Growth arrest homeobox gene

Chemistry: natural resins or derivatives; peptides or proteins; – Proteins – i.e. – more than 100 amino acid residues

Reexamination Certificate

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C435S069100, C536S023100, C536S023500, C536S023200, C530S399000, C530S358000

Reexamination Certificate

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06897293

ABSTRACT:
A novel growth arrest homeobox gene has been discovered and the nucleotide sequences have been determined in both the rat and the human. The expression of the novel homeobox gene inhibits vascular smooth muscle cell growth. The growth arrest homeobox gene hereinafter referred to as the “Gax gene” and its corresponding proteins are useful in the study of vascular smooth muscle cell proliferation and in the treatment of blood vessel diseases that result from excessive smooth muscle cell proliferation, particularly after balloon angioplasty.

REFERENCES:
patent: 5302706 (1994-04-01), Smith
patent: 5856121 (1999-01-01), Gorski et al.
patent: 6280969 (2001-08-01), Gorski et al.
Ngo et al., Computational Complexity, Protein Structure Prediction, and the Levinthal Paradox, in the Protein Folding Problem and Tertiary Structure Prediction, 1994, Merz et al. (ed.), Birkhauser, Boston, MA, pp. 433 and 492-495.*
“Molecular Cloning of a Homeobox Transcription Factor from Adult Aortic Smooth Muscle” by Patel, et al.,The Journal of Biological Chemistry, vol. 267, No. 36, Dec. 25, 1992, pp. 26085-26090.
“Molecular Cloning of a Diverged Homeobox Gene that is Rapidly Down-Regulated During the G0/G1Transition in Vascular Smooth Muscle Cells” by Gorski, et al.,Molecular and Cellular Biology, vol. 13, No. 6, Jun. 1993, pp. 3722-3733.
“Homeobox Transcription Factor Regulation in the Cardiovascular System” by Gorski, et al.,TCM, vol. 3, No. 5, 1993, pp. 184-190.
“Cloning and Sequence Analysis of Homeobox Transcriptio Factor cDNA's with an Inosine-Containing Probe” by Gorski, et al.,Short Technical Reports, vol. 15, No. 5, 1994.
“The Growth Arrest-Specific Gene,gas 1, Is Involved in Growth Suppression” by Del Sal, et al.,International Centre for Genetic Engineering and Biotechnology, Aug. 21, 1992, pp. 595-607.
“Cloning of Senescent Cell-Derived Inhibitors of DNA Synthesis Using an Expression Screen” by Noda, et al.,Experimental Cell Research, 211, 1994, pp. 90-98.
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“MOX-1andMOX-2define a novel homeobox gene subfamily and are differentially expressed during early mesodermal petterning in mouse embryos” by Candia, et al.,Development, 116, Aug. 28, 1992, pp. 1123-1136.
“Arterial Gene Transfer Using Pure DNA Applied Directly to a Hydrogel-Coated Anioplasty Balloon” by Riessen, et al.,Human Gene Therapy, 4, 1993, pp. 749-758.
“Antisense c-myboligonucleotides inhibit intimal arterial smooth muscle cell accumulation in vivo” by Simons, et al.,Nature, vol. 359, Sep. 3, 1992, pp. 67-70.
“Site-Specific Gene Expression in Vivo by Direct Gene Transfer into the Arterial Wall” by Nabel, et al.,Reports, Sep. 14, 1990, pp. 1285-1288.
“Low Level In Vivo Gene Transfer Into the Arterial Wall Through a Perforated Balloon Catheter” by Flugelman, et al.,Circulation, vol. 85, No. 3, Mar. 1992, pp. 1110-1117.
“Single-Step purification of polypeptides expressed inEscherichia colias fusions with glutathione S-transferase” by Smith, et al.,Gene, 67, 1988, pp. 31-40.
“Molecular Cloning and Localization of the HumanGaxGene to 7p21” by LePage, et al.,Genomics, 24, 1994, pp. 535-540.
“Amino acid sequence of Mox-2 and comparison to isXenopusand rat homologs” by Candia, et al.,Nucleic Acids Research, vol. 21, No. 21, 1993 p. 4982.
New Embl Database, Accession No.: 217223 rat Gax cDNA (2244 base pairs) submitted by Kenneth Walsh, Feb. 28, 1993.
Sequence for Mox-1 (2182 base pairs) (mistakenly designated “Mox-2”) submitted by A.F. Candia to New GenBank Accession No. 215103 and Sep. 25, 1992.
GenBank Database, Accession No.: 216406 mouse Mox-2A submitted by A.F. Candia to GenBank and created on Oct. 5, 1992.
Mouse Mox-2 sequence on Mar. 6, 1993 GenBank Database, Accession No.: 216406.

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