Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders

Author:

Tatsumi K,Saito M,Lin B,Iwamori M,Ichiseki H,Shimozawa N,Kamoshita S,Igarashi T,Sakakihara Y

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference27 articles.

1. P.B. Lazarow, H.W. Moser, Disorders of peroxisomal biogenesis, in: C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle (Eds.), The Metabolic and Molecular Basis of Inherited Diseases, McGraw-Hill, New York, 1995, pp. 2287–2324.

2. Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration;Volpe;Acta Neuropathol.,1972

3. The mechanism of arrest of neuronal migration in the Zellweger malformation: a hypothesis based upon cytoarchitectonic analysis;Evrard;Acta Neuropathol.,1978

4. Structural and chemical alterations in the cerebral maldevelopment of fetal cerebro-hepato-renal (Zellweger) syndrome;Powers;J. Neuropathol. Exp. Neurol.,1989

5. Cerebro-hepato-renal sydrome. Report of a case with histochemical and ultrastructural observations;Agammanolis;J. Neuropathol. Exp. Neurol.,1976

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