BIOMARKERS FOR BISPHOSPHONATE-RESPONSIVE BONE DISORDERS

DIAGNOSIS AND TREATMENT OF DISEASES CAUSED BY MISFOLDED PROTEINS

Polymorphisms in genes affecting ace-related disorders and uses thereof

Compositions and methods for the detection of topoisomerase II complexes with DNA

METHODS FOR IDENTIFICATION AND PREDICTION OF MULTIPLE SCLEROSIS DISEASE AND THERAPY RESPONSE

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

METHODS AND AGENTS FOR EVALUATING INFLAMMATORY BOWEL DISEASE, AND TARGETS FOR TREATMENT

Novel Method of Diagnosing, Monitoring, and Staging Prostate Cancer

Compositions and methods for determining whether a subject would benefit from co-receptor inhibitor therapy

Method for diagnosis of glutamate dehydrogenase disorders

METHOD OF DETECTING OCULAR DISEASES AND PATHOLOGIC CONDITIONS AND TREATMENT OF SAME

Genetic variants as markers for use in diagnosis, prognosis and treatment of eosinophilia, asthma, and myocardial infarction

In vitro fertilization

IL1RL-1 as a cardiovascular disease marker and therapeutic target

METHODS AND SYSTEMS FOR GENETIC ANALYSIS OF FETAL NUCLEATED RED BLOOD CELLS

Targets for use in diagnosis, prognosis and therapy of breast cancer

METHOD FOR PREDICTING THE RESPONSE TO A THERAPY

Methods for detecting TCR-gamma gene rearrangement

Genes involved in intestinal inflammatory diseases and use thereof

DPYD GENE VARIANTS AND USE THEREOF

Assessing brain aneurysms

Methods of monitoring conditions by sequence analysis

METHODS AND COMPOSITIONS FOR LOCATING SNP HETEROZYGOSITY FOR ALLELE SPECIFIC DIAGNOSIS AND THERAPY

Genetic markers for schizophrenia and bipolar disorder

MARKER FOR DETECTING THE PROPOSED EFFICACY OF TREATMENT

Parthenocarpic genetic elements derived from

Methods using PBK1 for identifying agents that treat metabolic disorders

Genomic classification of malignant melanoma based on patterns of gene copy number alterations

Genomic classification of colorectal cancer based on patterns of gene copy number alterations

Genomic classification of non-small cell lung carcinoma based on patterns of gene copy number alterations

Systems for rapid forensic analysis of mitochondrial DNA and characterization of mitochondrial DNA heteroplasmy

METHODS OF DIAGNOSIS AND TREATMENT OF CROHN'S DISEASE

METHODS OF TREATING PSYCHOSIS AND SCHIZOPHRENIA BASED ON POLYMORPHISMS IN THE ERBB4 GENE

USE OF SNPS FOR THE DIAGNOSIS OF A PAIN PROTECTIVE HAPLOTYPE IN THE GTP CYCLOHYDROLASE 1 GENE (GCH1)

Arrays, Systems, and Methods of Using Genetic Predictors of Polycystic Diseases

Methods for high throughput genotyping

GENEMAP OF THE HUMAN GENES ASSOCIATED WITH SCHIZOPHRENIA

CHD7 GENE POLYMORPHISMS ARE ASSOCIATED WITH SUSCEPTIBILITY TO IDIOPATHIC SCOLIOSIS

Polymorphisms in Genes Affecting Dopamine Transporter Disorders and Uses Thereof

Surfactant Protein D is a Biomarker for Steroid Responsiveness in Asthma and Chronic Obstructive Pulmonary Disease

TRANSLOCATION AND MUTANT ROS KINASE IN HUMAN NON-SMALL CELL LUNG CARCINOMA

Method for determination of presence of crossing with cultivated rose in wild rose

Multitag sequencing ecogenomics analysis-US

METHODS AND USES INVOLVING GENETIC ABNORMALITIES AT CHROMOSOME 12

Method for the genomic typing of erythrocyte systems, oligonucleotide probes and relative diagnostic kits

