azacitidine and Central Core Disease

azacitidine has been researched along with Central Core Disease in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Brockington, M; Jungbluth, H; Monk, D; Moore, GE; Muntoni, F; Sewry, CA; Stanier, P; Zhou, H	1

Other Studies

1 other study(ies) available for azacitidine and Central Core Disease

Article	Year
Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies. American journal of human genetics, 2006, Volume: 79, Issue:5 Topics: Alleles; Animals; Azacitidine; Base Sequence; Case-Control Studies; Cells, Cultured; CpG Islands; Decitabine; DNA Methylation; DNA Primers; Epigenesis, Genetic; Female; Fetus; Gene Silencing; Genes, Recessive; Genomic Imprinting; Humans; Hydroxamic Acids; Male; Mice; Mice, Inbred C57BL; Muscle, Skeletal; Myoblasts, Skeletal; Myopathy, Central Core; Pedigree; Point Mutation; Polymorphism, Single Nucleotide; Ryanodine Receptor Calcium Release Channel; Tissue Distribution	2006

Article

Year

Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.

American journal of human genetics, 2006, Volume: 79, Issue:5

Topics: Alleles; Animals; Azacitidine; Base Sequence; Case-Control Studies; Cells, Cultured; CpG Islands; Decitabine; DNA Methylation; DNA Primers; Epigenesis, Genetic; Female; Fetus; Gene Silencing; Genes, Recessive; Genomic Imprinting; Humans; Hydroxamic Acids; Male; Mice; Mice, Inbred C57BL; Muscle, Skeletal; Myoblasts, Skeletal; Myopathy, Central Core; Pedigree; Point Mutation; Polymorphism, Single Nucleotide; Ryanodine Receptor Calcium Release Channel; Tissue Distribution

2006