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Title	Description	Category
College Face Sheetⁱ	Routing Document for Grant and Clinical Trial application	Clinical Trials
Clinical Trials Process Flow Sheet	Flow sheet for Sponsored Clinical Trials	Clinical Trials
Clinical Trials for volunteers	What is a Clinical Trial For Volunteers	Clinical Trials
Clinical Trials Registration Policy	Guidelines/Policies	Clinical Trials
CTO Fee Schedule	Fact Sheet for Institutional fees	Clinical Trials
Pharmacy Service Fees	For use when negotiating a budget for Pharmacy Fees	Clinical Trials
Research Billing Form	Research Billing Form	Clinical Trials
Funding Update April 29-May 3, 2013	This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information.	Funding Update E-mail Alert
Funding Update April 15-19, 2013	This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information.	Funding Update E-mail Alert
Funding Update April 22-26, 2013	This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information.	Funding Update E-mail Alert
Funding Update May 6-10, 2013	This is a compilation of upcoming funding opportunities issued by the NIH and other sources. Also included are notices, conferences, Hot Topics programs, active collaborations and other research development information.	Funding Update E-mail Alert
Upstate Authorship Policy	This policy is based upon the ICMJE guidelines for granting authorship and contributorship	General Research Policies
PHS Policy Promoting Objectivity in Research	Policy establishes standards that provide a reasonable expectation that the design, conduct and reporting of research funded under PHS grants, cooperative agreements or contracts will be free from bias resulting from financial conflict of interest.	General Research Policies
Data Ownership Policy	Policy describes ownership of data produced at Upstate by faculty, staff, students, fellows, etc.	General Research Policies
DHHS Public Health Service Policies on Research Misconduct	Institutions that receive support from Public Health Services offices and agencies, such as NIH, are responsible for following these policies to assure the responsible conduct of research and respond to allegations of research misconduct.	General Research Policies
Research Conflict of Interest Committee Member Exclusion Policy.	Research Conflict of Interest Committee Member Exclusion Policy.	General Research Policies
Upstate Policy on Identification and Management of Conflicts of Interest and Commitment	This policy establishes standards for identification and management of conflicts of interest and commitment in research, education and patient care.	General Research Policies
Research Conflict of Interest Committee Membership	Research Conflict of Interest Committee Membership	General Research Policies
General Research Policies	An overview of regulatory and contractual policies that govern research and sponsored programs at Upstate and the Research Foundation of the State of New York.	General Research Policies
Upstate Research Misconduct Policy	Defines research misconduct and explains the process of assessing and invetigating allegations	General Research Policies
Charge for the Institutional Bio-Safety Committee	Guidelines/Policies	IBC—Institutional Biosafety Committee
Site Visit Checklist ⁱ	Checklist	IBC—Institutional Biosafety Committee
Application Form for Recombinant DNA, Bio-hazardous and Infectious Agent Researchⁱ	Application Form	IBC—Institutional Biosafety Committee
Instructions for writing a Biosafety manual	Instructions for writing a Biosafety manual	IBC—Institutional Biosafety Committee
Application Form for Handling, Packaging and Shipping Blood, Tissue or Body Fluids ⁱ	Application Form	IBC—Institutional Biosafety Committee
Policy and Procedures for Research Involving Human Blood, Fresh Human Tissue, or Body Fluids	Guidelines/Policies	IBC—Institutional Biosafety Committee
Summary of Guidelines for Research Involving Infectious Agents or Recombinant DNA Molecules	Guidelines/Policies	IBC—Institutional Biosafety Committee
Facility Safety Plan	Guidelines/Policies	IBC—Institutional Biosafety Committee
Exempt Experiments	Guidelines/Policies	IBC—Institutional Biosafety Committee
Biosafety Manual Template for Clinical Research	Templace	IBC—Institutional Biosafety Committee
