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Results: 1 to 20 of 94

1.

Cpd-1 null mice display a subtle neurological phenotype.

Kular RK, Gogliotti RG, Opal P.

PLoS One. 2010 Sep 9;5(9). pii: e12649. doi: 10.1371/journal.pone.0012649.

PMID:
20844742
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Generation and characterization of LANP/pp32 null mice.

Opal P, Garcia JJ, McCall AE, Xu B, Weeber EJ, Sweatt JD, Orr HT, Zoghbi HY.

Mol Cell Biol. 2004 Apr;24(8):3140-9.

PMID:
15060138
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Anp32e/Cpd1 regulates protein phosphatase 2A activity at synapses during synaptogenesis.

Costanzo RV, Vilá-Ortíz GJ, Perandones C, Carminatti H, Matilla A, Radrizzani M.

Eur J Neurosci. 2006 Jan;23(2):309-24.

PMID:
16420440
[PubMed - indexed for MEDLINE]
4.

Generation and characterization of the Anp32e-deficient mouse.

Reilly PT, Afzal S, Wakeham A, Haight J, You-Ten A, Zaugg K, Dembowy J, Young A, Mak TW.

PLoS One. 2010 Oct 26;5(10):e13597. doi: 10.1371/journal.pone.0013597.

PMID:
21049064
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Transgenic and knock-out mice: models of neurological disease.

Aguzzi A, Brandner S, Sure U, Rüedi D, Isenmann S.

Brain Pathol. 1994 Jan;4(1):3-20. Review.

PMID:
8025701
[PubMed - indexed for MEDLINE]
6.

Clorgyline-mediated reversal of neurological deficits in a Complexin 2 knockout mouse.

Glynn D, Gibson HE, Harte MK, Reim K, Jones S, Reynolds GP, Morton AJ.

Hum Mol Genet. 2010 Sep 1;19(17):3402-12. doi: 10.1093/hmg/ddq252. Epub 2010 Jun 28.

PMID:
20584925
[PubMed - indexed for MEDLINE]
Free Article
7.

Differential expression of CPD1 during postnatal development in the mouse cerebellum.

Radrizzani M, Vilá-Ortiz G, Cafferata EG, Di Tella MC, González-Guerrico A, Perandones C, Pivetta OH, Carminatti H, Idoyaga Vargas VP, Santa-Coloma TA.

Brain Res. 2001 Jul 13;907(1-2):162-74.

PMID:
11430900
[PubMed - indexed for MEDLINE]
8.

Acidic nuclear phosphoprotein 32kDa (ANP32)B-deficient mouse reveals a hierarchy of ANP32 importance in mammalian development.

Reilly PT, Afzal S, Gorrini C, Lui K, Bukhman YV, Wakeham A, Haight J, Ling TW, Cheung CC, Elia AJ, Turner PV, Mak TW.

Proc Natl Acad Sci U S A. 2011 Jun 21;108(25):10243-8. doi: 10.1073/pnas.1106211108. Epub 2011 Jun 2.

PMID:
21636789
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Depletion of Complexin II does not affect disease progression in a mouse model of Huntington's disease (HD); support for role for complexin II in behavioural pathology in a mouse model of HD.

Glynn D, Reim K, Brose N, Morton AJ.

Brain Res Bull. 2007 Apr 30;72(2-3):108-20. Epub 2006 Nov 13.

PMID:
17352934
[PubMed - indexed for MEDLINE]
10.

Complexin2 null mutation requires a 'second hit' for induction of phenotypic changes relevant to schizophrenia.

Radyushkin K, El-Kordi A, Boretius S, Castaneda S, Ronnenberg A, Reim K, Bickeböller H, Frahm J, Brose N, Ehrenreich H.

Genes Brain Behav. 2010 Aug;9(6):592-602. doi: 10.1111/j.1601-183X.2010.00590.x. Epub 2010 Apr 19.

PMID:
20412316
[PubMed - indexed for MEDLINE]
11.

The Anp32 family of proteins containing leucine-rich repeats.

Matilla A, Radrizzani M.

Cerebellum. 2005;4(1):7-18. Review.

PMID:
15895553
[PubMed - indexed for MEDLINE]
12.

Vertebrate Lrig3-ErbB interactions occur in vitro but are unlikely to play a role in Lrig3-dependent inner ear morphogenesis.

Abraira VE, Satoh T, Fekete DM, Goodrich LV.

PLoS One. 2010 Feb 1;5(2):e8981. doi: 10.1371/journal.pone.0008981.

PMID:
20126551
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Neurocan is dispensable for brain development.

Zhou XH, Brakebusch C, Matthies H, Oohashi T, Hirsch E, Moser M, Krug M, Seidenbecher CI, Boeckers TM, Rauch U, Buettner R, Gundelfinger ED, Fässler R.

Mol Cell Biol. 2001 Sep;21(17):5970-8.

PMID:
11486035
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Neurogranin null mutant mice display performance deficits on spatial learning tasks with anxiety related components.

Miyakawa T, Yared E, Pak JH, Huang FL, Huang KP, Crawley JN.

Hippocampus. 2001;11(6):763-75.

PMID:
11811671
[PubMed - indexed for MEDLINE]
15.

Generation and characterization of neuregulin-2-deficient mice.

Britto JM, Lukehurst S, Weller R, Fraser C, Qiu Y, Hertzog P, Busfield SJ.

Mol Cell Biol. 2004 Sep;24(18):8221-6.

PMID:
15340081
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Mice with combined gene knock-outs reveal essential and partially redundant functions of amyloid precursor protein family members.

Heber S, Herms J, Gajic V, Hainfellner J, Aguzzi A, Rülicke T, von Kretzschmar H, von Koch C, Sisodia S, Tremml P, Lipp HP, Wolfer DP, Müller U.

J Neurosci. 2000 Nov 1;20(21):7951-63.

PMID:
11050115
[PubMed - indexed for MEDLINE]
Free Article
17.

Fas/CD95 regulatory protein Faim2 is neuroprotective after transient brain ischemia.

Reich A, Spering C, Gertz K, Harms C, Gerhardt E, Kronenberg G, Nave KA, Schwab M, Tauber SC, Drinkut A, Harms K, Beier CP, Voigt A, Göbbels S, Endres M, Schulz JB.

J Neurosci. 2011 Jan 5;31(1):225-33. doi: 10.1523/JNEUROSCI.2188-10.2011.

PMID:
21209208
[PubMed - indexed for MEDLINE]
Free Article
18.

Neurons expressing the highest levels of gamma-synuclein are unaffected by targeted inactivation of the gene.

Ninkina N, Papachroni K, Robertson DC, Schmidt O, Delaney L, O'Neill F, Court F, Rosenthal A, Fleetwood-Walker SM, Davies AM, Buchman VL.

Mol Cell Biol. 2003 Nov;23(22):8233-45.

PMID:
14585981
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Targeted ANP32E mutant mice do not demonstrate obvious movement defects.

Wong P, Leo VI, Low M, Mak TW, Zhang X, Reilly PT.

PLoS One. 2013 May 13;8(5):e63815. doi: 10.1371/journal.pone.0063815. Print 2013.

PMID:
23675506
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Hepatic selenoprotein P (SePP) expression restores selenium transport and prevents infertility and motor-incoordination in Sepp-knockout mice.

Renko K, Werner M, Renner-Müller I, Cooper TG, Yeung CH, Hollenbach B, Scharpf M, Köhrle J, Schomburg L, Schweizer U.

Biochem J. 2008 Feb 1;409(3):741-9.

PMID:
17961124
[PubMed - indexed for MEDLINE]
Free Article

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