A high‐content drug screening strategy to identify protein level modulators for genetic diseases: A proof‐of‐principle in autosomal dominant leukodystrophy-Reference-Cited by-同舟云学术

A high‐content drug screening strategy to identify protein level modulators for genetic diseases: A proof‐of‐principle in autosomal dominant leukodystrophy

Published:2020-12-08 Issue:1 Volume:42 Page:102-116
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Giorgio Elisa¹²^ORCID,Pesce Emanuela³,Pozzi Elisa¹,Sondo Elvira³,Ferrero Marta¹,Morerio Cristina⁴,Borrelli Giusy¹,Della Sala Edoardo¹,Lorenzati Martina⁵,Cortelli Pietro⁶⁷,Buffo Annalisa⁵,Pedemonte Nicoletta³,Brusco Alfredo¹⁸^ORCID

Affiliation:

1. Department of Medical Sciences, Medical Genetics Unit University of Torino Turin Italy

2. Department of Molecular Medicine University of Pavia Pavia Italy

3. UOC Genetica Medica IRCCS Istituto Giannina Gaslini Genova Italy

4. UOC Laboratorio di Genetica Umana IRCCS Istituto Giannina Gaslini Genova Italy

5. Department of Neuroscience Rita Levi Montalcini and Neuroscience Institute Cavalieri Ottolenghi University of Torino Orbassano Torino Italy

6. Department of Biomedical and Neuromotor Sciences University of Bologna Bologna Italy

7. IRCCS Istituto delle Scienze Neurologiche di Bologna Bellaria Hospital Bologna Italy

8. Medical Genetics Unit Città della Salute e della Scienza University Hospital Turin Italy

Funder

Fondation Jérôme Lejeune

Fondazione Umberto Veronesi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24147

Reference44 articles.

1. Messenger RNA processing is altered in autosomal dominant leukodystrophy

2. Early phenotypic asymmetry of sister oligodendrocyte progenitor cells after mitosis and its modulation by aging and extrinsic factors

3. Nuclear pore complexes form immobile networks and have a very low turnover in live mammalian cells

4. The lamin protein family

5. Trisomy-driven overexpression of DYRK1A kinase in the brain of subjects with Down syndrome

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