Found: 6

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  • Protein Binding Partners of Dysregulated miRNAs in Parkinson's Disease Serum.

    Published in:
    Cells (2073-4409), 2021, v. 10, n. 4, p. 791, doi. 10.3390/cells10040791
    By:
    • Ruf, Wolfgang P.;
    • Freischmidt, Axel;
    • Grozdanov, Veselin;
    • Roth, Valerie;
    • Brockmann, Sarah J.;
    • Mollenhauer, Brit;
    • Martin, Dorothea;
    • Haslinger, Bernhard;
    • Fundel-Clemens, Katrin;
    • Otto, Markus;
    • Arnim, Christine von;
    • Holzmann, Karlheinz;
    • Ludolph, Albert C.;
    • Weishaupt, Jochen H.;
    • Danzer, Karin M.;
    • Sonntag, Kai-Christian
    Publication type:
    Article

  • Mitochondrial genome study in blood of maternally inherited ALS cases.

    Published in:
    Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00516-1
    By:
    • Brockmann, Sarah J.;
    • Buck, Eva;
    • Casoli, Tiziana;
    • Meirelles, João L.;
    • Ruf, Wolfgang P.;
    • Fabbietti, Paolo;
    • Holzmann, Karlheinz;
    • Weishaupt, Jochen H.;
    • Ludolph, Albert C.;
    • Conti, Fiorenzo;
    • Danzer, Karin M.
    Publication type:
    Article

  • A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosis.

    Published in:
    2021
    By:
    • Freischmidt, Axel;
    • Goswami, Anand;
    • Limm, Katharina;
    • Zimyanin, Vitaly L;
    • Demestre, Maria;
    • Glaß, Hannes;
    • Holzmann, Karlheinz;
    • Helferich, Anika M;
    • Brockmann, Sarah J;
    • Tripathi, Priyanka;
    • Yamoah, Alfred;
    • Poser, Ina;
    • Oefner, Peter J;
    • Böckers, Tobias M;
    • Aronica, Eleonora;
    • Ludolph, Albert C;
    • Andersen, Peter M;
    • Hermann, Andreas;
    • Weis, Joachim;
    • Reinders, Jörg
    Publication type:
    journal article

  • Dysregulation of a novel miR-1825/TBCB/TUBA4A pathway in sporadic and familial ALS.

    Published in:
    Cellular & Molecular Life Sciences, 2018, v. 75, n. 23, p. 4301, doi. 10.1007/s00018-018-2873-1
    By:
    • Helferich, Anika M.;
    • Brockmann, Sarah J.;
    • Reinders, Jörg;
    • Deshpande, Dhruva;
    • Holzmann, Karlheinz;
    • Brenner, David;
    • Andersen, Peter M.;
    • Petri, Susanne;
    • Thal, Dietmar R.;
    • Michaelis, Jens;
    • Otto, Markus;
    • Just, Steffen;
    • Ludolph, Albert C.;
    • Danzer, Karin M.;
    • Freischmidt, Axel;
    • Weishaupt, Jochen H.
    Publication type:
    Article

  • Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant.

    Published in:
    2016
    By:
    • Marroquin, Nicolai;
    • Stranz, Sebastian;
    • Müller, Kathrin;
    • Wieland, Thomas;
    • Ruf, Wolfgang P.;
    • Brockmann, Sarah J.;
    • Danzer, Karin M.;
    • Borck, Guntram;
    • Hübers, Annemarie;
    • Weydt, Patrick;
    • Meitinger, Thomas;
    • Strom, Tim-Matthias;
    • Rosenbohm, Angela;
    • Ludolph, Albert C.;
    • Weishaupt, Jochen H.
    Publication type:
    commentary

  • CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency.

    Published in:
    Human Molecular Genetics, 2018, v. 27, n. 4, p. 706, doi. 10.1093/hmg/ddx436
    By:
    • Brockmann, Sarah J.;
    • Freischmidt, Axel;
    • Oeckl, Patrick;
    • Müller, Kathrin;
    • Ponna, Srinivas K.;
    • Helferich, Anika M.;
    • Paone, Christoph;
    • Reinders, Jörg;
    • Kojer, Kerstin;
    • Orth, Michael;
    • Jokela, Manu;
    • Auranen, Mari;
    • Udd, Bjarne;
    • Hermann, Andreas;
    • Danzer, Karin M.;
    • Lichtner, Peter;
    • Walther, Paul;
    • Ludolph, Albert C.;
    • Andersen, Peter M.;
    • Otto, Markus
    Publication type:
    Article