-
1
-
-
0026735060
-
Biochemistry of peroxisomes
-
van den Bosch, H., Schutgens, R.B.H., Wanders, R.J.A., and Tager, J.M. (1992) Biochemistry of peroxisomes. Annu. Rev. Biochem. 61, 157-197
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 157-197
-
-
Van Den Bosch, H.1
Schutgens, R.B.H.2
Wanders, R.J.A.3
Tager, J.M.4
-
2
-
-
0034515057
-
The genetics of peroxisome biogenesis
-
Sacksteder, K.A. and Gould, S.J. (2000) The genetics of peroxisome biogenesis. Annu. Rev. Genet. 34, 623-652
-
(2000)
Annu. Rev. Genet.
, vol.34
, pp. 623-652
-
-
Sacksteder, K.A.1
Gould, S.J.2
-
3
-
-
0033787313
-
Import of peroxisomal matrix and membrane proteins
-
Subramani, S., Koller, A., and Snyder, W.B. (2000) Import of peroxisomal matrix and membrane proteins. Annu. Rev. Biochem. 63, 399-418
-
(2000)
Annu. Rev. Biochem.
, vol.63
, pp. 399-418
-
-
Subramani, S.1
Koller, A.2
Snyder, W.B.3
-
5
-
-
0036663192
-
Peroxisome biogenesis and protein import in plants, animals and yeasts: Enigma and variations?
-
Sparkes, I.A. and Baker, A. (2002) Peroxisome biogenesis and protein import in plants, animals and yeasts: enigma and variations? Mol. Membr. Biol. 19, 171-185
-
(2002)
Mol. Membr. Biol.
, vol.19
, pp. 171-185
-
-
Sparkes, I.A.1
Baker, A.2
-
6
-
-
0028817372
-
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
-
Dodt, G., Braverman, N., Wong, C., Moser, A., Moser, H.W., Watkins, P., Valle, D., and Gould, S.J. (1995) Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nat. Genet. 9, 115-125
-
(1995)
Nat. Genet.
, vol.9
, pp. 115-125
-
-
Dodt, G.1
Braverman, N.2
Wong, C.3
Moser, A.4
Moser, H.W.5
Watkins, P.6
Valle, D.7
Gould, S.J.8
-
7
-
-
0028916868
-
Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor
-
Fransen, M., Brees, C., Baumgart, E., Vanhooren, J.C.T., Baes, M., Mannaerts, G.P., and Van Veldhoven, P.P. (1995) Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor. J. Biol. Chem. 270, 7731-7736
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 7731-7736
-
-
Fransen, M.1
Brees, C.2
Baumgart, E.3
Vanhooren, J.C.T.4
Baes, M.5
Mannaerts, G.P.6
Van Veldhoven, P.P.7
-
8
-
-
0029024783
-
Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders
-
Wiemer, E.A.C., Nuttley, W.M., Bertolaet, B.L., Li, X., Francke, U., Wheelock, M.J., Anne, U.K., Johnson, K.R., and Subramani, S. (1995) Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders. J. Cell Biol. 130, 51-65
-
(1995)
J. Cell Biol.
, vol.130
, pp. 51-65
-
-
Wiemer, E.A.C.1
Nuttley, W.M.2
Bertolaet, B.L.3
Li, X.4
Francke, U.5
Wheelock, M.J.6
Anne, U.K.7
Johnson, K.R.8
Subramani, S.9
-
9
-
-
0030946632
-
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
-
Braverman, N., Steel, G., Obie, C., Moser, A., Moser, H., Gould, S.J., and Valle, D. (1997) Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata. Nat. Genet. 15, 369-376
-
(1997)
Nat. Genet.
, vol.15
, pp. 369-376
-
-
Braverman, N.1
Steel, G.2
Obie, C.3
Moser, A.4
Moser, H.5
Gould, S.J.6
Valle, D.7
-
10
-
-
0031003680
-
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
-
Motley, A.M., Hettema, E.H., Hogenhout, E.M., Brites, P., ten Asbroek, A.L.M.A., Wijburg, F.A., Baas, F., Heijmans, H.S., Tabak, H.F., Wanders, R.J.A., and Distel, B. (1997) Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor. Nat. Genet. 15, 377-380
-
(1997)
Nat. Genet.
