Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sumaira Zamurrad"'
Publikováno v:
Cell Reports, Vol 22, Iss 9, Pp 2359-2369 (2018)
Summary: Mutations in KDM5 family histone demethylases cause intellectual disability in humans. However, the molecular mechanisms linking KDM5-regulated transcription and cognition remain unknown. Here, we establish Drosophila as a model to understan
Externí odkaz:
https://doaj.org/article/b187904b04464079aec529b3a1b5186a
SummaryMutations in the genes encoding the KDM5 family of histone demethylases are observed in individuals with intellectual disability (ID). Despite clear evidence linking KDM5 function to neurodevelopmental pathways, how this family of proteins imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c5603199ea5ff9cefb94fbef6c2c9ac
https://doi.org/10.1101/2020.10.12.335711
https://doi.org/10.1101/2020.10.12.335711
Publikováno v:
SSRN Electronic Journal.
Mutations in the genes encoding the KDM5 family of histone demethylases are observed in individuals with intellectual disability (ID). Despite clear evidence linking KDM5 function to neurodevelopmental pathways, how this family of proteins impacts tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f67228efaa9477a575b143677f79a2b
https://doi.org/10.2139/ssrn.3717160
https://doi.org/10.2139/ssrn.3717160
Publikováno v:
Cell Reports, Vol 22, Iss 9, Pp 2359-2369 (2018)
Summary: Mutations in KDM5 family histone demethylases cause intellectual disability in humans. However, the molecular mechanisms linking KDM5-regulated transcription and cognition remain unknown. Here, we establish Drosophila as a model to understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5423075a246161da7bf7f8ebe9cde45
http://www.sciencedirect.com/science/article/pii/S2211124718301864
http://www.sciencedirect.com/science/article/pii/S2211124718301864
Publikováno v:
Cell reports
SUMMARY Mutations in the genes encoding the lysine demethylase 5 (KDM5) family of histone demethylases are observed in individuals with intellectual disability (ID). Despite clear evidence linking KDM5 function to neurodevelopmental pathways, how thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2698d36b5e3d9696cccddef5b301cda
https://doi.org/10.1016/j.celrep.2021.108753
https://doi.org/10.1016/j.celrep.2021.108753
Publikováno v:
G3: Genes | Genomes | Genetics. Dec2016, Vol. 6 Issue 12, p3765-3786. 22p.