392 results on '"Hollox, Edward"'
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2. Genetic variation of glycophorins and infectious disease
3. Human intelectin‐2 (ITLN2) is selectively expressed by secretory Paneth cells
4. SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
5. Extensive variation in the intelectin gene family in laboratory and wild mouse strains.
6. Human intelectin-1 (ITLN1) genetic variation and intestinal expression.
7. The Use of Microsatellites in the Management of Captive Gibbons
8. Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease
9. A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples
10. Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank
11. Balancing selection at the human salivary agglutinin gene (DMBT1) driven by host-microbe interactions
12. Association study of human leukocyte antigen (HLA) variants and idiopathic pulmonary fibrosis
13. Analysis of copy number variation at DMBT1 and age-related macular degeneration
14. Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment
15. Author Correction: Clonal architecture in mesothelioma is prognostic and shapes the tumour microenvironment
16. Evidence of Convergent Evolution in Humans and Macaques Supports an Adaptive Role for Copy Number Variation of the β-Defensin-2 Gene
17. Copy number variation of the beta defensin gene cluster on chromosome 8p influences the bacterial microbiota within the nasopharynx of otitis-prone children.
18. Gene fusions during the early evolution of mesothelioma correlate with impaired DNA repair and Hippo pathways.
19. Gene fusions during the early evolution of mesothelioma correlate with impaired DNA repair and Hippo pathways
20. Evolution and Diversity of Defensins in Vertebrates
21. Structural variation of the malaria-associated human glycophorin A-B-E region
22. DeepPheWAS: an R package for phenotype generation and association analysis for phenome-wide association studies
23. Molecular and population genetic analyses of variation within and surrounding the human lactase gene
24. Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease
25. Genetic variation of glycophorins and infectious disease
26. Evolution of the rapidly mutating human salivary agglutinin gene ( DMBT1 ) and population subsistence strategy
27. Genome-wide association study of ACE inhibitor-induced cough implicates neuropeptides and shows genetic overlap with chronic dry cough
28. Abstract 5693: Mesotheliomas harbor early clonal fusions involving both tumor suppressor drivers and novel oncogenic alterations
29. A comparison of software for analysis of rare and common short tandem repeat (STR) variation using human genome sequences from clinical and population-based samples
30. Analysis of Copy Number Variation Using the Paralogue Ratio Test (PRT)
31. Additional file 1 of Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank
32. β-defensin Genomic Copy Number Is Associated With HIV Load and Immune Reconstitution in Sub-Saharan Africans
33. No Evidence for Association of β‐Defensin Genomic Copy Number with HIV Susceptibility, HIV Load during Clinical Latency, or Progression to AIDS
34. Genome structural variation in human evolution
35. Human gene copy number variation and infectious disease
36. Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank
37. Extended Cohort for E-health, Environment and DNA (EXCEED) COVID-19 focus
38. Allelic Recombination between Distinct Genomic Locations Generates Copy Number Diversity in Human β-defensins
39. Maintenance of copy number variation at the human salivary agglutinin gene (DMBT1) by balancing selection driven by host-microbe interactions
40. P040 Identification and functional characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease
41. Haptoglobin (HP) and Haptoglobin-related protein (HPR) copy number variation, natural selection, and trypanosomiasis
42. Immunocytochemical detection of ERG expression in exfoliated urinary cells identifies with high specificity patients with prostate cancer
43. Fcγ receptors: genetic variation, function, and disease
44. Identification and functional characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease
45. Deleted in malignant brain tumor 1 genetic variation confers urinary tract infection risk in children and mice
46. Extensive variation in the mouse intelectin gene family: recent duplications, deletions and inactivating variants result in diversity in laboratory strains
47. Evolutionary genetics of the human Rh blood group system
48. Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntingtonʼs disease
49. Allelic recombination between distinct genomic locations generates copy number diversity in human [beta]-defensins
50. Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation
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