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Results: 13

Cited In for PubMed (Select 20226046)

1.

INS-gene mutations: From genetics and beta cell biology to clinical disease.

Liu M, Sun J, Cui J, Chen W, Guo H, Barbetti F, Arvan P.

Mol Aspects Med. 2015 Apr;42:3-18. doi: 10.1016/j.mam.2014.12.001. Epub 2014 Dec 24. Review.

PMID:
25542748
2.

Structural and functional study of the GlnB22-insulin mutant responsible for maturity-onset diabetes of the young.

Křížková K, Veverka V, Maletínská L, Hexnerová R, Brzozowski AM, Jiráček J, Žáková L.

PLoS One. 2014 Nov 25;9(11):e112883. doi: 10.1371/journal.pone.0112883. eCollection 2014.

3.

Transgenic zebrafish model of the C43G human insulin gene mutation.

Eames SC, Kinkel MD, Rajan S, Prince VE, Philipson LH.

J Diabetes Investig. 2013 Mar 18;4(2):157-67. doi: 10.1111/jdi.12015. Epub 2012 Nov 5.

4.

Insulin gene mutations and diabetes.

Nishi M, Nanjo K.

J Diabetes Investig. 2011 Apr 7;2(2):92-100. doi: 10.1111/j.2040-1124.2011.00100.x. Review.

5.

Inefficient translocation of preproinsulin contributes to pancreatic β cell failure and late-onset diabetes.

Guo H, Xiong Y, Witkowski P, Cui J, Wang LJ, Sun J, Lara-Lemus R, Haataja L, Hutchison K, Shan SO, Arvan P, Liu M.

J Biol Chem. 2014 Jun 6;289(23):16290-302. doi: 10.1074/jbc.M114.562355. Epub 2014 Apr 25.

PMID:
24770419
6.

Monogenic diabetes: a diagnostic algorithm for clinicians.

Carroll RW, Murphy R.

Genes (Basel). 2013 Sep 26;4(4):522-35. doi: 10.3390/genes4040522.

7.

Diabetes mellitus due to the toxic misfolding of proinsulin variants.

Weiss MA.

FEBS Lett. 2013 Jun 27;587(13):1942-50. doi: 10.1016/j.febslet.2013.04.044. Epub 2013 May 10. Review.

8.

Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.

Bonnefond A, Philippe J, Durand E, Dechaume A, Huyvaert M, Montagne L, Marre M, Balkau B, Fajardy I, Vambergue A, Vatin V, Delplanque J, Le Guilcher D, De Graeve F, Lecoeur C, Sand O, Vaxillaire M, Froguel P.

PLoS One. 2012;7(6):e37423. doi: 10.1371/journal.pone.0037423. Epub 2012 Jun 11.

9.

Impaired cleavage of preproinsulin signal peptide linked to autosomal-dominant diabetes.

Liu M, Lara-Lemus R, Shan SO, Wright J, Haataja L, Barbetti F, Guo H, Larkin D, Arvan P.

Diabetes. 2012 Apr;61(4):828-37. doi: 10.2337/db11-0878. Epub 2012 Feb 22.

10.

Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.

Greeley SA, Naylor RN, Philipson LH, Bell GI.

Curr Diab Rep. 2011 Dec;11(6):519-32. doi: 10.1007/s11892-011-0234-7. Review.

11.

Permanent diabetes during the first year of life: multiple gene screening in 54 patients.

Russo L, Iafusco D, Brescianini S, Nocerino V, Bizzarri C, Toni S, Cerutti F, Monciotti C, Pesavento R, Iughetti L, Bernardini L, Bonfanti R, Gargantini L, Vanelli M, Aguilar-Bryan L, Stazi MA, Grasso V, Colombo C, Barbetti F; ISPED Early Diabetes Study Group.

Diabetologia. 2011 Jul;54(7):1693-701. doi: 10.1007/s00125-011-2094-8. Epub 2011 Mar 10.

12.

Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.

Støy J, Steiner DF, Park SY, Ye H, Philipson LH, Bell GI.

Rev Endocr Metab Disord. 2010 Sep;11(3):205-15. doi: 10.1007/s11154-010-9151-3. Review. Erratum in: Rev Endocr Metab Disord. 2012 Mar;13(1):79-81.

13.

Proinsulin misfolding and diabetes: mutant INS gene-induced diabetes of youth.

Liu M, Hodish I, Haataja L, Lara-Lemus R, Rajpal G, Wright J, Arvan P.

Trends Endocrinol Metab. 2010 Nov;21(11):652-9. doi: 10.1016/j.tem.2010.07.001. Epub 2010 Aug 18. Review.

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