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1. Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations

2. Identification of Reduced Host Transcriptomic Signatures for Tuberculosis Disease and Digital PCR-Based Validation and Quantification

3. Identification of regulatory variants associated with genetic susceptibility to meningococcal disease

4. Modelling pathogen load dynamics to elucidate mechanistic determinants of host-Plasmodium falciparum interactions

5. Mycobacterium tuberculosis Exploits a Molecular OffSwitch of the Immune System for Intracellular Survival

6. Transcriptomic Studies of Malaria: a Paradigm for Investigation of Systemic Host-Pathogen Interactions

7. Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function

8. Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits

9. The Lin28/let-7 axis regulates glucose metabolism

10. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

11. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

12. Detection of Tuberculosis in HIV-Infected and -Uninfected African Adults Using Whole Blood RNA Expression Signatures: A Case-Control Study

13. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.

14. TreeFam: a curated database of phylogenetic trees of animal gene families

15. Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

16. A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

17. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women

18. Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

19. PLANNER: a multi-scale deep language model for the origins of replication site prediction.

20. Digerati - A multipath parallel hybrid deep learning framework for the identification of mycobacterial PE/PPE proteins.

21. Variation in CFHR3 determines susceptibility to meningococcal disease by controlling factor H concentrations.

22. Signatures of TSPAN8 variants associated with human metabolic regulation and diseases.

23. Identification of Reduced Host Transcriptomic Signatures for Tuberculosis Disease and Digital PCR-Based Validation and Quantification.

24. Nanopore sequencing as a scalable, cost-effective platform for analyzing polyclonal vector integration sites following clinical T cell therapy.

25. Modelling pathogen load dynamics to elucidate mechanistic determinants of host-Plasmodium falciparum interactions.

26. Identification of regulatory variants associated with genetic susceptibility to meningococcal disease.

27. Phase I Trial of Inducible Caspase 9 T Cells in Adult Stem Cell Transplant Demonstrates Massive Clonotypic Proliferative Potential and Long-term Persistence of Transgenic T Cells.

28. Integrated pathogen load and dual transcriptome analysis of systemic host-pathogen interactions in severe malaria.

29. Transcriptomic Studies of Malaria: a Paradigm for Investigation of Systemic Host-Pathogen Interactions.

30. Mycobacterium tuberculosis Exploits a Molecular Off Switch of the Immune System for Intracellular Survival.

31. Childhood tuberculosis is associated with decreased abundance of T cell gene transcripts and impaired T cell function.

32. Scaffolding and completing genome assemblies in real-time with nanopore sequencing.

33. Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities.

34. Diagnostic Test Accuracy of a 2-Transcript Host RNA Signature for Discriminating Bacterial vs Viral Infection in Febrile Children.

35. Streaming algorithms for identification of pathogens and antibiotic resistance potential from real-time MinION(TM) sequencing.

36. Realtime analysis and visualization of MinION sequencing data with npReader.

37. cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.

38. cnvOffSeq: detecting intergenic copy number variation using off-target exome sequencing data.

39. Diagnosis of childhood tuberculosis and host RNA expression in Africa.

40. YHap: a population model for probabilistic assignment of Y haplogroups from re-sequencing data.

41. Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response.

42. Detection of tuberculosis in HIV-infected and -uninfected African adults using whole blood RNA expression signatures: a case-control study.

43. Demographic and motor features associated with the occurrence of neuropsychiatric and sleep complications of Parkinson's disease.

44. A population model for genotyping indels from next-generation sequence data.

45. The effect of genomic inversions on estimation of population genetic parameters from SNP data.

46. Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.

47. cnvHiTSeq: integrative models for high-resolution copy number variation detection and genotyping using population sequencing data.

48. Bioinformatics: living on the edge.

49. Gene-targeted analysis of copy number variants identifies 3 novel associations with coronary heart disease traits.

50. An exome sequencing pipeline for identifying and genotyping common CNVs associated with disease with application to psoriasis.

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