, vol.15
, pp. 377-380
-
-
Motley, A.M.1
Hettema, E.H.2
Hogenhout, E.M.3
Brites, P.4
Ten Asbroek, A.L.M.A.5
Wijburg, F.A.6
Baas, F.7
Heijmans, H.S.8
Tabak, H.F.9
Wanders, R.J.A.10
Distel, B.11
-
11
-
-
1842335689
-
Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor
-
Purdue, P.E., Zhang, J.W., Skoneczny, M., and Lazarow, P.B. (1997) Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor. Nat. Genet. 15, 381-384
-
(1997)
Nat. Genet.
, vol.15
, pp. 381-384
-
-
Purdue, P.E.1
Zhang, J.W.2
Skoneczny, M.3
Lazarow, P.B.4
-
12
-
-
0034635364
-
Interaction of Pex5p, the type 1 peroxisomal targeting signal receptor, with the peroxisomal membrane proteins Pex14p and Pex13p
-
Urquhart, A.J., Kennedy, D., Gould, S.J., and Crane, D.I. (2000) Interaction of Pex5p, the type 1 peroxisomal targeting signal receptor, with the peroxisomal membrane proteins Pex14p and Pex13p. J. Biol. Chem. 275, 4127-4136
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 4127-4136
-
-
Urquhart, A.J.1
Kennedy, D.2
Gould, S.J.3
Crane, D.I.4
-
13
-
-
0035860787
-
The di-aromatic pentapeptide repeats of the human peroxisome import receptor PEX5 are separate high affinity binding sites for the peroxisomal membrane protein PEX14
-
Saidowsky, J., Dodt, G., Kirchberg, K., Wegner, A., Nastainczyk, W., Kunau, W.H., and Schliebs, W. (2001) The di-aromatic pentapeptide repeats of the human peroxisome import receptor PEX5 are separate high affinity binding sites for the peroxisomal membrane protein PEX14. J. Biol. Chem. 276, 34524-34529
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 34524-34529
-
-
Saidowsky, J.1
Dodt, G.2
Kirchberg, K.3
Wegner, A.4
Nastainczyk, W.5
Kunau, W.H.6
Schliebs, W.7
-
14
-
-
0036179374
-
Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: Conserved Pex5p WXXXF/Y motifs are critical for matrix protein import
-
Otera, H., Setoguchi, K., Hamasaki, M., Kumashiro, T., Shimizu, N., and Fujiki, Y. (2002) Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import. Mol. Cell. Biol. 22, 1639-1655
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 1639-1655
-
-
Otera, H.1
Setoguchi, K.2
Hamasaki, M.3
Kumashiro, T.4
Shimizu, N.5
Fujiki, Y.6
-
15
-
-
0035928730
-
Peroxisomes: The extended shuttle to the peroxisome matrix
-
Kunau, W.H. (2001) Peroxisomes: the extended shuttle to the peroxisome matrix. Current Biol. 11, 659-662
-
(2001)
Current Biol.
