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A mostrar 1 - 20 resultados de 38 para a pesquisa '(((( j la comida can netw ) OR ( j la combe can netw ))) OR ( j nat comparing cases new ))*', tempo de pesquisa: 1.50seg 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 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

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

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions

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