A mouse model for Zellweger syndrome

Baes, Myriam, Gressens, Pierre, Baumgart, Eveline, Carmeliet, Peter, Casteels, Minne, Fransen, Marc, Evrard, Philippe, Fahimi, Dariush, Declercq, Peter E., Collen, Désiré, van Veldhoven, Paul P., Mannaerts, Guy P.·1997·Nature Genetics
DOI 10.1038/ng0997-49

Cited by (275)

Items 101–200 of 275

  1. Peroxisome biogenesis disorders: Molecular basis for impaired peroxisomal membrane assembly
    Yukio Fujiki, Yuichi Yagita, Takashi Matsuzaki · 2012 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  2. Prenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouse
    Steven Huyghe, Minne Casteels, Anneleen Janssen, Liesbeth MEULDERS, Guy P. Mannaerts, Peter E Declercq, Paul P. Van Veldhoven, Myriam I Baes · 2001 · Biochemical Journal
  3. Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders
    Yukio Fujiki, Kanji Okumoto, Masanori Honsho, Yuichi Abe · 2022 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
  4. Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse
    Michael F. Wangler, Yu-Hsin Chao, Vafa Bayat, Νικόλαος Γιαγτζόγλου, Abhijit Babaji Shinde, Nagireddy Putluri, Cristian Coarfa, Taraka R. Donti, Brett H. Graham, Joseph E. Faust et al. · 2017 · PLoS Genetics
  5. Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes
    Minoru Nakayama, Hiroyasu Sato, Takayuki Okuda, Nao Fujisawa, Nozomu Kono, Hiroyuki Arai, Emiko Suzuki, Masato Umeda, Hiroyuki Ishikawa, Kenji Matsuno · 2011 · PLoS ONE
  6. The Neuronal Migration Defect in Mice with Zellweger Syndrome (Pex5Knockout) is not Caused by the Inactivity of Peroxisomal β-Oxidation
    Myriam I Baes, Pierre Gressèns, Steven Huyghe, Katelijne De Nys, C. Qi, Yunbing Jia, G P Mannaerts, Philippe Evrard, Paul P. Van Veldhoven, Peter E Declercq et al. · 2002 · Journal of Neuropathology & Experimental Neurology
  7. Peroxisomes and peroxisomal disorders: The main facts
    Marco Fidaleo · 2009 · Experimental and Toxicologic Pathology
  8. The expression of peroxisomal protein transcripts increased by retinoic acid during neural differentiation☆
    Maryam Ostadsharif, Kamran Ghaedi, Mohammad Hossein Nasr‐Esfahani, Marzieh Mojbafan, Somayeh Tanhaie, Khadijeh Karbalaie, Hossein Baharvand · 2010 · Differentiation
  9. Peroxisome biogenesis: from yeast to man
    Wolf‐H. Kunau · 1998 · Current Opinion in Microbiology
  10. Generalised and conditional inactivation of Pex genes in mice
    Myriam I Baes, Paul P. Van Veldhoven · 2006 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
  11. Peroxisomal Multifunctional Protein-2 Deficiency Causes Motor Deficits and Glial Lesions in the Adult Central Nervous System
    Steven Huyghe, H. Schmalbruch, Leen Hulshagen, Paul P. Van Veldhoven, Myriam I Baes, Dieter Hartmann · 2006 · American Journal Of Pathology
  12. Mass spectrometric analysis of ceramide perturbations in brain and fibroblasts of mice and human patients with peroxisomal disorders
    Benjamin J. Pettus, Myriam I Baes, Mark Busman, Yusuf Awni Hannun, Paul P. Van Veldhoven · 2004 · Rapid Communications in Mass Spectrometry
  13. Alpha‐oxidation of 3‐methyl‐substituted fatty acids and its thiamine dependence
    Minne Casteels, Veerle Foulon, Guy P. Mannaerts, Paul P. Van Veldhoven · 2003 · European Journal of Biochemistry
  14. Multiple paths to peroxisomes: Mechanism of peroxisome maintenance in mammals
    Rong Hua, Peter Kijun Kim · 2015 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
