Artykuły w czasopismach na temat „PEX1”
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Knoops, Kèvin, Rinse de Boer, Anita Kram i Ida J. van der Klei. "Yeast pex1 cells contain peroxisomal ghosts that import matrix proteins upon reintroduction of Pex1". Journal of Cell Biology 211, nr 5 (7.12.2015): 955–62. http://dx.doi.org/10.1083/jcb.201506059.
Pełny tekst źródłaVerner, Zdeněk, Vojtěch Žárský, Tien Le, Ravi Kumar Narayanasamy, Petr Rada, Daniel Rozbeský, Abhijith Makki i in. "Anaerobic peroxisomes in Entamoeba histolytica metabolize myo-inositol". PLOS Pathogens 17, nr 11 (15.11.2021): e1010041. http://dx.doi.org/10.1371/journal.ppat.1010041.
Pełny tekst źródłaAgrawal, Gaurav, Scott N. Fassas, Zhi-Jie Xia i Suresh Subramani. "Distinct requirements for intra-ER sorting and budding of peroxisomal membrane proteins from the ER". Journal of Cell Biology 212, nr 3 (1.02.2016): 335–48. http://dx.doi.org/10.1083/jcb.201506141.
Pełny tekst źródłaMiyata, Non, i Yukio Fujiki. "Shuttling Mechanism of Peroxisome Targeting Signal Type 1 Receptor Pex5: ATP-Independent Import and ATP-Dependent Export". Molecular and Cellular Biology 25, nr 24 (15.12.2005): 10822–32. http://dx.doi.org/10.1128/mcb.25.24.10822-10832.2005.
Pełny tekst źródłaGonzalez, Kim L., Sarah E. Ratzel, Kendall H. Burks, Charles H. Danan, Jeanne M. Wages, Bethany K. Zolman i Bonnie Bartel. "A pex1 missense mutation improves peroxisome function in a subset of Arabidopsis pex6 mutants without restoring PEX5 recycling". Proceedings of the National Academy of Sciences 115, nr 14 (19.03.2018): E3163—E3172. http://dx.doi.org/10.1073/pnas.1721279115.
Pełny tekst źródłaTitorenko, V. I., D. M. Ogrydziak i R. A. Rachubinski. "Four distinct secretory pathways serve protein secretion, cell surface growth, and peroxisome biogenesis in the yeast Yarrowia lipolytica." Molecular and Cellular Biology 17, nr 9 (wrzesień 1997): 5210–26. http://dx.doi.org/10.1128/mcb.17.9.5210.
Pełny tekst źródłaChang, C. C., S. South, D. Warren, J. Jones, A. B. Moser, H. W. Moser i S. J. Gould. "Metabolic control of peroxisome abundance". Journal of Cell Science 112, nr 10 (15.05.1999): 1579–90. http://dx.doi.org/10.1242/jcs.112.10.1579.
Pełny tekst źródłaKnoops, Kèvin, Selvambigai Manivannan, Małgorzata N. Cepińska, Arjen M. Krikken, Anita M. Kram, Marten Veenhuis i Ida J. van der Klei. "Preperoxisomal vesicles can form in the absence of Pex3". Journal of Cell Biology 204, nr 5 (3.03.2014): 659–68. http://dx.doi.org/10.1083/jcb.201310148.
Pełny tekst źródłaPlatta, Harald W., Fouzi El Magraoui, Bastian E. Bäumer, Daniel Schlee, Wolfgang Girzalsky i Ralf Erdmann. "Pex2 and Pex12 Function as Protein-Ubiquitin Ligases in Peroxisomal Protein Import". Molecular and Cellular Biology 29, nr 20 (17.08.2009): 5505–16. http://dx.doi.org/10.1128/mcb.00388-09.
Pełny tekst źródłaJudy, Ryan M., Connor J. Sheedy i Brooke M. Gardner. "Insights into the Structure and Function of the Pex1/Pex6 AAA-ATPase in Peroxisome Homeostasis". Cells 11, nr 13 (29.06.2022): 2067. http://dx.doi.org/10.3390/cells11132067.
