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Article ; Online: Monomorphic epitropic intestinal T-cell lymphoma presenting with intestinal perforation.

Zhang, Yong-Sheng / Kong, De-Tong / Zhang, Min / Liu, Xiang-Yu

2024 Volume 47, Issue 5, Page(s) 2494–2495

MeSH term(s)	Humans ; Intestinal Perforation/etiology ; Intestinal Perforation/surgery ; Lymphoma, T-Cell/complications ; Lymphoma, T-Cell/pathology ; Lymphoma, T-Cell/diagnosis ; Male ; Intestinal Neoplasms/complications ; Intestinal Neoplasms/surgery ; Intestinal Neoplasms/diagnostic imaging ; Intestinal Neoplasms/pathology ; Tomography, X-Ray Computed ; Middle Aged
Language	English
Publishing date	2024-01-30
Publishing country	Netherlands
Document type	Case Reports ; Letter
ZDB-ID	1068461-x
ISSN	0219-3108 ; 1015-9584
ISSN (online)	0219-3108
ISSN	1015-9584
DOI	10.1016/j.asjsur.2024.01.091
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Article: Chromosome Microarray Analysis Detection of a Single Exon Deletion of the Duchenne Muscular Dystrophy Gene in a Fetus: a Case Report.

Wang, Jing / Zhang, Yong-Sheng / Liu, Wan-Ru / Chen, Lin-Jiao

Clinical laboratory

2022 Volume 68, Issue 5

Abstract: Background: Amniocentesis was performed on a pregnant woman with a deletion of exon 45 of the Duchenne Muscular Dystrophy (DMD) gene.: Methods: Fetal Xp21.1 (31944831-32030363) x 0 was found by chromosome microarray analysis (CMA), i.e., 0.086 Mb ... ...

Abstract	Background: Amniocentesis was performed on a pregnant woman with a deletion of exon 45 of the Duchenne Muscular Dystrophy (DMD) gene. Methods: Fetal Xp21.1 (31944831-32030363) x 0 was found by chromosome microarray analysis (CMA), i.e., 0.086 Mb hemizygote deletion was detected in the Xp21.1 region of the fetal X chromosome, which contained exon 45 of the DMD gene. Results: The results verified by MLPA were consistent with those of CMA, which indicated that CMA was accurate in a single exon deletion in this fetus. This case suggests that CMA may become an essential method for the prenatal diagnosis of a fetus with DMD gene deletion/duplication. Conclusions: It can routinely detect chromosome copy number variation and analyze DMD diseases caused by exon duplication or deletion, which is enormously significant for new DMD exon deletion or duplication.
MeSH term(s)	Chromosomes ; DNA Copy Number Variations ; Dystrophin/genetics ; Exons/genetics ; Female ; Fetus ; Gene Deletion ; Humans ; Microarray Analysis ; Muscular Dystrophy, Duchenne/diagnosis ; Muscular Dystrophy, Duchenne/genetics ; Pregnancy
Chemical Substances	Dystrophin
Language	English
Publishing date	2022-05-10
Publishing country	Germany
Document type	Case Reports
ZDB-ID	1307629-2
ISSN	1433-6510 ; 0941-2131
ISSN	1433-6510 ; 0941-2131
DOI	10.7754/Clin.Lab.2021.210750
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Article: A broadband high frequency laser interferometer gravitational wave detector

Hu, Meng-Jun / Zhang, Yong-Sheng

Abstract: The gravitational wave detector of higher sensitivity and greater bandwidth is required for future gravitational wave astronomy and cosmology. Here we present a new type broadband high frequency laser interferometer gravitational wave detector utilizing ... ...

