):827-30. PubMed ID: 2176481
[TBL] [Abstract][Full Text] [Related]
8. Fibrillogenesis in gelsolin-related familial amyloidosis.
Maury CP; Nurmiaho-Lassila EL; Boysen G; Liljeström M
Amyloid; 2003 Aug; 10 Suppl 1():21-5. PubMed ID: 14640038
[TBL] [Abstract][Full Text] [Related]
9. Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.
Maury CP; Kere J; Tolvanen R; de la Chapelle A
FEBS Lett; 1990 Dec; 276(1-2):75-7. PubMed ID: 2176164
[TBL] [Abstract][Full Text] [Related]
10. Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.
Hiltunen T; Kiuru S; Hongell V; Heliö T; Palo J; Peltonen L
Am J Hum Genet; 1991 Sep; 49(3):522-8. PubMed ID: 1652889
[TBL] [Abstract][Full Text] [Related]
11. Mutation in gelsolin gene in Finnish hereditary amyloidosis.
Levy E; Haltia M; Fernandez-Madrid I; Koivunen O; Ghiso J; Prelli F; Frangione B
J Exp Med; 1990 Dec; 172(6):1865-7. PubMed ID: 2175344
[TBL] [Abstract][Full Text] [Related]
12. Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein.
Haltia M; Prelli F; Ghiso J; Kiuru S; Somer H; Palo J; Frangione B
Biochem Biophys Res Commun; 1990 Mar; 167(3):927-32. PubMed ID: 2157434
[TBL] [Abstract][Full Text] [Related]
13. Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.
de la Chapelle A; Kere J; Sack GH; Tolvanen R; Maury CP
Genomics; 1992 Jul; 13(3):898-901. PubMed ID: 1322359
[TBL] [Abstract][Full Text] [Related]
14. Solid-phase minisequencing test reveals Asp187----Asn (G654----A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis.
Paunio T; Kiuru S; Hongell V; Mustonen E; Syvänen AC; Bengström M; Palo J; Peltonen L
Genomics; 1992 May; 13(1):237-9. PubMed ID: 1315718
[No Abstract] [Full Text] [Related]
15. Immunohistochemical localization of amyloid in Finnish hereditary amyloidosis with antibodies to gelsolin peptides.
Maury CP
Lab Invest; 1991 Mar; 64(3):400-4. PubMed ID: 1848334
[TBL] [Abstract][Full Text] [Related]
16. Haplotype analysis in gelsolin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan.
Paunio T; Sunada Y; Kiuru S; Makishita H; Ikeda S; Weissenbach J; Palo J; Peltonen L
Hum Mutat; 1995; 6(1):60-5. PubMed ID: 7550233
[TBL] [Abstract][Full Text] [Related]
17. Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin.
Maury CP; Baumann M
Biochim Biophys Acta; 1990 Nov; 1096(1):84-6. PubMed ID: 2176550
[TBL] [Abstract][Full Text] [Related]
18. Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome.
Kivelä T; Tarkkanen A; Frangione B; Ghiso J; Haltia M
Invest Ophthalmol Vis Sci; 1994 Sep; 35(10):3759-69. PubMed ID: 8088963
[TBL] [Abstract][Full Text] [Related]
19. 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.
Maury CP; Nurmiaho-Lassila EL; Rossi H
Lab Invest; 1994 Apr; 70(4):558-64. PubMed ID: 8176895
[TBL] [Abstract][Full Text] [Related]
20. 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).
Maury CP; Liljeström M; Boysen G; Törnroth T; de la Chapelle A; Nurmiaho-Lassila EL
J Clin Pathol; 2000 Feb; 53(2):95-9. PubMed ID: 10767822
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]