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Items: 10

1.

Cell cycle arrest in Batten disease lymphoblast cells.

Kang S, Kim JB, Heo TH, Kim SJ.

Gene. 2013 May 1;519(2):245-50. doi: 10.1016/j.gene.2013.02.022. Epub 2013 Feb 28.

PMID:
23458879
2.

The genetic spectrum of human neuronal ceroid-lipofuscinoses.

Mole SE.

Brain Pathol. 2004 Jan;14(1):70-6. Review.

PMID:
14997939
3.
4.
5.

Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and update.

Rakheja D, Narayan SB, Bennett MJ.

Curr Mol Med. 2007 Sep;7(6):603-8. Review.

PMID:
17896996
6.

The function of CLN3P, the Batten disease protein.

Rakheja D, Narayan SB, Bennett MJ.

Mol Genet Metab. 2008 Mar;93(3):269-74. Review. No abstract available. Erratum in: Mol Genet Metab. 2008 Jun;94(2):270.

PMID:
18688960
7.

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

Phillips SN, Benedict JW, Weimer JM, Pearce DA.

J Neurosci Res. 2005 Mar 1;79(5):573-83. Review.

PMID:
15657902
8.

Moving towards therapies for juvenile Batten disease?

Cooper JD.

Exp Neurol. 2008 Jun;211(2):329-31. doi: 10.1016/j.expneurol.2008.02.016. Epub 2008 Mar 4. Review.

PMID:
18400221
9.

[From gene to disease; from CLN1, CLN2 and CLN3 to neuronal ceroid lipofuscinosis].

Taschner PE, Losekoot M, Breuning MH, Hofman I, van Diggelen OP.

Ned Tijdschr Geneeskd. 2005 Feb 5;149(6):300-3. Review. Dutch.

PMID:
15730038
10.

Large animal models for Batten disease: a review.

Weber K, Pearce DA.

J Child Neurol. 2013 Sep;28(9):1123-7. doi: 10.1177/0883073813493666. Review.

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