104 results on '"Jackson, A.P."'
Search Results
2. High-quality aluminum turbocharger impellers produced by thixocasting
3. Contribution of calcium-containing crystals to cartilage degradation and synovial inflammation in osteoarthritis
4. Development of some hypersonic benchmark flows using CFD and experiment
5. Gun tunnel flow calibration: defining input conditions for hypersonic flow computations
6. Cree encephalitis is allelic with Aicardi-Goutieres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism. (Short Report)
7. Receptor-mediated endocytosis
8. Managing the Team: A Guide to Successful Employee Involvement
9. Meier-Gorlin syndrome
10. Mutations in the NHEJ component XRCC4 cause primordial dwarfism
11. Meier-Gorlin syndrome Clinical genetics and genomics
12. Inclusion boy myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree
13. The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data
14. Extreme growth failure is a common presentation of ligase IV deficiency
15. A comprehensive evaluation of rodent malaria parasite genomes and gene expression
16. P801 DO SERUM MARKERS OF CELL INJURY AND DEATH HAVE POTENTIAL TO BECOME MECHANISTIC MARKERS IN NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD)?
17. Voltage-gated sodium channel beta3 subunit Ig domain
18. Meier-Gorlin syndrome: Growth and secondary sexual development of a microcephalic primordial dwarfism disorder
19. Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis.
20. Mutations in the pre-replication complex cause Meier-Gorlin syndrome
21. CEP152 is a genome maintenance protein disrupted in Seckel syndrome
22. Mammalian mitochondrial DNA replication intermediates are essentially duplex but contain extensive tracts of RNA/DNA hybrid.
23. Hippocampal Nabeta3 expression in patients with temporal lobe epilepsy.
24. Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.
25. Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
26. A second locus for Aicardi-Goutieres syndrome at chromosome 13q14-21.
27. Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus.
28. Structure of human PCNA bound to RNASEH2B PIP box peptide
29. Structure of the PCNA:RNase HII complex from Archaeoglobus fulgidus.
30. 17q21.31 Microdeletion Syndrome: Further Expanding the Clinical Phenotype
31. D.P.3.04. Inclusion body myopathy with Paget’s disease and frontotemporal dementia (IBMPFD): Extending the clinical features in a large pedigree
32. Aicardi-Goutieres syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21.
33. Safer fibreoptic intubation
34. Comparative study of the efficacy of eprinomectin versus ivermectin, and field efficacy of eprinomectin only, for the treatment of chorioptic mange in alpacas
35. The results from the 1999 sprites balloon campaign
36. An autosomal recessive exfoliative ichthyosis with linkage to chromosome 12q13
37. Development of a risk assessment methodology for evaluating potential impacts associated with contaminated mud disposal in the marine environment
38. Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21
39. Clathrin proteins and recognition memory
40. Thiopurine methyltransferase levels should be measured before commening patients on azathioprine
41. The Dangers of Taking ‘T in the Park’
42. Plant clathrin heavy chain: sequence analysis and restricted localisation in growing pollen tubes
43. Book Reviews
44. Simulation models for teaching endodonticsurgical procedures
45. Somatic cell mapping of bovine clathrin light chain genes: identification of a new bovine syntenic group
46. Characterisation of the gene for Drosophila amphiphysin
47. The kinetics of calcium binding to fura‐2 and indo‐1
48. Theory and meaning in counseling research: Comment on Strong (1991).
49. Somatic cell mapping of bovine clathrin light chain genes: identification of a new bovine synthenic group.
50. A physical model of nacre
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