Morten KJ - Search Results

1

Acetyl-leucine slows disease progression in lysosomal storage disorders.

Kaya E, Smith DA, Smith C, Morris L, Bremova-Ertl T, Cortina-Borja M, Fineran P, Morten KJ, Poulton J, Boland B, Spencer J, Strupp M, Platt FM. Kaya E, et al. Among authors: morten kj. Brain Commun. 2020 Dec 20;3(1):fcaa148. doi: 10.1093/braincomms/fcaa148. eCollection 2021. Brain Commun. 2020. PMID: 33738443 Free PMC article.

2

Mitophagy plays a central role in mitochondrial ageing.

Diot A, Morten K, Poulton J. Diot A, et al. Mamm Genome. 2016 Aug;27(7-8):381-95. doi: 10.1007/s00335-016-9651-x. Epub 2016 Jun 28. Mamm Genome. 2016. PMID: 27352213 Free PMC article. Review.

3

Unbiased yeast screens identify cellular pathways affected in Niemann-Pick disease type C.

Colaco A, Fernández-Suárez ME, Shepherd D, Gal L, Bibi C, Chuartzman S, Diot A, Morten K, Eden E, Porter FD, Poulton J, Platt N, Schuldiner M, Platt FM. Colaco A, et al. Life Sci Alliance. 2020 Jun 2;3(7):e201800253. doi: 10.26508/lsa.201800253. Print 2020 Jul. Life Sci Alliance. 2020. PMID: 32487688 Free PMC article.

4

Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype.

Morten KJ, Poulton J, Sykes B. Morten KJ, et al. Hum Mol Genet. 1995 Sep;4(9):1689-91. doi: 10.1093/hmg/4.9.1689. Hum Mol Genet. 1995. PMID: 8541865 No abstract available.

5

Functional mtDNA replication defect in a fibroblast line from a patient with mtDNA depletion.

Morten KJ, Freeman Emmerson C, Poulton J. Morten KJ, et al. J Inherit Metab Dis. 1996;19(2):123-6. doi: 10.1007/BF01799409. J Inherit Metab Dis. 1996. PMID: 8739945 No abstract available.

6

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

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

7

Leber's hereditary optic neuropathy: heteroplasmy is likely to be significant in the expression of LHON in families with the 3460 ND1 mutation.

Black GC, Morten K, Laborde A, Poulton J. Black GC, et al. Br J Ophthalmol. 1996 Oct;80(10):915-7. doi: 10.1136/bjo.80.10.915. Br J Ophthalmol. 1996. PMID: 8976705 Free PMC article.

8

Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?

Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L. Poulton J, et al. Among authors: morten kj. Hum Mol Genet. 1994 Jun;3(6):947-51. doi: 10.1093/hmg/3.6.947. Hum Mol Genet. 1994. PMID: 7951243 Clinical Trial.

9

A new point mutation associated with mitochondrial encephalomyopathy.

Morten KJ, Cooper JM, Brown GK, Lake BD, Pike D, Poulton J. Morten KJ, et al. Hum Mol Genet. 1993 Dec;2(12):2081-7. doi: 10.1093/hmg/2.12.2081. Hum Mol Genet. 1993. PMID: 8111377

10

Modulating mitochondrial quality in disease transmission: towards enabling mitochondrial DNA disease carriers to have healthy children.

Diot A, Dombi E, Lodge T, Liao C, Morten K, Carver J, Wells D, Child T, Johnston IG, Williams S, Poulton J. Diot A, et al. Biochem Soc Trans. 2016 Aug 15;44(4):1091-100. doi: 10.1042/BST20160095. Biochem Soc Trans. 2016. PMID: 27528757 Free PMC article.

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