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Imprinting
- Genomic imprinting and uniparental disomy are factors that influence how some genetic conditions are inherited. People inherit two copies ... s mother. This phenomenon is known as genomic imprinting. In genes that undergo genomic imprinting, the parent ...
- KCNK9 imprinting syndrome is a rare condition characterized by weak muscle tone (hypotonia) from birth. As a result, affected infants have a lack of energy ( ...
- ... gene activity results from a process called genomic imprinting.Most cases of Prader-Willi syndrome (about 70 ... Angelman syndrome deletion region: further evidence for regional imprinting control. Am J Hum Genet. 2000 Mar;66( ...
- Epigenomics (National Human Genome Research Institute)Genes and Gene Therapy/Related Issues ... Genes and Gene Therapy ... National Human Genome Research Institute ... From the National Institutes of Health ... Epigenomics is ...
- Prader-Willi Syndrome (PWS): Other FAQs (Eunice Kennedy Shriver National Institute of Child Health and Human Development)Prader-Willi Syndrome/Learn More ... Prader-Willi Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National ...
- The DNMT3A gene provides instructions for making an enzyme called DNA methyltransferase 3 alpha. This enzyme is involved in DNA methylation, which is the ...
- ... activation is caused by a phenomenon called genomic imprinting.IGF2 is part of a cluster of genes ... p) arm of chromosome 11 that undergoes genomic imprinting. Another gene in this cluster, H19, is also ...
- ... activation is caused by a phenomenon called genomic imprinting.H19 is part of a cluster of genes ... p) arm of chromosome 11 that undergoes genomic imprinting. Another gene in this cluster, IGF2, is also ...
- ... activation is caused by a phenomenon called genomic imprinting.The KCNQ1OT1 gene is part of a cluster ... p) arm of chromosome 11 that undergo genomic imprinting. KCNQ1OT1 and several other genes in this cluster ...
- ... s mother. This phenomenon is known as genomic imprinting. The KCNK9 gene is a maternally expressed imprinted ... channel protein, have been found to cause KCNK9 imprinting syndrome. This condition is characterized by weak muscle ...