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Items: 12


Retrospective Analysis of the Effects of Identification Procedures and Cage Changing by Using Data from Automated, Continuous Monitoring.

Lim MA, Defensor EB, Mechanic JA, Shah PP, Jaime EA, Roberts CR, Hutto DL, Schaevitz LR.

J Am Assoc Lab Anim Sci. 2019 Mar 1;58(2):126-141. doi: 10.30802/AALAS-JAALAS-18-000056. Epub 2019 Feb 14.


Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.

Bissonnette JM, Schaevitz LR, Knopp SJ, Zhou Z.

Neuroscience. 2014 May 16;267:166-76. doi: 10.1016/j.neuroscience.2014.02.043. Epub 2014 Mar 10.


MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.

Schaevitz LR, Gómez NB, Zhen DP, Berger-Sweeney JE.

Genes Brain Behav. 2013 Oct;12(7):732-40. doi: 10.1111/gbb.12070. Epub 2013 Aug 26.


Gene-environment interactions and epigenetic pathways in autism: the importance of one-carbon metabolism.

Schaevitz LR, Berger-Sweeney JE.

ILAR J. 2012;53(3-4):322-40. doi: 10.1093/ilar.53.3-4.322. Review.


Acetyl-L-carnitine improves behavior and dendritic morphology in a mouse model of Rett syndrome.

Schaevitz LR, Nicolai R, Lopez CM, D'Iddio S, Iannoni E, Berger-Sweeney JE.

PLoS One. 2012;7(12):e51586. doi: 10.1371/journal.pone.0051586. Epub 2012 Dec 5.


Preclinical research in Rett syndrome: setting the foundation for translational success.

Katz DM, Berger-Sweeney JE, Eubanks JH, Justice MJ, Neul JL, Pozzo-Miller L, Blue ME, Christian D, Crawley JN, Giustetto M, Guy J, Howell CJ, Kron M, Nelson SB, Samaco RC, Schaevitz LR, St Hillaire-Clarke C, Young JL, Zoghbi HY, Mamounas LA.

Dis Model Mech. 2012 Nov;5(6):733-45. doi: 10.1242/dmm.011007. Review.


Glutamate carboxypeptidase II and folate deficiencies result in reciprocal protection against cognitive and social deficits in mice: implications for neurodevelopmental disorders.

Schaevitz LR, Picker JD, Rana J, Kolodny NH, Shane B, Berger-Sweeney JE, Coyle JT.

Dev Neurobiol. 2012 Jun;72(6):891-905. doi: 10.1002/dneu.21000.


Cognitive and social functions and growth factors in a mouse model of Rett syndrome.

Schaevitz LR, Moriuchi JM, Nag N, Mellot TJ, Berger-Sweeney J.

Physiol Behav. 2010 Jun 1;100(3):255-63. doi: 10.1016/j.physbeh.2009.12.025. Epub 2010 Jan 5.


Phenotypic characterization of mice heterozygous for a null mutation of glutamate carboxypeptidase II.

Han L, Picker JD, Schaevitz LR, Tsai G, Feng J, Jiang Z, Chu HC, Basu AC, Berger-Sweeney J, Coyle JT.

Synapse. 2009 Aug;63(8):625-35. doi: 10.1002/syn.20649.


Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

Stearns NA, Schaevitz LR, Bowling H, Nag N, Berger UV, Berger-Sweeney J.

Neuroscience. 2007 May 25;146(3):907-21. Epub 2007 Mar 23.


Fezl regulates the differentiation and axon targeting of layer 5 subcortical projection neurons in cerebral cortex.

Chen B, Schaevitz LR, McConnell SK.

Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):17184-9. Epub 2005 Nov 11.


Neurogenesis of the cholinergic medial septum in female and male C57BL/6J mice.

Schaevitz LR, Berger-Sweeney J.

J Neurobiol. 2005 Dec;65(3):294-303.

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