Safety Product List	List of safety products	IBC—Institutional Biosafety Committee
Guidance for Research Using Lentiviral Vectors	Guidance	IBC—Institutional Biosafety Committee
Biosafety Level 2 Draft Door Sign	Door Sign	IBC—Institutional Biosafety Committee
Biosafety Manual Guidance and Template for Basic Science Research	Template	IBC—Institutional Biosafety Committee
Guidance for laboratory workers who work with vaccinia virus (from the CDC)	Vaccinia information	IBC—Institutional Biosafety Committee
Meeting Dates and Deadlines	Meeting Dates and Deadlines	IBC—Institutional Biosafety Committee
Transporting Biohazardous (including human blood, body fluids and tissue) Items	Guidelines/Policies	IBC—Institutional Biosafety Committee
Survey of Staff Use of Safety Medical Devices ⁱ	Form	IBC—Institutional Biosafety Committee
Policy and Procedures for Research Involving Recombinant DNA, and Infectious or Bio-Hazard Agents (Including Human Gene Transfer Research)	Guidelines/Policies	IBC—Institutional Biosafety Committee
Additional Study Personnel Form (Appendix A) ⁱ	Personnel Form	IBC—Institutional Biosafety Committee
Summary of NIH Guidlines for Research Involving Recombinant DNA Molecules	Guidelines/Policies	IBC—Institutional Biosafety Committee
Helpful References	References	IBC—Institutional Biosafety Committee
Memorandum of Understanding on Academic Exchange	MOU Academic Exchange	IIBMST—International Institute of Biomedical Sciences and Technology
IIBMST letter	IIBMST Focus Group Leaders announced	IIBMST—International Institute of Biomedical Sciences and Technology
IIBMST Electronic Membership Formⁱ	IIBMST Electronic Membership Form (interactive pdf)	IIBMST—International Institute of Biomedical Sciences and Technology
Memorandum of Understanding (MOU) between Upstate and Other International Universities	International Institute of Biomedical Sciences and Technology (IIBMST) Memorandum of Understanding	IIBMST—International Institute of Biomedical Sciences and Technology
Genetic Testing: Understanding Definitions and Key concepts	Education	IRB—Institutional Review Board (Human Subject)
Assessing Capacity to Consent for Research	Form	IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults Consent Template	Template	IRB—Institutional Review Board (Human Subject)
Genetic Testing & Banking Adults and Children Consent Template	Template	IRB—Institutional Review Board (Human Subject)
NCI CIRB Contact Information	Form	IRB—Institutional Review Board (Human Subject)
NCI Central IRB (CIRB) Guidelines	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
NCI CIRB Study Closure Information Formⁱ	Form	IRB—Institutional Review Board (Human Subject)
Conflict of Interest Policy for IRB Members	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Emergency Use of an Investigational Drug or Biologic	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Emergency Use Report Formⁱ	Form	IRB—Institutional Review Board (Human Subject)
Emergency Use of Unapproved Medical Devices	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Request Exemption from IRB Review	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Guidelines for Genetic Testing	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Upstate IRB Guidelines & Policies	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Research on Decedent's Information Requestⁱ	Form	IRB—Institutional Review Board (Human Subject)
HIPAA Review Prepatory to Research Request Form	Form	IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Consent Template	Template	IRB—Institutional Review Board (Human Subject)
HIPAA Required Section Spanish Consent Template	Template	IRB—Institutional Review Board (Human Subject)
Requesting an IND Consult from the FDA	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Investigator 101 Education Material	Education Material	IRB—Institutional Review Board (Human Subject)
Request for Tissue for Research Purposes (Pathology Department Form)ⁱ	Form	IRB—Institutional Review Board (Human Subject)
Meeting Dates and Deadlines	Dates and Deadlines	IRB—Institutional Review Board (Human Subject)
How to Register for the CITI Basic or Refresher Course	Step by step instructions on registering for the CITI Basic or Refresher Course	IRB—Institutional Review Board (Human Subject)
