32 results on '"Davies, Kay E."'
Search Results
2. Dysregulation of Tweak and Fn14 in skeletal muscle of spinal muscular atrophy mice
3. Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy
4. Deletion of AMPA receptor GluA1 subunit gene (Gria1) causes circadian rhythm disruption and aberrant responses to environmental cues
5. Surrogate gene therapy for muscular dystrophy
6. Absent sleep EEG spindle activity in GluA1 (Gria1) knockout mice: relevance to neuropsychiatric disorders
7. Evaluating the links between schizophrenia and sleep and circadian rhythm disruption
8. Identification of valid housekeeping genes for quantitative RT-PCR analysis of cardiosphere-derived cells preconditioned under hypoxia or with prolyl-4-hydroxylase inhibitors
9. Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia
10. The Robotic Mouse: Understanding the Role of AF4, a Cofactor of Transcriptional Elongation and Chromatin Remodelling, in Purkinje Cell Function
11. Analysis of skeletal muscle function in the C57BL6/SV129 syncoilin knockout mouse
12. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment: Third in Molecular Medicine Review Series
13. Pharmacological strategies for muscular dystrophy
14. Immunogold Confirmation that Utrophin is Localized to the Normal Position of Dystrophin in Dystrophin-negative Transgenic Mouse Muscle
15. Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd mdx and Dmd mdx3cv dystrophin-deficient mice
16. Genomic organization and refined mapping of the mouse β-dystrobrevin gene
17. Molecular Genetics of Autosomal Recessive Spinal Muscular Atrophy
18. EagI andNotI linking clones from human chromosomes 11 and Xp
19. Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle
20. Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle
21. New markers for linkage analysis of X-linked hypophosphataemic rickets
22. Three DNA markers for hypophosphataemic rickets
23. Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene
24. Muscular dystrophy: from gene to patient
25. Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease
26. Genotype mosaicism in fragile X fetal tissues
27. The application of DNA recombinant technology to the analysis of the human genome and genetic disease
28. MASA syndrome: further clinical delineation and chromosomal localisation
29. The mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease
30. Molecular analysis of muscular dystrophy
31. A study of genetic linkage heterogeneity in adult polycystic kidney disease
32. Linkage relationships between retinoschisis, Xg, and a cloned DNA sequence from the distal short arm of the X chromosome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.