Marc Fransen

Marc Fransen

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Marc Fransen

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Deciphering the potential involvement of PXMP2 and PEX11B in hydrogen peroxide permeation across the peroxisomal membrane reveals a role for PEX11B in protein sorting.

Biochim Biophys Acta Biomembr 2019 Oct 24;1861(10):182991. Epub 2019 May 24.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven - University of Leuven, Herestraat 49, box 601, B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bbamem.2019.05.013DOI Listing
October 2019

Peroxisomal Hydrogen Peroxide Metabolism and Signaling in Health and Disease.

Int J Mol Sci 2019 Jul 26;20(15). Epub 2019 Jul 26.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven-University of Leuven, 3000 Leuven, Belgium.

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http://dx.doi.org/10.3390/ijms20153673DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695606PMC
July 2019

Peroxisomes and Cellular Oxidant/Antioxidant Balance: Protein Redox Modifications and Impact on Inter-organelle Communication.

Subcell Biochem 2018;89:435-461

Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, Box 601, 3000, Louvain, Belgium.

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http://link.springer.com/10.1007/978-981-13-2233-4_19
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http://dx.doi.org/10.1007/978-981-13-2233-4_19DOI Listing
June 2019

Differential distribution of peroxisomal proteins points to specific roles of peroxisomes in the murine retina.

Mol Cell Biochem 2019 Jun 2;456(1-2):53-62. Epub 2019 Jan 2.

Department of Pharmaceutical and Pharmacological Sciences, Cell Metabolism, KU Leuven -University of Leuven, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s11010-018-3489-3DOI Listing
June 2019

Functional peroxisomes are required for β-cell integrity in mice.

Mol Metab 2019 Apr 8;22:71-83. Epub 2019 Feb 8.

KU Leuven - University of Leuven, Department of Pharmaceutical and Pharmacological Sciences, Laboratory of Cell Metabolism, B-3000, Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.molmet.2019.02.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437690PMC
April 2019

Peroxisomes as Modulators of Cellular Protein Thiol Oxidation: A New Model System.

Antioxid Redox Signal 2019 Jan 14;30(1):22-39. Epub 2017 Jul 14.

1 Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven-University of Leuven , Leuven, Belgium .

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http://dx.doi.org/10.1089/ars.2017.6997DOI Listing
January 2019

Redox Signaling from and to Peroxisomes: Progress, Challenges, and Prospects.

Antioxid Redox Signal 2019 Jan 22;30(1):95-112. Epub 2018 Mar 22.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven-University of Leuven , Leuven, Belgium .

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http://dx.doi.org/10.1089/ars.2018.7515DOI Listing
January 2019

Membrane topologies of PEX13 and PEX14 provide new insights on the mechanism of protein import into peroxisomes.

FEBS J 2019 01 28;286(1):205-222. Epub 2018 Nov 28.

Instituto de Investigação e Inovação em Saúde (i3S), Universidade do Porto, Portugal.

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http://doi.wiley.com/10.1111/febs.14697
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http://dx.doi.org/10.1111/febs.14697DOI Listing
January 2019

The peroxisomal import receptor PEX5 functions as a stress sensor, retaining catalase in the cytosol in times of oxidative stress.

Biochim Biophys Acta Mol Cell Res 2017 Oct 29;1864(10):1833-1843. Epub 2017 Jul 29.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven - University of Leuven, Herestraat 49, Box 601, B-3000 Leuven, Belgium. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01674889173019
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http://dx.doi.org/10.1016/j.bbamcr.2017.07.013DOI Listing
October 2017

Quantitative Monitoring of Subcellular Redox Dynamics in Living Mammalian Cells Using RoGFP2-Based Probes.

Methods Mol Biol 2017 ;1595:151-164

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, University of Leuven - KU Leuven, Herestraat 49 - box 601, Leuven, 3000, Belgium.

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http://link.springer.com/10.1007/978-1-4939-6937-1_14
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http://dx.doi.org/10.1007/978-1-4939-6937-1_14DOI Listing
May 2017

KillerRed as a Tool to Study the Cellular Responses to Peroxisome-Derived Oxidative Stress.

Methods Mol Biol 2017 ;1595:165-179

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven - University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1007/978-1-4939-6937-1_15DOI Listing
May 2017

The Peroxisome-Mitochondria Connection: How and Why?

Int J Mol Sci 2017 May 24;18(6). Epub 2017 May 24.

Department of Anatomy and Cell Biology, University of Western Ontario, London, ON N6A 3K7, Canada.

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http://dx.doi.org/10.3390/ijms18061126DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485950PMC
May 2017

Export-deficient monoubiquitinated PEX5 triggers peroxisome removal in SV40 large T antigen-transformed mouse embryonic fibroblasts.

Autophagy 2015 ;11(8):1326-40

a Laboratory of Lipid Biochemistry and Protein Interactions; Department of Cellular and Molecular Medicine; University of Leuven - KU Leuven ; Leuven , Belgium.

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http://dx.doi.org/10.1080/15548627.2015.1061846DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4590649PMC
June 2016

Peroxisome biogenesis in mammalian cells: The impact of genes and environment.

Biochim Biophys Acta 2016 May 21;1863(5):1049-60. Epub 2015 Aug 21.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven-University of Leuven, Herestraat 49 box 601, B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bbamcr.2015.08.011DOI Listing
May 2016

Antioxidant cytoprotection by peroxisomal peroxiredoxin-5.

Free Radic Biol Med 2015 Jul 13;84:215-226. Epub 2015 Mar 13.

Group of Animal Molecular and Cellular Biology, Institut des Sciences de la Vie, Université Catholique de Louvain, 1348 Louvain-la-Neuve, Belgium. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08915849150010
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http://dx.doi.org/10.1016/j.freeradbiomed.2015.02.032DOI Listing
July 2015

Redox interplay between mitochondria and peroxisomes.

