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2. Assessment of exposure to air pollution in children: Determining whether wearing a personal monitor affects physical activity.
3. Clinical Course of Non-Functional Pituitary Microadenoma in Children: A Single Center Experience: Supplemental Table
4. Effects of APOC3 Heterozygous Deficiency on Plasma Lipid and Lipoprotein Metabolism.
5. Enhanced and controlled chromatin extraction from FFPE tissues and the application to ChIP-seq
6. Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
7. Factors contributing to rapidly increasing rates of cesarean section in Armenia: a partially mixed concurrent quantitative-qualitative equal status study
8. Interaction between nectin-1 and the human natural killer cell receptor CD96
9. NanoMod: a computational tool to detect DNA modifications using Nanopore long-read sequencing data
10. The impact of childhood varicella vaccination on the incidence of herpes zoster in the general population: modelling the effect of exogenous and endogenous varicella-zoster virus immunity boosting
11. Tumor microenvironment modulation enhances immunologic benefit of chemoradiotherapy
12. Validation of Melanoma Immune Profile (MIP), a Prognostic Immune Gene Prediction Score for Stage II–III Melanoma
13. Abnormal Vertical Eye Movements as a Clue for Diagnosis of Niemann–Pick Type C
14. Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC)
15. Asymmetric PI3K Activity in Lymphocytes Organized by a PI3K-Mediated Polarity Pathway
16. BET bromodomain proteins regulate enhancer function during adipogenesis
17. Burnout and self-reported suboptimal patient care amongst health care workers providing HIV care in Malawi
18. Comparison of methods to assess onset of breast development in the LEGACY Girls Study: methodological considerations for studies of breast cancer
19. De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay
20. De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders
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