Chemistry: natural resins or derivatives; peptides or proteins; – Proteins – i.e. – more than 100 amino acid residues
Reexamination Certificate
2007-09-18
2007-09-18
Kam, Chih-Min (Department: 1656)
Chemistry: natural resins or derivatives; peptides or proteins;
Proteins, i.e., more than 100 amino acid residues
C435S069100, C435S325000, C435S252300, C435S320100, C435S006120, C536S023100
Reexamination Certificate
active
10643836
ABSTRACT:
The invention concerns GENSET polynucleotides and polypeptides. Such GENSET products may be used as reagents in forensic analyses, as chromosome markers, as tissue/cell/organelle-specific markers, in the production of expression vectors. In addition, they may be used in screening and diagnosis assays for abnormal GENSET expression and/or biological activity and for screening compounds that may be used in the treatment of GENSET-related disorders.
REFERENCES:
patent: 4914025 (1990-04-01), Manoil et al.
patent: 5019369 (1991-05-01), Presant et al.
patent: 5536637 (1996-07-01), Jacobs
patent: 5872141 (1999-02-01), Umbriet et al.
patent: 6034062 (2000-03-01), Thies et al.
patent: 6110490 (2000-08-01), Theirry
patent: 6204060 (2001-03-01), Mehtali et al.
patent: 6242179 (2001-06-01), Shah et al.
patent: 1130094 (2000-07-01), None
patent: H7-7182 (1999-01-01), None
patent: WO97/18826 (1995-07-01), None
patent: WO97/04097 (1997-02-01), None
patent: WO97/07198 (1997-02-01), None
patent: WO98/55614 (1998-12-01), None
Kedra et al., Human Genetics 103, 131-141 (1998).
Bougueleret, L. et al. “Extended cDNAs Useful for Expressing Secreted Proteins and to Obtain Specific Antibodies”, 2000, pp. 203-204, Accession No. AAY59685.
Cameron, C. et al. “Function and Protective Capacity ofTreponema pallidumSubsp.PallidumGlycerophosphodiester Phosphodiesterase”,Infection and Immunity, 1998, pp. 5763-5770, vol. 66, No. 12, American Society for Microbiology.
Downes, G. et al. “Structure and Mapping of the G Proteiny3 Subunit Gene and a Divergently Transcribed Novel Gene”,Gng31g, Genomics, 1998, pp. 220-230, vol. 53, Academic Press.
Inoue, S. et al. “Growth Suppression ofEscherichia coliby Induction of Expression of Mammalian Genes with Transmembrane or ATPase Domains”,Biochem. Biosphys. Reas. Comm., 2000, pp. 553-561, vol. 268, Academic Press.
Janson, H. et al. “Protein D, the Glycerophosphodiester Phosphodiesterase fromHaemophilus influenzaewith Affinity for Human Immunoglobulin D, Influences Virulence in a Rat Otitis Model”,Infection and Immunity, 1994, pp. 4848-4854, vol. 62, No. 11, American Society for Microbiology.
Larson, T. et al. “Periplasmic Glycerophosphodiester Phosphodiesterase ofEscherichia coli, a New Enzyme of theglpRegulon”,J. Biol. Chem., 1983, pp. 5428-5432, vol. 258, No. 9.
Magré, J. et al. “Identification Of The Gene Altered In Berardinelli-Seip Congenital Lipodystrophy On Chromosome 11q13”,Nature Genetics, 2001, pp. 365-370, vol. 28.
Meldrum, Brian “Glutamate as a Neurotransmitter in the Brain: Review of Physiology and Pathology”,The Journal of Nutrition—Supplement(presented at the International Symposium on Glutamate, 1998), 2000, pp. 1007S-1015S, Pub: American Society for Nutritional Sciences.
Munson, R. et al. “Protein D, a Putative Immunoglobulin D-Binding Protein Produced byHaemophilus influenzae, Is Glycerophosphodiester Phosphodiesterase”,J. Bacteriology, 1993, pp. 4569-4571, vol. 175, No. 14.
Neer, Eva “Heterotrimeric G Proteins: Organizers of Transmembrane Signals”,Cell, 1995, pp. 249-257, vol. 80, Cell Press.
Schoepp, D. et al. “Metabotropic Glutamate Receptors in Brain Function and Pathology”,TiPS, 1993, pp. 13-20, vol. 14, Elsevier Science Publishers, Ltd., UK.
Zheng, B. et al. “MIR16, a Putative Membrane Glycerophosphodiester Phosphodiesterase, Interacts with RGS16”,PNAS, 2000, pp. 3999-4004, vol. 97, No. 8.
Zheng, B. et al. “MIR16, a Putative Membrane Glycerophosphodiester Phosphodiesterase, Interacts with RGS16”,Proc. Natl. Acad. Sci. U.S.A., 2000, pp. 3999-4004, vol. 97, No. 8, Accession No. AAF65234 (bases 1 to 331).
Zheng, B. et al. “MIR16, a Putative Membrane Glycerophosphodiester Phosphodiesterase, interacts with RGS16”,Proc. Natl. Acad. Sci. U.S.A., 2000, pp. 3999-4004, vol. 97, No. 8, Accession No. AF212862 (bases 1 to 1200).
Glycerophosphoryl Diester PhosphodiesteraseEscherichia coli, 1989, NiceProt View of SWISS-PROT: P10908.
