Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hedwig Wariwoda"'
Autor:
Andreas Volz, Hedwig Wariwoda, I. Spoerri, Peter Itin, Bettina Burger, M. Aushev, Julia Reichelt, E. Imahorn, Oliver Patrick March, Patricia Renz, Sarah Von Arb
Publikováno v:
Journal of Cellular and Molecular Medicine
Ichthyosis with confetti (IWC) is a genodermatosis associated with dominant‐negative variants in keratin 10 (KRT10) or keratin 1 (KRT1). These frameshift variants result in extended aberrant proteins, localized to the nucleus rather than the cytopl
Autor:
Hedwig Wariwoda, Cornelia Imsand, Andrea Gubler, Severin R. Heynen, Marijana Samardzija, Christian Grimm, Philipp Huber
Publikováno v:
Experimental eye research
Blinding diseases of the retina are frequently characterized by loss of photoreceptor cells. The retinal degeneration 10 (rd10) mouse expresses a mutant form of rod phosphodiesterase leading to autosomal recessive photoreceptor degeneration. In contr
Autor:
Marijana Samardzija, Bruno Oesch, Naoyuki Tanimoto, Rico Frigg, Andreas Wenzel, Alexander A. Navarini, Mathias W. Seeliger, Christian Grimm, Hedwig Wariwoda, Charlotte E. Remé
Publikováno v:
Experimental eye research. 83(6)
A common feature of neurodegenerative disorders is acute or progressive loss of neurons due to apoptosis. The pathological isoform of the prion protein is associated with retinal apoptosis and the cellular isoform (PrPc) has been shown to mediate pro