Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Lagen Wan"'
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-10 (2019)
Abstract Background Although extensive use of tyrosine kinase inhibitors has resulted in high and durable response rate and prolonged survival time in patients with BCR-ABL1 positive chronic myeloid leukemia (CML) and acute leukemia, relapse and drug
Externí odkaz:
https://doaj.org/article/7ce142424892491d9ff74d3001f32171
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Objective The CYP2C19 genetic variation may be involved in the development of atherosclerotic cardiovascular disease (ASCVD). Serum lipid levels are important risk factors for ASCVD, but the effect of the CYP2C19 gene on serum lipid metabolism remain
Externí odkaz:
https://doaj.org/article/2bb3f0c1fe314892b5391463b3cc2904
Autor:
Wenjian Liao, Dan Long, Qisen Huang, Dandan Wei, Xiaobing Liu, Lagen Wan, Yuling Feng, Wei Zhang, Yang Liu
Publikováno v:
Frontiers in Microbiology, Vol 11 (2020)
ObjectivesTo establish a rapid molecular diagnostics of hvKp using the peg-344 loop-mediated isothermal amplification technique (LAMP).MethodsIn all, 28 K. pneumoniae strains isolated from the blood of patients were used for the peg-344 LAMP. K. pneu
Externí odkaz:
https://doaj.org/article/fe68828ace6148b1b201a5f832978a91
Publikováno v:
Platelets, Vol 28, Iss 8, Pp 829-831 (2017)
A 38-year-old female patient was diagnosed with anemia for 3 years. Medical examination showed slight splenomegaly (250 × 62 mm), thrombocytopenia (platelets 51 × 109/L), anemia (Hb levels 107 g/L), and β-glucocerebrosidase activity (GBA) in leuko
Externí odkaz:
https://doaj.org/article/a457331dbda742eabb0a969fbb3d7a00
Publikováno v:
Acta Haematologica. 143:472-477
Both congenital hypodysfibrinogenemia and factor XI deficiency are rare coagulopathies caused by mutations within the fibrinogen and F11 genes, respectively. To investigate the pathogenesis of combined congenital hypodysfibrinogenemia with factor XI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db0e1087b2cb9126dbafb4436c83ead1
https://doi.org/10.1159/000505012
https://doi.org/10.1159/000505012
Publikováno v:
Microbial drug resistance (Larchmont, N.Y.). 28(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70474e30f279886dbdf77da5868acf33
https://pubmed.ncbi.nlm.nih.gov/35021884
https://pubmed.ncbi.nlm.nih.gov/35021884
Publikováno v:
Cancer Management and Research
Meifang Liu, Jie Yang, Lagen Wan, Rui Zhao Department of Clinical Laboratory, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, 330006, People’s Republic of ChinaCorrespondence: Lagen Wan; Rui ZhaoDepartment of Clinical Labor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffa059af6e8d81bd1fd5de37db01352a
https://pubmed.ncbi.nlm.nih.gov/34188545
https://pubmed.ncbi.nlm.nih.gov/34188545
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
The Journal of International Medical Research
The Journal of International Medical Research
ObjectiveThe CYP2C19 genetic variation may be involved in the development of atherosclerotic cardiovascular disease (ASCVD). Serum lipid levels are important risk factors for ASCVD, but the effect of the CYP2C19 gene on serum lipid metabolism remains
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d316c02f3c3389ac44a61ba59346f0be
https://doaj.org/article/2bb3f0c1fe314892b5391463b3cc2904
https://doaj.org/article/2bb3f0c1fe314892b5391463b3cc2904
Autor:
Malik Peiris, Lagen Wan, Leo L.M. Poon, Tian Xin Xiang, Aiping Le, Jia Ming Liu, Wei Zhang, Li Meng Yan, Yang Liu
Publikováno v:
The Lancet Infectious Diseases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3506d2832c88ce8fb009289fc837c4d5
Additional file 1: Table S1. FISH signal details in BCR-ABL1 positive ALL patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7417fd3d6d070a5648fca0f2f152d3
