Autor:	Vineeta Bajaj, Lingegowda Krishna, Arun Kumar, M Markandaya
Rok vydání:	2004
Předmět:	Regulation of gene expression Genetics Chromosome Human genome Epigenetics Imprinting (psychology) Biology Genomic imprinting Gene Chromosome 22 Genetics (clinical)
Zdroj:	BMC Genetics. 5:13
ISSN:	1471-2156
DOI:	10.1186/1471-2156-5-13
Popis:	Background Genomic imprinting is an epigenetic chromosomal modification in the gametes or zygotes that results in a non-random monoallelic expression of specific autosomal genes depending upon their parent of origin. Approximately 44 human genes have been reported to be imprinted. A majority of them are clustered, including some on chromosome segment 11p15.5. We report here the imprinting status of the SLC22A1LS gene from the human chromosome segment 11p15.5
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::cbe6e4434a03d92a5fadc13e2e370f43 https://doi.org/10.1186/1471-2156-5-13 Zobrazit plný text záznamu Full text from SpringerLink