Mitchison HM - Search Results

1

Batten disease (JNCL) is linked to disturbances in mitochondrial, cytoskeletal, and synaptic compartments.

Luiro K, Kopra O, Blom T, Gentile M, Mitchison HM, Hovatta I, Törnquist K, Jalanko A. Luiro K, et al. Among authors: mitchison hm. J Neurosci Res. 2006 Oct;84(5):1124-38. doi: 10.1002/jnr.21015. J Neurosci Res. 2006. PMID: 16941499

2

Rapid diagnostic test for the major mutation underlying Batten disease.

Järvelä I, Mitchison HM, Munroe PB, O'Rawe AM, Mole SE, Syvänen AC. Järvelä I, et al. Among authors: mitchison hm. J Med Genet. 1996 Dec;33(12):1041-2. doi: 10.1136/jmg.33.12.1041. J Med Genet. 1996. PMID: 9004140 Free PMC article.

3

Developmental expression of palmitoyl protein thioesterase in normal mice.

Isosomppi J, Heinonen O, Hiltunen JO, Greene ND, Vesa J, Uusitalo A, Mitchison HM, Saarma M, Jalanko A, Peltonen L. Isosomppi J, et al. Among authors: mitchison hm. Brain Res Dev Brain Res. 1999 Dec 10;118(1-2):1-11. doi: 10.1016/s0165-3806(99)00115-7. Brain Res Dev Brain Res. 1999. PMID: 10611498

4

Spectrum of mutations in the Batten disease gene, CLN3.

Munroe PB, Mitchison HM, O'Rawe AM, Anderson JW, Boustany RM, Lerner TJ, Taschner PE, de Vos N, Breuning MH, Gardiner RM, Mole SE. Munroe PB, et al. Among authors: mitchison hm. Am J Hum Genet. 1997 Aug;61(2):310-6. doi: 10.1086/514846. Am J Hum Genet. 1997. PMID: 9311735 Free PMC article.

5

Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis.

Lauronen L, Munroe PB, Järvelä I, Autti T, Mitchison HM, O'Rawe AM, Gardiner RM, Mole SE, Puranen J, Häkkinen AM, Kirveskari E, Santavuori P. Lauronen L, et al. Among authors: mitchison hm. Neurology. 1999 Jan 15;52(2):360-5. doi: 10.1212/wnl.52.2.360. Neurology. 1999. PMID: 9932957

6

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected].

Mitchison HM, Bernard DJ, Greene ND, Cooper JD, Junaid MA, Pullarkat RK, de Vos N, Breuning MH, Owens JW, Mobley WC, Gardiner RM, Lake BD, Taschner PE, Nussbaum RL. Mitchison HM, et al. Neurobiol Dis. 1999 Oct;6(5):321-34. doi: 10.1006/nbdi.1999.0267. Neurobiol Dis. 1999. PMID: 10527801

7

Functional categorization of gene expression changes in the cerebellum of a Cln3-knockout mouse model for Batten disease.

Brooks AI, Chattopadhyay S, Mitchison HM, Nussbaum RL, Pearce DA. Brooks AI, et al. Among authors: mitchison hm. Mol Genet Metab. 2003 Jan;78(1):17-30. doi: 10.1016/s1096-7192(02)00201-9. Mol Genet Metab. 2003. PMID: 12559844

8

Loss of the Batten disease gene CLN3 prevents exit from the TGN of the mannose 6-phosphate receptor.

Metcalf DJ, Calvi AA, Seaman MNj, Mitchison HM, Cutler DF. Metcalf DJ, et al. Among authors: mitchison hm. Traffic. 2008 Nov;9(11):1905-14. doi: 10.1111/j.1600-0854.2008.00807.x. Epub 2008 Aug 4. Traffic. 2008. PMID: 18817525 Free article.

9

Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease).

Wavre-Shapton ST, Calvi AA, Turmaine M, Seabra MC, Cutler DF, Futter CE, Mitchison HM. Wavre-Shapton ST, et al. Among authors: mitchison hm. Hum Mol Genet. 2015 Dec 15;24(24):7060-74. doi: 10.1093/hmg/ddv406. Epub 2015 Oct 8. Hum Mol Genet. 2015. PMID: 26450516 Free PMC article.

10

A model for Batten disease protein CLN3: functional implications from homology and mutations.

Janes RW, Munroe PB, Mitchison HM, Gardiner RM, Mole SE, Wallace BA. Janes RW, et al. Among authors: mitchison hm. FEBS Lett. 1996 Dec 9;399(1-2):75-7. doi: 10.1016/s0014-5793(96)01290-2. FEBS Lett. 1996. PMID: 8980123 Free article.

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