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6. The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6. Matsumoto N; Tamura S; Moser A; Moser HW; Braverman N; Suzuki Y; Shimozawa N; Kondo N; Fujiki Y J Hum Genet; 2001; 46(5):273-7. PubMed ID: 11355018 [TBL] [Abstract][Full Text] [Related]
7. Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients. Maxwell MA; Allen T; Solly PB; Svingen T; Paton BC; Crane DI Hum Mutat; 2002 Nov; 20(5):342-51. PubMed ID: 12402331 [TBL] [Abstract][Full Text] [Related]
8. Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders. Zhang Z; Suzuki Y; Shimozawa N; Fukuda S; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Wanders RJ; Barth PG; Moser HW; Paton BC; Besley GT; Kondo N Hum Mutat; 1999; 13(6):487-96. PubMed ID: 10408779 [TBL] [Abstract][Full Text] [Related]
9. A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif. Fan W; Fujiki Y Biochem Biophys Res Commun; 2006 Jul; 345(4):1434-9. PubMed ID: 16723118 [TBL] [Abstract][Full Text] [Related]
11. Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease. Geisbrecht BV; Collins CS; Reuber BE; Gould SJ Proc Natl Acad Sci U S A; 1998 Jul; 95(15):8630-5. PubMed ID: 9671729 [TBL] [Abstract][Full Text] [Related]
12. Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels. Walter C; Gootjes J; Mooijer PA; Portsteffen H; Klein C; Waterham HR; Barth PG; Epplen JT; Kunau WH; Wanders RJ; Dodt G Am J Hum Genet; 2001 Jul; 69(1):35-48. PubMed ID: 11389485 [TBL] [Abstract][Full Text] [Related]
13. Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis. Fujiki Y; Miyata N; Matsumoto N; Tamura S Biochem Soc Trans; 2008 Feb; 36(Pt 1):109-13. PubMed ID: 18208396 [TBL] [Abstract][Full Text] [Related]
14. Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism. Gootjes J; Schmohl F; Mooijer PA; Dekker C; Mandel H; Topcu M; Huemer M; Von Schütz M; Marquardt T; Smeitink JA; Waterham HR; Wanders RJ Hum Mutat; 2004 Aug; 24(2):130-9. PubMed ID: 15241794 [TBL] [Abstract][Full Text] [Related]
15. Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex. Furuki S; Tamura S; Matsumoto N; Miyata N; Moser A; Moser HW; Fujiki Y J Biol Chem; 2006 Jan; 281(3):1317-23. PubMed ID: 16257970 [TBL] [Abstract][Full Text] [Related]
16. Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I. Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y Proc Natl Acad Sci U S A; 1998 Apr; 95(8):4350-5. PubMed ID: 9539740 [TBL] [Abstract][Full Text] [Related]
17. Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders. Reuber BE; Germain-Lee E; Collins CS; Morrell JC; Ameritunga R; Moser HW; Valle D; Gould SJ Nat Genet; 1997 Dec; 17(4):445-8. PubMed ID: 9398847 [TBL] [Abstract][Full Text] [Related]