The Impact of The HIPAA Privacy Rule on Research	Educational Presentation	IRB—Institutional Review Board (Human Subject)
Unanticipated Problems and Adverse Event Flow Chart	Determination Flow-chart	IRB—Institutional Review Board (Human Subject)
Reporting of Protocol Deviations	Protocol Deviation Policy	IRB—Institutional Review Board (Human Subject)
Case Reports Using Existing Data - Author Worksheetⁱ	Case Report Guide	IRB—Institutional Review Board (Human Subject)
FDA Guidance on In Vitro Diagnostics	Guidance	IRB—Institutional Review Board (Human Subject)
Security of Research Data: How to Protect Research Subjects	Overview of relevant FDA guidelines, HIPAA Security, and State Law; best practices to follow for protecting electronic information	IRB—Institutional Review Board (Human Subject)
Access to Patient Information for Research Purposes: Demystifying the Process	Educational Presentation	IRB—Institutional Review Board (Human Subject)
Bosnian Language HIPAA Section	HIPAA section translated into Bosnian	IRB—Institutional Review Board (Human Subject)
Bosnian Language Standard Consent Sections	In Case of Injury, Questions, Voluntary Participation, etc. translated in to Bosnian	IRB—Institutional Review Board (Human Subject)
Bosnian Language Signature Pages	Signature pages translated into Bosnian	IRB—Institutional Review Board (Human Subject)
"To Whom it May Concern" (Letter for Sponsors Regarding Adverse Events	AE Letter for Spnsors	IRB—Institutional Review Board (Human Subject)
Investigator Responsibilities for Research Involving a Significant Risk Device	Guidance	IRB—Institutional Review Board (Human Subject)
FDA Guidance on Consent for the use of In Vitro Diagnostics	Guidance	IRB—Institutional Review Board (Human Subject)
HIPAA and Research	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Guidelines for Scientific Reviewers	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Sample Assent Form	Form	IRB—Institutional Review Board (Human Subject)
Adult Subjects Consent Template	Template	IRB—Institutional Review Board (Human Subject)
Adult and/or Minor Subjects Consent Template	Template	IRB—Institutional Review Board (Human Subject)
Parental Permission Only Consent Template	Template	IRB—Institutional Review Board (Human Subject)
Adult Subjects Signature Page Template	Template	IRB—Institutional Review Board (Human Subject)
Adult & Minor Subjects Signature Page Template	Template	IRB—Institutional Review Board (Human Subject)
Minor Subjects Only Signature Page Template	Template	IRB—Institutional Review Board (Human Subject)
SOP for Obtaining Consent from Subjects who Enrolled as a Minor	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
SOP for Establishing Legal Guardianship for Pediatric Subjects	Guidelines/Policies	IRB—Institutional Review Board (Human Subject)
Spanish Language Version Signature Page Template	Template	IRB—Institutional Review Board (Human Subject)
Banking Specimens Section Consent Template	Template	IRB—Institutional Review Board (Human Subject)
University Hospital Patient Data Request Form	Form	IRB—Institutional Review Board (Human Subject)
University Hospital, Voluntary Faculty Request to Conduct Research which Requires the Use / Disclosure of IIHIⁱ	Form	IRB—Institutional Review Board (Human Subject)
Volunteer Recruitment Formⁱ	Form	IRB—Institutional Review Board (Human Subject)
Waiver of Authorization Request Formⁱ	Form	IRB—Institutional Review Board (Human Subject)
CITI Education Requirement Policy	Mandatory Human Subjects Education Program	IRB—Institutional Review Board (Human Subject)
Spanish Lanuage Standard Consent Sections	Standard language for the 'In Case of Injury', 'Questions', and 'Voluntary Participation' sections	IRB—Institutional Review Board (Human Subject)
Policy on IRB Review for Studies Pending Funding	Policy	IRB—Institutional Review Board (Human Subject)
In Vitro Diagnostocs Decision Tree	Guidance	IRB—Institutional Review Board (Human Subject)
Amended Informed Consent Regulations (FDA)	Amended informed consent regulations (FDA)	IRB—Institutional Review Board (Human Subject)
IRBNet New User Registration and instruction document	IRBNet New User Registration and instructions	IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 1	IRBNet Training Energizer 1	IRB—Institutional Review Board (Human Subject)