Abstract	The gravitational wave detector of higher sensitivity and greater bandwidth is required for future gravitational wave astronomy and cosmology. Here we present a new type broadband high frequency laser interferometer gravitational wave detector utilizing polarization of light as signal carrier. Except for Fabry-Perot cavity arms we introduce dual power recycling to further amplify the gravitational wave signals. A novel method of weak measurement amplification is used to amplify signals for detection and to guarantee the long-term run of detector. Equipped with squeezed light, the proposed detector is shown sensitive enough within the window from 100Hz to several kHz, making it suitable for the study of high frequency gravitational wave sources. With zero-area Sagnac topology, the detector has the potential to realize quantum non-demolition measurement. The detector presented here is expected to provide an alternative way of exploring the possible ground-base gravitational wave detector for the need of future research.
Keywords	covid19
Publisher	ArXiv
Document type	Article
Database	COVID19

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Article ; Online: Annual Variation of CO2 Absorption and Release in Caotang River of Three Gorges Reservoir

Zhang Yong-Sheng / Li Hai-Ying / Wu Lei-xiang

E3S Web of Conferences, Vol 185, p

2020 Volume 02029

Abstract: To analyze the annual variation of CO2 absorption and release in Caotang River of Three Gorges Reservoir, this paper selected six sections from the Yangtze River and Caotang River between July 2017 and June 2018, and monitored CO2 emission at the water- ... ...

Abstract	To analyze the annual variation of CO2 absorption and release in Caotang River of Three Gorges Reservoir, this paper selected six sections from the Yangtze River and Caotang River between July 2017 and June 2018, and monitored CO2 emission at the water-gas interface using static closed chamber. The results are as follows: during the investigation, the variation rate of CO2 averaged 0.66-2.05 ppm/Min in Caotang River, and the number was 1.02 ppm/Min and 2.67 ppm/Min in Yangtze River. In November, CO2 in Caotang River experienced dramatic variation as it was released from the water body to the atmosphere. The highest release rate occurred at the CT02 section, which was up to 42.58ppm/min. From July to October of 2017, most sections of the river absorbed CO2 without a fixed pattern in space. From January to March of 2018, the absorption and release rate of CO2 slowed down, with its absolute value between 0.20-2.28 ppm/min. The release or absorption rate of CO2 from April to June was slightly higher than that from January to March.
Keywords	Environmental sciences ; GE1-350
Subject code	333
Language	English
Publishing date	2020-01-01T00:00:00Z
Publisher	EDP Sciences
Document type	Article ; Online
Database	BASE - Bielefeld Academic Search Engine (life sciences selection)

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Article ; Online: Anisotropic Amorphization and Phase Transition in Na

Cheng, Lixun / Shen, Yaoling / Nan, Pengfei / Wu, Chuanqiang / Tai, Yilin / Luo, Xiaonan / Zhang, YongSheng / Ge, Binghui

Small (Weinheim an der Bergstrasse, Germany)

2023 Volume 20, Issue 6, Page(s) e2305655

Abstract: ... ...

Abstract	Na
Language	English
Publishing date	2023-09-28
Publishing country	Germany
Document type	Journal Article
ZDB-ID	2168935-0
ISSN	1613-6829 ; 1613-6810
ISSN (online)	1613-6829
ISSN	1613-6810
DOI	10.1002/smll.202305655
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Article ; Online: Glycogen phosphorylase of shrimp (Litopenaeus vannamei): Structure, expression and anti-WSSV function.

Zhang, Yong-Sheng / Li, Fei-Xiang / Yao, Cui-Luan

Fish & shellfish immunology

2019 Volume 91, Page(s) 275–283

Abstract: Glycogen phosphorylase (GP, EC 2.4.1.1) catalyze the rate-limiting step in glycogenolysis in animals, forming glucose-1-phosphate from the terminal alpha-1,4-glycosidic bond. Therefore, GP plays a crucial role in carbohydrate metabolism. In the present ... ...

