Tribble N - Search Results

1

Developmental validation of the ParaDNA(®) Intelligence System-A novel approach to DNA profiling.

Blackman S, Dawnay N, Ball G, Stafford-Allen B, Tribble N, Rendell P, Neary K, Hanson EK, Ballantyne J, Kallifatidis B, Mendel J, Mills DK, Wells S. Blackman S, et al. Among authors: tribble n. Forensic Sci Int Genet. 2015 Jul;17:137-148. doi: 10.1016/j.fsigen.2015.04.009. Epub 2015 May 6. Forensic Sci Int Genet. 2015. PMID: 25980941 Free article.

2

Applicability of the ParaDNA(®) Screening System to Seminal Samples.

Tribble ND, Miller JA, Dawnay N, Duxbury NJ. Tribble ND, et al. J Forensic Sci. 2015 May;60(3):690-2. doi: 10.1111/1556-4029.12742. Epub 2015 Mar 4. J Forensic Sci. 2015. PMID: 25739746

3

Assessing the impact of common forensic presumptive tests on the ability to obtain results using a novel rapid DNA platform.

Donachie GE, Dawnay N, Ahmed R, Naif S, Duxbury NJ, Tribble ND. Donachie GE, et al. Among authors: tribble nd. Forensic Sci Int Genet. 2015 Jul;17:87-90. doi: 10.1016/j.fsigen.2015.04.003. Epub 2015 Apr 11. Forensic Sci Int Genet. 2015. PMID: 25864157

4

The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver.

Beer NL, Tribble ND, McCulloch LJ, Roos C, Johnson PR, Orho-Melander M, Gloyn AL. Beer NL, et al. Among authors: tribble nd. Hum Mol Genet. 2009 Nov 1;18(21):4081-8. doi: 10.1093/hmg/ddp357. Epub 2009 Jul 30. Hum Mol Genet. 2009. PMID: 19643913 Free PMC article.

5

Glucokinase (GCK) and other susceptibility genes for beta-cell dysfunction: the candidate approach.

Gloyn AL, Tribble ND, van de Bunt M, Barrett A, Johnson PR. Gloyn AL, et al. Biochem Soc Trans. 2008 Jun;36(Pt 3):306-11. doi: 10.1042/BST0360306. Biochem Soc Trans. 2008. PMID: 18481947

6

Identification and functional characterisation of novel glucokinase mutations causing maturity-onset diabetes of the young in Slovakia.

Valentínová L, Beer NL, Staník J, Tribble ND, van de Bunt M, Hučková M, Barrett A, Klimeš I, Gašperíková D, Gloyn AL. Valentínová L, et al. Among authors: tribble nd. PLoS One. 2012;7(4):e34541. doi: 10.1371/journal.pone.0034541. Epub 2012 Apr 6. PLoS One. 2012. PMID: 22493702 Free PMC article.

7

Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.

Beer NL, Osbak KK, van de Bunt M, Tribble ND, Steele AM, Wensley KJ, Edghill EL, Colcough K, Barrett A, Valentínová L, Rundle JK, Raimondo A, Grimsby J, Ellard S, Gloyn AL. Beer NL, et al. Among authors: tribble nd. Diabetes Care. 2012 Jul;35(7):1482-4. doi: 10.2337/dc11-2420. Epub 2012 May 18. Diabetes Care. 2012. PMID: 22611063 Free PMC article.

8

Naturally occurring glucokinase mutations are associated with defects in posttranslational S-nitrosylation.

Ding SY, Tribble ND, Kraft CA, Markwardt M, Gloyn AL, Rizzo MA. Ding SY, et al. Among authors: tribble nd. Mol Endocrinol. 2010 Jan;24(1):171-7. doi: 10.1210/me.2009-0138. Epub 2009 Nov 24. Mol Endocrinol. 2010. PMID: 19934346 Free PMC article.

9

Permanent neonatal diabetes mellitus caused by a novel homozygous (T168A) glucokinase (GCK) mutation: initial response to oral sulphonylurea therapy.

Turkkahraman D, Bircan I, Tribble ND, Akçurin S, Ellard S, Gloyn AL. Turkkahraman D, et al. Among authors: tribble nd. J Pediatr. 2008 Jul;153(1):122-6. doi: 10.1016/j.jpeds.2007.12.037. Epub 2008 Mar 6. J Pediatr. 2008. PMID: 18571549

10

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.

Christesen HB, Tribble ND, Molven A, Siddiqui J, Sandal T, Brusgaard K, Ellard S, Njølstad PR, Alm J, Brock Jacobsen B, Hussain K, Gloyn AL. Christesen HB, et al. Eur J Endocrinol. 2008 Jul;159(1):27-34. doi: 10.1530/EJE-08-0203. Epub 2008 May 1. Eur J Endocrinol. 2008. PMID: 18450771

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