Ergebnisse einschränken

Nerve ultrasound for differentiation between amyotrophic lateral sclerosis and multifocal motor neuropathy

Grimm, Alexander ; Décard, Bernhard ; Athanasopoulou, Ioanna ; Schweikert, Kathi ; Sinnreich, Michael ; Axer, Hubertus

In: Journal of Neurology, 2015, vol. 262, no. 4, p. 870-880

Experimental determination of trace element partition coefficients between spinel and silicate melt: the influence of chemical composition and oxygen fugacity

Wijbrans, C. ; Klemme, S. ; Berndt, J. ; Vollmer, C.

In: Contributions to Mineralogy and Petrology, 2015, vol. 169, no. 4, p. 1-33

Schwann cells ER-associated degradation contributes to myelin maintenance in adult nerves and limits demyelination in CMT1B mice

Volpi, Vera G. ; Ferri, Cinzia ; Fregno, Ilaria ; Del Carro, Ubaldo ; Bianchi, Francesca ; Scapin, Cristina ; Pettinato, Emanuela ; Solda, Tatiana ; Feltri, M. Laura ; Molinari, Maurizio ; Wrabetz, Lawrence ; D’Antonio, Maurizio

In: PLOS genetics, 2019, vol. 15, no. 4, p. e1008069

In the peripheral nervous system (PNS) myelinating Schwann cells synthesize large amounts of myelin protein zero (P0) glycoprotein, an abundant component of peripheral nerve myelin. In humans, mutations in P0 cause the demyelinating Charcot-Marie-Tooth 1B (CMT1B) neuropathy, one of the most diffused genetic disorders of the PNS. We previously showed that several mutations, such as the...

Expression and localization of somatostatin receptor types 3, 4 and 5 in the wild-type, SSTR1 and SSTR1/SSTR2 knockout mouse cochlea

Radojevic, Vesna ; Bodmer, Daniel

In: Cell and Tissue Research, 2014, vol. 358, no. 3, p. 717-727

Phosphoinositides and Charcot-Marie-Tooth disease: New keys to old questions

Suter, U.

In: Cellular and Molecular Life Sciences, 2007, vol. 64, no. 24, p. 3261-3265

The causes of Charcot-Marie-Tooth disease

Young, P. ; Suter, U.

In: Cellular and Molecular Life Sciences CMLS, 2003, vol. 60, no. 12, p. 2547-2560

Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease

Niemann, Axel ; Berger, Philipp ; Suter, Ueli

In: NeuroMolecular Medicine, 2006, vol. 8, no. 1-2, p. 217-241

Wound-healing studies in transgenic and knockout mice

Grose, Richard ; Werner, Sabine

In: Molecular Biotechnology, 2004, vol. 28, no. 2, p. 147-166

Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2

Tersar, Kristian ; Boentert, Matthias ; Berger, Philipp ; Bonneick, Sonja ; Wessig, Carsten ; Toyka, Klaus V. ; Young, Peter ; Suter, Ueli

In: Human Molecular Genetics, 2007, vol. 16, no. 24, p. 2991-3001

PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease

Azzedine, Hamid ; Zavadakova, Petra ; Planté-Bordeneuve, Violaine ; Vaz Pato, Maria ; Pinto, Nuno ; Bartesaghi, Luca ; Zenker, Jennifer ; Poirot, Olivier ; Bernard-Marissal, Nathalie ; Arnaud Gouttenoire, Estelle ; Cartoni, Romain ; Title, Alexandra ; Venturini, Giulia ; Médard, Jean-Jacques ; Makowski, Edward ; Schöls, Ludger ; Claeys, Kristl G. ; Stendel, Claudia ; Roos, Andreas ; Weis, Joachim ; Dubourg, Odile ; Leal Loureiro, José ; Stevanin, Giovanni ; Said, Gérard ; Amato, Anthony ; Baraban, Jay ; LeGuern, Eric ; Senderek, Jan ; Rivolta, Carlo ; Chrast, Roman

In: Human Molecular Genetics, 2013, vol. 22, no. 20, p. 4224-4232