Polymorphism in the multi-phosphorylation domain of the human neurofilament heavy-subunit-encoding gene

This publication has 14 references indexed in Scilit:

• Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosis
  Cell, 1993
• Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
  Published by Elsevier ,1992
• Local modulation of neurofilament phosphorylation, axonal caliber, and slow axonal transport by myelinating Schwann cells
  Published by Elsevier ,1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
  Nature, 1991
• The effects of dephosphorylation on the structure of the projections of neurofilament
  Journal of Neuroscience, 1989
• Sequence and structure of the mouse gene coding for the largest neurofilament subunit
  Gene, 1988
• MAP2 is a component of crossbridges between microtubules and neurofilaments in the neuronal cytoskeleton: quick-freeze, deep-etch immunoelectron microscopy and reconstitution studies
  Journal of Neuroscience, 1988
• Organization of mammalian neurofilament polypeptides within the neuronal cytoskeleton.
  The Journal of cell biology, 1984
• Characteristics of the protein kinase activity associated with rat neurofilament preparations
  Biochimica et Biophysica Acta (BBA) - General Subjects, 1983