Genes differentially expressed in bipolar disorder and/or schizophrenia

Inbred corn line DE811ASR(BC5)

Non-invasive detection of fetal genetic traits

Complexity management of genomic DNA

USE OF HIGHLY PARALLEL SNP GENOTYPING FOR FETAL DIAGNOSIS

Novel Human Enzymes of the Metalloprotease Family

Methods and products for in vitro genotyping

CHR and POMC effects on animal growth

Methods for Predicting Therapeutic Response to Agents Acting on the Growth Hormone Receptor

PHYSIOGENOMIC METHOD FOR PREDICTING EFFECTS OF EXERCISE

Method for cancer detection and monitoring

Human DRG11-responsive axonal guidance and outgrowth of neurite (dragon) proteins and variants thereof

Proteins related to schizophrenia and uses thereof

Polymorphisms in ABCB1 associated with a lack of clinical response to medicaments

Autism Genes and Regulated Secretion

Methods and Nucleic Acids for Analyses of Colorectal Cell Proliferative Disorders

Ace genotype which correlates with improved success in sodium excretion in hypertensives with exercise

Method for producing nucleic acid probes

Defects in periaxin associated with myelinopathies

Nucleic acid molecules correlated with the Rhesus weak D phenotype

Genetic marker for prostate cancer

Polycystic xidney disease PKD2 gene and uses thereop

Means and methods for diagnosing and treating affective disorders

Method enabling the use of extracellular ribonucleic acid (RNA) extracted from plasma or serum to detect, monitor or evaluate cancer or premalignant conditions

Detection of extracellular tumor-associated nucleic acid in blood plasma or serum using nucleic acid amplification assay

Methods and compositions for predicting drug responses

Method of expressing human lysosomal protein in brain cells

Novel Muscle Growth Regulator

Genetic polymorphisms associated with Alzheimer's disease, methods of detection and uses thereof

LMNA gene and its involvement in Hutchinson-Gilford Progeria Syndrome (HGPS) and arteriosclerosis

ADH7 nucleic acids

Methods for tissue analysis

DIAGNOSIS OF FETAL ABNORMALITIES USING POLYMORPHISMS INCLUDING SHORT TANDEM REPEATS

Methods and compositions for predicting drug responses

Methods and compositions for predicting drug responses

Identification of Snps Associated with Hyperlipidemia, Dyslipidemia and Defective Carbohydrate Metabolism

ENA-78 Gene Polymorphisms and Protein Concentrations as Diagnostic and Prognostic Tools

Computational selection of probes for localizing chromosome breakpoints

NPH6 nucleic acids and proteins

Vitamin E supplementation for reducing cardiovascular events in individuals with DM and the Hp 2-2 genotype

Protein tyrosine phosphatase mutations in cancers

Genetic polymorphisms associated with body fat

SCREENING FOR DOWN SYNDROME

Method of diagnosis of a predisposition to develop thrombotic disease and its uses

TRPC6 involved in glomerulonephritis

Fluid flow meter body with high immunity to inlet/outlet flow disturbances

Method for detecting cancer and a method for suppressing cancer

Method and probe set for detecting cancer

Methods for the Detection of Ovarian Cancer

Method of haplotype-based genetic analysis for determining risk for developing insulin resistance, coronary artery disease and other phenotypes

Method for detecting and quantifying rare mutations/polymorphisms

Methods and applications of molecular beacon imaging for infectious disease and cancer detection

INTEGRATED MULTI-FORMAT AUDIO/VIDEO PRODUCTION SYSTEM

Markers for Salinity Tolerance in Wheat Plants and the Use Thereof in Breeding Programs

Human transferase family members and uses thereof

METHODS OF TREATING PSYCHOSIS AND SCHIZPHRENIA BASED ON POLYMORPHISMS IN THE CNTF GENE

METHOD AND NUCLEIC ACIDS FOR THE ANALYSIS OF ASTROCYTOMAS

Diagnosis of Fetal Abnormalities by Comparative Genomic Hybridization Analysis

IRF-5 HAPLOTYPES IN SYSTEMIC LUPUS ERYTHEMATOSUS

Chronic lymphocytic leukaemia

Prediction and prophylactic treatment of type 1 diabetes

Protein C And Endothelial Protein C Receptor Polymorphisms As Indicators Of Subject Outcome

