Literature DB >> 12882231

Ataxia Jackson (ax(J)): a genetic model for apoptotic neuronal cell death.

Makoto Ohgoh1, Kazuto Yamazaki.   

Abstract

Programmed cell death or apoptosis is an important process to form normal adult cytoarchitecture. But in vivo analysis of neuronal apoptosis has not been well advanced. Therefore, apoptotic cell death of a particular neuronal system or anatomical part in a mutant is an invaluable target to learn about a link between a gene and neuronal apoptosis. Ataxia (ax) is an autosomal recessive neurological mutant mouse. We recently investigated brains of homozygotes for ataxia Jackson (ax(J)), an allele of ax, using TUNEL method. A few TUNEL-positive cells were observed in the granular cell layer of the cerebellum, the dentate gyrus, and the olfactory bulb of phenotypically normal littermates (ax(J)/+ or +/+) aged at 23-38 days. In affected ax(J)/ax(J) mice, however, the number of TUNEL-positive cells was significantly increased in the cerebellum, particularly in the granular cell layer (p < 0.05). The ax(J) mouse will be an in vivo unique model for studies on the genetic basis of apoptotic neuronal cell death, and identification of the ax gene is desired to elucidate molecular basis of the apoptosis.

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Year:  2003        PMID: 12882231     DOI: 10.1080/14734220309422

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  25 in total

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Journal:  Nature       Date:  1997-08-21       Impact factor: 49.962

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  1 in total

1.  The ataxia (axJ) mutation causes abnormal GABAA receptor turnover in mice.

Authors:  Corinna Lappe-Siefke; Sven Loebrich; Wulf Hevers; Oliver B Waidmann; Michaela Schweizer; Susanne Fehr; Jean-Marc Fritschy; Ivan Dikic; Jens Eilers; Scott M Wilson; Matthias Kneussel
Journal:  PLoS Genet       Date:  2009-09-04       Impact factor: 5.917

  1 in total

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