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A mostrar 1 - 20 resultados de 41 para a pesquisa '(( j nat compared case new ) OR ((( j fast computer waste new ) OR ( j icat computer a new ))))', tempo de pesquisa: 1.53seg Refinar resultados
GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis
Materials informatics for the screening of multi-principal elements and high-entropy alloys

A new statistic and its power to infer membership and phenotype in a genome-wide association study using genotype frequencies
Association between the gut microbiome and atherosclerosis

Application and analysis of debris-flow early warning system in Wenchuan earthquake-affected area
Evaluation of the Procleix Ultrio Plus ID NAT assay for detection of HIV 1, HBV and HCV in blood donors

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
Homological scaffolds of brain functional networks

Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer
A New Protocol of Analyzing Isotope Coded Affinity Tag Data from High Resolution LC-MS Spectrometry

A novel, primate-specific, brain isoform of KCNH2 impacts cortical physiology, cognition, neuronal repolarization and risk for schizophrenia
Comparative analysis of detecting cervical lymph node metastasis with fine needle aspiration cytology

Comparative study of frequency of micronuclei in normal, potentially malignant diseases and oral squamous cell carcinoma
Hair Dye Use and Risk of Bladder Cancer in the New England Bladder Cancer Study

Case-Control Studies of Gene-Environment Interaction: Bayesian Design and Analysis
Wizard CD Plus and ProTaper Universal: analysis of apical transportation using new software

Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance

Incidental finding of two rare developmental anomalies: Fusion and dilaceration: A case report and literature review
Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis

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