Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Francys Alarcon"'
Autor:
Lina Zelinger, Charmeine Ko, Francys Alarcon, Samuel Koo, Kenneth Thomas, Hyunjun Nam, Fernando Lopez Diaz, Segun Jung, Fei Ye, Shashikant Kulkarni
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100109- (2023)
Externí odkaz:
https://doaj.org/article/b8d2249ccede4bd8bcf779e33c1c6d7b
Autor:
Lina Zelinger, Samuel Koo, Francys Alarcon, Charmeine Ko, Brad B Thomas, Segun C Jung, Ying Wang, Fei Ye, Shashikant Kulkarni
Publikováno v:
Blood. 140:11870-11871
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::493c0f2b1f00913b0f0955f0a72af32b
https://doi.org/10.1182/blood-2022-166932
https://doi.org/10.1182/blood-2022-166932
Abstract 219: Single-tube NGS profiling allows identification of molecular signature in ALL patients
Autor:
Lina Zelinger, Samuel Koo, Charmeine Ko, Francys Alarcon, Kenneth B. Thomas, Segun C. Jung, Fernando J. Lopez Diaz, Fei Ye, Shashikant Kulkarni
Publikováno v:
Cancer Research. 83:219-219
Background: Acute lymphoblastic leukemia (ALL) can be classified to subtypes by molecular signatures correlating to prognosis and treatment regimen, making accurate molecular profiling of interest for both clinical and research communities. NGS techn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::959a70513244c54b46d0e89ab4b7917e
https://doi.org/10.1158/1538-7445.am2023-219
https://doi.org/10.1158/1538-7445.am2023-219
Autor:
Fei Ye, Tibor Gyuris, Samuel Koo, Christophe Magnan, Ryan Bender, Brad B Thomas, Sally Agersborg, Archana Ramesh, Vincent Funari, Fernando J. Lopez-Diaz, Abhisek Ghosal, Hyunjun Nam, Paris Petersen, Francys Alarcon, Rudy Fabunan, Segun C Jung, Soo Jin Kang
Publikováno v:
Blood. 138:4925-4925
Background: Paired-box Pax gene family protein 5 (PAX5)/B-cell specific activator protein (BSAP) is a transcription factor encoded by the PAX5 gene and has an essential role in B-cell differentiation and maturation. High PAX5 expression is detected e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b8feebc405802bc00b7795d8cc00269
https://doi.org/10.1182/blood-2021-154043
https://doi.org/10.1182/blood-2021-154043
Autor:
Soo Jin Kang, Francys Alarcon, Fernando J. Lopez-Diaz, Tibor Gyuris, Hyunjun Nam, Samuel Koo, Archana Ramesh, Rudy Fabunan, Vincent Funari, Paris Petersen, Sally Agersborg, Christophe Magnan, Ryan Bender, Segun C Jung, Abhisek Ghosal, Fei Ye, Brad B Thomas
Publikováno v:
Blood. 138:1875-1875
Background: Acute Lymphocytic Leukemia (ALL) is the most common childhood cancer and accounts for about a quarter of adult acute leukemias. Current NCCN recommendations for clinical testing for risk stratification and treatment guidance include karyo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5e691f3b340e4e6269b41670b2fc034
https://doi.org/10.1182/blood-2021-148012
https://doi.org/10.1182/blood-2021-148012
Autor:
Samuel Koo, Paris Petersen, Hyunjun Nam, Susan Yamahata, Sally Agersborg, Francys Alarcon, Christophe Magnan, Fernando J. Lopez-Diaz, Rudy Fabunan, Tibor Gyuris, Brad B Thomas, Archana Ramesh, Ryan Bender, Soo Jin Kang, Fei Ye, Vincent Funari, Segun C Jung, Abhisek Ghosal
Publikováno v:
Blood. 138:2961-2961
Background: Multiple myeloma (MM) is a blood cancer type affecting plasma cell in bone marrow. MM is heterogenous in nature but t(11;14)(q13;q32) translocation is a common prognostic marker among MM patients. One of the most frequent oncogenic driver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60abfaf92d9b4f3e5cae74dbd7e0e557
https://doi.org/10.1182/blood-2021-153253
https://doi.org/10.1182/blood-2021-153253
Autor:
Lauryn Keeler, Christophe Magnan, Yongxin Yu, Shiping Jiang, Eve Shinbrot, Vincent Funari, Segun C Jung, Yanglong Mou, Fei Ye, Hyunjun Nam, Tessa Weiss, Ryan Bender, Brad B Thomas, Lawrence M. Weiss, Francys Alarcon, Sally Agersborg
Publikováno v:
Blood. 136:29-30
Background: A cost effective and comprehensive genomic profiling (CGP) approach for diagnosis, risk stratification and therapy would be useful for the evaluation of oncologic specimens. Available approaches involving additive testing for DNA and RNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d6ca387db417f3a5c43d4c69ee8ec7c
https://doi.org/10.1182/blood-2020-140460
https://doi.org/10.1182/blood-2020-140460
Autor:
Brad B Thomas, Christophe Magnan, Francys Alarcon, Fei Ye, Eve Shinbrot, Vincent Funari, Segun C Jung, Sally Agersborg, Yanglong Mou, Cynthie Wong, Ryan Bender, Lawrence M. Weiss, Tibor Gyuris
Publikováno v:
Cancer Research. 81:2208-2208
Background: To comprehensively profile mutations in hematologic malignancies, we developed a targeted multimodal NGS assay that can detect SNVs, InDels, fusions, gene expression, and copy number variations from total nucleic acid (TNA) in a single tu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c4ca285cc690700b7e8b29f579f0988
https://doi.org/10.1158/1538-7445.am2021-2208
https://doi.org/10.1158/1538-7445.am2021-2208