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1.
Boldt, K.* et al.: An organelle-specific protein landscape identifies novel diseases and molecular mechanisms. Nat. Commun. 7:11491 (2016)
2.
Wheway, G.* et al.: An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes. Nat. Cell Biol. 17, 1074-1087 (2015)
3.
Texier, Y. et al.: Elution profile analysis of SDS-induced subcomplexes by quantitative mass spectrometry. Mol. Cell. Proteomics 13, 1382-1391 (2014)
4.
Cevik, S.* et al.: Active transport and diffusion barriers restrict Joubert Syndrome-associated ARL13B/ARL-13 to an Inv-like ciliary membrane subdomain. PLoS Genet. 9:e1003977 (2013)
5.
Boldt, K. et al.: Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice. J. Clin. Invest. 121, 2169-2180 (2011)
6.
Coene, K.L.* et al.: The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase. Hum. Mol. Genet. 20, 3592-3605 (2011)