Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I. (Q42050552)

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scientific article published on February 1991

Language	Label	Description	Also known as
English	Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I.	scientific article published on February 1991

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scholarly article

1 reference

Europe PubMed Central

15 October 2017

Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I. (English)

1 reference

Europe PubMed Central

15 October 2017

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author name string

Yi S

1

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15 October 2017

Takahashi K

2

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Europe PubMed Central

15 October 2017

Naito M

3

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Europe PubMed Central

15 October 2017

Tashiro F

4

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Europe PubMed Central

15 October 2017

Wakasugi S

5

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Europe PubMed Central

15 October 2017

Maeda S

6

1 reference

Europe PubMed Central

15 October 2017

Shimada K

7

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Europe PubMed Central

15 October 2017

Yamamura K

8

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Europe PubMed Central

15 October 2017

Araki S

9

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Europe PubMed Central

15 October 2017

language of work or name

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publication date

1 February 1991

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15 October 2017

The American Journal of Pathology

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15 October 2017

138

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2

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403-412

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Europe PubMed Central

15 October 2017

A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves

1 reference

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Biology of serum amyloid P component

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5 June 2018

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

1 reference

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

1 reference

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Cloning and sequence analysis of cDNA for human prealbumin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

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Type I familial amyloidotic polyneuropathy (Japanese type)

1 reference

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Sequence of Deposition of Amyloid in Strain A Mice and Relationship to Renal Disease2

1 reference

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P-component (pentagonal unit) of amyloid: isolation, characterization, and sequence analysis.

1 reference

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Isolation and identification by sequence analysis of experimentally induced guinea pig amyloid fibrils

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HPRT-deficient (Lesch-Nyhan) mouse embryos derived from germline colonization by cultured cells

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Transthyretin: a choroid plexus-specific transport protein in human brain. The 1986 S. Weir Mitchell award

1 reference

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A molecular-pathologic approach to murine senile amyloidosis. Serum precursor-apolipoprotein A-II variant (Pro5----Gln) presents only in the senile amyloidosis-prone SAM-P/1 and SAM-P/2 mice.

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A potential animal model for Lesch-Nyhan syndrome through introduction of HPRT mutations into mice

1 reference

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5 June 2018

Transgenic mouse model of familial amyloidotic polyneuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Amyloidosis of the nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Familial amyloidotic polyneuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Potassium permanganate reaction in amyloidosis. A histologic method to assist in differentiating forms of this disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Spontaneous amyloidosis in LLC mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Amyloid fibril protein related to prealbumin in familial amyloidotic polyneuropathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Binding of serum amyloid P-component (SAP) by amyloid fibrils

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

5 June 2018

Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

17 August 2018

Polyneuritic amyloidosis in a Japanese family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1886191

17 August 2018

Introduction of Human γ1 Immunoglobulin Genes into Fertilized Mouse Eggs1

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

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Beta-pleated sheet fibrils. A comparison of native amyloid with synthetic protein fibrils

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

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The SJL/J mouse: a new model for spontaneous age-associated amyloidosis. I. Morphologic and immunochemical aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

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based on heuristic

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Evidence that the amyloid fibril protein in senile systemic amyloidosis is derived from normal prealbumin

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

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based on heuristic

inferred from PubMed ID database lookup

Senile amyloidosis in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies on familial amyloid polyneuropathy in Ogawa Village, Japan

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

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based on heuristic

inferred from PubMed ID database lookup

Senile cardiac amyloid is related to prealbumin

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

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PORTUGUESE POLYNEURITIC FAMILIAL TYPE OF AMYLOIDOSIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic senile amyloid in senescence-accelerated mice. A unique fibril protein demonstrated in tissues from various organs by the unlabeled immunoperoxidase method

1 reference

https://pubmed.ncbi.nlm.nih.gov/1992765

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

15 October 2017

1 reference

Europe PubMed Central

15 October 2017

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