Front Cell Dev Biol 2015 27;3:35. Epub 2015 May 27.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven - University of Leuven Leuven, Belgium.

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http://www.frontiersin.org/Mitochondrial_Research/10.3389/fc
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http://dx.doi.org/10.3389/fcell.2015.00035DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444963PMC
June 2015

The peroxisomal protein import machinery displays a preference for monomeric substrates.

Open Biol 2015 Apr;5(4):140236

Organelle Biogenesis and Function Group, Instituto de Biologia Celular e Molecular (IBMC), Universidade do Porto, Porto, Portugal Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto, Porto, Portugal

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http://dx.doi.org/10.1098/rsob.140236DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422123PMC
April 2015

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation.

Biochim Biophys Acta 2015 Feb 20;1853(2):285-98. Epub 2014 Nov 20.

KU Leuven - University of Leuven, Department of Pharmaceutical and Pharmacological Sciences, Laboratory of Cell Metabolism, B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bbamcr.2014.11.017DOI Listing
February 2015

HaloTag as a tool to investigate peroxisome dynamics in cultured mammalian cells.

Authors:
Marc Fransen

Methods Mol Biol 2014 ;1174:157-70

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, Faculty of Medicine, Katholieke Universiteit Leuven, Campus Gasthuisberg, Herestraat 49, 601, 3000, Leuven, Belgium,

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http://dx.doi.org/10.1007/978-1-4939-0944-5_10DOI Listing
January 2015

A cost-effective approach to microporate mammalian cells with the Neon Transfection System.

Anal Biochem 2014 Dec 27;466:49-50. Epub 2014 Aug 27.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU Leuven (University of Leuven), B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ab.2014.08.017DOI Listing
December 2014

Aging, age-related diseases and peroxisomes.

Subcell Biochem 2013 ;69:45-65

Department of Cellular and Molecular Medicine, KU Leuven, Herestraat 49, 601, B-3000, Leuven, Belgium,

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http://dx.doi.org/10.1007/978-94-007-6889-5_3DOI Listing
August 2014

A PEX7-centered perspective on the peroxisomal targeting signal type 2-mediated protein import pathway.

Mol Cell Biol 2014 Aug 27;34(15):2917-28. Epub 2014 May 27.

Organelle Biogenesis and Function Group, Instituto de Biologia Celular e Molecular (IBMC), Universidade do Porto, Porto, Portugal Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto, Porto, Portugal

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http://dx.doi.org/10.1128/MCB.01727-13DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135580PMC
August 2014

Peroxisomal metabolism and oxidative stress.

Biochimie 2014 Mar 9;98:56-62. Epub 2013 Aug 9.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, Campus Gasthuisberg, Herestraat 49, Box 601, B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.biochi.2013.07.026DOI Listing
March 2014

PEX5, the shuttling import receptor for peroxisomal matrix proteins, is a redox-sensitive protein.

Traffic 2014 Jan 31;15(1):94-103. Epub 2013 Oct 31.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, KU, Leuven, Belgium.

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http://doi.wiley.com/10.1111/tra.12129
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http://dx.doi.org/10.1111/tra.12129DOI Listing
January 2014

Mitochondria are targets for peroxisome-derived oxidative stress in cultured mammalian cells.

Free Radic Biol Med 2013 Dec 27;65:882-894. Epub 2013 Aug 27.

Laboratory of Lipid Biochemistry and Protein Interactions, Katholieke Universiteit Leuven, 3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.freeradbiomed.2013.08.173DOI Listing
December 2013

Peroxisome degradation in mammals: mechanisms of action, recent advances, and perspectives.

Front Physiol 2013 14;4:145. Epub 2013 Jun 14.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven Leuven, Vlaams-Brabant, Belgium.

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http://dx.doi.org/10.3389/fphys.2013.00145DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682127PMC
June 2013

Cyclophilin D: a therapeutic target to counteract reactive oxygen species-mediated damage in neurodegenerative disease?

Authors:
Marc Fransen

Brain 2012 Dec 28;135(Pt 12):3525-6. Epub 2012 Nov 28.

Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, Herestraat 49, Box 601, B-3000 Leuven, Belgium.

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https://academic.oup.com/brain/article-lookup/doi/10.1093/br
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http://dx.doi.org/10.1093/brain/aws304DOI Listing
December 2012

Role of peroxisomes in ROS/RNS-metabolism: implications for human disease.

Biochim Biophys Acta 2012 Sep 9;1822(9):1363-73. Epub 2011 Dec 9.

Department of Cellular and Molecular Medicine, Katholieke Universiteit Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.bbadis.2011.12.001DOI Listing
September 2012

Guidelines for the use and interpretation of assays for monitoring autophagy.

