Literature DB >> 9090374

PEX genes on the rise.

S Subramani.   

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Year:  1997        PMID： 9090374     DOI： 10.1038/ng0497-331

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  28 in total

Review 1.  Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview.

Authors:  P E Purdue; M Skoneczny; X Yang; J W Zhang; P B Lazarow
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

2.  Mutants of the Yarrowia lipolytica PEX23 gene encoding an integral peroxisomal membrane peroxin mislocalize matrix proteins and accumulate vesicles containing peroxisomal matrix and membrane proteins.

Authors:  T W Brown; V I Titorenko; R A Rachubinski
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

3.  Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Authors:  S Tamura; N Matsumoto; A Imamura; N Shimozawa; Y Suzuki; N Kondo; Y Fujiki
Journal:  Biochem J       Date:  2001-07-15       Impact factor: 3.857

Review 4.  The surprising complexity of peroxisome biogenesis.

Authors:  L J Olsen
Journal:  Plant Mol Biol       Date:  1998-09       Impact factor: 4.076

5.  Chondrodysplasia punctata and maternal systemic lupus erythematosus.

Authors:  H V Toriello
Journal:  J Med Genet       Date:  1998-08       Impact factor: 6.318

6.  Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1.

Authors:  T Harano; S Nose; R Uezu; N Shimizu; Y Fujiki
Journal:  Biochem J       Date:  2001-07-01       Impact factor: 3.857

7.  Pex17p is required for import of both peroxisome membrane and lumenal proteins and interacts with Pex19p and the peroxisome targeting signal-receptor docking complex in Pichia pastoris.

Authors:  W B Snyder; A Koller; A J Choy; M A Johnson; J M Cregg; L Rangell; G A Keller; S Subramani
Journal:  Mol Biol Cell       Date:  1999-12       Impact factor: 4.138

8.  Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris.

Authors:  W B Snyder; K N Faber; T J Wenzel; A Koller; G H Lüers; L Rangell; G A Keller; S Subramani
Journal:  Mol Biol Cell       Date:  1999-06       Impact factor: 4.138

9.  Yarrowia lipolytica cells mutant for the peroxisomal peroxin Pex19p contain structures resembling wild-type peroxisomes.

Authors:  G R Lambkin; R A Rachubinski
Journal:  Mol Biol Cell       Date:  2001-11       Impact factor: 4.138

10.  Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

Authors:  M Honsho; S Tamura; N Shimozawa; Y Suzuki; N Kondo; Y Fujiki
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025
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