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You searched for: Author/Creator Livneh, Ido

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1. A homozygous variant in CHMP3 is associated with complex hereditary spastic paraplegia. Issue 3 (16th June 2022)

3. Concomitant variants in NF1, LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitor. Issue 5 (20th December 2021)

4. Correction: In vivo modulation of ubiquitin chains by N-methylated non-proteinogenic cyclic peptides. Issue 3 (11th May 2021)

6. In-depth characterization of ubiquitin turnover in mammalian cells by fluorescence tracking. Issue 8 (19th August 2021)