, vol.11
, pp. 659-662
-
-
Kunau, W.H.1
-
16
-
-
0035805208
-
Peroxisomal protein import: The paradigm shifts
-
Smith, M.D. and Schnell, D.J. (2001) Peroxisomal protein import: The paradigm shifts. Cell 105, 293-296
-
(2001)
Cell
, vol.105
, pp. 293-296
-
-
Smith, M.D.1
Schnell, D.J.2
-
17
-
-
0035917528
-
The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol
-
Dammai, V. and Subramani, S. (2001) The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol. Cell 105, 187-196
-
(2001)
Cell
, vol.105
, pp. 187-196
-
-
Dammai, V.1
Subramani, S.2
-
18
-
-
0026064431
-
Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant
-
Tsukamoto, T., Miura, S., and Fujiki, Y. (1991) Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant. Nature 350, 77-81
-
(1991)
Nature
, vol.350
, pp. 77-81
-
-
Tsukamoto, T.1
Miura, S.2
Fujiki, Y.3
-
19
-
-
0031656796
-
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B
-
Okumoto, K., Itoh, R., Shimozawa, N., Suzuki, Y., Tamura, S., Kondo, N., and Fujiki, Y. (1998) Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B. Hum. Mol. Genet. 7, 1399-1405
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1399-1405
-
-
Okumoto, K.1
Itoh, R.2
Shimozawa, N.3
Suzuki, Y.4
Tamura, S.5
Kondo, N.6
Fujiki, Y.7
-
20
-
-
0032231872
-
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders
-
Warren, D.S., Morrell, J.C., Moser, H.W., Valle, D., and Gould, S.J. (1998) Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders. Am. J. Hum. Genet. 63, 347-359
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 347-359
-
-
Warren, D.S.1
Morrell, J.C.2
Moser, H.W.3
Valle, D.4
Gould, S.J.5
-
21
-
-
0030951104
-
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders
-
Chang, C.C., Lee, W.H., Moser, H., Valle, D., and Gould, S.J. (1997) Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders. Nat. Genet. 15, 385-388
-
(1997)
Nat. Genet.
, vol.15
, pp. 385-388
-
-
Chang, C.C.1
Lee, W.H.2
Moser, H.3
Valle, D.4
Gould, S.J.5
-
22
-
-
0031862579
-
PEX12, the pathogenic gene of group III Zellweger syndrome: CDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p
-
Okumoto, K., Shimozawa, N., Kawai, A., Tamura, S., Tsukamoto, T., Osumi, T., Moser, H., Wanders, R.J.A., Suzuki, Y., Kondo, N., and Fujiki, Y. (1998) PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p. Mol. Cell. Biol. 18, 4324-4336
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 4324-4336
-
-
Okumoto, K.1
Shimozawa, N.2
Kawai, A.3
Tamura, S.4
Tsukamoto, T.5
Osumi, T.6
Moser, H.7
Wanders, R.J.A.8
Suzuki, Y.9
Kondo, N.10
Fujiki, Y.11
-
23
-
-
0033571690
-
PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import
-
Chang, C.C., Warren, D.S., Sacksteder, K.A., and Gould, S.J. (1999) PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import. J. Cell Biol. 147, 761-774
-
(1999)
J. Cell Biol.
, vol.147
, pp. 761-774
-
-
Chang, C.C.1
Warren, D.S.2
Sacksteder, K.A.3
Gould, S.J.4
-
24
-
-
0031854532
-
An isoform of Pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes
-
Braverman, N., Dodt, G., Gould, S.J., and Valle, D. (1998) An isoform of Pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes. Hum. Mol. Genet. 7, 1195-1205
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1195-1205
-
-
Braverman, N.1
Dodt, G.2
Gould, S.J.3
Valle, D.4
-
25
-
-
0031962116
-
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: Studies with PEX5-defective CHO cell mutant
-
Otera, H., Okumoto, K., Tateishi, K., Ikoma, Y., Matsuda, E., Nishimura, M., Tsukamoto, T., Osumi, T., Ohashi, K., Higuchi, O., and Fujiki, Y. (1998) Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: Studies with PEX5-defective CHO cell mutant. Mol. Cell. Biol. 18, 388-399
