Walker M - Search Results

1

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

McFarland R, Schaefer AM, Gardner JL, Lynn S, Hayes CM, Barron MJ, Walker M, Chinnery PF, Taylor RW, Turnbull DM. McFarland R, et al. Among authors: walker m. Ann Neurol. 2004 Apr;55(4):478-84. doi: 10.1002/ana.20004. Ann Neurol. 2004. PMID: 15048886

2

Variation in the calpain-10 gene affects blood glucose levels in the British population.

Lynn S, Evans JC, White C, Frayling TM, Hattersley AT, Turnbull DM, Horikawa Y, Cox NJ, Bell GI, Walker M. Lynn S, et al. Among authors: walker m. Diabetes. 2002 Jan;51(1):247-50. doi: 10.2337/diabetes.51.1.247. Diabetes. 2002. PMID: 11756349

3

Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome.

Choo-Kang AT, Lynn S, Taylor GA, Daly ME, Sihota SS, Wardell TM, Chinnery PF, Turnbull DM, Walker M. Choo-Kang AT, et al. Among authors: walker m. Diabetes. 2002 Jul;51(7):2317-20. doi: 10.2337/diabetes.51.7.2317. Diabetes. 2002. PMID: 12086967

4

Diabetes and deafness: is it sufficient to screen for the mitochondrial 3243A>G mutation alone?

Whittaker RG, Schaefer AM, McFarland R, Taylor RW, Walker M, Turnbull DM. Whittaker RG, et al. Among authors: walker m. Diabetes Care. 2007 Sep;30(9):2238-9. doi: 10.2337/dc07-0466. Epub 2007 May 31. Diabetes Care. 2007. PMID: 17540956 No abstract available.

5

Does impaired mitochondrial function affect insulin signaling and action in cultured human skeletal muscle cells?

Brown AE, Elstner M, Yeaman SJ, Turnbull DM, Walker M. Brown AE, et al. Among authors: walker m. Am J Physiol Endocrinol Metab. 2008 Jan;294(1):E97-102. doi: 10.1152/ajpendo.00267.2007. Epub 2007 Oct 23. Am J Physiol Endocrinol Metab. 2008. PMID: 17957036 Free article.

6

Endocrine disorders in mitochondrial disease.

Schaefer AM, Walker M, Turnbull DM, Taylor RW. Schaefer AM, et al. Among authors: walker m. Mol Cell Endocrinol. 2013 Oct 15;379(1-2):2-11. doi: 10.1016/j.mce.2013.06.004. Epub 2013 Jun 13. Mol Cell Endocrinol. 2013. PMID: 23769710 Free PMC article. Review.

7

Age-related mitochondrial DNA depletion and the impact on pancreatic Beta cell function.

Nile DL, Brown AE, Kumaheri MA, Blair HR, Heggie A, Miwa S, Cree LM, Payne B, Chinnery PF, Brown L, Gunn DA, Walker M. Nile DL, et al. Among authors: walker m. PLoS One. 2014 Dec 22;9(12):e115433. doi: 10.1371/journal.pone.0115433. eCollection 2014. PLoS One. 2014. PMID: 25532126 Free PMC article.

8

Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms.

Nolden KA, Egner JM, Collier JJ, Russell OM, Alston CL, Harwig MC, Widlansky ME, Sasorith S, Barbosa IA, Douglas AG, Baptista J, Walker M, Donnelly DE, Morris AA, Tan HJ, Kurian MA, Gorman K, Mordekar S, Deshpande C, Samanta R, McFarland R, Hill RB, Taylor RW, Oláhová M. Nolden KA, et al. Among authors: walker m. Life Sci Alliance. 2022 Aug 1;5(12):e202101284. doi: 10.26508/lsa.202101284. Life Sci Alliance. 2022. PMID: 35914810 Free PMC article.

9

Endocrine Manifestations and New Developments in Mitochondrial Disease.

Ng YS, Lim AZ, Panagiotou G, Turnbull DM, Walker M. Ng YS, et al. Among authors: walker m. Endocr Rev. 2022 May 12;43(3):583-609. doi: 10.1210/endrev/bnab036. Endocr Rev. 2022. PMID: 35552684 Free PMC article.

10

Mitochondrial complex I subunit deficiency promotes pancreatic α-cell proliferation.

Yu X, Arden C, Berlinguer-Palmini R, Chen C, Bradshaw C, Smith AL, Whitehall J, White M, Anderson S, Kattner N, Shaw J, Turnbull D, Greaves LC, Walker M. Yu X, et al. Among authors: walker m. Mol Metab. 2022 Jun;60:101489. doi: 10.1016/j.molmet.2022.101489. Epub 2022 Apr 4. Mol Metab. 2022. PMID: 35390502 Free PMC article.

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