Diseases caused by mutations inORAI1andSTIM1-Reference-Cited by-同舟云学术

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Diseases caused by mutations inORAI1andSTIM1

Published:2015-10-15 Issue:1 Volume:1356 Page:45-79
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:Ann. N.Y. Acad. Sci.

Author:

Lacruz Rodrigo S.¹,Feske Stefan²

Affiliation:

1. Department of Basic Science and Craniofacial Biology; New York University College of Dentistry; New York New York

2. Department of Pathology; New York University School of Medicine; New York New York

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/nyas.12938/fullpdf

Reference167 articles.

1. A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function;Feske;Nature,2006

2. Mitogen-regulated Ca2+ current of T lymphocytes is activated by depletion of intracellular Ca2+ stores;Zweifach;Proc. Natl. Acad. Sci. U. S. A.,1993

3. Depletion of intracellular calcium stores activates a calcium current in mast cells;Hoth;Nature,1992

4. Mitogen-induced oscillations of cytosolic Ca2+ and transmembrane Ca2+ current in human leukemic T cells;Lewis;Cell Regul,1989

5. CRAC channels: activation, permeation, and the search for a molecular identity;Prakriya;Cell Calcium,2003

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1. The effect of genetic polymorphisms in STIM1 and ORAI1 on erythropoietin resistance in Egyptian patients with end-stage renal disease;Clinica Chimica Acta;2025-01

2. Discovery of selective Orai channel blockers bearing an indazole or a pyrazole scaffold;European Journal of Medicinal Chemistry;2024-11

3. Dynasore modulates store-operated calcium entry and mitochondrial calcium release in corneal epithelial cells;Experimental Eye Research;2024-10

4. A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease;Science Advances;2024-09-13

5. Phenotypic Heterogeneity in ORAI-1-Associated Congenital Myopathy;Global Medical Genetics;2024-09-05

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