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Year Number of Results
2015 1
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2019 1
2021 3
2022 1
2023 2
2024 2

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Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy.
Foronda H, Fu Y, Covarrubias-Pinto A, Bocker HT, González A, Seemann E, Franzka P, Bock A, Bhaskara RM, Liebmann L, Hoffmann ME, Katona I, Koch N, Weis J, Kurth I, Gleeson JG, Reggiori F, Hummer G, Kessels MM, Qualmann B, Mari M, Dikić I, Hübner CA. Foronda H, et al. Among authors: franzka p. Nature. 2023 Jun;618(7964):402-410. doi: 10.1038/s41586-023-06090-9. Epub 2023 May 24. Nature. 2023. PMID: 37225994 Free PMC article.
Altered Glycosylation in the Aging Heart.
Franzka P, Krüger L, Schurig MK, Olecka M, Hoffmann S, Blanchard V, Hübner CA. Franzka P, et al. Front Mol Biosci. 2021 May 28;8:673044. doi: 10.3389/fmolb.2021.673044. eCollection 2021. Front Mol Biosci. 2021. PMID: 34124155 Free PMC article.
GMPPA defects cause a neuromuscular disorder with α-dystroglycan hyperglycosylation.
Franzka P, Henze H, Jung MJ, Schüler SC, Mittag S, Biskup K, Liebmann L, Kentache T, Morales J, Martínez B, Katona I, Herrmann T, Huebner AK, Hennings JC, Groth S, Gresing L, Horstkorte R, Marquardt T, Weis J, Kaether C, Mutchinick OM, Ori A, Huber O, Blanchard V, von Maltzahn J, Hübner CA. Franzka P, et al. J Clin Invest. 2021 May 3;131(9):e139076. doi: 10.1172/JCI139076. J Clin Invest. 2021. PMID: 33755596 Free PMC article.
Knockdown of INPP5K compromises the differentiation of N2A cells.
Manzolillo A, Gresing L, Hübner CA, Franzka P. Manzolillo A, et al. Among authors: franzka p. Front Mol Neurosci. 2024 Mar 15;17:1356343. doi: 10.3389/fnmol.2024.1356343. eCollection 2024. Front Mol Neurosci. 2024. PMID: 38559586 Free PMC article.
Consequences of GMPPB deficiency for neuromuscular development and maintenance.
Schurig MK, Umeh O, Henze H, Jung MJ, Gresing L, Blanchard V, von Maltzahn J, Hübner CA, Franzka P. Schurig MK, et al. Among authors: franzka p. Front Mol Neurosci. 2024 Feb 14;17:1356326. doi: 10.3389/fnmol.2024.1356326. eCollection 2024. Front Mol Neurosci. 2024. PMID: 38419795 Free PMC article.
Mouse models for hereditary spastic paraplegia uncover a role of PI4K2A in autophagic lysosome reformation.
Khundadze M, Ribaudo F, Hussain A, Stahlberg H, Brocke-Ahmadinejad N, Franzka P, Varga RE, Zarkovic M, Pungsrinont T, Kokal M, Ganley IG, Beetz C, Sylvester M, Hübner CA. Khundadze M, et al. Among authors: franzka p. Autophagy. 2021 Nov;17(11):3690-3706. doi: 10.1080/15548627.2021.1891848. Epub 2021 Mar 9. Autophagy. 2021. PMID: 33618608 Free PMC article.
A mouse model for SPG48 reveals a block of autophagic flux upon disruption of adaptor protein complex five.
Khundadze M, Ribaudo F, Hussain A, Rosentreter J, Nietzsche S, Thelen M, Winter D, Hoffmann B, Afzal MA, Hermann T, de Heus C, Piskor EM, Kosan C, Franzka P, von Kleist L, Stauber T, Klumperman J, Damme M, Proikas-Cezanne T, Hübner CA. Khundadze M, et al. Among authors: franzka p. Neurobiol Dis. 2019 Jul;127:419-431. doi: 10.1016/j.nbd.2019.03.026. Epub 2019 Mar 28. Neurobiol Dis. 2019. PMID: 30930081
In Vivo Evidence for Lysosome Depletion and Impaired Autophagic Clearance in Hereditary Spastic Paraplegia Type SPG11.
Varga RE, Khundadze M, Damme M, Nietzsche S, Hoffmann B, Stauber T, Koch N, Hennings JC, Franzka P, Huebner AK, Kessels MM, Biskup C, Jentsch TJ, Qualmann B, Braulke T, Kurth I, Beetz C, Hübner CA. Varga RE, et al. Among authors: franzka p. PLoS Genet. 2015 Aug 18;11(8):e1005454. doi: 10.1371/journal.pgen.1005454. eCollection 2015 Aug. PLoS Genet. 2015. PMID: 26284655 Free PMC article.
11 results