Research Announcements

American Skin Association Funding Announcement

The American Skin Association’s (ASA) 2018 funding opportunities in dermatology have been announced.  ASA seeks to provide funding for top researchers, physicians, and medical students who are dedicated to the field of dermatology.  Through these grants, ASA hopes to broaden understanding and increase knowledge of various skin diseases.

ASA is currently inviting application submissions from medical students and established researchers alike.  The following grants are being offered this year:

  • Milstein Research Scholar Award in  Melanoma/Non-Melanoma Skin Cancer ($60,000)
  • Calder Research Scholar Award in Vitiligo/Pigment Cell Disorders ($60,000)
  • ASA Research Scholar Award in Dermatology ($60,000)
  • Research Grants in the areas of Childhood Skin diseases/Disfigurement, Psoriasis/Inflammatory Skin Diseases, Skin Cancer & Melanoma, and Quality of Life/health Services/Outcomes Studies ($15,000)
  • Hambrick Medical Student Grants for those students working in the area of Melanoma & Skin Cancer ($7,000)

Deadline

Submission deadline is Sunday, October 1, 2017 at 11:59 EST.  All applications should be completed online at americanskin.org.

For submission instructions and award information click here.

User-Fee Voucher Program for UNMC Advanced Microscopy Core Facility Announced

The Nebraska Center for Cellular Signaling is pleased to announce that funding through a voucher program is available to support usage of the UNMC Advanced Microscopy Core Facility. The facility encompasses microscopes with live-­cell capability as well as a new, state-­of-­the-­art Zeiss ELYRA PS.1 super-­resolution microscope capable of Super-­Resolution Structured Illumination Microscopy (SR-­SIM) and single-­molecule localization techniques such as direct Stochastic Optical Reconstruction Microscopy (dSTORM) and Photoactivatable Localization Microscopy (PALM). We support an applications specialist whose job is to promote the use of super-­resolution techniques so that a broader swath of the research community uses dSTORM or PALM.

Further information about the core facility and its capabilities may be found on our main website:
https://www.unmc.edu/vcr/cores/vcr-­cores/confocal-­microscopy/index.html

Purpose: The goals of this voucher program are to encourage and support usage of the microscopes by investigators for projects (1) to help acquire preliminary data for external grant applications that would use the core facility and (2) to promote utilization of microscopy in their research by users who are new to the technology.

Description: Vouchers in amounts up to $2,500 per project will be made on a competitive basis for a one-­year duration. These funds will not be allocated directly to the investigators’ laboratories, but would instead be held in an account by the Core Facility to be expended as needed to subsidize usage
fees for the Core for the applicable projects.

Eligibility and Qualifications: The voucher program is not limited to current NCCS investigators, but is available to any faculty members holding tenure ­leading appointments at UNMC, UNO, UNL or Creighton University. Individuals with transient commitments to or from their institutions will NOT be eligible; thus, post-­doctoral fellows and visiting professors and investigators with no more than adjunct appointments are not eligible.

Proposal Requirements: Submit a one-­page description of the entire project in the format of an NIH R-­type specific aims page accompanied by an NIH-­style Bio-Sketch of the Principal Investigator.  Include a cover letter summarizing your past experience with and the usage of microscopy in your research. Be sure to justify your proposed hours of use of the core facility relative to the requested funds. Blanket requests for $2,500 without a thoughtful projection of your likely needs will be given low priority for funding. In addition, you should state how your intended use of the voucher program would either enhance an ongoing project or improve the likelihood of acquiring external funding for a new project. The Executive Committee of the Core Facility will evaluate the proposals and awardees will be notified by email when decisions have been made.

Deadline for receipt of proposals: April 21, 2017
Earliest possible date vouchers would be available: May 15, 2017

For further Information:
Keith Johnson: 402-­559-­3890, kjohnsonr@unmc.edu
Rick MacDonald: 402-­559-­7824, rgmacdon@unmc.edu

Microbiome Research Seminar

Inflammation and dysbiosis in periodontitis: Mechanisms and therapeutic intervention
George Hajishengallis, DDS, PhD, Thomas W. Evans Centennial Professor, University of Pennsylvania, Penn Dental Medicine – Microbiology, Philadelphia, PA

Wednesday, March 8, 2017; 12:00 noon

Dixon Lecture Hall, UNMC, College of Dentistry
40th & Holdrege (UNL East Campus)
Lincoln, NE

Presentation will be livestreamed to CON 2017 on the UNMC campus in Omaha

Hosted by: Dr. Tom Petro

Recent human microbiome analyses and animal model-based mechanistic studies collectively suggest that the pathogenesis of periodontitis is not mediated by a select few bacteria (traditionally known as ‘periopathogens’) but rather involves polymicrobial synergy and dysbiosis. The dysbiosis of the periodontal microbiota represents an alteration in the relative abundance or influence of individual members of the polymicrobial community (relative to their abundance or influence in health) leading to dysregulated host-microbial interactions that mediate destructive inflammation and bone loss. Functional specialization of community participants has given rise to several newly appreciated designations within the commensal-to-pathogen spectrum (e.g., accessory pathogens, keystone pathogens, and pathobionts). Although necessary, the bacteria are not sufficient to cause periodontitis, as it is the host inflammatory response to this polymicrobial challenge that predominantly inflicts damage to the periodontium. It is now well appreciated that the control of periodontal inflammation can indirectly exert antimicrobial effects. This is because periodontitis-associated bacteria thrive in an inflammatory environment. Indeed, the release into the gingival crevicular fluid of inflammatory breakdown products of connective tissue favors the outgrowth of certain species (e.g., proteolytic and asaccharolytic) that can benefit from these microenvironmental alterations.  Briefly stated, an initial inflammatory response (e.g., due to incipient dysbsiosis associated with poor oral hygiene) may select for those bacteria that can give rise to full-blown dysbiosis, thereby exacerbating inflammation and ultimately causing clinically evident periodontitis in susceptible individuals. Therefore, the control of inflammation should not only inhibit tissue damage but also suppress a nutritionally favorable environment that fuels dysbiosis.

All interested faculty, staff and students are invited to attend this presentation. The seminar will be recorded and available for those who cannot attend.