-
1
-
-
0032545023
-
cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p
-
Abe, I. and Fujiki, Y. (1998). cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p. Biochem. Biophys. Res. Commun. 252, 529-533.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.252
, pp. 529-533
-
-
Abe, I.1
Fujiki, Y.2
-
2
-
-
0032563281
-
Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11
-
Abe, I., Okumoto, K., Tamura, S. and Fujiki, Y. (1998). Clofibrate-inducible, 28-kDa peroxisomal integral membrane protein is encoded by PEX11. FEBS Lett. 431, 468-472.
-
(1998)
FEBS Lett
, vol.431
, pp. 468-472
-
-
Abe, I.1
Okumoto, K.2
Tamura, S.3
Fujiki, Y.4
-
3
-
-
0034192231
-
Nuclear receptors arose from pre-existing protein modules during evolution
-
Barnett, P., Tabak, H. F. and Hettema, E. H. (2000). Nuclear receptors arose from pre-existing protein modules during evolution. Trends Biochem. Sci. 25, 227-228.
-
(2000)
Trends Biochem. Sci.
, vol.25
, pp. 227-228
-
-
Barnett, P.1
Tabak, H.F.2
Hettema, E.H.3
-
4
-
-
33845261493
-
A rapid method of total lipid extraction and purification
-
Bligh, E. G. and Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Can. J. Med. Sci. 37, 911-917.
-
(1959)
Can. J. Med. Sci.
, vol.37
, pp. 911-917
-
-
Bligh, E.G.1
Dyer, W.J.2
-
5
-
-
0033047785
-
Metabolic control of peroxisome abundance
-
Chang, C. C., South, S., Warren, D., Jones, J., Moser, A. B., Moser, H. W. and Gould, S. J. (1999). Metabolic control of peroxisome abundance. J. Cell Sci. 112, 1579-1590.
-
(1999)
J. Cell Sci.
, vol.112
, pp. 1579-1590
-
-
Chang, C.C.1
South, S.2
Warren, D.3
Jones, J.4
Moser, A.B.5
Moser, H.W.6
Gould, S.J.7
-
6
-
-
0022456326
-
The effect of clofibrate on the phospholipid composition of the peroxisomal membranes in mouse liver
-
Crane, D. I. and Masters, C. J. (1986). The effect of clofibrate on the phospholipid composition of the peroxisomal membranes in mouse liver. Biochim. Biophys. Acta. 876, 256-263.
-
(1986)
Biochim. Biophys. Acta.
, vol.876
, pp. 256-263
-
-
Crane, D.I.1
Masters, C.J.2
-
7
-
-
77956003976
-
Pex11pβ-mediated growth and division of mammalian peroxisomes follows a maturation pathway
-
Delille, H. K., Agricola, B., Guimaraes, S. C., Borta, H., Lüers, G. H., Fransen, M. and Schrader, M. (2010). Pex11pβ-mediated growth and division of mammalian peroxisomes follows a maturation pathway. J. Cell Sci. 123, 2750-2762.
-
(2010)
J. Cell Sci.
, vol.123
, pp. 2750-2762
-
-
Delille, H.K.1
Agricola, B.2
Guimaraes, S.C.3
Borta, H.4
Lüers, G.H.5
Fransen, M.6
Schrader, M.7
-
8
-
-
0035658316
-
Identification of the peroxisomal β-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid
-
Ferdinandusse, S., Denis, S., Mooijer, P. A., Zhang, Z., Reddy, J. K., Spector, A. A. and Wanders, R. J. (2001). Identification of the peroxisomal β-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid. J. Lipid Res. 42, 1987-1995.
-
(2001)
J. Lipid Res.
, vol.42
, pp. 1987-1995
-
-
Ferdinandusse, S.1
Denis, S.2
Mooijer, P.A.3
Zhang, Z.4
Reddy, J.K.5
Spector, A.A.6
Wanders, R.J.7
-
9
-
-
29944445799
-
Clinical and biochemical spectrum of D-bifunctional protein deficiency
-
Ferdinandusse, S., Denis, S., Mooijer, P. A., Dekker, C., Duran, M., Soorani-Lunsing, R. J., Boltshauser, E., Macaya, A., Gärtner, J., Majoie, C. B. et al. (2006). Clinical and biochemical spectrum of D-bifunctional protein deficiency. Ann. Neurol. 59, 92-104.
