hydrogen sulfite has been researched along with Angelman Syndrome in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 4 (66.67) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Arima, T; Hiura, H; John, RM; Kagami, M; Miyauchi, N; Nakai, K; Ogata, T; Okae, H; Sato, A; Sato, F; Soejima, H; Van De Pette, M | 1 |
Baumer, A; Hornby, DP; Matin, MM | 1 |
Cross, NC; Durston, VJ; Harvey, JF; White, HE | 1 |
Dikow, N; Hartmann, C; Janssen, B; Krämer, N; Nygren, AO; Schouten, JP; Zschocke, J | 1 |
Buiting, K; Dittrich, B; Doerfler, W; Horsthemke, B; Schmitz, B; Zeschnigk, M | 1 |
Aggerholm, A; Guldberg, P; Worm, J | 1 |
6 other study(ies) available for hydrogen sulfite and Angelman Syndrome
Article | Year |
---|---|
Characterization of DNA methylation errors in patients with imprinting disorders conceived by assisted reproduction technologies.
Topics: Angelman Syndrome; Beckwith-Wiedemann Syndrome; DNA Methylation; Epigenesis, Genetic; Female; Genomic Imprinting; Humans; Infant, Newborn; Japan; Male; Phenotype; Polymorphism, Single Nucleotide; Prader-Willi Syndrome; Pregnancy; Reproductive Techniques, Assisted; Risk Factors; Sequence Analysis, DNA; Silver-Russell Syndrome; Sulfites | 2012 |
An analytical method for the detection of methylation differences at specific chromosomal loci using primer extension and ion pair reverse phase HPLC.
Topics: Ampicillin Resistance; Angelman Syndrome; Base Sequence; Chromatography, High Pressure Liquid; Chromatography, Ion Exchange; CpG Islands; Cytosine; Deamination; DNA; DNA Methylation; DNA Primers; Genetic Markers; Genomic Imprinting; Humans; Molecular Sequence Data; Mutagenesis, Site-Directed; Nucleic Acid Amplification Techniques; Polymerase Chain Reaction; Prader-Willi Syndrome; Sulfites; Uracil | 2002 |
Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome.
Topics: Angelman Syndrome; Autoantigens; Chromosomes, Human, Pair 15; Cost-Benefit Analysis; CpG Islands; DNA Methylation; Female; Genomic Imprinting; Humans; Indicators and Reagents; Male; Polymerase Chain Reaction; Prader-Willi Syndrome; Reproducibility of Results; Ribonucleoproteins, Small Nuclear; Sensitivity and Specificity; Sequence Analysis, DNA; snRNP Core Proteins; Sulfites | 2006 |
Quantification of the methylation status of the PWS/AS imprinted region: comparison of two approaches based on bisulfite sequencing and methylation-sensitive MLPA.
Topics: Angelman Syndrome; Case-Control Studies; DNA Methylation; Genomic Imprinting; Humans; Nucleic Acid Amplification Techniques; Prader-Willi Syndrome; Sequence Analysis, DNA; Sulfites | 2007 |
Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
Topics: 5-Methylcytosine; Angelman Syndrome; Autoantigens; Chromosomes, Human, Pair 15; Cloning, Molecular; CpG Islands; Cytosine; Dinucleoside Phosphates; DNA Methylation; Female; Genomic Imprinting; Humans; Male; Plasmids; Polymerase Chain Reaction; Prader-Willi Syndrome; Promoter Regions, Genetic; Restriction Mapping; Ribonucleoproteins, Small Nuclear; Sequence Analysis, DNA; Sequence Deletion; snRNP Core Proteins; Sulfites | 1997 |
In-tube DNA methylation profiling by fluorescence melting curve analysis.
Topics: Acute Disease; Angelman Syndrome; Autoantigens; Bone Marrow; Carrier Proteins; Cell Cycle Proteins; Cyclin-Dependent Kinase Inhibitor p15; Cyclin-Dependent Kinase Inhibitor p16; DNA Fingerprinting; DNA Methylation; Fluorometry; Humans; Indicators and Reagents; Leukemia, Myeloid; Polymerase Chain Reaction; Prader-Willi Syndrome; Ribonucleoproteins, Small Nuclear; snRNP Core Proteins; Sulfites; Tumor Suppressor Proteins | 2001 |