  15. A novel missense variant in ACAA1 contributes to early-onset Alzheimer’s disease, impairs lysosomal function, and facilitates amyloid-β pathology and cognitive decline
    Rongcan Luo, Yu Fan, Jing Yang, Maosen Ye, Dengfeng Zhang, Kun Guo, Xiao Li, Rui Bi, Min Xu, Lu-Xiu Yang et al. · 2021 · Signal Transduction and Targeted Therapy
  16. α‐Synuclein abnormalities in mouse models of peroxisome biogenesis disorders
    Eugenia Yakunin, Ann B. Moser, Virginie Loeb, Ann Saada, Phyllis L. Faust, Denis I. Crane, Myriam I Baes, Ronit Sharon · 2009 · Journal of Neuroscience Research
  17. Molecular genetics of peroxisomal disorders
    W. Moser Hugo · 2000 · Frontiers in bioscience
  18. PEX5 regulates autophagy via the mTORC1-TFEB axis during starvation
    So Young Eun, Joon No Lee, In-Koo Nam, Zhiqiang Liu, Hong‐Seob So, Seong‐Kyu Choe, Raekil Park · 2018 · Experimental & Molecular Medicine
  19. Cre-Mediated Stress Affects Sirtuin Expression Levels, Peroxisome Biogenesis and Metabolism, Antioxidant and Proinflammatory Signaling Pathways
    Yu Xiao, Srikanth Karnati, Guofeng Qian, Anca Nenicu, Wei Fan, Svetlin Tchatalbachev, Anita Windhorst, Hamid Hossain, Florian Guillou, Georg H. Lüers et al. · 2012 · PLoS ONE
  20. Peroxisome deficient invertebrate and vertebrate animal models
    Paul P. Van Veldhoven, Myriam I Baes · 2013 · Frontiers in Physiology
  21. Peroxisomes as Modulators of Cellular Protein Thiol Oxidation: A New Model System
    Celien Lismont, Marcus Nordgren, Chantal Brees, Bernard Knoops, Paul P. Van Veldhoven, Marc Fransen · 2017 · Antioxidants and Redox Signaling
  22. Peroxisomal Membrane Contact Sites in Mammalian Cells
    Chao Chen, Jing Li, Xuhui Qin, Wei Wang · 2020 · Frontiers in Cell and Developmental Biology
  23. Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency
    Iris Oezen, Walter Rossmanith, Sonja Forss‐Petter, Stephan Kemp, Till Voigtländer, Karin Moser-Thier, Ronald J. A. Wanders, Reginald E. Bittner, Johannes Berger · 2005 · Human Molecular Genetics
  24. Functional studies on human Pex7p: subcellular localization and interaction with proteins containing a peroxisome-targeting signal type 2 and other peroxins
    Karen Ghys, Marc Fransen, Guy P. Mannaerts, Paul P. Van Veldhoven · 2002 · Biochemical Journal
  25. Identification of PEX5p-related novel peroxisome-targeting signal 1 (PTS1)-binding proteins in mammals
    Leen Amery, Hideki Sano, Guy P. Mannaerts, Jamie D. Snider, Jeroen van LOOY, Marc Fransen, Paul P. Van Veldhoven · 2001 · Biochemical Journal
  26. On the presence of C2-ceramide in mammalian tissues: possible relationship to etherphospholipids and phosphorylation by ceramide kinase
    Helena Van Overloop, Yves Denizot, Myriam I Baes, Paul P. Van Veldhoven · 2007 · Biological Chemistry
  27. Pex11a deficiency causes dyslipidaemia and obesity in mice
    Congcong Chen, Hongwei Wang, Bicheng Chen, Deyuan Chen, Chaosheng Lu, Haiyan Li, Yan Qian, Yi Tan, Huachun Weng, Lu Cai · 2018 · Journal of Cellular and Molecular Medicine
  28. Lipid droplet-associated kinase STK25 regulates peroxisomal activity and metabolic stress response in steatotic liver
    Annika Nerstedt, Yeshwant Kurhe, Emmelie Cansby, Mara Caputo, Lei Gao, Egor A. Vorontsov, Marcus Ståhlman, Esther Nuñez‐Durán, Jan Borén, Hanns–Ulrich Marschall et al. · 2019 · Journal of Lipid Research
  29. Generation of Pex5‐loxP mice allowing the conditional elimination of peroxisomes
