Mechanism of midline defect‐causing mutation P151L in MID 1 revealed-Reference-Cited by-同舟云学术

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Mechanism of midline defect‐causing mutation P151L in MID 1 revealed

Published:2017-07 Issue:14 Volume:284 Page:2167-2169
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:FEBS J

Author:

Nicholson Linda K.¹

Affiliation:

1. Department of Molecular Biology & Genetics Cornell University Ithaca NY USA

Funder

National Science Foundation

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.14149

Reference18 articles.

1. E3 Ubiquitin Ligases Neurobiological Mechanisms: Development to Degeneration

2. In the right place at the right time: visualizing and understanding mRNA localization

3. MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation

4. Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit 4

5. Active Transport of the Ubiquitin Ligase MID1 along the Microtubules Is Regulated by Protein Phosphatase 2A

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ubiquitin ligases: guardians of mammalian development;Nature Reviews Molecular Cell Biology;2022-01-25

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