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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 1
1998 2
1999 1
2000 5
2001 4
2002 8
2003 9
2004 9
2005 17
2006 15
2007 33
2008 26
2009 25
2010 21
2011 24
2012 27
2013 6
2014 3
2015 3
2016 1
2017 5
2018 6
2019 5
2020 3
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Similar Articles for PMID: 22187380

232 results
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Page 1
Coexpression of the type 2 diabetes susceptibility gene variants KCNJ11 E23K and ABCC8 S1369A alter the ATP and sulfonylurea sensitivities of the ATP-sensitive K(+) channel.
Hamming KS, Soliman D, Matemisz LC, Niazi O, Lang Y, Gloyn AL, Light PE. Hamming KS, et al. Diabetes. 2009 Oct;58(10):2419-24. doi: 10.2337/db09-0143. Epub 2009 Jul 8. Diabetes. 2009. PMID: 19587354 Free PMC article.
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes.
de Wet H, Rees MG, Shimomura K, Aittoniemi J, Patch AM, Flanagan SE, Ellard S, Hattersley AT, Sansom MS, Ashcroft FM. de Wet H, et al. Proc Natl Acad Sci U S A. 2007 Nov 27;104(48):18988-92. doi: 10.1073/pnas.0707428104. Epub 2007 Nov 19. Proc Natl Acad Sci U S A. 2007. PMID: 18025464 Free PMC article.
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11.
Edghill EL, Flanagan SE, Ellard S. Edghill EL, et al. Rev Endocr Metab Disord. 2010 Sep;11(3):193-8. doi: 10.1007/s11154-010-9149-x. Rev Endocr Metab Disord. 2010. PMID: 20922570 Review.
A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.
Tarasov AI, Nicolson TJ, Riveline JP, Taneja TK, Baldwin SA, Baldwin JM, Charpentier G, Gautier JF, Froguel P, Vaxillaire M, Rutter GA. Tarasov AI, et al. Diabetes. 2008 Jun;57(6):1595-604. doi: 10.2337/db07-1547. Epub 2008 Mar 17. Diabetes. 2008. PMID: 18346985 Free PMC article.
Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes.
Männikkö R, Flanagan SE, Sim X, Segal D, Hussain K, Ellard S, Hattersley AT, Ashcroft FM. Männikkö R, et al. Diabetes. 2011 Jun;60(6):1813-22. doi: 10.2337/db10-1583. Diabetes. 2011. PMID: 21617188 Free PMC article.
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes.
de Wet H, Proks P, Lafond M, Aittoniemi J, Sansom MS, Flanagan SE, Pearson ER, Hattersley AT, Ashcroft FM. de Wet H, et al. EMBO Rep. 2008 Jul;9(7):648-54. doi: 10.1038/embor.2008.71. Epub 2008 May 23. EMBO Rep. 2008. PMID: 18497752 Free PMC article.
Differential structure of atrial and ventricular KATP: atrial KATP channels require SUR1.
Flagg TP, Kurata HT, Masia R, Caputa G, Magnuson MA, Lefer DJ, Coetzee WA, Nichols CG. Flagg TP, et al. Circ Res. 2008 Dec 5;103(12):1458-65. doi: 10.1161/CIRCRESAHA.108.178186. Epub 2008 Oct 30. Circ Res. 2008. PMID: 18974387 Free PMC article.
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