-
1
-
-
41149158491
-
The peroxisome: still a mysterious organelle
-
Schrader M, Fahimi HD. The peroxisome: still a mysterious organelle. Histochem Cell Biol 2008;129:421-440.
-
(2008)
Histochem Cell Biol
, vol.129
, pp. 421-440
-
-
Schrader, M.1
Fahimi, H.D.2
-
2
-
-
33746366462
-
Biochemistry of mammalian peroxisomes revisited
-
Wanders RJ, Waterham HR. Biochemistry of mammalian peroxisomes revisited. Annu Rev Biochem 2006;75:295-332.
-
(2006)
Annu Rev Biochem
, vol.75
, pp. 295-332
-
-
Wanders, R.J.1
Waterham, H.R.2
-
3
-
-
33845336846
-
Peroxisome biogenesis disorders
-
Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW. Peroxisome biogenesis disorders. Biochim Biophys Acta 2006;1763:1733-1748.
-
(2006)
Biochim Biophys Acta
, vol.1763
, pp. 1733-1748
-
-
Steinberg, S.J.1
Dodt, G.2
Raymond, G.V.3
Braverman, N.E.4
Moser, A.B.5
Moser, H.W.6
-
4
-
-
14244267510
-
Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders
-
Wanders RJ, Waterham HR. Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders. Clin Genet 2005;67:107-133.
-
(2005)
Clin Genet
, vol.67
, pp. 107-133
-
-
Wanders, R.J.1
Waterham, H.R.2
-
5
-
-
0033970416
-
Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid alpha- and beta-oxidation systems in humans
-
Wanders RJ, van Grunsven EG, Jansen GA. Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid alpha- and beta-oxidation systems in humans. Biochem Soc Trans 2000;28:141-149.
-
(2000)
Biochem Soc Trans
, vol.28
, pp. 141-149
-
-
Wanders, R.J.1
van Grunsven, E.G.2
Jansen, G.A.3
-
7
-
-
0034515057
-
The genetics of peroxisome biogenesis
-
Sacksteder KA, Gould SJ. The genetics of peroxisome biogenesis. Annu Rev Genet 2000;34:623-652.
-
(2000)
Annu Rev Genet
, vol.34
, pp. 623-652
-
-
Sacksteder, K.A.1
Gould, S.J.2
-
8
-
-
0033794897
-
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. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G. Am J Hum Genet 2000;67:967-975.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 967-975
-
-
Muntau, A.C.1
Mayerhofer, P.U.2
Paton, B.C.3
Kammerer, S.4
Roscher, A.A.5
-
9
-
-
0033804750
-
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G
-
Ghaedi K, Honsho M, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G. Am J Hum Genet 2000;67:976-981.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 976-981
-
-
Ghaedi, K.1
Honsho, M.2
Shimozawa, N.3
Suzuki, Y.4
Kondo, N.5
Fujiki, Y.6
-
10
-
-
0033601767
-
Peroxisome synthesis in the absence of preexisting peroxisomes
-
South ST, Gould SJ. Peroxisome synthesis in the absence of preexisting peroxisomes. J Cell Biol 1999;144:255-266.
-
(1999)
J Cell Biol
, vol.144
, pp. 255-266
-
-
South, S.T.1
Gould, S.J.2
-
11
-
-
13044312086
-
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
-
Matsuzono Y, Kinoshita N, Tamura S, Shimozawa N, Hamasaki M, Ghaedi K, Wanders RJ, Suzuki Y, Kondo N, Fujiki Y. Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly. Proc Natl Acad Sci USA 1999;96:2116-2121.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2116-2121
-
-
Matsuzono, Y.1
Kinoshita, N.2
Tamura, S.3
Shimozawa, N.4
Hamasaki, M.5
Ghaedi, K.6
Wanders, R.J.7
Suzuki, Y.8
Kondo, N.9
Fujiki, Y.10
-
12
-
-
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, Fujiki Y. Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. Am J Hum Genet 1998;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
-
13
-
-
78650729949
-
A vesicle carrier that mediates peroxisome protein traffic from the endoplasmic reticulum
-
Lam SK, Yoda N, Schekman R. A vesicle carrier that mediates peroxisome protein traffic from the endoplasmic reticulum. Proc Natl Acad Sci USA 2010;107:21523-21528.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 21523-21528
-
-
Lam, S.K.1
Yoda, N.2
Schekman, R.3
-
14
-
-
27144457472
-
Pex3p initiates the formation of a preperoxisomal compartment from a subdomain of the endoplasmic reticulum in Saccharomyces cerevisiae
-
Tam YY, Fagarasanu A, Fagarasanu M, Rachubinski RA. Pex3p initiates the formation of a preperoxisomal compartment from a subdomain of the endoplasmic reticulum in Saccharomyces cerevisiae. J Biol Chem 2005;280:34933-34939.