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 388-399
-
-
Otera, H.1
Okumoto, K.2
Tateishi, K.3
Ikoma, Y.4
Matsuda, E.5
Nishimura, M.6
Tsukamoto, T.7
Osumi, T.8
Ohashi, K.9
Higuchi, O.10
Fujiki, Y.11
-
26
-
-
0034647529
-
Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals
-
Matsumura, T., Otera, H., and Fujiki, Y. (2000) Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. J. Biol. Chem. 275, 21715-21721
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 21715-21721
-
-
Matsumura, T.1
Otera, H.2
Fujiki, Y.3
-
27
-
-
0034678916
-
Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins
-
Ito, M., Ito, R., Huang, Y., Miura, S., Imamura, A., Suzuki, Y., and Shimozawa, N. (2000) Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteins. Biochim. Biophys. Acta 1496, 232-242
-
(2000)
Biochim. Biophys. Acta
, vol.1496
, pp. 232-242
-
-
Ito, M.1
Ito, R.2
Huang, Y.3
Miura, S.4
Imamura, A.5
Suzuki, Y.6
Shimozawa, N.7
-
28
-
-
0037042381
-
Different accumulations of 3-ketoacyl-CoA thiolase precursor in peroxisomes of Chinese hamster ovary cells harboring a dysfunction in the PEX2 protein
-
Huang, Y., Ito, R., Imanaka, T., Usuda, N., and Ito, M. (2002) Different accumulations of 3-ketoacyl-CoA thiolase precursor in peroxisomes of Chinese hamster ovary cells harboring a dysfunction in the PEX2 protein. Biochim. Biophys. Acta 1589, 273-284
-
(2002)
Biochim. Biophys. Acta
, vol.1589
, pp. 273-284
-
-
Huang, Y.1
Ito, R.2
Imanaka, T.3
Usuda, N.4
Ito, M.5
-
29
-
-
0035955305
-
Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 gene
-
Ito, R., Huang, Y., Yao, C., Shimozawa, N., Suzuki, Y., Kondo, N., Imanaka, T., Usuda, N., and Ito, M. (2001) Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 gene. Biochem. Biophys. Res. Commun. 288, 321-327
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.288
, pp. 321-327
-
-
Ito, R.1
Huang, Y.2
Yao, C.3
Shimozawa, N.4
Suzuki, Y.5
Kondo, N.6
Imanaka, T.7
Usuda, N.8
Ito, M.9
-
30
-
-
0028332245
-
Differential protein import deficiencies in human peroxisome assembly disorders
-
Motley, A., Hettema, E., Distel, B., and Tabak, H. (1994) Differential protein import deficiencies in human peroxisome assembly disorders. J. Cell Biol. 125, 755-767
-
(1994)
J. Cell Biol.
, vol.125
, pp. 755-767
-
-
Motley, A.1
Hettema, E.2
Distel, B.3
Tabak, H.4
-
31
-
-
0019363396
-
Organization and expression of eucaryotic split genes coding for proteins
-
Breathnach, R. and Chambon, P. (1981) Organization and expression of eucaryotic split genes coding for proteins. Annu. Rev. Biochem. 50, 349-383
-
(1981)
Annu. Rev. Biochem.
, vol.50
, pp. 349-383
-
-
Breathnach, R.1
Chambon, P.2
-
32
-
-
0034647937
-
The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p-PTS2 protein complex into peroxisomes via its initial docking site, Pex14p
-
Otera, H., Harano, T., Honsho, M., Ghaedi, K., Mukai, S., Tanaka, A., Kawai, A., Shimizu, N., and Fujiki, Y. (2000) The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p-PTS2 protein complex into peroxisomes via its initial docking site, Pex14p. J. Biol. Chem. 275, 21703-21714
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 21703-21714
-
-
Otera, H.1
Harano, T.2
Honsho, M.3
Ghaedi, K.4
Mukai, S.5
Tanaka, A.6
Kawai, A.7
Shimizu, N.8
Fujiki, Y.9
-
33
-
-
0025941962
-
A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase
-
Swinkels, B.W., Gould, S.J., Bodnar, A.G., Rachubinski, R.A., and Subramani, S. (1991) A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase. EMBO J. 10, 3255-3262
-
(1991)
EMBO J.