Authors:
Daniel J Klionsky Fabio C Abdalla Hagai Abeliovich Robert T Abraham Abraham Acevedo-Arozena Khosrow Adeli Lotta Agholme Maria Agnello Patrizia Agostinis Julio A Aguirre-Ghiso Hyung Jun Ahn Ouardia Ait-Mohamed Slimane Ait-Si-Ali Takahiko Akematsu Shizuo Akira Hesham M Al-Younes Munir A Al-Zeer Matthew L Albert Roger L Albin Javier Alegre-Abarrategui Maria Francesca Aleo Mehrdad Alirezaei Alexandru Almasan Maylin Almonte-Becerril Atsuo Amano Ravi Amaravadi Shoba Amarnath Amal O Amer Nathalie Andrieu-Abadie Vellareddy Anantharam David K Ann Shailendra Anoopkumar-Dukie Hiroshi Aoki Nadezda Apostolova Giuseppe Arancia John P Aris Katsuhiko Asanuma Nana Y O Asare Hisashi Ashida Valerie Askanas David S Askew Patrick Auberger Misuzu Baba Steven K Backues Eric H Baehrecke Ben A Bahr Xue-Yuan Bai Yannick Bailly Robert Baiocchi Giulia Baldini Walter Balduini Andrea Ballabio Bruce A Bamber Edward T W Bampton Gábor Bánhegyi Clinton R Bartholomew Diane C Bassham Robert C Bast Henri Batoko Boon-Huat Bay Isabelle Beau Daniel M Béchet Thomas J Begley Christian Behl Christian Behrends Soumeya Bekri Bryan Bellaire Linda J Bendall Luca Benetti Laura Berliocchi Henri Bernardi Francesca Bernassola Sébastien Besteiro Ingrid Bhatia-Kissova Xiaoning Bi Martine Biard-Piechaczyk Janice S Blum Lawrence H Boise Paolo Bonaldo David L Boone Beat C Bornhauser Karina R Bortoluci Ioannis Bossis Frédéric Bost Jean-Pierre Bourquin Patricia Boya Michaël Boyer-Guittaut Peter V Bozhkov Nathan R Brady Claudio Brancolini Andreas Brech Jay E Brenman Ana Brennand Emery H Bresnick Patrick Brest Dave Bridges Molly L Bristol Paul S Brookes Eric J Brown John H Brumell Nicola Brunetti-Pierri Ulf T Brunk Dennis E Bulman Scott J Bultman Geert Bultynck Lena F Burbulla Wilfried Bursch Jonathan P Butchar Wanda Buzgariu Sergio P Bydlowski Ken Cadwell Monika Cahová Dongsheng Cai Jiyang Cai Qian Cai Bruno Calabretta Javier Calvo-Garrido Nadine Camougrand Michelangelo Campanella Jenny Campos-Salinas Eleonora Candi Lizhi Cao Allan B Caplan Simon R Carding Sandra M Cardoso Jennifer S Carew Cathleen R Carlin Virginie Carmignac Leticia A M Carneiro Serena Carra Rosario A Caruso Giorgio Casari Caty Casas Roberta Castino Eduardo Cebollero Francesco Cecconi Jean Celli Hassan Chaachouay Han-Jung Chae Chee-Yin Chai David C Chan Edmond Y Chan Raymond Chuen-Chung Chang Chi-Ming Che Ching-Chow Chen Guang-Chao Chen Guo-Qiang Chen Min Chen Quan Chen Steve S-L Chen WenLi Chen Xi Chen Xiangmei Chen Xiequn Chen Ye-Guang Chen Yingyu Chen Yongqiang Chen Yu-Jen Chen Zhixiang Chen Alan Cheng Christopher H K Cheng Yan Cheng Heesun Cheong Jae-Ho Cheong Sara Cherry Russ Chess-Williams Zelda H Cheung Eric Chevet Hui-Ling Chiang Roberto Chiarelli Tomoki Chiba Lih-Shen Chin Shih-Hwa Chiou Francis V Chisari Chi Hin Cho Dong-Hyung Cho Augustine M K Choi DooSeok Choi Kyeong Sook Choi Mary E Choi Salem Chouaib Divaker Choubey Vinay Choubey Charleen T Chu Tsung-Hsien Chuang Sheau-Huei Chueh Taehoon Chun Yong-Joon Chwae Mee-Len Chye Roberto Ciarcia Maria R Ciriolo Michael J Clague Robert S B Clark Peter G H Clarke Robert Clarke Patrice Codogno Hilary A Coller María I Colombo Sergio Comincini Maria Condello Fabrizio Condorelli Mark R Cookson Graham H Coombs Isabelle Coppens Ramon Corbalan Pascale Cossart Paola Costelli Safia Costes Ana Coto-Montes Eduardo Couve Fraser P Coxon James M Cregg José L Crespo Marianne J Cronjé Ana Maria Cuervo Joseph J Cullen Mark J Czaja Marcello D'Amelio Arlette Darfeuille-Michaud Lester M Davids Faith E Davies Massimo De Felici John F de Groot Cornelis A M de Haan Luisa De Martino Angelo De Milito Vincenzo De Tata Jayanta Debnath Alexei Degterev Benjamin Dehay Lea M D Delbridge Francesca Demarchi Yi Zhen Deng Jörn Dengjel Paul Dent Donna Denton Vojo Deretic Shyamal D Desai Rodney J Devenish Mario Di Gioacchino Gilbert Di Paolo Chiara Di Pietro Guillermo Díaz-Araya Inés Díaz-Laviada Maria T Diaz-Meco Javier Diaz-Nido Ivan Dikic Savithramma P Dinesh-Kumar Wen-Xing Ding Clark W Distelhorst Abhinav Diwan Mojgan Djavaheri-Mergny Svetlana Dokudovskaya Zheng Dong Frank C Dorsey Victor Dosenko James J Dowling Stephen Doxsey Marlène Dreux Mark E Drew Qiuhong Duan Michel A Duchosal Karen Duff Isabelle Dugail Madeleine Durbeej Michael Duszenko Charles L Edelstein Aimee L Edinger Gustavo Egea Ludwig Eichinger N Tony Eissa Suhendan Ekmekcioglu Wafik S El-Deiry Zvulun Elazar Mohamed Elgendy Lisa M Ellerby Kai Er Eng Anna-Mart Engelbrecht Simone Engelender Jekaterina Erenpreisa Ricardo Escalante Audrey Esclatine Eeva-Liisa Eskelinen Lucile Espert Virginia Espina Huizhou Fan Jia Fan Qi-Wen Fan Zhen Fan Shengyun Fang Yongqi Fang Manolis Fanto Alessandro Fanzani Thomas Farkas Jean-Claude Farré Mathias Faure Marcus Fechheimer Carl G Feng Jian Feng Qili Feng Youji Feng László Fésüs Ralph Feuer Maria E Figueiredo-Pereira Gian Maria Fimia Diane C Fingar Steven Finkbeiner Toren Finkel