These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 2176164)

  • 21. [Gene analysis of Japanese patients with familial amyloidotic polyneuropathy type IV].
    Sunada Y; Nakase H; Shimizu T; Mannen T; Kanazawa I
    Rinsho Shinkeigaku; 1992 Aug; 32(8):840-4. PubMed ID: 1337024
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variant plasma gelsolin responsible for familial amyloidosis (Finnish type) has defective actin severing activity.
    Weeds AG; Gooch J; McLaughlin P; Maury CP
    FEBS Lett; 1993 Nov; 335(1):119-23. PubMed ID: 8243656
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 38. Altered platelet shape change in hereditary gelsolin Asp187Asn-related amyloidosis.
    Kiuru S; Javela K; Somer H; Kekomäki R
    Thromb Haemost; 2000 Mar; 83(3):491-5. PubMed ID: 10744159
    [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]  

  • 40. Inherited amyloidosis.
    Benson MD
    J Med Genet; 1991 Feb; 28(2):73-8. PubMed ID: 1848299
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.