SwePub
Sök i LIBRIS databas

  Extended search

id:"swepub:oai:DiVA.org:liu-79734"
 

Search: id:"swepub:oai:DiVA.org:liu-79734" > Extensive Intimal A...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Extensive Intimal Apolipoprotein A1-Derived Amyloid Deposits in a Patient with an Apolipoprotein A1 Mutation

Amarzguioui, Mohammed (author)
The Biotechnology Centre of Oslo, University of Oslo, Gaustadalleen 21, Oslo, Norway
Mucchiano, Gerd (author)
Linköpings universitet,Molekylär och immunologisk patologi,Hälsouniversitetet
Häggqvist, Bo (author)
Linköpings universitet,Molekylär och immunologisk patologi,Hälsouniversitetet
show more...
Westermark, Bo (author)
Linköpings universitet,Molekylär och immunologisk patologi,Hälsouniversitetet
Kavlie, Anita (author)
The Biotechnology Centre of Oslo, University of Oslo, Gaustadalleen 21, Oslo, Norway
Sletten, Knut (author)
The Biotechnology Centre of Oslo, University of Oslo, Gaustadalleen 21, Oslo, Norway
Prydz, Hans (author)
The Biotechnology Centre of Oslo, University of Oslo, Gaustadalleen 21, Oslo, Norway
show less...
 (creator_code:org_t)
Elsevier BV, 1998
1998
English.
In: Biochemical and Biophysical Research Communications - BBRC. - : Elsevier BV. - 0006-291X .- 1090-2104. ; 242:3, s. 534-539
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • In the aortic intima amyloid deposits are often associated with atherosclerotic plaques. In a recent study of one patient with aortic intimal amyloid the major fibril protein was an N-terminal fragment of apolipoprotein A1 (apoA1) consisting of 69 amino acid residues. In the present study, we have screened the apoA1 gene for mutations in autopsy cases with aortic intimal amyloid immunohistochemically positive for apoA1, using single stranded conformational polymorphism (SSCP) analysis and DNA sequencing. All cases except one had a normal apoA1 gene sequence. One case of exceptionally severe atherosclerosis combined with extensive intimal amyloid deposits showed an apoA1 deletion corresponding to Lys 107. Thus, wild type apoA1 is amyloidogenic but our findings suggest that the expression of a mutant apoA1-form may be associated with enhanced amyloidogenicity.

Keyword

MEDICINE
MEDICIN

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view