Table 1 lists the sequences in the Sequence Listing. Each is identified by a Five Prime Identification (FP ID) number, a SEQ ID NO. corresponding to the nucleotide coding sequence (SEQ ID NO. (N1)), a SEQ ID NO. corresponding to the encoded polypeptide sequence (SEQ ID NO. (P1)), and a SEQ ID NO. corresponding to the entire nucleotide sequence (SEQ ID NO. (N0)). Each is also identified by its public National Center for Information Biotechnology (NCBI) protein identification number (Protein ID).
Table 2 provides an annotated list of the sequences of the invention. Each sequence is identified by its FP ID and its NCBI protein identification number (Protein ID). An annotation is provided for each protein sequence, listing information about the protein and listing reference numbers through which more information about the protein can be obtained through the NCBI.
Table 3 provides information characteristic of each polypeptide. The polypeptides are identified by their FP ID. Each is classified according to its function, e.g., HG1014563 is a single transmembrane type 1 membrane protein (Classification). The length of the polypeptide is provided as the number of amino acid residues (Predicted Protein Length). Table 3 also specifies the result of an algorithm that predicts whether a sequence is secreted (TreeVote). This algorithm is constructed on the basis of a number of attributes that include hydrophobicity, two-dimensional structure, prediction of signal sequence cleavage site, and other parameters. This algorithm predicts whether the sequences listed in Table 3 are secreted as indicated in the classification column; a higher TreeVote indicates that the polypeptide is more likely to be secreted. The signal peptide coordinates (Signal Peptide Coords) are listed in terms of the amino acid residues beginning with “1” at the N-terminus of the polypeptide. The Mature Protein Coords refer to the coordinates of the amino acid residues of the mature polypeptide after cleavage of the signal peptide. Table 3 also specifies the coordinates of an alternative form of the mature protein (Alternate Mature Protein Coords). In instances where the mature protein start residue overlaps the signal peptide end residue, some of the amino acid residues may be cleaved off such that the mature protein does not start at the next amino acid residue from the signal peptides, resulting in the alternative mature protein coordinates. Finally, Table 3 provides the coordinates of the transmembrane and non-transmembrane sequences of the polypeptides. The transmembrane coordinates (TM Coords) refer to the transmembrane and are listed in terms of the amino acid residues beginning with “1” at the N-terminus of the polypeptide. The non-transmembrane coordinates (non-TM Coords) refer to the amino acids that are not transmembrane; these can include extracellular, cytoplasmic, and luminal sequences, and are listed in terms of the amino acid residues beginning with “1” at the N-terminus of the polypeptide.
Table 4 lists the coordinates of the Pfam domains of the polypeptides of the invention. Each is identified by a Five Prime Identification (FP ID) number, and the public NCBI protein identification number (Protein ID). The Pfam domains of those polypeptides that have at least one Pfam domain are listed (Pfam) and the Pfam coordinates are listed in terms of amino residues beginning with “1” at the N-terminus of the polypeptide, beginning at the beginning of the open reading frame.
The invention provides polynucleotides and polypeptides, listed in the Sequence Listing and Tables. These polypeptides and polynucleotides have novel functions, and provide methods of diagnosis, treatment, and prophylaxis for immune disorders and cancer, including cancers of the lung, bladder, prostate, breast, liver, pancreas, kidney, ovary, cervix, skin, bone, brain, and gastrointestinal tract, such as esophagus, stomach, colon, and rectum, as well as soft tissue sarcomas, leukemias, and lymphomas. Some of these polypeptides comprise regions that correspond to pfam domains. The regions of the polypeptides that correspond to a particular pfam domain can exhibit variations among polypeptides. For example, fibroblast growth factor receptors of the invention comprise epidermal growth factor (EGF) domains, which have variable polypeptide sequences and are encoded by variable nucleotide sequences.
