Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Audrey N, Jajosky"'
Autor:
Giby V. George, Diana G. Aldowitz, Audrey N. Jajosky, Danielle S. Wallace, W. Richard Burack, Jonathan W. Friedberg, Siba El Hussein
Publikováno v:
eJHaem, Vol 5, Iss 3, Pp 599-602 (2024)
Abstract Primary large B‐cell lymphomas of immune‐privileged sites (IP‐LBCLs) comprise LBCLs arising within “immune sanctuaries,” including the central nervous system (CNS), vitreoretina, and testes. Although patients present with localized
Externí odkaz:
https://doaj.org/article/58d783c3b450425c8cc31e067701e3ab
Mimicry of inherited red cell disorders: the result of somatic mutations in a clonal myeloid disease
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/c56dd4eb86074514b2888f7bc54d9d43
Publikováno v:
Genes, Vol 15, Iss 5, p 527 (2024)
BRAF mutation identification is important for the diagnosis and treatment of several tumor types, both solid and hematologic. Rapid identification of BRAF mutations is required to determine eligibility for targeted BRAF inhibitor therapy. The Idylla
Externí odkaz:
https://doaj.org/article/3649f3c00afd467595a0c5b5ed0a06bf
Autor:
Ryan Philip Jajosky, Shang-Chuen Wu, Leon Zheng, Audrey N. Jajosky, Philip G. Jajosky, Cassandra D. Josephson, Marie A. Hollenhorst, Robert Sackstein, Richard D. Cummings, Connie M. Arthur, Sean R. Stowell
Publikováno v:
iScience, Vol 26, Iss 1, Pp 105798- (2023)
Summary: Enzymes catalyze biochemical reactions and play critical roles in human health and disease. Enzyme variants and deficiencies can lead to variable expression of glycans, which can affect physiology, influence predilection for disease, and/or
Externí odkaz:
https://doaj.org/article/c164461cc1174391bb70a5dd7f22e7a3
Autor:
Audrey N. Jajosky, Anna L. Mitchell, Mahmut Akgul, Shashirekha Shetty, Jennifer M. Yoest, Stanton L. Gerson, Navid Sadri, Kwadwo A. Oduro
Publikováno v:
Genes, Vol 13, Iss 4, p 591 (2022)
Germline disruptive variants in Protection of Telomeres 1 (POT1) predispose to a wide variety of cancers, including melanoma, chronic lymphocytic leukemia (CLL), Hodgkin lymphoma, myeloproliferative neoplasms, and glioma. We report the first case of
Externí odkaz:
https://doaj.org/article/9dec03550765494599eb65a68ad49451
Autor:
Thomas D. Lee, Dara L. Aisner, Marjorie Parker David, Celeste C. Eno, Jeffrey Gagan, Christopher D. Gocke, Natalya V. Guseva, Lisa Haley, Audrey N. Jajosky, Daniel Jones, Mahesh M. Mansukhani, Pawel Mroz, Sarah S. Murray, Kimberly J. Newsom, Vera Ashley Paulson, Somak Roy, Chase Rushton, Jeremy P. Segal, T. Niroshini Senaratne, Alexa J. Siddon, Petr Starostik, Jessica A. G. Van Ziffle, David Wu, Rena R. Xian, Sophia Yohe, Annette S. Kim
Publikováno v:
Blood Advances.
While molecular testing of hematologic malignancies is now standard of care, there is variability in practice and testing capabilities between different academic laboratories, with common questions arising on how to best meet clinical expectations. A
Publikováno v:
Heliyon, Vol 5, Iss 9, Pp e02400- (2019)
From 2010 to 2019, 40.5% fewer senior students from United States (US) allopathic medical schools pursued pathology in the Main Residency Match. To possibly explain this trend, we sought to identify major concerns about pathology which were made duri
Externí odkaz:
https://doaj.org/article/e5ef21251b914d289923add4c27a5072
Publikováno v:
Journal of Nepal Health Research Council, Vol 16, Iss 1 (2018)
NA
Externí odkaz:
https://doaj.org/article/1e24f6809ebe4077ae25007e143318c3
Autor:
Siba El Hussein, Andrew G. Evans, John M. Fitzsimmons, Nufatt Leong, Meghan Buldo, Jeremy P. Segal, Audrey N. Jajosky, Paul G. Rothberg, Jane L. Liesveld, Zoltán N. Oltvai
Publikováno v:
Molecular Case Studies. 9:a006241
Autologous and allogeneic hematopoietic stem cell transplantation (HSCT) has revolutionized the therapy of hematolymphoid malignancies. Yet, how to best detect or predict the emergence of HSCT-related complications remain unresolved. Here, we describ
Autor:
Erika M. Moore, Kwadwo A. Oduro, Audrey N. Jajosky, Navid Sadri, Howard J. Meyerson, Rose Beck, Nathaniel P Havens
Publikováno v:
American Journal of Clinical Pathology. 156:433-444
Objectives We investigated the usefulness of a custom-designed 31-gene next-generation sequencing (NGS) panel implemented on a routine basis for the evaluation of low-grade lymphoproliferative disorders (LPDs). Methods In total, 147 blood, bone marro