Biochemical characterization of sporadic/familial hemiplegic migraine mutations-Reference-Cited by-同舟云学术

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Biochemical characterization of sporadic/familial hemiplegic migraine mutations

Published:2014-07 Issue:7 Volume:1838 Page:1693-1700
ISSN:0005-2736
Container-title:Biochimica et Biophysica Acta (BBA) - Biomembranes
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Biomembranes

Author:

Weigand Karl M.,Swarts Herman G.P.,Russel Frans G.M.,Koenderink Jan B.

Funder

Netherlands Organisation for Scientific Research

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry,Biophysics

Reference38 articles.

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3. Biology, structure and mechanism of P-type ATPases;Kuhlbrandt;Nat. Rev. Mol. Cell Biol.,2004

4. Endogenous cardiotonic steroids: physiology, pharmacology, and novel therapeutic targets;Bagrov;Pharmacol. Rev.,2009

5. Isozymes of the Na–K-ATPase: heterogeneity in structure, diversity in function;Blanco;Am. J. Physiol.,1998

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1. Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases;Neuroscience Research;2022-07

2. Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms;The Journal of Headache and Pain;2021-08-12

3. A Chinese family with familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2;Cephalalgia;2019-05-03

4. Molecular simulations and free-energy calculations suggest conformation-dependent anion binding to a cytoplasmic site as a mechanism for Na+/K+-ATPase ion selectivity;Journal of Biological Chemistry;2017-07

5. Free energy calculations suggest a mechanism for Na+/K+-ATPase ion selectivity;2017-02-07

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