157 results on '"Rubio, Justin P."'
Search Results
2. Background and Breakthrough Opioid Choice May Determine Different Pain Outcomes
3. Evidence for the role of FMR1 gray zone alleles as a risk factor for parkinsonism in females
4. Effect of gene variants on opioid dose, pain and adverse effect outcomes in advanced cancer: an explorative study
5. Opioid Switch Dosing in Chronic Cancer Pain: A Prospective Longitudinal Study.
6. Data from Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies
7. Supplementary Figures 1-5, Supplementary Tables 1-3, Full List of Authors and Affiliations from Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies
8. Exome array analysis suggests an increased variant burden in families with schizophrenia
9. Estimation of the Antirelapse Efficacy of Tafenoquine, Using Plasmodium vivax Genotyping
10. The mutational landscape of single neurons and oligodendrocytes reveals evidence of inflammation-associated DNA damage in multiple sclerosis
11. Leptin’s metabolic and immune functions can be uncoupled at the ligand/receptor interaction level
12. Effects of enzyme inducers efavirenz and tipranavir/ritonavir on the pharmacokinetics of the HIV integrase inhibitor dolutegravir
13. Transcriptomic effects of rs4845604, an IBD and allergy-associated RORC variant, in stimulated ex vivo CD4+ T cells
14. Common variation in the MOG gene influences transcript splicing in humans
15. Evaluation of the effect of UGT1A1 polymorphisms on dolutegravir pharmacokinetics
16. Analysis of extended HLA haplotypes in multiple sclerosis and narcolepsy families confirms a predisposing effect for the class I region in Tasmanian MS patients
17. Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data
18. Identifying nineteenth century genealogical links from genotypes
19. Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis
20. Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis
21. Deep Sequencing of The LRRK2 Gene in 14,002 Individuals Reveals Evidence of Purifying Selection and Independent Origin of the p.Arg1628pro Mutation in Europe
22. An 18-kDa Translocator Protein (TSPO) Polymorphism Explains Differences in Binding Affinity of the PET Radioligand PBR28
23. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
24. On the utility of data from the International HapMap Project for Australian association studies
25. Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinsonʼs Disease
26. An investigation of polymorphisms in the 17q11.2-12 CC chemokine gene cluster for association with multiple sclerosis in Australians
27. Histamine Receptor 3 negatively regulates oligodendrocyte differentiation and remyelination
28. Tafenoquine treatment of Plasmodium vivax malaria: suggestive evidence that CYP2D6 reduced metabolism is not associated with relapse in the Phase 2b DETECTIVE trial
29. Estimation of the Antirelapse Efficacy of Tafenoquine, UsingPlasmodium vivaxGenotyping
30. Leptin’s metabolic and immune functions can be uncoupled at the ligand/receptor interaction level
31. Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus
32. A genomewide association study of smoking relapse in four European population-based samples
33. Deep sequencing of theLRRK2gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe
34. A genome-wide association study in progressive multiple sclerosis
35. SIRT1 Activates MAO-A in the Brain to Mediate Anxiety and Exploratory Drive
36. An 18-kDa Translocator Protein (TSPO) Polymorphism Explains Differences in Binding Affinity of the PET Radioligand PBR28
37. Genetic Deficiency of Plasma Lipoprotein-Associated Phospholipase A2 (PLA2G7 V297F Null Mutation) and Risk of Alzheimer's Disease in Japan
38. CD127 immunophenotyping suggests altered CD4+ T cell regulation in primary progressive multiple sclerosis
39. Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data
40. Multiple Sclerosis: A Haplotype Association Study
41. McLeod neuroacanthocytosis: Genotype and phenotype
42. A conserved sorting-associated protein is mutant in chorea-acanthocytosis
43. McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene
44. Genomic Organization of the Human Gα14 and Gαq Genes and Mutation Analysis in Chorea–Acanthocytosis (CHAC)
45. Chorea-Acanthocytosis: Genetic Linkage to Chromosome 9q21
46. The chromosomal organization of the Plasmodium falciparum var gene family is conserved
47. A YAC contig map of Plasmodium falciparum chromosome 4: characterization of a DNA amplification between two recently separated isolates
48. Genetic Deficiency of Plasma Lipoprotein-Associated Phospholipase A2 (PLA2G7 V297F Null Mutation) and Risk of Alzheimer's Disease in Japan.
49. A Polymorphism in the HLA-DPB1 Gene Is Associated with Susceptibility to Multiple Sclerosis.
50. Multiple Sclerosis Susceptibility-Associated SNPs Do Not Influence Disease Severity Measures in a Cohort of Australian MS Patients.
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