National Institute of Dental & Craniofacial Research; Notice of Closed Meetings, 11997-11998 [05-4671]
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Federal Register / Vol. 70, No. 46 / Thursday, March 10, 2005 / Notices
in normal human myeloid lineage cells
and is believed to play a role in
allowing lymphocytes to differentiate
properly. It is believed that the gene
may play a role in human prostate
cancer, multiple myeloma, B-cell
chronic lymphocytic leukemia and
other types of cancer and can be used
diagnostically as well as in therapeutic
screening activities.
Tyrosyl-DNA Phosphodiesterases (TDP)
and Related Polypeptides, Nucleic
Acids, Vectors, TDP-Producing Host
Cell, Antibodies and Methods of Use
Jeffrey J. Pouliot and Howard A. Nash
(NIMH),
U.S. Patent Application No. 10/110,176
filed 05 Apr 2002 (DHHS Reference
No. E–281–1999/0–US–03), claiming
priority to U.S. Provisional
Application No. 60/157,690 filed 05
Oct 1999 (DHHS Reference No. E–
281–1999/0–US–01),
Licensing Contact: John Stansberry;
(301) 451–7337;
stansbej@mail.nih.gov.
Topisomerases are cellular enzymes
that are vital for replication of the
genome. However, if topisomerase and
DNA form covalent complexes that
prevent the resealing of DNA, this may
lead to cell death. Essentially, this
invention consists of a new isolated and
cloned enzyme, tyrosyl-DNA
phospodiesterase (TDP1) that is capable
of hydrolyzing the covalent complexes
between topisomerase and DNA,
allowing the DNA to reseal. The
mechanism that defines topiosomerases
is their capacity to break DNA and, after
an interval in which topological changes
may occur, to reseal the break without
the intervention of a high-energy
cofactor. The breakage of the DNA is
accompanied by the formation of a
covalent bond between topisomerase
and DNA to create an intermediate that
is resolved during the resealing step.
However, if the resealing step fails, the
covalent intermediates between
topoisomerase I and DNA can form
complexes that lead to cell death. The
failure of the resealing is increased by
some chemotherapies such as
camptothecin. Thus, this technology has
many potential commercial uses
including: a method for screening
camptothecin analogues or other
compounds for their resistance to repair
by this enzyme or to prescreen patients
for their sensitivity to topoisomerase
inhibitors, which could identify patients
most likely to respond to camptothecin
therapy. Further, this invention
provides for a vector comprising of the
nucleic acid molecule for TDP1 as well
as the method of altering the level of
TDP1 in a cell, a tissue, an organ or an
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organism. Finally, this invention
consists of a method for identifying a
compound that stabilizes a covalent
bond complex that forms between DNA
and topoisomerase I, wherein the
covalent bond cannot be cleaved.
Chromatin Insulator Protecting
Expressed Genes of Interest for Human
Gene Therapy or Other Mammalian
Transgenic Systems
Drs. Jay H. Chung and Gary Felsenfeld
(NIDDK),
U.S. Patent 5,610,053 issued 11 Mar
1997 (DHHS Reference No. E–206–
1992/1–US–01), Licensing Contact:
John Stansberry; (301) 435–5236;
stansbej@mail.nih.gov.
The technology provides the isolation
of a functional DNA sequence
comprising a chromatin insulating
element from a vertebrate system and
provides the first employment of the
pure insulator element as a functional
insulator in mammalian cells. The
technology further relates to a method
for insulating the expression of a gene
from the activity of cis-acting regulatory
sequences in eukaryotic chromatin.
This technology could be of major
importance in providing a mechanism
and a tool to restrict the action of cisacting regulatory elements on genes
whose activities or encoded products
are needed or desired to be expressed in
mammalian transgenic systems. This
technology provides the first pure
insulator element to function solely as
an insulator element in human cells.
Accordingly, this technology could have
tremendous practical implications for
transgenic technology and human gene
therapies, either in vitro or in vivo.
The technology further provides a
method and constructs for insulating the
expression of a gene or genes in
transgenic animals such that the
transfected genes will be protected and
stably expressed in the tissues of the
transgenic animal or its offspring. For
example, even if the DNA of the
construct integrates into areas of silent
chromatin in the genomic DNA of the
host animal, the gene will continue to
be expressed. The invention could
provide a means of improving the stable
integration and expression of any
transgenic construct of interest, with
efficiencies higher than are achieved
presently. Use of this invention may
represent a large potential savings for
licensee’s constructing transgenic cell
lines or animals.
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11997
Dated: March 2, 2005.
Steven M. Ferguson,
Director, Division of Technology Development
and Transfer, Office of Technology Transfer,
National Institutes of Health.
[FR Doc. 05–4675 Filed 3–9–05; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Dental &
Craniofacial Research; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice
is hereby given of the following
meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Dental and Craniofacial Research Special
Emphasis Panel, 05–59, Review F30s.
Date: March 30, 2005.
Time: 2 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Natcher Building, 45 Center Drive, Bethesda,
MD 20892 (Telephone Conference Call).
