Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kylie M Taylor"'
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:
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:
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:
Monique L. Howard, Matthew W. Spitzer, Xin Du, Terence Y. Pang, Stephen J. Palmer, Geoffrey J. Arthurson, Anthony J. Hannan, Thibault Renoir, Kylie M. Taylor, Edna C. Hardeman
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 huma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74c59ec963b35486fdd2bc0c124a3350
https://doi.org/10.1016/j.nbd.2011.12.010
https://doi.org/10.1016/j.nbd.2011.12.010
Publikováno v:
Cancer Research. 75:1647-1647
Melanoma is one the most commonly diagnosed cancers in Australia and while treatment is generally successful if the tumor is identified early, once the disease begins to spread the prognosis is considerably worse. The recent approval of new targeted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbf3947b0fba0eacc25ef57573c5119d
https://doi.org/10.1158/1538-7445.am2015-1647
https://doi.org/10.1158/1538-7445.am2015-1647
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49283 (2012)
PLoS ONE
PLoS ONE
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cca7077d9854e9e6118d46ca3d32b7f
https://doi.org/10.1371/journal.pone.0049283
https://doi.org/10.1371/journal.pone.0049283
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