-
(2005)
J Biol Chem
, vol.280
, pp. 34933-34939
-
-
Tam, Y.Y.1
Fagarasanu, A.2
Fagarasanu, M.3
Rachubinski, R.A.4
-
15
-
-
22144465170
-
Contribution of the endoplasmic reticulum to peroxisome formation
-
Hoepfner D, Schildknegt D, Braakman I, Philippsen P, Tabak HF. Contribution of the endoplasmic reticulum to peroxisome formation. Cell 2005;122:85-95.
-
(2005)
Cell
, vol.122
, pp. 85-95
-
-
Hoepfner, D.1
Schildknegt, D.2
Braakman, I.3
Philippsen, P.4
Tabak, H.F.5
-
16
-
-
46249130452
-
Dnm1p-dependent peroxisome fission requires Caf4p, Mdv1p and Fis1p
-
Motley AM, Ward GP, Hettema EH. Dnm1p-dependent peroxisome fission requires Caf4p, Mdv1p and Fis1p. J Cell Sci 2008;121:1633-1640.
-
(2008)
J Cell Sci
, vol.121
, pp. 1633-1640
-
-
Motley, A.M.1
Ward, G.P.2
Hettema, E.H.3
-
17
-
-
77953507085
-
Peroxisomal membrane proteins insert into the endoplasmic reticulum
-
van der Zand A, Braakman I, Tabak HF. Peroxisomal membrane proteins insert into the endoplasmic reticulum. Mol Biol Cell 2010;21:2057-2065.
-
(2010)
Mol Biol Cell
, vol.21
, pp. 2057-2065
-
-
van der Zand, A.1
Braakman, I.2
Tabak, H.F.3
-
18
-
-
79955505833
-
Peroxisome assembly: matrix and membrane protein biogenesis
-
Ma C, Agrawal G, Subramani S. Peroxisome assembly: matrix and membrane protein biogenesis. J Cell Biol 2011;193:7-16.
-
(2011)
J Cell Biol
, vol.193
, pp. 7-16
-
-
Ma, C.1
Agrawal, G.2
Subramani, S.3
-
19
-
-
68049105069
-
Pex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblasts
-
Toro AA, Araya CA, Cordova GJ, Arredondo CA, Cardenas HG, Moreno RE, Venegas A, Koenig CS, Cancino J, Gonzalez A, Santos MJ. Pex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblasts. J Cell Biochem 2009;107:1083-1096.
-
(2009)
J Cell Biochem
, vol.107
, pp. 1083-1096
-
-
Toro, A.A.1
Araya, C.A.2
Cordova, G.J.3
Arredondo, C.A.4
Cardenas, H.G.5
Moreno, R.E.6
Venegas, A.7
Koenig, C.S.8
Cancino, J.9
Gonzalez, A.10
Santos, M.J.11
-
20
-
-
33646791462
-
The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER
-
Kim PK, Mullen RT, Schumann U, Lippincott-Schwartz J. The origin and maintenance of mammalian peroxisomes involves a de novo PEX16-dependent pathway from the ER. J Cell Biol 2006;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
-
21
-
-
70350674903
-
Peroxisome dynamics in cultured mammalian cells
-
Huybrechts SJ, Van Veldhoven PP, Brees C, Mannaerts GP, Los GV, Fransen M. Peroxisome dynamics in cultured mammalian cells. Traffic 2009;10:1722-1733.
-
(2009)
Traffic
, vol.10
, pp. 1722-1733
-
-
Huybrechts, S.J.1
Van Veldhoven, P.P.2
Brees, C.3
Mannaerts, G.P.4
Los, G.V.5
Fransen, M.6
-
22
-
-
32144448220
-
In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p
-
Matsuzono Y, Fujiki Y. In vitro transport of membrane proteins to peroxisomes by shuttling receptor Pex19p. J Biol Chem 2006;281:36-42.