-
(2006)
Ann. Neurol.
, vol.59
, pp. 92-104
-
-
Ferdinandusse, S.1
Denis, S.2
Mooijer, P.A.3
Dekker, C.4
Duran, M.5
Soorani-Lunsing, R.J.6
Boltshauser, E.7
Macaya, A.8
Gärtner, J.9
Majoie, C.B.10
-
10
-
-
34848897852
-
Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency
-
Ferdinandusse, S., Denis, S., Hogenhout, E. M., Koster, J., van Roermund, C. W. T., Ijlst, L., Moser, A. B., Wanders, R. J. A. and Waterham, H. R. (2007). Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency. Hum. Mutat. 28, 904-912.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 904-912
-
-
Ferdinandusse, S.1
Denis, S.2
Hogenhout, E.M.3
Koster, J.4
van Roermund, C.W.T.5
Ijlst, L.6
Moser, A.B.7
Wanders, R.J.A.8
Waterham, H.R.9
-
11
-
-
0034733909
-
Peroxisome biogenesis and peroxisome biogenesis disorders
-
Fujiki, Y. (2000). Peroxisome biogenesis and peroxisome biogenesis disorders. FEBS Lett. 476, 42-46.
-
(2000)
FEBS Lett
, vol.476
, pp. 42-46
-
-
Fujiki, Y.1
-
12
-
-
33646086486
-
Aberrant peroxisome morphology in peroxisomal β-oxidation enzyme deficiencies
-
Funato, M., Shimozawa, N., Nagase, T., Takemoto, Y., Suzuki, Y., Imamura, Y., Matsumoto, T., Tsukamoto, T., Kojidani, T., Osumi, T. et al. (2006). Aberrant peroxisome morphology in peroxisomal β-oxidation enzyme deficiencies. Brain Dev. 5, 287-292.
-
(2006)
Brain Dev
, vol.5
, pp. 287-292
-
-
Funato, M.1
Shimozawa, N.2
Nagase, T.3
Takemoto, Y.4
Suzuki, Y.5
Imamura, Y.6
Matsumoto, T.7
Tsukamoto, T.8
Kojidani, T.9
Osumi, T.10
-
13
-
-
44649129342
-
The novel tail-anchored membrane protein Mff controls mitochondrial and peroxisomal fission in mammalian cells
-
Gandre-Babbe, S. and van der Bliek, A. M. (2008). The novel tail-anchored membrane protein Mff controls mitochondrial and peroxisomal fission in mammalian cells. Mol. Biol. Cell 19, 2402-2412.
-
(2008)
Mol. Biol. Cell
, vol.19
, pp. 2402-2412
-
-
Gandre-Babbe, S.1
van der Bliek, A.M.2
-
14
-
-
20244364534
-
Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator
-
Gondcaille, C., Depreter, M., Fourcade, S., Lecca, M. R., Leclercq, S., Martin, P. G., Pineau, T., Cadepond, F., ElEtr, M., Bertrand, N. et al. (2005). Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator. J. Cell Biol. 169, 93-104.
-
(2005)
J. Cell Biol.
, vol.169
, pp. 93-104
-
-
Gondcaille, C.1
Depreter, M.2
Fourcade, S.3
Lecca, M.R.4
Leclercq, S.5
Martin, P.G.6
Pineau, T.7
Cadepond, F.8
ElEtr, M.9
Bertrand, N.10
-
15
-
-
0034255179
-
Peroxisome biogenesis disorders: genetics and cell biology
-
Gould, S. J. and Valle, D. (2000). Peroxisome biogenesis disorders: genetics and cell biology. Trends in Genetics 16, 340-345.
-
(2000)
Trends in Genetics
, vol.16
, pp. 340-345
-
-
Gould, S.J.1
Valle, D.2
-
16
-
-
34247475252
-
A signal from inside the peroxisome initiates its division by promoting the remodeling of the peroxisomal membrane
-
Guo, T., Gregg, C., Boukh-Viner, T., Kyryakov, P., Goldberg, A., Bourque, S., Banu, F., Haile, S., Milijevic, S., San, K. H. et al. (2007). A signal from inside the peroxisome initiates its division by promoting the remodeling of the peroxisomal membrane. J. Cell Biol. 177, 289-303.