    Myriam I Baes, Mieke A. Dewerchin, A. Janssen, Désiré Collen, Peter Carmeliet · 2002 · genesis
  30. SIRT3 improved peroxisomes-mitochondria interplay and prevented cardiac hypertrophy via preserving PEX5 expression
    Minghui Wang, Yan-qing Ding, Yuehuai Hu, Zeyu Li, Wenwei Luo, Peiqing Liu, Zhuoming Li · 2023 · Redox Biology
  31. The rice peroxisomal receptor PEX5 negatively regulates resistance to rice blast fungus Magnaporthe oryzae
    Xiaoman You, Shanshan Zhu, Haowen Sheng, Zheng Liu, Dan Wang, Min Wang, Xiao Hui Xu, Feng He, Hong Fang, Fan Zhang et al. · 2023 · Cell Reports
  32. Peroxisomes in Different Skeletal Cell Types during Intramembranous and Endochondral Ossification and Their Regulation during Osteoblast Differentiation by Distinct Peroxisome Proliferator-Activated Receptors
    Guofeng Qian, Wei Fan, Barbara Ahlemeyer, Srikanth Karnati, Eveline Baumgart‐Vogt · 2015 · PLoS ONE
  33. LIS1—no more no less
    Orly Reiner, Aviv Cahana, Teresa Escámez, Salvador Martı́nez · 2002 · Molecular Psychiatry
  34. Zellweger Syndrome Knockout Mouse Models Challenge Putative Peroxisomal β-Oxidation Involvement in Docosahexaenoic Acid (22:6n-3) Biosynthesis
    Juan P. Infante, Virginia A. Huszagh · 2001 · Molecular Genetics and Metabolism
  35. Mitochondrial changes and oxidative stress in a mouse model of Zellweger syndrome neuropathogenesis
    Rani Sadia Rahim, Mo Chen, C. Cathrin Nourse, Adrian Cuda Banda Meedeniya, Denis I. Crane · 2016 · Neuroscience
  36. Peroxisomes Are Formed from Complex Membrane Structures inPEX6-deficient CHO Cells upon Genetic Complementation
    Noriyo Hashiguchi, Tomoko Kojidani, Tsuneo Imanaka, Tokuko Haraguchi, Yasushi Hiraoka, Eveline Baumgart‐Vogt, Sadaki Yokota, Toshiro Tsukamoto, Takashi Osumi · 2002 · Molecular Biology of the Cell
  37. Normal and abnormal neuronal migration in the developing cerebral cortex.
    Xue‐Zhi Sun, Sentaro Takahashi, Chun Cui, Rui Zhang, Hiromi Sakata‐Haga, Kazuhiko Sawada, Yoshihiro Fukui · 2002 · PubMed
  38. The peroxisomal targeting sequence type 1 receptor, Pex5p, and the peroxisomal import efficiency of alanine:glyoxylate aminotransferase
    Tracy G. Knott, Graeme M. Birdsey, Kirsty E. SINCLAIR, Imelda M. Gallagher, P. Edward Purdue, Christopher J. Danpure · 2000 · Biochemical Journal
  39. Comparison of the PTS1- and Rab8b-binding properties of Pex5p and Pex5Rp/TRIP8b
    Marc Fransen, Leen Amery, Andreas Hartig, Chantal Brees, Anja Rabijns, Guy P. Mannaerts, Paul P. Van Veldhoven · 2008 · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
  40. Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum
    Yuichi Abe, Masanori Honsho, Ryota Itoh, Ryoko Kawaguchi, Masashi Fujitani, Kazushirou Fujiwara, Masaaki Hirokane, Takashi Matsuzaki, Keiko Nakayama, Ryohei Ohgi et al. · 2018 · Life Science Alliance
  41. High content screening for nonclassical peroxisome proliferators
    Jonathan Z. Sexton · 2010 · International Journal of High Throughput Screening
  42. Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites
    Abhijit Babaji Shinde, Ritesh Kumar Baboota, Simone W. Denis, Ursula Loizides‐Mangold, Annelies Peeters, Marc Espeel, Ana Rita Malheiro, Howard Riezman, Stefan Vinckier, Frédéric Maxime Vaz et al. · 2017 · Mitochondrion
  43. Mouse Models and Genetic Modifiers in X-Linked Adrenoleukodystrophy