METHODS AND PRODUCTS FOR DIAGNOSING CANCER

FGFR4 Promotes Cancer Cell Resistance in Response to Chemotherapeutic Drugs

MIF AGONISTS AND ANTAGONIST AND THERAPEUTIC USES THEREOF

Compositions and methods for characterizing and regulating olfactory sensation

GSTP1 as teratogenic allele for autism and assays and methods based thereon

FIG4 gene mutations in neurodegeneration

NOVEL MAIZE PLANT

IDENTIFICATION OF GROUP OF HYPERTENSION-SUSCEPTIBILITY GENES

Noninvasive diagnosis of fetal aneuploidy by sequencing

Prediction and prophylactic treatment of type 1 diabetes

Nucleic acid encoding SCN1A variant

Compositions and Methods for Diagnosing Autism

Multivariate analysis involving genetic polymorphisms related to mediators of inflammatory response for prediction of outcome of critcally ill patients

Genetic Markers for Weight Management and Methods of Use Thereof

Integrated Analyses of Breast and Colorectal Cancers

Methods and compositions for DMXL-associated mental retardation

GENETIC MARKER FOR ADVERSE BEHAVIORAL CONDITIONS

Methods and compositions for characterizing patients for clinical outcome trials

AQP5 Polymorphism

Fetal cell analysis using sample splitting

Molecular signature and assay for fluoroquinoline resistance in bacillus anthracis

Marker mapping and resistance gene associations in soybean

Rice Mutant Allele

Methods and materials for determining pain sensitivity and predicting and treating related disorders

ACTN3 GENOTYPE SCREEN FOR ATHLETIC PERFORMANCE

LIPOPROTEIN LIPASE AND ITS EFFECT ON STATIN TREATMENTS

CYP2C9*8 Alleles Correlate With Decreased Warfarin Metabolism And Increased Warfarin Sensitivity

Methods for Disease Therapy

BBS10 related diagnostic methods for Bardet-Biedl syndrome

DNA CHIP FOR PREDICTION OF OCCURRENCE OF LATE ADVERSE REACTION IN URINARY ORGAN AFTER RADIOTHERAPY, AND METHOD FOR PREDICTION OF OCCURRENCE OF LATE ADVERSE REACTION IN URINARY ORGAN AFTER RADIO THERAPY USING THE SAME

Isolated nucleic acids and kits for identifying subjects susceptible to ataxic neurological disease

Broad range PCR-based compositions and methods for the detection and identification of fungal pathogens

Polymorphisms in Genes Affecting CYP2C9-Related Disorders and Uses Thereof

SLC1A1 ANTIPSYCHOTIC DRUG RESPONSE MARKERS

USE OF GENETIC MODIFICATIONS IN HUMAN GENE CHK1 WHICH CODES FOR CHECKPOINT KINASE 1

METHOD OF DETECTING OCULAR DISEASES AND PATHOLOGIC CONDITIONS AND TREATMENT OF SAME

Nucleotide and amino acid sequences, and assays and methods of use thereof for diagnosis of ovarian cancer

Non-invasive fetal genetic screening by digital analysis

Non-invasive fetal genetic screening by digital analysis

METHODS FOR DETECTING IgH/BCL-1 CHROMOSOMAL TRANSLOCATION

Nucleic acid molecules and other molecules associated with plants

Genetic loci associated with iron deficiency tolerance in soybean

Genetic loci associated with cell wall digestibility in maize

Certain human genomic DNA associated with total red-green colorblindness

Methods and sequences to preferentially suppress expression of mutated huntingtin

Tumor Repressor Genes in the Prevention of Cancer

GENEMAP OF THE HUMAN GENES ASSOCIATED WITH PSORIASIS

Tissue analysis and kits therefor

BIOMARKERS FOR SERIOUS SKIN RASH

Genetic markers for assessing risk of developing bipolar disorder

GENETIC VARIANTS USEFUL FOR RISK ASSESSMENTS OF CORONARY ARTERY DISEASE AND MYOCARDIAL INFARCTION

Genetic polymorphisms associated with coronary events and drug response, methods of detection and uses thereof

Mutagenesis of aspergillus fungi and genes essential for growth

Prognostic test for early stage non small cell lung cancer (NSCLC)