-
(2007)
J. Cell Biol.
, vol.177
, pp. 289-303
-
-
Guo, T.1
Gregg, C.2
Boukh-Viner, T.3
Kyryakov, P.4
Goldberg, A.5
Bourque, S.6
Banu, F.7
Haile, S.8
Milijevic, S.9
San, K.H.10
-
17
-
-
0032471611
-
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D
-
Honsho, M., Tamura, S., Shimozawa, N., Suzuki, Y., Kondo, N. and Fujiki, Y. (1998). Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. Am. J. Hum. Genet. 63, 1622-1630.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1622-1630
-
-
Honsho, M.1
Tamura, S.2
Shimozawa, N.3
Suzuki, Y.4
Kondo, N.5
Fujiki, Y.6
-
18
-
-
25444471534
-
Dnm1 forms spirals that are structurally tailored to fit mitochondria
-
Ingerman, E., Perkins, E. M., Marino, M., Mears, J. A., McCaffery, J. M., Hinshaw, J. E. and Nunnari, J. (2005). Dnm1 forms spirals that are structurally tailored to fit mitochondria. J. Cell Biol. 170, 1021-1027.
-
(2005)
J. Cell Biol.
, vol.170
, pp. 1021-1027
-
-
Ingerman, E.1
Perkins, E.M.2
Marino, M.3
Mears, J.A.4
McCaffery, J.M.5
Hinshaw, J.E.6
Nunnari, J.7
-
19
-
-
0031730433
-
Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy
-
Kemp, S., Wei, H.-M., Lu, J.-F., Braiterman, L. T., McGuinness, M. C., Moser, A. B., Watkins, P. A. and Smith, K. D. (1998). Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy. Nat. Med. 4, 1261-1268.
-
(1998)
Nat. Med.
, vol.4
, pp. 1261-1268
-
-
Kemp, S.1
Wei, H.-M.2
Lu, J.-F.3
Braiterman, L.T.4
McGuinness, M.C.5
Moser, A.B.6
Watkins, P.A.7
Smith, K.D.8
-
20
-
-
0035208916
-
ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations
-
Kemp, S., Pujol, A., Waterham, H. R., van Geel, B. M., Boehm, C. D., Raymond, G. V., Cutting, G. R., Wanders, R. J. and Moser, H. W. (2001). ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations. Hum. Mutat. 18, 499-515.
-
(2001)
Hum. Mutat.
, vol.18
, pp. 499-515
-
-
Kemp, S.1
Pujol, A.2
Waterham, H.R.3
van Geel, B.M.4
Boehm, C.D.5
Raymond, G.V.6
Cutting, G.R.7
Wanders, R.J.8
Moser, H.W.9
-
21
-
-
33646791462
-
The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER
-
Kim, P. K., Mullen, R. T., Schumann, U. and Lippincott-Schwartz, J. (2006). The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER. J. Cell Biol. 173, 521-532.
-
(2006)
J. Cell Biol.
, vol.173
, pp. 521-532
-
-
Kim, P.K.1
Mullen, R.T.2
Schumann, U.3
Lippincott-Schwartz, J.4
-
22
-
-
34247107180
-
Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis
-
Kobayashi, S., Tanaka, A. and Fujiki, Y. (2007). Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis. Exp. Cell Res. 313, 1675-1686.
-
(2007)
Exp. Cell Res.
, vol.313
, pp. 1675-1686
-
-
Kobayashi, S.1
Tanaka, A.2
Fujiki, Y.3
-
23
-
-
0037424490
-
Dynamin-like protein 1 is involved in peroxisomal fission
-
Koch, A., Thiemann, M., Grabenbauer, M., Yoon, Y., McNiven, M. A. and Schrader, M. (2003). Dynamin-like protein 1 is involved in peroxisomal fission. J. Biol. Chem. 278, 8597-8605.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 8597-8605
-
-
Koch, A.1
Thiemann, M.2
Grabenbauer, M.3
Yoon, Y.4
McNiven, M.A.5
Schrader, M.6
-
24
-
-
4444236087
-
Peroxisome elongation and constriction but not fission can occur independently of dynamin-like protein 1
-
Koch, A., Schneider, G., Lüers, G. H. and Schrader, M. (2004). Peroxisome elongation and constriction but not fission can occur independently of dynamin-like protein 1. J. Cell Sci. 117, 3995-4006.