    Ann K. Heinzer, Martina C. McGuinness, Jyh‐Feng Lu, Oscar Colin Stine, Heming Wei, Mark Van Der Vlies, Gao-Xiang Dong, James F. Powers, Paul A. Watkins, Kirby D. Smith · 2003 · Advances in experimental medicine and biology
  44. Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders
    Yasuyuki Suzuki, Nobuyuki Shimozawa, Atsushi Imamura, Seiji Fukuda, Zhongyi Zhang, Tadao Orii, Naoyuki Kondo · 2001 · Journal of Inherited Metabolic Disease
  45. Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes
    Tomoko Nagase, Nobuyuki Shimozawa, Yasuhiko Takemoto, Yasuyuki Suzuki, Masayuki Komori, Naomi Kondo · 2004 · Biochimica et Biophysica Acta (BBA) - General Subjects
  46. Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse model
    Ilse Vanhorebeek, Myriam I Baes, Peter E Declercq · 2001 · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
  47. Loss of functional peroxisomes leads to increased mitochondrial biogenesis and reduced autophagy that preserve mitochondrial function
    Lijun Chi, Dorothy Lee, Sharon Leung, Guanlan Hu, Bijun Wen, Paul Delgado-Olguı́n, Miluska Vissa, Ren Li, John Hunter Brumell, Peter Kijun Kim et al. · 2023 · Cellular and Molecular Life Sciences
  48. Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger Syndrome: A confocal laser scanning microscopy study
    Manuel J. Santos, Scott C. Henderson, Ann B. Moser, Hugo W. Moser, Paul B. Lazarow · 2000 · Biology of the Cell
  49. Peroxisome-Deficiency and HIF-2α Signaling Are Negative Regulators of Ketohexokinase Expression
    Tanja Eberhart, Miriam J. Schönenberger, Katharina Walter, Khanichi N. Charles, Phyllis L. Faust, Werner J. Kovacs · 2020 · Frontiers in Cell and Developmental Biology
  50. Peroxisome-localized hepatitis Bx protein increases the invasion property of hepatocellular carcinoma cells
    Jae-Min Han, Jung‐Ah Kang, Minhee Han, Kyung-Hun Chung, Chorong Lee, Woo-Keun Song, Youngsoo Jun, Sung‐Gyoo Park · 2014 · Archives of Virology
  51. Cholesterol Biosynthesis and Regulation: Role of Peroxisomes
    Werner J. Kovacs, Skaidrite K. Krisans · 2003 · Advances in experimental medicine and biology
  52. Tetratricopeptide repeat domain of Yarrowia lipolytica Pex5p is essential for recognition of the type 1 peroxisomal targeting signal but does not confer full biological activity on Pex5p
    Rachel K. Szilard, Richard A. Rachubinski · 2000 · Biochemical Journal
  53. Renal tubular peroxisomes are dispensable for normal kidney function
    Camille Ansermet, Gabriel Centeno, Sylvain Pradervand, Dušan Harmáček, Andy Garcia, Jean Daraspe, Sai Kocherlakota, Myriam I Baes, Yohan Bignon, Dmitri Firsov · 2022 · JCI Insight
  54. A review of morphological techniques for detection of peroxisomal (and mitochondrial) proteins and their corresponding mRNAs during ontogenesis in mice: Application to the PEX5‐knockout mouse with Zellweger syndrome
    Eveline Baumgart‐Vogt, H. Dariush Fahimi, Heike Steininger, Markus Grabenbauer · 2003 · Microscopy Research and Technique
  55. Peroxisome Deficiency in Cochlear Hair Cells Causes Hearing Loss by Deregulating BK Channels
    Xiaolong Fu, Peifeng Wan, Ling Lü, Yingcui Wan, Ziyi Liu, Guodong Hong, Shengda Cao, Xiuli Bi, Jing Zhou, Ruifeng Qiao et al. · 2023 · Advanced Science
  56. Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101
    Ryuichi Natsuyama, Kanji Okumoto, Yukio Fujiki · 2012 · Biochemical Journal
  57. Combined deficiency of peroxisomal β-oxidation and ether lipid synthesis in mice causes only minor cortical neuronal migration defects but severe hypotonia