Pełny tekst źródłaMotley, Alison M., Paul C. Galvin, Lakhan Ekal, James M. Nuttall i Ewald H. Hettema. "Reevaluation of the role of Pex1 and dynamin-related proteins in peroxisome membrane biogenesis". Journal of Cell Biology 211, nr 5 (7.12.2015): 1041–56. http://dx.doi.org/10.1083/jcb.201412066.
Pełny tekst źródłaBlok, Neil B., Dongyan Tan, Ray Yu-Ruei Wang, Pawel A. Penczek, David Baker, Frank DiMaio, Tom A. Rapoport i Thomas Walz. "Unique double-ring structure of the peroxisomal Pex1/Pex6 ATPase complex revealed by cryo-electron microscopy". Proceedings of the National Academy of Sciences 112, nr 30 (13.07.2015): E4017—E4025. http://dx.doi.org/10.1073/pnas.1500257112.
Pełny tekst źródłaIdnurm, Alexander, Steven S. Giles, John R. Perfect i Joseph Heitman. "Peroxisome Function Regulates Growth on Glucose in the Basidiomycete Fungus Cryptococcus neoformans". Eukaryotic Cell 6, nr 1 (13.10.2006): 60–72. http://dx.doi.org/10.1128/ec.00214-06.
Pełny tekst źródłaSchell-Steven, Annette, Katharina Stein, Mara Amoros, Christiane Landgraf, Rudolf Volkmer-Engert, Hanspeter Rottensteiner i Ralf Erdmann. "Identification of a Novel, Intraperoxisomal Pex14-Binding Site in Pex13: Association of Pex13 with the Docking Complex Is Essential for Peroxisomal Matrix Protein Import". Molecular and Cellular Biology 25, nr 8 (15.04.2005): 3007–18. http://dx.doi.org/10.1128/mcb.25.8.3007-3018.2005.
Pełny tekst źródłaHavali, Cengiz, Sevil Dorum, Yılmaz Akbaş, Orhan Görükmez i Tugba Hirfanoglu. "Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation". Journal of Pediatric Endocrinology and Metabolism 33, nr 3 (26.03.2020): 437–41. http://dx.doi.org/10.1515/jpem-2019-0194.
Pełny tekst źródłaSchieferdecker, Anne, i Petra Wendler. "Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex". International Journal of Molecular Sciences 20, nr 15 (1.08.2019): 3756. http://dx.doi.org/10.3390/ijms20153756.
Pełny tekst źródłaCollins, Cynthia S., Jennifer E. Kalish, James C. Morrell, J. Michael McCaffery i Stephen J. Gould. "The Peroxisome Biogenesis Factors Pex4p, Pex22p, Pex1p, and Pex6p Act in the Terminal Steps of Peroxisomal Matrix Protein Import". Molecular and Cellular Biology 20, nr 20 (15.10.2000): 7516–26. http://dx.doi.org/10.1128/mcb.20.20.7516-7526.2000.
Pełny tekst źródłaNuttall, James M., Alison M. Motley i Ewald H. Hettema. "Deficiency of the exportomer components Pex1, Pex6, and Pex15 causes enhanced pexophagy inSaccharomyces cerevisiae". Autophagy 10, nr 5 (18.03.2014): 835–45. http://dx.doi.org/10.4161/auto.28259.
Pełny tekst źródłaFujiki, Yukio, Non Miyata, Naomi Matsumoto i Shigehiko Tamura. "Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis". Biochemical Society Transactions 36, nr 1 (22.01.2008): 109–13. http://dx.doi.org/10.1042/bst0360109.
Pełny tekst źródłaSmith, Claire E. L., James A. Poulter, Alex V. Levin, Jenina E. Capasso, Susan Price, Tamar Ben-Yosef, Reuven Sharony i in. "Spectrum of PEX1 and PEX6 variants in Heimler syndrome". European Journal of Human Genetics 24, nr 11 (15.06.2016): 1565–71. http://dx.doi.org/10.1038/ejhg.2016.62.
Pełny tekst źródłaChang, Chia-Che, Daniel S. Warren, Katherine A. Sacksteder i Stephen J. Gould. "Pex12 Interacts with Pex5 and Pex10 and Acts Downstream of Receptor Docking in Peroxisomal Matrix Protein Import". Journal of Cell Biology 147, nr 4 (15.11.1999): 761–74. http://dx.doi.org/10.1083/jcb.147.4.761.
