Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Emily H. Pritchard"'
Autor:
Alan Cooper, Rachel Turkington, David T. F. Dryden, Margaret Nutley, Gareth A. Roberts, Emily H. Pritchard, Augoustinos S. Stephanou, Mark R. Tock
Publikováno v:
Biochemical and Biophysical Research Communications. 378:129-132
The ocr protein of bacteriophage T7 is a structural and electrostatic mimic of approximately 24 base pairs of double-stranded B-form DNA. As such, it inhibits all Type I restriction and modification (R/M) enzymes by blocking their DNA binding grooves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d66f03ff4f506fe56dac614d015c32c
https://doi.org/10.1016/j.bbrc.2008.11.014
https://doi.org/10.1016/j.bbrc.2008.11.014
Publikováno v:
Nolen, L D, Boyle, S, Ansari, M, Pritchard, E & Bickmore, W A 2013, ' Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF ', Human Molecular Genetics, vol. 22, no. 20, pp. 4180-93 . https://doi.org/10.1093/hmg/ddt265
Human Molecular Genetics
Human Molecular Genetics
Cornelia de Lange syndrome (CdLS) is a developmental disorder caused by mutations in NIPBL, a protein which has functionally been associated with the cohesin complex. Mutations in core cohesin complex components have also been reported in individuals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471e45ca2acc1f63fbbce5bf57012863
https://hdl.handle.net/20.500.11820/02ab2fe5-4ad8-43a3-9b2d-13abd3ed82e2
https://hdl.handle.net/20.500.11820/02ab2fe5-4ad8-43a3-9b2d-13abd3ed82e2
