A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons

Erstveröffentlichung
2010Authors
Braunstein, Kerstin E.
Eschbach, Judith
Rona-Voeroes, Krisztina
Soylu, Rana
Mikrouli, Elli
Wissenschaftlicher Artikel
Published in
Human Molecular Genetics ; 19 (2010), 22. - S. 4385-4398. - ISSN 0964-6906. - eISSN 1460-2083
Link to publication
https://dx.doi.org/10.1093/hmg/ddq361Institutions
UKU. Klinik für NeurologieSubject headings
[Free subject headings]: HUNTINGTIN-ASSOCIATED PROTEIN | AXONAL-TRANSPORT DEFECTS | DISEASE TRANSGENIC MICE | MOTOR-NEURONS | NEUROTROPHIC FACTOR | MOUSE MODEL | DYNEIN/DYNACTIN FUNCTION | VESICULAR TRANSPORT | SENSORY NEUROPATHY | MUTANT DYNACTIN[DDC subject group]: DDC 570 / Life sciences