Request for Proposals Frontotemporal Dementia Drug Discovery Program
Alzheimer’s Drug Discovery Foundation
All Regions
09/22/2008
$0
REQUEST FOR PROPOSALS
Frontotemporal Dementia Drug Discovery Program
The Alzheimer’s Drug Discovery Foundation (ADDF) and The Association for Frontotemporal Dementias (AFTD) seek to accelerate and support drug discovery for FTD and related dementias through this Request for Proposals (RFP.
Research investigating the pathologic mechanisms of neurodegeneration in frontotemporal dementia (FTD) and related disorders has advanced recently, creating new potential targets for drug discovery.
Examples of programs appropriate for this RFP include, but are not limited to:
• Identification and in vitro testing of potentially disease modifying lead compounds
• Development and testing of novel high throughput screening assays
• Medicinal chemistry on lead compounds
• Testing of lead compounds in a relevant animal model for preclinical proof of concept
• ADME, toxicology, pharmacokinetics, pharmacodynamics on lead compounds
• Development and testing of targeted gene delivery strategies
• Development of biomarkers to accelerate drug development and early diagnosis
PLEASE NOTE: THIS FUNDING WILL NOT SUPPORT APPLICATIONS FOR BASIC RESEARCH
MECHANISM(S) OF SUPPORT
ADDF/AFTD will provide individual grants for one year duration with the possibility of follow on funding. Applications may be submitted by non-profit academic institutions and for-profit biotechnology companies, both public and private, worldwide. Collaborative teams of neuroscientists and researchers in drug discovery disciplines such as medicinal chemistry and drug delivery are also encouraged to apply.
REVIEW PROCESS
The deadline date for applications is September 22nd, 2008. Applications will be confidentially reviewed by ADDF and an external Scientific Review Committee, including AFTD scientific advisors. Applications from biotechnology companies will also be reviewed by ADDF’s external Business Advisory Board. Award-winners will be publicly announced in April 2009.
APPLICATION PROCEDURE
All applications must be submitted electronically at www.AlzDiscovery.org.
Clinical Pharmacist, Medicinal Chemist, Neuroscientist, Scientist, Toxicologist
Novel Approaches to Drug Discovery for Alzheimer's Disease Request For Proposals
Alzheimer's Drug Discovery Foundation
All Regions
10/01/2008
$0
NOVEL APPROACHES TO DRUG DISCOVERY FOR ALZHEIMER’S DISEASE
REQUEST FOR PROPOSALS
Scope of the Program
The objective of this Request for Proposals (RFP) from the biotechnology industry and academia is to catalyze and accelerate the discovery and development of innovative and effective treatments for Alzheimer’s disease. The program will fund high throughput screening of novel targets to identify hits and leads, lead validation and optimization through medicinal chemistry, and pre-clinical in-vitro and in-vivo evaluation, including pharmacology, toxicology, pharmacokinetics, formulation chemistry and the conduct of pre-clinical “proof of concept” studies.
A KEY FUNDING PRIORITY IS THE SUPPORT OF AD DRUG DISCOVERY IN EMERGING BIOTECH COMPANIES
The total number of grants awarded will be dependent upon the numbers, quality and costs of applications received. Proposals covering two years may be submitted, although the second year of funding will be contingent upon progress of the completed work, the investigator’s second-year work-plan, and the numbers and quality of competing proposals. Only one year of funding will be guaranteed. Former recipients of ADDF and ISOA funding are eligible to apply.
Funding Mechanism
If the award recipient is a biotechnology company, ADDF shall provide the grant funding in the form of a convertible note, an equity investment or a recoverable grant based on mutually agreed and negotiated terms.
If the award recipient is an academic institution, then ADDF shall provide funding in the form of an academic grant with terms that provide the Foundation with a return on its investment in the event of commercial success as a result of the research program funded by the Award as negotiated and mutually agreed.
Reporting Requirements
Scientific and financial progress reports are due every six months after the start of the award. A final report of research activities and expenditures is due at the termination of the funding period.
Eligibility Criteria
The proposed research may be conducted at a registered public or private biotechnology company or at any type of not-for-profit academic setting and the Principal Investigator must hold an MD or PhD degree.
Application Guidelines and Selection Criteria
All applications and supporting materials must be received by October 1, 2008. Applications will be reviewed by a Scientific Review Committee (SRC) and a final decision will be made by December 31, 2008.
The following criteria will be used to determine the merit of an application:
• Merit and feasibility of the proposed research and its relevance to drug discovery and development for treatment of Alzheimer’s disease.
• Qualifications of the scientific staff conducting the studies.
• Excellence of the research environment, including the availability of a multidisciplinary research team comprised of neuroscientists, medicinal chemists, pharmaceutical scientists, and the necessary animal models, facilities and equipment required for drug discovery and drug development. Research can be outsourced and consultants employed where appropriate and adequately justified.
• Likelihood that the project will lead to advancement in the treatment of Alzheimer’s disease.
Application Procedures
Application forms are available at www.AlzDiscovery.org.
Medicinal Chemist, Clinical Chemist, Clinical Pharmacist, Laboratory Director, Neurologist, Neuroscientist, Pharmacist, Pharmacy Faculty
Commercialization Grants
Epilepsy Therapy Project
All Regions
08/01/2008
$100,000

