PuSH - Publication Server of Helmholtz Zentrum München

6 Records found.
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1.
Brockmann, S.J.* et al.: CHCHD10 mutations p. R15L and p. G66V cause motoneuron disease by haploinsufficiency. Hum. Mol. Genet. 27, 706-715 (2018)
2.
Hermann, A.* et al.: A case of beta-propeller protein-associated neurodegeneration due to a heterozygous deletion of WDR45. Tremor Other Hyperkinet. Mov. 7:465 (2017)
3.
Zhou, Q.* et al.: Antibodies inhibit transmission and aggregation of C9orf72 poly-GA dipeptide repeat proteins. EMBO Mol. Med. 9, 687-702 (2017)
4.
Siegl, C.* et al.: Alterations of red cell membrane properties in neuroacanthocytosis. PLoS ONE 8:e76715 (2013)
5.
Eilken, H. et al.: Continuous long-term detection of live cell surface markers by ‘in culture’ antibody staining. Protoc. Exch., DOI: 10.1038/protex.2011.205 (2011)
6.
Hermann, A.: Analysis of asymmetric division of hematopoietic stem cells by continuous single cell observation. München, Ludwig-Maximilians-Universität München, Fakultät für Biologie, Diss., 2009, 186 S.