    Krysko, Olga, Bottelbergs, Astrid, Veldhoven, Paul Van, Baes, Myriam · 2010 · Molecular Genetics and Metabolism
  58. Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder
    Kevin Berendse, Maxim Boek, Marion J. Gijbels, Nicole N. van der Wel, Femke C. C. Klouwer, Marius A. van den Bergh Weerman, Abhijit Babaji Shinde, Rob Ofman, Bwee Tien Poll‐The, Sander M. Houten et al. · 2019 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  59. Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders
    M. Gartz Hanson, Veronica L. Hood, Justin D. Vrana, Chandra L. Tucker, Lee Ann Niswander · 2014 · Developmental Biology
  60. Alterations of fatty acid metabolism and membrane fluidity in peroxisome‐defective mutant ZP102 cells
    Michiaki Nagura, Makiko Saito, Masao Iwamori, Yoichi Sakakihara, Takashi Igarashi · 2004 · Lipids
  61. A novel migration-related gene product, doublecortin, in neuronal migration disorder of fetuses and infants with Zellweger syndrome
    Jiali Qin, Masashi Mizuguchi, Masayuki Itoh, Sachio Takashima · 2000 · Acta Neuropathologica
  62. Peroxisomal Membrane Protein Import Does Not Require Pex17p
    Courtney C. Harper, Sarah T. South, J. Michael McCaffery, Stephen J. Gould · 2002 · Journal of Biological Chemistry
  63. Hepatitis C virus alters the morphology and function of peroxisomes
    Esther Martin de Fourchambault, Nathalie Callens, Jean‐Michel Saliou, Marie Fourcot, Océane Delos, Nicolas Barois, Quentin Thorel, Santseharay Ramírez, Jens Bukh, Laurence Cocquerel et al. · 2023 · Frontiers in Microbiology
  64. PEX3 promotes regenerative repair after myocardial injury in mice through facilitating plasma membrane localization of ITGB3
    Jia-Teng Sun, Zimu Wang, Liuhua Zhou, Tongtong Yang, Di Zhao, Yu-Lin Bao, Sibo Wang, Lingfeng Gu, Jiawen Chen, Tiankai Shan et al. · 2024 · Communications Biology
  65. PPAR-γImpairment Alters Peroxisome Functionality in Primary Astrocyte Cell Cultures
    Lorenzo Di Cesare Mannelli, Matteo Zanardelli, Laura Micheli, Carla Ghelardini · 2014 · BioMed Research International
  66. Impaired plasmalogen synthesis dysregulates liver X receptor-dependent transcription in cerebellum
    Masanori Honsho, Fabian Dorninger, Yuichi Abe, Daiki Setoyama, Ryohei Ohgi, Takeshi Uchiumi, Dongchon Kang, Johannes Berger, Yukio Fujiki · 2019 · The Journal of Biochemistry
  67. The surprising complexity of peroxisome biogenesis
    Laura J. Olsen · 1998 · Springer eBooks
  68. Control of mitochondrial dynamics and apoptotic pathways by peroxisomes
    Chenxing Jiang, Tomohiko Okazaki · 2022 · Frontiers in Cell and Developmental Biology
  69. In vivo labeling of peroxisomes by photoconvertible mEos2 in myelinating glia of mice
    Sarah Richert, Sandra Kleinecke, Jenniffer Günther, Florian Schaumburg, Julia M. Edgar, Gerd Ulrich Nienhaus, Klaus‐Armin Nave, Celia M. Kassmann · 2013 · Biochimie
  70. Zebrafish model of human Zellweger syndrome reveals organ-specific accumulation of distinct fatty acid species and widespread gene expression changes
    Shigeo Takashima, Shoko Takemoto, Kayoko Toyoshi, Akiko Ohba, Nobuyuki Shimozawa · 2021 · Molecular Genetics and Metabolism
  71. Genome-wide association study using haplotype libraries and repeated-measures model to identify candidate genomic regions for stillbirth in Holstein cattle
    Pablo Augusto de Souza Fonseca, Flávio Schramm Schenkel, Ángela Cánovas · 2022 · Journal of Dairy Science
