Difference between revisions of "Escande CC"
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{{Person | {{Person | ||
|lastname=Escande Castro | |lastname=Escande Castro | ||
|firstname=Carlos | |firstname=Carlos | ||
|title=PhD | |title=PhD | ||
|institution=Anesthesia Dept. | |||
Mayo Clinic | |||
|address=200 1st ST SW | |||
55905 MN | |area code=55905 | ||
|city=Rochester | |||
|state=Minnesota (MN) | |||
|country=USA | |||
}} | }} | ||
{{Labelingperson}} | |||
In our lab we are interested in how protein acetylation dynamics in the mitochondria affects ist function, and how these acetylation pathways are regulated. | In our lab we are interested in how protein acetylation dynamics in the mitochondria affects ist function, and how these acetylation pathways are regulated. | ||
Latest revision as of 15:02, 28 September 2016
| Name | Escande Castro Carlos, PhD |
|---|---|
| Institution | Anesthesia Dept.
Mayo Clinic |
| Address | 200 1st ST SW, 55905 |
| City | Rochester |
| State/Province | Minnesota (MN) |
| Country | USA |
| Weblink | |
| O2k-Network Lab |
Labels:
Publications
| Published | Reference | |
|---|---|---|
| Camacho-Pereira 2016 Cell Metab | 2016 | Camacho-Pereira J, Tarragó MG, Chini CC, Nin V, Escande C, Warner GM, Puranik AS, Schoon RA, Reid JM, Galina A, Chini EN (2016) CD38 dictates age-related NAD decline and mitochondrial dysfunction through an SIRT3-dependent mechanism. Cell Metab 23:1127-39. |
| Chini 2014 Clin Cancer Res | 2014 | Chini CC, Gonzalez Guerrico A, Nin V, Camacho-Pereira J, Escande C, Barbosa M, Chini EN (2014) Targeting of NAD metabolism in pancreatic cancer cells: potential novel therapy for pancreatic tumors. Clin Cancer Res 20:120-30. |
| Nin 2012 J Biol Chem | 2012 | Nin V, Escande C, Chini CC, Giri S, Camacho-Pereira J, Matalonga J, Lou Z, Chini EN (2012) Role of deleted in breast cancer 1 (DBC1) protein in SIRT1 deacetylase activation induced by protein kinase A and AMP-activated protein kinase. J Biol Chem 287:23489-501. |
Abstracts
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In our lab we are interested in how protein acetylation dynamics in the mitochondria affects ist function, and how these acetylation pathways are regulated.