The invention provides an isolated polynucleotide encoding a polypeptide or an isolated polypeptide encoded by the polynucleotide, wherein the polypeptide consists essentially of an amino acid sequence selected from among “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. The amino acid sequence can be a sequence of at least 6 contiguous amino acid residues.
The invention also provides a method of making the polypeptides comprising providing a nucleic acid molecule that comprises a polynucleotide sequence that encodes the polypeptide, introducing the nucleic acid molecule into an expression system, and allowing expression of the polypeptide. The expression system can be a cell-free system, such as wheat germ extract, a rabbit reticulocyte, or a frog oocyte expression system. It can also be a bacterial expression system, a yeast expression system, an insect cell expression system, or a mammalian cell expression system.
The invention provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier or excipient and the isolated polypeptide or isolated polynucleotide selected from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. The composition can comprise a phosphatidic acid phosphatase 2C polypeptide.
The invention also provides an isolated antibody specifically recognizing, binding to, and/or modulating the biological activity of at least one polypeptide or polynucleotide selected from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. The antibody can recognizing, bind to, and/or modulate the biological activity of phosphatidic acid phosphatase type 2 or variants thereof. The invention provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and such an antibody.
The antibody can be a monoclonal antibody, a polyclonal antibody, a single chain antibody, an antibody comprising a backbone of a molecule with an Ig domain or a TCR backbone, a targeting antibody, a neutralizing antibody, a stabilizing antibody, an enhancing antibody, an antibody agonist, an antibody antagonist, an antibody that promotes endocytosis of a target antigen, a cytotoxic antibody, an antibody that mediates ADCC, a human antibody, a non-human primate antibody, a non-primate animal antibody, a rabbit antibody, a mouse antibody, a rat antibody, a sheep antibody, a goat antibody, a horse antibody, a porcine antibody, a cow antibody, a chicken antibody, a humanized antibody, a primatized antibody, a chimeric antibody, an antigen binding fragment, a fragment comprising a variable region of a heavy chain or a light chain of an immunoglobulin, a fragment comprising a complementarity determining region or a framework region of an immunoglobulin, or other active fragments thereof, analogues thereof, and antagonists thereto. The antibody can comprise an antigen binding fragment of an immunoglobulin.
This antibody can be produced in a plant, an animal or in a cell. The cell can be a bacterial cell, a fungal cell, a plant cell, an insect cell, or a mammalian cell. The cell can also be a yeast cell, an Aspergillus cell, an SF9 cell, a High Five cell, a cereal plant cell, a tobacco cell, a tomato cell, or a CHO cell.
The antibody can comprise one or more cytotoxic component chosen from a radioisotope, a microbial toxin, a plant toxin, and a chemical compound. The antibody can function to specifically inhibit the binding of the polypeptide to a ligand, specifically inhibit the binding of the polypeptide to a substrate, specifically inhibit the binding of the polypeptide as a ligand specifically inhibit the binding of the polypeptide as a substrate, induce apoptosis, or induce ADCC or CDC.
The antibody can recognize, bind to, and/or modulate the biological activity of collagen type11 alpha1, carboxypeptidase D precursor, F-receptor linked protein tyrosine phosphatase, chromosome 1 open reading frame 9, ortholog of mouse plexin 3, KIAA0466, or beta-1,4-galactosyltransferase.
The antibody can specifically bind to or interfere with the activity of a polypeptide or a ligand of the polypeptide. It can be directed to a polypeptide sequence of at least 6, at least 8, at least 10, at least 12, at least 14, at least 16, at least 18, at least 20, or at least 22 contiguous amino acid residues chosen from the Sequence Listing and/or Tables. These contiguous residues can correspond to one or more extracellular domain of a polypeptide, or fragment thereof, analogue thereof, and/or antagonist thereto. These residues can correspond to a pfam domain. The antibody may recognize one or more antigenic epitope. It may specifically recognize one variant of the pfam domain, or more than one variant.
