Methods of identifying spike morphology and fusarium head blight resistance, and the use of these methods for improving barley and related triticeae plants

Methods and materials for canine breed identification

Mutagenesis of aspergillus fungi and identification of genes essential for growth

Sequences used to identify if a female mammal comprises a mutation in the alpha-fetoprotein sequence(S) or a partial or total deletion of the alpha-fetoprotein sequence(S)

Methods of treatment of type 2 diabetes

Methods of diagnosis

Id-1 and Id-2 genes and products as markers of epithelial cancer

Using gene panels to predict tissue sensitivity to ionizing radiation

Physiogenomic method for predicting clinical outcomes of treatments in patients

Methods of screening and compositions for life span modulators

Pathogenic gene for coronary artery disease

Modulation of insulin like growth factor I receptor expression

Nucleic acid amplification primers for PCR-based clonality studies

Method of detecting gene polymorphism

Biallelic markers of d-amino acid oxidase and uses thereof

Haplotype structures of chromosome 21

ADAMTS13 genes and proteins and variants and therapeutic compositions and methods utilizing the same

Corn event 3272 and methods for detection thereof

Arrays of nucleic acid probes for analyzing biotransformation genes

Genetic polymorphisms in the preprotachykinin gene

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

Differentiating homozygous, heterozygous and wild-type alleles using a multiplexed hybridization-mediated assay

Correcting for false positive signals from mismatched probe-target binding in a multiplexed hybridization-mediated assay

Correcting an assay image of an array of signals generated from a multiplexed hybridization-mediated assay

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

Genetic basis of Alzheimer's disease and diagnosis and treatment thereof

Compositions and methods for detecting and treating motor neuron disorders

Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof

Polynucleotides and methods for making plants resistant to fungal pathogens

Polynucleotides and methods for making plants resistant to fungal pathogens

Polynucleotides and methods for making plants resistant to fungal pathogens

Capturing sequences adjacent to type-IIS restriction sites for genomic library mapping

Genetic polymorphisms associated with coronary heart disease, methods of detection and uses thereof

Polynucleotides encoding human secreted proteins

Method of diagnosis of type 2 diabetes and early onset thereof

Rapid direct sequence analysis of multi-exon genes

IL1RL-1 as a cardiovascular disease marker and therapeutic target

SNPs in 5' regulatory region of MDR1 gene

Diagnostics and therapeutics for glaucoma

Polynucleotide associated with a type II diabetes mellitus comprising single nucleotide polymorphism, microarray and diagnostic kit comprising the same and method for analyzing polynucleotide using the same

Variants of cytochrome c and methods of diagnosis of thrombocytopenia

Method of diagnosins a genetic susceptibility for bone damage

Method of diagnosing breast cancer and compositions therefor

Methods for the diagnosis, prognosis and treatment of metabolic syndrome

Bovine CAST gene SNP and meat tenderness

Antibiotic susceptibility and virulence factor detection in Pseudomonas aeruginosa

Microarray and method for genotyping SHV beta lactamases

Determination of antibiotic resistance in staphylococcus aureus

Method for detecting the mutant genes of the major gene cacna1h relating to the childhood absence epilepsy and the cacna1h mutant genes

Methods of detecting gene expression in normal and cancerous cells

Bardet-Biedl susceptibility gene and uses thereof

Nucleic acid encoding an interleukin-9 receptor variant

Mammalian IAP gene family, primers, probes and detection methods

Human enzymes of the metalloprotease family

Alleles of the human mu opioid receptor, diagnostic methods using said alleles, and methods of treatment based thereon

Comparative analysis of extracellular RNA species

Chip-based speciation and phenotypic characterization of microorganisms

Genetic variations (SNPs) adjacent to the AKT1 gene locus, and diagnostic and prognostic uses thereof

Methods for identifying risk of breast cancer and treatments thereof

Associations of polymorphisms in the FRZB gene in obesity and osteoporosis

Molecular detection systems utilizing reiterative oligonucleotide synthesis

Genetic polymorphisms as predictive diagnostics for adverse drug reactions (adr) and drug efficacy

Reagents and methods for diagnosis of attention deficit hyperactivity disorder

Assay for human DNA for gender determination

Probe biochips and methods for use thereof

Molecular identification of bacteria of genus and related genera

Method of typing gene polymorphisms

Novel neurotrophic factor protein and uses thereof

MECP2E1 gene

Use of predetermined nucleotides having altered base pairing characteristics in the amplification of nucleic acid molecules

