A mostrar 1 - 20 resultados de 98 para a pesquisa '(( j i cooper jason n ) OR ((( 5 guest complex tear nlo ) OR ( 3.5 nacl mno carlos nojek ))))', tempo de pesquisa: 1.29seg Refinar resultados
Variability in Non-Cardiac Surgical Procedures in Children with Congenital Heart Disease
Inhibition of the Wnt/β-catenin pathway enhances antitumor immunity in ovarian cancer

Phase I study of intraventricular infusions of autologous ex vivo expanded NK cells in children with recurrent medulloblastoma and ependymoma
Allotransplantation for patients age 40 years and greater with non-Hodgkin Lymphoma (NHL): encouraging progression-free survival

Genomic and immune heterogeneity are associated with differential responses to therapy in melanoma
Report on the sixth blind test of organic crystal structure prediction methods

Analysis of protein-coding genetic variation in 60,706 humans
Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations

Congenital Titinopathy: Comprehensive characterization and pathogenic insights
A Meta-Analysis Identifies New Loci Associated with Body Mass index in Individuals of African Ancestry

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry
The Major Genetic Determinants of HIV-1 Control Affect HLA Class I Peptide Presentation

Proceedings of the 3rd Biennial Conference of the Society for Implementation Research Collaboration (SIRC) 2015: advancing efficient methodologies through community partnerships and team science: Seattle, WA, USA. 24-26 September 2015
COMPREHENSIVE AND INTEGRATED GENOMIC CHARACTERIZATION OF ADULT SOFT TISSUE SARCOMAS

Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease
Drosophila Muller F Elements Maintain a Distinct Set of Genomic Properties Over 40 Million Years of Evolution

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Aberrant septin 11 is associated with sporadic frontotemporal lobar degeneration

Common genetic determinants of vitamin D insufficiency: a genome-wide association study
The Genetic Landscape of Renal Complications in Type 1 Diabetes

Ferramentas de pesquisa: Obter Feed RSS — Enviar pesquisa por email — Guardar a pesquisa