Molnes J - Search Results

1

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway.

Njølstad PR, Sagen JV, Bjørkhaug L, Odili S, Shehadeh N, Bakry D, Sarici SU, Alpay F, Molnes J, Molven A, Søvik O, Matschinsky FM. Njølstad PR, et al. Among authors: molnes j. Diabetes. 2003 Nov;52(11):2854-60. doi: 10.2337/diabetes.52.11.2854. Diabetes. 2003. PMID: 14578306

2

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.

Gloyn AL, Pearson ER, Antcliff JF, Proks P, Bruining GJ, Slingerland AS, Howard N, Srinivasan S, Silva JM, Molnes J, Edghill EL, Frayling TM, Temple IK, Mackay D, Shield JP, Sumnik Z, van Rhijn A, Wales JK, Clark P, Gorman S, Aisenberg J, Ellard S, Njølstad PR, Ashcroft FM, Hattersley AT. Gloyn AL, et al. Among authors: molnes j. N Engl J Med. 2004 Apr 29;350(18):1838-49. doi: 10.1056/NEJMoa032922. N Engl J Med. 2004. PMID: 15115830 Free article.

3

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy.

Sagen JV, Raeder H, Hathout E, Shehadeh N, Gudmundsson K, Baevre H, Abuelo D, Phornphutkul C, Molnes J, Bell GI, Gloyn AL, Hattersley AT, Molven A, Søvik O, Njølstad PR. Sagen JV, et al. Among authors: molnes j. Diabetes. 2004 Oct;53(10):2713-8. doi: 10.2337/diabetes.53.10.2713. Diabetes. 2004. PMID: 15448106

4

Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions.

Tammaro P, Girard C, Molnes J, Njølstad PR, Ashcroft FM. Tammaro P, et al. Among authors: molnes j. EMBO J. 2005 Jul 6;24(13):2318-30. doi: 10.1038/sj.emboj.7600715. Epub 2005 Jun 16. EMBO J. 2005. PMID: 15962003 Free PMC article.

5

Allosteric activation of human glucokinase by free polyubiquitin chains and its ubiquitin-dependent cotranslational proteasomal degradation.

Bjørkhaug L, Molnes J, Søvik O, Njølstad PR, Flatmark T. Bjørkhaug L, et al. Among authors: molnes j. J Biol Chem. 2007 Aug 3;282(31):22757-64. doi: 10.1074/jbc.M700517200. Epub 2007 Jun 8. J Biol Chem. 2007. PMID: 17561510 Free article.

6

Catalytic activation of human glucokinase by substrate binding: residue contacts involved in the binding of D-glucose to the super-open form and conformational transitions.

Molnes J, Bjørkhaug L, Søvik O, Njølstad PR, Flatmark T. Molnes J, et al. FEBS J. 2008 May;275(10):2467-81. doi: 10.1111/j.1742-4658.2008.06391.x. Epub 2008 Apr 7. FEBS J. 2008. PMID: 18397317 Free article.

7

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry.

Sagen JV, Bjørkhaug L, Molnes J, Raeder H, Grevle L, Søvik O, Molven A, Njølstad PR. Sagen JV, et al. Among authors: molnes j. Pediatr Diabetes. 2008 Oct;9(5):442-9. doi: 10.1111/j.1399-5448.2008.00399.x. Epub 2008 Apr 9. Pediatr Diabetes. 2008. PMID: 18399931

8

Binding of ATP at the active site of human pancreatic glucokinase--nucleotide-induced conformational changes with possible implications for its kinetic cooperativity.

Molnes J, Teigen K, Aukrust I, Bjørkhaug L, Søvik O, Flatmark T, Njølstad PR. Molnes J, et al. FEBS J. 2011 Jul;278(13):2372-86. doi: 10.1111/j.1742-4658.2011.08160.x. Epub 2011 May 31. FEBS J. 2011. PMID: 21569204 Free PMC article.

9

HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease.

Gonc EN, Ozturk BB, Haldorsen IS, Molnes J, Immervoll H, Raeder H, Molven A, Søvik O, Njølstad PR. Gonc EN, et al. Among authors: molnes j. Pediatr Diabetes. 2012 Mar;13(2):e1-5. doi: 10.1111/j.1399-5448.2011.00773.x. Epub 2011 Jul 19. Pediatr Diabetes. 2012. PMID: 21767339

10

Exome sequencing and genetic testing for MODY.

Johansson S, Irgens H, Chudasama KK, Molnes J, Aerts J, Roque FS, Jonassen I, Levy S, Lima K, Knappskog PM, Bell GI, Molven A, Njølstad PR. Johansson S, et al. Among authors: molnes j. PLoS One. 2012;7(5):e38050. doi: 10.1371/journal.pone.0038050. Epub 2012 May 25. PLoS One. 2012. PMID: 22662265 Free PMC article.

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