Kim D Finley Filomena Fiorito Edward A Fisher Paul B Fisher Marc Flajolet Maria L Florez-McClure Salvatore Florio Edward A Fon Francesco Fornai Franco Fortunato Rati Fotedar Daniel H Fowler Howard S Fox Rodrigo Franco Lisa B Frankel Marc Fransen José M Fuentes Juan Fueyo Jun Fujii Kozo Fujisaki Eriko Fujita Mitsunori Fukuda Ruth H Furukawa Matthias Gaestel Philippe Gailly Malgorzata Gajewska Brigitte Galliot Vincent Galy Subramaniam Ganesh Barry Ganetzky Ian G Ganley Fen-Biao Gao George F Gao Jinming Gao Lorena Garcia Guillermo Garcia-Manero Mikel Garcia-Marcos Marjan Garmyn Andrei L Gartel Evelina Gatti Mathias Gautel Thomas R Gawriluk Matthew E Gegg Jiefei Geng Marc Germain Jason E Gestwicki David A Gewirtz Saeid Ghavami Pradipta Ghosh Anna M Giammarioli Alexandra N Giatromanolaki Spencer B Gibson Robert W Gilkerson Michael L Ginger Henry N Ginsberg Jakub Golab Michael S Goligorsky Pierre Golstein Candelaria Gomez-Manzano Ebru Goncu Céline Gongora Claudio D Gonzalez Ramon Gonzalez Cristina González-Estévez Rosa Ana González-Polo Elena Gonzalez-Rey Nikolai V Gorbunov Sharon Gorski Sandro Goruppi Roberta A Gottlieb Devrim Gozuacik Giovanna Elvira Granato Gary D Grant Kim N Green Aleš Gregorc Frédéric Gros Charles Grose Thomas W Grunt Philippe Gual Jun-Lin Guan Kun-Liang Guan Sylvie M Guichard Anna S Gukovskaya Ilya Gukovsky Jan Gunst Asa B Gustafsson Andrew J Halayko Amber N Hale Sandra K Halonen Maho Hamasaki Feng Han Ting Han Michael K Hancock Malene Hansen Hisashi Harada Masaru Harada Stefan E Hardt J Wade Harper Adrian L Harris James Harris Steven D Harris Makoto Hashimoto Jeffrey A Haspel Shin-ichiro Hayashi Lori A Hazelhurst Congcong He You-Wen He Marie-Joseé Hébert Kim A Heidenreich Miep H Helfrich Gudmundur V Helgason Elizabeth P Henske Brian Herman Paul K Herman Claudio Hetz Sabine Hilfiker Joseph A Hill Lynne J Hocking Paul Hofman Thomas G Hofmann Jörg Höhfeld Tessa L Holyoake Ming-Huang Hong David A Hood Gökhan S Hotamisligil Ewout J Houwerzijl Maria Høyer-Hansen Bingren Hu Chien-An A Hu Hong-Ming Hu Ya Hua Canhua Huang Ju Huang Shengbing Huang Wei-Pang Huang Tobias B Huber Won-Ki Huh Tai-Ho Hung Ted R Hupp Gang Min Hur James B Hurley Sabah N A Hussain Patrick J Hussey Jung Jin Hwang Seungmin Hwang Atsuhiro Ichihara Shirin Ilkhanizadeh Ken Inoki Takeshi Into Valentina Iovane Juan L Iovanna Nancy Y Ip Yoshitaka Isaka Hiroyuki Ishida Ciro Isidoro Ken-ichi Isobe Akiko Iwasaki Marta Izquierdo Yotaro Izumi Panu M Jaakkola Marja Jäättelä George R Jackson William T Jackson Bassam Janji Marina Jendrach Ju-Hong Jeon Eui-Bae Jeung Hong Jiang Hongchi Jiang Jean X Jiang Ming Jiang Qing Jiang Xuejun Jiang Xuejun Jiang Alberto Jiménez Meiyan Jin Shengkan Jin Cheol O Joe Terje Johansen Daniel E Johnson Gail V W Johnson Nicola L Jones Bertrand Joseph Suresh K Joseph Annie M Joubert Gábor Juhász Lucienne Juillerat-Jeanneret Chang Hwa Jung Yong-Keun Jung Kai Kaarniranta Allen Kaasik Tomohiro Kabuta Motoni Kadowaki Katarina Kagedal Yoshiaki Kamada Vitaliy O Kaminskyy Harm H Kampinga Hiromitsu Kanamori Chanhee Kang Khong Bee Kang Kwang Il Kang Rui Kang Yoon-A Kang Tomotake Kanki Thirumala-Devi Kanneganti Haruo Kanno Anumantha G Kanthasamy Arthi Kanthasamy Vassiliki Karantza Gur P Kaushal Susmita Kaushik Yoshinori Kawazoe Po-Yuan Ke John H Kehrl Ameeta Kelekar Claus Kerkhoff David H Kessel Hany Khalil Jan A K W Kiel Amy A Kiger Akio Kihara Deok Ryong Kim Do-Hyung Kim Dong-Hou Kim Eun-Kyoung Kim Hyung-Ryong Kim Jae-Sung Kim Jeong Hun Kim Jin Cheon Kim John K Kim Peter K Kim Seong Who Kim Yong-Sun Kim Yonghyun Kim Adi Kimchi Alec C Kimmelman Jason S King Timothy J Kinsella Vladimir Kirkin Lorrie A Kirshenbaum Katsuhiko Kitamoto Kaio Kitazato Ludger Klein Walter T Klimecki Jochen Klucken Erwin Knecht Ben C B Ko Jan C Koch Hiroshi Koga Jae-Young Koh Young Ho Koh Masato Koike Masaaki Komatsu Eiki Kominami Hee Jeong Kong Wei-Jia Kong Viktor I Korolchuk Yaichiro Kotake Michael I Koukourakis Juan B Kouri Flores Attila L Kovács Claudine Kraft Dimitri Krainc Helmut Krämer Carole Kretz-Remy Anna M Krichevsky Guido Kroemer Rejko Krüger Oleg Krut Nicholas T Ktistakis Chia-Yi Kuan Roza Kucharczyk Ashok Kumar Raj Kumar Sharad Kumar Mondira Kundu Hsing-Jien Kung Tino Kurz Ho Jeong Kwon Albert R La Spada Frank Lafont Trond Lamark Jacques Landry Jon D Lane Pierre Lapaquette Jocelyn F Laporte Lajos László Sergio Lavandero Josée N Lavoie Robert Layfield Pedro A Lazo Weidong Le Laurent Le Cam Daniel J Ledbetter Alvin J X Lee Byung-Wan Lee Gyun Min Lee Jongdae Lee Ju-Hyun Lee Michael Lee Myung-Shik Lee Sug Hyung Lee Christiaan Leeuwenburgh Patrick Legembre Renaud Legouis Michael Lehmann Huan-Yao Lei Qun-Ying Lei David A Leib José Leiro John J Lemasters Antoinette Lemoine Maciej S Lesniak Dina Lev Victor V Levenson Beth Levine Efrat Levy Faqiang Li Jun-Lin Li Lian Li Sheng Li Weijie Li Xue-Jun Li Yan-bo Li Yi-Ping Li Chengyu Liang Qiangrong Liang