[Federal Register: June 25, 2003 (Volume 68, Number 122)]
[Notices]
[Page 37853-37854]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr25jn03-68]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The inventions listed below are owned by agencies of the U.S.
Government and are available for licensing in the U.S. in accordance
with 35 U.S.C. 207 to achieve expeditious commercialization of results
of federally-funded research and development. Foreign patent
applications are filed on selected inventions to extend market coverage
for companies and may also be available for licensing.
ADDRESSES: Licensing information and copies of the U.S. patent
applications listed below may be obtained by writing to the indicated
licensing contact at the Office of Technology Transfer, National
Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville,
Maryland 20852-3804; telephone: 301/496-7057; fax: 301/402-0220. A
signed Confidential Disclosure Agreement will be required to receive
copies of the patent applications.
Zap70 Protein Expression as a Marker for Chronic Lymphocytic Leukemia
(CLL)
Louis M. Staudt et al. (NCI)
Serial No. 60/375,966 filed 25 Apr 2002 and Serial No. 10/309,548 filed
03 Dec 2002
Licensing Contact: Catherine Joyce; 301/435-5031; joycec@mail.nih.gov. The presence or absence of somatic mutations in the expressed
immunoglobulin heavy chain variable regions (IgVH) of chronic
lymphocytic leukemia (CLL) cells provides prognostic information.
Patients whose leukemic cells express unmutated IgVH regions (Ig-
unmutated CLL) often have progressive disease whereas patients whose
leukemic cells express mutated IgVH regions (Ig-mutated CLL) more often
have an indolent disease. Given the difficulty in performing IgVH
sequencing in a routine diagnostic laboratory, this prognostic
distinction is currently unavailable to most patients.
The present invention relates to the discovery that ZAP-70
expression also distinguishes the two CLL subtypes. Ig-unmutated CLL
expressed ZAP-70 5.54-fold more highly than Ig-mutated CLL. ZAP-70
expression correctly predicted IgVH mutation status in 93% of patients,
and ZAP-70 expression and IgVH mutation status were comparable in their
ability to predict time to treatment requirement following diagnosis.
Clinically applicable RNA and protein-based assays for ZAP-70
expression have been developed. These assays would yield important
prognostic information for CLL patients.
The above-mentioned invention is available for licensing on an
exclusive or non-exclusive basis.
ABCA13 Nucleic Acids and Proteins, and Uses Thereof
Michael Dean et al. (NCI)
DHHS Reference No. E-304-2000/0 filed August 20, 2003
Licensing Contact: Catherine Joyce; 301/435-5031; e-mail:
joycec@mail.nih.gov. This technology relates to the identification of a novel gene in
the ABC (ATP-binding cassette transporter) gene superfamily, the ABCA13
gene. The ABC proteins are involved in extra- and intracellular
membrane transport of various substrates such as ions, amino acids,
peptides, sugars, vitamins, or steroid hormones and at least 14 members
of the ABC gene superfamily have been described as associated with
human disease. ABCA13 has high similarity with other ABCA subfamily
genes that are associated with human inherited diseases. This includes
ABCA1, the gene responsible for the cholesterol transport disorders
Tangier disease and familial hypoalphalipoproteinemia, and ABCA4, the
gene responsible for several retinal degeneration disorders. The ABCA13
gene is expressed in trachea, testes, and bone marrow. The ABCA13 gene
maps to chromosome 7p12.3, a region that contains an inherited disorder
affecting the pancreas and bone marrow (Shwachman-Diamond syndrome) as
well as a locus involved in T-cell tumor invasion and metastasis
(INM7), and therefore is a positional candidate for these disorders.
The above-mentioned invention is available for licensing on an
exclusive or non-exclusive basis.
[[Page 37854]]
Dated: June 16, 2003.
Steven M. Ferguson,
Acting Director, Division of Technology Development and Transfer,
Office of Technology Transfer, National Institutes of Health.
[FR Doc. 03-15973 Filed 6-24-03; 8:45 am]
BILLING CODE 4140-01-P