Methods for genomic analysis

Cancer Detection Reagents And Uses In Pathology And Diagnostics And Cancer Cell Death

Tailored Treatment Suitable for Different Forms of Mastocytosis

Corn variety DE811ASR(BC5)

Method Of Evaluating Drug Sensitivity By Analyzing The Mu-Opioid Receptor Gene

IRON REGULATING PROTEIN-2 (IRP-2) AS A DIAGNOSTIC FOR NEURODEGENERATIVE DISEASE

Detecting fetal chromosomal abnormalities using tandem single nucleotide polymorphisms

BIOMARKER-OPTIMIZED ADHD TREATMENT

METHODS AND APPARATUS FOR GENOTYPING

Use Of A Genetic Modification In The Human Gnaq Gene For Predicting Risk Of Disease, The Course Of Disease, And Reaction To Treatments

Haplotype Markers And Methods Of Using The Same To Determine Response To Treatment

Method Of Adjudicating On Prostate Cancer

Polynucleotides and methods for making plants resistant to fungal pathogens

Method for detecting cancer and a method for suppressing cancer

Use of a Novel Polymorphism in the Hsgk1 Gene in the Diagnosis of Hypertonia an Use of the Sgk Gene Family in the Diagnosis and Therapy of the Long Qt Syndrome

Nucleic acid detection in pooled samples

Compositions and methods for detecting multidrug resistant strains of M. tuberculosis having mutations in genes of the mutT family

Method of Determining Gene Relating to Favorable Beef Taste and Texture

Polynucleotide

Compositions and Methods of Use for a Fibroblast Growth Factor

Nucleic acid molecules and other molecules associated with plants

Peptide nucleic acid probes for analysis of certain species

DIAGNOSIS OF TAMOXIFEN SENSITIVITY

Association of gene expression and psychiatric disoders

Method for conducting pharmacogenomics-based studies

Acetyl CoA Carboxylase Splice Variant and Uses Thereof

Method for Detecting the Risk of Cardiovascular Diseases Such as Acute Myocardial Infarction and Coronary Heart Disease By Analysing Defesin

Association of EDG5 polymorphism V286A with type II diabetes mellitus and venous thrombosis/pulmonary embolism and the use thereof

Gene methylation in cancer diagnosis

WARFARIN DOSAGE PREDICTION

Population scale HLA-typing and uses thereof

IDENTIFICATION OF MULTIPLE BIOLOGICAL (MICRO) ORGANISMS BY SPECIFIC AMPLIFICATION AND DETECTION OF THEIR NUCLEOTIDE SEQUENCES ON ARRAYS

Calpastatin markers for fertility and longevity

K-Ras Oligonucleotide Microarray and Method for Detecting K-Ras Mutations Employing the Same

Novel Target for Antiderpressant Therapy

Identifying a high oil phenotype in maize by detecting a marker locus genetically linked with a QTL6 region

Methods and compositions for genetic markers for autism

CYTOCHROME P450 GENETIC VARIATIONS

Association of Protein Polymorphisms With Coronary Heart Disease

Methods for Identifying Risk of Low Bmd and Treatments Thereof

Hormone Receptor Genes and Migraine Susceptibility

Detection of Human Papillomavirus

Genes and markers in type 2 diabetes and obesity

Biomarkers For The Prediction Of Drug-In Duced Diarrhea

Thrombomodulin (Thbd) Haplotypes Predict Outcome

Methods of diagnosing susceptibility to myocardial infarction and screening for an LTA4H haplotype

Nucleic acid molecules and other molecules associated with plants

Diagnosis and Prediction of Parkinson's Disease

Markers for prenatal diagnosis and monitoring

Polymorphisms in fatty acid binding protein 4 (''FABP4'') gene and their associations with carcass traits

Polymorphisms in the Epidermal Growth Factor Receptor Gene Promoter

Mutant sodium channel Na1.7 nucleic acid methods

Chromosome 5 Genetic Variants Related To Dyslexia

pDJA1, a cardiac specific gene, corresponding proteins, and uses thereof

Methods and compositions for producing vitamin K dependent proteins

Compositions and methods for viral resistance genes

Predicting and Diagnosing Patients With Autoimmune Disease

Methods for Genotyping

Mutational profiles in HIV-1 protease correlated with phenotypic drug resistance

Estimation method, human estrogen receptor alpha gene, genomic DNA, and diagnostic marker

