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Items: 20

1.

Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

Fukuda S, Shimozawa N, Suzuki Y, Zhang Z, Tomatsu S, Tsukamoto T, Hashiguchi N, Osumi T, Masuno M, Imaizumi K, Kuroki Y, Fujiki Y, Orii T, Kondo N.

Am J Hum Genet. 1996 Dec;59(6):1210-20.

2.

[Human peroxisome-deficient disorders and pathogenic gene].

Fujiki Y.

Rinsho Shinkeigaku. 1994 Dec;34(12):1219-21. Review. Japanese.

PMID:
7539728
3.
4.

[Molecular biology of peroxisome biogenesis].

Fujiki Y.

Nihon Rinsho. 1993 Sep;51(9):2336-42. Review. Japanese.

PMID:
8411711
5.

[Clinical and molecular aspects of peroxisome-deficient disorders].

Suzuki Y, Shimozawa N, Orii T.

Nihon Rinsho. 1993 Sep;51(9):2353-8. Review. Japanese.

PMID:
7692118
6.

Peroxisome biogenesis and molecular defects in peroxisome assembly disorders.

Fujiki Y, Okumoto K, Otera H, Tamura S.

Cell Biochem Biophys. 2000;32 Spring:155-64. Review.

PMID:
11330042
7.
8.

Peroxisome biogenesis disorders.

Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW.

Biochim Biophys Acta. 2006 Dec;1763(12):1733-48. Epub 2006 Sep 14. Review.

9.

PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders.

Crane DI, Maxwell MA, Paton BC.

Hum Mutat. 2005 Sep;26(3):167-75. Review.

PMID:
16086329
10.
11.

Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders.

Fujiki Y.

Ann N Y Acad Sci. 1996 Dec 27;804:491-501. Review. No abstract available.

PMID:
8993567
12.

Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis.

Aral B, Benelli C, Ait-Ghezala G, Amessou M, Fouque F, Maunoury C, Créau N, Kamoun P, Marsac C.

Am J Hum Genet. 1997 Dec;61(6):1318-26. Review.

13.

[Cloning of the holocarboxylase synthetase cDNA and identification of mutations prevalent in Japanese HCS-deficient patients].

Narisawa K, Suzuki Y, Aoki Y.

Nihon Rinsho. 1996 Jan;54(1):259-67. Review. Japanese.

PMID:
8587199
14.

[Biogenesis of peroxisomes and human peroxisomal disorders].

Fujiki Y.

Seikagaku. 1995 Mar;67(3):204-23. Review. Japanese. No abstract available.

PMID:
7602197
15.

Zellweger syndrome and associated phenotypes.

FitzPatrick DR.

J Med Genet. 1996 Oct;33(10):863-8. Review.

16.

Protein import deficiencies in human peroxisomal disorders.

Wiemer EA, Subramani S.

Mol Genet Med. 1994;4:119-52. Review. No abstract available.

PMID:
7981628
17.

Peroxisome biogenesis.

Lazarow PB.

Curr Opin Cell Biol. 1989 Aug;1(4):630-4. Review. No abstract available.

PMID:
2534044
18.

Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines.

Braverman NE, Raymond GV, Rizzo WB, Moser AB, Wilkinson ME, Stone EM, Steinberg SJ, Wangler MF, Rush ET, Hacia JG, Bose M.

Mol Genet Metab. 2016 Mar;117(3):313-21. doi: 10.1016/j.ymgme.2015.12.009. Epub 2015 Dec 23. Review.

PMID:
26750748
19.

Peroxisome biogenesis revisited.

Borst P.

Biochim Biophys Acta. 1989 Jun 1;1008(1):1-13. Review. No abstract available.

PMID:
2655706
20.

A unified nomenclature for peroxisome biogenesis factors.

Distel B, Erdmann R, Gould SJ, Blobel G, Crane DI, Cregg JM, Dodt G, Fujiki Y, Goodman JM, Just WW, Kiel JA, Kunau WH, Lazarow PB, Mannaerts GP, Moser HW, Osumi T, Rachubinski RA, Roscher A, Subramani S, Tabak HF, Tsukamoto T, Valle D, van der Klei I, van Veldhoven PP, Veenhuis M.

J Cell Biol. 1996 Oct;135(1):1-3. Review. No abstract available.

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