Pełny tekst źródłaTAMURA, Shigehiko, Naomi MATSUMOTO, Atsushi IMAMURA, Nobuyuki SHIMOZAWA, Yasuyuki SUZUKI, Naomi KONDO i Yukio FUJIKI. "Phenotype–genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p–Pex6p interaction". Biochemical Journal 357, nr 2 (9.07.2001): 417–26. http://dx.doi.org/10.1042/bj3570417.
Pełny tekst źródłaTitorenko, Vladimir I., i Richard A. Rachubinski. "Mutants of the Yeast Yarrowia lipolyticaDefective in Protein Exit from the Endoplasmic Reticulum Are Also Defective in Peroxisome Biogenesis". Molecular and Cellular Biology 18, nr 5 (1.05.1998): 2789–803. http://dx.doi.org/10.1128/mcb.18.5.2789.
Pełny tekst źródłaMauriac, Stephanie A., Thibault Peineau, Aamir Zuberi, Cathleen Lutz i Gwénaëlle S. G. Géléoc. "Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss". Cells 11, nr 24 (9.12.2022): 3982. http://dx.doi.org/10.3390/cells11243982.
Pełny tekst źródłaSaveria, Tracy, André Halbach, Ralf Erdmann, Rudolf Volkmer-Engert, Christiane Landgraf, Hanspeter Rottensteiner i Marilyn Parsons. "Conservation of PEX19-Binding Motifs Required for Protein Targeting to Mammalian Peroxisomal and Trypanosome Glycosomal Membranes". Eukaryotic Cell 6, nr 8 (22.06.2007): 1439–49. http://dx.doi.org/10.1128/ec.00084-07.
Pełny tekst źródłaMin, Kyunghun, Hokyoung Son, Jungkwan Lee, Gyung Ja Choi, Jin-Cheol Kim i Yin-Won Lee. "Peroxisome Function Is Required for Virulence and Survival of Fusarium graminearum". Molecular Plant-Microbe Interactions® 25, nr 12 (grudzień 2012): 1617–27. http://dx.doi.org/10.1094/mpmi-06-12-0149-r.
Pełny tekst źródłaMastalski, Thomas, Rebecca Brinkmeier i Harald W. Platta. "The Peroxisomal PTS1-Import Defect of PEX1- Deficient Cells Is Independent of Pexophagy in Saccharomyces cerevisiae". International Journal of Molecular Sciences 21, nr 3 (29.01.2020): 867. http://dx.doi.org/10.3390/ijms21030867.
Pełny tekst źródłaRinaldi, Mauro A., Wendell A. Fleming, Kim L. Gonzalez, Jaeseok Park, Meredith J. Ventura, Ashish B. Patel i Bonnie Bartel. "The PEX1 ATPase Stabilizes PEX6 and Plays Essential Roles in Peroxisome Biology". Plant Physiology 174, nr 4 (9.06.2017): 2231–47. http://dx.doi.org/10.1104/pp.17.00548.
Pełny tekst źródłaPedrosa, Ana G., Tânia Francisco, Diana Bicho, Ana F. Dias, Aurora Barros-Barbosa, Vera Hagmann, Gabriele Dodt, Tony A. Rodrigues i Jorge E. Azevedo. "Peroxisomal monoubiquitinated PEX5 interacts with the AAA ATPases PEX1 and PEX6 and is unfolded during its dislocation into the cytosol". Journal of Biological Chemistry 293, nr 29 (8.06.2018): 11553–63. http://dx.doi.org/10.1074/jbc.ra118.003669.
Pełny tekst źródłaWalter, Claudia, Jeannette Gootjes, Petra A. Mooijer, Herma Portsteffen, Christina Klein, Hans R. Waterham, Peter G. Barth i in. "Disorders of Peroxisome Biogenesis Due to Mutations in PEX1: Phenotypes and PEX1 Protein Levels". American Journal of Human Genetics 69, nr 1 (lipiec 2001): 35–48. http://dx.doi.org/10.1086/321265.
Pełny tekst źródłaTan, Dongyan, Neil B. Blok, Tom A. Rapoport i Thomas Walz. "Structures of the double-ring AAA ATPase Pex1-Pex6 involved in peroxisome biogenesis". FEBS Journal 283, nr 6 (12.11.2015): 986–92. http://dx.doi.org/10.1111/febs.13569.