Abstract	Glycogen phosphorylase (GP, EC 2.4.1.1) catalyze the rate-limiting step in glycogenolysis in animals, forming glucose-1-phosphate from the terminal alpha-1,4-glycosidic bond. Therefore, GP plays a crucial role in carbohydrate metabolism. In the present study, the full-length cDNA sequence of GP (LvGP) was cloned from shrimp, Litopenaeus vannamei. The obtained 3242-bp LvGP cDNA sequence included a 5'-terminal untranslated region (UTR) of 48 bp, an open reading frame (ORF) of 2559 bp encoding a polypeptide of 852 amino acids (aa) and a 3'-UTR of 635 bp. The predicted LvGP protein sequence contained a typical phosphorylase domain (113-829 aa) and shared 72%-97% identities with GP from other species. Phylogenetic analysis revealed that LvGP showed the closest relationship with GP from Marsupenaeus japonicus. Tissue expression profiles showed that LvGP existed in most examined tissues, with the most predominant expression in the brain, followed by the muscles and stomach. LvGP transcripts in hepatopancreas and hemocytes were up regulated after the WSSV challenge. Furthermore, the role of LvGP in shrimp defending against WSSV infection was investigated by RNA interference (RNAi). Our findings showed that WSSV proliferation and shrimp accumulative mortality increased significantly after LvGP RNAi (P < 0.01). The glycogen, glucose, and pyruvate content decreased in GP RNAi shrimp after WSSV injection, however, the lactate and ATP concentration enhanced. Moreover, lectin and anti-lipopolysaccharide factor2 (ALF2) were induced in LvGP silencing shrimp after WSSV infection, whereas the expression levels of crustin, ALF1 and ALF3 decreased. Our results suggested that the LvGP might play a crucial role in shrimp defending against WSSV infection by regulating metabolism and affecting the anti-infectious gene expression.
MeSH term(s)	Amino Acid Sequence ; Animals ; Arthropod Proteins/chemistry ; Arthropod Proteins/genetics ; Arthropod Proteins/immunology ; Base Sequence ; Gene Expression Profiling ; Gene Expression Regulation/immunology ; Glycogen Phosphorylase/chemistry ; Glycogen Phosphorylase/genetics ; Glycogen Phosphorylase/immunology ; Immunity, Innate/genetics ; Penaeidae/genetics ; Penaeidae/immunology ; Phylogeny ; RNA Interference ; Up-Regulation ; White spot syndrome virus 1/physiology
Chemical Substances	Arthropod Proteins ; Glycogen Phosphorylase (EC 2.4.1.-)
Language	English
Publishing date	2019-05-21
Publishing country	England
Document type	Journal Article
ZDB-ID	1067738-0
ISSN	1095-9947 ; 1050-4648
ISSN (online)	1095-9947
ISSN	1050-4648
DOI	10.1016/j.fsi.2019.05.043
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Article ; Online: Characterization and role of PGK from Litopenaeus vannamei in WSSV infection.

Li, Fei-Xiang / Zhang, Yong-Sheng / Yao, Cui-Luan

Fish & shellfish immunology

2019 Volume 93, Page(s) 144–152

Abstract: Phosphoglycerate kinase (EC 2.7.2.3, PGK) catalyses the reversible transfer of a phosphate group from 1,3-diphosphoglyceric acid and ADP to produce 3-phosphoglyceric acid and ATP, which represents the initial production of ATP during glycolysis; ... ...

