(Q41016239)

25 September 2017

Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs (English)

1 reference

25 September 2017

1 reference

Furuya H

1

1 reference

25 September 2017

Yoshioka K

2

1 reference

25 September 2017

Sasaki H

3

1 reference

25 September 2017

Sakaki Y

4

1 reference

25 September 2017

Nakazato M

5

1 reference

25 September 2017

Matsuo H

6

1 reference

25 September 2017

Nakadai A

7

1 reference

25 September 2017

Ikeda S

8

1 reference

25 September 2017

Yanagisawa N

9

1 reference

25 September 2017

language of work or name

English

0 references

publication date

1 December 1987

1 reference

Journal of Clinical Investigation

25 September 2017

1 reference

25 September 2017

80

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25 September 2017

6

1 reference

25 September 2017

1706-1711

1 reference

Familial cerebellar ataxia with cerebrovascular amyloid

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Primary structure of an amyloid prealbumin and its plasma precursor in a heredofamilial polyneuropathy of Swedish origin

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Chromosomal assignment of a family of human oncogenes

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Two RFLPs associated with the human prealbumin gene (PALB).

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Dideoxy sequencing method using denatured plasmid templates

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Localization of the human prealbumin gene to chromosome 18.

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Screening λgt Recombinant Clones by Hybridization to Single Plaques in Situ

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

A variant prealbumin-related low molecular weight amyloid fibril protein in familial amyloid polyneuropathy of Japanese origin

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Structure of the chromosomal gene for human serum prealbumin

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region 18q11.2-q12.1.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Structure of the human prealbumin gene.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Polymorphism of human plasma thyroxine binding prealbumin.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Polyneuritic amyloidosis in a Japanese family

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442443

Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA

19 August 2018

1 reference

12 December 2020

Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy

1 reference

12 December 2020

Hereditary generalized amyloidosis with polyneuropathy. Clinicopathological study of 65 Japanese patients

1 reference

12 December 2020

[A family of familial amyloidosis with cerebellar ataxia and pyramidal tract sign--clinical and genetic study (author's transl)]

1 reference

12 December 2020

Studies on familial amyloid polyneuropathy in Ogawa Village, Japan

1 reference

12 December 2020

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

1 reference

12 December 2020

Radioimmunoassay for detecting abnormal prealbumin in the serum for diagnosis of familial amyloidotic polyneuropathy (Japanese type)

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

Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Identifiers

DOI

10.1172/JCI113261

1 reference

25 September 2017

1 reference

25 September 2017

PubMed publication ID

3479441

1 reference