Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Kylie A, Taylor"'
Autor:
Fátima Valdés-Mora, Cathryn M. Gould, Yolanda Colino-Sanguino, Wenjia Qu, Jenny Z. Song, Kylie M. Taylor, Fabian A. Buske, Aaron L. Statham, Shalima S. Nair, Nicola J. Armstrong, James G. Kench, Kenneth M. L. Lee, Lisa G. Horvath, Minru Qiu, Alexei Ilinykh, Nicole S. Yeo-Teh, David Gallego-Ortega, Clare Stirzaker, Susan J. Clark
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
Acetylation of the histone variant H2A.Z at gene promoters is associated with oncogene activation; however, it is unclear if such modification has a role in regulating the function of enhancers. Here the authors show that acetylated H2A.Z is redistri
Externí odkaz:
https://doaj.org/article/d2ff8d2d6d19424694b455f94d09d58c
Autor:
Kylie M. Taylor, Monica Rossleigh, Daniel Christiadi, Zoltan H. Endre, Jonathan Erlich, Grant Luxton, Kate O'brien, Charles Simpson
Publikováno v:
Nephrology Dialysis Transplantation. 37:1118-1124
Background Kidney functional reserve (KFR), the only clinical kidney stress test, is not routinely measured because the complexity of measurement has limited clinical application. We investigated the utility of plasma cystatin C (CysC) after oral pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d252401689f0918193bff801c01ae020
https://doi.org/10.1093/ndt/gfab188
https://doi.org/10.1093/ndt/gfab188
Autor:
Monique L. Howard, Stephen J. Palmer, Kylie M. Taylor, Geoffrey J. Arthurson, Matthew W. Spitzer, Xin Du, Terence Y.C. Pang, Thibault Renoir, Edna C. Hardeman, Anthony J. Hannan
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 3, Pp 913-922 (2012)
Insufficiency of the transcriptional regulator GTF2IRD1 has become a strong potential explanation for some of the major characteristic features of the neurodevelopmental disorder Williams–Beuren syndrome (WBS). Genotype/phenotype correlations in hu
Externí odkaz:
https://doaj.org/article/e82c8a79eb184c809939e991a4f0bc8c
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49283 (2012)
GTF2IRD1 is one of the genes implicated in Williams-Beuren syndrome, a disease caused by haploinsufficiency of certain dosage-sensitive genes within a hemizygous microdeletion of chromosome 7. GTF2IRD1 is a prime candidate for some of the major featu
Externí odkaz:
https://doaj.org/article/cc747b992ae44ab4931d6407dc917a2f
Autor:
Yolanda Colino-Sanguino, Kylie M. Taylor, Lisa G. Horvath, Clare Stirzaker, Jenny Z. Song, Cathryn M. Gould, Wenjia Qu, Shalima S. Nair, James G. Kench, Nicola J. Armstrong, Fabian A. Buske, Nicole S. Yeo-Teh, Minru Qiu, Aaron L. Statham, David Gallego-Ortega, Fatima Valdes-Mora, Alexei Ilinykh, Susan J. Clark, Kenneth Lee
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
Nature Communications
Nature Communications
Acetylation of the histone variant H2A.Z (H2A.Zac) occurs at active promoters and is associated with oncogene activation in prostate cancer, but its role in enhancer function is still poorly understood. Here we show that H2A.Zac containing nucleosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::047fe950b18274b5b24ddd397bdbd31a
https://doaj.org/article/d2ff8d2d6d19424694b455f94d09d58c
https://doaj.org/article/d2ff8d2d6d19424694b455f94d09d58c
Autor:
Zoltan H. Endre, Jonathan Erlich, Sean E. Kennedy, Adam Jaffe, M. Coffey, S. Boardman, Kylie M. Taylor, Chee Y. Ooi
Publikováno v:
Journal of Cystic Fibrosis. 19:S7-S8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76ad705c72fadea0af992fed1eff0da3
https://doi.org/10.1016/s1569-1993(20)30187-9
https://doi.org/10.1016/s1569-1993(20)30187-9
Autor:
Jonathan Erlich, Adam Jaffe, Sean E. Kennedy, S. Boardman, M. Coffey, Kylie M. Taylor, Chee Y. Ooi, Zoltan H. Endre
Publikováno v:
Journal of Cystic Fibrosis. 19:S103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c67c2918d5b9c6ec5f404f5933455ac
https://doi.org/10.1016/s1569-1993(20)30501-4
https://doi.org/10.1016/s1569-1993(20)30501-4
Publikováno v:
Kidney International Reports. 4:S243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6151e85d6eba3ce2db04fbb1a15dd066
https://doi.org/10.1016/j.ekir.2019.05.606
https://doi.org/10.1016/j.ekir.2019.05.606
Autor:
Sara J. Bontempo, Edna C. Hardeman, Enoch S. E. Tay, Peter W. Gunning, Frances A. Lemckert, Nicole Santucci, Jocelyn Widagdo, Kylie M. Taylor, Stephen J. Palmer, Jeff Hook
Publikováno v:
Journal of Biological Chemistry. 285:4715-4724
The GTF2IRD1 gene is of principal interest to the study of Williams-Beuren syndrome (WBS). This neurodevelopmental disorder results from the hemizygous deletion of a region of chromosome 7q11.23 containing 28 genes including GTF2IRD1. WBS is thought
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dc15e30d0e4a51f08d7e41b0026a232
https://doi.org/10.1074/jbc.m109.086660
https://doi.org/10.1074/jbc.m109.086660
Autor:
Peter D, Massey, Glenn, Pearce, Kylie A, Taylor, Lisa, Orcher, Sherry, Saggers, David N, Durrheim
Publikováno v:
Rural and remote health. 9(3)
Aboriginal people are particularly vulnerable to pandemic influenza A, H1N109. This was first recognized in the First Nations of Canada. There have been calls for close planning with Aboriginal people to manage these risks. This article describes the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d84ad05085b7125a7c31bf59155ae733
https://pubmed.ncbi.nlm.nih.gov/19728766
https://pubmed.ncbi.nlm.nih.gov/19728766