Mitochondrial ND5 gene mutations in Parkinson's disease

Cancer markers and detection methods

Fast method for detecting micro-organisms in food samples

Autism gene

High throughput detection of glutathione s-transferase polymorphic alleles

Antibodies to tumor necrosis factor receptors 6α and 6β

Cystine-knot polypeptides: Cloaked-2 molecules and uses thereof

Databases for assessing nucleic acids

Gene causative of Rothmund-Thomson syndrome and its gene product

TCL-1 gene and protein and related methods and compositions

Business methods for assessing nucleic acids

Compositions and methods of use of standardized mixtures for determining an amount of a nucleic acid

Transposon mediated differential hybridisation

Method of detecting or quantitatively determining mitochondrial DNA 3243 variation, and kit therefor

Methods to predict ederma as a side effect of drug treatment

Human genomic polymorphisms

Atypical protein kinase C isoforms in disorders of the nervous system and cancer

Polymorphisms in the th clcn7 gene as genetic markers for bone mass

Methods for preventing and treating obesity in patients with mc4 receptor mutations

Kit for diagnosing and prognosticating matrix metalloproteinase-1 related disease via a matrix metalloproteinase-1 single nucleotide polymorphism

Tissue analysis and kits therefor

Genetic markers in the HLA-C gene associated with an adverse hematological response to drugs

Methods and compositions for assessing nucleic acids

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

Selection probe amplification

Use of silver gene for the authenication of the racial origin of animal populations and of the derivative products thereof

Fanc gene mutations in cancer

Method for determining predisposition to a physiological reaction in a patient

Screening for alzheimer's disease

Genetic markers in the CSF2RB gene associated with an adverse hematological response to drugs

Integrated biosensor and simulation system for diagnosis and therapy

Biallelic markers for use in constructing a high density disequilibrium map of the human genome

Genetic markers in the HLA-DQBI gene associated with an adverse hematological response to drugs

Genetic markers of schizophrenia spectrum disorders in the sulfotransferase 4a (sult4a) gene

Methods of identifying individuals at reduced risk of sepsis

Markers for metabolic syndrome obesity and insulin resistance

Bioarray chip reaction apparatus and its manufacture

Primers, probes and methods for nucleic acid amplification

Methods for treatment with bucindolol based on genetic targeting

Method of detection of predisposition to emphysema in chronic obstructive pulmonary disease

Association of the h2 haplotype of the p2y12 receptor with an increased risk for thrombosis and peripheral arterial disease

Use of neuronal apoptosis inhibitor protein (NAIP)

Method for detecting adverse reaction susceptibility to an HMG CoA reductase inhibitor

DNA markers for cattle growth

Methods of genotyping using differences in melting temperature

Mutations in the C7orf11 (TTDN1) gene causative of non-photosensitive trichothiodystrophy

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

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

Polymorphisms in the human gene for cytochrome P450 polypeptide 2C8 and their use in diagnostic applications

Effect of COMT genotype on frontal lobe function

APM1 biallelic markers and uses thereof

Converting diploidy to haploidy for genetic diagnosis

DNA markers for increased milk production in cattle

Genetic variants predicting warfarin sensitivity

Method enabling use of extracellular RNA extracted from plasma or serum to detect, monitor or evaluate cancer

Markers of alterations in the Y chromosome and uses therefor

NTRK1 genetic markers associated with progression of Alzheimer's disease

Genetic marker for coronary artery disease

Methodology of estimating the conformation of a protein by proteolysis

Growth hormone variations in humans and its uses

Hsan II related gene and expression products and uses thereof

Detecting the risk of cardiovascular disease by detecting mutations in genes, including genes encoding a2b-adrenoceptor and apoliporotein b

Parkinson's disease susceptibility haptotype as a tool for genetic screening

Methods of examining swine genetic resistance to rna virus-origin disease

Use of Fc receptor polymorphisms as diagnostics for treatment strategies for immune-response disorders

Genetic screening for improving treatment of patients diagnosed with depression

Method and probes for the detection of chromosome aberrations

Methods for the treatment of dementia based on apo e genotype

Pharmacogenetic DME detection assay methods and kits

Nucleotide sequence which encodes a flavin monooxygenase, the corresponding protein and their uses in the spheres of diagnosis and therapy