In another aspect, the invention provides a method for making an antibody by introducing a polypeptide; polynucleotide encoding the polypeptide, or a biologically active fragment thereof, into an animal in sufficient amount to elicit generation of antibodies specific to the polypeptide, wherein the polypeptide is described in the Sequence Listing or Tables, and recovering the antibodies. This method may further entail isolating a spleen from the animal injected with the polypeptide or polynucleotide or a fragment thereof, and recovering the antibodies from the spleen cells. It may also further entail making a hybridoma using spleen cells and selecting a hybridoma that secretes the antibodies. The invention provides making a polynucleotide library from the spleen cells, selecting a cDNA clone that produces the antibodies, and expressing the cDNA clone in an expression system to produce antibodies or fragments thereof. The cDNA clone, or a fragment thereof, can be introduced into an expression system to produce the antibody. This expression system can be an in vitro system, such as a cell-free system, a bacterial cell expression system, a yeast expression system, or a mammalian sell expression system.
The antibody can be produced either in vivo or in vitro, and can be produced by either a prokaryote or a eukaryote, such as a bacterial cell, a fungal cell, a plant cell, an insect cell, and a mammalian cell. Examples of suitable cells include yeast cells, Aspergillus cells, SF9 cells, High Five cells, CHO cells, cereal plant cells, tobacco cells, and tomato cells. The antibody can be isolated.
The antibody can function to specifically inhibit the binding of the polypeptide to a ligand, specifically inhibit the binding of the polypeptide to a substrate, specifically inhibit the binding of the polypeptide as a ligand, and/or specifically inhibit the binding of the polypeptide as a substrate.
The invention provides a host cell that produces an antibody that can recognize, bind to, and/or modulate the biological activity of from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. It also provides a bacteriophage, wherein such an antibody, or a fragment thereof, is displayed on the bacteriophage. The antibody may be displayed on the surface of the bacteriophage. The invention also provides a bacterial cell comprising the bacteriophage. It further provides a host cell that secretes an antibody of the invention.
The invention also provides a non-human animal injected with the polypeptide or polynucleotide from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing.
The invention further provides a method for determining the presence of a polypeptide specifically binding to an antibody in a sample by allowing the antibody as described above to interact with the sample; and determining whether interaction between the antibody and the polypeptide has occurred.
The invention provides a method for determining the presence of an antibody specifically binding to a polypeptide or a polynucleotide in a sample by allowing the polypeptide or polynucleotide from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. to interact with the sample; and determining whether interaction between the antibody and the polypeptide or polynucleotide has occurred.
The invention provides a method for modulating the biological activity of a first human or non-human animal host cell by providing an antibody as described above and contacting the antibody with a first host cell, wherein the activity of the first host cell, or a second host cell, is modulated. The modulation of biological activity can be chosen from enhancing cell activity directly, enhancing cell activity indirectly, inhibiting cell activity directly, inhibiting cell activity indirectly, inducing apoptosis, inducing ADCC, and inducing CDC. The cell activity that is modulated can be signal transduction, transcription, and/or translation. This modulation can result in cell death and/or inhibition of cell growth. Contacting the antibody with a first host cell can result in recruitment of at least one second host cell. The first host cell can be a cancer cell. The first or second host cell can be a T cell, B cell, NK cell, dendritic cell, macrophage, muscle cell, stem cell, skin cell, fat cell, blood cell, brain cell, bone marrow cell, endothelial cell, retinal cell, bone cell, kidney cell, pancreatic cell, liver cell, spleen cell, prostate cell, cervical cell, ovarian cell, breast cell, lung cell, soft tissue cell, colorectal cell, or a cell of the gastrointestinal tract.
In a further aspect, the invention provides a method for modulating biological activity by providing an antibody, such as one described above, and contacting this antibody with a first human or non-human host cell, thereby modulating the activity of a first human or non-human animal host cell, or a second host cell. Modulators also take the form of small molecule modulators. The modulation of biological activity can take the form of enhancing cell activity directly, enhancing cell activity indirectly, inhibiting cell activity directly, and/or inhibiting cell activity indirectly. It can also take the form of modulating signal transduction, transcription, and/or translation. Modulation can result in cell growth, inhibition of cell growth and/or cell death.
