Members of the Eph family of tyrosine kinase receptors have been implicated in the regulation of developmental processes and, in particular, axon guidance in the developing nervous system. The function of the EphA4 (Sek1) receptor was explored through creation of a null mutant mouse. Mice with a null mutation in the EphA4 gene are viable and fertile but have a gross motor dysfunction, which is evidenced by a loss of coordination of limb movement and a resultant hopping, kangaroo-like gait. Consistent with the observed phenotype, anatomical studies and anterograde tracing experiments reveal major disruptions of the corticospinal tract within the medulla and spinal cord in the null mutant animals. These results demonstrate a critical role for EphA4 in establishing the corticospinal projection.
机构:Sapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan
Oki, Mariko
Yamamoto, Hiroyuki
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Sapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, JapanSapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan
Yamamoto, Hiroyuki
Taniguchi, Hiroaki
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机构:Sapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan
Taniguchi, Hiroaki
Adachi, Yasushi
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机构:Sapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan
Adachi, Yasushi
Imai, Kohzoh
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Sapporo Med Univ, Sapporo, Hokkaido 0608556, JapanSapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan
Imai, Kohzoh
Shinomura, Yasuhisa
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机构:Sapporo Med Univ, Dept Internal Med 1, Chuo Ku, Sch Med, Sapporo, Hokkaido 0608543, Japan