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doi: 10.1038/ng0592-85
pmid: 1302014
Heterotrimeric guanine nucleotide binding proteins (G proteins) transduce extracellular signals received by transmembrane receptors to effector proteins. The multigene family of G protein alpha subunits, which interact with receptors and effectors, exhibit a high level of sequence diversity. In mammals, 15 G alpha subunit genes can be grouped by sequence and functional similarities into four classes. We have determined the murine chromosomal locations of all 15 G alpha subunit genes using an interspecific backcross derived from crosses of C57BL/6J and Mus spretus mice. These data, in combination with mapping studies in humans, have provided insight into the events responsible for generating the genetic diversity found in the mammalian alpha subunit genes and a framework for elucidating the role of the G alpha subunits in disease.
Male, 570, Base Sequence, Genetic Linkage, Molecular Sequence Data, 610, Chromosome Mapping, DNA, Biological Evolution, Invertebrates, Mice, GTP-Binding Proteins, Multigene Family, Animals, Humans, Female, DNA Probes, Crosses, Genetic
Male, 570, Base Sequence, Genetic Linkage, Molecular Sequence Data, 610, Chromosome Mapping, DNA, Biological Evolution, Invertebrates, Mice, GTP-Binding Proteins, Multigene Family, Animals, Humans, Female, DNA Probes, Crosses, Genetic
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 284 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 1% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
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