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Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5
Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5
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Lysine Glutarylation Is a Protein Posttranslational Modification Regulated by SIRT5

Tan, Minjia ; Peng, Chao ; Anderson, Kristin A. ; Chhoy, Peter ; Xie, Zhongyu ; Dai, Lunzhi ; Park, Jeongsoon ; Chen, Yue ; Huang, He ; Zhang, Yi ; Ro, Jennifer ; Wagner, Gregory R. ; Green, Michelle F. ; Madsen, Andreas S. ; Schmiesing, Jessica ; Peterson, Brett S. ; Xu, Guofeng ; Ilkayeva, Olga R. ; Muehlbauer, Michael J. ; Braulke, Thomas ; Mühlhausen, Chris ; Backos, Donald S. ; Olsen, Christian A. ; McGuire, Peter J. ; Pletcher, Scott D. ; Lombard, David B. ; Hirschey, Matthew D. ; Zhao, Yingming

Cell metabolism, 2014-04, Vol.19 (4), p.605-617 [Periódico revisado por pares]

United States: Elsevier Inc

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2
Cell biology and function of neuronal ceroid lipofuscinosis-related proteins
Cell biology and function of neuronal ceroid lipofuscinosis-related proteins
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Cell biology and function of neuronal ceroid lipofuscinosis-related proteins

Kollmann, Katrin ; Uusi-Rauva, Kristiina ; Scifo, Enzo ; Tyynelä, Jaana ; Jalanko, Anu ; Braulke, Thomas

Biochimica et biophysica acta, 2013-11, Vol.1832 (11), p.1866-1881 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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3
In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11
In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11
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In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11

Varga, Rita-Eva ; Khundadze, Mukhran ; Damme, Markus ; Nietzsche, Sandor ; Hoffmann, Birgit ; Stauber, Tobias ; Koch, Nicole ; Hennings, J Christopher ; Franzka, Patricia ; Huebner, Antje K ; Kessels, Michael M ; Biskup, Christoph ; Jentsch, Thomas J ; Qualmann, Britta ; Braulke, Thomas ; Kurth, Ingo ; Beetz, Christian ; Hübner, Christian A Cox, Gregory A.

PLoS genetics, 2015-08, Vol.11 (8), p.e1005454-e1005454 [Periódico revisado por pares]

United States: Public Library of Science

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4
Disease-Linked Glutarylation Impairs Function and Interactions of Mitochondrial Proteins and Contributes to Mitochondrial Heterogeneity
Disease-Linked Glutarylation Impairs Function and Interactions of Mitochondrial Proteins and Contributes to Mitochondrial Heterogeneity
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Disease-Linked Glutarylation Impairs Function and Interactions of Mitochondrial Proteins and Contributes to Mitochondrial Heterogeneity

Schmiesing, Jessica ; Storch, Stephan ; Dörfler, Ann-Cathrin ; Schweizer, Michaela ; Makrypidi-Fraune, Georgia ; Thelen, Melanie ; Sylvester, Marc ; Gieselmann, Volkmar ; Meyer-Schwesinger, Catherine ; Koch-Nolte, Friedrich ; Tidow, Henning ; Mühlhausen, Chris ; Waheed, Abdul ; Sly, William S. ; Braulke, Thomas

Cell reports (Cambridge), 2018-09, Vol.24 (11), p.2946-2956 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Sustained Neural Stem Cell-Based Intraocular Delivery of CNTF Attenuates Photoreceptor Loss in the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis
Sustained Neural Stem Cell-Based Intraocular Delivery of CNTF Attenuates Photoreceptor Loss in the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis
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Sustained Neural Stem Cell-Based Intraocular Delivery of CNTF Attenuates Photoreceptor Loss in the nclf Mouse Model of Neuronal Ceroid Lipofuscinosis

Jankowiak, Wanda ; Kruszewski, Katharina ; Flachsbarth, Kai ; Skevas, Christos ; Richard, Gisbert ; Rüther, Klaus ; Braulke, Thomas ; Bartsch, Udo Langmann, Thomas