Yung-Feng Liao Pawel P Liberski Andrew Lieberman Hyunjung J Lim Kah-Leong Lim Kyu Lim Chiou-Feng Lin Fu-Cheng Lin Jian Lin Jiandie D Lin Kui Lin Wan-Wan Lin Weei-Chin Lin Yi-Ling Lin Rafael Linden Paul Lingor Jennifer Lippincott-Schwartz Michael P Lisanti Paloma B Liton Bo Liu Chun-Feng Liu Kaiyu Liu Leyuan Liu Qiong A Liu Wei Liu Young-Chau Liu Yule Liu Richard A Lockshin Chun-Nam Lok Sagar Lonial Benjamin Loos Gabriel Lopez-Berestein Carlos López-Otín Laura Lossi Michael T Lotze Peter Lőw Binfeng Lu Bingwei Lu Bo Lu Zhen Lu Frédéric Luciano Nicholas W Lukacs Anders H Lund Melinda A Lynch-Day Yong Ma Fernando Macian Jeff P MacKeigan Kay F Macleod Frank Madeo Luigi Maiuri Maria Chiara Maiuri Davide Malagoli May Christine V Malicdan Walter Malorni Na Man Eva-Maria Mandelkow Stéphen Manon Irena Manov Kai Mao Xiang Mao Zixu Mao Philippe Marambaud Daniela Marazziti Yves L Marcel Katie Marchbank Piero Marchetti Stefan J Marciniak Mateus Marcondes Mohsen Mardi Gabriella Marfe Guillermo Mariño Maria Markaki Mark R Marten Seamus J Martin Camille Martinand-Mari Wim Martinet Marta Martinez-Vicente Matilde Masini Paola Matarrese Saburo Matsuo Raffaele Matteoni Andreas Mayer Nathalie M Mazure David J McConkey Melanie J McConnell Catherine McDermott Christine McDonald Gerald M McInerney Sharon L McKenna BethAnn McLaughlin Pamela J McLean Christopher R McMaster G Angus McQuibban Alfred J Meijer Miriam H Meisler Alicia Meléndez Thomas J Melia Gerry Melino Maria A Mena Javier A Menendez Rubem F S Menna-Barreto Manoj B Menon Fiona M Menzies Carol A Mercer Adalberto Merighi Diane E Merry Stefania Meschini Christian G Meyer Thomas F Meyer Chao-Yu Miao Jun-Ying Miao Paul A M Michels Carine Michiels Dalibor Mijaljica Ana Milojkovic Saverio Minucci Clelia Miracco Cindy K Miranti Ioannis Mitroulis Keisuke Miyazawa Noboru Mizushima Baharia Mograbi Simin Mohseni Xavier Molero Bertrand Mollereau Faustino Mollinedo Takashi Momoi Iryna Monastyrska Martha M Monick Mervyn J Monteiro Michael N Moore Rodrigo Mora Kevin Moreau Paula I Moreira Yuji Moriyasu Jorge Moscat Serge Mostowy Jeremy C Mottram Tomasz Motyl Charbel E-H Moussa Sylke Müller Sylviane Muller Karl Münger Christian Münz Leon O Murphy Maureen E Murphy Antonio Musarò Indira Mysorekar Eiichiro Nagata Kazuhiro Nagata Aimable Nahimana Usha Nair Toshiyuki Nakagawa Kiichi Nakahira Hiroyasu Nakano Hitoshi Nakatogawa Meera Nanjundan Naweed I Naqvi Derek P Narendra Masashi Narita Miguel Navarro Steffan T Nawrocki Taras Y Nazarko Andriy Nemchenko Mihai G Netea Thomas P Neufeld Paul A Ney Ioannis P Nezis Huu Phuc Nguyen Daotai Nie Ichizo Nishino Corey Nislow Ralph A Nixon Takeshi Noda Angelika A Noegel Anna Nogalska Satoru Noguchi Lucia Notterpek Ivana Novak Tomoyoshi Nozaki Nobuyuki Nukina Thorsten Nürnberger Beat Nyfeler Keisuke Obara Terry D Oberley Salvatore Oddo Michinaga Ogawa Toya Ohashi Koji Okamoto Nancy L Oleinick F Javier Oliver Laura J Olsen Stefan Olsson Onya Opota Timothy F Osborne Gary K Ostrander Kinya Otsu Jing-hsiung James Ou Mireille Ouimet Michael Overholtzer Bulent Ozpolat Paolo Paganetti Ugo Pagnini Nicolas Pallet Glen E Palmer Camilla Palumbo Tianhong Pan Theocharis Panaretakis Udai Bhan Pandey Zuzana Papackova Issidora Papassideri Irmgard Paris Junsoo Park Ohkmae K Park Jan B Parys Katherine R Parzych Susann Patschan Cam Patterson Sophie Pattingre John M Pawelek Jianxin Peng David H Perlmutter Ida Perrotta George Perry Shazib Pervaiz Matthias Peter Godefridus J Peters Morten Petersen Goran Petrovski James M Phang Mauro Piacentini Philippe Pierre Valérie Pierrefite-Carle Gérard Pierron Ronit Pinkas-Kramarski Antonio Piras Natik Piri Leonidas C Platanias Stefanie Pöggeler Marc Poirot Angelo Poletti Christian Poüs Mercedes Pozuelo-Rubio Mette Prætorius-Ibba Anil Prasad Mark Prescott Muriel Priault Nathalie Produit-Zengaffinen Ann Progulske-Fox Tassula Proikas-Cezanne Serge Przedborski Karin Przyklenk Rosa Puertollano Julien Puyal Shu-Bing Qian Liang Qin Zheng-Hong Qin Susan E Quaggin Nina Raben Hannah Rabinowich Simon W Rabkin Irfan Rahman Abdelhaq Rami Georg Ramm Glenn Randall Felix Randow V Ashutosh Rao Jeffrey C Rathmell Brinda Ravikumar Swapan K Ray Bruce H Reed John C Reed Fulvio Reggiori Anne Régnier-Vigouroux Andreas S Reichert John J Reiners Russel J Reiter Jun Ren José L Revuelta Christopher J Rhodes Konstantinos Ritis Elizete Rizzo Jeffrey Robbins Michel Roberge Hernan Roca Maria C Roccheri Stephane Rocchi H Peter Rodemann Santiago Rodríguez de Córdoba Bärbel Rohrer Igor B Roninson Kirill Rosen Magdalena M Rost-Roszkowska Mustapha Rouis Kasper M A Rouschop Francesca Rovetta Brian P Rubin David C Rubinsztein Klaus Ruckdeschel Edmund B Rucker Assaf Rudich Emil Rudolf Nelson Ruiz-Opazo Rossella Russo Tor Erik Rusten Kevin M Ryan Stefan W Ryter David M Sabatini Junichi Sadoshima Tapas Saha Tatsuya Saitoh Hiroshi Sakagami Yasuyoshi Sakai Ghasem Hoseini Salekdeh Paolo