Commercialization Grants

Letter of Intent due: AUGUST 1, 2008
If the LOI is accepted, APPLICATION is due: SEPTEMBER 15, 2008

The Epilepsy Therapy Project - Matching Grants Towards the Commercialization of Promising Therapies
The Epilepsy Therapy Project offers 1:1 matching grants of up to $100,000 to academic and commercial entities to support the commercialization of novel approaches to the treatment of epilepsy. These matching funds seek to leverage other resources, and accelerate the pace of therapeutic advance. Proposals will be evaluated by our Scientific Advisory Board together with our Business Advisory Board. We seek to fund discrete steps along the commercial pathway that if successful will enable a project to gain further funding. We welcome a broad span of proposals. Examples of the kind of work we would hope to support include: pre-clinical evaluation and testing of compounds or devices with novel mechanisms of action; and early clinical proof-of-principal trials of compounds or devices. Below are some specific project areas identified by our SAB, which illustrate the scope of our interests:

Directing a promising therapy towards epilepsy as a clinical pathway for regulatory approval. One example of this is work our founders have done with Cognetix, a Utah-based early stage drug development company utilizing conopeptides. While the company's compound had a number of potential therapeutic uses, the company chose to direct the initial clinical focus for its drug towards epilepsy.
Proof-of-principle trials, where a potentially valuable therapy is introduced to selected patients at leading epilepsy centers, under the close watch of leading epileptologists. A case here would be the use of a magnetic stimulation device therapy, which is being carried out in select leading epilepsy centers.
Helping to commercialize promising new epilepsy assays, which offer the ability to identify different targets using different mechanisms of action. An example here would be UCB Pharma's levetiracetam (Keppra), a new drug that failed earlier assays, but showed promise when screened with more recent assays.
Related to the previous example, we are exploring other promising compounds that have failed earlier assays, but may nonetheless offer value if screened against newer, better assays. While we cannot provide the funds necessary to carry a drug through clinical trials, our funds can help reduce risks in the pre-clinical stage, making subsequent clinical development more feasible. Armed with appropriate pre-clinical data, we can then introduce promising compounds to other investment capital sources for further funding and development.
Preference will be given to proposals that already have a commercial partner engaged to assist with development and to proposals that have committed or matched funding from the sponsoring institution, commercial partner or other third party source.

Proposals for research originating from outside the United States are welcome.

Address questions to grants@epilepsytherapyproject.org.

Investigators must submit a Letter of Intent by August 1, 2008.
The deadline for receipt of full Grant proposals is September 15, 2008.
Full proposals will be accepted only from Investigators whose Letter of Intent was approved.

New Therapy Grants Program
Epilepsy Research Foundation
All Regions
08/01/2008
$0
The New Therapy Grants Program seeks to advance the development of specific new therapies including new medicines and therapeutic devices. Consistent with the theme of translational research, all grant proposals must demonstrate a clear path from the lab to the patient.

Letter of Intent due: AUGUST 1, 2008
If the LOI is accepted, APPLICATION is due: SEPTEMBER 15, 2008
Background
The Epilepsy Research Foundation was created through a unique partnership between two leading epilepsy non-profit organizations, the Epilepsy Therapy Project and the Epilepsy Foundation. Additional support is provided by the Milken Family Foundation and Finding a Cure for Epilepsy and Seizures (FACES). The mission of the Epilepsy Research Foundation is to drive the development of new therapies for epilepsy, accelerating the advancement of research from the laboratory to the patient. The Epilepsy Research Foundation provides grants supporting the research and development of new therapies in both academic and commercial settings worldwide.

