Zobrazeno 1 - 10
of 270
pro vyhledávání: '"Owen M Rennert"'
Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment.
Autor:
Catherine A Ziats, Luke P Grosvenor, Sara M Sarasua, Audrey E Thurm, Susan E Swedo, Ahmed Mahfouz, Owen M Rennert, Mark N Ziats
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0213921 (2019)
Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder characterized by varying degrees of intellectual disability, severely delayed language development and specific facial features, and is caused by a deletion within chromosome 22q13.3. SH
Externí odkaz:
https://doaj.org/article/1bde7c760a064fb3a1eae980e5ebd04f
Autor:
Mark N Ziats, Owen M Rennert
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e24691 (2011)
The Autism Spectrum Disorders (ASD) represent a clinically heterogeneous set of conditions with strong hereditary components. Despite substantial efforts to uncover the genetic basis of ASD, the genomic etiology appears complex and a clear understand
Externí odkaz:
https://doaj.org/article/b34b61c5a96642319d974f5b0e6e2309
Autor:
Motonobu Saito, Kensuke Kumamoto, Ana I Robles, Izumi Horikawa, Bungo Furusato, Shu Okamura, Akiteru Goto, Taro Yamashita, Makoto Nagashima, Tin-Lap Lee, Vanessa J Baxendale, Owen M Rennert, Seiichi Takenoshita, Jun Yokota, Isabell A Sesterhenn, Glenwood E Trivers, S Perwez Hussain, Curtis C Harris
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e15541 (2010)
ING2 (inhibitor of growth family, member 2) is a member of the plant homeodomain (PHD)-containing ING family of putative tumor suppressors. As part of mSin3A-HDAC corepressor complexes, ING2 binds to tri-methylated lysine 4 of histone H3 (H3K4me3) to
Externí odkaz:
https://doaj.org/article/7c6a6aa2e45b4f58816bb1b60c02371a
Autor:
Yan A. Su, Owen M. Rennert, Jianxiong Zhao, Yuelin Jack Zhu, Ping He, Xuexi Wang, Qiuyang Zhang, David M. Su
Supplementary Table S4 from Two types of human malignant melanoma cell lines revealed by expression patterns of mitochondrial and survival-apoptosis genes: implications for malignant melanoma therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b0362761a069c36c6d22cbd8083e8d
https://doi.org/10.1158/1535-7163.22485230.v1
https://doi.org/10.1158/1535-7163.22485230.v1
Autor:
Yan A. Su, Owen M. Rennert, Jianxiong Zhao, Yuelin Jack Zhu, Ping He, Xuexi Wang, Qiuyang Zhang, David M. Su
Supplementary Fig. S2 from Two types of human malignant melanoma cell lines revealed by expression patterns of mitochondrial and survival-apoptosis genes: implications for malignant melanoma therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d84bf5757cfdf50b75f21a9b665cd6c
https://doi.org/10.1158/1535-7163.22485242.v1
https://doi.org/10.1158/1535-7163.22485242.v1
Autor:
Yan A. Su, Owen M. Rennert, Jianxiong Zhao, Yuelin Jack Zhu, Ping He, Xuexi Wang, Qiuyang Zhang, David M. Su
Human malignant melanoma has poor prognosis because of resistance to apoptosis and therapy. We describe identification of the expression profile of 1,037 mitochondria-focused genes and 84 survival-apoptosis genes in 21 malignant melanoma cell lines a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63010c51b166645aa555ed2bce1ff6a2
https://doi.org/10.1158/1535-7163.c.6531839.v1
https://doi.org/10.1158/1535-7163.c.6531839.v1
Publikováno v:
Pediatric Neurology. 98:46-52
Background The current classification system of neurodevelopmental disorders is based on clinical criteria; however, this method alone fails to incorporate what is now known about genomic similarities and differences between closely related clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c071268ca0a6d361f08f16b464e62bf7
https://doi.org/10.1016/j.pediatrneurol.2019.05.004
https://doi.org/10.1016/j.pediatrneurol.2019.05.004
Autor:
Cinzia Allegrucci, Amerikos Argyriou, Jérôme Caron, Hoi-Hung Cheung, Daria S. Chulpanova, M. Csobonyeiová, Anne Dubart-Kupperschmitt, Rachel Eiges, Jingping Ge, Kaomei Guan, Riikka H. Hämäläinen, Tayma Handal, Kristina V. Kitaeva, Jiesi Luo, Shalem R. Modi, Aysilu I. Mullagulova, George P. Murphy, Katie Newman, Patricia A. Olofsen, Mareike S. Poetsch, Owen M. Rennert, Albert A. Rizvanov, Ponlapat Rojnuckarin, Alisa A. Shaimardanova, Valeriya V. Solovyeva, Martin H. Steinberg, Ivo P. Touw, Kim Vanuytsel, Tao Wang, Anne Weber
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bb09dbf2a35c77efcc9d4bb35855ad6
https://doi.org/10.1016/b978-0-12-822227-0.01002-4
https://doi.org/10.1016/b978-0-12-822227-0.01002-4
Autor:
Jiajie Tu, Chao Wan, Fengjie Zhang, Lianbao Cao, Patrick Wai Nok Law, Yuyao Tian, Gang Lu, Owen M. Rennert, Wai‐Yee Chan, Hoi‐Hung Cheung
Publikováno v:
Aging Cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589ccee7fd3a0398bf04957053c48c63
https://doi.org/10.1111/acel.13227
https://doi.org/10.1111/acel.13227
Autor:
Hoi-Hung Cheung, Fengjie Zhang, Patrick Wai Nok Law, Chao Wan, Lianbao Cao, Owen M. Rennert, Jiajie Tu, Yuyao Tian, Wai-Yee Chan, Gang Lu
Publikováno v:
Aging Cell
WRN mutation causes a premature aging disease called Werner syndrome (WS). However, the mechanism by which WRN loss leads to progeroid features evident with impaired tissue repair and regeneration remains unclear. To determine this mechanism, we perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3187aa73e3b53e9dd6687299c1e1089
http://europepmc.org/articles/PMC7253065
http://europepmc.org/articles/PMC7253065