Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Vickie Hsuan"'
Autor:
Suzette Farber-Katz, Vickie Hsuan, Sitao Wu, Tyler Landrith, Huy Vuong, Dong Xu, Bing Li, Jayne Hoo, Stephanie Lam, Sarah Nashed, Deborah Toppmeyer, Phillip Gray, Ginger Haynes, Hsiao-Mei Lu, Aaron Elliott, Brigette Tippin Davis, Rachid Karam
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
Clinical genetic testing for hereditary breast and ovarian cancer (HBOC) is becoming widespread. However, the interpretation of variants of unknown significance (VUS) in HBOC genes, such as the clinically actionable genes BRCA1 and BRCA2, remain a ch
Externí odkaz:
https://doaj.org/article/ac330a471ac74523a1d861cc1c74206b
Autor:
Rachid Karam, Tina Pesaran, Phillip Gray, Pei Tsai, Adam C. Chamberlin, Hansook Kim Chong, Blair R. Conner, Vickie Hsuan, Aaron Elliott, Stephanie Lam, Sara Willett, Min-Sun Park, Wenbo Mu, Marcy E. Richardson
Publikováno v:
Genetics in Medicine
Purpose Gross duplications are ambiguous in terms of clinical interpretation due to the limitations of the detection methods that cannot infer their context, namely, whether they occur in tandem or are duplicated and inserted elsewhere in the genome.
Autor:
Sitao Wu, Yan Chang, Kefeng Lei, Jiaoti Huang, Yanjing Li, Qianben Wang, Yiping He, Qing Yang, Suzette Farber-Katz, Allen C. Gao, Qingfu Zhang, Hailiang Hu, John K. Lee, Donghui Cheng, Tyler Landrith, Qing Cheng, Yinglu Zhou, Shannon J. McCall, Matthew Rettig, Vickie Hsuan, Jung-Wook Park, Andrew S. Goldstein, Owen N. Witte, Rachid Karam, Bryan A. Smith, Xufeng Chen, Andrew J. Armstrong, Bing Li, Hong Zhang, Daniel G. Taylor, Melissa Flowers, Lingfan Xu, William Butler
Publikováno v:
Science translational medicine, vol 11, iss 521
Sci Transl Med
Sci Transl Med
Hormonal therapy targeting androgen receptor (AR) is initially effective to treat prostate cancer (PCa), but it eventually fails. It has been hypothesized that cellular heterogeneity of PCa, consisting of AR(+) luminal tumor cells and AR(−) neuroen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b724d9d759df256b9ea585ba7e770d5
https://escholarship.org/uc/item/1h73t7rk
https://escholarship.org/uc/item/1h73t7rk
Autor:
kConFab Investigators, Melissa C. Southey, John F. Pearson, Tina Pesaran, Logan C. Walker, Miguel de la Hoya, Sitao Wu, Dominique Vaur, Peter Devilee, Vickie Hsuan, Vanesa García-Barberán, Raphaël Leman, Patricia Llovet, Johan Vallon-Christersson, Irene López-Perolio, Raquel Behar, Alexandra Martins, Grégoire Davy, Anders Kvist, Vanessa Lattimore, Nicolas Goardon, Trinidad Caldés, Åke Borg, Laurent Castera, Pedro Pérez-Segura, Maaike P.G. Vreeswijk, Rachid Karam, Pilar Garre, Eduardo Díaz-Rubio, Eladio Velasco, Sophie Krieger, Kathleen S. Hruska, Alberto Valenzuela-Palomo, Amanda B. Spurdle
Publikováno v:
Journal of Medical Genetics, 56(7), 453-460. BMJ PUBLISHING GROUP
Journal of Medical Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Medical Genetics, BMJ Publishing Group, 2019, 56 (7), pp.453-460. ⟨10.1136/jmedgenet-2018-105834⟩
Journal of Medical Genetics
Digital.CSIC. Repositorio Institucional del CSIC
instname
Journal of Medical Genetics, BMJ Publishing Group, 2019, 56 (7), pp.453-460. ⟨10.1136/jmedgenet-2018-105834⟩
Cancer genetics: Original article.
