权威例句
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctataMutations in the gene encoding 3 beta-hydroxysteroid-delta 8, delta 7-isomerase cause X-linked dominant Conradi-Hünermann syndromeExpression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuliChangeable Slit to Control Uniformity of IlluminationMutations in the gene encoding 3β-hydroxysteroid-Δ 8,Δ7-isomerase cause X-linked dominant Conradi-Hünermann syndromeThe mechanism for synergism between phospholipase C- and adenylylcyclase-linked hormones in liver. Cyclic AMP-dependent kinase augme...Kainic acid alters the metabolism of Met5-enkephalin and the level of dynorphin A in the rat hippocampus.Amygdaloid kindling increases enkephalin-like immunoreactivity but decreases dynorphin-A-like immunoreactivity in rat hippocampus.Hyperornithinaemia-hyperammonaemia-homocitrullinuriasyndrome is caused by mutations in a gene encoding a mitochondrial ornithinetran...