-
(2004)
J. Cell Sci.
, vol.117
, pp. 3995-4006
-
-
Koch, A.1
Schneider, G.2
Lüers, G.H.3
Schrader, M.4
-
25
-
-
27144557499
-
A role for Fis1 in both mitochondrial and peroxisomal fission in mammalian cells
-
Koch, A., Yoon, Y., Bonekamp, N. A., McNiven, M. A. and Schrader, M. (2005). A role for Fis1 in both mitochondrial and peroxisomal fission in mammalian cells. Mol. Biol. Cell 16, 5077-5086.
-
(2005)
Mol. Biol. Cell
, vol.16
, pp. 5077-5086
-
-
Koch, A.1
Yoon, Y.2
Bonekamp, N.A.3
McNiven, M.A.4
Schrader, M.5
-
26
-
-
77955986557
-
PEX11 family members are membrane elongation factors that coordinate peroxisome proliferation and maintenance
-
Koch, J., Pranjic, K., Huber, A., Ellinger, A., Hartig, A., Kragler, F. and Brocard, C. (2010). PEX11 family members are membrane elongation factors that coordinate peroxisome proliferation and maintenance. J. Cell Sci. 123, 3389-3400.
-
(2010)
J. Cell Sci.
, vol.123
, pp. 3389-3400
-
-
Koch, J.1
Pranjic, K.2
Huber, A.3
Ellinger, A.4
Hartig, A.5
Kragler, F.6
Brocard, C.7
-
27
-
-
0030985318
-
Fatty acids, eicosanoids, and hypolipidemic agents identified as ligands of peroxisome proliferator-activated receptors by coactivator-dependent receptor ligand assay
-
Krey, G., Braissant, O., L'Horset, F., Kalkhoven, E., Perroud, M., Parker, M. G. and Wahli, W. (1997). Fatty acids, eicosanoids, and hypolipidemic agents identified as ligands of peroxisome proliferator-activated receptors by coactivator-dependent receptor ligand assay. Mol. Endocrinol. 11, 779-791.
-
(1997)
Mol. Endocrinol.
, vol.11
, pp. 779-791
-
-
Krey, G.1
Braissant, O.2
L'Horset, F.3
Kalkhoven, E.4
Perroud, M.5
Parker, M.G.6
Wahli, W.7
-
29
-
-
0037128209
-
PEX11 promotes peroxisome division independently of peroxisome metabolism
-
Li, X. and Gould, S. J. (2002). PEX11 promotes peroxisome division independently of peroxisome metabolism. J. Cell Biol. 156, 643-651.
-
(2002)
J. Cell Biol.
, vol.156
, pp. 643-651
-
-
Li, X.1
Gould, S.J.2
-
30
-
-
0037930873
-
The dynamin-like GTPase DLP1 is essential for peroxisome division and is recruited to peroxisomes in part by PEX11
-
Li, X. and Gould, S. J. (2003). The dynamin-like GTPase DLP1 is essential for peroxisome division and is recruited to peroxisomes in part by PEX11. J. Biol. Chem. 278, 17012-17020.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 17012-17020
-
-
Li, X.1
Gould, S.J.2
-
31
-
-
0036882106
-
PEX11 is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferation
-
Li, X., Baumgart, E., Dong, G. X., Morrell, J. C., Jimenez-Sanchez, G., Valle, D., Smith, K. D. and Gould, S. J. (2002a). PEX11 is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferation. Mol. Cell. Biol. 22, 8226-8240.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 8226-8240
-
-
Li, X.1
Baumgart, E.2
Dong, G.X.3
Morrell, J.C.4
Jimenez-Sanchez, G.5
Valle, D.6
Smith, K.D.7
Gould, S.J.8
-
32
-
-
0036261777
-
PEX11β deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function
-
Li, X., Baumgart, E., Morrell, J. C., Jimenez-Sanchez, G., Valle, D. and Gould, S. J. (2002b). PEX11β deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function. Mol. Cell. Biol. 22, 4358-4365.
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 4358-4365
-
-
Li, X.1
Baumgart, E.2
Morrell, J.C.3
Jimenez-Sanchez, G.4
Valle, D.5
Gould, S.J.6
-
33
-
-
33646892646
-
Dynasore, a cell-permeable inhibitor of dynamin
-
Macia, E., Ehrlich, M., Massol, R., Boucrot, E., Brunner, C. and Kirchhausen, T. (2006). Dynasore, a cell-permeable inhibitor of dynamin. Dev. Cell 10, 839-850.
