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  1. Article ; Online: Update on Omicron variant and its threat to vulnerable populations.

    Dai, Bowen / Ji, Wangquan / Zhu, Peiyu / Han, Shujie / Chen, Yu / Jin, Yuefei

    Public health in practice (Oxford, England)

    2024  Volume 7, Page(s) 100494

    Abstract: Objective: To reduce the incidence of severe illness and fatalities, and promote the awareness of protection and precaution, increased vaccination, strengthen the physical fitness, frequent ventilation, and health education should be enhanced among ... ...

    Abstract Objective: To reduce the incidence of severe illness and fatalities, and promote the awareness of protection and precaution, increased vaccination, strengthen the physical fitness, frequent ventilation, and health education should be enhanced among vulnerable populations as essential measures for the future control of COVID-19.
    Study design: Systematic review.
    Method: The search was done using PubMed, EMBASE and Web of Science for studies without language restrictions, published up through March 2023, since their authoritative and comprehensive literature search database. Eighty articles were included. Extraction of articles and quality assessment of included reviews was performed independently by two authors using the AMSTAR 2 score.
    Results: The articles in the final data set included research on epidemiological characteristics, pathogenicity, available vaccines, treatments and epidemiological features in special populations including the elders, pregnant women, kids, people with chronic diseases concerning Omicron.
    Conclusion: Although less pathogenic potential is found in Omicron, highly mutated forms have enhanced the ability of immune evasion and resistance to existing vaccines compared with former variants. Severe complications and outcomes may occur in vulnerable populations. Infected pregnant women are more likely to give birth prematurely, and fatal implications in children infected with Omicron are hyperimmune response and severe neurological disorders. In immunocompromised patients, there is a greater reported mortality and complication compared to patients with normal immune systems. Therefore, maintain social distancing, wear masks, and receive vaccinations are effective long-term measures.
    Language English
    Publishing date 2024-03-25
    Publishing country England
    Document type Journal Article ; Review
    ISSN 2666-5352
    ISSN (online) 2666-5352
    DOI 10.1016/j.puhip.2024.100494
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Investigating phase separation properties of chromatin-associated proteins using gradient elution of 1,6-hexanediol.

    Zhu, Peiyu / Hou, Chao / Liu, Manlin / Chen, Taoyu / Li, Tingting / Wang, Likun

    BMC genomics

    2023  Volume 24, Issue 1, Page(s) 493

    Abstract: Background: Chromatin-associated phase separation proteins establish various biomolecular condensates via liquid-liquid phase separation (LLPS), which regulates vital biological processes spatially and temporally. However, the widely used methods to ... ...

    Abstract Background: Chromatin-associated phase separation proteins establish various biomolecular condensates via liquid-liquid phase separation (LLPS), which regulates vital biological processes spatially and temporally. However, the widely used methods to characterize phase separation proteins are still based on low-throughput experiments, which consume time and could not be used to explore protein LLPS properties in bulk.
    Results: By combining gradient 1,6-hexanediol (1,6-HD) elution and quantitative proteomics, we developed chromatin enriching hexanediol separation coupled with liquid chromatography-mass spectrometry (CHS-MS) to explore the LLPS properties of different chromatin-associated proteins (CAPs). First, we found that CAPs were enriched more effectively in the 1,6-HD treatment group than in the isotonic solution treatment group. Further analysis showed that the 1,6-HD treatment group could effectively enrich CAPs prone to LLPS. Finally, we compared the representative proteins eluted by different gradients of 1,6-HD and found that the representative proteins of the 2% 1,6-HD treatment group had the highest percentage of IDRs and LCDs, whereas the 10% 1,6-HD treatment group had the opposite trend.
    Conclusion: This study provides a convenient high-throughput experimental method called CHS-MS. This method can efficiently enrich proteins prone to LLPS and can be extended to explore LLPS properties of CAPs in different biological systems.
    MeSH term(s) Humans ; Chromatin ; Chromatography, Liquid ; Corneal Dystrophies, Hereditary ; Glycols
    Chemical Substances hexamethylene glycol (ZIA319275I) ; Chromatin ; Glycols
    Language English
    Publishing date 2023-08-28
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041499-7
    ISSN 1471-2164 ; 1471-2164
    ISSN (online) 1471-2164
    ISSN 1471-2164
    DOI 10.1186/s12864-023-09600-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Essential Role of Non-Coding RNAs in Enterovirus Infection: From Basic Mechanisms to Clinical Prospects.

