An efficient screen for peroxisome-deficient mutants of Pichia pastoris
暂无分享,去创建一个
J. Cregg | X. Tan | M. Veenhuis | D. McCollum | H. Liu | Henry Liu
[1] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[2] G. Adam,et al. Control of peroxisome proliferation in Saccharomyces cerevisiae by ADR1, SNF1 (CAT1, CCR1) and SNF4 (CAT3) , 1992, Yeast.
[3] S. Subramani,et al. Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal , 1992, Molecular and cellular biology.
[4] T Hashimoto,et al. Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting. , 1991, Biochemical and biophysical research communications.
[5] G. N. Wilson. Structure-function relationships in the peroxisome: implications for human disease. , 1991, Biochemical medicine and metabolic biology.
[6] S. Subramani,et al. A novel, cleavable peroxisomal targeting signal at the amino‐terminus of the rat 3‐ketoacyl‐CoA thiolase. , 1991, The EMBO journal.
[7] C. Wang,et al. Evolutionary conservation of a microbody targeting signal that targets proteins to peroxisomes, glyoxysomes, and glycosomes , 1991, The Journal of cell biology.
[8] J. Schanstra,et al. Ethanol metabolism in a peroxisome-deficient mutant of the yeast Hansenula polymorpha , 1991 .
[9] M. Yaffe,et al. Temperature-sensitive yeast mutants defective in mitochondrial inheritance , 1990, The Journal of cell biology.
[10] J. Cregg,et al. Peroxisome‐deficient mutants of Hansenula polymorpha , 1990 .
[11] T. Tsukamoto,et al. Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes , 1990, The Journal of cell biology.
[12] M. Veenhuis,et al. Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[13] H. Moser,et al. Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines from 19 Patients , 1989, Pediatric Research.
[14] P. Borst. Peroxisome biogenesis revisited. , 1989, Biochimica et biophysica acta.
[15] H. Shio,et al. Peroxisomal integral membrane proteins in control and Zellweger fibroblasts. , 1988, The Journal of biological chemistry.
[16] R. Wanders,et al. Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis. , 1988, The Journal of clinical investigation.
[17] H. Shio,et al. Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly. , 1988, Science.
[18] S. Gould,et al. Identification of a peroxisomal targeting signal at the carboxy terminus of firefly luciferase , 1987, The Journal of cell biology.
[19] P. Lazarow,et al. Translocation of acyl-CoA oxidase into peroxisomes requires ATP hydrolysis but not a membrane potential , 1987, The Journal of cell biology.
[20] M. Veenhuis,et al. Proliferation of microbodies in Saccharomyces cerevisiae , 1987, Yeast.
[21] H. Moser,et al. Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome). , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[22] R. Wanders,et al. Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[23] C. Raetz,et al. Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[24] T. Hashimoto,et al. Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome. , 1986, Clinica chimica acta; international journal of clinical chemistry.
[25] J. Cregg,et al. Pichia pastoris as a host system for transformations , 1985, Molecular and cellular biology.
[26] T. Gingeras,et al. Isolation of alcohol oxidase and two other methanol regulatable genes from the yeast Pichia pastoris , 1985, Molecular and cellular biology.
[27] R. Rachubinski,et al. Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[28] C. W. Scott,et al. Alcohol oxidase assembles post-translationally into the peroxisome of Candida boidinii. , 1984, The Journal of biological chemistry.
[29] N. Shimamoto,et al. Absence of DNA in peroxisomes of Candida tropicalis , 1982, Journal of bacteriology.
[30] W. Kunau,et al. Degradation of unsaturated fatty acids in peroxisomes. Existence of a 2,4-dienoyl-CoA reductase pathway. , 1981, The Journal of biological chemistry.
[31] M. M. Bradford. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.
[32] R. Winkelmann. The Metabolic Basis of Inherited Diseases , 1972 .
[33] U. K. Laemmli,et al. Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.
[34] I. J. van der Klei,et al. Alcohol oxidase from Hansenula polymorpha CBS 4732. , 1990, Methods in enzymology.
[35] M. Ueda,et al. Catalase from Candida boidinii 2201. , 1990, Methods in enzymology.
[36] J. Cregg. Genetics of Methylotrophic Yeasts , 1987 .
[37] M. Veenhuis,et al. Metabolic Significance and Biogenesis of Microbodies in Yeasts , 1987 .
[38] Gleeson Mag. The genetic analysis of the methylotrophic yeast Hansenula polymorpha. , 1986 .
[39] Y. Fujiki,et al. Biogenesis of peroxisomes. , 1985, Annual review of cell biology.
[40] N. Tolbert. Isolation of subcellular organelles of metabolism on isopycnic sucrose gradients. , 1974, Methods in enzymology.