Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Gordana Raca"'
Autor:
Andy W. C. Pang, Karena Kosco, Nikhil S. Sahajpal, Arthi Sridhar, Jen Hauenstein, Benjamin Clifford, Joey Estabrook, Alex D. Chitsazan, Trilochan Sahoo, Anwar Iqbal, Ravindra Kolhe, Gordana Raca, Alex R. Hastie, Alka Chaubey
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3263 (2023)
Structural variations (SVs) play a key role in the pathogenicity of hematological malignancies. Standard-of-care (SOC) methods such as karyotyping and fluorescence in situ hybridization (FISH), which have been employed globally for the past three dec
Externí odkaz:
https://doaj.org/article/c634aea7b1764212a52720e1928fe2f0
Autor:
Jason Saliba, Arpad Danos, Kilannin Krysiak, Adam Coffman, Susanna Kiwala, Joshua McMichael, Cameron Grisdale, Ian King, Shamini Selvarajah, Xinjie Xu, Rashmi Kanagal-Shamanna, Laveniya Satgunaseelan, David Meredith, Mark Evans, Charles Mullighan, Yassmine Akkari, Gordana Raca, Angshumoy Roy, Alex Wagner, Ramaswamy Govindan, Obi Griffith, Malachi Griffith
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100098- (2023)
Externí odkaz:
https://doaj.org/article/24351fa03483446cb567a340e61249e1
Autor:
Arpad M. Danos, Kilannin Krysiak, Erica K. Barnell, Adam C. Coffman, Joshua F. McMichael, Susanna Kiwala, Nicholas C. Spies, Lana M. Sheta, Shahil P. Pema, Lynzey Kujan, Kaitlin A. Clark, Amber Z. Wollam, Shruti Rao, Deborah I. Ritter, Dmitriy Sonkin, Gordana Raca, Wan-Hsin Lin, Cameron J. Grisdale, Raymond H. Kim, Alex H. Wagner, Subha Madhavan, Malachi Griffith, Obi L. Griffith
Publikováno v:
Genome Medicine, Vol 11, Iss 1, Pp 1-12 (2019)
Abstract Manually curated variant knowledgebases and their associated knowledge models are serving an increasingly important role in distributing and interpreting variants in cancer. These knowledgebases vary in their level of public accessibility, a
Externí odkaz:
https://doaj.org/article/39ec4aa7be3443f3b794858501c8d184
Autor:
Michael W. Drazer, Sabah Kadri, Madina Sukhanova, Sushant A. Patil, Allison H. West, Simone Feurstein, Dalein A. Calderon, Matthew F. Jones, Caroline M. Weipert, Christopher K. Daugherty, Adrián A. Ceballos-López, Gordana Raca, Mark W. Lingen, Zejuan Li, Jeremy P. Segal, Jane E. Churpek, Lucy A. Godley
Publikováno v:
Blood Advances, Vol 2, Iss 2, Pp 146-150 (2018)
Abstract: Next-generation sequencing (NGS)–based targeted gene capture panels are used to profile hematopoietic malignancies to guide prognostication and treatment decisions. Because these panels include genes associated with hereditary hematopoiet
Externí odkaz:
https://doaj.org/article/9d39cfe2ed3a40e9bed4f702d8809afc
Publikováno v:
Leukemia Research Reports, Vol 6, Iss C, Pp 29-32 (2016)
Congenital leukemia is a rare event with a poor prognosis. We report a case of congenital leukemia with a cryptic rearrangement of MLL demonstrable only with RT-PCR. Interestingly, with treatment, the patient showed lineage plasticity of the leukemia
Externí odkaz:
https://doaj.org/article/c7a6f3ed76a149d6bb5b1d00627ddf77
Publikováno v:
Case Reports in Hematology, Vol 2015 (2015)
The RCSD1 gene has recently been identified as a novel gene fusion partner of the ABL1 gene in cases of B-cell Acute Lymphoblastic Leukemia (B-ALL). The RCSD1 gene is located at 1q23 and ABL1 is located at 9q34, so that the RCSD1-ABL1 fusion typicall
Externí odkaz:
https://doaj.org/article/18db3864d08840c58945d49917def023
Publikováno v:
Case Reports in Pathology, Vol 2015 (2015)
Angiosarcoma arising in association with an arteriovenous graft (AVG) or fistula is a unique clinicopathologic scenario that appears to be gaining recognition in the literature. Among reported cases, none has described high-level MYC gene amplificati
Externí odkaz:
https://doaj.org/article/42e779694a684a278c066769dfddc2a0
Autor:
Heesun J. Rogers, James W. Vardiman, John Anastasi, Gordana Raca, Natasha M. Savage, Athena M. Cherry, Daniel Arber, Erika Moore, Jennifer JD. Morrissette, Adam Bagg, Yen-Chun Liu, Susan Mathew, Attilio Orazi, Pei Lin, Sa A. Wang, Carlos E. Bueso-Ramos, Kathryn Foucar, Robert P. Hasserjian, Ramon V. Tiu, Matthew Karafa, Eric D. Hsi
Publikováno v:
Haematologica, Vol 99, Iss 5 (2014)
Acute myeloid leukemia and myelodysplastic syndrome with inv(3)(q21q26.2)/t(3;3)(q21;q26.2) have a poor prognosis. Indeed, the inv(3)(q21q26.2)/t(3;3)(q21;q26.2) has been recognized as a poor risk karyotype in the revised International Prognostic Sco
Externí odkaz:
https://doaj.org/article/d9f87de7034c45ec8554cbe976bf06a7
Publikováno v:
Case Reports in Hematology, Vol 2013 (2013)
Posttransplant lymphoproliferative disorder (PTLD) comprises a spectrum ranging from polyclonal hyperplasia to aggressive monoclonal lymphomas. The majority of PTLDs are of B-cell origin while T-cell PTLDs and Hodgkin lymphoma-like PTLDs are uncommon
Externí odkaz:
https://doaj.org/article/1684fac4908a40dbbe7e715d3c21e4f8
Autor:
Alexandra E. Kovach, Gordana Raca
Publikováno v:
Surgical Pathology Clinics. 16:249-266