Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Shannon Skarshaug"'
Autor:
Caoimhe Egan, Alina Nicolae, Justin Lack, Hye-Jung Chung, Shannon Skarshaug, Thu Anh Pham, Winnifred Navarro, Zied Abdullaev, Nadine S. Aguilera, Liqiang Xi, Svetlana Pack, Stefania Pittaluga, Elaine S. Jaffe, Mark Raffeld
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Histiocytic sarcoma is a rare malignant neoplasm that may occur de novo or in the context of a previous hematologic malignancy or mediastinal germ cell tumor. Here, we performed whole exome sequencing and RNA-sequencing (RNA-Seq) on 21 archival cases
Externí odkaz:
https://doaj.org/article/95046bccf4214eeb8ab9261f884d1be1
Autor:
Martha Quezado, Hye-Jung Chung, Lola Saidkhodjaeva, Manoj Tyagi, Zhichao Wu, Sushma Nagaraj, Mark R. Gilbert, Andreas von Deimling, Rust Turakulov, Shannon Skarshaug, Michael Newford, Antonios Papanicolau-Sengos, Drew Pratt, Kenneth Aldape, Kayla O’Donnell, Abigail K. Suwala, Candice Perry, Svetlana Pack, Vineela Gangalapudi, Shirin Karimi, Farshad Nassiri, Yasin Mamatjan, Zied Abdullaev, Felix Sahm, Valerie Zgonc, Liqiang Xi, Gelareh Zadeh, Mark Raffeld, Kristin Valdez, Eytan Ruppin
Publikováno v:
Neuro Oncol
Background Accurate CNS tumor diagnosis can be challenging, and methylation profiling can serve as an adjunct to classify diagnostically difficult cases. Methods An integrated diagnostic approach was employed for a consecutive series of 1258 surgical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5482cffe1dcc272c160e68427c43dc78
https://doi.org/10.1093/neuonc/noab227
https://doi.org/10.1093/neuonc/noab227
Autor:
Martha Quezado, Mark R. Gilbert, Andreas von Deimling, Kayla O’Donnell, Joseph Chinquee, Felix Sahm, Antonios Papanicolau-Sengos, Manoj Tyagi, Abigail K. Suwala, Svetlana Pack, Michael Newford, Sushma Nagaraj, Drew Pratt, Valerie Zgonc, Shannon Skarshaug, Zhichao Wu, Liqiang Xi, Hye-Jung Chung, Gelareh Zadeh, Lola Saidkhodjaeva, Kenneth Aldape, Mark Raffeld, Candice Perry, Zied Abdullaev, Eytan Ruppin, Farshad Nassiri
Publikováno v:
Neuro Oncol
DNA methylation profiling coupled with the application of CNS tumor methylation classifier has contributed to precise and accurate diagnostics for a range of tumor types involving the central nervous system. The impact and characteristics of methylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7478c6c721f5c54228d53aed23ad858
https://europepmc.org/articles/PMC8598573/
https://europepmc.org/articles/PMC8598573/
Autor:
Svetlana Pack, Elaine S. Jaffe, Zied Abdullaev, Shannon Skarshaug, Alina Nicolae, Justin B. Lack, Caoimhe Egan, Thu Anh Pham, Hye-Jung Chung, Mark Raffeld, Liqiang Xi, Winnifred Navarro, Stefania Pittaluga, Nadine S. Aguilera
Publikováno v:
Haematologica. 105:951-960
Histiocytic sarcoma is a rare malignant neoplasm that may occur de novo or in the context of a previous hematologic malignancy or mediastinal germ cell tumor. Here, we performed whole exome sequencing and RNA-sequencing (RNA-Seq) on 21 archival cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b65be2899ea082eea41933b01c7ae7
https://doi.org/10.3324/haematol.2019.230375
https://doi.org/10.3324/haematol.2019.230375
Autor:
Svetlana Pack, Elaine S. Jaffe, Zied Abdullaev, Shannon Skarshaug, Stefania Pittaluga, Liqiang Xi, Caoimhe Egan, Mark Raffeld, Thu Anh Pham, Justin B. Lack
Publikováno v:
Mod Pathol
Histiocytic sarcoma and tumors with dendritic cell differentiation (HDT) are uncommon neoplasms often with an aggressive clinical course that may occur in association with another hematologic malignancy or mediastinal germ cell tumor (secondary HDT,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4daaff0ffe346e547c170ec75ac75a1d
https://europepmc.org/articles/PMC9161669/
https://europepmc.org/articles/PMC9161669/
Autor:
Michael Blaese, Fred S. Rosen, Robin Parmley, Jurg Ott, L. A. Sandkuyl, Louis M. Kunkel, Gail A. P. Bruns, David C. Page, Sau-Ping Kwan, Shannon Skarshaug
Publikováno v:
Genomics. 3(1)
The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive genetic disease in which the molecular defect is unknown. In 15 families with WAS, seven restriction fragment length polymorphic loci from the X chromosome were used to map the disease locus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::931903d758fbdb5ea6a678f9d27be545
https://pubmed.ncbi.nlm.nih.gov/2906042
https://pubmed.ncbi.nlm.nih.gov/2906042