Zobrazeno 1 - 10
of 1 739
pro vyhledávání: '"L Jeffrey Medeiros"'
Autor:
Jie Xu, Swaminathan Iyer, Mahsa Khanlari, Shaoying Li, Roberto N Miranda, Cameron Yin, Pei Lin, Guilin Tang, Sergej N Konoplev, L Jeffrey Medeiros
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 8, Iss Suppl 3 (2020)
Externí odkaz:
https://doaj.org/article/aa4af7e9d3f34045b449e1cf478af334
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0238477 (2020)
Somatic copy number alterations (CNA) are common in endometrial serous carcinoma (ESC). We used the Tumor Cancer Genome Atlas Pan Cancer dataset (TCGA Pan Can) to explore the impact of somatic CNA and gene expression levels (mRNA) of cancer-related g
Externí odkaz:
https://doaj.org/article/fbefc4544e3a4ed5942e499b5e8ab8f1
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 23, p 9314 (2020)
Hydroa vacciniforme (HV) is a rare form of photosensitivity disorder in children and is frequently associated with Epstein–Barr virus (EBV) infection, whereas HV-like lymphoproliferative disorders (HVLPD) describe a spectrum of EBV-associated T-cel
Externí odkaz:
https://doaj.org/article/78fa77538a6f4ef9a1cbc3b28c1f72ae
Autor:
Santiago Montes-Moreno, Mark J Routbort, Elijah J Lohman, Bedia A Barkoh, Rashmi Kanagal-Shamanna, Carlos E Bueso-Ramos, Rajesh R Singh, L Jeffrey Medeiros, Raja Luthra, Keyur P Patel
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0204218 (2018)
ASXL1 (additional sex combs like 1) is a gene that is mutated in a number of hematological neoplasms. The most common genetic alteration is c.1934dupG p.Gly646fs. Previous publications have shown that ASXL1 mutations have a negative prognostic impact
Externí odkaz:
https://doaj.org/article/211084062a8445818fd012187eafcc83
Autor:
Dai Chihara, Michelle A Fanale, Roberto N Miranda, Mansoor Noorani, Jason R Westin, Loretta J Nastoupil, Fredrick B Hagemeister, Luis E Fayad, Jorge E Romaguera, Felipe Samaniego, Francesco Turturro, Hun J Lee, Sattva S Neelapu, M Alma Rodriguez, Michael Wang, Nathan H Fowler, Richard E Davis, L Jeffrey Medeiros, Yasuhiro Oki
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0191461 (2018)
We performed a retrospective analysis to identify risk factors and survival outcome for central nervous system (CNS) relapse of peripheral T-cell lymphoma (PTCL) by histologic type. Records of 600 PTCL patients diagnosed between 1999 and 2014 were an
Externí odkaz:
https://doaj.org/article/73ceca117ba94c9caecbd4ff828737e7
Autor:
Meenakshi Mehrotra, Dzifa Yawa Duose, Rajesh R Singh, Bedia A Barkoh, Jawad Manekia, Michael A Harmon, Keyur P Patel, Mark J Routbort, L Jeffrey Medeiros, Ignacio I Wistuba, Rajyalakshmi Luthra
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0181968 (2017)
Next generation sequencing based tumor tissue genotyping involves complex workflow and a relatively longer turnaround time. Semiconductor based next generation platforms varied from low throughput Ion PGM to high throughput Ion Proton and Ion S5XL se
Externí odkaz:
https://doaj.org/article/bb549dfe68a64ba9828eeddd3a89200d
Publikováno v:
eJHaem, Vol 5, Iss 2, Pp 379-382 (2024)
Abstract Nucleophosmin 1 (NPM1) mutations occur in approximately one‐third cases of adult de novo acute myeloid leukemia (AML). Identification of NPM1 mutations is important for classification, risk stratification, tailored therapy, and monitoring
Externí odkaz:
https://doaj.org/article/7ca035fc4517481587956fc20e45efb4
Autor:
Ting Zhou, Choladda V. Curry, Mahsa Khanlari, Min Shi, Wei Cui, Deniz Peker, Weina Chen, Endi Wang, Juehua Gao, Qi Shen, Wei Xie, Fatima Z. Jelloul, Rebecca L. King, Ji Yuan, Xiaoqiong Wang, Chen Zhao, Ifeyinwa E. Obiorah, Elizabeth L. Courville, Eric Nomura, Sindhu Cherian, Mina L. Xu, W. Richard Burack, Hong-xing Liu, Elias J. Jabbour, Koichi Takahashi, Wei Wang, Sa A. Wang, Joseph D. Khoury, L. Jeffrey Medeiros, Shimin Hu
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-6 (2024)
Externí odkaz:
https://doaj.org/article/58cbb20b1ddb45959fc162e418099f3a
Autor:
Anjanaa Vijayanarayanan, Sa A. Wang, Sofia Garces, Karan Saluja, L. Jeffrey Medeiros, Beenu Thakral
Publikováno v:
eJHaem, Vol 5, Iss 1, Pp 266-268 (2024)
Externí odkaz:
https://doaj.org/article/6e78721b23a640a786ac13d9fc0e145d
Publikováno v:
Frontiers in Oncology, Vol 3 (2013)
Approximately 20% of unselected cases and 30% cytogenetically diploid cases of acute myeloid leukemia (AML) and 80% of grade II-III gliomas and secondary glioblastomas carry mutations in the isocitrate dehydrogenase (IDH) 1 and 2 genes. IDH1/2 mutati
Externí odkaz:
https://doaj.org/article/6fbf123f22974fe8a9176426fcf1a93c