PMC Links for Nucleotide (Select 1700660485) - PMC

Select item 66961641.

Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex

Anne Schieferdecker, Petra Wendler

Int J Mol Sci. 2019 Aug; 20(15): 3756. Published online 2019 Aug 1. doi: 10.3390/ijms20153756

PMCID:: PMC6696164

Select item 60651972.

Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol

Ana G. Pedrosa, Tânia Francisco, Diana Bicho, Ana F. Dias, Aurora Barros-Barbosa, Vera Hagmann, Gabriele Dodt, Tony A. Rodrigues, Jorge E. Azevedo

J Biol Chem. 2018 Jul 20; 293(29): 11553–11563. Published online 2018 Jun 8. doi: 10.1074/jbc.RA118.003669

PMCID:: PMC6065197

Abstract Article PDF–1.5M

Select item 58128953.

Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder

Kim D. Falkenberg, Nancy E. Braverman, Ann B. Moser, Steven J. Steinberg, Femke C.C. Klouwer, Agatha Schlüter, Montserrat Ruiz, Aurora Pujol, Martin Engvall, Karin Naess, FrancJan van Spronsen, Irene Körver-Keularts, M. Estela Rubio-Gozalbo, Sacha Ferdinandusse, Ronald J.A. Wanders, Hans R. Waterham

Am J Hum Genet. 2017 Dec 7; 101(6): 965–976. Published online 2017 Dec 7. doi: 10.1016/j.ajhg.2017.11.007

PMCID:: PMC5812895

Abstract Article PDF–1.2M

Select item 19148644.

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

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

Am J Hum Genet. 1996 Dec; 59(6): 1210–1220.

PMCID:: PMC1914864

Summary Page Browse PDF–2.5M

Select item 4502315.

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor.

T Yahraus, N Braverman, G Dodt, J E Kalish, J C Morrell, H W Moser, D Valle, S J Gould

EMBO J. 1996 Jun 17; 15(12): 2914–2923.

PMCID:: PMC450231

Summary Page Browse PDF–2.7M

Select item 211276.

Disruption of a PEX1–PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease

Brian V. Geisbrecht, Cynthia S. Collins, Bernadette E. Reuber, Stephen J. Gould

Proc Natl Acad Sci U S A. 1998 Jul 21; 95(15): 8630–8635. doi: 10.1073/pnas.95.15.8630

PMCID:: PMC21127

Abstract Article PDF–320K

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