Topographic genotyping

Novel coding sequence haplotypes of the human BRCA2 gene

LDLR genetic markers associated with age of onset of Alzheimer's Disease

Method for determining susceptibility of an individual to allergen induced hypersensitivity

Method and kit for detecting a risk for diabetes or a metabolic syndrome

Novel enzymes and metabolites involved in skatole metabolism

Stem cell growth factor-like ployeptides

Mycobacterial rpoB sequences

Genotype test

Method to determine responsiveness of cancer to epidermal growth factor receptor targeting treatments

Genetic alterations associated with prostate cancer

Methods of diagnosing cardiovascular disease

CFTR allele detection assays

Method of detection

Method of judging inflammatory disease

Disease risk estimating method fusing sequence polymorphisms in a specific region of chromosome 19

Method for characterizing primary tumors

Methods for detection of promoter polymorphism in a UGT gene promoter

Method for augmenting the effects of serotonin reuptake inhibitors

Gene expression and genetic changes implicated in alcoholism

Genetic marker for coronary artery disease

Methods for the treatment of metabolic disorders, including obesity and diabetes

Compositions and methods for diagnosing autism

Methods of determining human egg competency

Molecular analysis of cellular fluid and liquid cytology specimens for clinical diagnosis, characterization, and integration with microscopic pathology evaluation

Polymorphic markers and methods of genotyping corn

Methods for detecting a polymorphism in the NFKB1 gene promoter

Medical use of ras antagonists for the treatment of capillary malformation

Method of detecting bone paget's disease

Human type II diabetes gene-slit-3 located on chromosome 5q35

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

Genetic loci associated with tolerance in soybean

Soybean polymorphisms and methods of genotyping

Real-time polymerase chain reaction-based genotyping assay for single nucleotide polymorphism

Differential expression of genes in microsatellite instability

Bardet-Biedl susceptibility gene and uses thereof

Notch1 variants associated with cardiovascular disease

Method for determining susceptibility to schizophrenia

Diagnostic test for attention deficit hyperactivity disorder

Screens for altered immune response capability

Marker gene

G protein coupled receptors and uses thereof

Oligonucleotides useful in methods for detecting and characterizing Aspergillus fumigatus

Methods and compositions for treating and diagnosing mood disorders, schizophrenia, and neuro-psychiatric disorders

Mammalian IAP gene family, primers, probes, and detection methods

Gene mutation associated with age-related macular degeneration

Cancer associated plexin B1 mutations

Method for detecting increased susceptibility to tumors

Delete sequence in , method for detecting mycobacteria using these sequences and vaccines

Protein associated with cell growth, differentiation, and death

Quantitative diagnostic analysis of hypertonia

Functional correction of the C/T-variance of the human eNOS-gene

Method for rapid detection and identification of bioagents

Detection of nucleic acids from multiple types of human papillomaviruses

BMPR2 mutations in pulmonary arterial hypertension related to congenital heart disease

Methods for disease detection

Haplotype partitioning

ACTN3 genotype screen for athletic performance

Method for determining the allelic state of the 5'-end of the $g(a)s1- casein gene

Allelic variation in human gene expression

Compositions and methods in cancer associated with altered expression of KCNJ9

Methods for detection of genetic disorders

Polynucleotides, polypeptides and method for screening for useful dog candidates

Methods for identifying an individual at increased risk of developing coronary artery disease

Enhanced amplifiability of minute fixative-treated tissue samples, minute stained cytology samples, and other minute sources of DNA

Diagnostic test for collie eye anomaly

Method for the carry-over protection in DNA amplification systems targeting methylation analysis achieved by a modified pre-treatment of nucleic acids

Methods for monitoring genomic DNA of organisms

Genetic markers for predicting disease and treatment outcome

Primer and probe for detecting vibrio cholerae or vibrio mimicus and detection method using the same

Diagnostic and therapeutic means for kidney stone related pathologies

Genotyping assay to predict cytochrome P4503A5 exression

Large-scale parallelized DNA sequencing

Porcine reproductive and respiratory syndrome virus receptor components and uses thereof

Identification of a gene causing the most common form of Bardet-Biedl syndrome and uses thereof

Large-scale parallelized DNA sequencing

Method and kit for detecting a risk of essential arterial hypertension

Carrier tests for polycystic kidney disease in the cat

Diagnosis of Shwachman-Diamond Syndrome

Coded nucleic acid carriers

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

Means and methods for diagnosing and treating affective disorders

High yielding soybean plants with low linolenic acid

Method of nucleic acid typing for selecting registered donors for cross-matching to transfusion recipients

