BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Maggi L, Bonanno S, Altamura C, Desaphy JF. Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy. Cells 2021;10:1521. [PMID: 34208776 DOI: 10.3390/cells10061521] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 He S, Lim GE. The Application of High‐Throughput Approaches in Identifying Novel Therapeutic Targets and Agents to Treat Diabetes. Advanced Biology 2022. [DOI: 10.1002/adbi.202200151] [Reference Citation Analysis]
2 Rossi D, Catallo MR, Pierantozzi E, Sorrentino V. Mutations in proteins involved in E-C coupling and SOCE and congenital myopathies. J Gen Physiol 2022;154:e202213115. [PMID: 35980353 DOI: 10.1085/jgp.202213115] [Reference Citation Analysis]
3 Altamura C, Conte E, Campanale C, Laghetti P, Saltarella I, Camerino GM, Imbrici P, Desaphy J. Chaperone activity of niflumic acid on ClC-1 chloride channel mutants causing myotonia congenita. Front Pharmacol 2022;13:958196. [DOI: 10.3389/fphar.2022.958196] [Reference Citation Analysis]
4 Lee M, Lin P, Lin M, Chiou HC, Wang K, Huang C. Kinetic Alterations in Resurgent Sodium Currents of Mutant Nav1.4 Channel in Two Patients Affected by Paramyotonia Congenita. Biology 2022;11:613. [DOI: 10.3390/biology11040613] [Reference Citation Analysis]
5 Kim S, Mun S, Shin W, Han K, Kim MY. Identification of Potentially Pathogenic Variants Associated with Recurrence in Medication-Related Osteonecrosis of the Jaw (MRONJ) Patients Using Whole-Exome Sequencing. J Clin Med 2022;11:2145. [PMID: 35456240 DOI: 10.3390/jcm11082145] [Reference Citation Analysis]
6 Wnek GE, Costa ACS, Kozawa SK. Bio-Mimicking, Electrical Excitability Phenomena Associated With Synthetic Macromolecular Systems: A Brief Review With Connections to the Cytoskeleton and Membraneless Organelles. Front Mol Neurosci 2022;15:830892. [DOI: 10.3389/fnmol.2022.830892] [Reference Citation Analysis]
7 Yim J, Kim KB, Kim M, Lee GD, Kim M. Andersen–Tawil Syndrome With Novel Mutation in KCNJ2: Case Report. Front Pediatr 2022;9:790075. [DOI: 10.3389/fped.2021.790075] [Reference Citation Analysis]
8 Nicole S, Lory P. New Challenges Resulting From the Loss of Function of Nav1.4 in Neuromuscular Diseases. Front Pharmacol 2021;12:751095. [PMID: 34671263 DOI: 10.3389/fphar.2021.751095] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Brugnoni R, Canioni E, Filosto M, Pini A, Tonin P, Rossi T, Canavese C, Eoli M, Siciliano G, Lauria G, Mantegazza R, Maggi L. Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes. Neurogenetics 2021. [PMID: 34608571 DOI: 10.1007/s10048-021-00673-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]