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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Proteinuria and CUBN[original query]
Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients.
Nephron 2019 141 (3): 156-165.
Albert Christian, Kube Johanna, Albert Annemarie, Schanze Denny, Zenker Martin, Mertens Peter
Sequence variants associating with urinary biomarkers. GWAS Catalog
Human molecular genetics 2019 04 28 (7): 1199-1211.
Benonisdottir Stefania, Kristjansson Ragnar P, Oddsson Asmundur, Steinthorsdottir Valgerdur, Mikaelsdottir Evgenia, Kehr Birte, Jensson Brynjar O, Arnadottir Gudny A, Sulem Gerald, Sveinbjornsson Gardar, Kristmundsdottir Snaedis, Ivarsdottir Erna V, Tragante Vinicius, Gunnarsson Bjarni, Runolfsdottir Hrafnhildur Linnet, Arthur Joseph G, Deaton Aimee M, Eyjolfsson Gudmundur I, Davidsson Olafur B, Asselbergs Folkert W, Hreidarsson Astradur B, Rafnar Thorunn, Thorleifsson Gudmar, Edvardsson Vidar, Sigurdsson Gunnar, Helgadottir Anna, Halldorsson Bjarni V, Masson Gisli, Holm Hilma, Onundarson Pall T, Indridason Olafur S, Benediktsson Rafn, Palsson Runolfur, Gudbjartsson Daniel F, Olafsson Isleifur, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka
Not all proteinuria is created equal.
The Journal of clinical investigation 2019 12 130 (1): 74-76.
Beenken Andrew, Barasch Jonathan M, Gharavi Ali
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.
The Journal of clinical investigation 2019 10 130 (1): 335-344.
Bedin Mathilda, Boyer Olivia, Servais Aude, Li Yong, Villoing-Gaudé Laure, Tête Marie-Josephe, Cambier Alexandra, Hogan Julien, Baudouin Veronique, Krid Saoussen, Bensman Albert, Lammens Florie, Louillet Ferielle, Ranchin Bruno, Vigneau Cecile, Bouteau Iseline, Isnard-Bagnis Corinne, Mache Christoph J, Schäfer Tobias, Pape Lars, Gödel Markus, Huber Tobias B, Benz Marcus, Klaus Günter, Hansen Matthias, Latta Kay, Gribouval Olivier, Morinière Vincent, Tournant Carole, Grohmann Maik, Kuhn Elisa, Wagner Timo, Bole-Feysot Christine, Jabot-Hanin Fabienne, Nitschké Patrick, Ahluwalia Tarunveer S, Köttgen Anna, Andersen Christian Brix Folsted, Bergmann Carsten, Antignac Corinne, Simons Mati
Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans.
Frontiers in endocrinology 2023 3 14 1081741.
Uglebjerg Nicoline, Ahmadizar Fariba, Aly Dina M, Cañadas-Garre Marisa, Hill Claire, Naber Annemieke, Oddsson Asmundur, Singh Sunny S, Smyth Laura, Trégouët David-Alexandre, Chaker Layal, Ghanbari Mohsen, Steinthorsdottir Valgerdur, Ahlqvist Emma, Hadjadj Samy, Van Hoek Mandy, Kavousi Maryam, McKnight Amy Jayne, Sijbrands Eric J, Stefansson Kari, Simons Matias, Rossing Peter, Ahluwalia Tarunveer
Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease.
International journal of molecular sciences 2024 5 25 (10): .
Veerle Labarque, Emmanuel Chide Okocha,
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