Nucleotide and amino acid sequences, and assays and methods of use thereof for diagnosis

Genetic Markers for Assessing Risk of Developing Schizophrenia

Genetic markers of schizophrenia endophenotypes

CHRONIC OBSTRUCTIVE PULMONARY DISEASE SUSCEPTIBILITY AND RELATED COMPOSITIONS AND METHODS

Plant cyclopropane fatty acid synthase genes, proteins, and uses thereof

Insect resistant plant

SYSTEM AND METHOD FOR INFERRING STR ALLELIC GENOTYPE FROM SNPS

BCR-ABL variants

Gene polymorphisms as predictors of tumor progression and their use in cancer therapy

Diagnosing fetal chromosomal aneuploidy using genomic sequencing

ALLELE-ALLELE INTERACTIONS OF MTHFR GENE VARIANTS, AND USES THEREOF IN PREDICTING DISEASE RISK

DIAGNOSIS OF FETAL ABNORMALITIES BY COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS

Means and methods for haplotyping MHC-DRB loci in mammals and uses thereof

Noninvasive Diagnosis of Fetal Aneuploidy by Sequencing

Method for the simultaneous determination of blood group and platelet antigen genotypes

COMPOSITIONS AND METHODS FOR DETECTING MUTATIONS IN JAK2 NUCLEIC ACID

Genetic Markers for Weight Management and Methods of Use Thereof

Methods, kits, and reaction mixtures for high resolution melt genotyping

Mutation Implicated in Abnormality of Cardiac Sodium Channel Function

Probes for detecting obesity gene

Method for the diagnosis of colorectal cancer

METHOD OF SCREENING TEST SUBSTANCES FOR TREATING OR PREVENTING A DISEASE MEDIATED BY PLASMA CELLS

Genetic Markers for Optimizing Treatment for Schizophrenia

HUMAN DIABETES SUSCEPTIBILITY TNFRSF10D GENE

Method for the Simultaneous Determination of Blood Group and Platelet Antigen Genotypes

REAGENTS AND METHODS FOR DETECTING CYP2D6 POLYMORPHISMS

GENETIC MARKERS FOR WEIGHT MANAGEMENT AND METHODS OF USE THEREOF

Detecting and treating dementia

Detection of nucleic acids from multiple types of human papillomaviruses

TREX1 AS A MARKER FOR LUPUS ERYTHEMATOSUS

NUCLEIC ACID MOLECULES AND OTHER MOLECULES ASSOCIATED WITH THE TOCOPHEROL PATHWAY

Gene Polymorphisms as Sex-Specific Predictors in Cancer Therapy

Genetic test for the identification of carriers of complex vertebral malformations in cattle

METHODS FOR TREATING, DIAGNOSING, AND MONITORING LUPUS

GENETIC COMPONENT OF COMPLICATIONS IN TYPE 2 DIABETES

GENE SEQUENCE VARIANCES IN GENES RELATED TO FOLATE METABOLISM HAVING UTILITY IN DETERMINING THE TREATMENT OF DISEASE

DETECTION OF NPM1 NUCLEIC ACID IN ACELLULAR BODY FLUIDS

CROHN DISEASE SUSCEPTIBILITY GENE

Allele Detection

Method for typing HLA alleles

GENETIC MARKER WEIGHT MANAGEMENT

DETECTING GENETIC PREDISPOSITION TO OSTEOARTHRITIS ASSOCIATED CONDITIONS

27877, 18080, 14081, 32140, 50352, 16658, 14223, 16002, 50566, 65552 and 65577 molecules and uses therefor

Genetic loci associated with northern leaf blight resistance in maize

Method of modulating cell resistance

Polynucleotide associated with a colon cancer comprising single nucleotide polymorphism, microarray and diagnostic kit comprising the same and method for diagnosing a colon cancer using the polynucleotide

Nucleic acids encoding sodium channel SCN1A alpha subunit proteins and mutations associated with epilepsy