, vol.10
, pp. 3255-3262
-
-
Swinkels, B.W.1
Gould, S.J.2
Bodnar, A.G.3
Rachubinski, R.A.4
Subramani, S.5
-
34
-
-
0026326482
-
Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting
-
Osumi, T., Tsukamoto, T., Hata, S., Yokota, S., Miura, S., Fujiki, Y., Hijikata, M., Miyazawa, S., and Hashimoto, T. (1991) Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting. Biochem. Biophys. Res. Commun. 181, 947-954
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.181
, pp. 947-954
-
-
Osumi, T.1
Tsukamoto, T.2
Hata, S.3
Yokota, S.4
Miura, S.5
Fujiki, Y.6
Hijikata, M.7
Miyazawa, S.8
Hashimoto, T.9
-
35
-
-
0019028350
-
Purification and properties of acyl-CoA oxidase from rat liver
-
Osumi, T., Hashimoto, T., and Ui, N. (1980) Purification and properties of acyl-CoA oxidase from rat liver. J. Biochem. 87, 1735-1746
-
(1980)
J. Biochem.
, vol.87
, pp. 1735-1746
-
-
Osumi, T.1
Hashimoto, T.2
Ui, N.3
-
36
-
-
0034711253
-
Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder
-
Fujiwara, C., Imamura, A., Hashiguchi, N., Shimozawa, N., Suzuki, Y., Kondo, N., Imanaka, T., Tsukamoto, T., and Osumi, T. (2000) Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder. J. Biol. Chem. 275, 37271-37277
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 37271-37277
-
-
Fujiwara, C.1
Imamura, A.2
Hashiguchi, N.3
Shimozawa, N.4
Suzuki, Y.5
Kondo, N.6
Imanaka, T.7
Tsukamoto, T.8
Osumi, T.9
-
37
-
-
0037414755
-
Characterization of the peroxisomal cycling receptor, Pex5p, using a cell-free in vitro import system
-
Gouveia, A.M., Guimaraes, C.P., Oliveira, M.E., Reguenga, C., Sa-Miranda, C., and Azevedo, J.E. (2003) Characterization of the peroxisomal cycling receptor, Pex5p, using a cell-free in vitro import system. J. Biol. Chem. 278, 226-232
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 226-232
-
-
Gouveia, A.M.1
Guimaraes, C.P.2
Oliveira, M.E.3
Reguenga, C.4
Sa-Miranda, C.5
Azevedo, J.E.6
-
38
-
-
0035805574
-
Recognition of peroxisomal targeting signal type 1 by the import receptor Pex5p
-
Klein, A.T.J., Barnett, P., Bottger, G., Konings, D., Tabak, H.F., and Distel, B. (2001) Recognition of peroxisomal targeting signal type 1 by the import receptor Pex5p. J. Biol. Chem. 276, 15034-15041
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 15034-15041
-
-
Klein, A.T.J.1
Barnett, P.2
Bottger, G.3
Konings, D.4
Tabak, H.F.5
Distel, B.6
-
39
-
-
0034693260
-
Characterization of peroxisomal Pex5p from rat liver. Pex5p in the Pex5p-Pex14p membrane complex is a transmembrane protein
-
Gouveia, A.M.M., Reguenga, C., Oliveira, M.E.M., Sa-Miranda, C., and Azevedo, J.E. (2000) Characterization of peroxisomal Pex5p from rat liver. Pex5p in the Pex5p-Pex14p membrane complex is a transmembrane protein. J. Biol. Chem. 275, 32444-32451
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 32444-32451
-
-
Gouveia, A.M.M.1
Reguenga, C.2
Oliveira, M.E.M.3
Sa-Miranda, C.4
Azevedo, J.E.5
-
40
-
-
0035839442
-
Characterization of the mammalian peroxisomal import machinery: Pex2p, Pex5p, Pex12p, and Pex14p are subunits of the same protein assembly
-
