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  • Author: Kubisch C
  • References

Author: Kubisch C


References 6 references


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  • Fiedler MRM, et al. (2018) Conditional Expression of the Small GTPase ArfA Impacts Secretion, Morphology, Growth, and Actin Ring Position in Aspergillus niger. Front Microbiol 9:878 PMID:29867795
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  • Fazeli W, et al. (2017) A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction. Hum Mol Genet 26(20):4055-4066 PMID:29016863
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  • Sowada N, et al. (2016) Increased copper toxicity in Saccharomyces cerevisiae lacking VPS35, a component of the retromer and monogenic Parkinson disease gene in humans. Biochem Biophys Res Commun 476(4):528-533 PMID:27262440
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  • Borck G, et al. (2015) BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies. Genome Res 25(2):155-66 PMID:25561519
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  • Borck G, et al. (2012) eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation. Mol Cell 48(4):641-6 PMID:23063529
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  • Kornak U, et al. (2000) Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis. Hum Mol Genet 9(13):2059-63 PMID:10942435
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