Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kristianne M. Oristian"'
Autor:
Alexander R. Kovach, Kristianne M. Oristian, David G. Kirsch, Rex C. Bentley, Changde Cheng, Xiang Chen, Po‐Han Chen, Jen‐Tsan Ashley Chi, Corinne M. Linardic
Publikováno v:
Molecular Oncology, Vol 16, Iss 20, Pp 3587-3605 (2022)
Rhabdomyosarcoma (RMS), a cancer characterized by features of skeletal muscle, is the most common soft‐tissue sarcoma of childhood. With 5‐year survival rates among high‐risk groups at
Externí odkaz:
https://doaj.org/article/0db7f3865e1540b1a057d18db74bc12c
Autor:
Cara E. Shields, Sindhu Potlapalli, Selma M. Cuya‐Smith, Sarah K. Chappell, Dongdong Chen, Daniel Martinez, Jennifer Pogoriler, Komal S. Rathi, Shiv A. Patel, Kristianne M. Oristian, Corinne M. Linardic, John M. Maris, Karmella A. Haynes, Robert W. Schnepp
Publikováno v:
Molecular Oncology, Vol 15, Iss 8, Pp 2156-2171 (2021)
Rhabdomyosarcoma (RMS) is an aggressive pediatric soft tissue sarcoma. There are two main subtypes of RMS, alveolar rhabdomyosarcoma (ARMS) and embryonal rhabdomyosarcoma. ARMS typically encompasses fusion‐positive rhabdomyosarcoma, which expresses
Externí odkaz:
https://doaj.org/article/54ae8d279f04470ca6884d0bbba468ac
Autor:
Jenny J. Li, Alexander R. Kovach, Margaret DeMonia, Katherine K. Slemmons, Kristianne M. Oristian, Candy Chen, Corinne M. Linardic
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma. The two predominant histologic variants of RMS, embryonal and alveolar rhabdomyosarcoma (eRMS and aRMS, respectively), carry very different prognoses. While eRMS is ass
Externí odkaz:
https://doaj.org/article/e07c4697734344668dbd9b9c8ec6c4f3
Autor:
Katherine K. Slemmons, Michael D. Deel, Yi-Tzu Lin, Kristianne M. Oristian, Nina Kuprasertkul, Katia C. Genadry, Po-Han Chen, Jen-Tsan Ashley Chi, Corinne M. Linardic
Publikováno v:
Biology Open, Vol 10, Iss 2 (2021)
The development of three-dimensional cell culture techniques has allowed cancer researchers to study the stemness properties of cancer cells in in vitro culture. However, a method to grow PAX3-FOXO1 fusion-positive rhabdomyosarcoma (FP-RMS), an aggre
Externí odkaz:
https://doaj.org/article/daca80c943474799ab9e57d405f1f363
Autor:
Yuning J. Tang, Jianguo Huang, Hidetoshi Tsushima, Ga I. Ban, Hongyuan Zhang, Kristianne M. Oristian, Vijitha Puviindran, Nerissa Williams, Xiruo Ding, Jianhong Ou, Sin-Ho Jung, Chang-Lung Lee, Yiqun Jiao, Benny J. Chen, David G. Kirsch, Benjamin A. Alman
Publikováno v:
Cell Reports, Vol 28, Iss 11, Pp 2837-2850.e5 (2019)
Summary: Cellular heterogeneity is frequently observed in cancer, but the biological significance of heterogeneous tumor clones is not well defined. Using multicolor reporters and CRISPR-Cas9 barcoding, we trace clonal dynamics in a mouse model of sa
Externí odkaz:
https://doaj.org/article/7903da5dab684dbe9e99ae031438d1ef
Autor:
Corinne M. Linardic, Rex C. Bentley, Kristianne M. Oristian, Nina Kuprasertkul, Lisa E.S. Crose, Breanne A. Burgess, Katia C. Genadry, Ashley R. Hinson, Katherine K. Slemmons, Michael D. Deel
Additional analysis of xenograft tumors and drug studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643385277ea4ba55a1561a9104b64fde
https://doi.org/10.1158/1078-0432.22465064
https://doi.org/10.1158/1078-0432.22465064
Autor:
Corinne M. Linardic, Rex C. Bentley, Kristianne M. Oristian, Nina Kuprasertkul, Lisa E.S. Crose, Breanne A. Burgess, Katia C. Genadry, Ashley R. Hinson, Katherine K. Slemmons, Michael D. Deel
PCR Primers for quantitative qRT-PCR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258cd9e002efe534f70dbfb5f165f9d6
https://doi.org/10.1158/1078-0432.22465055
https://doi.org/10.1158/1078-0432.22465055
Autor:
Corinne M. Linardic, Rex C. Bentley, Kristianne M. Oristian, Nina Kuprasertkul, Lisa E.S. Crose, Breanne A. Burgess, Katia C. Genadry, Ashley R. Hinson, Katherine K. Slemmons, Michael D. Deel
Supplementary Table and Figure Legends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ab1767b28202764a3125d43b7d05cd2
https://doi.org/10.1158/1078-0432.22465058
https://doi.org/10.1158/1078-0432.22465058
Autor:
Corinne M. Linardic, Rex C. Bentley, Kristianne M. Oristian, Nina Kuprasertkul, Lisa E.S. Crose, Breanne A. Burgess, Katia C. Genadry, Ashley R. Hinson, Katherine K. Slemmons, Michael D. Deel
Purpose: Alveolar rhabdomyosarcoma (aRMS) is a childhood soft tissue sarcoma driven by the signature PAX3-FOXO1 (P3F) fusion gene. Five-year survival for aRMS is Experimental Design: After determining from publicly available datasets that TAZ is upre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44251c255f4b67cd301e77691184a0e2
https://doi.org/10.1158/1078-0432.c.6525911.v1
https://doi.org/10.1158/1078-0432.c.6525911.v1
Autor:
Katherine K. Slemmons, Margaret DeMonia, Kristianne M. Oristian, Alexander R. Kovach, Candy Chen, Jenny J. Li, Corinne M. Linardic
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Scientific Reports
Scientific Reports
Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma. The two predominant histologic variants of RMS, embryonal and alveolar rhabdomyosarcoma (eRMS and aRMS, respectively), carry very different prognoses. While eRMS is associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18165d80918b3735cd83e8ea91bd0911
https://doaj.org/article/e07c4697734344668dbd9b9c8ec6c4f3
https://doaj.org/article/e07c4697734344668dbd9b9c8ec6c4f3