Pharmacy Research Policy	Pharmacy Research Policy	IRB—Institutional Review Board (Human Subject)
IRBNet Training Energizer 2	IRBNet Training Energizer 2	IRB—Institutional Review Board (Human Subject)
Adverse Event Guideline	Requirements for notifying the IRB of Unanticipated Events	IRB—Institutional Review Board (Human Subject)
Intramural Bridge Grant Applicationⁱ	Intramural Research Bridge Grant Application Form	Intramural Research Funding/Grants
Intramural Research Grant Guidelines	Guidelines for Eligibility and Use of Intramural Research Grant Funds	Intramural Research Funding/Grants
Intramural Postdoctoral Fellowship Applicationⁱ	Intramural Postdoctoral Research Fellowship Application Form	Intramural Research Funding/Grants
Intramural Pilot Collaborative Grant Applicationⁱ	Intramural Research Pilot Collaborative Research Grant Application Form	Intramural Research Funding/Grants
Intramural Pilot Grant Applicationⁱ	Intramural Research Pilot Grant Application Form	Intramural Research Funding/Grants
New Technology Disclosure (NTD) Formⁱ	Form	Patent/New Technology Transfer
New Technology Disclosure (NTD) Procedure	Guidelines	Patent/New Technology Transfer
New Company Formation	How to Create A New Company	Patent/New Technology Transfer
Upstate Core Facilities-Center for Research and Evaluation (CRE)	Services of and how to access the Center for Research and Evaluation	Presentations
Upstate Core Facilities-Flow Cytometry Core	Information regarding research supported by and how to access the Core Facility for Flow Cytometry	Presentations
Upstate Core Facilities-Microarray-Based Research Core	Information regarding the types of research supported by and how to access the Microarray-Based Research Core at Upstate	Presentations
Upstate Core Facilities-MRI Research Core	Information regarding research supported by and how to access teh MRI Research Core	Presentations
Major Changes to NIH Applications	Information and instructions regarding NIH applications on/after January 25, 2010	Presentations
Finding and Applying for Funding	Information about identifying government and foundation funding and how to apply through Upstate and SU	Presentations
Investigator Training Program-Mechanics of Performing a Clinical Trial Part I	Part II of how to conduct a clinical trial at Upstate Medical University	Presentations
Investigator Training Program-Overall Project Management	Managing a clinical trial, including responsibilities of the PI and the project team	Presentations
Investigator Training Program-Research Integrity Part I	Importance of conflict of interest and the new Upstate Medical University Policy on Relations with the Pharmaceutical, Medical Device & BIotechnology Industry	Presentations
Investigator Training Program-Research Integrity Part II	Provides information about research misconduct	Presentations
NIH Public Access-PubMed, PubMed Central, Open Access, and Public Access	NIH new Public Access policy and resources for researchers to use to comply with this policy	Presentations
NIH Public Access-Upstate & the NIH Public Access Policy	information about the NIH Public Access policy and Upstate resources to assist researchers comply with this policy	Presentations
Tech Transfer-From Discovery to Patent Application Filing...and Beyond	Steps in taking a discovery (invention) from initial disclosure to obtaining a patent and/or license	Presentations
Tech Transfer-Find Funding to Commercialize Technology using SBIR & STTR Programs	Information about the SBIR and STTR programs for researchers to find funding to commercialize their discoveries	Presentations
Tech Transfer-What Happens After You Invent	Information about turning inventions into assets, protecting and managing asset rights, and turning IP assets into gain	Presentations
Upstate Core Facilities-Confocal & 2-photon Core	Research supported by and how to access Upstate's Confocal & 2 Photon Core Facility	Presentations
Upstate Core Facilities-Clinical Research Unit	Services and capacity of and how to access the Clinical Research Unit at the IHP	Presentations
Upstate Core Facilities-DNA Sequencing Core	information about research supported by and how to access the Core Facility for DNA Sequencing	Presentations
What Research Administration Can Do for YOU	Information about services of research development, sponsored programs office,post award, and research accounting	Presentations