-
(2006)
J Biol Chem
, vol.281
, pp. 36-42
-
-
Matsuzono, Y.1
Fujiki, Y.2
-
23
-
-
3042724871
-
Peroxisomal membrane proteins contain common Pex19p-binding sites that are an integral part of their targeting signals
-
Rottensteiner H, Kramer A, Lorenzen S, Stein K, Landgraf C, Volkmer-Engert R, Erdmann R. Peroxisomal membrane proteins contain common Pex19p-binding sites that are an integral part of their targeting signals. Mol Biol Cell 2004;15:3406-3417.
-
(2004)
Mol Biol Cell
, vol.15
, pp. 3406-3417
-
-
Rottensteiner, H.1
Kramer, A.2
Lorenzen, S.3
Stein, K.4
Landgraf, C.5
Volkmer-Engert, R.6
Erdmann, R.7
-
24
-
-
77955430895
-
The peroxisomal receptor Pex19p forms a helical mPTS recognition domain
-
Schueller N, Holton SJ, Fodor K, Milewski M, Konarev P, Stanley WA, Wolf J, Erdmann R, Schliebs W, Song YH, Wilmanns M. The peroxisomal receptor Pex19p forms a helical mPTS recognition domain. EMBO J 2010;29:2491-2500.
-
(2010)
EMBO J
, vol.29
, pp. 2491-2500
-
-
Schueller, N.1
Holton, S.J.2
Fodor, K.3
Milewski, M.4
Konarev, P.5
Stanley, W.A.6
Wolf, J.7
Erdmann, R.8
Schliebs, W.9
Song, Y.H.10
Wilmanns, M.11
-
25
-
-
0345861756
-
PEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteins
-
Jones JM, Morrell JC, Gould SJ. PEX19 is a predominantly cytosolic chaperone and import receptor for class 1 peroxisomal membrane proteins. J Cell Biol 2004;164:57-67.
-
(2004)
J Cell Biol
, vol.164
, pp. 57-67
-
-
Jones, J.M.1
Morrell, J.C.2
Gould, S.J.3
-
26
-
-
4644250692
-
Domain architecture and activity of human Pex19p, a chaperone-like protein for intracellular trafficking of peroxisomal membrane proteins
-
Shibata H, Kashiwayama Y, Imanaka T, Kato H. Domain architecture and activity of human Pex19p, a chaperone-like protein for intracellular trafficking of peroxisomal membrane proteins. J Biol Chem 2004;279:38486-38494.
-
(2004)
J Biol Chem
, vol.279
, pp. 38486-38494
-
-
Shibata, H.1
Kashiwayama, Y.2
Imanaka, T.3
Kato, H.4
-
27
-
-
13844281618
-
Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis
-
Fransen M, Vastiau I, Brees C, Brys V, Mannaerts GP, Van Veldhoven PP. Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis. J Mol Biol 2005;346:1275-1286.
-
(2005)
J Mol Biol
, vol.346
, pp. 1275-1286
-
-
Fransen, M.1
Vastiau, I.2
Brees, C.3
Brys, V.4
Mannaerts, G.P.5
Van Veldhoven, P.P.6
-
28
-
-
33749392686
-
Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation
-
Matsuzono Y, Matsuzaki T, Fujiki Y. Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation. J Cell Sci 2006;119:3539-3550.
-
(2006)
J Cell Sci
, vol.119
, pp. 3539-3550
-
-
Matsuzono, Y.1
Matsuzaki, T.2
Fujiki, Y.3
-
29
-
-
1642394134
-
PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins
-
Fang Y, Morrell JC, Jones JM, Gould SJ. PEX3 functions as a PEX19 docking factor in the import of class I peroxisomal membrane proteins. J Cell Biol 2004;164:863-875.
-
(2004)
J Cell Biol
, vol.164
, pp. 863-875
-
-
Fang, Y.1
Morrell, J.C.2
Jones, J.M.3
Gould, S.J.4
-
30
-
-
0042130361
-
The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis
-
Muntau AC, Roscher AA, Kunau WH, Dodt G. The interaction between human PEX3 and PEX19 characterized by fluorescence resonance energy transfer (FRET) analysis. Eur J Cell Biol 2003;82:333-342.
-
(2003)
Eur J Cell Biol
, vol.82
, pp. 333-342
-
-
Muntau, A.C.1
Roscher, A.A.2
Kunau, W.H.3
Dodt, G.4
-
31
-
-
33845318535
-
Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions
-
Fujiki Y, Matsuzono Y, Matsuzaki T, Fransen M. Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions. Biochim Biophys Acta 2006;1763:1639-1646.