Pełny tekst źródłaSKONECZNY, Marek, i Joanna RYTKA. "Oxygen and haem regulate the synthesis of peroxisomal proteins: catalase A, acyl-CoA oxidase and Pex1p in the yeast Saccharomyces cerevisiae; the regulation of these proteins by oxygen is not mediated by haem". Biochemical Journal 350, nr 1 (9.08.2000): 313–19. http://dx.doi.org/10.1042/bj3500313.
Pełny tekst źródłaKiel, J. A. K. W., R. E. Hilbrands, R. A. L. Bovenberg i M. Veenhuis. "Isolation of Penicillium chrysogenum PEX1 and PEX6 encoding AAA proteins involved in peroxisome biogenesis". Applied Microbiology and Biotechnology 54, nr 2 (15.08.2000): 238–42. http://dx.doi.org/10.1007/s002530000378.
Pełny tekst źródłaDi Pietro, Erminia, Catherine Argyriou, Panteha Saberian, Ellen Crushell, Steven Steinberg, Yasmin D’Souza i Nancy Braverman. "A PEX1 terminal deletion retains partial PEX1 protein function resulting in an attenuated Zellweger spectrum phenotype". Molecular Genetics and Metabolism 132 (kwiecień 2021): S164. http://dx.doi.org/10.1016/s1096-7192(21)00344-9.
Pełny tekst źródłaMbekeani, Alison, Will Stanley, Vishal Kalel, Noa Dahan, Einat Zalckvar, Lilach Sheiner, Wolfgang Schliebs, Ralf Erdmann, Ehmke Pohl i Paul Denny. "Functional Analyses of a Putative, Membrane-Bound, Peroxisomal Protein Import Mechanism from the Apicomplexan Protozoan Toxoplasma gondii". Genes 9, nr 9 (29.08.2018): 434. http://dx.doi.org/10.3390/genes9090434.
Pełny tekst źródłaGoto, Shino, Shoji Mano, Chihiro Nakamori i Mikio Nishimura. "Arabidopsis ABERRANT PEROXISOME MORPHOLOGY9 Is a Peroxin That Recruits the PEX1-PEX6 Complex to Peroxisomes". Plant Cell 23, nr 4 (kwiecień 2011): 1573–87. http://dx.doi.org/10.1105/tpc.110.080770.
Pełny tekst źródłaGardner, Brooke M., Saikat Chowdhury, Gabriel C. Lander i Andreas Martin. "The Pex1/Pex6 Complex Is a Heterohexameric AAA + Motor with Alternating and Highly Coordinated Subunits". Journal of Molecular Biology 427, nr 6 (marzec 2015): 1375–88. http://dx.doi.org/10.1016/j.jmb.2015.01.019.
Pełny tekst źródłaRatbi, Ilham, Kim D. Falkenberg, Manou Sommen, Nada Al-Sheqaih, Soukaina Guaoua, Geert Vandeweyer, Jill E. Urquhart i in. "Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6". American Journal of Human Genetics 97, nr 4 (październik 2015): 535–45. http://dx.doi.org/10.1016/j.ajhg.2015.08.011.
Pełny tekst źródłaPedrosa, Ana G., Tânia Francisco, Maria J. Ferreira, Tony A. Rodrigues, Aurora Barros-Barbosa i Jorge E. Azevedo. "A Mechanistic Perspective on PEX1 and PEX6, Two AAA+ Proteins of the Peroxisomal Protein Import Machinery". International Journal of Molecular Sciences 20, nr 21 (23.10.2019): 5246. http://dx.doi.org/10.3390/ijms20215246.
Pełny tekst źródłaMichelakakis, Helen M., Dimitrios I. Zafeiriou, Marina S. Moraitou, Jeannette Gootjes i Ronald J. A. Wanders. "PEX1 deficiency presenting as Leber congenital amaurosis". Pediatric Neurology 31, nr 2 (sierpień 2004): 146–49. http://dx.doi.org/10.1016/j.pediatrneurol.2004.01.013.
Pełny tekst źródłaGunduz, Mehmet, i Ozlem Unal. "Dysmorphic Facial Features and Other Clinical Characteristics in Two Patients with PEX1 Gene Mutations". Case Reports in Pediatrics 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/5175709.