ERF grant awards are supplemented by support from: Finding a Cure for Epilepsy and Seizures (FACES) and the Milken Family Foundation Translational Research Awards.

New Therapy Grants Program
The New Therapy Grants Program seeks to advance the development of specific new therapies including new medicines and therapeutic devices. Consistent with the theme of translational research, all grant proposals must demonstrate a clear path from the lab to the patient. Other areas of consideration include but are not limited to:

Seed funding for preliminary and targeted work deemed necessary to explore novel therapeutic approaches
Projects which if successful offer a clear path to downstream development
Proposals that support the commercialization of exceptional academic research projects
Research to bring new approaches and therapy to children
Preference will be given to proposals that already have a commercial partner engaged to assist with development and to proposals that have committed or matched funding from the sponsoring institution, commercial partner or other third party source. Proposals for research originating from outside the United States are welcome.

Address questions to grants@epilepsytherapyproject.org.

Investigators must submit a Letter of Intent by August 1, 2008.
The deadline for receipt of full Grant proposals is September 15, 2008.
Neurologist, Neuroscientist, Physician Researcher
Clinical Research Training Grant
Muscular Dystrophy Association
All Regions
08/01/2008
$180,000

Muscular Dystrophy Association

Clinical Research Training Grant (CRTG)

Summary: The CRTG is designed to provide promising young clinicians the research training opportunities needed to become productive clinical investigators in neuromuscular disease research. This training opportunity is designed to be compatible with the requirements of a traditional clinical fellowship in neuromuscular disease and any forthcoming requirements for certification in neuromuscular disease. Trainees will be expected to design their own educational plans and to participate, under the supervision of a mentor, in the development and/or coordination of a clinical research project. At minimum, trainees should gain experience in the basic epidemiological methods of clinical research, ethical and legal issues, and the principles involved in monitoring patient-oriented research, including regulatory requirements and quality assurance. Recipients are also encouraged to acquire knowledge of and exposure to research technologies, large dataset management, bioinformatics and other research tools, as well as to develop the communication and collaboration skills necessary for successful investigator development. Clinical Research Training Grants will be awarded annually to no more than two qualified recipients for the amount of $90,000 per year for two years.

Deadlines*

*Potential applicants are strongly encouraged to contact MDA staff before submitting a letter of intent for this grant.

2009:
Letter of Intent: August 1, 2008
Grant Application: September 1, 2008
Start Date: July 1, 2009

FOR ONLINE SUBMISSION OF THE "REQUEST FOR GRANT APPLICATiON" go to: https://proposalcentral.altum.com

Frequently Asked Questions

What is the funding level and percent commitment for this grant?
This Fellowship is funded at up to $90,000 per year, with a cap of $85,000 to be applied to salary and benefits, and a cap of $10,000 to be applied to coursework, travel and a laptop computer. Applicants are expected to commit 100% of their time to this Fellowship.

Who can apply?
To apply for the CRTG, you must hold a Doctor of Medicine or Doctor of Osteopathy degree and be licensed to practice medicine in the state or province in which the grant will be given; be board eligible or board certified in neurology, child neurology or physical medicine and rehabilitation at the time of the award. Clinicians who have been in a practice focused on neuromuscular diseases for not more than 5 years are also eligible to submit an application. See the CRTG Policy Manual for further requirements.

Do you need to be a U.S. citizen to apply?
U.S. or Canadian citizens, resident aliens, or nonresident aliens with a valid employment authorization are eligible for this training opportunity. Strong preference will be given to applicants who intend to remain in the U.S. or Canada after completing training.

How are applications reviewed?
Applications are reviewed by members of MDA’s Medical Advisory Committee (MAC) at its October meeting. Review criteria include: quality of applicant; quality of mentor and training environment; and quality of educational plan. See the CRTG Policy Manual for more detail.

How many grants are awarded each year?
No more than two grants will be awarded annually.