Fluorogenic Nucleic Acid Probes Including Lna for Methods to Detect and/or Quantify Nucleic Acid Analytes

Methods of Generating Stem Cells and Embryonic Bodies Carrying Disease-Causing Mutations and Methods of Using same for Studying Genetic Disorders

Method of diagnosing breast cancer

Compositions related to the quantitative trait locus 6 (QTL6) in maize and methods of use

Single Nucleotide Polymorphisms as Prognostic Tool to Diagnose Adverse Drug Reactions (Adr) and Drug Efficacy

Dna Oligomer, Genetic Marker and Dna Oligomer Set for Prediction of Onset of Side-Effect from Radiation Therapy, and Method for Predicting Onset of Side-Effect

IL-1 gene cluster and associated inflammatory polymorphisms and haplotypes

Identification of Echinacea and its imposters using genetic variations

11q DELETION AS A MOLECULAR GENETIC MARKER IN BREAST CANCER

Method of judging risk for onset of drug-induced granulocytopenia

Animal genotyping method

Human hemojuvelin (HJV) or dragon-like 1 (DL-1) polypeptides and variants and uses thereof

Regulation of glucose and insulin levels by GnT-4 glycosyltransferase activity

DETECTION OF MUTATIONAL FREQUENCY AND RELATED METHODS

Markers for addiction

Dep2 and its uses in major depressive disorder and other related disorders

DEP2 and its uses in major depressive disorder and other related disorders

Method of determining genetic predisposition for deficiency in health functions using SNP analysis

KCNQ2 and KCNQ3—potassium channel genes which are mutated in benign familial neonatal convulsions (BFNC) and other epilepsies

Genetic polymorphisms in the corticotropin-releasing hormone (CRH) gene as markers for improving beef marbling score and/or subcutaneous fat depth

Genetic polymorphisms associated with Alzheimer's Disease, methods of detection and uses thereof

Diagnostic methods for pain sensitivity and chronicity and for tetrahydrobiopterin-related disorders

Compositions and Methods for Treating Mental Disorders

Identification of a novel gene underlying familial spastic paraplegia

COMPOSITIONS FOR USE IN IDENTIFICATION OF BACTERIA

Methods for detecting mutations in JAK2 nucleic acid

Genetic markers for obesity

Methods and Compositions for Autism Risk Assessment

Use Of Genetic Polymorphisms To Predict Drug-Induced Hepatotoxicity

Primers for Use in Detecting Beta-Lactamases

Individualized cancer therapy

Regulation of the serotonin reuptake transporter and disease

Compositions for use in identification of bacteria

Rapid and efficient capture of DNA from sample without using cell lysing reagent

GENETIC VARIANTS OF HUMAN INOSITOL POLYPHOSPHATE-4-PHOSPHATASE, TYPE I (INPP4A) USEFUL FOR PREDICTION AND THERAPY OF IMMUNOLOGICAL DISORDER

Methods for identification of alport syndrome

Methods for detecting polymorphisms using arms or rflp

Methods of identifying and isolating stem cells and cancer stem cells

COMPOSITIONS FOR USE IN IDENTIFICATION OF BACTERIA

Genetic test for the identification of dwarfism in cattle

Genetic markers for prognosis of antifolate treatment efficacy

Antigen Receptor Variable Region Typing

Method and Kit for Predicting Adverse Side Effects of Paclitaxel Therapy

Detection of Lethality Gene for Improved Fertility in Mammals

Hemojuvelin or dragon-like 2 (DL-2) polypeptides and variants and uses thereof

Methods and compositions for detecting polynucleotides

Fcgr3a Gebotype and Methods for Evaluating Treatment Response to Non-Depleting Antibodies

Predicting negative symptom change during drug treatment

Antibodies against SUMO4 polypeptides

Method of detecting expanded CAG repeat region in spinocerebellar ataxia-2 gene

Simplified QTL mapping approach for screening and mapping novel markers associated with beef marbling

Apolipoprotein E genotyping and accompanying internet-based health management system

Compositions for use in identification of bacteria

INTERACTION OF STRESSFUL LIFE EVENTS AND A SEROTONIN TRANSPORTER POLYMORPHISM IN THE PREDICTION OF EPISODES OF MAJOR DEPRESSION

