(Q35593224)

9 August 2017

Lactoferrin Glu561Asp facilitates secondary amyloidosis in the cornea (English)

1 reference

9 August 2017

Araki-Sasaki K

1

1 reference

9 August 2017

Ando Y

2

1 reference

9 August 2017

Nakamura M

3

1 reference

9 August 2017

Kitagawa K

4

1 reference

9 August 2017

Ikemizu S

5

1 reference

9 August 2017

Kawaji T

6

1 reference

9 August 2017

Yamashita T

7

1 reference

9 August 2017

Ueda M

8

1 reference

9 August 2017

Hirano K

9

1 reference

9 August 2017

Yamada M

10

1 reference

9 August 2017

Matsumoto K

11

1 reference

9 August 2017

Kinoshita S

12

1 reference

9 August 2017

Tanihara H

13

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 June 2005

1 reference

British Journal of Ophthalmology

9 August 2017

1 reference

9 August 2017

89

1 reference

9 August 2017

684-688

1 reference

9 August 2017

6

1 reference

A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy

9 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Identification of the gene responsible for gelatinous drop-like corneal dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Exposure of cryptic epitopes on transthyretin only in amyloid and in amyloidogenic mutants

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Structure of the human lactoferrin gene and its chromosomal localization.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Ocular manifestations of familial amyloidotic polyneuropathy type I: long-term follow up.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Ocular amyloidosis, with special reference to the hereditary forms with vitreous involvement

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Idiopathic AA amyloidosis manifested by autonomic neuropathy, vestibulocochleopathy, and lattice corneal dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Secondary localized amyloidosis of the cornea associated with tertiary syphilis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Amyloid, amyloidosis, and amyloidogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Amyloid fibril protein nomenclature -- 2002.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

A novel localized amyloidosis associated with lactoferrin in the cornea.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Corneal amyloidosis complicated by trichiasis. Immunohistochemical identification of the amyloid light chain protein

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

A histopathological study of corneal amyloidosis secondary to trichiasis

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1772658

Secondary localized amyloidosis of the cornea caused by trichiasis

26 September 2018

1 reference

12 December 2020

Three-dimensional structure of lactoferrin. Implications for function, including comparisons with transferrin

1 reference

12 December 2020

Amyloidosis due to a mutation of the gelsolin gene in an American family with lattice corneal dystrophy type II

1 reference

12 December 2020

Familial subepithelial corneal amyloidosis--a lactoferrin-related amyloidosis

1 reference

12 December 2020

[A case of corneal lactoferrin amyloidosis secondary to trichiasis]

1 reference

12 December 2020

Endocrine cells in rectal biopsy specimens from patients with familial amyloidotic polyneuropathy

1 reference

12 December 2020

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA

1 reference

12 December 2020

Secondary Amyloidosis in Ocular Leprosy

1 reference

12 December 2020

1 reference

12 December 2020

FAP mutations destabilize transthyretin facilitating conformational changes required for amyloid formation

1 reference

12 December 2020

Secondary localized amyloidosis in interstitial keratitis. Clinicopathologic findings

1 reference

12 December 2020

Identifiers

DOI

10.1136/BJO.2004.056804

1 reference

9 August 2017

1 reference

9 August 2017

1 reference