Salomoni Paul M Salvaterra Guy Salvesen Rosa Salvioli Anthony M J Sanchez José A Sánchez-Alcázar Ricardo Sánchez-Prieto Marco Sandri Uma Sankar Poonam Sansanwal Laura Santambrogio Shweta Saran Sovan Sarkar Minnie Sarwal Chihiro Sasakawa Ausra Sasnauskiene Miklós Sass Ken Sato Miyuki Sato Anthony H V Schapira Michael Scharl Hermann M Schätzl Wiep Scheper Stefano Schiaffino Claudio Schneider Marion E Schneider Regine Schneider-Stock Patricia V Schoenlein Daniel F Schorderet Christoph Schüller Gary K Schwartz Luca Scorrano Linda Sealy Per O Seglen Juan Segura-Aguilar Iban Seiliez Oleksandr Seleverstov Christian Sell Jong Bok Seo Duska Separovic Vijayasaradhi Setaluri Takao Setoguchi Carmine Settembre John J Shacka Mala Shanmugam Irving M Shapiro Eitan Shaulian Reuben J Shaw James H Shelhamer Han-Ming Shen Wei-Chiang Shen Zu-Hang Sheng Yang Shi Kenichi Shibuya Yoshihiro Shidoji Jeng-Jer Shieh Chwen-Ming Shih Yohta Shimada Shigeomi Shimizu Takahiro Shintani Orian S Shirihai Gordon C Shore Andriy A Sibirny Stan B Sidhu Beata Sikorska Elaine C M Silva-Zacarin Alison Simmons Anna Katharina Simon Hans-Uwe Simon Cristiano Simone Anne Simonsen David A Sinclair Rajat Singh Debasish Sinha Frank A Sinicrope Agnieszka Sirko Parco M Siu Efthimios Sivridis Vojtech Skop Vladimir P Skulachev Ruth S Slack Soraya S Smaili Duncan R Smith Maria S Soengas Thierry Soldati Xueqin Song Anil K Sood Tuck Wah Soong Federica Sotgia Stephen A Spector Claudia D Spies Wolfdieter Springer Srinivasa M Srinivasula Leonidas Stefanis Joan S Steffan Ruediger Stendel Harald Stenmark Anastasis Stephanou Stephan T Stern Cinthya Sternberg Björn Stork Peter Strålfors Carlos S Subauste Xinbing Sui David Sulzer Jiaren Sun Shi-Yong Sun Zhi-Jun Sun Joseph J Y Sung Kuninori Suzuki Toshihiko Suzuki Michele S Swanson Charles Swanton Sean T Sweeney Lai-King Sy Gyorgy Szabadkai Ira Tabas Heinrich Taegtmeyer Marco Tafani Krisztina Takács-Vellai Yoshitaka Takano Kaoru Takegawa Genzou Takemura Fumihiko Takeshita Nicholas J Talbot Kevin S W Tan Keiji Tanaka Kozo Tanaka Daolin Tang Dingzhong Tang Isei Tanida Bakhos A Tannous Nektarios Tavernarakis Graham S Taylor Gregory A Taylor J Paul Taylor Lance S Terada Alexei Terman Gianluca Tettamanti Karin Thevissen Craig B Thompson Andrew Thorburn Michael Thumm FengFeng Tian Yuan Tian Glauco Tocchini-Valentini Aviva M Tolkovsky Yasuhiko Tomino Lars Tönges Sharon A Tooze Cathy Tournier John Tower Roberto Towns Vladimir Trajkovic Leonardo H Travassos Ting-Fen Tsai Mario P Tschan Takeshi Tsubata Allan Tsung Boris Turk Lorianne S Turner Suresh C Tyagi Yasuo Uchiyama Takashi Ueno Midori Umekawa Rika Umemiya-Shirafuji Vivek K Unni Maria I Vaccaro Enza Maria Valente Greet Van den Berghe Ida J van der Klei Wouter van Doorn Linda F van Dyk Marjolein van Egmond Leo A van Grunsven Peter Vandenabeele Wim P Vandenberghe Ilse Vanhorebeek Eva C Vaquero Guillermo Velasco Tibor Vellai Jose Miguel Vicencio Richard D Vierstra Miquel Vila Cécile Vindis Giampietro Viola Maria Teresa Viscomi Olga V Voitsekhovskaja Clarissa von Haefen Marcela Votruba Keiji Wada Richard Wade-Martins Cheryl L Walker Craig M Walsh Jochen Walter Xiang-Bo Wan Aimin Wang Chenguang Wang Dawei Wang Fan Wang Fen Wang Guanghui Wang Haichao Wang Hong-Gang Wang Horng-Dar Wang Jin Wang Ke Wang Mei Wang Richard C Wang Xinglong Wang Xuejun Wang Ying-Jan Wang Yipeng Wang Zhen Wang Zhigang Charles Wang Zhinong Wang Derick G Wansink Diane M Ward Hirotaka Watada Sarah L Waters Paul Webster Lixin Wei Conrad C Weihl William A Weiss Scott M Welford Long-Ping Wen Caroline A Whitehouse J Lindsay Whitton Alexander J Whitworth Tom Wileman John W Wiley Simon Wilkinson Dieter Willbold Roger L Williams Peter R Williamson Bradly G Wouters Chenghan Wu Dao-Cheng Wu William K K Wu Andreas Wyttenbach Ramnik J Xavier Zhijun Xi Pu Xia Gengfu Xiao Zhiping Xie Zhonglin Xie Da-zhi Xu Jianzhen Xu Liang Xu Xiaolei Xu Ai Yamamoto Akitsugu Yamamoto Shunhei Yamashina Michiaki Yamashita Xianghua Yan Mitsuhiro Yanagida Dun-Sheng Yang Elizabeth Yang Jin-Ming Yang Shi Yu Yang Wannian Yang Wei Yuan Yang Zhifen Yang Meng-Chao Yao Tso-Pang Yao Behzad Yeganeh Wei-Lien Yen Jia-jing Yin Xiao-Ming Yin Ook-Joon Yoo Gyesoon Yoon Seung-Yong Yoon Tomohiro Yorimitsu Yuko Yoshikawa Tamotsu Yoshimori Kohki Yoshimoto Ho Jin You Richard J Youle Anas Younes Li Yu Long Yu Seong-Woon Yu Wai Haung Yu Zhi-Min Yuan Zhenyu Yue Cheol-Heui Yun Michisuke Yuzaki Olga Zabirnyk Elaine Silva-Zacarin David Zacks Eldad Zacksenhaus Nadia Zaffaroni Zahra Zakeri Herbert J Zeh Scott O Zeitlin Hong Zhang Hui-Ling Zhang Jianhua Zhang Jing-Pu Zhang Lin Zhang Long Zhang Ming-Yong Zhang Xu Dong Zhang Mantong Zhao Yi-Fang Zhao Ying Zhao Zhizhuang J Zhao Xiaoxiang Zheng Boris Zhivotovsky Qing Zhong Cong-Zhao Zhou Changlian Zhu Wei-Guo Zhu Xiao-Feng Zhu Xiongwei Zhu Yuangang Zhu Teresa Zoladek Wei-Xing Zong Antonio Zorzano Jürgen Zschocke Brian Zuckerbraun