Abstract	Phosphoglycerate kinase (EC 2.7.2.3, PGK) catalyses the reversible transfer of a phosphate group from 1,3-diphosphoglyceric acid and ADP to produce 3-phosphoglyceric acid and ATP, which represents the initial production of ATP during glycolysis; therefore, PGK is a key enzyme in the energy metabolism. To study the role of PGK in the resistance to WSSV infection in shrimp, the full-length cDNA of the PGK gene (LvPGK) from Litopenaeus vannamei was obtained by using homology cloning and RACE amplification. The tissue distribution of LvPGK and its expression changes in the main immune tissues after WSSV stimulation were obtained by quantitative real-time PCR. Furthermore, RNA interference (RNAi) was used to study the role of LvPGK in shrimp defending against WSSV infection. The results showed that the full-length cDNA sequence of LvPGK was 1855 bp, contained a 1248 bp open reading frame (ORF) encoding 415 amino acids, and included a conserved PGK domain. LvPGK presented ubiquitous expression in most examined tissues, with the most predominant expression in the muscle and the weakest expression in the intestine. LvPGK transcripts could be induced in the hemocytes and hepatopancreas by injection with WSSV. Both the replication of WSSV and the shrimp cumulative mortality decreased significantly after LvPGK knockdown (P < 0.01). After challenging LvPGK RNAi shrimp with WSSV, the concentration of glucose in the hepatopancreas and muscle tissue did not show significant change; however, the content of pyruvate and lactate decreased significantly (P < 0.05). Moreover, significant decreases in the expression levels of crustin, ALF1, ALF2 and ALF3 were also detected. The results suggested that LvPGK might be involved in WSSV replication by increasing host aerobic and anaerobic metabolism.
MeSH term(s)	Amino Acid Sequence ; Animals ; Arthropod Proteins/chemistry ; Arthropod Proteins/genetics ; Arthropod Proteins/immunology ; Base Sequence ; Gene Expression Profiling ; Gene Expression Regulation/immunology ; Immunity, Innate/genetics ; Penaeidae/enzymology ; Penaeidae/genetics ; Penaeidae/immunology ; Phosphoglycerate Kinase/chemistry ; Phosphoglycerate Kinase/genetics ; Phosphoglycerate Kinase/immunology ; Phylogeny ; Sequence Alignment ; White spot syndrome virus 1/physiology
Chemical Substances	Arthropod Proteins ; Phosphoglycerate Kinase (EC 2.7.2.3)
Language	English
Publishing date	2019-07-18
Publishing country	England
Document type	Journal Article
ZDB-ID	1067738-0
ISSN	1095-9947 ; 1050-4648
ISSN (online)	1095-9947
ISSN	1050-4648
DOI	10.1016/j.fsi.2019.07.048
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Article ; Online: Prenatal diagnosis of 6pter-p24 deletion syndrome in a fetus from a Han Chinese family: A case report.

Shi, Qing-Yang / Liu, Yan-Hong / Zhang, Yong-Sheng / Yu, Xiao-Wei

Medicine

2020 Volume 99, Issue 8, Page(s) e19246

Abstract: Introduction: Chromosome 6pter-p24 deletion syndrome (OMIM #612582) is a rare genetic disorder characterized by deletion of the distal part of 6p. Human 6p deletion syndromes result in a variety of congential malformations.: Patient concerns: The ... ...

Abstract	Introduction: Chromosome 6pter-p24 deletion syndrome (OMIM #612582) is a rare genetic disorder characterized by deletion of the distal part of 6p. Human 6p deletion syndromes result in a variety of congential malformations. Patient concerns: The fetus was the fourth child born to healthy non-consanguineous parents with no relevant family history. Diagnosis: The fetus was diagnosed with 6pter-p24 deletion syndrome through prenatal ultrasound, magnetic resonance imaging, and chromosomal microarray analysis. The fetus had brain, skeletal, and heart malformations. The fetus was cytogenetically normal. Chromosomal microarray analysis detected an interstitial 7.999Mb deletion within the 6p25.1p24.3 region of chromosome 6. Interventions: There was no treatment for the fetus. Outcomes: Pregnancy was terminated. Conclusions: To the author's knowledge, the present case is one of the first to report the prenatal diagnosis of 6pter-p24 deletion syndrome in a fetus. No published reports have described the diagnosis of 6pter-p24 deletion syndrome using multiple technologies during the antenatal period; therefore, our findings may provide a reference for other clinicians. The clinical features and pathophysiology of this prenatal diagnosis are discussed.
MeSH term(s)	Chromosome Deletion ; Chromosomes, Human, Pair 6 ; Eye Abnormalities/diagnosis ; Female ; Fetus ; Hearing Loss/diagnosis ; Heart Defects, Congenital/diagnosis ; Humans ; Hypertelorism/diagnosis ; Pregnancy ; Prenatal Diagnosis/methods
Language	English
Publishing date	2020-02-20
Publishing country	United States
Document type	Case Reports ; Journal Article
ZDB-ID	80184-7
ISSN	1536-5964 ; 0025-7974
ISSN (online)	1536-5964
ISSN	0025-7974
DOI	10.1097/MD.0000000000019246
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Article: Application of a nurse-led multidisciplinary health problem assessment tool on patients undergoing peritoneal dialysis at home: A cross-sectional study.

