Literature DB >> 3514227

Peroxisomal disorders: a newly recognised group of genetic diseases.

R B Schutgens, H S Heymans, R J Wanders, H van den Bosch, J M Tager.   

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Year:  1986        PMID： 3514227     DOI： 10.1007/bf00441734

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  98 in total

1.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

2.  Refsum's disease, adrenoleucodystrophy, and the Zellweger syndrome.

Authors:  O Stokke; S Skrede; J Ek; I Björkhem
Journal:  Scand J Clin Lab Invest       Date:  1984-09       Impact factor: 1.713

3.  Oxidation of spermidine and spermine in rat liver: purification and properties of polyamine oxidase.

Authors:  E Hölttä
Journal:  Biochemistry       Date:  1977-01-11       Impact factor: 3.162

4.  Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome.

Authors:  H S Heymans; H vd Bosch; R B Schutgens; W H Tegelaers; J U Walther; J Müller-Höcker; P Borst
Journal:  Eur J Pediatr       Date:  1984-04       Impact factor: 3.183

5.  A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells.

Authors:  R J Wanders; G Schrakamp; H van den Bosch; J M Tager; R B Schutgens
Journal:  Eur J Pediatr       Date:  1986-04       Impact factor: 3.183

6.  Serum very long chain fatty acid pattern in Zellweger syndrome.

Authors:  J A Bakkeren; L A Monnens; J M Trijbels; J M Maas
Journal:  Clin Chim Acta       Date:  1984-04-27       Impact factor: 3.786

7.  Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and females.

Authors:  R Jaffe; P Crumrine; Y Hashida; H W Moser
Journal:  Am J Pathol       Date:  1982-07       Impact factor: 4.307

8.  Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy.

Authors:  I Singh; A E Moser; S Goldfischer; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

9.  Subcellular localization of acyl coenzyme A: dihydroxyacetone phosphate acyltransferase in rat liver peroxisomes (microbodies).

Authors:  A K Hajra; C L Burke; C L Jones
Journal:  J Biol Chem       Date:  1979-11-10       Impact factor: 5.157

10.  Peroxisomal defects in neonatal-onset and X-linked adrenoleukodystrophies.

Authors:  S Goldfischer; J Collins; I Rapin; B Coltoff-Schiller; C H Chang; M Nigro; V H Black; N B Javitt; H W Moser; P B Lazarow
Journal:  Science       Date:  1985-01-04       Impact factor: 47.728
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  82 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

Review 2.  Import of proteins into peroxisomes and other microbodies.

Authors:  M J de Hoop; G Ab
Journal:  Biochem J       Date:  1992-09-15       Impact factor: 3.857

3.  Adrenoleucodystrophy.

Authors:  S H Green
Journal:  Arch Dis Child       Date:  1991-07       Impact factor: 3.791

4.  Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease.

Authors:  A W Schram; A Strijland; T Hashimoto; R J Wanders; R B Schutgens; H van den Bosch; J M Tager
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

5.  An efficient positive selection procedure for the isolation of peroxisomal import and peroxisome assembly mutants of Saccharomyces cerevisiae.

Authors:  Y Elgersma; M van den Berg; H F Tabak; B Distel
Journal:  Genetics       Date:  1993-11       Impact factor: 4.562

Review 6.  The inborn errors of peroxisomal beta-oxidation: a review.

Authors:  R J Wanders; C W van Roermund; R B Schutgens; P G Barth; H S Heymans; H van den Bosch; J M Tager
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

7.  A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy.

Authors:  T Mito; K Takada; S Akaboshi; S Takashima; K Takeshita; Y Origuchi
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

8.  Isolation of peroxisome-deficient mutants of Saccharomyces cerevisiae.

Authors:  R Erdmann; M Veenhuis; D Mertens; W H Kunau
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

9.  Establishment of a normal range of morphometric values for peroxisomes in paediatric liver.

Authors:  J L Hughes; A J Bourne; A Poulos
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1993

10.  Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome).

Authors:  P B Lazarow; Y Fujiki; G M Small; P Watkins; H Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205
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