-
1
-
-
0030725335
-
Molecular defects in genetic diseases of peroxisomes
-
Fujiki, Y. (1997) Molecular defects in genetic diseases of peroxisomes. Biochim. Biophys. Acta 1361, 235-250
-
(1997)
Biochim. Biophys. Acta
, vol.1361
, pp. 235-250
-
-
Fujiki, Y.1
-
2
-
-
15444353327
-
Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (peroxisomal ghosts), representing a novel complementation group in mammals
-
Kinoshita, N., Ghaedi, K., Shimozawa, N., Wanders, R.J.A., Matsuzono, Y., Imanaka, T., Okumoto, K., Suzuki, Y., Kondo, N., and Fujiki, Y. (1998) Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (peroxisomal ghosts), representing a novel complementation group in mammals. J. Biol. Chem. 273, 24122-24130
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 24122-24130
-
-
Kinoshita, N.1
Ghaedi, K.2
Shimozawa, N.3
Wanders, R.J.A.4
Matsuzono, Y.5
Imanaka, T.6
Okumoto, K.7
Suzuki, Y.8
Kondo, N.9
Fujiki, Y.10
-
3
-
-
0033134119
-
Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals
-
Ghaedi, K., Itagaki, A., Toyama, R., Tamura, S., Matsumura, T., Kawai, A., Shimozawa, N., Suzuki, Y., Kondo, N., and Fujiki, Y. (1999) Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals. Exp. Cell Res. 248, 482-488
-
(1999)
Exp. Cell Res.
, vol.248
, pp. 482-488
-
-
Ghaedi, K.1
Itagaki, A.2
Toyama, R.3
Tamura, S.4
Matsumura, T.5
Kawai, A.6
Shimozawa, N.7
Suzuki, Y.8
Kondo, N.9
Fujiki, Y.10
-
4
-
-
0033134180
-
Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein
-
Ghaedi, K., Kawai, A., Okumoto, K., Tamura, S., Shimozawa, N., Suzuki, Y., Kondo, N., and Fujiki, Y. (1999) Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein. Exp. Cell Res. 248, 489-497
-
(1999)
Exp. Cell Res.
, vol.248
, pp. 489-497
-
-
Ghaedi, K.1
Kawai, A.2
Okumoto, K.3
Tamura, S.4
Shimozawa, N.5
Suzuki, Y.6
Kondo, N.7
Fujiki, Y.8
-
5
-
-
0032471958
-
Genetic basis of peroxisome assembly mutants of humans, CHO cells and yeast: Identification of a new complementation group of peroxisome biogenesis disorders, absent from peroxisomal membrane ghosts
-
Shimozawa, N., Suzuki, Y., Zhang, Z., Imamura, A., Kondo, N., Kinoshita, N., Fujiki, Y., Tsukamoto, T., Osumi, T., Imanaka, T., Orii, T., Beemer, F., Mooijer, P., Dekker, C., and Wanders, R.J.A. (1998) Genetic basis of peroxisome assembly mutants of humans, CHO cells and yeast: identification of a new complementation group of peroxisome biogenesis disorders, absent from peroxisomal membrane ghosts. Am. J. Hum. Genet. 63, 1898-1903
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1898-1903
-
-
Shimozawa, N.1
Suzuki, Y.2
Zhang, Z.3
Imamura, A.4
Kondo, N.5
Kinoshita, N.6
Fujiki, Y.7
Tsukamoto, T.8
Osumi, T.9
Imanaka, T.10
Orii, T.11
Beemer, F.12
Mooijer, P.13
Dekker, C.14
Wanders, R.J.A.15
-
6
-
-
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
-
7
-
-
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
-
8
-
-
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. (1992) 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
-
9
-
-
0028324958
-
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization
-
Masuno, M., Shimozawa, N., Suzuki, Y., Kondo, N., Orii, T., Tsukamoto, T., Osumi, T., Fujiki, Y., Imaizumi, K., and Kuroki, Y. (1994) Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization. Genomics 20, 141-142
-
(1994)
Genomics
, vol.20
, pp. 141-142
-
-