    Zhu, Peiyu / Chen, Shuaiyin / Zhang, Weiguo / Duan, Guangcai / Jin, Yuefei

    International journal of molecular sciences

    2021  Volume 22, Issue 6

    Abstract: Enteroviruses (EVs) are common RNA viruses that can cause various types of human diseases and conditions such as hand, foot, and mouth disease (HFMD), myocarditis, meningitis, sepsis, and respiratory disorders. Although EV infections in most patients are ...

    Abstract Enteroviruses (EVs) are common RNA viruses that can cause various types of human diseases and conditions such as hand, foot, and mouth disease (HFMD), myocarditis, meningitis, sepsis, and respiratory disorders. Although EV infections in most patients are generally mild and self-limiting, a small number of young children can develop serious complications such as encephalitis, acute flaccid paralysis, myocarditis, and cardiorespiratory failure, resulting in fatalities. Established evidence has suggested that certain non-coding RNAs (ncRNAs) such as microRNAs (miRNAs), long ncRNAs (lncRNAs), and circular RNAs (circRNAs) are involved in the occurrence and progression of many human diseases. Recently, the involvement of ncRNAs in the course of EV infection has been reported. Herein, the authors focus on recent advances in the understanding of ncRNAs in EV infection from basic viral pathogenesis to clinical prospects, providing a reference basis and new ideas for disease prevention and research directions.
    MeSH term(s) Antigens, Viral/genetics ; Child ; Enterovirus/genetics ; Enterovirus/pathogenicity ; Enterovirus Infections/genetics ; Enterovirus Infections/virology ; Humans ; MicroRNAs/genetics ; RNA, Circular/genetics ; RNA, Long Noncoding/genetics ; RNA, Untranslated/genetics
    Chemical Substances Antigens, Viral ; MicroRNAs ; RNA, Circular ; RNA, Long Noncoding ; RNA, Untranslated
    Language English
    Publishing date 2021-03-12
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms22062904
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Current status of hand-foot-and-mouth disease.

    Zhu, Peiyu / Ji, Wangquan / Li, Dong / Li, Zijie / Chen, Yu / Dai, Bowen / Han, Shujie / Chen, Shuaiyin / Jin, Yuefei / Duan, Guangcai

    Journal of biomedical science

    2023  Volume 30, Issue 1, Page(s) 15

    Abstract: Hand-foot-and-mouth disease (HFMD) is a viral illness commonly seen in young children under 5 years of age, characterized by typical manifestations such as oral herpes and rashes on the hands and feet. These symptoms typically resolve spontaneously ... ...

    Abstract Hand-foot-and-mouth disease (HFMD) is a viral illness commonly seen in young children under 5 years of age, characterized by typical manifestations such as oral herpes and rashes on the hands and feet. These symptoms typically resolve spontaneously within a few days without complications. Over the past two decades, our understanding of HFMD has greatly improved and it has received significant attention. A variety of research studies, including epidemiological, animal, and in vitro studies, suggest that the disease may be associated with potentially fatal neurological complications. These findings reveal clinical, epidemiological, pathological, and etiological characteristics that are quite different from initial understandings of the illness. It is important to note that HFMD has been linked to severe cardiopulmonary complications, as well as severe neurological sequelae that can be observed during follow-up. At present, there is no specific pharmaceutical intervention for HFMD. An inactivated Enterovirus A71 (EV-A71) vaccine that has been approved by the China Food and Drug Administration (CFDA) has been shown to provide a high level of protection against EV-A71-related HFMD. However, the simultaneous circulation of multiple pathogens and the evolution of the molecular epidemiology of infectious agents make interventions based solely on a single agent comparatively inadequate. Enteroviruses are highly contagious and have a predilection for the nervous system, particularly in child populations, which contributes to the ongoing outbreak. Given the substantial impact of HFMD around the world, this Review synthesizes the current knowledge of the virology, epidemiology, pathogenesis, therapy, sequelae, and vaccine development of HFMD to improve clinical practices and public health efforts.
    MeSH term(s) Animals ; Foot-and-Mouth Disease/complications ; Foot-and-Mouth Disease/epidemiology ; Hand, Foot and Mouth Disease/epidemiology ; Enterovirus ; Enterovirus Infections ; Disease Outbreaks ; China/epidemiology ; Enterovirus A, Human
    Language English
    Publishing date 2023-02-24
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 1193378-1
    ISSN 1423-0127 ; 1021-7770
    ISSN (online) 1423-0127
    ISSN 1021-7770
    DOI 10.1186/s12929-023-00908-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: VIPpred: a novel model for predicting variant impact on phosphorylation events driving carcinogenesis.