Human Subjects Research-Unanticipated Problems & Adverse Events	clinical, human subjects research unexpected problems and adverse events	Presentations
Upstate Core Facilities-Musculoskeletal Core	Information about the types of research supported by and how to access teh Musculoskeletal Core	Presentations
Upstate Core Facilitites-Proteomics Core	Information regarding research supported by and how to access the Proteomics Core Facility	Presentations
Upstate Core Facilities-Cetner for Humanized SCID Mouse Models & Stem Cell Processing Lab	information regarding research supported by the Center for Humanized SCID mouse models and Stem Cell processing lab	Presentations
Upstate Core Facilities-In vivo Micro CT Core Laboratory	Provides information about the research supported and how to access the In vivo MicroCT Core Facility	Presentations
Investigator Training Program-Mechanics of Performing a Clinical Trial Part II	Information about pre-award and initial decisions, study start-up, trial progression, and study close out	Presentations
Investigator Training Program-New Initiatives to Promote Clinical Research	Updates regarding Clinical Research Unit, Clinical Trials Office, and availability of inpatient beds for Phase I trials	Presentations
Investigator Training Program-Patient Needs Come First	Information about patient needs and safety in clinical research	Presentations
Investigator Training Program-Considerations for Conducting Studies at Upstate	Information regarding the importance of clinical research and conducting clinical research at Upstate Medical University	Presentations
Study Initiation Key Points	Key Points include: Informed Consent, Continuing Review Submission to the IRB, Confidentiality and HIPAA Issues, Amendments to Approved Protocols, Adverse Event Reporting to the IRB, Protocol Deviation Reporting to the IRB,DSMB Submission to the IRB	QAIP—Quality Assessment & Improvement Program
QAIP Compliance Tips	Tips and Best Practices	QAIP—Quality Assessment & Improvement Program
Informed Consent Compliance Checklistⁱ	Informed Consent Checklist	QAIP—Quality Assessment & Improvement Program
Study Initiation Visit: Preventive Care for Your Study Site	Education	QAIP—Quality Assessment & Improvement Program
Narrative (notes-to-file) Formⁱ	Note-to-File Form	QAIP—Quality Assessment & Improvement Program
Investigator Self-Assessment Checklistⁱ	Self-assessment Checklist	QAIP—Quality Assessment & Improvement Program
Ways to Prepare for a QAIP Study Site Visit	Prepare for Site Visit	QAIP—Quality Assessment & Improvement Program
Research Compliance Reference List	Education	QAIP—Quality Assessment & Improvement Program
QAIP Site Visit Schematic Chart	QAIP Schematic	QAIP—Quality Assessment & Improvement Program
Subject Eligibility Checklistⁱ	Eligibility Checklist	QAIP—Quality Assessment & Improvement Program
Subject Enrollment Logⁱ	Enrollment Log	QAIP—Quality Assessment & Improvement Program
Study Team Signature and Delegation of Responsibility Logⁱ	Responsibility Log	QAIP—Quality Assessment & Improvement Program
QAIP Site Visit Formⁱ	Site Visit Form	QAIP—Quality Assessment & Improvement Program
Instructions for IRB Protocols Involving Ionizing Radiation Exposure to Human Subjects	Guidelines/Policies	RSC—Radiation Safety Committee
2013-2014 Golisano Children's Hospital Grant Guidelines	Guidelines for applying for research or program funding from the Golisano Children's Hospital Grant Program	Research Administration
2013-2014 Golisano Children's Hospital Research Grant Application	Application form to be used to apply for research funding under the Golisano Children's Hospital Program	Research Administration
Deans' Grand Rounds 2011	Grand Rounds Schedule	Research Administration
Research Strategic Plan Implementation Schedule	Research Strategic Plan Implementation Schedule	Research Administration
Deans Grand Rounds Wright 2012	Dr. Wright	Research Administration
FCOI Memo from Dr. Goodman	FCOI Memo from Dr. Goodman	Research Administration
Conflict of Interest Formⁱ	Disclosure of Significant Financial Interests and Obligations	Research Administration
Indirect Cost Rate Agreement	Federally negotiated Indirect Cost Rates	Research Administration
