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Items: 1 to 20 of 94

1.

Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in mice.

Hunsaker MR, von Leden RE, Ta BT, Goodrich-Hunsaker NJ, Arque G, Kim K, Willemsen R, Berman RF.

Behav Brain Res. 2011 Sep 12;222(1):117-21. doi: 10.1016/j.bbr.2011.03.039. Epub 2011 Mar 31.

2.

Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching task.

Diep AA, Hunsaker MR, Kwock R, Kim K, Willemsen R, Berman RF.

Neurobiol Learn Mem. 2012 Feb;97(2):229-34. doi: 10.1016/j.nlm.2011.12.006. Epub 2011 Dec 21.

3.

Temporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.

Hunsaker MR, Goodrich-Hunsaker NJ, Willemsen R, Berman RF.

Behav Brain Res. 2010 Dec 1;213(2):263-8. doi: 10.1016/j.bbr.2010.05.010. Epub 2010 May 15.

4.

Spatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation.

Borthwell RM, Hunsaker MR, Willemsen R, Berman RF.

Behav Brain Res. 2012 Jul 15;233(1):29-34. doi: 10.1016/j.bbr.2012.04.029. Epub 2012 Apr 26.

5.

FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.

Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, Hagerman PJ.

Neurology. 2008 Apr 15;70(16 Pt 2):1397-402. Epub 2007 Dec 5.

6.

CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation.

Hunsaker MR, Kim K, Willemsen R, Berman RF.

Hippocampus. 2012 Dec;22(12):2260-75. doi: 10.1002/hipo.22043. Epub 2012 Jun 18.

7.

Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses.

Careaga M, Rose D, Tassone F, Berman RF, Hagerman R, Ashwood P.

PLoS One. 2014 Apr 9;9(4):e94475. doi: 10.1371/journal.pone.0094475. eCollection 2014.

8.

Progressive spatial processing deficits in a mouse model of the fragile X premutation.

Hunsaker MR, Wenzel HJ, Willemsen R, Berman RF.

Behav Neurosci. 2009 Dec;123(6):1315-24. doi: 10.1037/a0017616.

9.

Cognitive decline, neuromotor and behavioural disturbances in a mouse model for fragile-X-associated tremor/ataxia syndrome (FXTAS).

Van Dam D, Errijgers V, Kooy RF, Willemsen R, Mientjes E, Oostra BA, De Deyn PP.

Behav Brain Res. 2005 Jul 30;162(2):233-9.

PMID:
15876460
10.

Cerebral protein synthesis in a knockin mouse model of the fragile X premutation.

Qin M, Huang T, Liu Z, Kader M, Burlin T, Xia Z, Zeidler Z, Hukema RK, Smith CB.

ASN Neuro. 2014 Sep 23;6(5). pii: 1759091414551957. doi: 10.1177/1759091414551957. Print 2014.

11.

The role of AGG interruptions in the transcription of FMR1 premutation alleles.

Yrigollen CM, Tassone F, Durbin-Johnson B, Tassone F.

PLoS One. 2011;6(7):e21728. doi: 10.1371/journal.pone.0021728. Epub 2011 Jul 19.

12.

Early mitochondrial abnormalities in hippocampal neurons cultured from Fmr1 pre-mutation mouse model.

Kaplan ES, Cao Z, Hulsizer S, Tassone F, Berman RF, Hagerman PJ, Pessah IN.

J Neurochem. 2012 Nov;123(4):613-21. doi: 10.1111/j.1471-4159.2012.07936.x. Epub 2012 Sep 28.

13.

Impaired sensorimotor gating in Fmr1 knock out and Fragile X premutation model mice.

Renoux AJ, Sala-Hamrick KJ, Carducci NM, Frazer M, Halsey KE, Sutton MA, Dolan DF, Murphy GG, Todd PK.

Behav Brain Res. 2014 Jul 1;267:42-5. doi: 10.1016/j.bbr.2014.03.013. Epub 2014 Mar 19.

14.

Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development.

Cunningham CL, Martínez Cerdeño V, Navarro Porras E, Prakash AN, Angelastro JM, Willemsen R, Hagerman PJ, Pessah IN, Berman RF, Noctor SC.

Hum Mol Genet. 2011 Jan 1;20(1):64-79. doi: 10.1093/hmg/ddq432. Epub 2010 Oct 8.

15.

A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis.

Qin M, Entezam A, Usdin K, Huang T, Liu ZH, Hoffman GE, Smith CB.

Neurobiol Dis. 2011 Apr;42(1):85-98. doi: 10.1016/j.nbd.2011.01.008. Epub 2011 Jan 8.

16.

Ubiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation.

Wenzel HJ, Hunsaker MR, Greco CM, Willemsen R, Berman RF.

Brain Res. 2010 Mar 8;1318:155-66. doi: 10.1016/j.brainres.2009.12.077. Epub 2010 Jan 4.

17.

Fragile X-associated tremor/ataxia syndrome: influence of the FMR1 gene on motor fiber tracts in males with normal and premutation alleles.

Wang JY, Hessl D, Schneider A, Tassone F, Hagerman RJ, Rivera SM.

JAMA Neurol. 2013 Aug;70(8):1022-9. doi: 10.1001/jamaneurol.2013.2934.

18.

Mouse models of fragile X-associated tremor ataxia.

Berman RF, Willemsen R.

J Investig Med. 2009 Dec;57(8):837-41. doi: 10.231/JIM.0b013e3181af59d6. Review.

19.

CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome.

Brouwer JR, Huizer K, Severijnen LA, Hukema RK, Berman RF, Oostra BA, Willemsen R.

J Neurochem. 2008 Dec;107(6):1671-82. doi: 10.1111/j.1471-4159.2008.05747.x. Epub 2008 Nov 10.

20.

Size bias of fragile X premutation alleles in late-onset movement disorders.

Jacquemont S, Leehey MA, Hagerman RJ, Beckett LA, Hagerman PJ.

J Med Genet. 2006 Oct;43(10):804-9. Epub 2006 May 24.

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