(Q48669949)

14 February 2018

title

Comparison of amyloid deposition in two lines of transgenic mouse that model familial amyloidotic polyneuropathy, type I. (English)

1 reference

14 February 2018

author name string

Y Takaoka

1

1 reference

14 February 2018

F Tashiro

2

1 reference

14 February 2018

S Yi

3

1 reference

14 February 2018

S Maeda

4

1 reference

14 February 2018

K Shimada

5

1 reference

14 February 2018

K Takahashi

6

1 reference

14 February 2018

Y Sakaki

7

1 reference

14 February 2018

K Yamamura

8

1 reference

14 February 2018

publication date

1 July 1997

1 reference

14 February 2018

published in

Transgenic Research

1 reference

14 February 2018

volume

6

1 reference

14 February 2018

issue

4

1 reference

14 February 2018

page(s)

261-269

1 reference

14 February 2018

https://scigraph.springernature.com/pub.10.1023/a:1018454527309

exact match

0 references

cites work

Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Structure of the chromosomal gene for human serum prealbumin

1 reference

12 December 2020

Tissue-specific and developmental expression of human transthyretin gene in transgenic mice

1 reference

12 December 2020

Variant apolipoprotein AI as a major constituent of a human hereditary amyloid

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial amyloidotic polyneuropathy type 1 in Kumamoto, Japan: A clinicopathologic, histochemical, immunohistochemical, and ultrastructural study

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of carriers of mutant prealbumin gene associated with familial amyloidotic polyneuropathy type I by Southern blot procedures: study of six pedigrees in the Arao district of Japan

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A 6-kb upstream region of the human transthyretin gene can direct developmental, tissue-specific, and quantitatively normal expression in transgenic mouse.

1 reference

12 December 2020

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein

1 reference

12 December 2020

Peripheral nerve fibre changes in asymptomatic children of patients with familial amyloid polyneuropathy

1 reference

12 December 2020

Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy

1 reference

12 December 2020

Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences

1 reference

12 December 2020

Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement

1 reference

12 December 2020

Familial amyloid polyneuropathy: an electron microscope study of the peripheral nerve in five cases. I. Interstitial changes

1 reference

12 December 2020

A new isoleucine substitution of Val-20 in transthyretin tetramers selectively impairs dimer-dimer contacts and causes systemic amyloidosis

1 reference

12 December 2020

Partial denaturation of transthyretin is sufficient for amyloid fibril formation in vitro

1 reference

12 December 2020

PORTUGUESE POLYNEURITIC FAMILIAL TYPE OF AMYLOIDOSIS

1 reference

12 December 2020

Diagnostic radioimmunoassay and DNA-analysis in Swedish and Japanese patients with familial amyloidotic polyneuropathy. Homozygosity for the TTR met30 gene

1 reference

12 December 2020

Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline

1 reference

12 December 2020

Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA

1 reference

12 December 2020

Transgenic mouse model of familial amyloidotic polyneuropathy.

1 reference

12 December 2020

Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy

1 reference

12 December 2020

Structure of the human prealbumin gene.

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1018454527309

1 reference

14 February 2018

Dimensions Publication ID

0 references

1 reference

14 February 2018