-
(2006)
Dev. Cell
, vol.10
, pp. 839-850
-
-
Macia, E.1
Ehrlich, M.2
Massol, R.3
Boucrot, E.4
Brunner, C.5
Kirchhausen, T.6
-
34
-
-
0029792856
-
Redoxsensitive homodimerization of Pex11p: a proposed mechanism to regulate peroxisomal division
-
Marshall, P. A., Dyer, J. M., Quick, M. E. and Goodman, J. M. (1996). Redoxsensitive homodimerization of Pex11p: a proposed mechanism to regulate peroxisomal division. J. Cell Biol. 135, 123-137.
-
(1996)
J. Cell Biol.
, vol.135
, pp. 123-137
-
-
Marshall, P.A.1
Dyer, J.M.2
Quick, M.E.3
Goodman, J.M.4
-
35
-
-
0029584553
-
Polyunsaturated fatty acids in the developing human brain, erythrocytes and plasma in peroxisomal disease: therapeutic implications
-
Martinez, M. (1995). Polyunsaturated fatty acids in the developing human brain, erythrocytes and plasma in peroxisomal disease: therapeutic implications. J. Inherit. Metab. Dis. 18 Suppl. 1, 61-75.
-
(1995)
J. Inherit. Metab. Dis.
, vol.18
, Issue.SUPPL. 1
, pp. 61-75
-
-
Martinez, M.1
-
36
-
-
0027532282
-
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters
-
Mosser, J., Douar, A.-M., Sarde, C.-O., Kioschis, P. R. F., Moser, H., Poustka, A.-M., Mandel, J.-L. and Aubourg, P. (1993). Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters. Nature 361, 726-730.
-
(1993)
Nature
, vol.361
, pp. 726-730
-
-
Mosser, J.1
Douar, A.-M.2
Sarde, C.-O.3
Kioschis, P.R.F.4
Moser, H.5
Poustka, A.-M.6
Mandel, J.-L.7
Aubourg, P.8
-
37
-
-
33845982949
-
Molecular mechanisms of import of peroxisometargeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL
-
Mukai, S. and Fujiki, Y. (2006). Molecular mechanisms of import of peroxisometargeting signal type 2 (PTS2) proteins by PTS2 receptor Pex7p and PTS1 receptor Pex5pL. J. Biol. Chem. 281, 37311-37320.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 37311-37320
-
-
Mukai, S.1
Fujiki, Y.2
-
38
-
-
0037088664
-
Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells
-
Mukai, S., Ghaedi, K. and Fujiki, Y. (2002). Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells. J. Biol. Chem. 277, 9548-9561.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 9548-9561
-
-
Mukai, S.1
Ghaedi, K.2
Fujiki, Y.3
-
39
-
-
0031656796
-
Mutation 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. (1998a). Mutation 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
-
40
-
-
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. et al. (1998b). 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
-
41
-
-
0032734577
-
The dynamin-like protein DLP1 is essential for normal distribution and morphology of the endoplasmic reticulum and mitochondria in mammalian cells
-
Pitts, K. R., Yoon, Y., Krueger, E. W. and McNiven, M. A. (1999). The dynamin-like protein DLP1 is essential for normal distribution and morphology of the endoplasmic reticulum and mitochondria in mammalian cells. Mol. Biol. Cell 10, 4403-4417.
-
(1999)
Mol. Biol. Cell
, vol.10
, pp. 4403-4417
-
-
Pitts, K.R.1
Yoon, Y.2
Krueger, E.W.3
McNiven, M.A.4
-
42
-
-
0023878166
-
A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)
-
Poll-The, B. T., Roels, E., Ogier, H., Scotto, J., Vamecq, J., Schutgens, R. B. H., van Roermund, C. W. T., van Wijland, M. J. A., Schram, A. W., Tager, J. M. et al. (1988). A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy). Am. J. Hum. Genet. 42, 422-434.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 422-434
-
-
Poll-The, B.T.1
Roels, E.2
Ogier, H.3
Scotto, J.4
Vamecq, J.5
Schutgens, R.B.H.6
van Roermund, C.W.T.7
van Wijland, M.J.A.8
Schram, A.W.9
Tager, J.M.10
-
43
-
-
0023932509
-
Peroxisomal membrane ghosts in Zellweger syndrome- aberrant organelle assembly
-
Santos, M. J., Imanaka, T., Shio, H., Small, G. M. and Lazarow, P. B. (1988). Peroxisomal membrane ghosts in Zellweger syndrome- aberrant organelle assembly. Science 239, 1536-1538.
