Structure and Functional Characterization of Human Histidine Triad Nucleotide-Binding Protein 1 Mutations Associated with Inherited Axonal Neuropathy with Neuromyotonia-Reference-Cited by-同舟云学术

Structure and Functional Characterization of Human Histidine Triad Nucleotide-Binding Protein 1 Mutations Associated with Inherited Axonal Neuropathy with Neuromyotonia

Published:2018-08 Issue:17 Volume:430 Page:2709-2721
ISSN:0022-2836
Container-title:Journal of Molecular Biology
language:en
Short-container-title:Journal of Molecular Biology

Author:

Shah Rachit M.,Maize Kimberly M.,West Harrison T.,Strom Alexander M.,Finzel Barry C.,Wagner Carston R.

Funder

University of Minnesota Endowment

University of Minnesota Frieda Martha Kunze Fellowship

American Foundation for Pharmaceutical Education

DOE Office of Science

Publisher

Elsevier BV

Subject

Molecular Biology,Structural Biology

Reference34 articles.

1. Inherited peripheral neuropathies;Saporta;Neurol. Clin.,2013

2. Autosomal-recessive and X-linked forms of hereditary motor and sensory neuropathy in childhood;Ouvrier;Muscle Nerve,2007

3. Disease mechanisms in inherited neuropathies;Suter;Nat. Rev. Neurosci.,2003

4. Charcot–Marie–Tooth disease subtypes and genetic testing strategies;Saporta;Ann. Neurol.,2011

5. Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations;Wuttke;Neurology,2007

Cited by 10 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. HINT1 Inhibitors as Selective Modulators of MOR-NMDAR Cross Regulation and Non-Opioid Analgesia;2024-07-17

2. In-depth characterization of HINT1 pathogenic variants;2023-12-02

3. The Many Faces of Histidine Triad Nucleotide Binding Protein 1 (HINT1);ACS Pharmacology & Translational Science;2023-07-20

4. Dynamic Long-Range Interactions Influence Substrate Binding and Catalysis by Human Histidine Triad Nucleotide-Binding Proteins (HINTs), Key Regulators of Multiple Cellular Processes and Activators of Antiviral ProTides;Biochemistry;2022-11-18

5. HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling;Orphanet Journal of Rare Diseases;2022-10-14