Pełny tekst źródłaGuerrero-Solano, José Antonio, Mirandeli Bautista, Josué Vidal Espinosa-Juárez, Luis Alfonso Moreno-Rocha, Gabriel Betanzos-Cabrera, Liana Claudia Salanță, Minarda De la O Arciniega, Elena G. Olvera-Hernández i Osmar Antonio Jaramillo-Morales. "Differential Antinociceptive Efficacy of Peel Extracts and Lyophilized Juices of Three Varieties of Mexican Pomegranate (Punica granatum L.) in the Formalin Test". Plants 12, nr 1 (27.12.2022): 131. http://dx.doi.org/10.3390/plants12010131.
Pełny tekst źródłaImamura, Atsushi, Nobuyuki Shimozawa, Yasuyuki Suzuki, Zhongyi Zhang, Toshiro Tsukamoto, Yukio Fujiki, Tadao Orii, Takashi Osumi, Ronald J. A. Wanders i Naomi Kondo. "Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1". Pediatric Research 48, nr 4 (październik 2000): 541–45. http://dx.doi.org/10.1203/00006450-200010000-00020.
Pełny tekst źródłaShiozawa, Kumiko, Nobuo Maita, Kentaro Tomii, Azusa Seto, Natsuko Goda, Yutaka Akiyama, Toshiyuki Shimizu, Masahiro Shirakawa i Hidekazu Hiroaki. "Crystallographic characterization of the N-terminal domain of PEX1". Acta Crystallographica Section D Biological Crystallography 60, nr 11 (20.10.2004): 2098–99. http://dx.doi.org/10.1107/s090744490402428x.
Pełny tekst źródłaGaliani, Silvia, Dominic Waithe, Katharina Reglinski, Luis Daniel Cruz-Zaragoza, Esther Garcia, Mathias P. Clausen, Wolfgang Schliebs, Ralf Erdmann i Christian Eggeling. "Super-resolution Microscopy Reveals Compartmentalization of Peroxisomal Membrane Proteins". Journal of Biological Chemistry 291, nr 33 (16.06.2016): 16948–62. http://dx.doi.org/10.1074/jbc.m116.734038.
Pełny tekst źródłaPan, Ronghui, John Satkovich i Jianping Hu. "E3 ubiquitin ligase SP1 regulates peroxisome biogenesis in Arabidopsis". Proceedings of the National Academy of Sciences 113, nr 46 (31.10.2016): E7307—E7316. http://dx.doi.org/10.1073/pnas.1613530113.
Pełny tekst źródłaTAMURA, Shigehiko, Naomi MATSUMOTO, Atsushi IMAMURA, Nobuyuki SHIMOZAWA, Yasuyuki SUZUKI, Naomi KONDO i Yukio FUJIKI. "Phenotype‒genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p‒Pex6p interaction". Biochemical Journal 357, nr 2 (15.07.2001): 417. http://dx.doi.org/10.1042/0264-6021:3570417.
Pełny tekst źródłaPark, Na Yeon, Doo Sin Jo, So Jung Park, Heejin Lee, Ji-Eun Bae, Youlim Hong, Joon Bum Kim i in. "Depletion of HNRNPA1 induces peroxisomal autophagy by regulating PEX1 expression". Biochemical and Biophysical Research Communications 545 (marzec 2021): 69–74. http://dx.doi.org/10.1016/j.bbrc.2021.01.083.
Pełny tekst źródłaZhang, R., L. Chen, S. Jiralerspong, A. Snowden, S. Steinberg i N. Braverman. "Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compounds". Proceedings of the National Academy of Sciences 107, nr 12 (8.03.2010): 5569–74. http://dx.doi.org/10.1073/pnas.0914960107.
Pełny tekst źródłaShiozawa, K., N. Maita, K. Tomii, A. Seto, N. Goda, Y. Akiyama, T. Shimizu, M. Shirakawa i H. Hiroaki. "Structure of the N-terminal domain of PEX1 AAA-ATPase". Acta Crystallographica Section A Foundations of Crystallography 61, a1 (23.08.2005): c268. http://dx.doi.org/10.1107/s0108767305088574.
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