Pearce DA - Search Results

1

Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.

Ramirez-Montealegre D, Chattopadhyay S, Curran TM, Wasserfall C, Pritchard L, Schatz D, Petitto J, Hopkins D, She JX, Rothberg PG, Atkinson M, Pearce DA. Ramirez-Montealegre D, et al. Among authors: pearce da. Neurology. 2005 Feb 22;64(4):743-5. doi: 10.1212/01.WNL.0000151973.08426.7E. Neurology. 2005. PMID: 15728308

2

BTN1, a yeast gene corresponding to the human gene responsible for Batten's disease, is not essential for viability, mitochondrial function, or degradation of mitochondrial ATP synthase.

Pearce DA, Sherman F. Pearce DA, et al. Yeast. 1997 Jun 30;13(8):691-7. doi: 10.1002/(SICI)1097-0061(19970630)13:8<691::AID-YEA123>3.0.CO;2-D. Yeast. 1997. PMID: 9219333

3

A yeast model for the study of Batten disease.

Pearce DA, Sherman F. Pearce DA, et al. Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):6915-8. doi: 10.1073/pnas.95.12.6915. Proc Natl Acad Sci U S A. 1998. PMID: 9618513 Free PMC article.

4

Localization and processing of CLN3, the protein associated to Batten disease: where is it and what does it do?

Pearce DA. Pearce DA. J Neurosci Res. 2000 Jan 1;59(1):19-23. J Neurosci Res. 2000. PMID: 10658181 Review.

5

Neural and extraneural expression of the neuronal ceroid lipofuscinoses genes CLN1, CLN2, and CLN3: functional implications for CLN3.

Chattopadhyay S, Pearce DA. Chattopadhyay S, et al. Among authors: pearce da. Mol Genet Metab. 2000 Sep-Oct;71(1-2):207-11. doi: 10.1006/mgme.2000.3056. Mol Genet Metab. 2000. PMID: 11001812 Free article. Review.

6

The yeast model for batten disease: mutations in BTN1, BTN2, and HSP30 alter pH homeostasis.

Chattopadhyay S, Muzaffar NE, Sherman F, Pearce DA. Chattopadhyay S, et al. Among authors: pearce da. J Bacteriol. 2000 Nov;182(22):6418-23. doi: 10.1128/JB.182.22.6418-6423.2000. J Bacteriol. 2000. PMID: 11053386 Free PMC article.

7

Searching for interacting partners of CLN1, CLN2 and Btn1p with the two-hybrid system.

Cottone CD, Chattopadhyay S, Pearce DA. Cottone CD, et al. Among authors: pearce da. Eur J Paediatr Neurol. 2001;5 Suppl A:95-8. doi: 10.1053/ejpn.2000.0442. Eur J Paediatr Neurol. 2001. PMID: 11589016

8

An autoantibody inhibitory to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.

Chattopadhyay S, Ito M, Cooper JD, Brooks AI, Curran TM, Powers JM, Pearce DA. Chattopadhyay S, et al. Among authors: pearce da. Hum Mol Genet. 2002 Jun 1;11(12):1421-31. doi: 10.1093/hmg/11.12.1421. Hum Mol Genet. 2002. PMID: 12023984

9

Altered flurothyl seizure induction latency, phenotype, and subsequent mortality in a mouse model of juvenile neuronal ceroid lipofuscinosis/batten disease.

Kriscenski-Perry E, Applegate CD, Serour A, Mhyre TR, Leonardo CC, Pearce DA. Kriscenski-Perry E, et al. Among authors: pearce da. Epilepsia. 2002 Oct;43(10):1137-40. doi: 10.1046/j.1528-1157.2002.16002.x. Epilepsia. 2002. PMID: 12366726 Free article.

10

Interaction with Btn2p is required for localization of Rsglp: Btn2p-mediated changes in arginine uptake in Saccharomyces cerevisiae.

Chattopadhyay S, Pearce DA. Chattopadhyay S, et al. Among authors: pearce da. Eukaryot Cell. 2002 Aug;1(4):606-12. doi: 10.1128/EC.1.4.606-612.2002. Eukaryot Cell. 2002. PMID: 12456008 Free PMC article.

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