Weimer JM - Search Results

1

Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis.

Geraets RD, Koh Sy, Hastings ML, Kielian T, Pearce DA, Weimer JM. Geraets RD, et al. Among authors: weimer jm. Orphanet J Rare Dis. 2016 Apr 16;11:40. doi: 10.1186/s13023-016-0414-2. Orphanet J Rare Dis. 2016. PMID: 27083890 Free PMC article. Review.

2

The neuronal ceroid lipofuscinoses: mutations in different proteins result in similar disease.

Weimer JM, Kriscenski-Perry E, Elshatory Y, Pearce DA. Weimer JM, et al. Neuromolecular Med. 2002;1(2):111-24. doi: 10.1385/NMM:1:2:111. Neuromolecular Med. 2002. PMID: 12025857 Review.

3

CLN3, the protein associated with batten disease: structure, function and localization.

Phillips SN, Benedict JW, Weimer JM, Pearce DA. Phillips SN, et al. Among authors: weimer jm. J Neurosci Res. 2005 Mar 1;79(5):573-83. doi: 10.1002/jnr.20367. J Neurosci Res. 2005. PMID: 15657902 Review.

4

Elevation of Hook1 in a disease model of Batten disease does not affect a novel interaction between Ankyrin G and Hook1.

Weimer JM, Chattopadhyay S, Custer AW, Pearce DA. Weimer JM, et al. Biochem Biophys Res Commun. 2005 May 20;330(4):1176-81. doi: 10.1016/j.bbrc.2005.03.103. Biochem Biophys Res Commun. 2005. PMID: 15823567

5

Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotype.

Kwon JM, Rothberg PG, Leman AR, Weimer JM, Mink JW, Pearce DA. Kwon JM, et al. Among authors: weimer jm. Neurosci Lett. 2005 Oct 21;387(2):111-4. doi: 10.1016/j.neulet.2005.07.023. Neurosci Lett. 2005. PMID: 16087292

6

Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons.

Weimer JM, Custer AW, Benedict JW, Alexander NA, Kingsley E, Federoff HJ, Cooper JD, Pearce DA. Weimer JM, et al. Neurobiol Dis. 2006 May;22(2):284-93. doi: 10.1016/j.nbd.2005.11.008. Epub 2006 Jan 18. Neurobiol Dis. 2006. PMID: 16412658 Free PMC article.

7

Selectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten disease.

Kovács AD, Weimer JM, Pearce DA. Kovács AD, et al. Among authors: weimer jm. Neurobiol Dis. 2006 Jun;22(3):575-85. doi: 10.1016/j.nbd.2005.12.018. Epub 2006 Feb 17. Neurobiol Dis. 2006. PMID: 16483786

8

Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosis.

Weimer JM, Benedict JW, Elshatory YM, Short DW, Ramirez-Montealegre D, Ryan DA, Alexander NA, Federoff HJ, Cooper JD, Pearce DA. Weimer JM, et al. Brain Res. 2007 Aug 8;1162:98-112. doi: 10.1016/j.brainres.2007.05.018. Epub 2007 May 21. Brain Res. 2007. PMID: 17617387 Free PMC article.

9

Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis.

Weimer JM, Benedict JW, Getty AL, Pontikis CC, Lim MJ, Cooper JD, Pearce DA. Weimer JM, et al. Brain Res. 2009 Apr 17;1266:93-107. doi: 10.1016/j.brainres.2009.02.009. Epub 2009 Feb 20. Brain Res. 2009. PMID: 19230832 Free PMC article.

10

A murine model of variant late infantile ceroid lipofuscinosis recapitulates behavioral and pathological phenotypes of human disease.

Morgan JP, Magee H, Wong A, Nelson T, Koch B, Cooper JD, Weimer JM. Morgan JP, et al. Among authors: weimer jm. PLoS One. 2013 Nov 1;8(11):e78694. doi: 10.1371/journal.pone.0078694. eCollection 2013. PLoS One. 2013. PMID: 24223841 Free PMC article.

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