    Xu, Xiaofeng / Li, Ying / Chen, Taoyu / Hou, Chao / Yang, Liang / Zhu, Peiyu / Zhang, Yi / Li, Tingting

    Briefings in bioinformatics

    2023  Volume 25, Issue 1

    Abstract: Disrupted protein phosphorylation due to genetic variation is a widespread phenomenon that triggers oncogenic transformation of healthy cells. However, few relevant phosphorylation disruption events have been verified due to limited biological ... ...

    Abstract Disrupted protein phosphorylation due to genetic variation is a widespread phenomenon that triggers oncogenic transformation of healthy cells. However, few relevant phosphorylation disruption events have been verified due to limited biological experimental methods. Because of the lack of reliable benchmark datasets, current bioinformatics methods primarily use sequence-based traits to study variant impact on phosphorylation (VIP). Here, we increased the number of experimentally supported VIP events from less than 30 to 740 by manually curating and reanalyzing multi-omics data from 916 patients provided by the Clinical Proteomic Tumor Analysis Consortium. To predict VIP events in cancer cells, we developed VIPpred, a machine learning method characterized by multidimensional features that exhibits robust performance across different cancer types. Our method provided a pan-cancer landscape of VIP events, which are enriched in cancer-related pathways and cancer driver genes. We found that variant-induced increases in phosphorylation events tend to inhibit the protein degradation of oncogenes and promote tumor suppressor protein degradation. Our work provides new insights into phosphorylation-related cancer biology as well as novel avenues for precision therapy.
    MeSH term(s) Humans ; Phosphorylation ; Proteomics ; Oncogenes ; Carcinogenesis/genetics ; Neoplasms/metabolism
    Language English
    Publishing date 2023-12-29
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2068142-2
    ISSN 1477-4054 ; 1467-5463
    ISSN (online) 1477-4054
    ISSN 1467-5463
    DOI 10.1093/bib/bbad480
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Design, synthesis and biological evaluation of isoxazole-containing biphenyl derivatives as small-molecule inhibitors targeting the programmed cell death-1/ programmed cell death-ligand 1 immune checkpoint.

    Zhu, Peiyu / Zhang, Jian / Yang, Yifei / Wang, Lixun / Zhou, Jinpei / Zhang, Huibin

    Molecular diversity

    2021  Volume 26, Issue 1, Page(s) 245–264

    Abstract: Monoclonal antibodies targeting the programmed cell death-1/ programmed cell death-ligand 1 (PD-1/PD-L1) immune checkpoint have achieved enormous success in cancer immunotherapy. But the antibody-based immunotherapies carry a number of unavoidable ... ...

