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SEPALLATA (SEP) genes form an integral part of models that outline the molecular basis of floral organ determination and are hypothesized to act as co-factors with ABCD floral homeotic genes in specifying different floral whorls.
The three vertebrate neurexin genes form an orthologous group with the one invertebrate neurexin gene (Figure 1.2).
This indicates that network neighbors of known disease genes form an important class of candidates for identifying novel genes for the same disease.
Functional analyses of these associated genes, including a monoterpene cyclase gene and a SAM-dependent methyltransferase gene, demonstrated that these genes form an operon and are responsible for the transformation of GPP to 2-MIB.
The three cyclostome ENC genes form an independent group (48/0.65; fig. 1 B).
The 31 genes form an amphioxus-specific clade, suggesting that gene expansion has occurred in the amphioxus lineage.
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Genes form a biological blueprint that is largely reactive in nature, and the TCF7L2 gene was apparently quiescent during most of our evolution.
The resulting genes form a sequence.
Indeed the autotrophic arsenite oxidase genes form a distinct phylogenetic group, separated from previously described heterotrophic arsenite oxidase genes, with the exception of the heterotroph Agrobacterium tumefaciens.
The Caenorhabditis elegans GluClα1 and GluClβ genes form a functional glutamate and ivermectin-gated chloride channel when expressed in Xenopus oocytes, but expression is weak in mammalian cells.
The elephant γ genes form a distinct cluster.
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