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Keyword [Nonsense]
Result: 41 - 60 | Page: 3 of 4
41. Whole Exome Sequencing Identifies The Causative Gene Mutation In A Chinese Family With Hereditary Multiple Exostoses
42. Screening Compounds That Induce Readthrough Of Nonsense Mutations By High-throughput PTT-ELISA And Luciferase Reporter System
43. Study On The Nonsense Mutation Readthrough Activity Of 5-methoxyflavone
44. Clinical And Genetic Analysis Of Angelman Syndrome In A Family
45. A Case Report Of SRY Gene Mutation In Sexual Development Disorder And A Study On The Correlation Between Osteocalcin And Glycorelic Disease
46. Mechanisms by which nonsense codons downregulate T-cell receptor transcripts
47. Human nonsense-mediated mRNA decay is a cytoplasmic process triggered by aberrant 3'-untranslated regions
48. T-cell receptor nonsense-associated altered splicing
49. Discovery and analysis of components of nonsense mediated decay in Drosophila
50. Characterization of genomic targets of chromosomal aberrations and an in vivo model of disrupted nonsense mediated decay
51. Nonsense mRNA reducing factor-1: Insight into its function through an unpredicted interacting factor
52. Nonsense-mediated mRNA decay of the human HEXA mRNA
53. No Nonsense: The Protection of Wild-Type mRNAs From Nonsense-Mediated mRNA Decay in Saccharomyces cerevisiae
54. Analysis of nonsense-mediatedmRNA decay in Caenorhabditis elegans
55. Nonsense suppressortRNAs in the study of class II and class III gene expression and regulation
56. The suppression of nonsense mutations in plants
57. Nonsense-mediated decay and neuronal ceroid lipofuscinosis: Utilizing nonsense suppression as a therapeutic tool to enhance functional protein activity
58. Research Of The Mechanisms Of The Effects Of ER-α36, LOC147710 And Omentin-1 On The Regulation Of Bone Metabolism
59. Genetic And Molecular Investigation For Distinct Scoliotic Phenotypes Conveyed By Allelic Mutations Implicated In FBN1
60. Impact Of Genetic Factors In The Pathogenesis Of Parkinson’s Disease And Paroxysmal Kinesigenic Dyskinesias
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