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Results: 1 to 20 of 170

Related Citations for PubMed (Select 2157434)

1.

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 30;167(3):927-32.

PMID:
2157434
2.

Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type.

Ghiso J, Haltia M, Prelli F, Novello J, Frangione B.

Biochem J. 1990 Dec 15;272(3):827-30.

4.

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.

5.

Demonstration of a circulating 65K gelsolin variant specific for familial amyloidosis, Finnish type.

Maury CP, Rossi H.

Biochem Biophys Res Commun. 1993 Feb 26;191(1):41-4.

PMID:
8383491
6.
7.

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 1;172(6):1865-7.

8.

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 1;42(3):357-9.

PMID:
1311149
10.

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 14;1096(1):84-6. Erratum in: Biochim Biophys Acta 1991 Jun 5;1096(4):361.

PMID:
2176550
12.

Creation of amyloid fibrils from mutant Asn187 gelsolin peptides.

Maury CP, Nurmiaho-Lassila EL.

Biochem Biophys Res Commun. 1992 Feb 28;183(1):227-31.

PMID:
1311922
13.

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.

14.

Gelsolin immunoreactivity in corneal amyloid, wound healing, and macular and granular dystrophies.

Rodrigues MM, Rajagopalan S, Jones K, Nirankari V, Wisniewski T, Frangione B, Gorevic PD.

Am J Ophthalmol. 1993 May 15;115(5):644-52.

PMID:
7683843
15.

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 Jr, Tolvanen R, Maury CP.

Genomics. 1992 Jul;13(3):898-901.

PMID:
1322359
16.

An immunohistochemical study of gelsolin immunoreactivity in corneal amyloidosis.

Loeffler KU, Edward DP, Tso MO.

Am J Ophthalmol. 1992 May 15;113(5):546-54.

PMID:
1315488
17.

[Familial amyloidotic polyneuropathy type IV (Finnish type)--the first description of a large kindred in Japan].

Sunada Y, Shimizu T, Mannen T, Kanazawa I.

Rinsho Shinkeigaku. 1992 Aug;32(8):826-33. Japanese.

PMID:
1337023
19.
20.

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 10;276(1-2):75-7.

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