Luo, YiXin / Huang, YanLin / Cui, MiaoLing / Zhang, JiLiang / Zhang, YongSheng

Clinical nephrology

2021 Volume 96, Issue 6, Page(s) 317–327

Abstract: Objective: To identify and analyze the most prominent problems of peritoneal dialysis (PD) patients by applying a nurse-led multidisciplinary health problem assessment tool.: Methods: 170 PD patients were recruited from the PD center of the First ... ...

Abstract	Objective: To identify and analyze the most prominent problems of peritoneal dialysis (PD) patients by applying a nurse-led multidisciplinary health problem assessment tool. Methods: 170 PD patients were recruited from the PD center of the First Affiliated Hospital of GuangXi Medical University from January 2019 to June 2019, and their information was collected from July 2019 to June 2020 through telephone interviews, Wechat interviews, outpatient visits, and home visits; their health problems were classified and analyzed with regard to physiological, psychosocial, health-related behavior, and environment categories based on the Omaha Problem Classification System, and their knowledge, behavior, and status related to these problems were evaluated by the Omaha Knowledge-Behavior-Status Scale. Results: 165 of the eligible patients completed the follow-up, and their ten most prominent health problems were "Income", "Social contact", "Pain", "Neuro-musculo-skeletal function", "Digestion-hydration" and "Edema", "Nutrition", "Physical activity", "Fluid and diet restriction", and "Symptom management". As for the Knowledge-Behavior-Status scale, they got the lowest scores in knowledge of "Symptom management", behavior of "Fluid and diet restriction" and Status of "Nutrition", while they scored the best in knowledge of "Nutrition" and "Edema", behavior of "Income" and "Pain", and Status of "Pain" and "Edema". Conclusion: The multidisciplinary problem assessment tool based on the Omaha Problem Classification System serves as an effective and instructive tool to identify the prominent health problems of PD patients and provides a basis for the development of subsequent targeted interventions.
MeSH term(s)	China ; Cross-Sectional Studies ; Humans ; Nurse's Role ; Nutritional Status ; Peritoneal Dialysis/adverse effects
Language	English
Publishing date	2021-10-04
Publishing country	Germany
Document type	Journal Article
ZDB-ID	185101-9
ISSN	0301-0430
ISSN	0301-0430
DOI	10.5414/CN110497
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Article: The untold story between enhancers and skeletal muscle development

ZHANG, Yong-sheng / LU, Dan / LIU, Yu-wen / YI, Guo-qiang / TANG, Zhong-lin

CAAS. Publishing services by Elsevier B.V Journal of integrative agriculture. 2020 Sept., v. 19, no. 9

2020

Abstract: Currently, enhancers have key transcriptional regulatory roles in muscle development. Skeletal muscle formation involves various molecules, and in animals, enhancers are one of the main types of transcriptional regulatory regions that are of great ... ...

Abstract	Currently, enhancers have key transcriptional regulatory roles in muscle development. Skeletal muscle formation involves various molecules, and in animals, enhancers are one of the main types of transcriptional regulatory regions that are of great importance to regulate myogenic gene expression. In muscle development, enhancers can generate enhancer RNAs (eRNAs) that are involved in the regulation of gene transcription. The regulation of gene expression by eRNAs offers great potential in improving animal production traits. Herein we comprehensively review the roles of enhancers in muscle formation and its potential function in skeletal muscle development. This review will describe the future application of enhancers in skeletal muscle development and discuss the prospects that enhancer studies offer for agriculture, biotechnology, and animal breeding.
Keywords	agriculture ; animal production ; animals ; biotechnology ; gene expression ; gene expression regulation ; muscle development ; muscles ; skeletal muscle ; transcription (genetics)
Language	English
Dates of publication	2020-09
Size	p. 2137-2149.
Publishing place	Elsevier B.V.
Document type	Article
Note	NAL-AP-2-clean
ZDB-ID	2660426-7
ISSN	2095-3119
ISSN	2095-3119
DOI	10.1016/S2095-3119(20)63235-X
Database	NAL-Catalogue (AGRICOLA)

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