Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Lawrence J, Jennings"'
Autor:
Lawrence J. Jennings
Publikováno v:
eJHaem, Vol 3, Iss 4, Pp 1343-1345 (2022)
Abstract Current guidelines recommend that Acute Myeloid Leukemia (AML) patients with NPM1 mutations should be monitored for measurable residual disease by quantifying the transcripts and normalizing them to ABL1 transcripts. In this short report, a
Externí odkaz:
https://doaj.org/article/59249ebe6a18402faf2b69627af9db9c
Autor:
Samuel D. Racette, Borislav A. Alexiev, Michael P. Angarone, Ajay Bhasin, Kaitlin Lima, Lawrence J. Jennings, Senthil Balasubramanian, Akihiro J. Matsuoka
Publikováno v:
BMC Infectious Diseases, Vol 21, Iss 1, Pp 1-4 (2021)
Abstract Background We present a yet to be described association of SARS-CoV-2 infection with Kikuchi-Fujimoto disease. Case presentation A 32-year-old physician with history of SARS-CoV-2 infection presented to the emergency department with 2 weeks
Externí odkaz:
https://doaj.org/article/45a7f7dc8efb410c98881ce919ac83a6
Autor:
Ramon Lorenzo-Redondo, Hannah H. Nam, Scott C. Roberts, Lacy M. Simons, Lawrence J. Jennings, Chao Qi, Chad J. Achenbach, Alan R. Hauser, Michael G. Ison, Judd F. Hultquist, Egon A. Ozer
Publikováno v:
EBioMedicine, Vol 62, Iss , Pp 103112- (2020)
Background: The rapid spread of SARS-CoV-2, the causative agent of Coronavirus disease 2019 (COVID-19), has been accompanied by the emergence of distinct viral clades, though their clinical significance remains unclear. Here, we aimed to investigate
Externí odkaz:
https://doaj.org/article/8cc5b77272e341439e4973f8a4665fcd
Autor:
Omar Bushara, James R. Wester, Danielle Jacobsen, Leyu Sun, Samuel Weinberg, Juehua Gao, Lawrence J. Jennings, Lu Wang, Shannon M. Lauberth, Feng Yue, Jie Liao, Guang-Yu Yang
Publikováno v:
Human Pathology. 131:9-16
With the advent of next-generation sequencing (NGS), identifying and better understanding genetic mutations in cancer pathways has become more feasible. A mutation now commonly reported in NGS panels is the SETD2 gene (H3K36 trimethyltransferase). Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e98b3b32f9b0bdcc9961d7b146736d2
https://doi.org/10.1016/j.humpath.2022.12.001
https://doi.org/10.1016/j.humpath.2022.12.001
Autor:
Omar Bushara, Samuel Edward Weinberg, Brian Steven Finkelman, Hongmei Jiang, Katrina Krogh, Leyu Sun, Amy L. Halverson, Lawrence J. Jennings, Jie Liao, Guang-Yu Yang
Publikováno v:
Human Pathology. 128:20-30
Anal squamous cell carcinoma (SCC) is a human papillomavirus (HPV)-mediated malignancy with increasing incidence. Human immunodeficiency virus (HIV) infection is a significant risk factor for anal SCC; however, it is unknown if HIV infection alters a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40adfdc1401b26afde1488cb29d0dce0
https://doi.org/10.1016/j.humpath.2022.06.025
https://doi.org/10.1016/j.humpath.2022.06.025
Autor:
Pouya Jamshidi, Matthew McCord, Kristyn Galbraith, Lucas Santana-Santos, Lawrence J. Jennings, Matija Snuderl, Craig Horbinski
Publikováno v:
Acta Neuropathologica. 145:365-367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b1b84504eb0fda746cfe4059f5b751e
https://doi.org/10.1007/s00401-023-02542-8
https://doi.org/10.1007/s00401-023-02542-8
Autor:
Ted Ling Hu, Lacy Simons, Taylor J. Dean, Estefany Rios Guzman, Matthew T. Caputo, Arghavan Alisoltani, Chao Qi, Michael Malczynski, Timothy Blanke, Lawrence J. Jennings, Michael Ison, Chad J. Achenbach, Paige M. Larkin, Karen L. Kaul, Ramon Lorenzo-Redondo, Egon A. Ozer, Judd Hultquist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54209e56e72d93413c40d2aff10374c9
https://doi.org/10.2139/ssrn.4323726
https://doi.org/10.2139/ssrn.4323726
Autor:
Masha Kocherginsky, Yi Hua Chen, Taylor Zak, Olga Frankfurt, Firas Wehbe, Xinyan Lu, Peng Ji, Qing Chen, Juehua Gao, Jessica K. Altman, Lawrence J. Jennings, Madina Sukhanova, Sandeep Gurbuxani
Publikováno v:
Genes, Chromosomes and Cancer. 61:71-80
MECOM rearrangements are recurrent in myeloid neoplasms and associated with poor prognosis. However, only inv(3)(q21q26.2) and t(3;3)(q21;q26.2), the classic MECOM rearrangements resulting in RPN1-MECOM rearrangement with Mecom overexpression and GAT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0015c3d28a7f2ea9eab79a71415a261f
https://doi.org/10.1002/gcc.23004
https://doi.org/10.1002/gcc.23004
Autor:
Min Yu, Tiziana Bachetti, Virginia Speare, Casey M. Rand, Isabella Ceccherini, Amy Zhou, Kai Lee Yap, Patrick Reineke, Lawrence J. Jennings, Debra E. Weese-Mayer, Sara M. Hockney, Lili Zhou, Melanie Pennock, Elizabeth Berry-Kravis, Grace Niewijk
Publikováno v:
Genetics in Medicine. 23:1656-1663
Purpose CCHS is an extremely rare congenital disorder requiring artificial ventilation as life support. Typically caused by heterozygous polyalanine repeat expansion mutations (PARMs) in the PHOX2B gene, identification of a relationship between PARM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddba4abca4a84e89251cc011b0d5343b
https://doi.org/10.1038/s41436-021-01178-x
https://doi.org/10.1038/s41436-021-01178-x
Publikováno v:
American journal of hematology. 98(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7ce93b026b24196bf3bc5a388a61e8
https://pubmed.ncbi.nlm.nih.gov/36288429
https://pubmed.ncbi.nlm.nih.gov/36288429