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2. DNMT3B PWWP mutations cause hypermethylation of heterochromatin

3. ALDH1A3-acetaldehyde metabolism potentiates transcriptional heterogeneity in melanoma

6. Author Reply to Peer Reviews of DNMT3B PWWP mutations cause hypermethylation of heterochromatin

7. Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis

8. Author response: Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis

9. DNMT3B PWWP mutations cause hypermethylation of heterochromatin

11. Ciliary tip actin dynamics regulate the cadence of photoreceptor disc formation

12. Non‐fitting FLIM‐FRET facilitates analysis of protein interactions in live zebrafish embryos.

13. DISC1 regulates N-methyl-D-aspartate receptor dynamics: abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness

14. Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis.

15. A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia

16. Author response: A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia

17. Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability

18. Functional Predictors of Causative Cis-Regulatory Mutations in Mendelian Disease

19. Fluorescentin vivoediting reporter (FIVER): A novel multispectral reporter ofin vivogenome editing

24. Variation in the autism candidate gene GABRB3 modulates tactile sensitivity in typically developing children

25. DISC1 regulates N-Methyl-D-Aspartate receptor dynamics: Abnormalities induced by a Disc1 mutation modelling a translocation linked to major mental illness

28. Identification and functional modelling of plausibly causative cis-regulatory variants in a highly-selected cohort with X-linked intellectual disability

29. The crucial role of bioimage analysts in scientific research and publication.

30. Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.

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