Zobrazeno 1 - 10
of 163
pro vyhledávání: '"Lynn C. Moscinski"'
Autor:
Xiaohong Zhao, Tint Lwin, Ariosto Silva, Bijal Shah, Jiangchuan Tao, Bin Fang, Liang Zhang, Kai Fu, Chengfeng Bi, Jiannong Li, Huijuan Jiang, Mark B. Meads, Timothy Jacobson, Maria Silva, Allison Distler, Lancia Darville, Ling Zhang, Ying Han, Dmitri Rebatchouk, Maurizio Di Liberto, Lynn C. Moscinski, John M. Koomen, William S. Dalton, Kenneth H. Shain, Michael Wang, Eduardo Sotomayor, Jianguo Tao
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-15 (2017)
Ibrutinib has demonstrated high response rates in B-cell lymphomas but a lot of ibrutinib-treated patients relapse with resistance. This study unified TME-mediatedde novoand acquired drug resistance through B-cell receptor signalling and PI3K-AKT-mTO
Externí odkaz:
https://doaj.org/article/87b74c23a81c4b28a5b297ad5bef630b
Autor:
Kathy L. McGraw, Johnny Nguyen, Rami S. Komrokji, David Sallman, Najla H. Al Ali, Eric Padron, Jeffrey E. Lancet, Lynn C. Moscinski, Alan F. List, Ling Zhang
Publikováno v:
Haematologica, Vol 101, Iss 8 (2016)
Externí odkaz:
https://doaj.org/article/5fb82e67babe49b4976bdd4b16a1a3ab
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 2, Iss 2, Pp e2010028-e2010028 (2010)
We report a case of phenytoin-induced pseudolymphoma in a 28-year-old male with a history of autism and seizure disorder. The patient presented with bilateral cervical lymphadenopathy that was shown to be moderately to markedly FDG-avid on a whole bo
Externí odkaz:
https://doaj.org/article/0544ac366e4b4fabbcc1fa9eaaef621f
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 2, Iss 2, Pp e2010028-e2010028 (2010)
We report a case of phenytoin-induced pseudolymphoma in a 28-year-old male with a history of autism and seizure disorder. The patient presented with bilateral cervical lymphadenopathy that was shown to be moderately to markedly FDG-avid on a whole bo
Externí odkaz:
https://doaj.org/article/54afd88d7a3a47e894d35d9cd4e21cee
Autor:
Curtis Gravenmier, Yumeng Zhang, Nagehan Pakasticali, Lynn C. Moscinski, Jinming Song, Ling Zhang
Publikováno v:
Blood. 140:12248-12249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9ddadbc29309e0068e121567200614c
https://doi.org/10.1182/blood-2022-170665
https://doi.org/10.1182/blood-2022-170665
Publikováno v:
Blood. 140:4026-4027
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90f8ac3ce6856715ab9f29318006cd15
https://doi.org/10.1182/blood-2022-165241
https://doi.org/10.1182/blood-2022-165241
Autor:
Alan F. List, Jeffrey E. Lancet, Xiaohui Zhang, Evans Roberts, Lynn C. Moscinski, Lynh Nguyen, Ivo Abraham, David A. Sallman, Eric Padron, Dahui Qin, Diana Braswell, Seongseok Yun, Kathy L. McGraw, Ling Zhang, Jinming Song
Publikováno v:
Leukemia & Lymphoma. 61:1395-1405
Studies comparing the prognostic role of RUNX1 mutations (RUNX1mut) in acute myeloid leukemia (AML) and acute myeloid leukemia-with myelodysplasia-related changes (AML-MRC) are limited. Our study e...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1aabdb484fd0c9b2e35216d542ad1717
https://doi.org/10.1080/10428194.2020.1723016
https://doi.org/10.1080/10428194.2020.1723016
Publikováno v:
Cancer Genomics - Proteomics. 16:91-98
Background Mutations in splicing factor 3b subunit 1 (SF3B1) have been reported to be associated with a favorable prognosis, while the prognostic impact of tet methylcytosine dioxygenase 2 (TET2) mutations is still controversial. The clinical signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::419da4a822b3aa3943817015f1e2b18d
https://doi.org/10.21873/cgp.20115
https://doi.org/10.21873/cgp.20115
Autor:
Hailing Zhang, David Gajzer, Pukhraz Basra, Xiaohui Zhang, Jinming Song, Lynn C. Moscinski, Dahui Qin, Ling Zhang, Mohammad Hussaini, Haipeng Shao
Publikováno v:
American journal of clinical pathology. 154(1)
Objectives To compare the clinical significance of SF3B1/DNMT3A Comutations with SF3B1 or DNMT3A mutation alone in myelodysplastic syndrome (MDS) and clonal cytopenia of undetermined significance (CCUS). Methods We identified and compared 31 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb5113fd7bd3708c29a5f51a6be1ba0f
https://pubmed.ncbi.nlm.nih.gov/32112088
https://pubmed.ncbi.nlm.nih.gov/32112088
Autor:
Lynh, Nguyen, Xiaohui, Zhang, Evans, Roberts, Seongseok, Yun, Kathy, McGraw, Ivo, Abraham, Jinming, Song, Diana, Braswell, Dahui, Qin, David A, Sallman, Jeffrey E, Lancet, Alan F, List, Lynn C, Moscinski, Eric, Padron, Ling, Zhang
Publikováno v:
Leuk Lymphoma
Studies comparing the prognostic role of RUNX1 mutations (RUNX1(mut)) in acute myeloid leukemia (AML) and acute myeloid leukemia-with myelodysplasia-related changes (AML-MRC) are limited. Our study examines the genetic profile of 118 RUNX1(mut) AML p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fe03158e4014badc0e8247bfc051f95
https://pubmed.ncbi.nlm.nih.gov/32091281
https://pubmed.ncbi.nlm.nih.gov/32091281