How should the “classwork” requirement be met?
Applicants are asked to design an “educational program” including formal classwork in clinical research. The classwork requirement can be satisfied through many different mechanisms including classes in relevant areas offered at the applicant’s own institution or classes offered by government or private organizations, or some combination of both. Both certificate and credit hour classes may be counted toward the educational requirement. Examples of appropriate topics for classwork include, but are not limited to epidemiology, ethics/responsible conduct of research, study design/clinical trials design, use of human subjects, scientific writing/grantsmanship, and good clinical practice. Your application will be reviewed, in part, on the breadth and depth of the educational plan that you develop.

What is meant by "development or coordination of a clinical research project"?
Your second-year project should allow you to apply information that you gained from the first-year coursework in a clinical research setting. Planning for this project should begin in year one. Appropriate projects might include, for example, participating in a clinical trial, conducting a restrospective chart review study, or designing and implementing a small epidemiological study. Your role in the design, execution, and/or data anaylsis for the research project should be clearly delineated. The project should not be a laboratory research project. It is expected that a publication or presentation at a scientific meeting will result from the research project.

Is this program compatible with certification in neuromuscular disease?
Certification requirements for neuromuscular training are currently under development. This fellowship is meant to be compatible with requirements for such certification. If you plan to seek certification in neuromuscular training, please indicate this in your applicant statement and educational plan, and include the requirements for certification in your educational plan.

How will progress be judged?
Progress reports will be required at six months, twelve months and eighteen months. Applicants who are not judged to be making satisfactory progress will be subject to cancellation.

Contact:
Elizabeth Habeeb-Louks
MDA Research Department
(520) 529-2000, ext. 6021
crtg@mdausa.org

Neurologist, Osteopath, Physiatrist , Physician, Physician Researcher
Spasmodic Dysphonia Grants
National Spasmodic Dysphonia Association
All Regions
01/15/2009
$20,000

The National Spasmodic Dysphonia Association is seeking research applications for new investigator startup grants or post doctoral study focused on research aimed at increasing understanding of Spasmodic Dysphonia, a focal dystonia with that affects speech.

Small seed money grants to new or established investigators for up to $20,000 (excluding indirect costs) per year will be awarded. These can be for startup grants enabling successful applicants to subsequently seek funding from the National Institutes of Health or may provide partial support for post doctoral research training relating to Spasmodic Dysphonia.

We are interested in hypothesis-driven research related to new approaches aimed at increasing understanding of Spasmodic Dysphonia that focuses on the following areas:

Endogenous and environmental risk factors for the development of Spasmodic Dysphonia
Pathophysiology of central nervous system dysfunction in Spasmodic Dysphonia
Animal models for Spasmodic Dysphonia
Novel approaches to the treatment of Spasmodic Dysphonia
Diagnostic tools for Spasmodic Dysphonia
Controlled studies of treatment outcomes in Spasmodic Dysphonia
The deadline to submit an application is January 15, 2009.

National Spasmodic Dysphonia Association
300 Park Boulevard, Suite 415, Itasca, IL 60143
Phone: 800-795-6732 Fax: 630-250-4505
Website: www.dysphonia.org

Established Investigator, Neurologist, Physician Researcher
Grant requests
Multiple Sclerosis Foundation
All Regions
11/01/2008
$0

Grant requests
For all grant requests other than the Brighter Tomorrow grant

The initial contact should be made by letter of inquiry stating the amount sought, purpose of the grant, and nature of the organization requesting the grant. Please include an e-mail address if available. The letter should be sent to:

The Grant Committee
c/o Managing Director
Multiple Sclerosis Foundation
6350 North Andrews Avenue
Ft. Lauderdale, Fl. 33309

If you are awarded a grant we do ask as a minimum that you provide us with semi-annual progress reports however additional criteria may apply depending on the amount and type of grant.

FUNDING CYCLE

All grant requests excluding the Brighter Tomorrow grant, must be received prior to November 1 of each year. If your request is funded, funding will occur prior to January 15 of the following year.

LIMITATIONS AND EXCLUSIONS

The Multiple Sclerosis Foundation, at its sole discretion, has the right to limit, refuse or cancel any grants made. The awarding of grants is at the determination of the Multiple Sclerosis Foundation.

