Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kelly, Erikson"'
Autor:
Burak Uzunparmak, Meng Gao, Antje Lindemann, Kelly Erikson, Li Wang, Eric Lin, Steven J. Frank, Frederico O. Gleber-Netto, Mei Zhao, Heath D. Skinner, Jared Newton, Andrew G. Sikora, Jeffrey N. Myers, Curtis R. Pickering
Publikováno v:
JCI Insight, Vol 5, Iss 23 (2020)
Caspase-8 (CASP8) is one of the most frequently mutated genes in head and neck squamous carcinomas (HNSCCs), and CASP8 mutations are associated with poor survival. The distribution of these mutations in HNSCCs suggests that they are likely to be inac
Externí odkaz:
https://doaj.org/article/14760ca81f2f40509561c39f19dd2321
Autor:
Kelly Erikson, Curtis R. Pickering, Burak Uzunparmak, Eric Lin, Meng Gao, Jared M. Newton, Jeffrey N. Myers, Heath D. Skinner, Li Wang, Andrew G. Sikora, Antje Lindemann, Mei Zhao, Frederico O. Gleber-Netto, Steven J. Frank
Publikováno v:
JCI Insight, Vol 5, Iss 23 (2020)
JCI Insight
JCI Insight
Caspase-8 (CASP8) is one of the most frequently mutated genes in head and neck squamous carcinomas (HNSCCs), and CASP8 mutations are associated with poor survival. The distribution of these mutations in HNSCCs suggests that they are likely to be inac
Autor:
Burak Uzunparmak, Meng Gao, Antje Lindemann, Kelly Erikson, Li Wang, Eric Lin, Steven J. Frank, Frederico O. Gleber-Netto, Mei Zhao, Heath D. Skinner, Jared Newton, Andrew G. Sikora, Jeffrey N. Myers, Curtis R. Pickering
Caspase-8 (CASP8) is one of the most frequently mutated genes in head and neck squamous carcinomas (HNSCC), and mutations ofCASP8are associated with poor overall survival. The distribution of these mutations in HNSCC suggests that they are likely to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::089d1e63ccd8bc74436a0800bea4ff05
https://doi.org/10.1101/2020.04.17.039040
https://doi.org/10.1101/2020.04.17.039040
Autor:
Kathleen M. Fisch, Jeffrey N. Myers, Li Shen, Meng Gao, Nene N. Kalu, Heath D. Skinner, Faye M. Johnson, Jing Wang, Yuanxin Xi, Shuling Ren, Curtis R. Pickering, Keiko Akagi, Theresa Guo, Maura L. Gillison, Tanguy Y. Seiwert, Guorong Xu, Joseph A. Califano, Kelly Erikson, Frederico O. Gleber-Netto, Mitchell J. Frederick, Xiayu Rao
Publikováno v:
JCI insight, vol 4, iss 1
Incidence of HPV(+) oropharyngeal squamous cell carcinoma (OPSCC) has been increasing dramatically. Although long-term survival rates for these patients are high, they often suffer from permanent radiotherapy-related morbidity. This has prompted the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a0b98190d0249cfaecc5b2dd290d6f
https://europepmc.org/articles/PMC6485353/
https://europepmc.org/articles/PMC6485353/
Autor:
Ivan F M Lo, James R. Lupski, Claudia M.B. Carvalho, HM Luk, Curtis R. Pickering, Kelly Erikson, Bo Yuan, Jennifer E. Posey, Shen Gu, Gordon K.C. Leung, Brian H.Y. Chung
Publikováno v:
Human Mutation. 37:160-164
Germline copy-number variants (CNVs) involving quadruplications are rare and the mechanisms generating them are largely unknown. Previously, we reported a 20-week gestation fetus with split-hand malformation; clinical microarray detected two maternal
Autor:
Kelly Erikson, Albert Mulenga
Publikováno v:
Gene. 482:78-93
Parasitic encoded proteases are essential to regulating interactions between parasites and their hosts and thus they represent attractive anti-parasitic druggable and/or vaccine target. We have utilized annotations of Ixodes scapularis proteases in g
Autor:
Kelly Erikson, Faye M. Johnson, Frederico O. Gleber-Netto, Maura L. Gillison, Curtis R. Pickering, Joseph A. Califano, Jeffrey N. Myers, Xiayu Rao, Jing Wang, Keiko Akagi
Publikováno v:
Cancer Research. 78:4621-4621
Determining which HPV+ oropharyngeal squamous cell carcinoma (OPSCC) patients will respond to therapy is of utmost important for implementation of treatment de-escalation to reduce morbidity or testing of novel therapeutic approaches. Due to the lack
Autor:
Shen, Gu, Jennifer E, Posey, Bo, Yuan, Claudia M B, Carvalho, H M, Luk, Kelly, Erikson, Ivan F M, Lo, Gordon K C, Leung, Curtis R, Pickering, Brian H Y, Chung, James R, Lupski
Publikováno v:
Human mutation. 37(2)
Germline copy-number variants (CNVs) involving quadruplications are rare and the mechanisms generating them are largely unknown. Previously, we reported a 20-week gestation fetus with split-hand malformation; clinical microarray detected two maternal