Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Galia Konfortova"'
Publikováno v:
Genome research. 13(4)
A characteristic of imprinted genes is that the maternal and paternal alleles show differences in methylation. To perform a genome-wide screen for novel imprinted loci, we applied methylation-sensitive representational difference analysis (Me-RDA) to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3e9a1097fdafaf12ceb8104d4944483
https://pubmed.ncbi.nlm.nih.gov/12670997
https://pubmed.ncbi.nlm.nih.gov/12670997
Autor:
Grazyna Ptak, Kenneth J. McCreath, Ian Wilmut, Lorraine E. Young, Sébastien Wieckowski, Angelika Schnieke, Alex J. Kind, Galia Konfortova, Kenneth Fernandes, Robert Feil, Pasqualino Loi
Publikováno v:
Mechanisms of Development
Mechanisms of Development, Elsevier, 2003, 120 (12), pp.1433--42. ⟨10.1016/j.mod.2003.09.006⟩
Mechanisms of Development, Elsevier, 2003, 120 (12), pp.1433--42. ⟨10.1016/j.mod.2003.09.006⟩
In different mammalian species, in vitro culture and manipulation can lead to aberrant fetal and peri-natal development. It has been postulated that these diverse abnormalities are caused by epigenetic alterations and that these could affect genes th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d155d5dfc3177e242e49b29f02b7b698
http://hdl.handle.net/11575/16350
http://hdl.handle.net/11575/16350
Autor:
Philippe Arnaud, Rachel J. Smith, Galia Konfortova, Gavin Kelsey, Colin V. Beechey, Wendy Dean
Publikováno v:
Gene
Gene, 2002, pp.101-12
Gene, Elsevier, 2002, pp.101-12
Gene, 2002, pp.101-12
Gene, Elsevier, 2002, pp.101-12
International audience; We identified a maternally methylated CpG island at the mouse Zac1 locus on chromosome (Chr.) 10 in a screen for imprinted genes. The homologous human gene ZAC (also known as LOT1 and PLAGLI) is a candidate gene for transient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8810ca23bb8f7da3b2d360113ac0adc
https://pubmed.ncbi.nlm.nih.gov/12119104
https://pubmed.ncbi.nlm.nih.gov/12119104
Autor:
Wolf Reik, Richard I. Gregory, Robert Feil, Samantha L. Thompson, Galia Konfortova, Wendy Dean
Publikováno v:
Toxicology Letters
Toxicology Letters, Elsevier, 2001, 120 (1-3), pp.143--150. ⟨10.1016/S0378-4274(01)00292-2⟩
Toxicology Letters, Elsevier, 2001, 120 (1-3), pp.143--150. ⟨10.1016/S0378-4274(01)00292-2⟩
Genomic imprinting is an epigenetic marking mechanism by which certain genes become repressed on one of the two parental alleles. Imprinting plays important roles in mammalian development, and in humans its deregulation may result in disease and carc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9f24b54cff3cfdf3edbaf4d2e49437c
https://hal.archives-ouvertes.fr/hal-02197469
https://hal.archives-ouvertes.fr/hal-02197469