-
(1988)
Science
, vol.239
, pp. 1536-1538
-
-
Santos, M.J.1
Imanaka, T.2
Shio, H.3
Small, G.M.4
Lazarow, P.B.5
-
44
-
-
78249268827
-
RhoA regulates peroxisome association to microtubules and the actin cytoskeleton
-
Schollenberger, L., Gronemeyer, T., Huber, C. M., Lay, D., Wiese, S., Meyer, H. E., Warscheid, B., Saffrich, R., Peränen, J., Gorgas, K. et al. (2010). RhoA regulates peroxisome association to microtubules and the actin cytoskeleton. PLoS ONE 5, e13886.
-
(2010)
PLoS ONE
, vol.5
-
-
Schollenberger, L.1
Gronemeyer, T.2
Huber, C.M.3
Lay, D.4
Wiese, S.5
Meyer, H.E.6
Warscheid, B.7
Saffrich, R.8
Peränen, J.9
Gorgas, K.10
-
45
-
-
0032491315
-
Expression of PEX11β mediates peroxisome proliferation in the absence of extracellular stimuli
-
Schrader, M., Reuber, B. E., Morrell, J. C., Jimenez-Sanchez, G., Obie, C., Stroh, T. A., Valle, D., Schroer, T. A. and Gould, S. J. (1998). Expression of PEX11β mediates peroxisome proliferation in the absence of extracellular stimuli. J. Biol. Chem. 273, 29607-29614.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 29607-29614
-
-
Schrader, M.1
Reuber, B.E.2
Morrell, J.C.3
Jimenez-Sanchez, G.4
Obie, C.5
Stroh, T.A.6
Valle, D.7
Schroer, T.A.8
Gould, S.J.9
-
46
-
-
0033617195
-
The peroxin Pex14p: cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis
-
Shimizu, N., Itoh, R., Hirono, Y., Otera, H., Ghaedi, K., Tateishi, K., Tamura, S., Okumoto, K., Harano, T., Mukai, S. et al. (1999). The peroxin Pex14p: cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis. J. Biol. Chem. 274, 12593-12604.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 12593-12604
-
-
Shimizu, N.1
Itoh, R.2
Hirono, Y.3
Otera, H.4
Ghaedi, K.5
Tateishi, K.6
Tamura, S.7
Okumoto, K.8
Harano, T.9
Mukai, S.10
-
47
-
-
1642458359
-
Tissue-selective, bidirectional regulation of PEX11α and perilipin genes through a common peroxisome proliferator response element
-
Shimizu, M., Takeshita, A., Tsukamoto, T., Gonzalez, F. J. and Osumi, T. (2004). Tissue-selective, bidirectional regulation of PEX11α and perilipin genes through a common peroxisome proliferator response element. Mol. Cell. Biol. 24, 1313-1323.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 1313-1323
-
-
Shimizu, M.1
Takeshita, A.2
Tsukamoto, T.3
Gonzalez, F.J.4
Osumi, T.5
-
48
-
-
33745098383
-
Cytosolic phospholipase A2: biochemical properties and physiological roles
-
Shimizu, T., Ohto, T. and Kita, Y. (2006). Cytosolic phospholipase A2: biochemical properties and physiological roles. IUBMB Life 58, 328-333.
-
(2006)
IUBMB Life
, vol.58
, pp. 328-333
-
-
Shimizu, T.1
Ohto, T.2
Kita, Y.3
-
49
-
-
0026492894
-
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome
-
Shimozawa, N., Tsukamoto, T., Suzuki, Y., Orii, T. and Fujiki, Y. (1992a). Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome. J. Clin. Invest. 90, 1864-1870.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 1864-1870
-
-
Shimozawa, N.1
Tsukamoto, T.2
Suzuki, Y.3
Orii, T.4
Fujiki, Y.5
-
50
-
-
0026523576
-
A human gene responsible for Zellweger syndrome that affects peroxisome assembly
-
Shimozawa, N., Tsukamoto, T., Suzuki, Y., Orii, T., Shirayoshi, Y., Mori, T. and Fujiki, Y. (1992b). A human gene responsible for Zellweger syndrome that affects peroxisome assembly. Science 255, 1132-1134.
