Literature DB >> 1405476

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder.

R J Wanders1, H Schumacher, J Heikoop, R B Schutgens, J M Tager.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1992        PMID： 1405476     DOI： 10.1007/bf02435984

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


× No keyword cloud information.
  5 in total

1.  Peroxisomal enzyme activities in the human hepatoblastoma cell line HepG2 as compared to human liver.

Authors:  R J Wanders; C W van Roermund; M Griffioen; L Cohen
Journal:  Biochim Biophys Acta       Date:  1991-11-14

2.  Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders.

Authors:  R J Wanders; C W van Roermund; M J van Wijland; J Heikoop; R B Schutgens; A W Schram; J M Tager; H van den Bosch; B T Poll-Thé; J M Saudubray
Journal:  Clin Chim Acta       Date:  1987-07-15       Impact factor: 3.786

Review 3.  Peroxisomal disorders in neurology.

Authors:  R J Wanders; H S Heymans; R B Schutgens; P G Barth; H van den Bosch; J M Tager
Journal:  J Neurol Sci       Date:  1988-12       Impact factor: 3.181

4.  Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

Authors:  H S Heymans; J W Oorthuys; G Nelck; R J Wanders; R B Schutgens
Journal:  N Engl J Med       Date:  1985-07-18       Impact factor: 91.245

5.  Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.

Authors:  G Schrakamp; C F Roosenboom; R B Schutgens; R J Wanders; H S Heymans; J M Tager; H van den Bosch
Journal:  J Lipid Res       Date:  1985-07       Impact factor: 5.922
  5 in total
  40 in total

1.  Analysis of plasmenylethanolamines using electrospray tandem mass spectrometry and its application in screening for peroxisomal disorders.

Authors:  P Vreken; F Valianpour; H Overmars; P G Barth; J J Selhorst; A H van Gennip; R J Wanders
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

Review 2.  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 3.  Peroxisomal disorders: clinical, biochemical, and molecular aspects.

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

4.  Lipids-Я-Us: peroxisome generation of iNKT ligands.

Authors:  Randy R Brutkiewicz; Alexander L Dent
Journal:  Nat Immunol       Date:  2012-04-18       Impact factor: 25.606

Review 5.  Diagnostic work-up of a peroxisomal patient.

Authors:  J G Leroy; M Espeel; J F Gadisseux; H Mandel; M Martinez; B T Poll-The; R J Wanders; F Roels
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

6.  Plasmalogens and oxidative stress: evidence against a major role of plasmalogens in protection against the superoxide anion radical.

Authors:  G A Jansen; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1997-03       Impact factor: 4.982

Review 7.  Peroxisome Biogenesis Disorders.

Authors:  Masanori Honsho; Kanji Okumoto; Shigehiko Tamura; Yukio Fujiki
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

Review 8.  Plasmalogens, phospholipase A2, and docosahexaenoic acid turnover in brain tissue.

Authors:  A A Farooqui; L A Horrocks
Journal:  J Mol Neurosci       Date:  2001 Apr-Jun       Impact factor: 3.444

Review 9.  Peroxisomal disorders: a review.

Authors:  B Fournier; J A Smeitink; L Dorland; R Berger; J M Saudubray; B T Poll-The
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

10.  Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.

Authors:  D G Barr; J M Kirk; M al Howasi; R J Wanders; R B Schutgens
Journal:  Arch Dis Child       Date:  1993-03       Impact factor: 3.791
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.