Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 74

1.

Lipofuscin accumulation and gene expression in different tissues of mnd mice.

Traina G, Bigini P, Federighi G, Sitia L, Paroni G, Fiordaliso F, Salio M, Bendotti C, Brunelli M.

Mol Neurobiol. 2012 Apr;45(2):247-57. doi: 10.1007/s12035-012-8248-y. Epub 2012 Mar 8.

PMID:
22399241
2.

Different early ER-stress responses in the CLN8(mnd) mouse model of neuronal ceroid lipofuscinosis.

Galizzi G, Russo D, Deidda I, Cascio C, Passantino R, Guarneri R, Bigini P, Mennini T, Drago G, Guarneri P.

Neurosci Lett. 2011 Jan 25;488(3):258-62. doi: 10.1016/j.neulet.2010.11.041. Epub 2010 Nov 19.

PMID:
21094208
3.

The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8.

Ranta S, Zhang Y, Ross B, Lonka L, Takkunen E, Messer A, Sharp J, Wheeler R, Kusumi K, Mole S, Liu W, Soares MB, Bonaldo MF, Hirvasniemi A, de la Chapelle A, Gilliam TC, Lehesjoki AE.

Nat Genet. 1999 Oct;23(2):233-6.

PMID:
10508524
4.

Deficient mitochondrial Ca(2+) buffering in the Cln8(mnd) mouse model of neuronal ceroid lipofuscinosis.

Kolikova J, Afzalov R, Surin A, Lehesjoki AE, Khiroug L.

Cell Calcium. 2011 Dec;50(6):491-501. doi: 10.1016/j.ceca.2011.08.004. Epub 2011 Sep 13.

PMID:
21917311
5.

Localization of wild-type and mutant neuronal ceroid lipofuscinosis CLN8 proteins in non-neuronal and neuronal cells.

Lonka L, Salonen T, Siintola E, Kopra O, Lehesjoki AE, Jalanko A.

J Neurosci Res. 2004 Jun 15;76(6):862-71.

PMID:
15160397
6.

Gene disruption of Mfsd8 in mice provides the first animal model for CLN7 disease.

Damme M, Brandenstein L, Fehr S, Jankowiak W, Bartsch U, Schweizer M, Hermans-Borgmeyer I, Storch S.

Neurobiol Dis. 2014 May;65:12-24. doi: 10.1016/j.nbd.2014.01.003. Epub 2014 Jan 11.

PMID:
24423645
7.

You say lipofuscin, we say ceroid: defining autofluorescent storage material.

Seehafer SS, Pearce DA.

Neurobiol Aging. 2006 Apr;27(4):576-88. Epub 2006 Feb 7. Review.

PMID:
16455164
8.
9.

CNS-expressed cathepsin D prevents lymphopenia in a murine model of congenital neuronal ceroid lipofuscinosis.

Shevtsova Z, Garrido M, Weishaupt J, Saftig P, Bähr M, Lühder F, Kügler S.

Am J Pathol. 2010 Jul;177(1):271-9. doi: 10.2353/ajpath.2010.091267. Epub 2010 May 20.

10.

Cellular pathology and pathogenic aspects of neuronal ceroid lipofuscinoses.

Kida E, Golabek AA, Wisniewski KE.

Adv Genet. 2001;45:35-68. Review.

PMID:
11332776
11.

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.

Bronson RT, Donahue LR, Johnson KR, Tanner A, Lane PW, Faust JR.

Am J Med Genet. 1998 May 26;77(4):289-97.

PMID:
9600738
12.

The intracellular location and function of proteins of neuronal ceroid lipofuscinoses.

Ezaki J, Kominami E.

Brain Pathol. 2004 Jan;14(1):77-85. Review.

PMID:
14997940
13.

Molecular basis of the neuronal ceroid lipofuscinoses: mutations in CLN1, CLN2, CLN3, and CLN5.

Mole SE, Mitchison HM, Munroe PB.

Hum Mutat. 1999;14(3):199-215. Review.

PMID:
10477428
14.
15.

The development of behavioral abnormalities in the motor neuron degeneration (mnd) mouse.

Bolivar VJ, Scott Ganus J, Messer A.

Brain Res. 2002 May 24;937(1-2):74-82.

PMID:
12020865
16.

Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin in mouse CNS neurons.

Koike M, Nakanishi H, Saftig P, Ezaki J, Isahara K, Ohsawa Y, Schulz-Schaeffer W, Watanabe T, Waguri S, Kametaka S, Shibata M, Yamamoto K, Kominami E, Peters C, von Figura K, Uchiyama Y.

J Neurosci. 2000 Sep 15;20(18):6898-906.

17.

Mitochondrial oxidative metabolism in motor neuron degeneration (mnd) mouse central nervous system.

Bertamini M, Marzani B, Guarneri R, Guarneri P, Bigini P, Mennini T, Curti D.

Eur J Neurosci. 2002 Dec;16(12):2291-6.

PMID:
12492423
18.
19.

Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze.

Wendt KD, Lei B, Schachtman TR, Tullis GE, Ibe ME, Katz ML.

Behav Brain Res. 2005 Jun 20;161(2):175-82.

PMID:
15885820
20.

Rate of accumulation of Luxol Fast Blue staining material and mitochondrial ATP synthase subunit 9 in motor neuron degeneration mice.

Rodman JS, Lipman R, Brown A, Bronson RT, Dice JF.

Neurochem Res. 1998 Oct;23(10):1291-6.

PMID:
9804285

Supplemental Content

Support Center