(Q69919076)

English

Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy

scientific article published on 01 May 1988

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Restriction fragment analysis confirms the position 33 mutation in transthyretin from an Israeli patient (SKO) with familial amyloidotic polyneuropathy (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

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D R Jacobson

1

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6 October 2019

F Santiago-Schwartz

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

J N Buxbaum

3

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6 October 2019

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1 May 1988

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6 October 2019

Biochemical and Biophysical Research Communications

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

153

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6 October 2019

1

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6 October 2019

198-202

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

Structure of the chromosomal gene for human serum prealbumin

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

Polymorphism of human plasma thyroxine binding prealbumin.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

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%2888%2981208-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

Cloning and sequence analysis of cDNA for human prealbumin

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

A general method for isolation of high molecular weight DNA from eukaryotes

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

Oncogene alterations in primary human colon tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2888%2981208-7

7 January 2021

Identifiers

10.1016/S0006-291X(88)81208-7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2897849%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

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