Biological material pre-fixation treatment |
| OF PREFERRED EMBODIMENTS In one aspect, the present invention relates to an improved bioprosthetic ... |
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Diagnosis of Williams syndrome |
| OF THE INVENTION The present invention is directed to the determination that SVAS and Williams ... |
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Biological material pre-fixation treatment |
| OF PREFERRED EMBODIMENTS In one aspect, the present invention relates to an improved bioprosthetic ... |
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Method for bonding or fusion of biological tissue and material |
| Biological materials are joined, repaired or fused by heating the material in proximity to a ... |
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Diagnosis and treatment of supravalvular aortic stenosis and Williams syndrome |
| OF THE INVENTION The present invention is directed to the determination that SVAS and Williams ... |
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Biological material pre-fixation treatment |
| OF PREFERRED EMBODIMENTS In one aspect, the present invention relates to an improved bioprosthetic ... |
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Matrix substrate for a viable body tissue-derived prosthesis and method for making the same |
| OF THE INVENTION The present invention covers a process that thoroughly removes intact cells from ... |
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Barrier webs having bioactive surfaces |
| What is claimed is: 1. A bioactive substrate comprising: a support; and a bioactive surface thereon,... |
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Biopolymer foams for use in tissue repair and reconstruction |
| OF THE INVENTION The present invention features biopolymer foams, composite biopolymer foams, ... |
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Periodate oxidative method for attachment of biomolecules to medical device surfaces |
| OF THE INVENTION As used in the specification and claims hereof, the following terms have the ... |
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Interleukin-1 beta converting enzyme like apoptotic protease-6
| Details |
Inventors: Dixit, Vishva M.; He, Wei-Wu; Kikly, Kristine K.; Ruben, Steven M.;
Assignee: Human Genome Sciences, Inc. (Rockville, MD); SmithKline Beecham Corporation (Philadelphia, PA); University of Michigan (Ann Arbor, MI)
Primary Examiner: Low; Christopher S. F.
Assistant Examiner: Bugaisky; Gabriele E.
Attorney, Agent or Firm: Human Genome Sciences, Inc.
Human ICE LAP-6 polypeptides and DNA (RNA) encoding such ICE LAP-6 and a procedure for producing such polypeptides by recombinant techniques is disclosed. Also disclosed are methods for utilizing such ICE LAP-6 for the treatment of a susceptibility to viral infection, tumorogenesis and to diseases and defects in the control embryogenesis and tissue homeostasis, and the nucleic acid sequences described above may be employed in an assay for ascertaining such susceptibility. Antagonists against such ICE LAP-6 and their use as a therapeutic to treat Alzheimer's disease, Parkinson's disease, rheumatoid arthritis, septic shock, sepsis, stroke, chronic inflammation, acute inflammation, CNS inflammation, osteoporosis, ischemia reperfusion injury, cell death associated with cardiovascular disease, polycystic kidney disease, apoptosis of endothelial cells in cardiovascular disease, degenerative liver disease, MS, ALS, cererbellar degeneration, ischemic injury, myocardial infarction, AIDS, myelodysplastic syndromes, aplastic anemia, male pattern baldness, and head injury damage are also disclosed. Also disclosed are diagnostic assays for detecting diseases related to mutations in the nucleic acid sequences and altered concentrations of the polypeptides. Also disclosed are diagnostic assays for detecting mutations in the polynucleotides encoding the interleukin-1 beta converting enzyme apoptosis proteases and for detecting altered levels of the polypeptide in a host. |
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DETAILED DESCRIPTION Toward these ends, and others, it is an object of the present invention to provide polypeptides, inter alia, that have been identified as novel ICE LAP-6 by homology between the amino acid sequence set out in FIG. 1 or the polypeptide encoded by the deposited clone and known amino acid sequences of other proteins such as those sequences set out in FIG. 2. , It is a further object of the invention, moreover, to provide polynucleotides that encode ICE LAP-6, particularly polynucleotides that encode the polypeptide herein designated ICE LAP-6 and the polynucleotide of the deposited clone. In a particular preferred embodiment of this aspect of the invention the polynucleotide comprises the region encoding human ICE LAP-6 set forth in FIGS. 2A, 2B and 2C. In accordance with this aspect of the present invention there is provided an isolated nucleic acid molecule encoding a mature polypeptide expressed by the human cDNA in FIGS. 2A, 2B and 2C or derived using the primers set forth in Example 1, or a polynucleotide encoding the polypeptide in FIG. 1 or derived from the polypeptide encoded by the deposited clone. In accordance with this aspect of the invention there are provided isolated nucleic acid molecules encoding human ICE LAP-6, including mRNAs, cDNAs, genomic DNAs and, in further embodiments of this aspect of the invention, biologically, diagnostically, clinically or therapeutically useful variants, analogs or derivatives thereof, or fragments thereof, including fragments of the variants, analogs and derivatives. Among the particularly preferred embodiments of this aspect of the invention are naturally occurring allelic variants of human ICE LAP-6. It also is an object of the invention to provide ICE LAP-6 polypeptides, particularly human ICE LAP-6 polypeptides, that may be employed for therapeutic purposes, for example, to treat viral infection, as an anti-tumor agent and to control embryonic development and tissue homeostasis. In accordance with this aspect of the invention there are provided novel polypeptides of human origin referred to herein as ICE LAP-6 as well as biologically, diagnostically or therapeutically useful fragments, variants and derivatives thereof, variants and derivatives of the fragments, and analogs of the foregoing
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