[Background] PALB2 monoallelic loss-of-function germ-line variants confer a breast cancer risk comparable to the average BRCA2 pathogenic variant. Recommendations for risk reduction strategies in carriers are s
[Background] PALB2 monoallelic loss-of-function germ-line variants confer a breast cancer risk comparable to the average BRCA2 pathogenic variant. Recommendations for risk reduction strategies in carriers are s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf122896e2ef86221ef12014cfcfc9cb
http://hdl.handle.net/1887/121881
http://hdl.handle.net/1887/121881
Autor:
Phillip Gray, Swati Shah, Lisa Uyeda, Elizabeth R. Plimack, Matthew Zibelman, Marijo Bilusic, Lavinia Dobrea, Hsaio Mei Lu, Huy Gia Vuong, Vickie Hsuan, Aaron Elliott, Mike Janicek, Wenbo Mu, Lawrence D. Wagman, Jayne Hoo, Erica A. Golemis, Harshil Patel, Susanne Fox, Pei Tsai, Sandra Brown, Ranee Mehra
Publikováno v:
Oncotarget
The development of targeted therapies for both germline and somatic DNA mutations has increased the need for molecular profiling assays to determine the mutational status of specific genes. Moreover, the potential of off-label prescription of targete
Autor:
Sitao Wu, Suzette Farber-Katz, Dong Xu, Deborah Toppmeyer, Ginger Haynes, Rachid Karam, Vickie Hsuan, Aaron Elliott, Bing Li, Jayne Hoo, Hsiao Mei Lu, Brigette Tippin Davis, Sarah Nashed, Tyler Landrith, Huy Gia Vuong, Phillip Gray, Stephanie Lam
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
Frontiers in Oncology
Frontiers in Oncology
Clinical genetic testing for hereditary breast and ovarian cancer (HBOC) is becoming widespread. However, the interpretation of variants of unknown significance (VUS) in HBOC genes, such as the clinically actionable genes BRCA1 and BRCA2, remain a ch
Autor:
Marcy E. Richardson, Hansook Chong, Wenbo Mu, Blair R. Conner, Vickie Hsuan, Sara Willett, Stephanie Lam, Pei Tsai, Tina Pesaran, Adam C. Chamberlin, Min-Sun Park, Phillip Gray, Rachid Karam, Aaron Elliott
Publikováno v:
Genetics in Medicine
Gross duplications are ambiguous in terms of clinical interpretation due to the limitations of the detection methods that cannot infer their context, namely, whether they occur in tandem or are duplicated and inserted elsewhere in the genome. We inve
Autor:
Matthew Tripp, Nancy F. Hansen, Qimin Chao, Mani Gurjal, Carolyn C. Tang, Shelise Brooks, Maiko Nakajima, Motoaki Seki, Audrey Southwick, Hank C. Wu, Ronald W. Davis, Cecilia Wong, Rosa Cheuk, Yuki Yamamura, Michelle Nguyen, Kazuo Shinozaki, Andrew D. Goldsmith, Marie M. H. Chan, Christopher Kim, Joseph R. Ecker, Eric Koesema, Kayoko Yamada, Akiko Enju, Yoshihide Hayashizaki, Chanda Johnson-Hopson, Charlie H. Chang, Erika Wallender, Tetsuya Sakurai, Justine M. Deng, Paul Shinn, Vickie Hsuan, Takahiro Arakawa, Kei Iida, Asako Kamiya, Huaming Chen, Masakazu Satou, Shirley X. Liu, Bao Lam, Joseph M. Dale, Courtney Onodera, Meagan Karnes, Jun Lim, Racquel Tamse, Jenny Banh, Shiaulou Yuan, George Karlin-Newmann, Nathan Choy, Ted Jones, Paul X. Jiang, Troy Wu, Leah Bowser, Junko Ishida, Yasser Ansari, Kenji Akiyama, Guixia Yu, Maria Vaysberg, Mitsue J. Toriumi, Jeong M. Lee, Paul K. Pham, Cristina C. Meyers, Curtis J. Palm, Piero Carninci, Hitomi Sakano, Molly Miranda, Hong L. Quach, Mari Narusaka, Jun Kawai, Fumika Banno, Shehnaz Khan, Athanasios Theologis
Publikováno v:
ResearcherID
Functional analysis of a genome requires accurate gene structure information and a complete gene inventory. A dual experimental strategy was used to verify and correct the initial genome sequence annotation of the reference plant Arabidopsis . Sequen
Autor:
Jayne Hoo, Suzette Farber-Katz, Dong Xu, Sitao Wu, Vickie Hsuan, Rachid Karam, Aaron Elliott, Phillip Gray, Huy Gia Vuong, Hsiao-Mei Lu
Publikováno v:
Cancer Research. 77:1450-1450
Genetic testing for hereditary breast and ovarian cancer (HBOC) is becoming increasingly widespread in the era of precision medicine. The implementation of next-generation sequencing (NGS) has resulted in an explosion of genetic data. While the major
BDNF, which acts through tropomyosin-related kinase B (TrkB) receptors during mammalian development, also enhances long-term synaptic facilitation (LTF) in adult Aplysia . Because LTF is a substrate for long-term memory (LTM) in Aplysia , we examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03fe2ecbaa19ea97201ba7be6bce769f
https://europepmc.org/articles/PMC1599935/
https://europepmc.org/articles/PMC1599935/