Grant Application Checklist	Checklist of important steps for grant application	Research Administration
RF Fringe Benefit Rates	Research Foundation Fringe Benefit Rates	Research Administration
Upstate Financial Disclosure Formⁱ	This form is completed by Upstate faculty, staff and students applying for extramural research funding who will participate in the design, conduct or reporting of the research	Research Administration
Research Implementation Plan 2012 Update	Strategic Plan: Research Implementation Plan 2012 Update	Research Administration
Advancing Clinical Research at Upstate-Investigator Training Program	an in-depth course for faculty who conduct human subject research	Research Administration
Signature Authorization Formⁱ	Post Awards document for PI to authorize funds	Research Administration
Flow Cytometry Fee Schedule	Fee schedule for ust of Flow Cytometry Core Facility updated 2/2/10.	Research Administration
Strategic Plan: Research Implementation Plan	A detailed series of events required to strengthen and grow our research enterprise.	Research Administration
Research Misconduct Policy	Guidelines/Policies for responding to allegations of research misconduct, updated August, 2011	Research Administration
Strategic Plan for Strengthening Research	This plan details SUNY Upstate's four research pillars and is the blueprint for the future.	Research Administration
Guidelines: Cell Phone Purchases and Monthly Charges on Sponsored Accounts	Guidelines	Research Administration
Mandatory Responsible Conduct of Research Education Program	To assure that all Upstate research is performed in a responsible and ethical fashion, all researchers, students, staff, and research personnel musttake a Responsible Conduct of Research course offered by the Collaborative Institutional Training Initiative (CITI)	Research Administration
Conversations in Entrepreneurship	Conversations in Entrepreneurship	Research Administration
IHP MRI Policy	IHP MRI Core Policy January,2011 update	Research Facilities
Proteomics Core Research Facility SERVICES and PRICING	Proteomics Core Research Facility SERVICES and PRICING info	Research Facilities
IHP MRI User Request Formⁱ	Use this form to request services from the IHP MRI Core Facility	Research Facilities
IHP MRI Request Formⁱ	Use this form to request the services of the IHP MRI Core Research Facility	Research Facilities
Core Flow Cell Sorter	Core Flow Cell Sorter	Research Facilities
Core Flow Fortessa Cell Analyzer	Fortessa Cell Analyzer	Research Facilities
Using the Clinical Research Unit	Policies and procedures for using the Upstate Medical University Clinical Research Unit	Research Facilities
Flow Core Fee Schedule	Flow Core Fee Schedule	Research Facilities
Core Flow Useful Links	Core Flow Useful Links	Research Facilities
core flow training	core flow training	Research Facilities
Requesting Use of CRU Application	Application to request use of the Upstate Medical University Clinical Research Unit	Research Facilities
Core Flow LSRII	Flow	Research Facilities
Core Flow Aria Cell Sorter	Core Flow Aria Cell Sorter	Research Facilities
Core Flow Sort Questionaire	Core Flow Sort Questionaire	Research Facilities
Research Forum: Issue 37	Research Forum Newsletter Spring 2010	Research Forum Newsletters
Research Forum: Issue 41	Research Forum Newsletter Spring 2011	Research Forum Newsletters
Research Forum: Issue 40	Research Forum Newsletter Winter 2010-2011	Research Forum Newsletters
Research Forum: Issue 36	Research Forum Newsletter Winter 2009-2010	Research Forum Newsletters
Research Forum: Issue 35	Research Forum Newsletter Fall 2009	Research Forum Newsletters
Research Forum: Issue 39	Research Forum Newsletter Fall 2010	Research Forum Newsletters
Research Forum: Issue 38	Research Forum Newsletter Summer 2010	Research Forum Newsletters
Student Work/Research Mentor Directory	Student Summer Research List of Mentors and Supervisors	Student Research
2013 Summer Student Research/Work Fact Sheet	Provides information to students about summer work and research opportunities	Student Research
2013 Summer Student Research Fellowship Application	application to be completed by MS1 students in order to be considered for a research fellowship	Student Research
This Week in Research @ Upstate	Highlights of Biomedical Research Seminars for the current week.	This Week in Research at Upstate