System and method for detection of mutations in JAK2 polynucleotides

COMPOSITIONS FOR USE IN IDENTIFICATION OF BACTERIA

Identifying organisms by detecting intronic nucleic acid or encoded proteins

Association of PDE4D allelic variants with stroke

Novel mutations in hexosaminidase A

Methods for rapid identification and quantitation of nucleic acid variants

Method of Predicting a Benefit of Antioxidant Therapy for Prevention of Cardiovascular Disease in Hiperglycemic Patients

Human Autism Predisposition Gene Encoding a Transcription Factor and Uses Thereof

Human Obesity Susceptibility Gene and Uses Thereof

Method of determining the susceptibility of a subject to developing insulin-dependent diabetes

Novel genes and markers associated with high-density lipoprotein-cholesterol (HDL-C)

Polymorphisms in growth hormone receptor, ghrelin, leptin, neuropeptide Y, and uncoupling protein 2 genes and their associations with measures of performance and carcass merit in beef cattle

COMPETITIVE HYBRIDIZATION OF DNA PROBES AND METHOD OF USING THE SAME

Recurrent gene fusions in prostate cancer

Polymorphisms in the NOD2/CARD15 gene

Prenatal Diagnosis Using Cell-Free Fetal DNA in Amniotic Fluid

Methods And Compositions For The Prevention And Treatment Of Gentiourinary Disorders Including Pre-Term Labor And Leiomyomas

ribulose bisphosphate carboxylase activase promoter

Adrenergic Receptor SNP for Improved Milking Characteristics

Method for identifying altered vitamin D metabolism

Angiogenesis pathway gene polymorphisms for therapy selection

Promoter polymorphisms of the BLyS gene and use in diagnostic methods

Identifying susceptibility to cardiac hypertrophy

12 kb sequence immediately adjacent to and upstream of the AKT1 gene locus containing multiple genetic variations associated with changes in metabolic syndrome, and methods of use

Method for non-invasive prenatal diagnosis

Method for diagnosing renal diseases or predispositions

Methods of seed breeding using high throughput nondestructive seed sampling

CD38 as a prognostic indicator in B cell chronic lymphocytic leukemia

Genotyping result evaluation method and system

Non-invasive fetal genetic screening by digital analysis

Physiogenomic method for predicting statin injury to muscle and muscle side effects

Human single nucleotide polymorphisms associated with dose-dependent weight gain and methods of use thereof

Methods for diagnosing and treating kidney cancer

Single nucleotide polymorphisms predicting cardiovascular disease

Assay For Bipolar Affective Disorder

Methylated gene biomarkers for detecting cancer

Use of antibodies to the gamma 2 chain of laminin 5 to inhibit tumor growth and metastasis

Method Of Diagnosing Breast Cancer

Method of diagnosis of obesity

Hepoxilins and modulators of ichthyin for treatment skin disorders

Methods for predicting irinotecan toxicity

Identification of aging genes through large-scale analysis

Method for identification and monitoring of epigenetic modifications

PHYSIOGENOMIC METHOD FOR PREDICTING RESPONSE TO DIET

METHOD OF DETERMINING OUTCOME OF NON SMALL-CELL LUNG CANCER ACCORDING TO XRCC3 POLYMORPHISM

TAT-039 and methods of assessing and treating cancer

Cancer Therapy and Prevention Based on Modulation of Complement activity

Methods of assessing susceptibility to drug-induced thrombocytopenia

Methods and compositions for vitamin K epoxide reductase

Nucleic acid encoding an interleukin-9 receptor variant

Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)

Human MLR single nucleotide polymorphisms associated with dose-dependent congestive heart failure and methods of use thereof

Method of judging imflammatory disease by using single nucleotide polymorphism in galectin -2 gene

Use of single nucleotide polymorphism in the coding region of the porcine leptin receptor gene to enhance pork production

Follistatin gene as a genetic marker for reproductive and performance traits in pigs

Identification of a gene and mutation responsible for autosomal recessive congenital hydrocephalus

Lafora's disease gene

Genetic markers of food allergy

Method of promoting delivery of an antioxidant agent to a cell expression neuroligin

Kits and methods for assessing skin health

3714, 16742, 23546, and 13887 novel protein kinase molecules and uses therefor

METHODS OF DETERMINING RELATIVE GENETIC LIKELIHOODS OF AN INDIVIDUAL MATCHING A POPULATION

Identification

Alterations in the copy number of the SULT1A1 gene

Method for amplification of nucleic acids of low complexity

WDR36 Gene Alterations and Glaucoma

Use of deletion polymorphisms to predict, prevent, and manage histoincompatibility

