553 results on '"Lovett M"'
Search Results
2. The Reverse Genetic Approach to the Etiology of Schizophrenia
3. Efficacy of a Medical Directive to Reduce Inappropriate Indwelling Urinary Catheter Use on Orthopedic Wards
4. Genetic Linkage of Autosomal Recessive Canine Narcolepsy with a μ Immunoglobulin Heavy-Chain Switch-Like Segment
5. The Structure and Expression of the Integrated Viral DNA in Mouse Cells Transformed by Simian Virus 40
6. Interactions of Treponema pallidum with Endothelial Cell Monolayers
7. New Technologies for Use in the Surveillance and Control of Yaws
8. Association of the ROBO1 gene with reading disabilities in a family-based analysis
9. Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problems
10. Support for EKN1 as the susceptibility locus for dyslexia on 15q21
11. A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1
12. Comparative gene expression analysis of avian embryonic facial structures reveals new candidates for human craniofacial disorders
13. The synthesis of viral tumour antigens in SV40-transformed mouse cells
14. Bradykinin increases intracellular calcium levels in a human bronchial epithelial cell line via the B2 receptor subtype
15. ASSOCIATION STUDY OF DEVELOPMENTAL DYSLEXIA AND THE GENES FOR VMP, DCDC2, KIAA0319, TTRAP AND THEM2 ON CHROMOSOME 6p
16. EVIDENCE FOR THE 8Q CANDIDATE REGION IN SUSCEPTIBILITY TO ADOLESCENT IDIOPATHIC SCOLIOSIS.
17. Language-Based Difficulties in School-Age Children with Reading Disabilities
18. A management system for protecting compressed air tunnelling workers during operations through contaminated soil.
19. High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts
20. Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer
21. Bringing maths and science teaching into the 21st century.
22. ASSOCIATION STUDY OF DEVELOPMENTAL DYSLEXIA AND THE GENES FOR VMP, DCDC2, KIAA0319, TTRAP AND THEM2 ON CHROMOSOME 6p
23. Determination of technetium-99 in environmental material with rhenium as a yield monitor
24. Physical mapping of the beige critical region on mouse Chromosome 13
25. ISOLATION AND ANALYSIS OF NOVEL GENES MAPPING TO THE CRITICAL REGION OF THE 5Q-SYNDROME
26. PRESENILIN 1 INTERACTS IN BRAIN WITH A NOVEL MEMBER OF THE ARMADILLO FAMILY
27. The Reverse Genetic Approach to the Etiology of Schizophrenia
28. ISOLATION OF NOVEL CDNA CLONES MAPPING TO THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
29. Cytomegalovirus Infection With Lymphadenopathy
30. Technologies for generating, normalizing and subtracting cDNA libraries from small quantities of mRNA
31. Genomic approaches for identifying genes involved in auditory hair cell regeneration
32. Mutations in CD2BP1 that disrupt PTP PEST binding cause the allelic disorders familial recurrent arthritis and PAPA syndrome
33. Large scale gene expression profiling of early human craniofacial development
34. Transcript map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759
35. Linkage study of reading disabilities and attention-deficit hyperactivity disorder in the chromosome 6p region
36. Positional candidate gene identification for keratolytic winter erythema (KWE) on 8p22-23
37. Localization of a novel form of juvenile rheumatoid arthritis (familial recurrent arthritis) to human chromosome 15q
38. Characterization of the BEM 46 gene, a candidate for the mouse deafness (dn) and human DFNB7/DFNB11 genes
39. Evidence of Susceptibility Loci in Genome Wide Searches of Familial Idiopathic Scoliosis
40. Gene expression profiles from early stages of human craniofacial development
41. Isolation of transcribed DNA sequences from chromosome 21 using mouse fetal cDNA
42. Some experiences in controlling contamination of environmental materials during sampling and processing for low-level actinide analysis
43. Transuranic nuclides in plaice (Pleuronectes platessa) from the North-Eastern Irish Sea
44. Modeling the ability to reason about oneself and others in educational contexts
45. Association of theROBO1gene with reading disabilities in a family-based analysis
46. Homozygosity mapping applied to hereditary hearing impairment: localizing recessive deafness genes
47. The applications of single-cell genomics
48. Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21
49. A new gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p
50. Primary transcription map of the critical region of the 5q-syndrome
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