Contact Person: Lynn M. King, PhD,
Scientific Review Administrator, Scientific
Review Branch, 45 Center Dr., Rm 4AN–38K,
National Institute of Dental & Craniofacial
Research, National Institutes of Health,
Bethesda, MD 20892–6402, (301) 594–5006.
Name of Committee: National Institute of
Dental and Craniofacial Research Special
Emphasis Panel, 05–55, Review of R21s.
Date: April 11, 2005.
Time: 11 a.m. to 12 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Natcher Building, 45 Center Drive, Bethesda,
MD 20892 (Telephone Conference Call).
Contact Person: Rebecca Roper, MS, MPH,
Scientific Review Administrator, Scientific
Review Branch, Division of Extramural
Research, National Inst of Dental &
Craniofacial Research, National Institutes of
Health, 45 Center Dr., room 4AN32E,
Bethesda, MD 20892, (301) 451–5096.
Name of Committee: National Institute of
Dental and Craniofacial Research Special
Emphasis Panel, 05–56, Review R21s.
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11998
Federal Register / Vol. 70, No. 46 / Thursday, March 10, 2005 / Notices
Date: April 22, 2005.
Time: 2 p.m. to 3 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Natcher Building, 45 Center Drive, Bethesda,
MD 20892 (Telephone Conference Call).
Contact Person: Rebecca Roper, MS, MPH,
Scientific Review Administrator, Scientific
Review Branch, Division of Extramural
Research, National Inst of Dental &
Craniofacial Research, National Institutes of
Health, 45 Center Dr., room 4AN32E,
Bethesda, MD 20892, (301) 451–5096
(Catalogue of Federal Domestic Assistance
Program Nos. 93.121, Oral Diseases and
Disorders Research, National Institutes of
Health, HHS)
Dated: March 3, 2005.
Anna Snouffer,
Acting Director, Office of Federal Advisory
Committee Policy.
[FR Doc. 05–4671 Filed 3–9–05; 8:45 am]
BILLING CODE 4140–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Toxicology Program (NTP);
NTP Liaison and Scientific Review
Office; Announcement of Availability
of NTP Roadmap for the 21st Century
and NTP Celebration of its History
National Institute of
Environmental Health Sciences
(NIEHS); National Institutes of Health
(NIH), HHS.
ACTION: Announcement of availability of
a document and a symposium.
AGENCY:
SUMMARY: The National Toxicology
Program (NTP) announces availability of
the document, ‘‘A National Toxicology
Program for the 21st Century: A
Roadmap for the Future,’’ and invites
attendance at the symposium, ‘‘The
National Toxicology Program: A Quarter
Century of Toxicology for Public
Health’’ on May 10–11, 2005, at the
National Academy of Sciences in
Washington, DC. This meeting will
reflect on the history of the NTP and its
impact on public health since its
establishment in 1978 and unveil the
NTP’s plans and directions for the
future.
DATES: The symposium will be held on
May 10–11, 2005.
ADDRESSES: The symposium will be
held at the National Academy of
Sciences, 2100 C Street, NW.,
Washington, DC. Registration
information and other details for the
symposium are available on the NTP
Web site (https://ntp.niehs.nih.gov select
‘‘NTP 25 Years’’) or by contacting Nan
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Cushing (see FOR FURTHER INFORMATION
below). The NTP Roadmap
document is available electronically on
the NTP Web site, (select ‘‘NTP Vision
& Roadmap’’) or in printed text from the
NTP Liaison and Scientific Review
Office, P.O. Box 12233, MD A3–01, 111
TW Alexander Drive, Research Triangle
Park, NC 27709 (mail); (919) 541–0530
(telephone); (919) 541–0530 (fax).
FOR FURTHER INFORMATION CONTACT: Nan
Cushing, NTP Liaison and Scientific
Review Office, 919–541–0530
(telephone), cushing1@niehs.nih.gov (email).
SUPPLEMENTARY INFORMATION:
CONTACT
Background
The NTP was established in 1978 to
coordinate toxicological testing
programs within the Department of
Health and Human Services, develop
and validate improved testing methods,
develop approaches and generate data to
strengthen scientific knowledge about
potentially hazardous substances, and
communicate with stakeholders. In its
more than 25 years of existence, NTP
has become a world leader in providing
scientific information that improves our
nation’s ability to evaluate potential
human health effects from chemical and
physical exposures. The NTP maintains
a number of complex, interrelated
research and testing programs that
provide unique and critical information
needed by health regulatory and
research agencies to protect public
health. The NTP is hosting a symposium
on May 10–11, 2005, to celebrate its
leadership and contributions in
protecting public health and present the
NTP’s roadmap for the 21st century.
