Localization of Menkes gene expression in the mouse brain; its association with neurological manifestations in Menkes model mice

[1]  P. Lockhart,et al.  Expression of the Menkes gene homologue in mouse tissues lack of effect of copper on the mRNA levels , 1994, FEBS letters.

[2]  Y. Boyd,et al.  RFLVs in mottled dappled alleles , 1994, Nature Genetics.

[3]  D. Pellegrini-Giampietro,et al.  Kainate-induced status epilepticus alters glutamate and GABAA receptor gene expression in adult rat hippocampus: an in situ hybridization study , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  S. Packman,et al.  The mottled gene is the mouse homologue of the Menkes disease gene , 1994, Nature Genetics.

[5]  P. Lockhart,et al.  Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice , 1994, Nature Genetics.

[6]  N. Yoshimura.  Histochemical localization of copper in various organs of brindled mice , 1994, Pathology international.

[7]  I. Takahashi,et al.  Histochemical localization of copper in the intestine and kidney of macular mice: light and electron microscopic study. , 1993, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[8]  M. Evenson,et al.  Deficiency of copper can cause neuronal degeneration. , 1992, Medical hypotheses.

[9]  D. Tolbert,et al.  Preliminary characterization of hereditary cerebellar ataxia in rats. , 1992, Laboratory animal science.

[10]  A. Kuroiwa,et al.  Chicken homeobox gene Msx-1: structure, expression in limb buds and effect of retinoic acid. , 1991, Development.

[11]  M. Shimada,et al.  Copper Contents and Pathological Changes in Various Organs of Macular Mouse , 1988 .

[12]  M. Shimada,et al.  Light and electron microscopic study on cerebellar cortex of macular mutant mouse as a model of Menkes kinky hair disease , 1987, Brain and Development.

[13]  M T Davisson,et al.  X-linked genetic homologies between mouse and man. , 1987, Genomics.

[14]  D. Danks,et al.  Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old mice. , 1986, The Biochemical journal.

[15]  K. Suzuki,et al.  Neuronal degeneration in the brain of the brindled mouse. II. Ultrastructure of neuronal inclusions in the cerebral cortex. , 1979, Acta neuropathologica.

[16]  D. Danks,et al.  Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development. , 1979, The Biochemical journal.

[17]  D. Danks,et al.  Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice. , 1979, The Biochemical journal.

[18]  K. Yajima,et al.  NEURONAL DEGENERATION IN THE BRAIN OF THE BRINDLED MOUSE—A LIGHT MICROSCOPE STUDY , 1979, Journal of neuropathology and experimental neurology.

[19]  M. Alter,et al.  A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. , 1962, Pediatrics.

[20]  Thomas W. Glover,et al.  Isolation of a partial candidate gene for Menkes disease by positional cloning , 1993, Nature Genetics.

[21]  S. Packman,et al.  Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPase , 1993, Nature Genetics.

[22]  Anthony P. Monaco,et al.  Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein , 1993, Nature Genetics.

[23]  J. Swann,et al.  The ontogeny of hippocampal local circuits and focal epileptogenesis. , 1992, Epilepsy research. Supplement.

[24]  Charles R.scriver.  The Metabolic basis of inherited disease , 1989 .