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Items: 1 to 20 of 422

1.

Temporal gene expression profiling reveals CEBPD as a candidate regulator of brain disease in prosaposin deficient mice.

Sun Y, Jia L, Williams MT, Zamzow M, Ran H, Quinn B, Aronow BJ, Vorhees CV, Witte DP, Grabowski GA.

BMC Neurosci. 2008 Aug 1;9:76. doi: 10.1186/1471-2202-9-76.

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Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and alpha-hydroxy ceramide accumulation, and altered prosaposin trafficking.

Sun Y, Witte DP, Zamzow M, Ran H, Quinn B, Matsuda J, Grabowski GA.

Hum Mol Genet. 2007 Apr 15;16(8):957-71. Epub 2007 Mar 12.

PMID:
17353235
4.

Cell death pathways differ in several mouse models with motoneurone disease: analysis of pure motoneurone populations at a presymptomatic age.

Perrin FE, Boisset G, Lathuilière A, Kato AC.

J Neurochem. 2006 Sep;98(6):1959-72. Epub 2006 Jul 11.

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Altered expression of randomly selected genes in mouse hippocampus after traumatic brain injury.

Long Y, Zou L, Liu H, Lu H, Yuan X, Robertson CS, Yang K.

J Neurosci Res. 2003 Mar 1;71(5):710-20.

PMID:
12584729
7.

Transcriptome analysis reveals altered cholesterol metabolism during the neurodegeneration in mouse scrapie model.

Xiang W, Hummel M, Mitteregger G, Pace C, Windl O, Mansmann U, Kretzschmar HA.

J Neurochem. 2007 Aug;102(3):834-47. Epub 2007 Apr 16.

8.

D-Serine exposure resulted in gene expression changes implicated in neurodegenerative disorders and neuronal dysfunction in male Fischer 344 rats.

Davidson ME, Kerepesi LA, Soto A, Chan VT.

Arch Toxicol. 2009 Aug;83(8):747-62. doi: 10.1007/s00204-009-0405-3. Epub 2009 Feb 11.

PMID:
19212759
9.

Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases.

von Schantz C, Saharinen J, Kopra O, Cooper JD, Gentile M, Hovatta I, Peltonen L, Jalanko A.

BMC Genomics. 2008 Mar 28;9:146. doi: 10.1186/1471-2164-9-146.

10.

Down-regulation of Bcl-2 in the fetal brain of the Gaucher disease mouse model: a possible role in the neuronal loss.

Hong YB, Kim EY, Jung SC.

J Hum Genet. 2004;49(7):349-54. Epub 2004 Jun 4.

PMID:
15179559
11.
12.

Global transcriptome analysis of genetically identified neurons in the adult cortex.

Rossner MJ, Hirrlinger J, Wichert SP, Boehm C, Newrzella D, Hiemisch H, Eisenhardt G, Stuenkel C, von Ahsen O, Nave KA.

J Neurosci. 2006 Sep 27;26(39):9956-66.

13.

Metallothionein I and II mitigate age-dependent secondary brain injury.

Natale JE, Knight JB, Cheng Y, Rome JE, Gallo V.

J Neurosci Res. 2004 Nov 1;78(3):303-14.

PMID:
15389833
14.

Genes and pathways differentially expressed in the brains of Fxr2 knockout mice.

Cavallaro S, Paratore S, Fradale F, de Vrij FM, Willemsen R, Oostra BA.

Neurobiol Dis. 2008 Dec;32(3):510-20. doi: 10.1016/j.nbd.2008.09.008. Epub 2008 Sep 30.

PMID:
18930145
15.

Monocular visual deprivation in macaque monkeys: a profile in the gene expression of lateral geniculate nucleus by laser capture microdissection.

Cheng G, Kaminski HJ, Gong B, Zhou L, Hatala D, Howell SJ, Zhou X, Mustari MJ.

Mol Vis. 2008 Aug 4;14:1401-13.

16.

Altered expression of type 1 inositol 1,4,5-trisphosphate receptor in the Ngsk Prnp deficient mice.

Lee HP, Choi JK, Shin HY, Jeon YC, Jeong BH, Lee HG, Kim JI, Choi EK, Carp RI, Kim YS.

Neuroscience. 2010 May 19;167(3):799-808. doi: 10.1016/j.neuroscience.2010.02.052. Epub 2010 Feb 26.

PMID:
20219645
17.

A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging.

Kopra O, Vesa J, von Schantz C, Manninen T, Minye H, Fabritius AL, Rapola J, van Diggelen OP, Saarela J, Jalanko A, Peltonen L.

Hum Mol Genet. 2004 Dec 1;13(23):2893-906. Epub 2004 Sep 30.

PMID:
15459177
18.

Gene expression profiling during the embryonic development of mouse brain using an oligonucleotide-based microarray system.

Matsuki T, Hori G, Furuichi T.

Brain Res Mol Brain Res. 2005 May 20;136(1-2):231-54. Epub 2005 Mar 23.

PMID:
15893606
19.

Quantitative gene expression profiling of mouse brain regions reveals differential transcripts conserved in human and affected in disease models.

Brochier C, Gaillard MC, Diguet E, Caudy N, Dossat C, Ségurens B, Wincker P, Roze E, Caboche J, Hantraye P, Brouillet E, Elalouf JM, de Chaldée M.

Physiol Genomics. 2008 Apr 22;33(2):170-9. doi: 10.1152/physiolgenomics.00125.2007. Epub 2008 Feb 5.

20.

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.

Mol Genet Metab. 2003 Jan;78(1):17-30.

PMID:
12559844

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