  72. Longitudinal study of Pex1-G844D NMRI mouse model: A robust pre-clinical model for mild Zellweger spectrum disorder
    Tanguy Demaret, Martin Roumain, Jérôme Ambroise, Jonathan Evraerts, Joachim Ravau, Caroline Bouzin, Bertrand Bearzatto, Jean‐Luc Gala, Hedwig C.M. Stepman, Sandrine Marie et al. · 2020 · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  73. A peroxisome deficiency–induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway
    Yuichi Abe, Masanori Honsho, Ryoko Kawaguchi, Takashi Matsuzaki, Yayoi Ichiki, Masashi Fujitani, Kazushirou Fujiwara, Masaaki Hirokane, Masahide Oku, Yasuyoshi Sakai et al. · 2020 · Journal of Biological Chemistry
  74. Role of peroxisomes in the pathogenesis and therapy of renal fibrosis
    Dan Zhang, Yang-He Zhang, Bin Liu, Hongxia Yang, Guangtao Li, Honglan Zhou, Yishu Wang · 2025 · Metabolism
  75. Central serotonergic neuron deficiency in a mouse model of Zellweger syndrome
    Rani Sadia Rahim, Adrian Cuda Banda Meedeniya, Denis I. Crane · 2014 · Neuroscience
  76. Viperin interacts with PEX19 to mediate peroxisomal augmentation of the innate antiviral response
    Onruedee Khantisitthiporn, Byron Shue, Nicholas S. Eyre, Colt W Nash, Lynne Turnbull, Cynthia B. Whitchurch, Kylie H. Van der Hoek, Karla J. Helbig, Michael R. Beard · 2021 · Life Science Alliance
  77. Genetic and molecular bases of peroxisome biogenesis disorders
    Yasuyuki Suzuki, Nobuyuki Shimozawa, Tadao Orii, Toshiro Tsukamoto, Takashi Osumi, Yukio Fujiki, Naomi Kondo · 2001 · Genetics in Medicine
  78. Developmental Roles of D-bifunctional Protein-A Zebrafish Model of Peroxisome Dysfunction
    Yong‐Il Kim, Sushil Bhandari, Joon No Lee, Kyeong‐Won Yoo, Se-Jin Kim, Gi‐Su Oh, Hyungjin Kim, Meyoung Cho, Jong-Young Kwak, Hong‐Seob So et al. · 2014 · Molecules and Cells
  79. Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures
    Marianne Depreter, Tom O. G. Tytgat, Sonja Beken, Marc Espeel, Karen De Smet, Vera Rogiers, Frank Roels · 2000 · Journal of Hepatology
  80. Neuronal Migration Disorders
    Pierre Gressèns · 2005 · Journal of Child Neurology
  81. Loss of pex5 sensitizes zebrafish to fasting due to deregulated mitochondria, mTOR, and autophagy
    Sushil Bhandari, Yong‐Il Kim, In-Koo Nam, KwangHeum Hong, Yunju Jo, Kyeong‐Won Yoo, Weifang Liao, Jae‐Young Lim, Seong‐Jin Kim, Jae‐Young Um et al. · 2023 · Cellular and Molecular Life Sciences
  82. Peroxisomes in dental tissues of the mouse
    Ingra Stelzig, Srikanth Karnati, Klaus Peter Valerius, Eveline Baumgart‐Vogt · 2013 · Histochemistry and Cell Biology
  83. Pathogenesis of peroxisomal deficiency disorders (Zellweger syndrome) may be mediated by misregulation of the GABAergic system viathe diazepam binding inhibitor
    Rainer Breitling · 2004 · BMC Pediatrics
  84. In Situ Hybridization: General Principles and Application of Digoxigenin-Labeled cRNA for the Detection of mRNAs
    Eveline Baumgart‐Vogt, Arno Schad, Markus Grabenbauer · 2001 · Birkhäuser Boston eBooks
  85. Isolation and Biochemical Characterization of Peroxisomes from Cultured Rat Glial Cells
    Inderjit Singh, Oscar Carillo, Aryan M. A. Namboodiri · 2000 · Neurochemical Research
  86. Alterations in peroxisome-mitochondria interplay in skeletal muscle accelerate muscle dysfunction
    Marco Scalabrin, Eloisa Turco, Ilaria Davigo, Riccardo Filadi, Leonardo Nogara, Gaia Gherardi, Lucia Barazzuol, Andrea Armani, Giulia Trani, Samuele Negro et al. · 2025 · Nature Communications
