345 results on '"Wheeler, Vanessa"'
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2. Contributors
3. The instability of the Huntington's disease CAG repeat mutation
4. CircHTT(2,3,4,5,6) — co-evolving with the HTT CAG-repeat tract — modulates Huntington's disease phenotypes
5. Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset
6. Genetic modifiers of Huntington disease differentially influence motor and cognitive domains
7. Correction to: Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat
8. Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat
9. Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington’s disease
10. Polyglutamine-Expanded Huntingtin Exacerbates Age-Related Disruption of Nuclear Integrity and Nucleocytoplasmic Transport
11. Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease
12. Somatic CAG Repeat Stability in a Transgenic Sheep Model of Huntington’s Disease
13. Modification of Huntington's disease by short tandem repeats
14. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset
15. Base editing strategies to convert CAG to CAA diminish the disease-causing mutation in Huntington’s disease.
16. Posttranscriptional regulation of FAN1 by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease.
17. CAG repeat expansion in the Huntington’s disease gene shapes linear and circular RNAs biogenesis
18. A State's Reach Cannot Exceed its Grasp : Territorial Limitations on State Franchise Statutes
19. Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.
20. Chapter 4 - The instability of the Huntington's disease CAG repeat mutation
21. Base editing strategies to convert CAG to CAA diminish the disease-causing mutation in Huntington's disease
22. Assessing average somatic CAG repeat instability at the protein level
23. Delineating regional vulnerability in the neurodegenerative disease SCA1 using a conditional mutant ATXN1 mouse
24. Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease
25. Franchising & Distribution Currents
26. Transcriptional Consequences of 16p11.2 Deletion and Duplication in Mouse Cortex and Multiplex Autism Families
27. Intangible Cruelty: The History, Risks, and Challenges of the Prejudgment Attachment of Intellectual Property and Its Implications for Franchisors.
28. Transcriptional regulatory networks underlying gene expression changes in Huntington's disease
29. D12 Faulty linear and back-splicing in Huntington’s disease: novel players in the pathologic process hint at innovative RNA biomarkers
30. A22 Medium-sized spiny neurons diversity in Huntington’s disease pathology
31. A modifier of Huntingtonʼs disease onset at the MLH1 locus
32. High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntingtonʼs disease CAG knock-in mice across multiple genetic backgrounds
33. LADR Case Notes (August 2022-October 2022) and FLJ Currents (Winter 2023).
34. Chromosome substitution strain assessment of a Huntington’s disease modifier locus
35. Early Alterations of Brain Cellular Energy Homeostasis in Huntington Disease Models
36. Additional file 1 of Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat
37. Additional file 2 of Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat
38. Motivational, proteostatic and transcriptional deficits precede synapse loss, gliosis and neurodegeneration in the B6.HttQ111/+ model of Huntington’s disease
39. Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat
40. Genetic modifiers of Huntington’s disease differentially influence motor and cognitive domains
41. Defective linear and circular RNAs biogenesis in Huntington’s disease: CAG repeat expansion hijacks neuronal splicing
42. Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models
43. Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes
44. Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington’s Disease
45. A04 Circhtt, a circular rna from the huntington’s disease gene locus: functional characterization and possible implications for disease modulation
46. FAN1, a DNA Repair Nuclease, as a Modifier of Repeat Expansion Disorders
47. Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirection
48. Huntington’s Disease Pathogenesis: Two Sequential Components
49. Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation
50. Special Issue: DNA Repair and Somatic Repeat Expansion in Huntington’s Disease
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