D Jaarsma

Summary

Affiliation: Erasmus University
Country: The Netherlands

Publications

  1. ncbi Light-microscopic distribution and parasagittal organisation of muscarinic receptors in rabbit cerebellar cortex
    D Jaarsma
    Department of Anatomy, Erasmus University Medical School, Rotterdam, Netherlands
    J Chem Neuroanat 9:241-59. 1995
  2. ncbi Induction of c-Jun immunoreactivity in spinal cord and brainstem neurons in a transgenic mouse model for amyotrophic lateral sclerosis
    D Jaarsma
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neurosci Lett 219:179-82. 1996
  3. ncbi Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SO
    D Jaarsma
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neurobiol Dis 7:623-43. 2000
  4. ncbi CuZn superoxide dismutase (SOD1) accumulates in vacuolated mitochondria in transgenic mice expressing amyotrophic lateral sclerosis-linked SOD1 mutations
    D Jaarsma
    Department of Anatomy, Erasmus University Rotterdam, The Netherlands
    Acta Neuropathol 102:293-305. 2001
  5. ncbi Expression of the low affinity neurotrophin receptor p75 in spinal motoneurons in a transgenic mouse model for amyotrophic lateral sclerosis
    J C V M Copray
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neuroscience 116:685-94. 2003

Detail Information

Publications5

  1. ncbi Light-microscopic distribution and parasagittal organisation of muscarinic receptors in rabbit cerebellar cortex
    D Jaarsma
    Department of Anatomy, Erasmus University Medical School, Rotterdam, Netherlands
    J Chem Neuroanat 9:241-59. 1995
    ..Their functional significance is puzzling, since their distribution does not correspond to that of markers of cholinergic innervation...
  2. ncbi Induction of c-Jun immunoreactivity in spinal cord and brainstem neurons in a transgenic mouse model for amyotrophic lateral sclerosis
    D Jaarsma
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neurosci Lett 219:179-82. 1996
    ..This c-Jun may be involved in the neurodegenerative processes both in ALS and in motoneuron disease in SOD1(G93A) mice...
  3. ncbi Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SO
    D Jaarsma
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neurobiol Dis 7:623-43. 2000
    ....
  4. ncbi CuZn superoxide dismutase (SOD1) accumulates in vacuolated mitochondria in transgenic mice expressing amyotrophic lateral sclerosis-linked SOD1 mutations
    D Jaarsma
    Department of Anatomy, Erasmus University Rotterdam, The Netherlands
    Acta Neuropathol 102:293-305. 2001
    ..In sum, our data suggest that both fALS-mutant and wild-type SOD1 may cross the mitochondrial outer membrane, and by doing so induce the degeneration of these mitochondria...
  5. ncbi Expression of the low affinity neurotrophin receptor p75 in spinal motoneurons in a transgenic mouse model for amyotrophic lateral sclerosis
    J C V M Copray
    Department of Anatomy, Erasmus University, Rotterdam, The Netherlands
    Neuroscience 116:685-94. 2003
    ....