-
(1992)
Science
, vol.255
, pp. 1132-1134
-
-
Shimozawa, N.1
Tsukamoto, T.2
Suzuki, Y.3
Orii, T.4
Shirayoshi, Y.5
Mori, T.6
Fujiki, Y.7
-
51
-
-
58649098789
-
Acyl-CoA:lysophospholipid acyltransferases
-
Shindou, H. and Shimizu, T. (2009). Acyl-CoA:lysophospholipid acyltransferases. J. Biol. Chem. 284, 1-5.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 1-5
-
-
Shindou, H.1
Shimizu, T.2
-
52
-
-
0032893407
-
X-linked adrenoleukodystrophy: genes, mutations, and phenotypes
-
Smith, K. D., Kemp, S., Braiterman, L. T., Lu, J. F., Wei, H. M., Geraghty, M., Stetten, G., Bergin, J. S., Pevsner, J. and Watkins, P. A. (1999). X-linked adrenoleukodystrophy: genes, mutations, and phenotypes. Neurochem. Res. 24, 521-535.
-
(1999)
Neurochem. Res.
, vol.24
, pp. 521-535
-
-
Smith, K.D.1
Kemp, S.2
Braiterman, L.T.3
Lu, J.F.4
Wei, H.M.5
Geraghty, M.6
Stetten, G.7
Bergin, J.S.8
Pevsner, J.9
Watkins, P.A.10
-
53
-
-
0035851141
-
Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis
-
Su, H. M., Moser, A. B., Moser, H. W. and Watkins, P. A. (2001). Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis. J. Biol. Chem. 276, 38115-38120.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 38115-38120
-
-
Su, H.M.1
Moser, A.B.2
Moser, H.W.3
Watkins, P.A.4
-
54
-
-
0031941276
-
Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement
-
Subramani, S. (1998). Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement. Physiol. Rev. 78, 171-188.
-
(1998)
Physiol. Rev.
, vol.78
, pp. 171-188
-
-
Subramani, S.1
-
55
-
-
0025977715
-
Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases
-
Suzuki, Y., Shimozawa, N., Yajima, S., Yamaguchi, S., Orii, T. and Hashimoto, T. (1991). Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases. Biochem. Pharmacol. 41, 453-456.
-
(1991)
Biochem. Pharmacol.
, vol.41
, pp. 453-456
-
-
Suzuki, Y.1
Shimozawa, N.2
Yajima, S.3
Yamaguchi, S.4
Orii, T.5
Hashimoto, T.6
-
56
-
-
0031279890
-
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder
-
Suzuki, Y., Jiang, L. L., Souri, M., Miyazawa, S., Fukuda, S., Zhang, Z., Une, M., Shimozawa, N., Kondo, N., Orii, T. and Hashimoto, T. (1997). D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. Am. J. Hum. Genet. 61, 1153-1162.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1153-1162
-
-
Suzuki, Y.1
Jiang, L.L.2
Souri, M.3
Miyazawa, S.4
Fukuda, S.5
Zhang, Z.6
Une, M.7
Shimozawa, N.8
Kondo, N.9
Orii, T.10
Hashimoto, T.11
-
57
-
-
0037462961
-
cDNA cloning and characterization of the third isoform of human peroxin Pex11p
-
Tanaka, A., Okumoto, K. and Fujiki, Y. (2003). cDNA cloning and characterization of the third isoform of human peroxin Pex11p. Biochem. Biophys. Res. Commun. 300, 819-823.
-
(2003)
Biochem. Biophys. Res. Commun.
, vol.300
, pp. 819-823
-
-
Tanaka, A.1
Okumoto, K.2
Fujiki, Y.3
-
58
-
-
33646136227
-
Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene
-
Tanaka, A., Kobayashi, S. and Fujiki, Y. (2006). Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene. Exp. Cell Res. 312, 1671-1684.
-
(2006)
Exp. Cell Res.
, vol.312
, pp. 1671-1684
-
-
Tanaka, A.1
Kobayashi, S.2
Fujiki, Y.3
-
59
-
-
0025342563
-
Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes
-
Tsukamoto, T., Yokota, S. and Fujiki, Y. (1990). Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes. J. Cell Biol. 110, 651-660.
