Zobrazeno 1 - 10
of 3 967
pro vyhledávání: '"Duplication mutation"'
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Publikováno v:
Iraqi Journal of Hematology, Vol 12, Iss 2, Pp 159-163 (2023)
BACKGROUND: Mutations in the FLT3 gene are very common in acute myeloid leukemia (AML). These mutations are linked to a high chance of the disease relapse and decrease overall survival. This study aimed to investigate this mutation in AML cases and t
Externí odkaz:
https://doaj.org/article/7f86d122d3b345a291b87e2772472524
Autor:
Huang C; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Huang Y; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Pan L; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Li L; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Ling X; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Wang C; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Xiao Q; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Zhai N; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Long Y; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China., Mo W; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China. Electronic address: mown16300@126.com., Lin F; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China. Electronic address: fqlin1998@163.com., Huang Y; Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning 530021, Guangxi, China. Electronic address: YFY004462@sr.gxmu.edu.cn.
Publikováno v:
Gene [Gene] 2024 Dec 30; Vol. 931, pp. 148889. Date of Electronic Publication: 2024 Aug 29.
Autor:
Rasool, Sarween1 (AUTHOR), Mohammad, Nawsherwan2 (AUTHOR), Hamza, Hiwa1 (AUTHOR), Alnuaimy, Sarah1 (AUTHOR)
Publikováno v:
Iraqi Journal of Hematology. Jul-Dec2023, Vol. 12 Issue 2, p159-163. 5p.
Autor:
Sumiyoshi, Ritsu, Tashiro, Haruko *, Shirasaki, Ryosuke, Matsuo, Takuji, Yamamoto, Tadashi, Matsumoto, Kensuke, Ooi, Jun, Shirafuji, Naoki
Publikováno v:
In Leukemia Research February 2022 113
Autor:
Klimtchuk, Elena S., Prokaeva, Tatiana, Frame, Nicholas M., Abdullahi, Hassan A., Spencer, Brian, Dasari, Surendra, Cui, Haili, Berk, John L., Kurtin, Paul J., Connors, Lawreen H., Gursky, Olga
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2018 Jul 01. 115(28), E6428-E6436.
Externí odkaz:
https://www.jstor.org/stable/26510924
Akademický článek
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Publikováno v:
Case Reports in Neurology, Vol 12, Iss 2, Pp 255-259 (2020)
Mutations in the myelin protein zero (MPZ) gene can cause a variety of clinical and electrophysiological forms of genetic neuropathies including Charcot-Marie-Tooth (CMT) type 1B disease which is characterized by demyelinating features. We present a
Externí odkaz:
https://doaj.org/article/78118e3cd9b84f7c98b13f274be961e9