Literature DB >> 9199576

Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome.

B C Paton, S E Heron, P V Nelson, C P Morris, A Poulos.   

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Year:  1997        PMID： 9199576      PMCID： PMC1716138          DOI： 10.1016/S0002-9297(07)64247-5

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  21 in total

Review 1.  ABC transporters: from microorganisms to man.

Authors:  C F Higgins
Journal:  Annu Rev Cell Biol       Date:  1992

2.  Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.

Authors:  S Yajima; Y Suzuki; N Shimozawa; S Yamaguchi; T Orii; Y Fujiki; T Osumi; T Hashimoto; H W Moser
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

3.  Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE.

Authors:  B Budowle; R Chakraborty; A M Giusti; A J Eisenberg; R C Allen
Journal:  Am J Hum Genet       Date:  1991-01       Impact factor: 11.025

4.  A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1).

Authors:  J Gärtner; C Obie; H Moser; D Valle
Journal:  Hum Mol Genet       Date:  1992-11       Impact factor: 6.150

5.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Authors:  M Orita; H Iwahana; H Kanazawa; K Hayashi; T Sekiya
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

6.  Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.

Authors:  N Shimozawa; Y Suzuki; S Tomatsu; T Tsukamoto; T Osumi; Y Fujiki; K Kamijo; T Hashimoto; N Kondo; T Orii
Journal:  Pediatr Res       Date:  1996-05       Impact factor: 3.756

7.  Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.

Authors:  N Shimozawa; Y Suzuki; T Orii; A Moser; H W Moser; R J Wanders
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

8.  Nucleotide sequence of the human 70 kDa peroxisomal membrane protein: a member of ATP-binding cassette transporters.

Authors:  K Kamijo; T Kamijo; I Ueno; T Osumi; T Hashimoto
Journal:  Biochim Biophys Acta       Date:  1992-02-11

9.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

10.  The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily.

Authors:  K Kamijo; S Taketani; S Yokota; T Osumi; T Hashimoto
Journal:  J Biol Chem       Date:  1990-03-15       Impact factor: 5.157
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  2 in total

1.  Identification of ectodysplasin-A receptor gene deletion at 2q12.2 and a potential autosomal MR locus.

Authors:  Bradley L Griggs; Sydney Ladd; Amy Decker; Barbara R DuPont; Alexander Asamoah; Anand K Srivastava
Journal:  Eur J Hum Genet       Date:  2008-10-15       Impact factor: 4.246

Review 2.  Peroxisomal ABC Transporters: An Update.

Authors:  Ali Tawbeh; Catherine Gondcaille; Doriane Trompier; Stéphane Savary
Journal:  Int J Mol Sci       Date:  2021-06-05       Impact factor: 5.923
  2 in total

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