1996
DOI: 10.1006/abbi.1996.0389
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cDNA Cloning of a Chick Homologue of Human ATPase Complex Subunit 4, Quantitative Tissue Distribution and Tertiary Structure Comparison of the ATPase Domain to RecA

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Cited by 4 publications
(2 citation statements)
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“…Several of the cDNAs identified in the screen but not confirmed by QPCR to be differentially expressed, also belong to intriguing gene families with proven functions in the developing nervous system. These include another protein involved in selective protein degradation, ATPase complex subunit 4 (S4) one of several different subunits of the multimeric regulatory complex that combines with the 20S proteolytic core to form the 26S proteasome (Dubiel et al, 1992;Singh et al, 1996, Hutson et al, 1997. Regulation of cellular proliferation through ubiquitin-mediated proteolytic degradation of cell cycle components is a crucial function of the proteasome, and its levels are particularly high in immature and mitotically active cells (Ichihara and Tanaka, 1995).…”
Section: Discussionmentioning
confidence: 99%
“…Several of the cDNAs identified in the screen but not confirmed by QPCR to be differentially expressed, also belong to intriguing gene families with proven functions in the developing nervous system. These include another protein involved in selective protein degradation, ATPase complex subunit 4 (S4) one of several different subunits of the multimeric regulatory complex that combines with the 20S proteolytic core to form the 26S proteasome (Dubiel et al, 1992;Singh et al, 1996, Hutson et al, 1997. Regulation of cellular proliferation through ubiquitin-mediated proteolytic degradation of cell cycle components is a crucial function of the proteasome, and its levels are particularly high in immature and mitotically active cells (Ichihara and Tanaka, 1995).…”
Section: Discussionmentioning
confidence: 99%
“…The insert DNA was sequenced to confirm the deletion. The shortened insert then was transcribed in vitro to generate the internal standard RNA for the S7 fragment as described previously (Singh, Cai and Wagner, 1996). RNA was purified by phenol\chloroform extraction and precipitation.…”
Section: Molecular Cloning and Generating Internal Standard Rnas Of Smentioning
confidence: 99%