Retinal degeneration in choroideremia: deficiency of rab geranylgeranyl transferase.
暂无分享,去创建一个
[1] T. Südhof,et al. Purification of component A of Rab geranylgeranyl transferase: Possible identity with the choroideremia gene product , 1992, Cell.
[2] T. Südhof,et al. Rab geranylgeranyl transferase. A multisubunit enzyme that prenylates GTP-binding proteins terminating in Cys-X-Cys or Cys-Cys. , 1992, The Journal of biological chemistry.
[3] P. Humphries,et al. On the molecular genetics of retinitis pigmentosa. , 1992, Science.
[4] F. Cremers,et al. An autosomal homologue of the choroideremia gene colocalizes with the Usher syndrome type II locus on the distal part of chromosome 1q. , 1992, Human molecular genetics.
[5] J. Gibbs,et al. Steady-state kinetic mechanism of Ras farnesyl:protein transferase. , 1992, Biochemistry.
[6] R. Nussbaum,et al. Isolation of a candidate gene for choroideremia. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[7] B. Kinsella,et al. rab GTP-binding proteins with three different carboxyl-terminal cysteine motifs are modified in vivo by 20-carbon isoprenoids. , 1992, The Journal of biological chemistry.
[8] S. Pfeffer. GTP-binding proteins in intracellular transport. , 1992, Trends in cell biology.
[9] P. Humphries,et al. A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa , 1991, Nature.
[10] T. Dryja,et al. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa , 1991, Nature.
[11] M. Gelb,et al. C terminus of the small GTP-binding protein smg p25A contains two geranylgeranylated cysteine residues and a methyl ester. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[12] C. Der,et al. Isoprenoid modification of rab proteins terminating in CC or CXC motifs. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[13] P. Bahn. Cannibalism in the Neolithic , 1991, Nature.
[14] Frank McCormick,et al. The GTPase superfamily: conserved structure and molecular mechanism , 1991, Nature.
[15] T. Südhof,et al. A small GTP-binding protein dissociates from synaptic vesicles during exocytosis , 1991, Nature.
[16] W. Balch. Small GTP-binding proteins in vesicular transport. , 1990, Trends in biochemical sciences.
[17] F. Cremers,et al. Cloning of a gene that is rearranged in patients with choroideraemia , 1990, Nature.
[18] Y. Hata,et al. Molecular cloning and characterization of a novel type of regulatory protein (GDI) for smg p25A, a ras p21-like GTP-binding protein , 1990, Molecular and cellular biology.
[19] P. Casey,et al. Inhibition of purified p21 ras farnesyl:protein transferase by Cys-AAX tetrapeptides , 1990, Cell.
[20] M. Leppert,et al. Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q. , 1990, Genomics.
[21] C. Möller,et al. Localization of Usher syndrome type II to chromosome 1q. , 1990, Genomics.
[22] Oliver H. Lowry,et al. Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.