Calpastatin (CAST) alleles

Method for conducting non-invasive early detection of colon cancer and/or of colon cancer precursor cells

Transgenic mouse expressing an APP 670/671 mutation

Compositions and methods for genetic analysis of polycystic kidney disease

Methods for Measuring Therapy Resistance

Markers for breast cancer

Nucleic acids and associated diagnostics

Juvenile hemochromatosis gene (hfe2a), expression products and uses thereof

Identification of polynucleotides and polypeptide for predicting activity of compounds that interact with protein tyrosine kinases and/or protein tyrosine kinase pathways

Methods and sequences to preferentially suppress expression of mutated huntingtin

Method for identifying progressive rod-cone degeneration in dogs

Profiling tumor specific markers for the diagnosis and treatment of neoplastic disease

Method for detecting cancer and a method for suppressing cancer

Method for detecting cancer and a method for suppressing cancer

Methods of diagnosis of androgen-dependent prostate cancer, prostate cancer undergoing androgen withdrawal, and androgen-independent prostate cancer

Cystic fibrosis transmembrane conductance regulator gene mutations

Single nucleotide polymorphisms in protein-tyrosine phosphatase receptor-type delta for the diagnosis of susceptibility to infection and asthma

Quantifying and profiling antibody and t cell receptor gene expression

Thrombosis diagnosis/prognosis method

Repertoire determination of a lymphocyte b population

Method of detecting mutations associated with thrombosis

Use of genetic polymorphisms that associate with efficacy of treatment of inflammatory disease

HUMAN OBESITY SUSCEPTIBILITY GENE AND USES THEREOF

Methods of diagnosis of ovarian cancer, compositions and methods of screening for modulators of ovarian cancer

Method for detecting cancer and a method for suppressing cancer

Method for detecting cancer and a method for suppressing cancer

2′-terminator related pyrophosphorolysis activated polymerization

Detection of mutations in a gene associated with resistance to viral infection, OAS1

C3-Convertase Inhibitors for the Prevention and Treatment of Age-Related Macular Degeneration in Patients With At Risk Variants Of Complement Factor H

Antibody to human enzymes of the metalloprotease family

LSAMP Gene Associated With Cardiovascular Disease

Method for detecting the risk of cancer, coronary heart disease, and stroke by analysing a catalase gene

Nucleic acid sequencing methods, kits and reagents

Treatment of Huntington's Disease with EPA

Method for detecting gene specifying allergic predisposition

Method of screening for drug hypersensitivity reaction

Nucleic acid molecules associated with the tocopherol pathway

Methods for testing for the development of Huntington's disease

Screening and Therapy for Lymphatic Disorders Involving the FLT4 Receptor Tyrosine Kinase (VEGFR-3)

Altered gene expression profiles in stable versus acute childhood asthma

Method and kit for detection of early cancer or pre-cancer using blood and body fluids

Method

Association of polymorphic kinase anchor proteins with cardiac phenotypes and related methods

Polymerase chain reaction assays for monitoring antiviral therapy and making therapeutic decisions in the treatment of acquired immunodeficiency syndrome

Usages of MTHFR gene polymorphisms in predicting homocysteine level, disease risk, and treatment effects and related methods and kit

Method and markers for determining the genotype of horned/polled cattle

METHODS AND COMPOSITIONS FOR DETERMINING WHETHER A SUBJECT CARRIES A GENE MUTATION ASSOCIATED WITH HEREDITARY HEARING LOSS

Diagnosis of systemic onset juvenile idiopathic arthritis through blood leukocyte microarray analysis

Alterations in the copy number of the SULT1A1 gene

Diagnosis method and kits for inherited neuropathies caused by duplication or deletion of chromosome 17p11.2-p12 region

Simultneous analytical method for oxidatively damaged guanine compound and concentration correcting substance thereof, and analyzer used for this analytical method

Human autism susceptibility gene and uses thereof

Identification of fetal DNA and fetal cell markers in maternal plasma or serum

Anti-p53 Antibodies

Methods for high throughput genotyping

Class I sequence based typing of HLA-A, -B, and -C alleles by direct DNA sequencing

Assessing response to anti-CD20 therapy by genotyping C1q components