Literature DB >> 9354782

PEX12 encodes an integral membrane protein of peroxisomes.

K Okumoto, Y Fujiki.   

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Year:  1997        PMID: 9354782     DOI: 10.1038/ng1197-265

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


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  16 in total

Review 1.  Peroxisomal disorders: clinical, biochemical, and molecular aspects.

Authors:  R J Wanders
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

Review 2.  The surprising complexity of peroxisome biogenesis.

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

3.  A novel mutation in the PEX12 gene causing a peroxisomal biogenesis disorder.

Authors:  Jana Konkoľová; Robert Petrovič; Ján Chandoga; Edita Halasová; Petra Jungová; Daniel Böhmer
Journal:  Mol Biol Rep       Date:  2015-06-21       Impact factor: 2.316

4.  Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.

Authors:  Y Matsuzono; N Kinoshita; S Tamura; N Shimozawa; M Hamasaki; K Ghaedi; R J Wanders; Y Suzuki; N Kondo; Y Fujiki
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

5.  Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants.

Authors:  H Otera; K Okumoto; K Tateishi; Y Ikoma; E Matsuda; M Nishimura; T Tsukamoto; T Osumi; K Ohashi; O Higuchi; Y Fujiki
Journal:  Mol Cell Biol       Date:  1998-01       Impact factor: 4.272

6.  Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders.

Authors:  C C Chang; S J Gould
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

7.  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

8.  Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.

Authors:  D S Warren; J C Morrell; H W Moser; D Valle; S J Gould
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

9.  Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.

Authors:  Wing Yan Yik; Steven J Steinberg; Ann B Moser; Hugo W Moser; Joseph G Hacia
Journal:  Hum Mutat       Date:  2009-03       Impact factor: 4.878

10.  Topogenesis and homeostasis of fatty acyl-CoA reductase 1.

Authors:  Masanori Honsho; Shunsuke Asaoku; Keiko Fukumoto; Yukio Fujiki
Journal:  J Biol Chem       Date:  2013-10-09       Impact factor: 5.157

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