Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Hai-feng NI"'
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28985- (2024)
Background: Nephronophthisis (NPHP) is a rare autosomal recessive inherited tubulointerstitial nephropathy, the most prevalent genetic cause of end-stage renal disease (ESRD) in children. Convincing evidence indicated that the overall prevalence of N
Externí odkaz:
https://doaj.org/article/4d2a7a51cd174788b9bc15663a78f831
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-18 (2023)
Abstract Objective Investigating the impact of centromere protein N (CENP-N) on radiosensitivity of nasopharyngeal carcinoma (NPC) cells. Methods Using immunohistochemistry and immunofluorescence to detect CENP-N expression in tissues from 35 patient
Externí odkaz:
https://doaj.org/article/6868de2ba4444561856966d8b00cd57f
Publikováno v:
Cell Communication and Signaling, Vol 21, Iss 1, Pp 1-18 (2023)
Abstract Background Pyroptosis is crucial for controlling various immune cells. However, the role of allergen-induced CD11c + dendritic cell (DC) pyroptosis in allergic rhinitis (AR) remains unclear. Methods Mice were grouped into the control group,
Externí odkaz:
https://doaj.org/article/387c5ad8e9374618961d16ade6b33af9
Autor:
Lin-Li Lv, Cui Wang, Zuo-Lin Li, Jing-Yuan Cao, Xin Zhong, Ye Feng, Jun Chen, Tao-Tao Tang, Hai-Feng Ni, Qiu-Li Wu, Bin Wang, Hui-Yao Lan, Bi-Cheng Liu
Publikováno v:
Cell Death and Disease, Vol 12, Iss 10, Pp 1-11 (2021)
Abstract Tubules injury and immune cell activation are the common pathogenic mechanisms in acute kidney injury (AKI). However, the exact modes of immune cell activation following tubule damage are not fully understood. Here we uncovered that the rele
Externí odkaz:
https://doaj.org/article/50af5ecc5f8d457b96f1414b614b6a16
Autor:
Ye Feng, Xin Zhong, Hai-Feng Ni, Cui Wang, Tao-Tao Tang, Li-Ting Wang, Kai-Yun Song, Ri-Ning Tang, Hong Liu, Bi-Cheng Liu, Lin-Li Lv
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-13 (2021)
Abstract Background Diabetic nephropathy (DN) is a leading cause of renal failure, whereas the effective and early diagnostic biomarkers are still lacking. Methods Fourteen cytokines and chemokines mRNA were detected in urinary extracellular vesicles
Externí odkaz:
https://doaj.org/article/e27aa031852b4dc9a60e12388fffb176
Autor:
Le-Ting Zhou, Lin-Li Lv, Ming-Ming Pan, Yu-Han Cao, Hong Liu, Ye Feng, Hai-Feng Ni, Bi-Cheng Liu
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0167334 (2016)
Adverse outcome of chronic kidney disease, such as end stage renal disease, is a significant burden on personal health and healthcare costs. Urinary tubular injury markers, such as NGAL, KIM-1 and NAG, could provide useful prognostic value for the ea
Externí odkaz:
https://doaj.org/article/e338f5f13b6d45dea189fa341617cfcc
Autor:
Jun-Feng Chen, Hong Liu, Hai-Feng Ni, Lin-Li Lv, Ming-Hui Zhang, Ai-Hua Zhang, Ri-Ning Tang, Ping-Sheng Chen, Bi-Cheng Liu
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e83593 (2013)
Dysfunctional mitochondria participate in the progression of chronic kidney disease (CKD). Pirfenidone is a newly identified anti-fibrotic drug. However, its mechanism remains unclear. Mitochondrial dysfunction is an early event that occurs prior to
Externí odkaz:
https://doaj.org/article/75cdb78dd4e545d79ac8f03090792978
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20431 (2011)
BACKGROUND: Podocyte injury and subsequent excretion in urine play a crucial role in the pathogenesis and progression of diabetic nephropathy (DN). Quantification of messenger RNA (mRNA) expression in urinary sediment by real-time PCR is emerging as
Externí odkaz:
https://doaj.org/article/fcf78d95f588469ab91dd2c45faa31cc
Publikováno v:
Neurological Sciences. 43:1809-1815
Neuronal intranuclear inclusion disease (NIID) is a rare progressive neurodegenerative disorder, with complex and diverse of clinical manifestations characterized by eosinophilic hyaline inclusions in neurons and somatic cells. Due to the improvement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac28a7ff922005eb208c8e8c69f4b991
https://doi.org/10.1007/s10072-021-05526-2
https://doi.org/10.1007/s10072-021-05526-2
Publikováno v:
Clinical Kidney Journal
Immunoglobulin A (IgA) nephropathy, in the presence of myeloid bodies, has been reported in Fabry disease (FD). In this case, we excluded the diagnosis of FD by demonstrating the absence of mutation in the α-galactosidase A（GLA）gene. Our patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f4042be909845aab5f9c85cf454ccb2
http://europepmc.org/articles/PMC8162858
http://europepmc.org/articles/PMC8162858