PloS one, 2015-05, Vol.10 (5), p.e0127204-e0127204 [Periódico revisado por pares]

United States: Public Library of Science

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6
Repurposing of tamoxifen ameliorates CLN3 and CLN7 disease phenotype
Repurposing of tamoxifen ameliorates CLN3 and CLN7 disease phenotype
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Repurposing of tamoxifen ameliorates CLN3 and CLN7 disease phenotype

Soldati, Chiara ; Lopez‐Fabuel, Irene ; Wanderlingh, Luca G ; Garcia‐Macia, Marina ; Monfregola, Jlenia ; Esposito, Alessandra ; Napolitano, Gennaro ; Guevara‐Ferrer, Marta ; Scotto Rosato, Anna ; Krogsaeter, Einar K ; Paquet, Dominik ; Grimm, Christian M ; Montefusco, Sandro ; Braulke, Thomas ; Storch, Stephan ; Mole, Sara E ; De Matteis, Maria A ; Ballabio, Andrea ; Sampaio, Julio L ; McKay, Tristan ; Johannes, Ludger ; Bolaños, Juan P ; Medina, Diego L

EMBO molecular medicine, 2021-10, Vol.13 (10), p.n/a [Periódico revisado por pares]

Frankfurt: EMBO Press

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7
Protein kinase a dependent phosphorylation of apical membrane antigen 1 plays an important role in erythrocyte invasion by the malaria parasite
Protein kinase a dependent phosphorylation of apical membrane antigen 1 plays an important role in erythrocyte invasion by the malaria parasite
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Protein kinase a dependent phosphorylation of apical membrane antigen 1 plays an important role in erythrocyte invasion by the malaria parasite

Leykauf, Kerstin ; Treeck, Moritz ; Gilson, Paul R ; Nebl, Thomas ; Braulke, Thomas ; Cowman, Alan F ; Gilberger, Tim W ; Crabb, Brendan S Kim, Kami

PLoS pathogens, 2010-06, Vol.6 (6), p.e1000941-e1000941 [Periódico revisado por pares]

United States: Public Library of Science

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8
Neuronal ceroid lipofuscinoses
Neuronal ceroid lipofuscinoses
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Neuronal ceroid lipofuscinoses

Jalanko, Anu ; Braulke, Thomas

Biochimica et biophysica acta, 2009-04, Vol.1793 (4), p.697-709 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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9
Early enzyme replacement therapy prevents dental and craniofacial abnormalities in a mouse model of mucopolysaccharidosis type VI
Early enzyme replacement therapy prevents dental and craniofacial abnormalities in a mouse model of mucopolysaccharidosis type VI
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Early enzyme replacement therapy prevents dental and craniofacial abnormalities in a mouse model of mucopolysaccharidosis type VI

Nagpal, Rohit ; Georgi, Gina ; Knauth, Sarah ; Schmid-Herrmann, Carmen ; Muschol, Nicole ; Braulke, Thomas ; Kahl-Nieke, Bärbel ; Amling, Michael ; Schinke, Thorsten ; Koehne, Till ; Petersen, Julian

Frontiers in physiology, 2022-09, Vol.13, p.998039-998039 [Periódico revisado por pares]

Frontiers Media S.A

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10
A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system
A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system
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A hereditary spastic paraplegia mouse model supports a role of ZFYVE26/SPASTIZIN for the endolysosomal system

Khundadze, Mukhran ; Kollmann, Katrin ; Koch, Nicole ; Biskup, Christoph ; Nietzsche, Sandor ; Zimmer, Geraldine ; Hennings, J Christopher ; Huebner, Antje K ; Symmank, Judit ; Jahic, Amir ; Ilina, Elena I ; Karle, Kathrin ; Schöls, Ludger ; Kessels, Michael ; Braulke, Thomas ; Qualmann, Britta ; Kurth, Ingo ; Beetz, Christian ; Hübner, Christian A Barsh, Gregory S.

PLoS genetics, 2013-12, Vol.9 (12), p.e1003988-e1003988 [Periódico revisado por pares]

United States: Public Library of Science

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