Masuno, M.1
Shimozawa, N.2
Suzuki, Y.3
Kondo, N.4
Orii, T.5
Tsukamoto, T.6
Osumi, T.7
Fujiki, Y.8
Imaizumi, K.9
Kuroki, Y.10
-
10
-
-
0027535994
-
Prenatal diagnosis of Zellweger syndrome using DNA analysis
-
Shimozawa, N., Tsukamoto, T., Suzuki, Y., Orii, T., and Fujiki, Y. (1993) Prenatal diagnosis of Zellweger syndrome using DNA analysis. Prenat. Diagnosis 13, 149
-
(1993)
Prenat. Diagnosis
, vol.13
, pp. 149
-
-
Shimozawa, N.1
Tsukamoto, T.2
Suzuki, Y.3
Orii, T.4
Fujiki, Y.5
-
11
-
-
0027965618
-
Peroxisome assembly factor 1: Nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis
-
Tsukamoto, T., Shimozawa, N., and Fujiki, Y. (1994) Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis. Mol. Cell. Biol. 14, 5458-5465
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 5458-5465
-
-
Tsukamoto, T.1
Shimozawa, N.2
Fujiki, Y.3
-
12
-
-
0027319019
-
Peroxisome-deficient Chinese hamster ovary cells with point mutations in peroxisome assembly factor-1
-
Thieringer, R. and Raetz, C.R.H. (1993) Peroxisome-deficient Chinese hamster ovary cells with point mutations in peroxisome assembly factor-1. J. Biol. Chem. 268, 12631-12636
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 12631-12636
-
-
Thieringer, R.1
Raetz, C.R.H.2
-
13
-
-
0030003144
-
Does this have a familiar RING?
-
Saurin, A.J., Borden, K.L.B., Boddy, M.N., and Freemont, P.S. (1996) Does this have a familiar RING? Trends Biochem. Sci. 21, 208-214
-
(1996)
Trends Biochem. Sci.
, vol.21
, pp. 208-214
-
-
Saurin, A.J.1
Borden, K.L.B.2
Boddy, M.N.3
Freemont, P.S.4
-
15
-
-
0029990950
-
The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1
-
Waterham, H.R., de Vries, Y., Russel, K.A., Xie, W., Vennhuis, M., and Cregg, J.M. (1996) The Pichia pastoris PER6 gene product is a peroxisomal integral membrane protein essential for peroxisome biogenesis and has sequence similarity to the Zellweger syndrome protein PAF-1. Mol. Cell. Biol. 16, 2527-2536
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 2527-2536
-
-
Waterham, H.R.1
De Vries, Y.2
Russel, K.A.3
Xie, W.4
Vennhuis, M.5
Cregg, J.M.6
-
16
-
-
0029833897
-
The Yarrowia lipolytica gene PAY5 encodes a peroxisomal integral membrane protein homologous to the mammalian peroxisome assembly factor PAF-1
-
Eitzen, G.A., Titorenko, V.I., Smith, J.J., Veenhuis, M., Szilard, R.K., and Rachubinski, R.A. (1996) The Yarrowia lipolytica gene PAY5 encodes a peroxisomal integral membrane protein homologous to the mammalian peroxisome assembly factor PAF-1. J. Biol. Chem. 271, 20300-20306
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 20300-20306
-
-
Eitzen, G.A.1
Titorenko, V.I.2
Smith, J.J.3
Veenhuis, M.4
Szilard, R.K.5
Rachubinski, R.A.6
-
17
-
-
0028999113
-
A nonmammalian homolog of the PAF1 gene (Zellweger syndrome) discovered as a gene involved in caryogamy in the fungus Podospora anserina
-
Berteaux-Lecellier, V., Picard, M., Thompson-Coffe, C., Zickler, D., Panvier-Adoutte, A., and Simonet, J.-M. (1995) A nonmammalian homolog of the PAF1 gene (Zellweger syndrome) discovered as a gene involved in caryogamy in the fungus Podospora anserina. Cell 81, 1043-1051
-
(1995)
Cell
, vol.81
, pp. 1043-1051
-
-
Berteaux-Lecellier, V.1
Picard, M.2
Thompson-Coffe, C.3
Zickler, D.4
Panvier-Adoutte, A.5
Simonet, J.-M.6
-
18
-
-
0031018416
-