IRF-5 haplotypes in systemic lupus erythematosus

DETERMINING THE PHASE OF DUPLICATED CYP2D6 ALLELES

GENETIC VARIATIONS ASSOCIATED WITH TUMORS

Methods and compositions for detection of Cowden Syndrome (CS) and CS-like syndrome

Single nucleotide polymorphisms as genetic markers for childhood leukemia

Impdh2 snp associated with acute rejection

METHOD FOR PREDICTING THERAPEUTIC RESPONSIVENESS TO TNF-ALPHA BLOCKING AGENTS

Soy protein adhesive and uses thereof

Methods of Treatment, and Diagnosis of Epilepsy by Detecting Mutations in the SCN1A Gene

METHODS FOR PREDICTING AND DETECTING INTOLERANCE TO AN HYPOLIPIDEMIC AGENT

Methods of prognosing a rheumatoid arthritis remission phenotype

Method to determine the risk for side effects of an SSRI treatment in a person

Nanosensors and related technologies

Automated seed sampler and methods of sampling, testing and bulking seeds

Assessment of chromosomal alterations to predict clinical outcome of bortezomib treatment

GENETIC SUSCEPTIBILITY VARIANTS OF TYPE 2 DIABETES MELLITUS

HIGH RESOLUTION, HIGH THROUGHPUT HLA GENOTYPING BY CLONAL SEQUENCING

AZGP Gene Single Nucleotide Polymorphisms (SNPs)

Determining Age Ranges of Skin Samples

Compositions and methods for assaying markers tightly linked to resistance locus Bs2 of pepper

Single nucleotide polymorphisms and use of same predicting male-specific prenatal loss

Methods of Detecting Root Knot Nematodes

Genemap of the human genes associated with crohn's disease

Soybean transgenic event MON87705 and methods for detection thereof

MO-1, A Gene Associated With Morbid Obesity

COLORIMETRIC METHOD AND KIT FOR THE DETECTION OF SPECIFIC NUCLEIC ACID SEQUENCES USING METAL NANOPARTICLES FUNCTIONALIZED WITH MODIFIED OLIGONUCLEOTIDES

Apparatus and methods for parallel processing of micro-volume liquid reactions

PAXILLIN MUTATIONS, METHODS OF ASSESSING RISK OF METASTASIS AND METHODS OF STAGING TUMORS

METHOD FOR IDENTIFYING ALTERED VITAMIN D METABOLISM

POLYMORPHISMS IN GENES AFFECTING CNS DISORDERS AND USES THEREOF

Assays for resistance to echinocandin-class drugs

Detection and use of antiviral resistance mutations

Systems and methods for rapid identification of nucleic acid variants

Diagnostic method

Markers and Methods for Assessing and Treating Ulcerative Colitis and Related Disorders Using a 20 Gene Panel

Juvenile hemochromatosis gene (HFE2A), expression products and uses thereof

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

PROBE FOR DETECTING MUTATION IN JAK2 GENE AND USE THEREOF

Methods of PCR-Based Detection of "Ultra Short" Nucleic Acid Sequences

Specific gene polymorphisms in breast cancer diagnosis, prevention and treatment

Corn event 3272 and methods of detection thereof

METHODS FOR THE ADMINISTRATION OF ILOPERIDONE

Methods and kits for early detection of cancer or predisposition thereto

Methods for Identifying Cancer Risk

Chromosome 1p36 polymorphisms and low bone mineral density

USE OF ADAMTS4 GENE AND PROTEIN POLYMORPHISMS

METHOD AND KIT FOR MOLECULAR CHROMOSOMAL QUANTIFICATION

Methods for collecting and detecting oligonucleotides

METHOD FOR DETECTING DISEASE-ASSOCIATED MUTATIONS

CAT ALLERGEN

METHODS FOR SCREENING AND TREATMENT INVOLVING THE GENES GYPC, AGPAT3, AGL, PVRL2, HMGB 3, HSDL2 AND/OR LDB2

Sequence Variations in PNPLA3 Associated with Hepatic Steatosis

Tubulin Mutation Diagnostic

Screening methods for transfusion related acute lung injury (TRALI)