-
(2006)
Biochim Biophys Acta
, vol.1763
, pp. 1639-1646
-
-
Fujiki, Y.1
Matsuzono, Y.2
Matsuzaki, T.3
Fransen, M.4
-
32
-
-
44449122442
-
Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of Trp-104 in Pex3p as a critical residue for the interaction
-
Sato Y, Shibata H, Nakano H, Matsuzono Y, Kashiwayama Y, Kobayashi Y, Fujiki Y, Imanaka T, Kato H. Characterization of the interaction between recombinant human peroxin Pex3p and Pex19p: identification of Trp-104 in Pex3p as a critical residue for the interaction. J Biol Chem 2008;283:6136-6144.
-
(2008)
J Biol Chem
, vol.283
, pp. 6136-6144
-
-
Sato, Y.1
Shibata, H.2
Nakano, H.3
Matsuzono, Y.4
Kashiwayama, Y.5
Kobayashi, Y.6
Fujiki, Y.7
Imanaka, T.8
Kato, H.9
-
33
-
-
77955491804
-
Insights into peroxisome function from the structure of PEX3 in complex with a soluble fragment of PEX19
-
Schmidt F, Treiber N, Zocher G, Bjelic S, Steinmetz MO, Kalbacher H, Stehle T, Dodt G. Insights into peroxisome function from the structure of PEX3 in complex with a soluble fragment of PEX19. J Biol Chem 2010;285:25410-25417.
-
(2010)
J Biol Chem
, vol.285
, pp. 25410-25417
-
-
Schmidt, F.1
Treiber, N.2
Zocher, G.3
Bjelic, S.4
Steinmetz, M.O.5
Kalbacher, H.6
Stehle, T.7
Dodt, G.8
-
34
-
-
78650269198
-
Structural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3p
-
Sato Y, Shibata H, Nakatsu T, Nakano H, Kashiwayama Y, Imanaka T, Kato H. Structural basis for docking of peroxisomal membrane protein carrier Pex19p onto its receptor Pex3p. EMBO J 2010;29:4083-4093.
-
(2010)
EMBO J
, vol.29
, pp. 4083-4093
-
-
Sato, Y.1
Shibata, H.2
Nakatsu, T.3
Nakano, H.4
Kashiwayama, Y.5
Imanaka, T.6
Kato, H.7
-
35
-
-
0032979799
-
Identification and characterization of the human peroxin PEX3
-
Soukupova M, Sprenger C, Gorgas K, Kunau WH, Dodt G. Identification and characterization of the human peroxin PEX3. Eur J Cell Biol 1999;78:357-374.
-
(1999)
Eur J Cell Biol
, vol.78
, pp. 357-374
-
-
Soukupova, M.1
Sprenger, C.2
Gorgas, K.3
Kunau, W.H.4
Dodt, G.5
-
36
-
-
0032486364
-
Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p
-
Kammerer S, Holzinger A, Welsch U, Roscher AA. Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p. FEBS Lett 1998;429:53-60.
-
(1998)
FEBS Lett
, vol.429
, pp. 53-60
-
-
Kammerer, S.1
Holzinger, A.2
Welsch, U.3
Roscher, A.A.4
-
37
-
-
33845955999
-
The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step
-
Pinto MP, Grou CP, Alencastre IS, Oliveira ME, Sa-Miranda C, Fransen M, Azevedo JE. The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step. J Biol Chem 2006;281:34492-34502.
-
(2006)
J Biol Chem
, vol.281
, pp. 34492-34502
-
-
Pinto, M.P.1
Grou, C.P.2
Alencastre, I.S.3
Oliveira, M.E.4
Sa-Miranda, C.5
Fransen, M.6
Azevedo, J.E.7
-
38
-
-
0027759463
-
In vitro insertion of the 22-kD peroxisomal membrane protein into isolated rat liver peroxisomes
-
Diestelkötter P, Just WW. In vitro insertion of the 22-kD peroxisomal membrane protein into isolated rat liver peroxisomes. J Cell Biol 1993;123:1717-1725.
-
(1993)
J Cell Biol
, vol.123
, pp. 1717-1725
-
-
Diestelkötter, P.1
Just, W.W.2
-
39
-
-
0034122564
-
The peroxin pex3p initiates membrane assembly in peroxisome biogenesis
-
Ghaedi K, Tamura S, Okumoto K, Matsuzono Y, Fujiki Y. The peroxin pex3p initiates membrane assembly in peroxisome biogenesis. Mol Biol Cell 2000;11:2085-2102.