Best's macular dystrophy gene

Methods of transforming corn

Method for diagnosing inflammatory bowel disease

Human FcgammaRIIB gene polymorphisms for assessing development of systemic lupus erythematosus and compositions for use thereof

12 human secreted proteins

Analysis of DNA

Method and kit for detecting a risk of acute myocardial infarction

Method of predicting genetic risk for hypertension

Method of diagnosing risk of restenosis after coronary angioplasty

Method for analysis of methylated nucleic acids

Mitochondrial biology expression arrays

Diagnosis of fetal aneuploidy

Proteins related to schizophrenia and uses thereof

Determination of methylation of nucleic acid sequences

Methods and compositions for analyzing comprised sample using single nucleotide polymorphism panels

Mutation associated with epilepsy

Methods for SMN genes and spinal muscular atrophy carriers screening

Dynamic genomic deletion expansion and formulation of molecular marker panels for integrated molecular pathology diagnosis and characterization of tissue, cellular fluid, and pure fluid specimens

Topographic genotyping for determining the diagnosis, malignant potential, and biologic behavior of pancreatic cysts and related conditions

Schizophrenia associated genes

Polycystic kidney disease nucleic acids and proteins

Methods for the detection of kidney cancer

Compositions, methods, and systems for determining bovine parentage and identity

Methods for diagnosing episodic movement disorders and related conditions

Methods and compositions for predicting drug responses

Methods and kits for the selection of animals having certain milk production capabilities, based on the analysis of a polymorphism in the somatotropin receptor gene

Method for the amplification of genetic information

Identifying agents for decreasing cellular toxicity associated with huntingin polypeptide

Drug targets for the treatment of neurodegenerative disorders

Methods and compositions for detecting VKORC1 single nucleotide polymorphisms

Solid support assay systems and methods utilizing non-standard bases

Primers, methods and kits for amplifying or detecting human leukocyte antigen alleles

Methods for detecting chromosome aberrations

Method and kit for detection of mutations in mitochondrial dna

Polymorphisms in the human gene for tpmt and their use in diagnostic and therapeutic applications

Methods of assessing the risk for the development of sporadic prostate cancer

Alpha-2 adrenergic receptor polymorphisms

Juvenile hemochromatosis gene (HFE2A) cleavage products and uses thereof

Prediction and predisposition of MBL gene to bronchial asthma with allergic rhinitis

Single nucleotide polymorphisms and combinations thereof predictive for paclitaxel responsiveness

Atlastin

Compositions and methods for the therapy and diagnosis of breast cancer

Compositions to ameliorate protein misfolding and aggregation

Biological markers for longevity and diseases and uses thereof

Identification of genetic markers associated with parkinson disease

Complexity management of genomic DNA by locus specific amplification

Genetic marker for endocrine disorders

Assay for detecting and quantifying HIV-1

Novel serine threonine kinase member, h2520-59

Human GAK-related gene variants associated with lung cancer

Methods and probes for the detection of cancer

Methods for detection of pathogens in red blood cells

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

Detection of nucleic acid sequence differences by comparative genomic hybridization

Nucleic acids of the human ABCC12 gene, vectors containing such nucleic acids and uses thereof

Concatameric ligation products: compositions, methods and kits for same

Complexity management and anaylysis of genomic data

Genetic loci associated with phytophthora tolerance in soybean

Human g protein coupled receptor

Assessment of CTLA-4 polymorphisms in CTLA-4 blockade therapy

Mutant met and uses therefor

Risk prediction for hypertension, elevated plasma triglyceride and metabolic syndrome

Methods for diagnosing osteoporosis or a susceptibility to osteoporosis based on haplotype association

Methods for predicting methotrexate polyglutamate levels using pharmacogenetics

Method for detecting cystic fibrosis

Method for predicting a drug transport capability by abcg2 polymorphisms

Method of testing food

Identification and mapping of single nucleotide polymorphisms in the human genome

Diagnostic and therapeutic means for pathologies associated with alpha 2 subunit of the na, k pump

Hybrid expression of neisserial proteins

Kit for diagnosing GH deficiency

Mutations associated with iron disorders

Methods and compositions relating to COL2A1 gene mutations and osteonecrosis

Genetic risk factor for neurodegenerative disease

Administration of FGF2 for treamtent of anxiety

Polymorphic Plasminogen genes and uses thereof