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In JoVE (1)
- In vivo Bioluminescence Imaging of Tumor Hypoxia Dynamics of Breast Cancer Brain Metastasis in a Mouse Model
Other Publications (2)
Articles by Henry Dunn in JoVE
In vivo Bioluminescence Imaging of Tumor Hypoxia Dynamics of Breast Cancer Brain Metastasis in a Mouse Model
Debabrata Saha1, Henry Dunn2, Heling Zhou2, Hiroshi Harada3, Masahiro Hiraoka3, Ralph P. Mason2, Dawen Zhao2
1Department of Radiation Oncology, University of Texas Southwestern Medical Center, 2Department of Radiology, University of Texas Southwestern Medical Center, 3Department of Radiation Oncology, Kyoto University Graduate School of Medicine
Bioluminescence imaging of hypoxia inducible factor-1α activity is applied to monitor intracranial tumor hypoxia development in a breast cancer brain metastasis mouse model.
Other articles by Henry Dunn on PubMed
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. Nov, 2002 | Pubmed ID: 12463490
We describe nine females with Rett Syndrome (RS), aged 14 to 26 years. All had had developmental delay before the end of their first year and had subsequently regressed to profound dementia with apraxia, ataxia, irregular respirations and often also seizures.
REGULATION OF G PROTEIN-COUPLED RECEPTOR ACTIVITY, TRAFFICKING AND LOCALIZATION BY GPCR-INTERACTING PROTEINS
British Journal of Pharmacology. Jun, 2011 | Pubmed ID: 21699508
G protein-coupled receptors (GPCRs) represent the largest family of integral membrane proteins and were first identified as receptor proteins that coupled via heterotrimeric G proteins to regulate a vast variety of effector proteins to modulate cellular function. It is now recognized that GPCRs interact with a myriad of proteins that not only function to attenuate their signalling but also function to couple these receptors to heterotrimeric G protein-independent signalling pathways. In addition, intracellular and transmembrane proteins associate with GPCRs and regulate their processing in the endoplasmic reticulum, trafficking to the cell surface, compartmentalization to plasma membrane microdomains, endocytosis, and trafficking between intracellular membrane compartments. The present review will overview the functional consequence of β-arrestin, receptor activity-modifying proteins (RAMPS), regulators of G protein signalling (RGS), G protein-coupled receptor associated sorting proteins (GASPs), Homer, small GTPases, PSD95/Disc Large/Zona Occludens (PDZ), spinophilin, protein phosphatases, calmodulin, optineurin and Src homology 3 (SH3) containing protein interactions with GPCRs.