-
(1990)
J. Cell Biol.
, vol.110
, pp. 651-660
-
-
Tsukamoto, T.1
Yokota, S.2
Fujiki, Y.3
-
60
-
-
4744371532
-
Peroxisomes, lipid metabolism, and peroxisomal disorders
-
Wanders, R. J. (2004). Peroxisomes, lipid metabolism, and peroxisomal disorders. Mol. Genet. Metab. 83, 16-27.
-
(2004)
Mol. Genet. Metab.
, vol.83
, pp. 16-27
-
-
Wanders, R.J.1
-
61
-
-
33845304296
-
Peroxisomal disorders: the single peroxisomal enzyme deficiencies
-
Wanders, R. J. and Waterham, H. R. (2006). Peroxisomal disorders: the single peroxisomal enzyme deficiencies. Biochim. Biophys. Acta 1763, 1707-1720.
-
(2006)
Biochim. Biophys. Acta
, vol.1763
, pp. 1707-1720
-
-
Wanders, R.J.1
Waterham, H.R.2
-
62
-
-
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
-
63
-
-
34247525092
-
A lethal defect of mitochondrial and peroxisomal fission
-
Waterham, H. R., Koster, J., van Roermund, C. W. T., Mooyer, P. A. W., Wanders, R. J. A. and Leonard, J. V. (2007). A lethal defect of mitochondrial and peroxisomal fission. N. Engl. J. Med. 356, 1736-1741.
-
(2007)
N. Engl. J. Med.
, vol.356
, pp. 1736-1741
-
-
Waterham, H.R.1
Koster, J.2
van Roermund, C.W.T.3
Mooyer, P.A.W.4
Wanders, R.J.A.5
Leonard, J.V.6
-
64
-
-
0034059821
-
Pharmacological induction of peroxisomes in peroxisome biogenesis disorders
-
Wei, H., Kemp, S., McGuinness, M. C., Moser, A. B. and Smith, K. D. (2000). Pharmacological induction of peroxisomes in peroxisome biogenesis disorders. Ann. Neurol. 47, 286-296.
-
(2000)
Ann. Neurol.
, vol.47
, pp. 286-296
-
-
Wei, H.1
Kemp, S.2
McGuinness, M.C.3
Moser, A.B.4
Smith, K.D.5
-
65
-
-
0031030969
-
Visualization of the peroxisomal compartment in living mammalian cells: dynamic behavior and association with microtubules
-
Wiemer, E. A. C., Wenzel, T., Deerinck, T. J., Ellisman, M. H. and Subramani, S. (1997). Visualization of the peroxisomal compartment in living mammalian cells: dynamic behavior and association with microtubules. J. Cell Biol. 136, 71-80.
-
(1997)
J. Cell Biol.
, vol.136
, pp. 71-80
-
-
Wiemer, E.A.C.1
Wenzel, T.2
Deerinck, T.J.3
Ellisman, M.H.4
Subramani, S.5
-
66
-
-
0037860757
-
Identification of hepatic peroxisomal phospholipase A(2) and characterization of arachidonic acid-containing choline glycerophospholipids in hepatic peroxisomes
-
Yang, J., Han, X. and Gross, R. W. (2003). Identification of hepatic peroxisomal phospholipase A(2) and characterization of arachidonic acid-containing choline glycerophospholipids in hepatic peroxisomes. FEBS Lett. 546, 247-250.
-
(2003)
FEBS Lett
, vol.546
, pp. 247-250
-
-
Yang, J.1
Han, X.2
Gross, R.W.3
-
67
-
-
33749265862
-
Formation of elongated giant mitochondria in DFO-induced cellular senescence: involvement of enhanced fusion process through modulation of Fis1
-
Yoon, Y. S., Yoon, D. S., Lim, I. K., Yoon, S. H., Chung, H. Y., Rojo, M., Malka, F., Jou, M. J., Martinou, J. C. and Yoon, G. (2006). Formation of elongated giant mitochondria in DFO-induced cellular senescence: involvement of enhanced fusion process through modulation of Fis1. J. Cell Physiol. 209, 468-480.
-
(2006)
J. Cell Physiol.
, vol.209
, pp. 468-480
-
-
Yoon, Y.S.1
Yoon, D.S.2
Lim, I.K.3
Yoon, S.H.4
Chung, H.Y.5
Rojo, M.6
Malka, F.7
Jou, M.J.8
Martinou, J.C.9
Yoon, G.10
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