Zobrazeno 1 - 10
of 1 072
pro vyhledávání: '"M. Chisholm"'
Autor:
Nisha Patel, Adam Lamble, Ilan Kirsch, Haneen Shalabi, Hao-Wei Wang, Sara K. Silbert, Samantha Scanlon, Constance M Yuan, Alyssa Doverte, Jake Wellek, Raul Braylan, Mark Ahlman, Evrim B Turkbey, Sandra D Bohling, Karen M Chisholm, Murat Alp Oztek, Mike LaLoggia, Anupam Verma, Alexandra E Kovach, Brent L Wood, Kasey Leger, Nirali N. Shah
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 12, Iss 10 (2024)
Lineage switch (LS) refers to the immunophenotypic transformation of one leukemia lineage to another (ie, lymphoid to myeloid) with retention of baseline genetics. This phenomenon was originally observed in infants with B-lymphoblastic leukemia (B-AL
Externí odkaz:
https://doaj.org/article/c7eef0e46fe34bf3a2c08de396cd97b7
Autor:
Eline J.M. Bertrums, Jenny L. Smith, Lauren Harmon, Rhonda E. Ries, Yi-Cheng J. Wang, Todd A. Alonzo, Andrew J. Menssen, Karen M. Chisholm, Amanda R. Leonti, Katherine Tarlock, Fabiana Ostronoff, Era L. Pogosova-Agadjanyan, Gertjan J.L. Kaspers, Henrik Hasle, Michael Dworzak, Christiane Walter, Nora Muhlegger, Cristina Morerio, Laura Pardo, Betsy Hirsch, Susana Raimondi, Todd M. Cooper, Richard Aplenc, Alan S. Gamis, Edward A. Kolb, Jason E. Farrar, Derek Stirewalt, Xiaotu Ma, Tim I. Shaw, Scott N. Furlan, Lisa Eidenschink Brodersen, Michael R. Loken, Marry M. van den Heuvel-Eibrink, C. Michel Zwaan, Timothy J. Triche, Bianca F. Goemans, Soheil Meshinchi
Publikováno v:
Haematologica, Vol 108, Iss 8 (2023)
NUP98 fusions comprise a family of rare recurrent alterations in AML, associated with adverse outcomes. In order to define the underlying biology and clinical implications of this family of fusions, we performed comprehensive transcriptome, epigenome
Externí odkaz:
https://doaj.org/article/831b66d955b24822ab485927eae2ccd2
Publikováno v:
Microbiology Spectrum, Vol 11, Iss 1 (2023)
ABSTRACT There is growing evidence that shows Clostridium (Clostridioides) difficile is a pathogen of One Health importance with a complex dissemination pathway involving animals, humans, and the environment. Thus, environmental discharge and agricul
Externí odkaz:
https://doaj.org/article/a3d63e4f58404d21ba53c32e37fb61da
Mutations in JAK/STAT and NOTCH1 Genes Are Enriched in Post-Transplant Lymphoproliferative Disorders
Autor:
Alexandra Butzmann, Kaushik Sridhar, Diwash Jangam, Hanbing Song, Amol Singh, Jyoti Kumar, Karen M. Chisholm, Benjamin Pinsky, Franklin Huang, Robert S. Ohgami
Publikováno v:
Frontiers in Oncology, Vol 11 (2022)
Post-transplant lymphoproliferative disorders (PTLD) are diseases occurring in immunocompromised patients after hematopoietic stem cell transplantation (HCT) or solid organ transplantation (SOT). Although PTLD occurs rarely, it may be associated with
Externí odkaz:
https://doaj.org/article/16330ea7f6f941179cf86195dd2203b7
Autor:
S.F Gordon, J. Lam, J.T. Vasquez, R. Cercone, N. Tenneti, J. Hart, M. Chisholm, M. Heland, M. Hoq, J. Kaufman, M. Danchin
Publikováno v:
Vaccine. 41:3436-3445
Autor:
Zeinab A. M. Afify, Mary M. Taj, Manuela Orjuela‐Grimm, Kavitha Srivatsa, Tamara P. Miller, Holly J. Edington, Mansi Dalal, Joanna Robles, James B. Ford, Matthew J. Ehrhardt, Tonya J. Ureda, Jeremy D. Rubinstein, Sarah McCormack, Julie M. Rivers, Karen M. Chisholm, Madison K. Kavanaugh, Andrew J. Bukowinski, Erika D. Friehling, Maegan C. Ford, Sonika N. Reddy, Lianna J. Marks, Christine Moore Smith, Clinton C. Mason
Publikováno v:
Cancer. 129:780-789
Pediatric Epstein-Barr virus-negative monomorphic post solid organ transplant lymphoproliferative disorder [EBV(-)M-PTLD] comprises approximately 10% of M-PTLD. No large multi-institutional pediatric-specific reports on treatment and outcome are avai
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Publikováno v:
Pediatric and Developmental Pathology. 25:538-547
Background Kikuchi-Fujimoto disease (KFD) is a rare, benign, and self-limited disease that presents with cervical lymphadenopathy and systemic symptoms. Histologic evaluation is often necessary to differentiate KFD from other entities. Methods Electr
Hemophagocytic lymphohistiocytosis as a paraneoplastic syndrome associated with ovarian dysgerminoma
Publikováno v:
Gynecologic Oncology Reports, Vol 17, Iss C, Pp 38-41 (2016)
Externí odkaz:
https://doaj.org/article/8d31d7ce049e4d99a3b0e51d09c7f1be
Autor:
Karen M. Chisholm, Jenny Smith, Amy E. Heerema‐McKenney, John K. Choi, Rhonda E. Ries, Betsy A. Hirsch, Susana C. Raimondi, Yi‐Cheng Wang, Alice Dang, Todd A. Alonzo, Lillian Sung, Richard Aplenc, Alan S. Gamis, Soheil Meshinchi, Samir B. Kahwash
Publikováno v:
Pediatric Blood & Cancer. 70