Reguenga, C., Oliveira, M.E.M., Gouveia, A.M.M., Sa-Miranda, C., and Azevedo, J.E. (2001) Characterization of the mammalian peroxisomal import machinery: Pex2p, Pex5p, Pex12p, and Pex14p are subunits of the same protein assembly. J. Biol. Chem. 276, 29935-29942
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 29935-29942
-
-
Reguenga, C.1
Oliveira, M.E.M.2
Gouveia, A.M.M.3
Sa-Miranda, C.4
Azevedo, J.E.5
-
41
-
-
0037349250
-
Pex8p: An intraperoxisomal organizer of the peroxisomal import machinery
-
Agne, B., Meindl, N.M., Niederhoff, K., Einwachter, H., Rehling, P., Sickmann, A., Meyer, H.E., Girzalsky, W., and Kunau, W.H. (2003) Pex8p: an intraperoxisomal organizer of the peroxisomal import machinery. Mol. Cell 11, 635-646
-
(2003)
Mol. Cell
, vol.11
, pp. 635-646
-
-
Agne, B.1
Meindl, N.M.2
Niederhoff, K.3
Einwachter, H.4
Rehling, P.5
Sickmann, A.6
Meyer, H.E.7
Girzalsky, W.8
Kunau, W.H.9
-
42
-
-
16944361876
-
A mouse model for Zellweger syndrome
-
Baes, M., Gressens, P., Baumgart, E., Carmeliet, P., Casteels, M., Fransen, M., Evrard, P., Fahimi, D., Declercq, P.E., Collen, D., van Veldhoven, P.P., and Mannaerts, G.P. (1997) A mouse model for Zellweger syndrome. Nat. Genet. 17, 49-57
-
(1997)
Nat. Genet.
, vol.17
, pp. 49-57
-
-
Baes, M.1
Gressens, P.2
Baumgart, E.3
Carmeliet, P.4
Casteels, M.5
Fransen, M.6
Evrard, P.7
Fahimi, D.8
Declercq, P.E.9
Collen, D.10
Van Veldhoven, P.P.11
Mannaerts, G.P.12
-
43
-
-
0028110118
-
Saccharomyces cerevisiae peroxisomal thiolase is imported as a dimer
-
Glover, J.R., Andrews, D.W., and Rachubinski, R.A. (1994) Saccharomyces cerevisiae peroxisomal thiolase is imported as a dimer. Proc. Natl. Acad. Sci. USA 91, 10541-10545
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 10541-10545
-
-
Glover, J.R.1
Andrews, D.W.2
Rachubinski, R.A.3
-
44
-
-
0028033934
-
An oligomeric protein is imported into peroxisomes in vivo
-
McNew, J.A. and Goodman, J.M. (1994) An oligomeric protein is imported into peroxisomes in vivo. J. Cell Biol. 127, 1245-1257
-
(1994)
J. Cell Biol.
, vol.127
, pp. 1245-1257
-
-
McNew, J.A.1
Goodman, J.M.2
-
45
-
-
0034469382
-
Insulin-degrading enzyme exists inside of rat liver peroxisomes and degrades oxidized proteins
-
Morita, M., Kurochikin, I.V., Motojima, K., Goto, S., Takano, T., Okamura, S., Sato, R., Yokota, S., and Imanaka, T. (2000) Insulin-degrading enzyme exists inside of rat liver peroxisomes and degrades oxidized proteins. Cell Struct. Funct. 25, 309-315
-
(2000)
Cell Struct. Funct.
, vol.25
, pp. 309-315
-
-
Morita, M.1
Kurochikin, I.V.2
Motojima, K.3
Goto, S.4
Takano, T.5
Okamura, S.6
Sato, R.7
Yokota, S.8
Imanaka, T.9
-
46
-
-
0345791524
-
Proteomic analysis of rat liver peroxisome. Presence of peroxisome-specific isozyme of lon protease
-
Kikuchi, M., Hatano, N., Yokota, S., Shimozawa, N., Imanaka, T., and Taniguchi, H. (2004) Proteomic analysis of rat liver peroxisome. Presence of peroxisome-specific isozyme of lon protease. J. Biol. Chem. 279, 421-428
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 421-428
-
-
Kikuchi, M.1
Hatano, N.2
Yokota, S.3
Shimozawa, N.4
Imanaka, T.5
Taniguchi, H.6
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