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Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease

Autor: Smyth, Laura J, Dahlström, Emma H, Syreeni, Anna, Kerr, Katie, Kilner, Jill, Doyle, Ross, Brennan, Eoin, Nair, Viji, Fermin, Damian, Nelson, Robert G, Looker, Helen C, Wooster, Christopher, Andrews, Darrell, Anderson, Kerry, McKay, Gareth J, Cole, Joanne B, Salem, Rany M, Conlon, Peter J, Kretzler, Matthias, Hirschhorn, Joel N, Sadlier, Denise, Godson, Catherine, Florez, Jose C, GENIE consortium, Forsblom, Carol, Maxwell, Alexander P, Groop, Per-Henrik, Sandholm, Niina, McKnight, Amy Jayne

Publikováno v: Smyth, L J, Dahlström, E H, Syreeni, A, Kerr, K, Kilner, J, Doyle, R, Brennan, E, Nair, V, Fermin, D, Nelson, R G, Looker, H C, Wooster, C, Andrews, D, Anderson, K, McKay, G J, Cole, J B, Salem, R M, Conlon, P J, Kretzler, M, Hirschhorn, J N, Sadlier, D, Godson, C, Florez, J C, GENIE Consortium, Forsblom, C, Maxwell, A P, Groop, P H, Sandholm, N & McKnight, A J 2022, ' Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease ', Nature Communications, vol. 13, 7891 . https://doi.org/10.1038/s41467-022-34963-6
Nature communications, vol 13, iss 1

Type 1 diabetes affects over nine million individuals globally, with approximately 40% developing diabetic kidney disease. Emerging evidence suggests that epigenetic alterations, such as DNA methylation, are involved in diabetic kidney disease. Here

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93872e02e57d5287f43ad757fb5f5e30
https://pure.qub.ac.uk/en/publications/4a97ab7f-894d-4f4e-9ed7-f7ebb2e90205

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Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

Autor: Balachandar, Srimmitha, Graves, Tamara J, Shimonty, Anika, Kerr, Katie, Kilner, Jill, Xiao, Sihao, Slade, Richard, Sroya, Manveer, Alikian, Mary, Curetean, Emanuel, Thomas, Ellen, McConnell, Vivienne, McKee, Shane, Boardman-Pretty, Freya, Devereau, Andrew, Fowler, Tom A, Caulfield, Mark J, Alton, Eric W, Ferguson, Teena, Redhead, Julian, McKnight, Amy J., Thomas, Geraldine A, Research Consortium, Genomics England, Aldred, Micheala A, Shovlin, Claire L

Publikováno v: Balachandar, S, Graves, T J, Shimonty, A, Kerr, K, Kilner, J, Xiao, S, Slade, R, Sroya, M, Alikian, M, Curetean, E, Thomas, E, McConnell, V, McKee, S, Boardman-Pretty, F, Devereau, A, Fowler, T A, Caulfield, M J, Alton, E W, Ferguson, T, Redhead, J, McKnight, A J, Thomas, G A, Research Consortium, G E, Aldred, M A & Shovlin, C L 2022, ' Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations ', American Journal of Medical Genetics A, vol. 188, no. 3, pp. 959-964 . https://doi.org/10.1002/ajmg.a.62584

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multisystemic vascular dysplasia, characterized by arteriovenous malformations (AVMs), mucocutaneous telangiectasia and nosebleeds. HHT is caused by a heterozygous null allele in AC

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2607::9ba662d2a30f6a66ae792b6d17757213
https://pure.qub.ac.uk/en/publications/b57c8db3-e414-4c81-802f-d796d520de2e

Making Peace with Criminals: An Economic Approach to Assessing Punishment Options in the Colombian Peace Process

Autor: Kerr, Katie

Publikováno v: The University of Miami Inter-American Law Review, 2005 Oct 01. 37(1), 53-117.

Externí odkaz: https://www.jstor.org/stable/40176604