Sigma-1 receptor chaperones at the ER-mitochondrion interface regulate Ca(2+) signaling and cell survival.

By Teruo Hayashi, T. Su. Cell, 2007

1,738 citations recorded by the source corpus.

Subfields: Biological Psychiatry, Cellular and Molecular Neuroscience, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/efb52f0f0871ebba1eb0755210521effe7814e8f

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Biological Psychiatry

1. R. Rizzuto
2. G. Hajnóczky
3. C. Giorgi
4. P. Pinton
5. T. Su
6. Teruo Hayashi

In Cellular and Molecular Neuroscience

1. R. Rizzuto
2. T. Su
3. G. Hajnóczky
4. C. Giorgi
5. P. Pinton
6. Teruo Hayashi
7. T. Maurice

In Molecular Biology

1. R. Rizzuto
2. T. Su
3. C. Giorgi
4. P. Pinton
5. G. Hajnóczky
6. Teruo Hayashi
7. T. Maurice

Citations in the corpus

• Calcium and apoptosis: ER-mitochondria Ca2+ transfer in the control of apoptosis (2008, positive): “Mitochondria appear to be the downstream effectors of this pathway, as knockdown of IP3R-3 significantly decreased agonist-induced mitochondrial Ca2þ uptake (Hayashi and Su, 2007).”
• The Pharmacology of Sigma-1 Receptors (2009, background): “Related to this point is another important question concerning the chaperone activity of sigma-1 receptors (Hayashi & Su, 2007): Do sigma-1 receptors regulate ion channels through their chaperone activities or by some other mechanism?”
• MAM (2009, methodology): “Two recent studies demonstrate that the MAM uses chaperone machineries to regulate Ca2+ signaling [12,37].”