SEARCH

SEARCH BY CITATION

References

  • Burright E. N., Clark H. B., Servadio A., Matilla T., Feddersen R. M., Yunis W. S., Duvick L. A., Zoghbi H. Y. and Orr H. T. (1995) SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat. Cell 82, 937948.
  • Clark H. B., Burright E. N., Yunis W. S., Larson S., Wilcox C., Hartman B., Matilla A., Zoghbi H. Y. and Orr H. T. (1997) Purkinje cell expression of a mutant allele of SCA1 in transgenic mice leads to disparate effects on motor behaviors, followed by a progressive cerebellar dysfunction and histological alterations. J. Neurosci. 17, 73857395.
  • Cudalbu C., McLin V. A., Lei H., Duarte J. M. N., Rougemont A.-L., Oldani G., Terraz S., Toso C. and Gruetter R. (2013) The C57BL/6J mouse exhibits sporadic congenital portosystemic shunts. PLoS ONE 8, e69782.
  • Eder K., Kish S. J., Kirchgessner M. and Ross B. M. (1998) Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1. Mov. Disord. 13, 813819.
  • Garwood M. and DelaBarre L. (2001) The return of the frequency sweep: designing adiabatic pulses for contemporary NMR. J. Magn. Reson. 153, 155177.
  • Gruetter R. and Tkáč I. (2000) Field mapping without reference scan using asymmetric echo-planar techniques. Magn. Reson. Med. 43, 319323.
  • Hennig J., Nauerth A. and Friedburg H. (1986) RARE imaging: a fast imaging method for clinical MR. Magn. Reson. Med. 3, 823833.
  • Klockgether T. (2011) Update on degenerative ataxias. Curr. Opin. Neurol. 24, 339345.
  • Klockgether T. and Paulson H. (2011) Milestones in ataxia. Mov. Disord. 26, 11341141.
  • Michaeli S., Garwood M., Zhu X. H., DelaBarre L., Andersen P., Adriany G., Merkle H., Ugurbil K. and Chen W. (2002) Proton T2 relaxation study of water, N-acetylaspartate, and creatine in human brain using Hahn and Carr-Purcell spin echoes at 4T and 7T. Magn. Reson. Med. 47, 629633.
  • Miller T. J., Hanson R. D. and Yancey P. H. (2000) Developmental changes in organic osmolytes in prenatal and postnatal rat tissues. Comp. Biochem. Physiol., Part A Mol. Integr. Physiol. 125, 4556.
  • Mountford C. E., Stanwell P., Lin A., Ramadan S. and Ross B. (2010) Neurospectroscopy: the past, present and future. Chem. Rev. 110, 30603086.
  • Ottersen O. P., Madsen S., Storm-Mathisen J., Somogyi P., Scopsi L. and Larsson L. I. (1988) Immunocytochemical evidence suggests that taurine is colocalized with GABA in the Purkinje cell terminals, but that the stellate cell terminals predominantly contain GABA: a light- and electronmicroscopic study of the rat cerebellum. Exp. Brain Res. 72, 407416.
  • Öz G. (2013) MR Spectroscopy in Health and Disease, in Handbook of the Cerebellum and Cerebellar Disorders (Manto M., Gruol D. L., Schmahmann J. D., Koibuchi N.and Rossi F. and Rossi F. eds), Vol. 1, pp. 713733. Springer Dordrecht, Netherlands.
  • Öz G., Hutter D., Tkáč I., Clark H. B., Gross M. D., Jiang H., Eberly L. E., Bushara K. O. and Gomez C. M. (2010a) Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status. Mov. Disord. 25, 12531261.
  • Öz G., Nelson C. D., Koski D. M. et al. (2010b) Noninvasive detection of presymptomatic and progressive neurodegeneration in a mouse model of spinocerebellar ataxia type 1. J. Neurosci. 30, 38313838.
  • Öz G., Vollmers M. L., Nelson C. D., Shanley R., Eberly L. E., Orr H. T. and Clark H. B. (2011) In vivo monitoring of recovery from neurodegeneration in conditional transgenic SCA1 mice. Exp. Neurol. 232, 290298.
  • Petroff O. A., Pleban L. A. and Spencer D. D. (1995) Symbiosis between in vivo and in vitro NMR spectroscopy: the creatine, N-acetylaspartate, glutamate, and GABA content of the epileptic human brain. Magn. Reson. Imaging 13, 11971211.
  • Provencher S. W. (1993) Estimation of metabolite concentrations from localized in vivo proton NMR spectra. Magn. Reson. Med. 30, 672679.
  • Provencher S. W. (2001) LCModel & LCMgui User's Manual.
  • Ross B. M., Eder K., Moszczynska A. et al. (2000) Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1. Mov. Disord. 15, 294300.
  • Schöls L., Bauer P., Schmidt T., Schulte T. and Riess O. (2004) Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 3, 291304.
  • Storm-Mathisen J., Danbolt N. C., Rothe F., Torp R., Zhang N., Aas J. E., Kanner B. I., Langmoen I. and Ottersen O. P. (1992) Ultrastructural immunocytochemical observations on the localization, metabolism and transport of glutamate in normal and ischemic brain tissue. Prog. Brain Res. 94, 225241.
  • Swanson R. A., Sagar S. M. and Sharp F. R. (1989) Regional brain glycogen stores and metabolism during complete global ischaemia. Neurol. Res. 11, 2428.
  • Tkáč I., Zacharoff L. and Dubinsky J. M. (2011) Longitudinal study of neurochemical changes in Q140 mouse model of Huntington's disease, in Nineteenth Scientific Meeting of the ISMRM pp. 2288. Montreal, Canada.
  • Watase K., Weeber E. J., Xu B. et al. (2002) A long CAG repeat in the mouse Sca1 locus replicates SCA1 features and reveals the impact of protein solubility on selective neurodegeneration. Neuron 34, 905919.
  • Wu J. Y. and Prentice H. (2010) Role of taurine in the central nervous system. J. Biomed. Sci. 17(Suppl 1), S1.
  • Wüllner U., Reimold M., Abele M., Burk K., Minnerop M., Dohmen B. M., Machulla H. J., Bares R. and Klockgether T. (2005) Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6. Arch. Neurol. 62, 12801285.
  • Xin L., Gambarota G., Mlynárik V. and Gruetter R. (2008) Proton T2 relaxation time of J-coupled cerebral metabolites in rat brain at 9.4 T. NMR Biomed. 21, 396401.
  • Zoghbi H. Y. and Orr H. T. (2000) Glutamine repeats and neurodegeneration. Annu. Rev. Neurosci. 23, 217247.
  • Zu T., Duvick L. A., Kaytor M. D., Berlinger M. S., Zoghbi H. Y., Clark H. B. and Orr H. T. (2004) Recovery from polyglutamine-induced neurodegeneration in conditional SCA1 transgenic mice. J. Neurosci. 24, 88538861.