Proline

fibrillin 1 ; Homo sapiens







6 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 29845260 Two rare missense mutations in the fibrillin‑1 gene associated with atypical cardiovascular manifestations in a Chinese patient affected by Marfan syndrome. 2018 Jul 1
2 17158461 Effects of fibrillin-1 degradation on microfibril ultrastructure. 2007 Feb 9 1
3 12402346 Mutation screening of the fibrillin-1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the identification of 11 novel and three previously reported mutations. 2002 Nov 1
4 10825173 Interaction of tropoelastin with the amino-terminal domains of fibrillin-1 and fibrillin-2 suggests a role for the fibrillins in elastic fiber assembly. 2000 Aug 11 1
5 11083269 Autoantibodies to fibrillin 1 in systemic sclerosis: ethnic differences in antigen recognition and lack of correlation with specific clinical features or HLA alleles. 2000 Nov 1
6 9792099 Effects of proline cis-trans isomerization on TB domain secondary structure. 1998 Oct 1