Organism-Specific Hybridizable Nucleic Acid Molecule

DRG11-Responsive (DRAGON) Gene Family

METHOD FOR SELECTION OF HOP STRAIN, BLEEDING MARKER FOR USE IN SELECTION OF HOP STRAIN, AND PRIMER SET

Mutations in the Bcr-Abl tyrosine kinase associated with resistance to ST1-571

Genetic variations associated with tumors

Genetic loci associated with head smut resistance in maize

Growth factor which acts through ErbB-4 RTK

GENETIC VARIANTS ASSOCIATED WITH PERIODIC LIMB MOVEMENTS AND RESTLESS LEGS SYNDROME

Probes for detecting immune-related gene polymorphisms and applications of the same

BIOMARKERS FOR ACETAMINOPHEN TOXICITY

Reagents and Methods for Detecting CYP2C9 Polymorphisms

ADENOSINE A1 AND A3 RECEPTOR GENE SEQUENCE VARIATIONS FOR PREDICTING DISEASE OUTCOME AND TREATMENT OUTCOME

METHOD OF SURFACE PLASMON RESONANCE (SPR) TO DETECT GENOMIC DISORDERS FOR POSTNATAL DIAGNOSIS

METHOD AND KIT FOR DIAGNOSIS AND MONITORING OF THE TREATMENT OF CHRONIC TRIPANOSSOMIASIS AND CHAGAS DISEASE

DNA-based test for detection of annual and intermediate ryegrass

PKD mutations and evaluation of same

SMALL MOLECULE MODULATORS OF P53 FAMILY SIGNALING

METHODS FOR IDENTIFYING MUTATIONS IN CODING AND NON-CODING DNA

Method of identifying individuals at risk of perioperative myocardial injury, major adverse cardiac events, cognitive decline, arrhythmias, depression or bleeding

Variants of hepatitis B virus with resistance to anti-viral nucleoside agents and applications thereof

INTERFERON GAMMA POLYMORPHISMS AS INDICATORS OF SUBJECT OUTCOME IN CRITICALLY ILL SUBJECTS

Methods for identification of alleles using allele-specific primers for amplification

Juvenile hemochromatosis gene (HFE2A), expression products and uses thereof

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

METHOD OF PREDICTING A BENEFIT OF ANTIOXIDANT THERAPY FOR PREVENTION OF CARDIOVASCULAR DISEASE IN HYPERGLYCEMIC PATIENTS

Circulating Mutant DNA to Assess Tumor Dynamics

Method for the diagnosis of schizophrenia

Breeding and milking cows for milk free of β-casein A

Genetic variants contributing to risk of prostate cancer

METHODS OF ASSESSING CORONARY ARTERY DISEASE

Methods for detecting attention-deficit/hyperactivity disorder

METHODS AND COMPOSITIONS FOR BREEDING PLANTS WITH ENHANCED YIELD

Genetic polymorphisms associated with cardiovascular diseases, methods of detection and uses thereof

Method for detecting oral squamous-cell carcinoma

Variants of human taste receptor genes

Methods for Assessing Risk of Alzheimer's Disease in a Patient

Biomarkers for Drug-Induced Liver Injury

Method for detecting thyroid carcinoma

METHOD AND KIT FOR ASSESSING RISK OF GOUT AND HYPERURICEMIA

BioMarkers for the Progression of Alzheimer's Disease

Methods and Kits for Analyzing Genetic Material of a Fetus

Methods and nucleic acids for the detection of metastasis of colon cell proliferative disorders

GENETIC VARIATIONS ASSOCIATED WITH TUMORS

Method For Identification of Compound Having Anti-Anxiety Effect

Screening methods and sequences relating thereto

METHODS AND COMPOSITIONS FOR PHARMACOGENETIC ANALYSIS OF ANTI-INFLAMMATORY DRUGS IN THE TREATMENT OF RHEUMATOID ARTHRITIS AND OTHER INFLAMMATORY DISEASES

Detection of penicillin tolerance in Group B : single nucleotide polymorphisms in penicillin binding protein 4

