Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emily M. Traxler"'
Publikováno v:
Hepatology Communications, Vol 6, Iss 8, Pp 2132-2146 (2022)
Abstract Beckwith‐Wiedemann Syndrome (BWS) is the most common human overgrowth disorder caused by structural and epigenetic changes to chromosome 11p15. Patients with BWS are predisposed to developing hepatoblastoma (HB). To better understand the m
Externí odkaz:
https://doaj.org/article/e4f4d915f01b4c0eba8c33c55ec13943
Autor:
Yahan Li, Darren Erich Hagen, Tieming Ji, Mohammad Reza Bakhtiarizadeh, Whitney M. Frederic, Emily M. Traxler, Jennifer M. Kalish, Rocío Melissa Rivera
Publikováno v:
Epigenetics, Vol 14, Iss 9, Pp 850-876 (2019)
The use of assisted reproductive technologies (ART) can induce a congenital overgrowth condition in humans and ruminants, namely Beckwith-Wiedemann syndrome (BWS) and large offspring syndrome (LOS), respectively. Shared phenotypes and epigenotypes ha
Externí odkaz:
https://doaj.org/article/ac001e9389484b93a3317259e3e7acc6
Autor:
Emily M Traxler, Arupa Ganguly, Yemin Lan, Daniel F. Deegan, Nora Engel, Natali S Sobel Naveh, Rosanna Weksberg, Jennifer M. Kalish, Jacklyn M. Huhn
Publikováno v:
Nucleic Acids Research
DNA methylation, chromatin-binding proteins, and DNA looping are common components regulating genomic imprinting which leads to parent-specific monoallelic gene expression. Loss of methylation (LOM) at the human imprinting center 2 (IC2) on chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3bf78238cddbcb08d49eb5832cd433
https://doi.org/10.1093/nar/gkab475
https://doi.org/10.1093/nar/gkab475
Autor:
Darren E. Hagen, Whitney M Frederic, Yahan Li, Mohammad Reza Bakhtiarizadeh, Tieming Ji, Emily M Traxler, Jennifer M. Kalish, Rocío Melissa Rivera
Publikováno v:
Epigenetics
The use of assisted reproductive technologies (ART) can induce a congenital overgrowth condition in humans and ruminants, namely Beckwith-Wiedemann syndrome (BWS) and large offspring syndrome (LOS), respectively. Shared phenotypes and epigenotypes ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96317ba3cb8b6c8babf4d0d18aa9b455
https://pubmed.ncbi.nlm.nih.gov/31144574
https://pubmed.ncbi.nlm.nih.gov/31144574