Autophagy 2012 Apr;8(4):445-544

Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

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April 2012

Identification of a novel PEX14 mutation in Zellweger syndrome.

BMJ Case Rep 2009 23;2009. Epub 2009 Jan 23.

K.U.Leuven, Moleculaire Celbiologie, Campust Gasthuisberg ON1, Herestraat 49 box 601, Leuven, 3000, Belgium.

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November 2011

Intraperoxisomal redox balance in mammalian cells: oxidative stress and interorganellar cross-talk.

Mol Biol Cell 2011 May 3;22(9):1440-51. Epub 2011 Mar 3.

Laboratory of Lipid Biochemistry and Protein Interactions, Department of Molecular Cell Biology, Katholieke Universiteit Leuven, 3000 Leuven, Belgium.

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May 2011

Pex11pbeta-mediated growth and division of mammalian peroxisomes follows a maturation pathway.

J Cell Sci 2010 Aug 20;123(Pt 16):2750-62. Epub 2010 Jul 20.

Centre for Cell Biology and Department of Biology, University of Aveiro, Aveiro, Portugal.

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August 2010

Peroxisomes in zebrafish: distribution pattern and knockdown studies.

Histochem Cell Biol 2010 Jul 17;134(1):39-51. Epub 2010 Jun 17.

Department of Pharmaceutical Sciences, KU Leuven, Leuven, Belgium.

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July 2010

The cytosolic domain of PEX3, a protein involved in the biogenesis of peroxisomes, binds membrane lipids.

Biochim Biophys Acta 2009 Nov 26;1793(11):1669-75. Epub 2009 Aug 26.

Instituto de Biologia Molecular e Celular (IBMC), Universidade do Porto, 4150-180 Porto, Portugal.

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November 2009

Peroxisome dynamics in cultured mammalian cells.

Traffic 2009 Nov 4;10(11):1722-33. Epub 2009 Aug 4.

