Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Qiuwang, Zhang"'
Publikováno v:
Journal of Biological Engineering, Vol 17, Iss 1, Pp 1-15 (2023)
Abstract Background Thrombosis is a common cause of vascular prosthesis failure. Antibody coating of prostheses to capture circulating endothelial progenitor cells to aid endothelialization on the device surface appears a promising solution to preven
Externí odkaz:
https://doaj.org/article/92522e3d914c41f3b53cc49a8c10f50a
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/5e4eaab196214a198d5f6c33b46ab106
Publikováno v:
Stem Cells International, Vol 2022 (2022)
Endothelial cell (EC) dysfunction has been implicated in a variety of pathological conditions. The collection of ECs from patients is typically conducted postmortem or through invasive procedures, such as surgery and interventional procedures, hamper
Externí odkaz:
https://doaj.org/article/884abb813a6c4fd2b61e4f80112112d4
Autor:
Weirong Jin, Qiuwang Zhang, Bei Wang, Lili Pan, Hongyou Qin, Daying Yang, Xiangqun Zhou, Yongcai Du, Ling Lin, Michael J. Kutryk
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Familial hypercholesterolemia (FH), an autosomal dominant genetic disorder, is underdiagnosed and undertreated. The majority of FH cases are caused by low density lipoprotein receptor (LDL-R) gene mutations. The C308Y mutation in
Externí odkaz:
https://doaj.org/article/0bae859ad7bb4dceb0293d73903c0262
Autor:
Fushun Lin, Qian Wang, Lingwei Meng, Yongfeng Liang, Xiangjin Kong, Kaiming Wei, Qiuwang Zhang, Xinghua Gu
Publikováno v:
International Journal of Cardiology. 375:57-65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1431688be8b28202451778e7a7d2810a
https://doi.org/10.1016/j.ijcard.2023.01.023
https://doi.org/10.1016/j.ijcard.2023.01.023
Autor:
Bei Wang, Qiuwang Zhang, Ling Lin, Li-li Pan, Cheng-yu He, Xiang-xin Wan, Zhi-ang Zheng, Zheng-xin Huang, Chao-bao Zou, Ming-chang Fu, Michael J. Kutryk
Publikováno v:
Lipids in Health and Disease, Vol 17, Iss 1, Pp 1-7 (2018)
Abstract Background Achilles tendons are the most common sites of tendon xanthomas that are commonly caused by disturbance of lipid metabolism. Achilles tendon thickening is the early characteristic of Achilles tendon xanthomas. The relationship betw
Externí odkaz:
https://doaj.org/article/dcef752b28564b5fb43257d906b36a8d
Publikováno v:
European Journal of Pharmaceutics and Biopharmaceutics. 181:218-226
This study was designed to test the ability of ex vivo antibody-coated intravascular devices to capture genetically engineered pig endothelial colony-forming cells (ECFCs) as proof of concept for their potential for in vivo targeted drug delivery. Hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33d70e4b7f023e45e0bb7368bc140a0c
https://doi.org/10.1016/j.ejpb.2022.11.015
https://doi.org/10.1016/j.ejpb.2022.11.015
Publikováno v:
Stem Cells International. 2022:1-14
Endothelial cell (EC) dysfunction has been implicated in a variety of pathological conditions. The collection of ECs from patients is typically conducted postmortem or through invasive procedures, such as surgery and interventional procedures, hamper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af0b30e6a395fd91cc9b41cba2bf5259
https://doi.org/10.1155/2022/4460041
https://doi.org/10.1155/2022/4460041
Publikováno v:
International Journal of Molecular Sciences
Volume 24
Issue 5
Pages: 4916
Volume 24
Issue 5
Pages: 4916
Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disease characterized by aberrant angiogenesis and vascular malformations. Mutations in the transforming growth factor beta co-receptor, endoglin (ENG), account for approximately half of k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0c6004742dffbe17f820081657ef7e
Publikováno v:
Transl Res
Hereditary hemorrhagic telangiectasia (HHT) is a genetic disease characterized by vascular dysplasia. Mutations of the endoglin (ENG) gene that encodes a co-receptor of the transforming growth factor β1 signaling pathway cause type I HHT. ENG is pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79d4f11817b5d67ceace06f860119165
https://doi.org/10.1016/j.trsl.2021.04.005
https://doi.org/10.1016/j.trsl.2021.04.005