Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ji-shi Liu"'
Autor:
Shuai Guo, Yi Dong, Ran Du, Yu-Xing Liu, Shu Liu, Qin Wang, Ji-Shi Liu, Hui Xu, Yu-Jie Jiang, Huang Hao, Liang-Liang Fan, Rong Xiang
Publikováno v:
Molecular Biomedicine, Vol 5, Iss 1, Pp 1-17 (2024)
Abstract Chronic kidney disease (CKD) poses a significant global health dilemma, emerging from complex causes. Although our prior research has indicated that a deficiency in Reticulon-3 (RTN3) accelerates renal disease progression, a thorough examina
Externí odkaz:
https://doaj.org/article/b1214927b9f14e828954359a36c32f71
Publikováno v:
Linchuang shenzangbing zazhi, Vol 24, Iss 1, Pp 84-88 (2024)
Externí odkaz:
https://doaj.org/article/4cd47d4732314a2cbc5c58a5c5cc7e6f
Autor:
Jie‐Yuan Jin, Si‐Hua Chang, Ya‐Qin Chen, Meng‐Wei Liu, Yi Dong, Ji‐Shi Liu, Qin Wang, Hao Huang, Liang‐Liang Fan, Rong Xiang
Publikováno v:
MedComm, Vol 5, Iss 2, Pp n/a-n/a (2024)
Abstract The discovery of the endothelium as a major regulator of vascular tone triggered intense research among basic and clinical investigators to unravel the physiologic and pathophysiologic significance of this phenomenon. Sphingosine‐l‐phosp
Externí odkaz:
https://doaj.org/article/9cf2b655352d4c2d8424062dd91d5331
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
7q terminal deletion syndrome is a rare condition presenting with multiple congenital malformations, including abnormal brain and facial structures, developmental delay, intellectual disability, abnormal limbs, and sacral anomalies. At least 40 OMIM
Externí odkaz:
https://doaj.org/article/7737368f2aa148bf9959d1557658fa17
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)
Abstract Background Focal segmental glomerulosclerosis (FSGS), as the frequent primary glomerular diseases in adults, accounts for symptomless proteinuria or nephrotic syndrome with or without renal insufficiency. As the crucial lesion of chronic kid
Externí odkaz:
https://doaj.org/article/8f328df919c343378e913d0c503feedd
Autor:
Liang-Liang Fan, Ran Du, Ji-Shi Liu, Jie-Yuan Jin, Chen-Yu Wang, Yi Dong, Wan-Xia He, Ri-Qiang Yan, Rong Xiang
Publikováno v:
Experimental & Molecular Medicine. 54:653-661
Reticulon 3 (RTN3) is an endoplasmic reticulum protein that has previously been shown to play roles in neurodegenerative diseases, but little is known about its function in the kidneys. The aim of the present study was to clarify the roles of RTN3 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a867d708f0d04d86860f8d09b07148
https://doi.org/10.1038/s12276-022-00763-7
https://doi.org/10.1038/s12276-022-00763-7
Publikováno v:
Mol Syndromol
Loss of function of arginine vasopressin receptor 2 (AVPR2) may affect the recognition and binding of arginine vasopressin (AVP) which, in turn, may prevent the activation of Gs/adenylate cyclase and reduce the reabsorption of water by renal tubules
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73031ba46004c4465fcaf58dc929403
https://europepmc.org/articles/PMC7445547/
https://europepmc.org/articles/PMC7445547/
Publikováno v:
The American Journal of Cardiology. 119:1485-1489
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare heart disorder characterized by myocyte loss and fibro-fatty tissue replacement. With the progress of ARVC, patient can present serious ventricular arrhythmias, heart failure, and even
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d26b963cd12f16635458ba65ecd6aa6
https://doi.org/10.1016/j.amjcard.2017.01.011
https://doi.org/10.1016/j.amjcard.2017.01.011
Autor:
Kun Xia, Liang-Liang Fan, Rong Xiang, Hao Zhang, Xiaoxian Liu, Li-Jian Tao, Hao Huang, Ji-Shi Liu
Publikováno v:
Cardiology. 136:10-14
Objectives: Dilated cardiomyopathy (DCM) is a leading cause of sudden cardiac death. So far, only 127 mutations of Titin(TTN) have been reported in patients with different phenotypes such as isolated cardiomyopathies, purely skeletal muscle phenotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4ffb77a0ce1d6df1240a99b169937da
https://doi.org/10.1159/000447422
https://doi.org/10.1159/000447422
Publikováno v:
International journal of clinical and experimental pathology. 10(8)
Background: Alport syndrome (AS) is a genetic disease characterized by progressive glomerulonephritis with a high life-time risk for end-stage renal disease (ESRD), sensorineural hearing loss and ocular abnormalities. So far, a lot of mutations were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1501c36a704cb25dfc4a1b18973661ff
https://pubmed.ncbi.nlm.nih.gov/31966729
https://pubmed.ncbi.nlm.nih.gov/31966729