Items where Author is "Neidhardt, John"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 11.

Article

Song, Fei and Owczarek-Lipska, Marta and Ahmels, Tim and Book, Marius and Aisenbrey, Sabine and Menghini, Moreno and Barthelmes, Daniel and Schrader, Stefan and Spital, Georg and Neidhardt, John (2021) High-throughput sequencing to identify mutations associated with retinal dystrophies. Genes (Basel), 12 (8). pp. 1-16. ISSN 2073-4425

Breuel, Saskia and Vorm, Mariann and Bräuer, Anja U. and Owczarek-Lipska, Marta and Neidhardt, John (2019) Combining engineered U1 snRNA and antisense oligonucleotides to improve the treatment of a BBS1 splice site mutation. Molecular Therapy / Nucleic Acids, 17. pp. 123-130. ISSN 2162-2531

Vagts, Jannes and Weiten, Arne and Scheve, Sabine and Kalvelage, Kristin and Swirski, Sebastian and Wöhlbrand, Lars and Neidhardt, John and Winklhofer, Michael and Rabus, Ralf (2019) Nanomolar responsiveness of an anaerobic degradation specialist to alkylphenol pollutants. Journal of bacteriology, 202 (5). e00595-19. ISSN 1098-5530

Courage, Carolina and Jackson, Christopher B. and Owczarek-Lipska, Marta and Jamsheer, Aleksander and Sowińska-Seidler, Anna and Piotrowicz, Małgorzata and Jakubowski, Lucjusz and Dallèves, Fanny and Riesch, Erik and Neidhardt, John and Lemke, Johannes R. (2019) Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome. American journal of medical genetics, 179 (12). pp. 2447-2453. ISSN 1552-4833

Owczarek-Lipska, Marta and Mulahasanovic, Lejla and Obermaier, Carolin D. and Hörtnagel, Konstanze and Neubauer, Bernd A. and Korenke, Georg-Christoph and Biskup, Saskia and Neidhardt, John (2019) Novel mutations in the GJC2 gene associated with Pelizaeus-Merzbacher-like disease. Molecular biology reports, 46 (4). pp. 4507-4516. ISSN 1573-4978

Neßlauer, Anna-Maria and Gläser, Anne and Gräler, Markus and Engelmann, Robby and Müller-Hilke, Brigitte and Frank, Marcus and Burstein, Christine and Rolfs, Arndt and Neidhardt, John and Wree, Andreas and Witt, Martin and Bräuer, Anja U. (2019) A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1. Lipids in Health and Disease, 18 (1). ISSN 1476-511X

Neßlauer, Anna-Maria and Gläser, Anne and Gräler, Markus and Engelmann, Robby and Müller-Hilke, Brigitte and Frank, Marcus and Burstein, Christine and Rolfs, Arndt and Neidhardt, John and Wree, Andreas and Witt, Martin and Bräuer, Anja U. (2019) A therapy with miglustat, 2-hydroxypropyl-ß-cyclodextrin and allopregnanolone restores splenic cholesterol homeostasis in Niemann-pick disease type C1. Lipids in health and disease, 18. p. 146. ISSN 1476-511X

Schlegel, J. and Hoffmann, J. and Röll, D. and Müller, B. and Günther, S. and Zhang, W. and Janise, A. and Vössing, Christine and Fühler, B. and Neidhardt, John and Khanna , H. and Lorenz, B. and Stieger, K. (2019) Toward genome editing in X-linked RP: development of a mouse model with specific treatment relevant features. Translational research, 203. pp. 57-72. ISSN 1878-1810

Swirski, Sebastian and Röger, Carsten and Pienkowska-Schelling, Aldona and Ihlenburg, Cynthia and Fischer, Gösta and May, Oliver and Vorm, Mariann and Owczarek-Lipska, Marta and Neidhardt, John (2018) A Novel C-Terminal Mutation in Gsdma3 (C+/H−) Leads to Alopecia and Corneal Inflammatory Response in Mice. Investigative Opthalmology & Visual Science, 59 (1). p. 561. ISSN 1552-5783

Da Costa, Romain and Röger, Carsten and Segelken, Jasmin and Barben, Maya and Grimm, Christian and Neidhardt, John (2016) A Novel Method Combining Vitreous Aspiration and Intravitreal AAV2/8 Injection Results in Retina-Wide Transduction in Adult Mice. Investigative Opthalmology & Visual Science, 57 (13). p. 5326. ISSN 1552-5783

Reiff, Charlotte and Owczarek-Lipska, Marta and Spital, Georg and Röger, Carsten and Hinz, Hebke and Jüschke, Christoph and Thiele, Holger and Altmüller, Janine and Nürnberg, Peter and Da Costa, Romain and Neidhardt, John (2016) The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Scientific Reports, 6 (1). ISSN 2045-2322

This list was generated on Mon Jul 15 08:50:46 2024 CEST.