The proteinopathy of D169G and K263E mutants at the RNA Recognition Motif (RRM) domain of tar DNA-binding protein (tdp43) causing neurological disorders: A computational study-Reference-Cited by-同舟云学术

The proteinopathy of D169G and K263E mutants at the RNA Recognition Motif (RRM) domain of tar DNA-binding protein (tdp43) causing neurological disorders: A computational study

Published:2017-04-07 Issue:4 Volume:36 Page:1075-1093
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Bhandare Vishwambhar Vishnu¹^ORCID,Ramaswamy Amutha¹^ORCID

Affiliation:

1. Centre for Bioinformatics, Pondicherry University, Pondicherry 605014, India

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/07391102.2017.1310670

Reference76 articles.

1. Effects of Disease Causing Mutations on the Essential Motions in Proteins

2. Predicting Functional Effect of Human Missense Mutations Using PolyPhen‐2

3. Sporadic and hereditary amyotrophic lateral sclerosis (ALS)

4. Axonal Transport of TDP-43 mRNA Granules Is Impaired by ALS-Causing Mutations

5. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

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