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Results: 13

1.

Ca2+ binding by domain 2 plays a critical role in the activation and stabilization of gelsolin.

Nag S, Ma Q, Wang H, Chumnarnsilpa S, Lee WL, Larsson M, Kannan B, Hernandez-Valladares M, Burtnick LD, Robinson RC.

Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13713-8. doi: 10.1073/pnas.0812374106. Epub 2009 Aug 4.

PMID:
19666512
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Corneal melt in lattice corneal dystrophy type II after cataract surgery.

Papathanassiou M, Liarakos VS, Vaikousis E, Paschalidis T, Agrogiannis G, Vergados I.

J Cataract Refract Surg. 2009 Jan;35(1):185-9. doi: 10.1016/j.jcrs.2008.07.039.

PMID:
19101443
[PubMed - indexed for MEDLINE]
3.

Lattice corneal dystrophy type II: clinical, pathologic, and molecular study in a Spanish family.

Huerva V, Velasco A, Sánchez MC, Mateo AJ, Matías-Guiu X.

Eur J Ophthalmol. 2007 May-Jun;17(3):424-9.

PMID:
17534828
[PubMed - indexed for MEDLINE]
4.

Loss of a metal-binding site in gelsolin leads to familial amyloidosis-Finnish type.

Kazmirski SL, Isaacson RL, An C, Buckle A, Johnson CM, Daggett V, Fersht AR.

Nat Struct Biol. 2002 Feb;9(2):112-6.

PMID:
11753432
[PubMed - indexed for MEDLINE]
5.

The disintegration of a molecule: the role of gelsolin in FAF, familial amyloidosis (Finnish type).

Robinson RC, Choe S, Burtnick LD.

Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2117-8. No abstract available.

PMID:
11226199
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Elucidating the mechanism of familial amyloidosis- Finnish type: NMR studies of human gelsolin domain 2.

Kazmirski SL, Howard MJ, Isaacson RL, Fersht AR.

Proc Natl Acad Sci U S A. 2000 Sep 26;97(20):10706-11.

PMID:
10995458
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV.

Akiya S, Nishio Y, Ibi K, Uozumi H, Takahashi H, Hamada T, Onishi A, Ishiguchi H, Hoshii Y, Nakazato M.

Ophthalmology. 1996 Jul;103(7):1106-10.

PMID:
8684801
[PubMed - indexed for MEDLINE]
8.

Apolipoprotein E increases the fibrillogenic potential of synthetic peptides derived from Alzheimer's, gelsolin and AA amyloids.

Soto C, Castaño EM, Prelli F, Kumar RA, Baumann M.

FEBS Lett. 1995 Sep 4;371(2):110-4.

PMID:
7672107
[PubMed - indexed for MEDLINE]
Free Article
9.

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 29;335(1):119-23.

PMID:
8243656
[PubMed - indexed for MEDLINE]
Free Article
10.

Lattice corneal dystrophy type II with familial amyloid polyneuropathy type IV.

Asaoka T, Amano S, Sunada Y, Sawa M.

Jpn J Ophthalmol. 1993;37(4):426-31.

PMID:
8145387
[PubMed - indexed for MEDLINE]
11.

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 Jr, Rodrigues M, Ghiso J, Levy E, Haltia M, Frangione B.

N Engl J Med. 1991 Dec 19;325(25):1780-5. No abstract available.

PMID:
1658654
[PubMed - indexed for MEDLINE]
Free Article
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 30;167(3):927-32.

PMID:
2157434
[PubMed - indexed for MEDLINE]
13.

Inherited systemic amyloidosis (Finnish type): ultrastructure of the skin.

Collan Y, Meretoja J.

Ann Clin Res. 1978 Feb;10(1):43-7.

PMID:
677801
[PubMed - indexed for MEDLINE]

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