    Abstract Monoclonal antibodies targeting the programmed cell death-1/ programmed cell death-ligand 1 (PD-1/PD-L1) immune checkpoint have achieved enormous success in cancer immunotherapy. But the antibody-based immunotherapies carry a number of unavoidable deficiencies such as poor pharmacokinetic properties and immunogenicity. Small-molecule PD-1/PD-L1 inhibitors offer the superiority of complementarity with monoclonal antibodies and represent an appealing alternative. A novel series of isoxazole-containing biphenyl compounds were designed, synthesized and evaluated as PD-1/PD-L1 inhibitors in this paper. The structure-activity relationship of the novel synthesized compounds indicated that the ring-closure strategy of introducing isoxazole could be employed and the 3-cyanobenzyl group was significant for the inhibitory activity against the PD-1/PD-L1 protein-protein interactions. Molecular docking studies were performed to help understand the binding mode of the small-molecule inhibitor with the PD-L1 dimer. In particular, compound II-12 was a promising anti-PD-1/PD-L1 inhibitor with the IC
    MeSH term(s) Apoptosis ; B7-H1 Antigen/chemistry ; B7-H1 Antigen/metabolism ; Biphenyl Compounds/chemistry ; Biphenyl Compounds/pharmacology ; Isoxazoles/pharmacology ; Ligands ; Molecular Docking Simulation ; Programmed Cell Death 1 Receptor/chemistry ; Programmed Cell Death 1 Receptor/metabolism
    Chemical Substances B7-H1 Antigen ; Biphenyl Compounds ; Isoxazoles ; Ligands ; Programmed Cell Death 1 Receptor ; diphenyl (2L9GJK6MGN)
    Language English
    Publishing date 2021-03-30
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1376507-3
    ISSN 1573-501X ; 1381-1991
    ISSN (online) 1573-501X
    ISSN 1381-1991
    DOI 10.1007/s11030-021-10208-4
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  7. Article ; Online: Analysis of miRNAs Involved in Mouse Heart Injury Upon Coxsackievirus A2 Infection.

    Wu, Zhaoke / Zhu, Shenshen / Qian, Juanfeng / Hu, Yanmin / Ji, Wangquan / Li, Dong / Zhu, Peiyu / Liang, Ruonan / Jin, Yuefei

    Frontiers in cellular and infection microbiology

    2022  Volume 12, Page(s) 765445

    Abstract: Coxsackievirus A2 (CVA2) has recently been constantly detected, and is associated with viral myocarditis in children. Our previous study demonstrated that CVA2 led to heart damage in a neonatal murine model. However, the molecular mechanism of heart ... ...

    Abstract Coxsackievirus A2 (CVA2) has recently been constantly detected, and is associated with viral myocarditis in children. Our previous study demonstrated that CVA2 led to heart damage in a neonatal murine model. However, the molecular mechanism of heart injury caused by CVA2 remains largely unknown. Emerging evidence suggests the significant functions of miRNAs in Coxsackievirus infection. To investigate potential miRNAs involved in heart injury caused by CVA2, our study, for the first time, conducted a RNA-seq
    MeSH term(s) Animals ; Apoptosis ; Coxsackievirus Infections/pathology ; Gene Expression Profiling ; Heart Injuries ; Mice ; MicroRNAs/genetics ; MicroRNAs/metabolism ; RNA, Messenger/genetics
    Chemical Substances MicroRNAs ; RNA, Messenger
    Language English
    Publishing date 2022-01-28
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2619676-1
    ISSN 2235-2988 ; 2235-2988
    ISSN (online) 2235-2988
    ISSN 2235-2988
    DOI 10.3389/fcimb.2022.765445
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The CXCL10/CXCR3 Axis Promotes Disease Pathogenesis in Mice upon CVA2 Infection.

    Liang, Ruonan / Chen, Shuaiyin / Jin, Yuefei / Tao, Ling / Ji, Wangquan / Zhu, Peiyu / Li, Dong / Zhang, Yu / Zhang, Weiguo / Duan, Guangcai

    Microbiology spectrum

    2022  Volume 10, Issue 3, Page(s) e0230721

    Abstract: Coxsackievirus A2 (CVA2) is an emerging pathogen that results in hand-foot-and-mouth disease (HFMD) outbreaks. Systemic inflammatory response and central nervous system inflammation are the main pathological features of fatal HFMD. However, the ... ...

