Cutis laxa in hereditary gelsolin amyloidosis. - Wikidata - awgldk - TriplyDB

Cutis laxa in hereditary gelsolin amyloidosis.

Cutis laxa in hereditary gelsolin amyloidosis.

http://www.wikidata.org/entity/Q34396968

about

The 8 and 5 kDa fragments of plasma gelsolin form amyloid fibrils by a nucleated polymerization mechanism, while the 68 kDa fragment is not amyloidogenic Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report.Heparin accelerates gelsolin amyloidogenesis.Amyloidogenesis of natively unfolded proteins.Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention.Gender differences in the clinical course of Finnish gelsolin amyloidosis.Natural course of Finnish gelsolin amyloidosis.Familial Amyloid Polyneuropathy Type IV (FINNISH) with Rapid Clinical Progression in an Iranian Woman: A Case Report Heparin binds 8 kDa gelsolin cross-β-sheet oligomers and accelerates amyloidogenesis by hastening fibril extension.Gelsolin amyloid angiopathy causes severe disruption of the arterial wall.Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis.Familial amyloidotic polyneuropathy type IV – gelsolin amyloidosis Xerostomia in hereditary gelsolin amyloidosis Withdrawn: Severe ataxia with neuropathy in hereditary gelsolin amyloidosis

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P2860

Cutis laxa in hereditary gelsolin amyloidosis.

http://www.wikidata.org/entity/Q34396968

description

2005 nî lūn-bûn

@nan

2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի փետրվարին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Cutis laxa in hereditary gelsolin amyloidosis.

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Cutis laxa in hereditary gelsolin amyloidosis.

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Cutis laxa in hereditary gelsolin amyloidosis.

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type

label

Cutis laxa in hereditary gelsolin amyloidosis.

@ast

Cutis laxa in hereditary gelsolin amyloidosis.

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Cutis laxa in hereditary gelsolin amyloidosis.

@nl

prefLabel

Cutis laxa in hereditary gelsolin amyloidosis.

@ast

Cutis laxa in hereditary gelsolin amyloidosis.

@en

Cutis laxa in hereditary gelsolin amyloidosis.

@nl

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P356

J.1365-2133.2004.06276.X

P1433

British Journal of Dermatology

P1476

Cutis laxa in hereditary gelsolin amyloidosis.

@en

P2093

Haltia M

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Keski-Oja J

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Kiuru-Enari S

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P2860

Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN)

An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxa

Genetic heterogeneity of cutis laxa: a heterozygous tandem duplication within the fibulin-5 (FBLN5) gene.

Dendritic cells and the control of immunity

Targeted pharmacological depletion of serum amyloid P component for treatment of human amyloidosis

Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa

Hemostatic, inflammatory, and fibroblast responses are blunted in mice lacking gelsolin

Functions of gelsolin: motility, signaling, apoptosis, cancer.

Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Review: immunoglobulin light chain amyloidosis--the archetype of structural and pathogenic variability.

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250-257

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scholarly article

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10.1111/J.1365-2133.2004.06276.X

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2

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15727635

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