Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Suhee Chang"'
Autor:
Suhee Chang, Stella K. Hur, Natali S. Sobel Naveh, Joanne L. Thorvaldsen, Deborah L. French, Alyssa L Gagne, Chintan D. Jobaliya, Montserrat C. Anguera, Marisa S. Bartolomei, Jennifer M Kalish
Publikováno v:
Epigenetics, Vol 16, Iss 12, Pp 1295-1305 (2021)
Genomic imprinting is a rare form of gene expression in mammals in which a small number of genes are expressed in a parent-of-origin-specific manner. The aetiology of human imprinting disorders is diverse and includes chromosomal abnormalities, mutat
Externí odkaz:
https://doaj.org/article/03d418f378ec4d8dbddcd0b45ec27f03
Autor:
Suhee Chang, Diana Fulmer, Stella K Hur, Joanne L Thorvaldsen, Li Li, Yemin Lan, Eric A Rhon-Calderon, Nicolae Adrian Leu, Xiaowen Chen, Jonathan A Epstein, Marisa S Bartolomei
Publikováno v:
eLife, Vol 11 (2022)
Dysregulation of the imprinted H19/IGF2 locus can lead to Silver-Russell syndrome (SRS) in humans. However, the mechanism of how abnormal H19/IGF2 expression contributes to various SRS phenotypes remains unclear, largely due to incomplete understandi
Externí odkaz:
https://doaj.org/article/6e1ce1ff28534687a37e77cf4367e911
Modeling human epigenetic disorders in mice: Beckwith-Wiedemann syndrome and Silver-Russell syndrome
Autor:
Suhee Chang, Marisa S. Bartolomei
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 5 (2020)
Genomic imprinting, a phenomenon in which the two parental alleles are regulated differently, is observed in mammals, marsupials and a few other species, including seed-bearing plants. Dysregulation of genomic imprinting can cause developmental disor
Externí odkaz:
https://doaj.org/article/0a56dd9710b04361a0dad05fd6b829d8
Autor:
Suhee Chang, Diana Fulmer, Stella K Hur, Joanne L Thorvaldsen, Li Li, Yemin Lan, Eric A Rhon-Calderon, Nicolae Adrian Leu, Xiaowen Chen, Jonathan A Epstein, Marisa S Bartolomei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2486457cd9cb1cb518bad21f891e224
https://doi.org/10.7554/elife.78754.sa2
https://doi.org/10.7554/elife.78754.sa2
Autor:
Deborah L. French, Joanne L. Thorvaldsen, Suhee Chang, Jennifer M. Kalish, Alyssa L. Gagne, Marisa S. Bartolomei, Montserrat C. Anguera, Stella K. Hur, Chintan D Jobaliya, Natali S Sobel Naveh
Publikováno v:
Epigenetics
Genomic imprinting is a rare form of gene expression in mammals in which a small number of genes are expressed in a parent-of-origin-specific manner. The aetiology of human imprinting disorders is diverse and includes chromosomal abnormalities, mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fba878ea7aca5f9aa1651cd15a90700
https://doi.org/10.1080/15592294.2020.1861172
https://doi.org/10.1080/15592294.2020.1861172
Autor:
Suhee Chang, Diana Fulmer, Stella K. Hur, Joanne L. Thorvaldsen, Li Li, Yemin Lan, Eric A. Rhon-Calderon, N Adrian Leu, Xiaowen Chen, Jonathan A. Epstein, Marisa S. Bartolomei
Dysregulation of the imprintedH19/IGF2locus can lead to Silver-Russell Syndrome (SRS) in humans. However, the mechanism of how abnormalH19/IGF2expression contributes to various SRS phenotypes remains unclear, largely due to incomplete understanding o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f0cf7b3f2822a8e237515277bbf545d
https://doi.org/10.1101/2022.03.28.486058
https://doi.org/10.1101/2022.03.28.486058
Autor:
Suhee, Chang, Diana, Fulmer, Stella K, Hur, Joanne L, Thorvaldsen, Li, Li, Yemin, Lan, Eric A, Rhon-Calderon, Nicolae Adrian, Leu, Xiaowen, Chen, Jonathan A, Epstein, Marisa S, Bartolomei
Publikováno v:
eLife. 11
Dysregulation of the imprinted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0fa8b68d926269779393023bf2939c7b
https://pubmed.ncbi.nlm.nih.gov/36441651
https://pubmed.ncbi.nlm.nih.gov/36441651
Autor:
Stella K. Hur, Jennifer M. Kalish, Carolyn Lye, Alice Yu, Suhee Chang, Monserrat C. Anguera, Joanne L. Thorvaldsen, Marisa S. Bartolomei
Publikováno v:
Cancer Research. 77:1936-1936
Beckwith-Wiedemann Syndrome (BWS) is a cancer predisposition syndrome that affects at least 1 in 10,500 children. Up to 25% of children with BWS develop tumors, primarily Wilms tumor and hepatoblastoma. BWS is due to genetic or epigenetic changes tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae0ca4fe46a1e6a4530c47fb0b8d2263
https://doi.org/10.1158/1538-7445.am2017-1936
https://doi.org/10.1158/1538-7445.am2017-1936