Glycerophosphoryl Diester Phosphodiesterase, periplasmic [Precursor]Escherichia coli, 1991, NiceProt View of SWISS-PROT: P09394.
Glycerophosphoryl Diester Phosphodiesterase [Precursor]Haemophilus influenzae, 1995, NiceProt View of SWISS-PROT: Q06282.
Similar to G Protein Gamma 3 Linked GeneHomo Sapiens, 2001, NiceProt View of SWISS-PROT: Q9BSQ0.
Hypothetical 43.1 kDa proteinMus musculus, 2000, NiceProt View of SWISS-PROT: Q9JMF1.
Bork, P. “Powers and Pitfalls in Sequence Analysis: The 70% Hurdle”,Genome Research, 2000, pp. 398-400, vol. 10.
Broun, P. et al., “Catalytic Plasticity of Fatty Acid Modification Enzymes Underlying Chemical Diversity of Plant Lipids”,Science, 1998, pp. 1315-1317, vol. 282.
Seffernick,J.L. et al., “Melamine Deaminase and Atrazine Chlorohydrolase: 98 Percent Identical but Functionally Different”,Journal of Bacteriology, 2001, pp. 2405-2410, vol. 183, No. 8, American Society for Microobiology.
Van De Loo, F. J. et al., “An Oleate 12-hydroxylase from Ricinus Communis L. is a Fatty Acyl Desaturase Homolog”,Proc. Natl. Acad. Sci. USA, 1995, pp. 6743-6747, vol. 92.
Witkowski, A. et al., “Conversion of β-Ketoacyl Synthase to a Malonyl Decarboxylase by Replacement of the Active-Site Cysteine with Glutamine”,Biochemistry, 1999, pp. 11643-11650, vol. 38.
Attwood, T. “Genomics: The Babel of Bioinformatics”,Science, 2000, pp. 471-473, vol. 290, No. 5491.
Ruben S.M. et al. “Human Secreted Protein Encoded by Gene 21”,Database Geneseq[online], Mar. 23, 2000, AC No. Y76144, XP002163702.
Ruben S.M. et al. “Human Secreted Protein Encoded by Gene 21”,Database Geneseq[online], Mar. 23, 2000, AC No. Z65270, XP002163703.
DATABASE EMBL[online], AC No. Al911546, Jul. 30, 1999, Natl. Cancer Inst., “ty73d05.x1 NCI—CGAP—Kid11Homo sapienscDNA Clone IMAGE: 2284713”, XP002163704.
DATABASE EMBL[online], AC No. Al361251, Jan. 7, 1999, Natl. Cancer Inst., “qy42e02.x1 NCI—CGAP—Bm23Homo sapienscDNA Clone IMAGE: 2014682”, XP002163705.
Jacobs, K.A. et al. “A Genetic Selection for Isolating cDNAs Encoding Secreted Proteins”,Gene, NL, Elsevier, Oct. 1987, pp. 289-296, vol. 198, Biomedical Press, Amsterdam, XP002045919.
Tashiro, K. et al. “Signal Sequence Trap: A Cloning Strategy for Secreted Proteins and Type I Membrane Proteins”,Science, Jul. 30, 1993, pp. 600-603, vol. 261, American Association for the Advancement of Science, XP000673204.
Lim, E.M. et al. “Identification of Mycobacterium Tuberculosis DNA Sequences Encoding Exported Proteins by Using phoA Gene Fusions”,Journal of Bacteriology, Jan. 1995, pp. 59-650021-9193/95, vol. 177, No. 1.
Miyake et al. “RP105, a Novel B Cell Surface Molecule Implicated in B Cell Activation, is a Member of the Leucine-Rich Repeat Protein Family”,The Journal of Immunology, pp. 3333-3340, The American Association of Immunologists, 0022-1767/95.
Jacobs et al. “A Novel Method for Isolating Eukaryotic cDNA Clones Encoding Secreted Proteins”,Dendritic Cells: Antigen Presenting Cells of T and B Lymphocytes, Mar. 10-16, 1995, C1-207.
Fujiwara, T. et al. “HUM309B01B Clontech Human Aorta PolyA+ mRNA (#6572)Homo sapienscDNA Clone GEN-309B01 5′, mRNA Sequence”, XP002032351, Accession No. D62634.
Marra, M. et al. “The WashU-HHMI Mouse EST Project”, XP002032348, Accession No. W08383.
Marra, M. et al. “The WashU-HHMI Mouse EST Project”, XP002032350, Accession No. W11170.
Marra, M. et al. “The WashU-HHMI Mouse EST Project”, XP002032349, Accession No. W17930.
Marra, M. et al. “The Wash U-HHMI Mouse EST Project”, XP002032347, Accession No. W67046.
Abraham, E., et al., “Phosphatidic Acid Signaling Mediates Lung Cytokine Expression and Lung Inflammatory Injury After Hemorrhage in Mice”,J. Exp. Me
Bougueleret Lydie
Dumas Milne Edwards Jean-Baptiste
Jobert Severin
Kam Chih-Min
Saliwanchik Lloyd & Saliwanchik
Serono Genetics Institute S.A.
LandOfFree
Full-length human cDNAs encoding potentially secreted proteins does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Full-length human cDNAs encoding potentially secreted proteins, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Full-length human cDNAs encoding potentially secreted proteins will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3749429