Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Yanhui, Jin"'
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-4 (2023)
Abstract Background Preeclampsia complicated with hypofibrinogenemia is a rare disorder. We report two cases of severe preeclampsia complicated with hypofibrinogenemia followed by postpartum haemorrhage (PPH). Case Two women diagnosed as preeclampsia
Externí odkaz:
https://doaj.org/article/0631700a411a4bed9b4ce5c6bbaef5cf
Publikováno v:
SAGE Open, Vol 13 (2023)
This study examines the impact of institutional investors on the readability of corporate social responsibility (CSR) reports in the Chinese polluting industry. All available CSR reports in the listed polluting industries in China from 2010 to 2019 a
Externí odkaz:
https://doaj.org/article/dd88580f2628463fa7a568b45be84db1
Publikováno v:
IEEE Access, Vol 11, Pp 42191-42203 (2023)
In order to solve the resource allocation problem in scenarios of centralized wireless cellular communication with multiple cells, users and channels, a novel resource allocation algorithm based on joint Deep Deterministic Policy Gradient (DDPG) rein
Externí odkaz:
https://doaj.org/article/ea094cbf95604a12af8dd33f6168688f
Publikováno v:
Entropy, Vol 24, Iss 12, p 1722 (2022)
Device-to-device (D2D) technology enables direct communication between devices, which can effectively solve the problem of insufficient spectrum resources in 5G communication technology. Since the channels are shared among multiple D2D user pairs, it
Externí odkaz:
https://doaj.org/article/3a7bd325c48041f0a1c1518d82acafc5
Autor:
Manlin Zeng, Kaiqi Jia, Haixiao Xie, Yaosheng Xie, Lihong Yang, Yuan Chen, Yanhui Jin, Mingshan Wang
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b65a7359cdbadedbeb80c3b24808f00
https://doi.org/10.1007/s12288-023-01666-x
https://doi.org/10.1007/s12288-023-01666-x
Publikováno v:
Blood Coagulation & Fibrinolysis. 33:61-66
The aim of this study was to explore the molecular pathogenesis of two families with compound heterozygous hereditary factor XI deficiency. All the exons, flanking sequences, 5' and 3' untranslated regions of the F11 gene were analysed by direct DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab0648c61b1c656f26f4415f1c5ad29
https://doi.org/10.1097/mbc.0000000000001105
https://doi.org/10.1097/mbc.0000000000001105
Publikováno v:
Journal of Clinical Laboratory Analysis. 36
Inherited AT deficiency is an autosomal-dominant thrombophilic disorder usually caused by various SERPINC1 defects associated with a high risk of recurrent venous thromboembolism. In this article, the phenotype, gene mutation, and molecular pathogeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1b974285cf622fffa0a2a711aa6ad9f
https://doi.org/10.1002/jcla.24732
https://doi.org/10.1002/jcla.24732
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 33(6)
The objective of the study was to analyse a novel F13A1 gene mutation in a Chinese patient with factor XIII (FXIII) deficiency and explore the molecular mechanism. Pedigree investigation, clinical diagnosis, phenotypic and genetic analysis were condu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6422a34b3d15c3945d138ab92875e318
https://pubmed.ncbi.nlm.nih.gov/35981255
https://pubmed.ncbi.nlm.nih.gov/35981255
Autor:
Haixiao, Xie, Lihong, Yang, Huinan, Xia, Yanhui, Jin, Xiaolong, Li, Shuting, Jiang, Yaoyao, Xu, Mingshan, Wang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 39(7)
To explore the genetic basis for a patient with factor VIII deficiency.All exons of the F13A1 and F13B genes were amplified by PCR and sequenced directly. The sequencing was performed with a reverse primer if a variant was found. Conservation of vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9449247301a3f264a6ba60f2e46eb9e6
https://pubmed.ncbi.nlm.nih.gov/35810426
https://pubmed.ncbi.nlm.nih.gov/35810426