Functional identification of a Leishmania gene related to the peroxin 2 gene reveals common ancestry of glycosomes and peroxisomes
-
Flaspohler, J.A., Rickoll, W.L., Beverley, S.M., and Parsons, M. (1997) Functional identification of a Leishmania gene related to the peroxin 2 gene reveals common ancestry of glycosomes and peroxisomes. Mol. Cell. Biol. 17, 1093-1101
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 1093-1101
-
-
Flaspohler, J.A.1
Rickoll, W.L.2
Beverley, S.M.3
Parsons, M.4
-
19
-
-
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
-
20
-
-
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., and Fujiki, Y. (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
Fujiki, Y.11
-
21
-
-
0031962116
-
Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: Studies with PEX5-defective CHO cell mutants
-
Otera, H., Tateishi, K., Okumoto, 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 mutants. Mol. Cell. Biol. 18, 388-399
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 388-399
-
-
Otera, H.1
Tateishi, K.2
Okumoto, 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
-
22
-
-
0026643496
-
Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal
-
Miura, S., Kasuya-Arai, I., Mori, H., Miyazawa, S., Osumi, T., Hashimoto, T., and Fujiki, Y. (1992) Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal. J. Biol. Chem. 267, 14405-14411
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 14405-14411
-
-
Miura, S.1
Kasuya-Arai, I.2
Mori, H.3
Miyazawa, S.4
Osumi, T.5
Hashimoto, T.6
Fujiki, Y.7
-
23
-
-
0020039866
-
Isolation of intracellular membranes by means of sodium carbonate treatment: Application to endoplasmic reticulum
-
Fujiki, Y., Hubbard, A.L., Fowler, S., and Lazarow, P.B. (1982) Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum. J. Cell Biol. 93, 97-102
-
(1982)
J. Cell Biol.
, vol.93
, pp. 97-102
-
-
Fujiki, Y.1
Hubbard, A.L.2
Fowler, S.3
Lazarow, P.B.4
-
24
-
-
0030890954
-
Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways
-
Albertini, M., Rehling, P., Erdmann, R., Girzalsky, W., Kiel, J.A.K.W., Veenhuis, M., and Kunau, W.-H. (1997) Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways. Cell 89, 83-92
-
(1997)
Cell
, vol.89
, pp. 83-92
-
-
Albertini, M.1
Rehling, P.2
Erdmann, R.3
Girzalsky, W.4
Kiel, J.A.K.W.5
Veenhuis, M.6
Kunau, W.-H.7
-
25
-
-
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. (1998) 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
-
26
-
-
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
-
27
-
-
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. Nature Genet. 15, 385-388
-
(1997)
Nature Genet.
, vol.15
, pp. 385-388
-
-
Chang, C.-C.1
Lee, W.-H.2
Moser, H.3
Valle, D.4
Gould, S.J.5
-
28
-
-
0031279088
-
PEX12 encodes an integral membrane protein of peroxisomes
-
Okumoto, K. and Fujiki, Y. (1997) PEX12 encodes an integral membrane protein of peroxisomes. Nature Genet. 17, 265-266
-
(1997)
Nature Genet.
, vol.17
, pp. 265-266
-
-
Okumoto, K.1
Fujiki, Y.2
-
29
-
-
0018088549
-
Presence of NADPH-cytochrome P-450 reductase in rat liver Golgi membranes. Evidence obtained by immunoadsorption method
-
Ito, A. and Palade, G. E. (1978) Presence of NADPH-cytochrome P-450 reductase in rat liver Golgi membranes. Evidence obtained by immunoadsorption method. J. Cell Biol. 79, 590-597
-
(1978)
J. Cell Biol.
, vol.79
, pp. 590-597
-
-
Ito, A.1
Palade, G.E.2
|