One way this modulation can occur is by contacting the antibody with a first human or non-human host cell to result in the recruitment of the second host cell. The first host cell can, for example, be a cancer cell. Either the first or second host cell can be a T cell, B cell; NK cell, dendritic cell, macrophage, muscle cell, stem cell, skin cell, fat cell, blood cell, brain cell, bone marrow cell, endothelial cell, retinal cell, bone cell, kidney cell, pancreatic cell, liver cell, spleen cell, prostate cell, cervical cell, ovarian cell, breast cell, lung cell, liver cell, soft tissue cell, colorectal cell; or gastrointestinal tract cell.
The invention provides a method for screening for a modulator of polypeptide activity by providing a composition comprising a polypeptide or an active fragment thereof, wherein the polypeptide is chosen from the Sequence Listing or Table 1, allowing at least one modulator to contact the polypeptide, and selecting a modulator that binds to the polypeptide or interferes with the activity of the polypeptide. The polypeptide can be expressed on a cell surface. It can be an antibody. A modulator selected in this manner can be present in a composition with a pharmaceutically acceptable carrier.
The invention provides a method for identifying a modulator that modulates the biological activity of a polypeptide comprising providing at least one polypeptide chosen from among Table 1, the Pfam Coords in Table 4, the non-TM Coords in Table 3, and active fragments thereof by allowing at least one agent to contact the polypeptide; and selecting an agent that binds the polypeptide or affects the biological activity of the polypeptide. The polypeptide can be phosphatidic acid phosphatase type 2C. The polypeptide can also be collagen type11 alpha1, carboxypeptidase D precursor, F-receptor linked protein tyrosine phosphatase, chromosome 1 open reading frame 9, ortholog of mouse plexin 3, KIAA0466, or beta-1,4-galactosyltransferase. The modulator can be an antibody, a small molecule drug, a soluble receptor, or an extracellular fragment of the polypeptide.
The invention provides a modulator composition comprising a modulator and a pharmaceutically acceptable carrier, wherein the modulator is chosen from among one obtainable by the methods and antibodies described above a soluble receptor that competes for ligand binding to the polypeptide of claim 1 an extracellular fragment that competes for ligand binding to the polypeptide of claim 1, a RNAi molecule, an anti-sense molecule, or a ribozyme that inhibits the transcription or translation of the polynucleotide.
In yet a further aspect, the invention provides a method for diagnosing a proliferative disease such as cancer, psoriasis, and ulcerative colitis, or an immune or inflammatory disease such as rheumatoid arthritis, osteoarthritis, psoriasis, inflammatory bowel disease, and multiple sclerosis, by providing an antibody, allowing the antibody to contact a patient sample, and detecting specific binding between the antibody and an antigen in the sample to determine whether the subject has proliferative disease such as cancer. The invention also provides a method for diagnosing a proliferative disease, by providing a polypeptide that specifically binds the antibody, allowing the polypeptide to contact a patient sample and detecting specific binding between the polypeptide and any interacting molecule in the sample to determine whether the subject has a proliferative disease.
The invention provides a method for diagnosing cancer in a patient by providing an antibody described above, and allowing it to contact a patient sample, and detecting specific binding between the antibody and an antigen in the sample to determine whether the subject has cancer.
The invention also provides a method for diagnosing cancer in a patient by providing a method for diagnosing cancer in a patient, by providing a polypeptide that specifically binds an antibody as described above, allowing the polypeptide to contact a patient sample; and detecting specific binding between the polypeptide and any interacting molecule in the sample to determine whether the subject has cancer.
The invention provides a kit comprising a pharmaceutical composition comprising a pharmaceutically acceptable carrier, an antibody as described above, and instructions for administration into a human or non-human animal.
