Acknowledgements for Grant Writers
Investigators who are writing grant applications and need a description of the Cellular Imaging shared resource can find options below. Descriptions of the overall Fred Hutchinson Cancer Center Shared Resources program are available on the main Shared Resources grant information page.
Publications by Cellular Imaging staff and grant awards to the core are listed below.
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Citations & Statements | Grand Descriptions | Publications and Grants
Citations & Statements
All publications, press releases, or other documents that cite results from CCSG-supported research must include acknowledgement of the grant and maintain compliance with NIH Public Access Policy. All manuscripts accepted for publication must be submitted to PubMed Central and be assigned a PMCID. Additionally, please reference the Research Resource Identifier (RRID). RRIDs are assigned to cores to help researchers cite key resources in the biomedical literature to improve transparency of research methods.
“This research was supported by the Cellular Imaging Shared Resource, RRID:SCR_022609, of the Fred Hutch/University of Washington/Seattle Children’s Cancer Consortium (P30 CA015704).”
Additionally, we would like to thank the Fred Hutchinson Cancer Center Cellular Imaging Shared Resource for assistance with microscopy and image analysis.
*Highlighting specific staff members is a great way to acknowledge personalized support.
Required Statement for MJ Murdock Charitable Trust
"Acknowledgement of the use of instruments acquired through other funding mechanisms, e.g. M. J. Murdock Charitable Trust, NIH S10 Shared Instrumentation Grant."
Cellular Imaging Shared Resouce Grant Descriptions
Short Grant Description
The Cellular Imaging shared resource provides researchers with customized light microscopy support. Staff support the entire imaging workflow including microscope selection, training, independent use, and image analysis on our widefield, confocal, and super-resolution microscopes.
Long Grant Description
Cellular Imaging is a comprehensive microscopy facility which supports fundamental and preclinical projects. Staff members work directly with investigators from experimental design and instrument selection through data analysis. The team enables researchers to visualize biological structures at the molecular, cellular, tissue, and organism level.
The Cellular Imaging core facility supports imaging capabilities including brightfield imaging, widefield and confocal fluorescence imaging modalities, lightsheet microscopy, and super-resolution microscopy. Types of services can include time lapse imaging, image-based screening, photoconversion, laser ablation techniques, multi-photon microscopy, FRET, and FRAP. In addition to imaging support, staff work with researchers to develop image analysis workflows using commercial software or custom-written code.
Publications Made Possible by Cellular Imaging
Our services and technologies have made possible many high-impact publications, such as the following:
- Hui J, Nakamura M, Dubrulle J, Parkhurst SM. Coordinated efforts of different actin filament populations are needed for optimal cell wound repair. Mol Biol Cell. 2023. doi: 10.1091/mbc.E22-05-0155. PMCID: PMC10011732.
- Galeano Niño JL, Wu H, LaCourse KD, Kempchinsky AG, Baryiames A, Barber B, Futran N, Houlton J, Sather C, Sicinska E, Taylor A, Minot SS, Johnston CD, Bullman S. Effect of the intratumoral microbiota on spatial and cellular heterogeneity in cancer. Nature. 2022. doi: 10.1038/s41586-022-05435-0. PMCID: PMC9684076.
- Pattwell SS, Arora S, Nuechterlein N, Zager M, Loeb KR, Cimino PJ, Holland NC, Reche-Ley N, Bolouri H, Almiron Bonnin DA, Szulzewsky F, Phadnis VV, Ozawa T, Wagner MJ, Haffner MC, Cao J, Shendure J, Holland EC. Oncogenic role of a developmentally regulated NTRK2 splice variant. Sci Adv. 2022. doi: 10.1126/sciadv.abo6789. PMCID: PMC9544329.
- Kelly KP, Alassaf M, Sullivan CE, Brent AE, Goldberg ZH, Poling ME, Dubrulle J, Rajan A. Fat body phospholipid state dictates hunger-driven feeding behavior. Elife. 2022. doi: 10.7554/eLife.80282. PMCID: PMC9566863.
- Lynch KL, Dillon MR, Bat-Erdene M, Lewis HC, Kaai RJ, Arnold EA, Avgousti DC. A viral histone-like protein exploits antagonism between linker histones and HMGB proteins to obstruct the cell cycle. Curr Biol. 2021. doi: 10.1016/j.cub.2021.09.050. PMCID: PMC8665055.
- Isabella AJ, Stonick JA, Dubrulle J, Moens CB. Intrinsic positional memory guides target-specific axon regeneration in the zebrafish vagus nerve. Development. 2021. doi: 10.1242/dev.199706. PMCID: PMC8489019.
- Steenkiste EM, Berndt JD, Pilling C, Simpkins C, Cooper JA. A Cas-BCAR3 co-regulatory circuit controls lamellipodia dynamics. Elife. 2021. doi: 10.7554/eLife.67078. PMCID: PMC8266394.
- Eichholz K, Li AZ, Diem K, Jensen MC, Zhu J, Corey L. A CAR RNA FISH assay to study functional and spatial heterogeneity of chimeric antigen receptor T cells in tissue. Sci Rep. 2021. doi: 10.1038/s41598-021-92196-x. PMCID: PMC8217486.
- Raiders S, Black EC, Bae A, MacFarlane S, Klein M, Shaham S, Singhvi A. Glia actively sculpt sensory neurons by controlled phagocytosis to tune animal behavior. Elife. 2021. doi: 10.7554/eLife.63532. PMCID: PMC8079151.