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Genomics publications search

2,677 publications found

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Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy.

Polymorphisms in translesion polymerase genes influence treatment outcome in malignant mesothelioma

A Common Polymorphism Within MSLN Affects miR-611 Binding Site and Soluble Mesothelin Levels in Healthy People

Identification of an MLL4-GPS2 fusion as an oncogenic driver of undifferentiated spindle cell sarcoma in a child

Four individually druggable MET hotspots mediate HGF-driven tumor progression

Pyrosequencing reveals diverse fecal microbiota in Simmental calves during early development.

A candidate gene association study for nine economically important traits in Italian Holstein cattle

In frame exon skipping in UBE3B is associated with developmental disorders and increased mortality in cattle

Characterization of Cellular and Humoral Immune Responses After IBV Infection in Chicken Lines Differing in MBL Serum Concentration

Nocardia vulneris sp. nov., isolated from wounds of human patients in North America

Genetic Predisposition to In Situ and Invasive Lobular Carcinoma of the Breast

IL1B and DEFB1 Polymorphisms Increase Susceptibility to Invasive Mold Infection After Solid Organ Transplantation.

Endogenous IFNλ in Viral Hepatitis Patients

Genetic variation in the TLR and NF‐κB pathways and cervical and vulvar cancer risk: A population‐based case–control study

Polymorphisms in microRNA genes as predictors of clinical outcomes in colorectal cancer patients

Feeding rates and prey selectivity of planktonic decapod larvae in the Western English Channel

A single strain of Tetratrichomonas gallinarum causes fatal typhlohepatitis in red-legged partridges (Alectoris rufa) to be distinguished from histomonosis

Effect of oral infection with Kashmir bee virus and Israeli acute paralysis virus on bumblebee (Bombus terrestris) reproductive success

TREM2 Variant p. R47H as a Risk Factor for Sporadic Amyotrophic Lateral Sclerosis

UBQLN2 mutations are not a frequent cause of amyotrophic lateral sclerosis in Ireland

Association of tardive dyskinesia with variation in CYP2D6: Is there a role for active metabolites?

High-Resolution Genetic Mapping of Complex Traits from a Combined Analysis of F2 and Advanced Intercross Mice

Loss of tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy

Genetic Association Analysis of ATP Binding Cassette Protein Family Reveals a Novel Association of ABCB1 Genetic Variants with Epilepsy Risk, but Not with Drug-Resistance

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects

Inherited variation in the PARP1 gene and survival from melanoma

Age-Specific Incidence Rates for Dementia and Alzheimer Disease in NIA-LOAD/NCRAD and EFIGA Families

Loss-of-Function Mutations in APOC3 and Risk of Ischemic Vascular Disease

Genetic variants conferring susceptibility to Alzheimer's disease in the general population; do they also predispose to dementia in Down's syndrome

The triggering receptor expressed on myeloid cells 2 (< i> TREM2) is associated with enhanced inflammation, neuropathological lesions and increased risk for Alzheimer's dementia.

Plasma estrogen levels, estrogen receptor gene variation and ischemic arterial disease in postmenopausal women: the Three-City prospective Cohort Study

Remnant Cholesterol, Low-Density Lipoprotein Cholesterol, and Blood Pressure as Mediators from Obesity to Ischemic Heart Disease.

EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa.

Interaction between c-Src Tyrosine Kinase Gene Variant and Fish Oil Intake Influences Blood Pressure in Healthy Adults

Revision of the Pelvicachromis taeniatus-group (Perciformes), with revalidation of the taxon Pelvicachromis kribensis (Boulenger, 1911) and description of a new species

A transcriptome approach to ecdysozoan phylogeny

Phylogenetic position of Myriapoda revealed by 454 transcriptome sequencing.

The evolutionary history of holometabolous insects inferred from transcriptome-based phylogeny and comprehensive morphological data

A SNP-based approach for rapid and cost-effective genetic wolf monitoring in Europe based on non-invasively collected samples

Contribution of syndecan-4 genetic variants to hypertension, the TAMRISK study.

Mitochondrial DNA Variants in Obesity

Effects of established BMI-associated loci on obesity-related traits in a French representative population sample

Associations between avoidant focused coping strategies and polymorphisms in genes coding for brain-derived neurotrophic factor and vascular endothelial growth factor in suicide attempters: a preliminary study

Genetic variants in or near ADH1B and ADH1C affect susceptibility to alcohol dependence in a British and Irish population

Pubertal Onset in Girls is Strongly Influenced by Genetic Variation Affecting FSH Action

Early life adversity and serotonin transporter gene variation interact at the level of the adrenal gland to affect the adult hypothalamo-pituitary-adrenal axis

Groundnut

In Arabidopsis thaliana two co‐adapted cyto‐nuclear systems correlate with distinct ccmC transcript sizes.

Characterization of a phosphotriesterase-like lactonase from the hyperthermoacidophilic crenarchaeon Vulcanisaeta moutnovskia

Quantification of bacterial and archaeal symbionts in high and low microbial abundance sponges using real-time PCR

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