Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Juha R M, Ojala"'
Autor:
Christine-Maria Horejs, Jean-Philippe St-Pierre, Juha R. M. Ojala, Joseph A. M. Steele, Patricia Barros da Silva, Angela Rynne-Vidal, Stephanie A. Maynard, Catherine S. Hansel, Clara Rodríguez-Fernández, Manuel M. Mazo, Amanda Y. F. You, Alex J. Wang, Thomas von Erlach, Karl Tryggvason, Manuel López-Cabrera, Molly M. Stevens
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
Matrix metalloproteinase enzymes are widely known to contribute to the breakdown of tissues. Here, the authors utilise a biomaterial substrate functionalised with a laminin fragment to modulate the expression of these enzymes, subsequently controllin
Externí odkaz:
https://doaj.org/article/6f96d69568c34d5fb8957a8cd8f04a9a
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56414 (2013)
We have previously reported genetic association of a single nucleotide polymorphism (SNP), rs1866813, at 3q locus with increased risk of diabetic nephropathy (DN). The SNP is located approximately 70 kb downstream of a cluster of four genes. This rai
Externí odkaz:
https://doaj.org/article/dd7f1ab8f90b4df39f92ceaa3a131f02
Autor:
Christine-Maria, Horejs, Jean-Philippe, St-Pierre, Juha R M, Ojala, Joseph A M, Steele, Patricia Barros, da Silva, Angela, Rynne-Vidal, Stephanie A, Maynard, Catherine S, Hansel, Clara, Rodríguez-Fernández, Manuel M, Mazo, Amanda Y F, You, Alex J, Wang, Thomas, von Erlach, Karl, Tryggvason, Manuel, López-Cabrera, Molly M, Stevens
Publikováno v:
Nature Communications
Matrix metalloproteinases (MMPs) contribute to the breakdown of tissue structures such as the basement membrane, promoting tissue fibrosis. Here we developed an electrospun membrane biofunctionalized with a fragment of the laminin β1-chain to modula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d52998d3eae2e801bb973f23ab0b599
https://pubmed.ncbi.nlm.nih.gov/28593951
https://pubmed.ncbi.nlm.nih.gov/28593951
Autor:
Norhashimah, Abu Seman, Bing, He, Juha R M, Ojala, Wan Nazaimoon, Wan Mohamud, Claes-Göran, Östenson, Kerstin, Brismar, Harvest F, Gu
Publikováno v:
American journal of nephrology. 40(5)
Solute carrier family 12 member 3 (SLC12A3) encodes a sodium/chloride transporter in kidneys. Previous reports suggest that Arg913Gln polymorphism in this gene is associated with diabetic nephropathy (DN), but the data appear to be inconsistent. Up t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8a47c0bc083b0f9a7bdfcb21f49647ab
https://pubmed.ncbi.nlm.nih.gov/25401745
https://pubmed.ncbi.nlm.nih.gov/25401745