(Q48205324)

English

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis.

scientific article published in October 1991

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scholarly article

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis. (English)

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

author name string

Saeki Y

1

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Ueno S

2

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Yorifuji S

3

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Sugiyama Y

4

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Ide Y

5

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Matsuzawa Y

6

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

language of work or name

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publication date

1 October 1991

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

Biochemical and Biophysical Research Communications

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

180

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

1

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

380-385

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

DNA sequence polymorphisms in Alu repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

A novel variant of transthyretin (Tyr114 to Cys) deduced from the nucleotide sequences of gene fragments from familial amyloidotic polyneuropathy in Japanese sibling cases

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg)

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Chemiluminescent detection of DNA: application for DNA sequencing and hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Nonradioactive DNA detection on Southern blots by enzymatically triggered chemiluminescence

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Recent advances in the molecular pathology of familial amyloid polyneuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2805%2981304-X

7 January 2021

Identifiers

10.1016/S0006-291X(05)81304-X

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

1 reference

Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/1656975

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