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23. Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Haltia M; Ghiso J; Prelli F; Gallo G; Kiuru S; Somer H; Palo J; Frangione B Am J Pathol; 1990 Jun; 136(6):1223-8. PubMed ID: 2162627 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. Structure of gelsolin segment 1-actin complex and the mechanism of filament severing. McLaughlin PJ; Gooch JT; Mannherz HG; Weeds AG Nature; 1993 Aug; 364(6439):685-92. PubMed ID: 8395021 [TBL] [Abstract][Full Text] [Related]
27. Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II. Gorevic PD; Munoz PC; Gorgone G; Purcell JJ; Rodrigues M; Ghiso J; Levy E; Haltia M; Frangione B N Engl J Med; 1991 Dec; 325(25):1780-5. PubMed ID: 1658654 [No Abstract] [Full Text] [Related]
28. Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families. Mustonen T; Schmidt EK; Valori M; Tienari PJ; Atula S; Kiuru-Enari S Eur J Hum Genet; 2018 Jan; 26(1):117-123. PubMed ID: 29167514 [TBL] [Abstract][Full Text] [Related]
29. Nanobody interaction unveils structure, dynamics and proteotoxicity of the Finnish-type amyloidogenic gelsolin variant. Giorgino T; Mattioni D; Hassan A; Milani M; Mastrangelo E; Barbiroli A; Verhelle A; Gettemans J; Barzago MM; Diomede L; de Rosa M Biochim Biophys Acta Mol Basis Dis; 2019 Mar; 1865(3):648-660. PubMed ID: 30625383 [TBL] [Abstract][Full Text] [Related]
30. Danish type gelsolin-related amyloidosis in a Brazilian family: case reports. Solari HP; Ventura MP; Antecka E; Belfort Junior R; Burnier MN Arq Bras Oftalmol; 2011; 74(4):286-8. PubMed ID: 22068858 [TBL] [Abstract][Full Text] [Related]
31. A novel GSN variant outside the G2 calcium-binding domain associated with Amyloidosis of the Finnish type. Mullany S; Souzeau E; Klebe S; Zhou T; Knight LSW; Qassim A; Berry EC; Marshall H; Hussey M; Dubowsky A; Breen J; Hassall MM; Mills RA; Craig JE; Siggs OM Hum Mutat; 2021 Jul; 42(7):818-826. PubMed ID: 33973672 [TBL] [Abstract][Full Text] [Related]
32. Asp187Asn mutation of gelsolin in an American kindred with familial amyloidosis, Finnish type (FAP IV). Steiner RD; Paunio T; Uemichi T; Evans JP; Benson MD Hum Genet; 1995 Mar; 95(3):327-30. PubMed ID: 7868127 [TBL] [Abstract][Full Text] [Related]
33. Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutation. Cabral-Macias J; Garcia-Montaño LA; Pérezpeña-Díazconti M; Aguilar MC; Garcia G; Vencedor-Meraz CI; Graue-Hernandez EO; Chacón-Camacho OF; Zenteno JC Mol Vis; 2020; 26():345-354. PubMed ID: 32368002 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Finnish hereditary amyloidosis: a mutation in the gelsolin gene]. Maury P Duodecim; 1994; 110(7):675-80. PubMed ID: 8542822 [No Abstract] [Full Text] [Related]
36. Expression of human plasma gelsolin in Escherichia coli and dissection of actin binding sites by segmental deletion mutagenesis. Way M; Gooch J; Pope B; Weeds AG J Cell Biol; 1989 Aug; 109(2):593-605. PubMed ID: 2547804 [TBL] [Abstract][Full Text] [Related]
37. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies. Conceição I; Sales-Luis ML; De Carvalho M; Evangelista T; Fernandes R; Paunio T; Kangas H; Coutinho P; Neves C; Saraiva MJ Muscle Nerve; 2003 Dec; 28(6):715-21. PubMed ID: 14639586 [TBL] [Abstract][Full Text] [Related]
39. In vitro expression analysis shows that the secretory form of gelsolin is the sole source of amyloid in gelsolin-related amyloidosis. Kangas H; Paunio T; Kalkkinen N; Jalanko A; Peltonen L Hum Mol Genet; 1996 Sep; 5(9):1237-43. PubMed ID: 8872462 [TBL] [Abstract][Full Text] [Related]