364 related articles for article (PubMed ID: 23716570)
1. Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.
Krause C; Rosewich H; Woehler A; Gärtner J
Hum Mol Genet; 2013 Oct; 22(19):3844-57. PubMed ID: 23716570
[TBL] [Abstract][Full Text] [Related]
2. Identification of a novel, intraperoxisomal pex14-binding site in pex13: association of pex13 with the docking complex is essential for peroxisomal matrix protein import.
Schell-Steven A; Stein K; Amoros M; Landgraf C; Volkmer-Engert R; Rottensteiner H; Erdmann R
Mol Cell Biol; 2005 Apr; 25(8):3007-18. PubMed ID: 15798189
[TBL] [Abstract][Full Text] [Related]
3. Saccharomyces cerevisiae PTS1 receptor Pex5p interacts with the SH3 domain of the peroxisomal membrane protein Pex13p in an unconventional, non-PXXP-related manner.
Bottger G; Barnett P; Klein AT; Kragt A; Tabak HF; Distel B
Mol Biol Cell; 2000 Nov; 11(11):3963-76. PubMed ID: 11071920
[TBL] [Abstract][Full Text] [Related]
4. Peroxisomal protein PEX13 functions in selective autophagy.
Lee MY; Sumpter R; Zou Z; Sirasanagandla S; Wei Y; Mishra P; Rosewich H; Crane DI; Levine B
EMBO Rep; 2017 Jan; 18(1):48-60. PubMed ID: 27827795
[TBL] [Abstract][Full Text] [Related]
5. Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Toyama R; Mukai S; Fujiki Y; Tsukamoto T; Osumi T; Orii T; Wanders RJ; Kondo N
Hum Mol Genet; 1999 Jun; 8(6):1077-83. PubMed ID: 10332040
[TBL] [Abstract][Full Text] [Related]
6. Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
Shimozawa N; Tsukamoto T; Nagase T; Takemoto Y; Koyama N; Suzuki Y; Komori M; Osumi T; Jeannette G; Wanders RJ; Kondo N
Hum Mutat; 2004 Jun; 23(6):552-8. PubMed ID: 15146459
[TBL] [Abstract][Full Text] [Related]
7. PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.
Liu Y; Björkman J; Urquhart A; Wanders RJ; Crane DI; Gould SJ
Am J Hum Genet; 1999 Sep; 65(3):621-34. PubMed ID: 10441568
[TBL] [Abstract][Full Text] [Related]
8. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.
Slawecki ML; Dodt G; Steinberg S; Moser AB; Moser HW; Gould SJ
J Cell Sci; 1995 May; 108 ( Pt 5)():1817-29. PubMed ID: 7544797
[TBL] [Abstract][Full Text] [Related]
9. Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.
Maxwell M; Bjorkman J; Nguyen T; Sharp P; Finnie J; Paterson C; Tonks I; Paton BC; Kay GF; Crane DI
Mol Cell Biol; 2003 Aug; 23(16):5947-57. PubMed ID: 12897163
[TBL] [Abstract][Full Text] [Related]
10. The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport to peroxisomes.
Mano S; Nakamori C; Nito K; Kondo M; Nishimura M
Plant J; 2006 Aug; 47(4):604-18. PubMed ID: 16813573
[TBL] [Abstract][Full Text] [Related]
11. Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations.
Al-Dirbashi OY; Shaheen R; Al-Sayed M; Al-Dosari M; Makhseed N; Abu Safieh L; Santa T; Meyer BF; Shimozawa N; Alkuraya FS
Am J Med Genet A; 2009 Jun; 149A(6):1219-23. PubMed ID: 19449432
[TBL] [Abstract][Full Text] [Related]
12. Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance.
Nguyen T; Bjorkman J; Paton BC; Crane DI
J Cell Sci; 2006 Feb; 119(Pt 4):636-45. PubMed ID: 16449325
[TBL] [Abstract][Full Text] [Related]
13. Pex13, the mouse ortholog of the human peroxisome biogenesis disorder PEX13 gene: gene structure, tissue expression, and localization of the protein to peroxisomes.
Björkman J; Gould SJ; Crane DI
Genomics; 2002 Feb; 79(2):162-8. PubMed ID: 11829486
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel PEX14 mutation in Zellweger syndrome.
Huybrechts SJ; Van Veldhoven PP; Hoffman I; Zeevaert R; de Vos R; Demaerel P; Brams M; Jaeken J; Fransen M; Cassiman D
J Med Genet; 2008 Jun; 45(6):376-83. PubMed ID: 18285423
[TBL] [Abstract][Full Text] [Related]
15. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
[TBL] [Abstract][Full Text] [Related]
16. Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene.
Björkman J; Stetten G; Moore CS; Gould SJ; Crane DI
Genomics; 1998 Dec; 54(3):521-8. PubMed ID: 9878256
[TBL] [Abstract][Full Text] [Related]
17. Quantitative analysis of peroxisomal targeting signal type-1 binding to wild-type and pathogenic mutants of Pex5p supports an affinity threshold for peroxisomal protein targeting.
Maynard EL; Berg JM
J Mol Biol; 2007 May; 368(5):1259-66. PubMed ID: 17399738
[TBL] [Abstract][Full Text] [Related]
18. Modulation of peroxisomal import by the PEX13 SH3 domain and a proximal FxxxF binding motif.
Gaussmann S; Peschel R; Ott J; Zak KM; Sastre J; Delhommel F; Popowicz GM; Boekhoven J; Schliebs W; Erdmann R; Sattler M
Nat Commun; 2024 Apr; 15(1):3317. PubMed ID: 38632234
[TBL] [Abstract][Full Text] [Related]
19. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.
Nito K; Kamigaki A; Kondo M; Hayashi M; Nishimura M
Plant Cell Physiol; 2007 Jun; 48(6):763-74. PubMed ID: 17478547
[TBL] [Abstract][Full Text] [Related]
20. PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import.
Chang CC; Warren DS; Sacksteder KA; Gould SJ
J Cell Biol; 1999 Nov; 147(4):761-74. PubMed ID: 10562279
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