Critical Challenges in Parkinson’s Disease 2008
Michael J. Fox Foundation for Parkinson’s Research
All Regions
07/24/2008
$0
Critical Challenges in PD 2008

06/03/2008

The Michael J. Fox Foundation for Parkinson’s Research (MJFF) is launching this funding initiative to promote development and testing of technologies to image alpha-synuclein and/or Lewy body-related pathology associated with Parkinson’s disease (PD) in living brain tissue. Projects can include the development and/or testing of specific probes (e.g., small molecule compounds or modified peptides/antibodies) or methods for detecting alpha-synuclein/Lewy body components appropriate for use in MRI, PET/SPECT or other imaging modality. Depending on the stage of technology development, work can include pre-clinical or clinical studies. However, the ultimate deliverable of the study must include an in vivo test of the imaging approach either in a PD-relevant mammalian model or human PD patient.

Studies appropriate for this RFP may include:
• Development of technologies (e.g., small molecule ligands, peptide/antibody approaches, etc.) that can be used to visualize alpha-synuclein/Lewy body pathological features and are detectable with an appropriate imaging modality.
• Examination of the sensitivity and selectivity of alpha-synuclein/Lewy body imaging technologies to detect alpha-synuclein in human PD postmortem samples.
• Optimization studies to make technologies appropriate for eventual in vivo preclinical or clinical testing, including for example determination of pharmacokinetic parameters, toxicity, blood-brain barrier permeability, target engagement, and clearance times.
• In vivo testing of technologies in preclinical animal models of alpha-synuclein/Lewy body pathology.
• Clinical testing of technologies in living human PD patients, including possible ‘Hospice studies’ to confirm imaging results to postmortem examination.

A strong, collaborative and appropriately skilled investigator team will be a major criterion for successful funding in this program.

Applicants may request a project period of up to two years and direct costs appropriate and justifiable for the work proposed, in addition to indirect costs of up to 25 percent of direct costs.

Please note that a ‘Technology Summary’ is a required element of this program’s application process and is different from a standard pre-proposal. All Technology Summaries received in response to this MJFF RFP will be subjected to a review process. Only a small subset of applicants will ultimately be selected to work with MJFF staff to develop full proposals for final funding consideration.
MJFF employs an expedited, abbreviated granting mechanism to accelerate discoveries and ultimately translate findings to PD patients more quickly. 

For additional information about this initiative, contact the Foundation at research@michaeljfox.org.

Conference Call
MJFF will hold a 45 minute long conference call on June 19, 2008 at 12:00 PM U.S. Eastern Time to clarify and explain the Critical Challenges in PD 2008 program and to answer applicants' questions. To participate in this call, you must RSVP via email to conferencecalls@michaeljfox.org. Participants will receive a reply with call-in details.

For additional information about this initiative, contact the Foundation at research@michaeljfox.org.
Imaging Professional, Molecular Biologist , Neurologist, Neuroradiologist , Neuroscientist, Physician Researcher, Radiologic Technologist, Radiologist
Fondation Leducq Transatlantic Fellowships
Fondation Leducq
All Regions
08/18/2008
$150,000

Fondation Leducq has established a two-year Transatlantic Fellowship Award that will allow four outstanding young researchers per year--two from North America and two from Europe--to work internationally with one of the scientific teams already assembled under the Leducq Foundation Transatlantic Networks of Excellence program. The fellowship is designed to provide support to program fellows to work on the other side of the Atlantic from his or her country of origin with a member of a Leducq network. Fellows must commit to spending at least one of the two years abroad; they can work at other sites in the network as the needs of the research program dictate, including, for a maximum of one year, in their country of origin.

The objectives of the Leducq Transatlantic Fellowship Program are to develop outstanding researchers capable of performing original and innovative cardiovascular or neurovascular research in an international and collaborative context; to train young investigators in translational research through interactive investigation with a Leducq network comprised of basic science and clinical researchers; to support the career development of these young investigators; and to reinforce the objectives of the Transatlantic Networks of Excellence Program. 

The deadline for application submission will be September 18, 2008. The start date will be in the autumn of 2009.

Candidates must apply through an eligible, continuing Fondation Leducq Transatlantic Network. Interested applicants can contact the investigators directly, or contact the Leducq Foundation (info@fondationleducq.org) for further information.

Cardiologist, Young Investigator, Young Scientist
Research grants-Huntington's Disease
Hereditary Disease Foundation
All Regions
10/15/2008
$50,000
Research grants

The focus of the Hereditary Disease Foundation is on Huntington's disease. Support will be for research projects that will contribute to identifying and understanding the basic defect in Huntington's disease. Areas of interest include trinucleotide expansions, animal models, gene therapy, neurobiology and development of the basal ganglia, cell survival and death, and intercellular signaling in striatal neurons.