-
(2000)
Mol Biol Cell
, vol.11
, pp. 2085-2102
-
-
Ghaedi, K.1
Tamura, S.2
Okumoto, K.3
Matsuzono, Y.4
Fujiki, Y.5
-
40
-
-
59449104113
-
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway
-
Matsuzaki T, Fujiki Y. The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway. J Cell Biol 2008;183:1275-1286.
-
(2008)
J Cell Biol
, vol.183
, pp. 1275-1286
-
-
Matsuzaki, T.1
Fujiki, Y.2
-
42
-
-
0027074320
-
Thermal stability comparison of purified empty and peptide-filled forms of a class I MHC molecule
-
Fahnestock ML, Tamir I, Narhi L, Bjorkman PJ. Thermal stability comparison of purified empty and peptide-filled forms of a class I MHC molecule. Science 1992;258:1658-1662.
-
(1992)
Science
, vol.258
, pp. 1658-1662
-
-
Fahnestock, M.L.1
Tamir, I.2
Narhi, L.3
Bjorkman, P.J.4
-
43
-
-
0031953508
-
Structural characterization of a soluble and partially folded class I major histocompatibility heavy chain/beta 2m heterodimer
-
Bouvier M, Wiley DC. Structural characterization of a soluble and partially folded class I major histocompatibility heavy chain/beta 2m heterodimer. Nat Struct Biol 1998;5:377-384.
-
(1998)
Nat Struct Biol
, vol.5
, pp. 377-384
-
-
Bouvier, M.1
Wiley, D.C.2
-
44
-
-
79959370908
-
Cell-free sorting of peroxisomal membrane proteins from the endoplasmic reticulum
-
Agrawal G, Joshi S, Subramani S. Cell-free sorting of peroxisomal membrane proteins from the endoplasmic reticulum. Proc Natl Acad Sci USA 2011;108:9113-9118.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 9113-9118
-
-
Agrawal, G.1
Joshi, S.2
Subramani, S.3
-
45
-
-
77956003976
-
Pex11pbeta-mediated growth and division of mammalian peroxisomes follows a maturation pathway
-
Delille HK, Agricola B, Guimaraes SC, Borta H, Luers GH, Fransen M, Schrader M. Pex11pbeta-mediated growth and division of mammalian peroxisomes follows a maturation pathway. J Cell Sci 2010;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
Luers, G.H.5
Fransen, M.6
Schrader, M.7
-
46
-
-
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, Brocard C. PEX11 family members are membrane elongation factors that coordinate peroxisome proliferation and maintenance. J Cell Sci 2010;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
-
47
-
-
0028840636
-
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group
-
Poulos A, Christodoulou J, Chow CW, Goldblatt J, Paton BC, Orii T, Suzuki Y, Shimozawa N. Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group. J Pediatr 1995;127:596-599.
-
(1995)
J Pediatr
, vol.127
, pp. 596-599
-
-
Poulos, A.1
Christodoulou, J.2
Chow, C.W.3
Goldblatt, J.4
Paton, B.C.5
Orii, T.6
Suzuki, Y.7
Shimozawa, N.8
-
48
-
-
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 HW, Watkins P, Valle D, Gould SJ. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Nat Genet 1995;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
-
49
-
-
0033020663
-
Identification and characterization of the human orthologue of yeast Pex14p
-
Will GK, Soukupova M, Hong X, Erdmann KS, Kiel JA, Dodt G, Kunau WH, Erdmann R. Identification and characterization of the human orthologue of yeast Pex14p. Mol Cell Biol 1999;19:2265-2277.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 2265-2277
-
-
Will, G.K.1
Soukupova, M.2
Hong, X.3
Erdmann, K.S.4
Kiel, J.A.5
Dodt, G.6
Kunau, W.H.7
Erdmann, R.8
-
50
-
-
0034972812
-
Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences
-
Fransen M, Wylin T, Brees C, Mannaerts GP, Van Veldhoven PP. Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences. Mol Cell Biol 2001;21:4413-4424.
-
(2001)
Mol Cell Biol
, vol.21
, pp. 4413-4424
-
-
Fransen, M.1
Wylin, T.2
Brees, C.3
Mannaerts, G.P.4
Van Veldhoven, P.P.5
|