    Abstract Coxsackievirus A2 (CVA2) is an emerging pathogen that results in hand-foot-and-mouth disease (HFMD) outbreaks. Systemic inflammatory response and central nervous system inflammation are the main pathological features of fatal HFMD. However, the immunopathogenesis of CVA2 infection is poorly understood. We first detected the transcriptional levels of 81 inflammation-related genes in neonatal mice with CVA2 infection. Remarkably, CVA2 induced higher expression of chemokine (C-X-C motif) ligand 10 (CXCL10) in multiple organs and tissues. CXCL10 acts through its cognate receptor chemokine (C-X-C motif) receptor 3 (CXCR3) and regulates immune responses. CXCL10/CXCR3 activation contributes to the pathogenesis of many inflammatory diseases. Next, we found CXCL10 and CXCR3 expression to be significantly elevated in the organs and tissues from CVA2-infected mice at 5 days postinfection (dpi) using immunohistochemistry (IHC). To further explore the role of CXCL10/CXCR3 in CVA2 pathogenesis, an anti-CXCR3 neutralizing antibody (αCXCR3) or IgG isotype control antibody was used to treat CVA2-infected mice on the same day as infection and every 24 h until 5 dpi. Our results showed that αCXCR3 therapy relieved the clinical manifestations and pathological damage and improved the survival rate of CVA2-infected mice. Additionally, αCXCR3 treatment reduced viral loads and reversed the proinflammatory cytokine (interleukin 6 [IL-6], tumor necrosis factor alpha [TNF-α], and IL-1β) expression, apoptosis, and inflammatory cell infiltration induced by CVA2. Collectively, our study presents evidence for the involvement of the CXCL10/CXCR3 axis in CVA2 pathogenesis. The activation of CXCL10/CXCR3 contributes to CVA2 pathogenesis by inducing apoptosis, proinflammatory cytokine expression, and inflammatory cell infiltration, which can be reversed by αCXCR3 therapy. This study provides new insight into the pathogenesis of HFMD, which has an important guiding significance for the treatment of HFMD.
    MeSH term(s) Animals ; Antibodies, Neutralizing ; Chemokine CXCL10/genetics ; Chemokine CXCL10/metabolism ; Coxsackievirus Infections ; Inflammation ; Interleukin-6 ; Mice ; Receptors, CXCR3/metabolism ; Systemic Inflammatory Response Syndrome ; Tumor Necrosis Factor-alpha
    Chemical Substances Antibodies, Neutralizing ; Chemokine CXCL10 ; Cxcl10 protein, mouse ; Cxcr3 protein, mouse ; Interleukin-6 ; Receptors, CXCR3 ; Tumor Necrosis Factor-alpha
    Language English
    Publishing date 2022-05-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2807133-5
    ISSN 2165-0497 ; 2165-0497
    ISSN (online) 2165-0497
    ISSN 2165-0497
    DOI 10.1128/spectrum.02307-21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: PhaSepDB in 2022: annotating phase separation-related proteins with droplet states, co-phase separation partners and other experimental information.

    Hou, Chao / Wang, Xinxin / Xie, Haotai / Chen, Taoyu / Zhu, Peiyu / Xu, Xiaofeng / You, Kaiqiang / Li, Tingting

    Nucleic acids research

    2022  Volume 51, Issue D1, Page(s) D460–D465

    Abstract: Phase separation (PS) proteins form droplets to regulate myriad membraneless organelles (MLOs) and cellular pathways such as transcription, signaling transduction and protein degeneration. PS droplets are usually liquid-like and can convert to hydrogel/ ... ...