Anyone accepting funding from the Hereditary Disease Foundation must agree to abide by the following policy: Propagatable materials (including monoclonal antibodies and recombinant DNAs) should be freely available to other investigators following publication. The Foundation's position is that there be no restrictions or proprietary rights in materials produced with our support.

Deadlines for applications are February 15, June 15 and October 15. Applications will be reviewed in May, September and January. To obtain an application, please submit a letter of intent no more than one page long. It may be submitted at any time to following address,

Hereditary Disease Foundation
Attn: Carl D. Johnson, PhD
3960 Broadway, 6th Floor
New York, NY 10032
USA

The maximum award for research grants is $50,000. Grants are usually for one year with a possibility of renewal. Grants are considered seed money. If the project shows promise, it is hoped that other institutions will fund it thereafter. The Foundation does not generally include the salary of the principle investigator. Indirect costs are not allowed, but fringe benefits are considered part of personnel costs and are allowed.

Grant applications should be submitted by email and five hard copies. Supplemental material and reprints should be submitted with a file type of PDF(.pdf).

Applicants are notified of funding decisions by letter only.

To apply:

· Submit a letter of intent: There is no deadline – submit anytime, electronically using the form on the Foundation’s website:
http://www.hdfoundation.org/funding/intent.php.

The letter of intent should include:

o Contact information

o A summary of your proposed research project – 500 words or less

· Letter of Intent Review: Letters of intent are reviewed by a triage group. Turn-around is usually less than two weeks and the primary consideration is relevance to finding treatments and cures for Huntington’s disease. If a proposal is accepted, an application form for a full proposal is sent to the applicant by email. Applicants are encouraged to interact by email or phone with Carl Johnson, Ph.D., the Executive Director for Science, while preparing their application

Applications require:

· Administrative contact: Name, title, email address, phone & fax numbers and mailing address of the institutional representative who will manage the project. The application must be approved and signed by the institution.

· Project summary: Not to exceed 200 words.

· Budget (for Grants only): Grant funding is limited to $50,000. Except in unusual circumstances, salary support is not provided for the Principal Investigator. The Foundation does not provide funds for indirect costs or overhead. Postdoctoral Fellowship salaries are determined by the Foundation, based on number of years after receipt of a doctoral degree. Postdoctoral Fellowship Awards include $8,000 for supplies.

· Other current and pending support: Please provide a complete list (NIH format) indicating aims of each project and potential overlap with the current proposal.

· Biographical sketch: Attach a two-page biographical sketch (NIH format) for the Principal Investigator and other professional personnel. Include training, experience, recent publications and patent filings. Any supplemental materials, manuscripts or papers should be submitted electronically in PDF format.

· Protection of Human Subjects: Any study using human subjects must be approved by the Institutional Review Board (IRB) of the applicant institution. Please attach the completed “Protection of Human Subjects Assurance/Certification/Declaration” form.

· Protection of Animal Subjects: The transportation, care, and use of animals must be in accordance with the Animal Welfare Act (7 U.S.C. 2131 et. seq.) and other applicable Federal laws, guidelines, and policies.

· Study Proposal: Not to exceed 10 pages, including references. There is no need for an extensive, NIH style, introduction, but be sure to include a description of critical details of the proposed plan as well as documentation of research experience. Particular attention should be paid to the aims and anticipated outcomes of the study and on how they will help discover or develop treatments for Huntington’s disease.

Application Review:

Applications are reviewed by the Scientific Advisory Board of the Hereditary Disease Foundation. The SAB meets three times each year: in January, May and October. Applications received at least six weeks prior to the meeting are considered. Applicants will receive written notification of the funding decision shortly after the review meeting.

Award Payment:

If the application is approved for funding, payment will be made in two equal installments. Awardees must arrange, via email or in writing, activation of the Award. The first payment is sent immediately; the second will be made six months later, upon receipt of a progress report via email. A final report including a financial statement is also required.

Please submit completed applications both by email and five hard copies to:

Hereditary Disease Foundation
Attn: Carl D. Johnson, Ph.D.
Executive Director for Science
3960 Broadway, 6th Floor
New York, NY 10032
Cell Biologist, Molecular Biologist , Neurologist, Neuroscientist, Physician Researcher

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