Katholieke Universiteit Leuven, Faculteit Geneeskunde, Departement Moleculaire Celbiologie, LIPIT, Campus Gasthuisberg (O&N 1), Leuven, Belgium.

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November 2009

Mapping the cargo protein membrane translocation step into the PEX5 cycling pathway.

J Biol Chem 2009 Oct 23;284(40):27243-51. Epub 2009 Jul 23.

Instituto de Biologia Molecular e Celular (IBMC), Universidade do Porto, 4150-180 Porto, Portugal.

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October 2009

Properties of the ubiquitin-pex5p thiol ester conjugate.

J Biol Chem 2009 Apr 10;284(16):10504-13. Epub 2009 Feb 10.

Instituto de Biologia Molecular e Celular (IBMC), Universidade do Porto, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.

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April 2009

Comparison of the PTS1- and Rab8b-binding properties of Pex5p and Pex5Rp/TRIP8b.

Biochim Biophys Acta 2008 May 29;1783(5):864-73. Epub 2008 Feb 29.

Katholieke Universiteit Leuven, Campus Gasthuisberg (O&N 1), Departement Moleculaire Celbiologie, LIPIT, Leuven, Belgium.

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May 2008

Ubiquitination of mammalian Pex5p, the peroxisomal import receptor.

J Biol Chem 2007 Oct 28;282(43):31267-72. Epub 2007 Aug 28.

Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua do Campo Alegre 823, 4150-180 Porto, Portugal.

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October 2007

Functional characterization of two missense mutations in Pex5p - C11S and N526K.

Biochim Biophys Acta 2007 Jul 29;1773(7):1141-8. Epub 2007 Apr 29.

Instituto de Biologia Molecular e Celular (IBMC), Porto, Portugal.

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July 2007

Targeting signals in peroxisomal membrane proteins.

Biochim Biophys Acta 2006 Dec 25;1763(12):1629-38. Epub 2006 Aug 25.

Katholieke Universiteit Leuven, Faculty of Medicine, Department of Molecular Cell Biology, Division of Pharmacology, Campus Gasthuisberg, Herestraat 49 bus 601, 3000 Leuven, Belgium.

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December 2006

Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions.

Biochim Biophys Acta 2006 Dec 26;1763(12):1639-46. Epub 2006 Sep 26.

Department of Biology, Faculty of Sciences, Kyushu University Graduate School, 6-10-1 Hakozaki, Fukuoka 812-8581, Japan.

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December 2006

The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step.

J Biol Chem 2006 Nov 15;281(45):34492-502. Epub 2006 Sep 15.

Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.

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November 2006

Trypanosoma brucei glycosomal ABC transporters: identification and membrane targeting.

Mol Membr Biol 2006 Mar-Apr;23(2):157-72

Research Unit for Tropical Diseases, Christian de Duve Institute of Cellular Pathology and Laboratory of Biochemistry, Université catholique de Louvain, Brussels, Belgium.

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July 2006

Localization of a portion of the liver isoform of fatty-acid-binding protein (L-FABP) to peroxisomes.

Biochem J 2006 Mar;394(Pt 2):475-84

Department of Biochemistry, Biocenter Oulu, University of Oulu, Linnanmaa, P.O. Box 3000, FIN-90014 Oulu, Finland.

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http://dx.doi.org/10.1042/BJ20051058DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1408678PMC
March 2006

The N-terminal half of the peroxisomal cycling receptor Pex5p is a natively unfolded domain.

J Mol Biol 2006 Mar 19;356(4):864-75. Epub 2005 Dec 19.

Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.

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http://dx.doi.org/10.1016/j.jmb.2005.12.002DOI Listing
March 2006

Pex5p, the peroxisomal cycling receptor, is a monomeric non-globular protein.

J Biol Chem 2005 Jul 2;280(26):24404-11. Epub 2005 May 2.

Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Portugal.

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http://dx.doi.org/10.1074/jbc.M501985200DOI Listing
July 2005

Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis.

J Mol Biol 2005 Mar 28;346(5):1275-86. Epub 2005 Jan 28.

Departement Moleculaire Celbiologie, Afdeling Farmacologie, Katholieke Universiteit Leuven, Faculteit Geneeskunde, Campus Gasthuisberg (O/N 6, box 601), Herestraat 49, 3000 Leuven, Belgium.

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March 2005

The N terminus of the peroxisomal cycling receptor, Pex5p, is required for redirecting the peroxisome-associated peroxin back to the cytosol.

J Biol Chem 2004 Nov 24;279(45):46573-9. Epub 2004 Aug 24.

Instituto de Biologia Molecular e Celular, Rua do Campo Alegre, 823, 4150-180 Porto, Instituto de Ciências Biomédicas de Abel Salazar, Largo do Professor Abel Salazar, 2, 4099-003 Porto, Portugal.

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November 2004

Potential role for Pex19p in assembly of PTS-receptor docking complexes.

J Biol Chem 2004 Mar 10;279(13):12615-24. Epub 2004 Jan 10.

Katholieke Universiteit Leuven, Faculteit Geneeskunde, Campus Gasthuisberg (O/N), Departement Moleculaire Celbiologie, Afdeling Farmacologie, Herestraat 49, B-3000 Leuven, Belgium.

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March 2004

Functional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxins.

Biochem J 2002 Jul;365(Pt 1):41-50

Katholieke Universiteit Leuven, Fakulteit Geneeskunde, Campus Gasthuisberg (O/N), Afdeling Farmakologie, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1042/BJ20011432DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1222642PMC
July 2002

Analysis of mammalian peroxin interactions using a non-transcription-based bacterial two-hybrid assay.

Mol Cell Proteomics 2002 Mar;1(3):243-52

Departement Moleculaire Celbiologie, Afdeling Farmacologie, Katholieke Universiteit Leuven, Campus Gasthuisberg, Herestraat 49 (O/N), B-3000 Leuven, Belgium.

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March 2002