Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Damian B Yap"'
Autor:
Damian B Yap, David C Walker, Leah M Prentice, Steven McKinney, Gulisa Turashvili, Katrin Mooslehner-Allen, Teresa Ruiz de Algara, John Fee, Xavier d'Anglemont de Tassigny, William H Colledge, Samuel Aparicio
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27127 (2011)
Mll5 is currently a member of the Mll family of SET domain histone methyltransferase proteins but studies have also showed that it could be part of the SET3 branch of proteins. Recently, constitutive knock out animal studies have shown that Mll5 is r
Externí odkaz:
https://doaj.org/article/2896489fe9d34f38bb80962b782ea739
Autor:
Damian B. Yap, Ilaria Nisoli, Yonit Tsatskis, Ann Boija, Martin Hirst, Edvin Karlsson, Alireza Lorzadeh, Samuel Aparicio, Per-Henrik Holmqvist, Michelle Moksa, Manolis Fanto, Helen McNeill, Mattias Mannervik, Kelvin Yeung, Per Stenberg
Publikováno v:
eLife
eLife, Vol 6 (2017)
Yeung, K, Boija, A, Karlsson, E, Holmqvist, P H, Tsatskis, Y, Nisoli, I, Yap, D, Lorzadeh, A, Moksa, M, Hirst, M, Aparicio, S, Fanto, M, Stenberg, P, Mannervik, M & McNeill, H 2017, ' Atrophin controls developmental signaling pathways via interactions with Trithorax-like ', eLife, vol. 6, no. 0, e23084 . https://doi.org/10.7554/eLife.23084
eLife, Vol 6 (2017)
Yeung, K, Boija, A, Karlsson, E, Holmqvist, P H, Tsatskis, Y, Nisoli, I, Yap, D, Lorzadeh, A, Moksa, M, Hirst, M, Aparicio, S, Fanto, M, Stenberg, P, Mannervik, M & McNeill, H 2017, ' Atrophin controls developmental signaling pathways via interactions with Trithorax-like ', eLife, vol. 6, no. 0, e23084 . https://doi.org/10.7554/eLife.23084
Mutations in human Atrophin1, a transcriptional corepressor, cause dentatorubral-pallidoluysian atrophy, a neurodegenerative disease. Drosophila Atrophin (Atro) mutants display many phenotypes, including neurodegeneration, segmentation, patterning an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb558ed67f90c04c83ae85380d90324a
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-135291
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-135291
Autor:
Ana S A Cohen, Valentina Milano, Natália Tkachenko, M I Van Allen, Damian B. Yap, Chieko Chijiwa, María A Ramos-Arroyo, M. E. Suzanne Lewis, Katelin N. Townsend, Margaret L. McKinnon, Mélanie Fradin, Colin J. D. Ross, Jieqing Xu, William B. Dobyns, William T. Gibson, David D. Weaver
Publikováno v:
Human Mutation
Human Mutation, 2016, 37 (3), pp.301-307. ⟨10.1002/humu.22946⟩
Human Mutation, Wiley, 2016, 37 (3), pp.301-307. ⟨10.1002/humu.22946⟩
Human Mutation, 2016, 37 (3), pp.301-307. ⟨10.1002/humu.22946⟩
Human Mutation, Wiley, 2016, 37 (3), pp.301-307. ⟨10.1002/humu.22946⟩
International audience; Weaver syndrome (WS) is a rare congenital disorder characterized by generalized overgrowth, macrocephaly, specific facial features, accelerated bone age, intellectual disability, and susceptibility to cancers. De novo mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::814236f1583257cf6d65363ece7b1382
https://univ-rennes.hal.science/hal-01255849/document
https://univ-rennes.hal.science/hal-01255849/document
Autor:
Samuel Aparicio, Steven McKinney, Damian B. Yap, Teresa Ruiz de Algara, John Dixon, Mark B. L. Carlton, Rosemary Thresher, R. Keith Humphries, Alaeddin Tafech, Bill Colledge, Michael Heuser, Malina Leung
Publikováno v:
Blood. 113:1432-1443
MLL5 is a divergent member of the Drosophila Trithorax-related (SET) domain and plant homeodomain (PHD) domain-containing chromatin regulators that are involved in the regulation of transcriptional “memory” during differentiation. Human MLL5 is l