The invention provides a method for treating uncontrolled proliferative growth in a subject comprising administering a composition comprising an isolated antibody that specifically recognizes, binds to, and/or modulates the biological activity of at least one polypeptide or polynucleotide selected from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing.
The invention provides a method for treating uncontrolled proliferative growth in a subject comprising administering a modulator to a subject, wherein the modulator binds to or interferes with the activity of at least one polypeptide or polynucleotide selected from the Tables, the “non-TM Coords” in Table 3, “Pfam Coords” in Table 4, or the Sequence Listing. The polypeptide can be phosphatidic acid phosphatase type 2C or COL11A1. The uncontrolled proliferative growth can be a tumor or psoriasis. The tumor can be a lung tumor, a colon tumor, a bladder tumor, a liver tumor, an ovarian tumor, a breast tumor, a kidney tumor, or a pancreatic tumor. The composition can administered, for example, orally, parenterally, by implantation, by inhalation, intranasally, intravenously, intra-arterially, intracardiacally, subcutaneously, intraperitoneally, transdermally, intraventricularly, intracranially, and intrathecally.
The invention yet also provides a method of treating a proliferative disease by providing an antibody composition that comprises a first antibody or fragment thereof that specifically binds to a first epitope of a first polypeptide or a biologically active fragment thereof, wherein the first polypeptide is encoded by a polynucleotide sequence or polypeptide sequence found in Table 1 and/or the Sequence Listing, and administering the antibody composition to a subject in need of such treatment. The antibody composition can further comprise a second antibody that binds specifically to or interferes with the activity of a second epitope of the first polypeptide or to a first epitope of a second polypeptide. The second polypeptide can be chosen from the Sequence Listing and/or Tables.
The invention provides therapeutic agent screening, such as small molecule drug screening; therapeutic applications, such as in the treatment of a variety of diseases and conditions, including, e.g., cancer, proliferative disorders, immune disorders, inflammatory disorders, and other metabolic disorders.
The invention further provides a kit comprising an antibody as described above, and instructions for its use.
The invention yet further provides method of gene therapy, comprising providing a polynucleotide comprising a nucleic acid molecule encoding the antibody, of claim 1, and administering the polynucleotide to a subject in need of such treatment.
The invention provides a method for prophylactically or therapeutically treating a subject by providing a vaccine and administering the vaccine to the subject; wherein the vaccine comprises a polynucleotide or a polypeptide found in the Sequence Listing or Tables, or a fragment thereof, an analogue thereof, or an antagonist thereto. The vaccine can be a cancer vaccine, and the polypeptide can be a cancer antigen. Therapeutic vaccines can be in the form of nucleic acid or polypeptide vaccines, and can be administered alone, such as naked DNA, or can be facilitated, such as via the use of a viral vector, microsomes, or liposomes.
The invention also provides a method of inhibiting transcription or translation of a first polynucleotide encoding a first polypeptide by providing a second polynucleotide that hybridizes to the first polynucleotide, wherein the first polynucleotide comprises a polynucleotide sequence chosen from a polynucleotide or a polypeptide found in the Sequence Listing or Tables, or a fragment thereof, an analogue thereof, or an antagonist thereto, and allowing the first polynucleotide to contact the second polynucleotide. The second polynucleotide can comprise an antisense molecule, a ribozyme, and/or an interfering RNA (iRNA) molecule.
The invention yet also provides a method of treating a proliferative disorder by administering a modulator to a subject in need of such treatment, wherein the modulator binds to a cell surface molecule that is overexpressed in the disorder. The modulator can be an antibody, for example, one that is capable of initiating ADCC.
The invention provides a method of treating a lung tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, binds to, or modulate the biological activity of a polypeptide, and the polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a breast tumor in a subject by providing the modulator composition as described above and administering the modulator composition to the subject. This modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of a polypeptide, and the polypeptide can be PAP2C or COL11A1
The invention provides a method of treating a colon tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a liver tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating an ovarian tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a pancreatic tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a kidney tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a stomach tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating a tumor in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
The invention provides a method of treating an immune disorder in a subject by providing a modulator composition as described above and administering the modulator composition to the subject. The modulator can be an antibody. The antibody can specifically recognize, bind to, or modulate the biological activity of the polypeptide. The polypeptide can be PAP2C or COL11A1.
Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.
The examples, which are intended to be purely exemplary of the invention and should therefore not be considered to limit the invention in any way, also describe and detail aspects and embodiments of the invention discussed above, The examples are not intended to represent that the experiments below are all or the only experiments performed. Efforts have been made to ensure accuracy with respect to numbers used (e.g. amounts, temperature, etc.) but some experimental errors and deviations should be accounted for. Unless indicated otherwise, parts are parts by weight, molecular weight is weight average molecular weight, temperature is in degrees Centigrade, and pressure is at or near atmospheric.
While the present invention has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the invention. In addition, many modifications can be made to adapt a particular situation, material, composition of matter, process, process step or steps, to the objective, spirit and scope of the present invention. All such modifications are intended to be within the scope of the claims appended hereto.
PAP2C can be expressed in vitro in a cell free expression system, using wheat germ lysate or E. coli lysate. Alternatively, PAP2C can be expressed in a baculovirus system (Doerfler, W., Bohm, P., eds. 1987; Luckow, V. and Summers, M. 1988). The expressed protein can be substantially purified (Deutscher, M. P., et al., eds. 1990) and used for injection into mice for production of antibodies. The mice can be normal mice, in which case, the resulting monoclonal antibodies can be made in accordance to conventional techniques, but will be humanized for use in the treatment of humans. The expressed protein can also be used for injection into XenoMouse or other similar mice owned by Abgenix, Inc. (Fremont, Calif., USA), Medarex, Inc. (Princeton, N.J., USA) or Kirin (Japan), which are capable of producing human antibodies.
The expressed protein can also be used to screen for binding with Fab fragments of antibodies displayed on bacteriophages, using phage display libraries, such as is available from Cambridge Antibody Technology (Cambridge, U.K.), MorphoSys (Martinsried/Munich, Germany) or Dyax Corp. (Cambridge, Mass., USA). The Fab fragments that bind the PAP2C polypeptide with high affinity can be validated by immunohistochemistry as binding to tumor tissues. The desired Fab fragment can fused to an appropriate Fc fragment to make a synthetic antibody.
The compositions and methods of the invention are useful in the diagnosis, treatment, or prevention of proliferative and immune disorders.
The specification is most thoroughly understood in light of the following references, all of which are hereby incorporated in their entireties. The disclosures of the patents and other references cited above are also hereby incorporated by reference.
A sequence listing transmittal sheet and a sequence listing in paper format accompanies this application.
sapiens]
sapiens]
perfringens enterotoxin receptor 1 [Homo sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
sapiens]
This application is related to U.S. application Ser. No. 60/444,944, “Methods of Use of Human Lung-Expressed Polypeptides Encoded by Polynucleotides and Antibodies Thereto,” filed Jan. 31, 2003; U.S. application Ser. No. 60/444,913, “Methods of Use of Human Lung-Expressed Polypeptides Encoded by Polynucleotides and Antibodies Thereto,” filed Feb. 3, 2003; U.S. application Ser. No. 60/446,647, “Methods of Use of Human Lung-Expressed Polypeptides Encoded by Polynucleotides and Antibodies Thereto,” filed Feb. 10, 2003; and U.S. application Ser. No. 60/448,837, “Methods of Use of Human Lung-Expressed Polypeptides Encoded by Polynucleotides and Antibodies Thereto,” filed Feb. 18, 2003, the contents of all of which are incorporated herein by reference in their entirety.
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/US04/02655 | 1/30/2004 | WO | 00 | 2/23/2007 |
Number | Date | Country | |
---|---|---|---|
60443944 | Jan 2003 | US | |
60444913 | Feb 2003 | US | |
60446647 | Feb 2003 | US | |
60448837 | Feb 2003 | US |