(Q35585176)

9 August 2017

title

Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis (English)

1 reference

nucleic acid sequence analysis

9 August 2017

main subject

1 reference

M R Wallace

1

1 reference

9 August 2017

F E Dwulet

2

1 reference

9 August 2017

E C Williams

3

1 reference

9 August 2017

P M Conneally

4

1 reference

9 August 2017

M D Benson

5

1 reference

9 August 2017

language of work or name

English

0 references

publication date

1 January 1988

1 reference

Journal of Clinical Investigation

9 August 2017

published in

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9 August 2017

volume

81

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9 August 2017

issue

1

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9 August 2017

page(s)

189-193

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Hereditary cerebral haemorrhage with amyloidosis

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Chemical and clinical classification of amyloidosis 1985.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Structure of the human prealbumin gene.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Localization of the human prealbumin gene to chromosome 18.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Structure of prealbumin: secondary, tertiary and quaternary interactions determined by Fourier refinement at 1.8 A

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Thyroxine Transport Proteins of Plasma. Molecular Properties and Biosynthesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Polymorphism of human plasma thyroxine binding prealbumin.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442492

26 September 2018

Hereditary amyloidosis

1 reference

12 December 2020

Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)

1 reference

12 December 2020

Prealbumin and retinol binding protein serum concentrations in the Indiana type hereditary amyloidosis

1 reference

12 December 2020

Amino acid analysis by reverse-phase high-performance liquid chromatography: precolumn derivatization with phenylisothiocyanate

1 reference

12 December 2020

Revised analysis of amino acid replacement in a prealbumin variant (SKO-III) associated with familial amyloidotic polyneuropathy of Jewish origin

1 reference

12 December 2020

Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Amyloidotic polyneuropathy in a Jewish family. Evidence for the genetic heterogeneity of the lower limb familial amyloidotic neuropathies

1 reference

12 December 2020

Hereditary cerebral amyloid angiopathy: the amyloid fibrils contain a protein which is a variant of cystatin C, an inhibitor of lysosomal cysteine proteases

1 reference

12 December 2020

Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Hereditary amyloidosis: description of a new American kindred with late onset cardiomyopathy. Appalachian amyloid

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

Identifiers

DOI

10.1172/JCI113293

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9 August 2017

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9 August 2017

1 reference