Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis-Reference-Cited by-同舟云学术

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Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis

Published:2014-03-03 Issue:11 Volume:111 Page:4197-4202
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Nesin V.,Wiley G.,Kousi M.,Ong E.-C.,Lehmann T.,Nicholl D. J.,Suri M.,Shahrizaila N.,Katsanis N.,Gaffney P. M.,Wierenga K. J.,Tsiokas L.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference50 articles.

1. Store-Operated Calcium Channels

2. The second messenger linking receptor activation to internal Ca release in liver

3. Depletion of intracellular calcium stores activates a calcium current in mast cells

4. Molecular Basis of Calcium Signaling in Lymphocytes: STIM and ORAI

5. STIM proteins: dynamic calcium signal transducers

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3. Constitutive, Muscle-Specific Orai1 Knockout Results in the Incomplete Assembly of Ca2+ Entry Units and a Reduction in the Age-Dependent Formation of Tubular Aggregates;Biomedicines;2024-07-24

4. Exome sequencing in undiagnosed congenital myopathy reveals new genes and refines genes–phenotypes correlations;Genome Medicine;2024-07-09

5. Identification of Glucosidase II that regulates STIM1 activation dynamics;2024-04-22

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