Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Poshi Xu"'
Publikováno v:
Frontiers in Microbiology, Vol 12 (2021)
The emergence of hypervirulent carbapenem-resistant Klebsiella pneumoniae (hv-CRKP) was regarded as an emerging threat in clinical settings. Here, we investigated the prevalence of CRKP strains among inpatients in a new hospital over 1 year since its
Externí odkaz:
https://doaj.org/article/6cb3df0410cb432690d9d497c70c9a16
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 11 (2021)
The spread of plasmid-mediated carbapenem-resistant clinical isolates is a serious threat to global health. In this study, an emerging NDM-encoding IncHI5-like plasmid from Klebsiella pneumoniae of infant patient origin was characterized, and the pla
Externí odkaz:
https://doaj.org/article/36fca1efe43348b5bd6cdd8845ad8bbf
Publikováno v:
Open Medicine
Open Medicine, Vol 15, Iss 1, Pp 396-402 (2020)
Open Medicine, Vol 15, Iss 1, Pp 396-402 (2020)
Multiple myeloma (MM) is an immunoglobulin-producing tumor of plasma cells, which occurs commonly in the elderly. The incidence of myocardial amyloidosis with MM is extremely low and early clinical manifestations are nonspecific. The diversity of cli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55c52fe5b5da7b775ccd47782db513e
http://europepmc.org/articles/PMC7706130
http://europepmc.org/articles/PMC7706130
Publikováno v:
European Journal of Clinical Microbiology & Infectious Diseases. 39:1785-1788
Methylobacterium radiotolerans has only been identified in blood samples from end-stage renal failure or leukaemia patients in clinic. Here, we report a case of infective endocarditis (IE) caused by M. radiotolerans. 16S rRNA sequencing and matrix-as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f22aa05ff06b369af0561b0a65ebe58
https://doi.org/10.1007/s10096-020-03896-7
https://doi.org/10.1007/s10096-020-03896-7
Publikováno v:
Open Medicine, Vol 15, Iss 1, Pp 769-773 (2020)
Open Medicine
Open Medicine
Congenital dysfibrinogenemia (CD) is a rare hereditary fibrinogen disorder characterized by normal fibrinogen antigen levels associated with lower functional activities. The aim of this study is to analyze the phenotype and genotype of a family of CD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::deff23911451b4d869ddaf30a97bb291
https://doi.org/10.1515/med-2020-0214
https://doi.org/10.1515/med-2020-0214
Publikováno v:
Disease Markers.
LncRNAs are known to regulate a plethora of key events of cellular processes; however, little is known about the function of lncRNAs in autophagy. Here in the current study, we report lncRNA-IGFBP4 which has previously been known to regulate the prol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::586281aa6bb19ec0ae54a3b50378b4f0
Publikováno v:
RSC Advances. 9:1451-1459
Hypoxia is a major hallmark of solid tumors and is associated with malignant phenotypes. Exosomal miRNAs derived from hypoxia tumor cells are implicated in the modulation of cancer progression, whereas, the mechanisms underlying the association betwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dacfef55a43de1069e31ff6a12e3c44e
https://doi.org/10.1039/c8ra06750c
https://doi.org/10.1039/c8ra06750c
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(2)
To carry out genetic testing and prenatal diagnosis for 90 families affected with spinal muscular atrophy (SMA), and discuss the necessity for carrier screening.All families were subjected to multiplex ligation-dependent probe amplification (MLPA) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4426e1f3ae6147b5247e11798c16cff5
https://pubmed.ncbi.nlm.nih.gov/32034734
https://pubmed.ncbi.nlm.nih.gov/32034734
Autor:
Jin He, Wen Yin, Xiaohong Li, Poshi Xu, Daniel C. Nelson, Yujing Gong, Qiong Li, Dehua Luo, Hongping Wei, Irina V. Etobayeva, Hang Yang, Shujuan Wang
Publikováno v:
Antimicrob Agents Chemother
Streptococcus pneumoniae is a leading human pathogen uniquely characterized by choline moieties on the bacterial surface. Our previous work reported a pneumococcus-specific chimeric lysin, ClyJ, which combines the CHAP (cysteine, histidine-dependent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67597ffb3aff10b960b4d048ee9f0b82
https://pubmed.ncbi.nlm.nih.gov/31767724
https://pubmed.ncbi.nlm.nih.gov/31767724
Autor:
Zhengmin Li, Guangxia Yang, Lei Zhang, Zongshan Zhang, Xiaoyu Wang, Poshi Xu, Panpan Liu, Wenxin Zhao
Publikováno v:
Journal of cellular biochemistry. 120(10)
Primary Sjogren's syndrome (pSS) is a chronic systemic autoimmune disease that affects exocrine glands. To study the molecular mechanism and identify crucial genes/pathways in pSS pathogenesis, the microarray-based whole-genome gene expression profil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74398924e302aee06cea2d2a3af2f3a1
https://pubmed.ncbi.nlm.nih.gov/31125139
https://pubmed.ncbi.nlm.nih.gov/31125139