NTP Roadmap for the Future
In August 2003, the NTP defined its
vision for the 21st century and
undertook a yearlong process to refine
that vision and develop a roadmap for
its implementation. The NTP Vision is
to support the evolution of toxicology
from a predominately observational
science at the level of disease-specific
models to a predominately predictive
science focused upon a broad inclusion
of target-specific, mechanism-based,
biological observations. The NTP
Roadmap described in the document,
‘‘A National Toxicology Program for the
21st Century: A Roadmap for the
Future,’’ was developed with input from
numerous groups including the NTP’s
Federal partners, its advisory
committees, and the public. The NTP
Roadmap identifies the challenges and
opportunities confronting the program
today and discusses the directions
envisioned for the NTP in the 21st
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century in three main areas: (1) Refining
traditional toxicology assays, (2)
developing rapid, mechanism-based
predictive screens for environmentally
induced diseases, and (3) improving the
overall utility of NTP products for
public health decisions. Once
implemented, it will strategically
position the NTP at the forefront for
providing scientific data and the
interpretation of those data for public
health decisionmaking. Presentation of
the NTP’s vision and roadmap will be
a focus at the May symposium. The
document is available electronically in
PDF on the NTP Web site (https://
ntp.niehs.nih.gov select ‘‘NTP Vision
and Roadmap’’) or in printed text by
contacting the NTP Liaison and
Scientific Review Office (see FOR
FURTHER INFORMATION CONTACT above).
Preliminary Agenda
The symposium begins each day at 9
a.m. and adjourns at 4:30 p.m. on May
10 and noon on May 11. The
preliminary agenda topics are identified
below.
May 10, 2005
• Welcome
• Implications of Health Policy and
Health Legislation: Why Is the NTP
Needed?
• Public Health in the 21st Century:
NTP’s Contributions and Challenges
• Invited Remarks
• NTP Goals: Their Importance to
Public Health
—Coordination of Toxicology Testing
—Strengthening the Science Base in
Toxicology
—Evolution of the NTP in Other
Areas
—Partnerships and Communication
• Public Health Impact of the NTP
—Role of Safety Information on
Agents with Environmental
Exposure in Guiding Public Health
Decisions
—Role of the Report on Carcinogens
and the Center for the Evaluation of
Risks to Human Reproduction in
Guiding Public Health Decisions
May 11, 2005
• Welcome
• Toxicology’s Role in Public Health
Decisionmaking in the 21st Century
—Molecular Biology in Public Health
Decisions
—Functional Genomics in Public
Health Decisions
—Systems Biology in Public Health
Decisions
• NTP in the 21st Century
• The Future of Environmental Health
Research
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Agencies
[Federal Register Volume 70, Number 46 (Thursday, March 10, 2005)]
[Notices]
[Pages 11997-11998]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-4671]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
National Institute of Dental & Craniofacial Research; Notice of
Closed Meetings
Pursuant to section 10(d) of the Federal Advisory Committee Act, as
amended (5 U.S.C. Appendix 2), notice is hereby given of the following
meetings.
The meetings will be closed to the public in accordance with the
provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5
U.S.C., as amended. The grant applications and the discussions could
disclose confidential trade secrets or commercial property such as
patentable material, and personal information concerning individuals
associated with the grant applications, the disclosure of which would
constitute a clearly unwarranted invasion of personal privacy.
Name of Committee: National Institute of Dental and Craniofacial
Research Special Emphasis Panel, 05-59, Review F30s.
Date: March 30, 2005.
Time: 2 p.m. to 3:30 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institutes of Health, Natcher Building, 45
Center Drive, Bethesda, MD 20892 (Telephone Conference Call).
Contact Person: Lynn M. King, PhD, Scientific Review
Administrator, Scientific Review Branch, 45 Center Dr., Rm 4AN-38K,
National Institute of Dental & Craniofacial Research, National
Institutes of Health, Bethesda, MD 20892-6402, (301) 594-5006.
Name of Committee: National Institute of Dental and Craniofacial
Research Special Emphasis Panel, 05-55, Review of R21s.
Date: April 11, 2005.
Time: 11 a.m. to 12 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institutes of Health, Natcher Building, 45
Center Drive, Bethesda, MD 20892 (Telephone Conference Call).
Contact Person: Rebecca Roper, MS, MPH, Scientific Review
Administrator, Scientific Review Branch, Division of Extramural
Research, National Inst of Dental & Craniofacial Research, National
Institutes of Health, 45 Center Dr., room 4AN32E, Bethesda, MD
20892, (301) 451-5096.
Name of Committee: National Institute of Dental and Craniofacial
Research Special Emphasis Panel, 05-56, Review R21s.
[[Page 11998]]
Date: April 22, 2005.
Time: 2 p.m. to 3 p.m.
Agenda: To review and evaluate grant applications.
Place: National Institutes of Health, Natcher Building, 45
Center Drive, Bethesda, MD 20892 (Telephone Conference Call).
Contact Person: Rebecca Roper, MS, MPH, Scientific Review
Administrator, Scientific Review Branch, Division of Extramural
Research, National Inst of Dental & Craniofacial Research, National
Institutes of Health, 45 Center Dr., room 4AN32E, Bethesda, MD
20892, (301) 451-5096
(Catalogue of Federal Domestic Assistance Program Nos. 93.121, Oral
Diseases and Disorders Research, National Institutes of Health, HHS)
Dated: March 3, 2005.
Anna Snouffer,
Acting Director, Office of Federal Advisory Committee Policy.
[FR Doc. 05-4671 Filed 3-9-05; 8:45 am]
BILLING CODE 4140-01-M