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G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.
Published in:
Diabetes, 2008, v. 57, n. 10, p. 2843, doi. 10.2337/db08-0073
By:
- Trégouet, David-Alexandre;
- Groop, Per-Henrik;
- McGinn, Steven;
- Forsblom, Carol;
- Hadjadj, Samy;
- Marre, Michel;
- Parving, Hans-Henrik;
- Tarnow, Lise;
- Telgmann, Ralph;
- Godefroy, Tiphaine;
- Nicaud, Viviane;
- Rousseau, Rachel;
- Parkkonen, Maikki;
- Hoverfält, Anna;
- Gut, Ivo;
- Heath, Simon;
- Matsuda, Fumihiko;
- Cox, Roger;
- Kazeem, Gbenga;
- Farrall, Martin
Publication type:
Article
A Functional Polymorphism in the Manganese Superoxide Dismutase Gene and Diabetic Nephropathy.
Published in:
Diabetes, 2007, v. 56, n. 1, p. 265, doi. 10.2337/db06-0698
By:
- Möllsten, Anna;
- Marklund, Stefan L.;
- Wessman, Maija;
- Svensson, Maria;
- Forsblom, Carol;
- Parkkonen, Maikki;
- Brismar, Kerstin;
- Groop, Per-Henrik;
- Dahlquist, Gisela
Publication type:
Article
Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 19, p. 2257, doi. 10.1093/hmg/11.19.2257
By:
- Saarela, Janna;
- Schoenberg Fejzo, Marlena;
- Chen, Daniel;
- Finnilä, Saara;
- Parkkonen, Maikki;
- Kuokkanen, Satu;
- Sobel, Eric;
- Tienari, Pentti J.;
- Sumelahti, Marja-Liisa;
- Wikström, Juhani;
- Elovaara, Irina;
- Koivisto, Keijo;
- Pirttilä, Tuula;
- Reunanen, Mauri;
- Palotie, Aarno;
- Peltonen, Leena
Publication type:
Article
Genetic Examination of SETD7 and SUV39H1/H2 Methyltransferases and the Risk of Diabetes Complications in Patients With Type 1 Diabetes.
Published in:
Diabetes, 2011, v. 60, n. 11, p. 3073, doi. 10.2337/db11-0073
By:
- Syreeni, Anna;
- El-Osta, Assam;
- Forsblom, Carol;
- Sandholm, Niina;
- Parkkonen, Maikki;
- Tarnow, Lise;
- Parving, Hans-Henrik;
- McKnight, Amy J.;
- Maxwell, Alexander P.;
- Cooper, Mark E.;
- Groop, Per-Henrik
Publication type:
Article

Found: 4

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.

A Functional Polymorphism in the Manganese Superoxide Dismutase Gene and Diabetic Nephropathy.

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24.

Genetic Examination of SETD7 and SUV39H1/H2 Methyltransferases and the Risk of Diabetes Complications in Patients With Type 1 Diabetes.