(Q41865259)

13 October 2017

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

1 reference

13 October 2017

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J Ghiso

1

1 reference

13 October 2017

M Haltia

2

1 reference

13 October 2017

F Prelli

3

1 reference

13 October 2017

J Novello

4

1 reference

13 October 2017

B Frangione

5

1 reference

13 October 2017

language of work or name

English

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publication date

1 December 1990

1 reference

13 October 2017

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13 October 2017

272

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13 October 2017

3

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13 October 2017

827-830

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

An hereditary syndrome consisting of peripheral polyneuropathy, skin changes and lattice-shaped corneal dystrophy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Amyloid fibrils in hereditary cerebral hemorrhage with amyloidosis of Icelandic type is a variant of gamma-trace basic protein (cystatin C)

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Nonmuscle actin-binding proteins

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Reversibility of gelsolin/actin interaction in macrophages. Evidence of Ca2+-dependent and Ca2+-independent pathways

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

The actin filament-severing domain of plasma gelsolin

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Plasma and cytoplasmic gelsolins are encoded by a single gene and contain a duplicated actin-binding domain

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Nucleotide sequence of pig plasma gelsolin. Comparison of protein sequence with human gelsolin and other actin-severing proteins shows strong homologies and evidence for large internal repeats

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Gelsolin has three actin-binding sites

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Localization of gelsolin proximal to ABL on chromosome 9

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

The gelsolin (GSN) cDNA clone, from 9q32-34, identifies BclI and StuI RFLPs

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Stroke in Icelandic patients with hereditary amyloid angiopathy is related to a mutation in the cystatin C gene, an inhibitor of cysteine proteases

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Expression of a normal and variant Alzheimer's beta-protein gene in amyloid of hereditary cerebral hemorrhage, Dutch type: DNA and protein diagnostic assays.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Coexistence of Alzheimer's amyloid precursor protein and amyloid protein in cerebral vessel walls.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Mutation of the Alzheimer's disease amyloid gene in hereditary cerebral hemorrhage, Dutch type

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1149782

Comparative histopathological and clinical findings in eyes with lattice corneal dystrophy of two different types

5 June 2018

1 reference

12 December 2020

Three forms of dominant amyloid neuropathy

1 reference

12 December 2020

Structure and biosynthesis of cytoplasmic and secreted variants of gelsolin

1 reference

12 December 2020

Haplotype analysis of familial amyloidotic polyneuropathy

1 reference

12 December 2020

Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

1 reference

12 December 2020

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

1 reference

12 December 2020

Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation. Report on three cases

1 reference

12 December 2020

Lattice corneal dystrophy associated with familial systemic amyloidosis (Meretoja's syndrome)

1 reference

12 December 2020

Familial amyloidosis with cranial neuropathy and corneal lattice dystrophy

1 reference

12 December 2020

Modulation of gelsolin function by phosphatidylinositol 4,5-bisphosphate

1 reference

12 December 2020

Quantitative measurement of plasma gelsolin and its incorporation into fibrin clots

1 reference

12 December 2020

Renal biopsy findings in familial amyloidosis with corneal lattice dystrophy. An immuno-histochemical, light-microscopical and electron-microscopical study

1 reference

12 December 2020

Identifiers

DOI

10.1042/BJ2720827

1 reference

release_244ejw2vs5a4bodpqz6a3vwvt4

13 October 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/244ejw2vs5a4bodpqz6a3vwvt4

24 November 2022

mapped directly with Wikidata item

1 reference

13 October 2017

PubMed publication ID

2176481

1 reference