Poulton J - Search Results

1

Pancreatic pathology in non-insulin dependent diabetes (NIDDM).

Clark A, de Koning EJ, Hattersley AT, Hansen BC, Yajnik CS, Poulton J. Clark A, et al. Among authors: poulton j. Diabetes Res Clin Pract. 1995 Aug;28 Suppl:S39-47. doi: 10.1016/0168-8227(95)01075-o. Diabetes Res Clin Pract. 1995. PMID: 8529518 Review.

2

Mitochondrial DNA, diabetes and pancreatic pathology in Kearns-Sayre syndrome.

Poulton J, O'Rahilly S, Morten KJ, Clark A. Poulton J, et al. Diabetologia. 1995 Jul;38(7):868-71. doi: 10.1007/s001250050366. Diabetologia. 1995. PMID: 7556992

3

Fetal and neonatal exposure to AZT and low-protein diet affects glucose homeostasis: a model with implications for AIDS prevention.

Morten K, Field P, Ashley N, Williams KA, Harris D, Hartley M, Clark A, Poulton J. Morten K, et al. Among authors: poulton j. Am J Physiol Endocrinol Metab. 2005 Dec;289(6):E1115-8. doi: 10.1152/ajpendo.00226.2005. Epub 2005 Jul 12. Am J Physiol Endocrinol Metab. 2005. PMID: 16014351 Free article.

4

A common mitochondrial DNA variant is associated with insulin resistance in adult life.

Poulton J, Brown MS, Cooper A, Marchington DR, Phillips DI. Poulton J, et al. Diabetologia. 1998 Jan;41(1):54-8. doi: 10.1007/s001250050866. Diabetologia. 1998. PMID: 9498630

5

Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study.

Poulton J, Luan J, Macaulay V, Hennings S, Mitchell J, Wareham NJ. Poulton J, et al. Hum Mol Genet. 2002 Jun 15;11(13):1581-3. doi: 10.1093/hmg/11.13.1581. Hum Mol Genet. 2002. PMID: 12045211

6

Do sequence variants in the major non-coding region of the mitochondrial genome influence mitochondrial mutations associated with disease?

Marchington DR, Poulton J, Sellar A, Holt IJ. Marchington DR, et al. Among authors: poulton j. Hum Mol Genet. 1996 Apr;5(4):473-9. doi: 10.1093/hmg/5.4.473. Hum Mol Genet. 1996. PMID: 8845839

7

Prospects for DNA-based prenatal diagnosis of mitochondrial disorders.

Poulton J, Marchington DR. Poulton J, et al. Prenat Diagn. 1996 Dec;16(13):1247-56. doi: 10.1002/(SICI)1097-0223(199612)16:13<1247::AID-PD99>3.0.CO;2-P. Prenat Diagn. 1996. PMID: 9061755 Review.

8

Mitochondrial gene mutations.

Poulton J. Poulton J. Eur J Paediatr Neurol. 1998;2(2):99-103. doi: 10.1016/s1090-3798(98)80049-4. Eur J Paediatr Neurol. 1998. PMID: 10724104 No abstract available.

9

Mitochondrial DNA and genetic disease.

Poulton J. Poulton J. Arch Dis Child. 1988 Aug;63(8):883-5. doi: 10.1136/adc.63.8.883. Arch Dis Child. 1988. PMID: 3046511 Free PMC article. Review. No abstract available.

10

Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.

Black GC, Craig IW, Oostra RJ, Norby S, Rosenberg T, Morten K, Laborde A, Poulton J. Black GC, et al. Among authors: poulton j. Eye (Lond). 1995;9 ( Pt 4):513-6. doi: 10.1038/eye.1995.117. Eye (Lond). 1995. PMID: 7498577

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