  87. A Novel FRET Approach Quantifies the Interaction Strength of Peroxisomal Targeting Signals and Their Receptor in Living Cells
    Bernhard Hochreiter, Cheng‐Shoong Chong, Andreas Hartig, Sebastian Maurer‐Stroh, Johannes Berger, Johannes A. Schmid, Markus Kunze · 2020 · Cells
  88. A Pex7 Deficient Mouse Series Correlates Biochemical and Neurobehavioral Markers to Genotype Severity—Implications for the Disease Spectrum of Rhizomelic Chondrodysplasia Punctata Type 1
    Wedad Fallatah, Wei Cui, Erminia Di Pietro, Grace T. Carter, Brittany Pounder, Fabian Dorninger, Christian Pifl, Ann B. Moser, Johannes Berger, Nancy Braverman · 2022 · Frontiers in Cell and Developmental Biology
  89. Differential activities of peroxisomes along the mouse intestinal epithelium
    Petruta Lavinia Morvay, Myriam I Baes, Paul P. Van Veldhoven · 2017 · Cell Biochemistry and Function
  90. Peroxisomes: 40 years of histochemical staining, personal reminiscences
    H. Dariush Fahimi · 2009 · Histochemistry and Cell Biology
  91. Microporation is an efficient method for siRNA-induced knockdown of PEX5 in HepG2 cells: evaluation of the transfection efficiency, the PEX5 mRNA and protein levels and induction of peroxisomal deficiency
    Barbara Ahlemeyer, Julia-Franziska Vogt, Vera Michel, Petra Hahn-Kohlberger, Eveline Baumgart‐Vogt · 2014 · Histochemistry and Cell Biology
  92. Maturation of the liver-specific peroxisome versus laminin, collagen IV and integrin expression
    Marianne Depreter · 1998 · Biology of the Cell
  93. Peroxisome Biogenesis Disorders
    Yukio Fujiki · 2006 · Encyclopedia of Life Sciences
  94. Peroxisome Deficiency Impairs BDNF Signaling and Memory
    Yuichi Abe, Yoshiki Nishimura, Kaori Nakamura, Shigehiko Tamura, Masanori Honsho, Hiroshi Udo, Toshihide Yamashita, Yukio Fujiki · 2020 · Frontiers in Cell and Developmental Biology
  95. Lessons from Knockout Mice. I: Phenotypes of Mice with Peroxisome Biogenesis Disorders
    Myriam I Baes, Paul P. Van Veldhoven · 2003 · Advances in experimental medicine and biology
  96. Experimental evidence that pristanic acid disrupts mitochondrial homeostasis in brain of young rats
    Estela Natacha Brandt Busanello, Alexandre Umpierrez Amaral, Anelise Miotti Tonin, Mateus Grings, Alana Pimentel Moura, Paula Eichler, Carmen Regla Vargas, Moaçir Wajner · 2011 · Journal of Neuroscience Research
  97. Pex13, the Mouse Ortholog of the Human Peroxisome Biogenesis Disorder PEX13 Gene: Gene Structure, Tissue Expression, and Localization of the Protein to Peroxisomes
    Jonas Björkman, Stephen J. Gould, Denis I. Crane · 2002 · Genomics
  98. PEX5 prevents cardiomyocyte hypertrophy via suppressing the redox-sensitive signaling pathways MAPKs and STAT3
    Minghui Wang, Jingyan Li, Yan-qing Ding, Sidong Cai, Zhuoming Li, Peiqing Liu · 2021 · European Journal of Pharmacology
  99. Peroxisome biogenesis factor PEX14 is crucial for survival and fecundity of female brown planthopper, Nilaparvata lugens (Stål)
    Yuqiong Liu, Huan Dai, Anfu Bamu, Xinda Lin · 2024 · Insect Biochemistry and Molecular Biology
  100. The mouse gene encoding the peroxisomal membrane protein 1‐like protein (PXMP1‐L): cDNA cloning, genomic organization and comparative expression studies1
    Andreas Holzinger, Ania Carolina Muntau, Peter Mayerhofer, Stefan Kammerer, Sabrina Albet, Maurice Bugaut, Adelbert Anton Roscher · 1998 · FEBS Letters