METHODS FOR DIAGNOSING OSTEOARTHRITIS

METHOD FOR DIAGNOSING CANCER BY DETECTING THE METHYLATION OF TRANSITIONAL ZONES

Methods for the Detection of Cancer

METHOD TO ASSESS SUSCEPTIBILITY TO ANDROGENIC ALOPECIA

Responsiveness to Therapy for Liver Disorders

Probe set and method for identifying HLA allele

METHOD OF DIAGNOSING A NEURODEGENERATIVE DISEASE

Molecular markers linked to PPO inhibitor tolerance in soybeans

VH4 codon signature for multiple sclerosis

Methods and Systems for Universal Carrier Screening

MICROSATELLITE-BASED FINGERPRINTING SYSTEM FOR SACCHARUM COMPLEX

Use of Genetic Determinants in Cardiovascular Risk Assessment

RGS2 GENOTYPES ASSOCIATED WITH EXTRAPYRAMIDAL SYMPTOMS INDUCED BY ANTIPSYCHOTIC MEDICATION

Using genetic polymorphisms of the BICD1 gene as a method for diagnosing and treating myopia

Screening for disease susceptibility by genotyping the CCR5 and CCR2 genes

Compositions comprising MG29 nucleic acids, polypeptides, and associated methods of use

Filaggrin

Quantitative Trait Loci and Somatostatin

DNA fragment used as attached to 5′ end of primer used in nucleic acid amplification reaction and use of DNA fragment

Systems and Methods for Improving Protein and Milk Production of Dairy Herds

DIAGNOSIS OF INFLAMMATORY BOWEL DISEASE IN CHILDREN

Methods of using F-spondin as a biomarker for cartilage degenerative conditions and bone diseases

METHODS AND COMPOSITIONS FOR THE ASSESSMENT OF CARDIOVASCULAR FUNCTION AND DISORDERS

Micro RNAs and their methods of use for the treatment and diagnosis of schizophrenia and schizophrenia spectrum disorders

Compositions and methods for detecting Noonan syndrome

Method for the detection of EGFR mutations in blood samples

Lafora's disease gene

GENETIC POLYMORPHISMS ASSOCIATED WITH AUTOINFLAMMATORY DISEASES, METHODS OF DETECTION AND USES THEREOF

Diagnostic and Therapeutic Target Adarb2 Proteins for Neurodegenerative Diseases

Detection of nucleic acid sequence differences using coupled ligase detection and polymerase chain reactions

GENE EXPRESSION MARKERS FOR INFLAMMATORY BOWEL DISEASE

Methods for identifying genomic deletions

Genetic Markers Associated with Degenerative Disc Disease and Uses Thereof

Method of screening for LRRK2-related parkinsonism inheritance

SINGLE COPY GENOMIC HYBRIDIZATION PROBES AND METHODS OF GENERATING SAME

GENE POLYMORPHISM USEFUL FOR ASSISTANCE/THERAPY FOR SMOKING CESSATION

Qtls for Mastitis Resistance in Cattle

Gene and methods for diagnosing neuropsychiatric disorders and treating such disorders

CDNA FOR HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE AND USES THEREOF

Nucleotide primer set and nucleotide probe for detecting genotype of N-acetyltransferase-2 (NAT2)

CHARACTERIZING PROSTATE CANCER

Methods of assessing the risk of reproductive failure by measuring telomere length

Genetic analyses predictive of asthma

Methods for prenatal diagnosis of chromosomal abnormalities

Methods and Compositions for Producing Active Vitamin K-Dependent Proteins

METHODS FOR DETECTING A CYCLOPHILIN B SNP ASSOCIATED WITH HERDA

Methods and kits useful for detecting an alteration in a locus copy number

Genetic markers for risk management of atrial fibrillation, atrial flutter, and stroke

MATERIALS AND METHODS FOR ABCB1 POLYMORPHIC VARIANT SCREENING, DIAGNOSIS, AND TREATMENT

Pharmacogenomics of blood pressure lowering agents

METHODOLOGY FOR ANALYSIS OF SEQUENCE VARIATIONS WITHIN THE HCV NS5B GENOMIC REGION

GENE ASSOCIATED WITH ARTERIOSCLEROTIC DISEASE, AND USE THEREOF

Novel human protein kinase, phosphatase, and protease family members and uses thereof