    Abstract Phase separation (PS) proteins form droplets to regulate myriad membraneless organelles (MLOs) and cellular pathways such as transcription, signaling transduction and protein degeneration. PS droplets are usually liquid-like and can convert to hydrogel/solid-like under certain conditions. The PS behavior of proteins is regulated by co-PS partners and mutations, modifications, oligomerizations, repeat regions and alternative splicing of the proteins. With growing interest in PS condensates and associated proteins, we established PhaSepDB 1.0, which provided experimentally verified PS proteins and MLO-related proteins. The past few years witnessed a surge in PS-related research works; thus, we kept updating PhaSepDB. The current PhaSepDB contains 1419 PS entries, 770 low-throughput MLO-related entries and 7303 high-throughput MLO-related entries. We provided more detailed annotations of PS proteins, including PS verification experiments, regions used in experiments, phase diagrams of different experimental conditions, droplet states, co-PS partners and PS regulatory information. We believe that researchers can go further in studying PS proteins with the updated PhaSepDB (http://db.phasep.pro/).
    MeSH term(s) Organelles/chemistry ; Proteins/chemistry ; Biomechanical Phenomena ; Cells/chemistry ; Cells/cytology
    Chemical Substances Proteins
    Language English
    Publishing date 2022-09-16
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 186809-3
    ISSN 1362-4962 ; 1362-4954 ; 0301-5610 ; 0305-1048
    ISSN (online) 1362-4962 ; 1362-4954
    ISSN 0301-5610 ; 0305-1048
    DOI 10.1093/nar/gkac783
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Impedimetric Immunosensor Utilizing Polyaniline/Gold Nanocomposite-Modified Screen-Printed Electrodes for Early Detection of Chronic Kidney Disease.

    Shaikh, Muhammad Omar / Srikanth, Boyanagunta / Zhu, Pei-Yu / Chuang, Cheng-Hsin

    Sensors (Basel, Switzerland)

    2019  Volume 19, Issue 18

    Abstract: The presence of small amounts of human serum albumin (HSA) in urine or microalbuminuria (30-300 µg/mL) is a valuable clinical biomarker for the early detection of chronic kidney disease (CKD). Herein, we report on the development of an inexpensive and ... ...

    Abstract The presence of small amounts of human serum albumin (HSA) in urine or microalbuminuria (30-300 µg/mL) is a valuable clinical biomarker for the early detection of chronic kidney disease (CKD). Herein, we report on the development of an inexpensive and disposable immunosensor for the sensitive, specific, and label-free detection of HSA using electrochemical impedance spectroscopy (EIS). We have utilized a simple one-step screen-printing protocol to fabricate the carbon-based three-electrode system on flexible plastic substrates. To enable efficient antibody immobilization and improved sensitivity, the carbon working electrode was sequentially modified with electropolymerized polyaniline (PANI) and electrodeposited gold nanocrystals (AuNCs). The PANI matrix serves as an interconnected nanostructured scaffold for homogeneous distribution of AuNCs and the resulting PANI/AuNCs nanocomposite synergically improved the immunosensor response. The PANI/AuNCs-modified working electrode surface was characterized using scanning electron microscopy (SEM) and the electrochemical response at each step was analyzed using EIS in a ferri/ferrocyanide redox probe solution. The normalized impedance variation during immunosensing increased linearly with HSA concentration in the range of 3-300 µg/mL and a highly repeatable response was observed for each concentration. Furthermore, the immunosensor displayed high specificity when tested using spiked sample solutions containing different concentrations of actin protein and J82 cell lysate (a complex fluid containing a multitude of interfering proteins). Consequently, these experimental results confirm the feasibility of the proposed immunosensor for early diagnosis and prognosis of CKD at the point of care.
    MeSH term(s) Aniline Compounds/chemistry ; Biosensing Techniques/methods ; Carbon/chemistry ; Cell Line, Tumor ; Dielectric Spectroscopy ; Electrodes ; Gold/chemistry ; Humans ; Metal Nanoparticles/chemistry ; Nanocomposites/chemistry ; Renal Insufficiency, Chronic/diagnosis ; Serum Albumin, Human/analysis ; Surface Properties
    Chemical Substances Aniline Compounds ; polyaniline ; Carbon (7440-44-0) ; Gold (7440-57-5) ; Serum Albumin, Human (ZIF514RVZR)
    Language English
    Publishing date 2019-09-16
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2052857-7
    ISSN 1424-8220 ; 1424-8220
    ISSN (online) 1424-8220
    ISSN 1424-8220
    DOI 10.3390/s19183990
    Database MEDical Literature Analysis and Retrieval System OnLINE

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