Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Zheng Kun Xia"'
Autor:
Ying-chao Peng, Zhi-qiang Zhang, Mei-qiu Wang, Xiang Fang, Chun-lin Gao, Tao Sun, Zheng-kun Xia
Publikováno v:
Linchuang shenzangbing zazhi, Vol 24, Iss 2, Pp 108-115 (2024)
ObjectiveTo evaluate the efficacy and safety of rituximab (RTX) for steroid-resistant idiopathic focal segmental glomerulosclerosis (FSGS) in children.MethodsFrom 2014 to 2020, the relevant clinical data were retrospectively reviewed for 12 children
Externí odkaz:
https://doaj.org/article/4a82c3cbd90b4c2c9f9eda55a887a4ee
Publikováno v:
Renal Failure, Vol 45, Iss 2 (2023)
Background Acute interstitial nephritis (AIN) is a relatively rare cause of acute kidney injury (AKI) in children. Immune complex (IC) deposition was rare in renal pathology of AIN.Methods Based on the status and position of IC deposition, a total of
Externí odkaz:
https://doaj.org/article/e365a42553aa4d6792b1e9e9b56423f8
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundCrescentic glomerulonephritis (CrGN) is a relatively rare but severe condition in childhood with the clinical feature of rapidly progressive glomerulonephritis (RPGN). The aim of this study is to investigate the clinicopathological features
Externí odkaz:
https://doaj.org/article/51de584a43454f34bfc8f2a765a7da76
Publikováno v:
Journal of Receptors and Signal Transduction. 40:273-280
Objective: The aim of our study is to investigate the relationship between podocyte autophagy and apoptosis induced by Puromycin Aminonucleoside (PAN) and to clarify its mechanism.Methods: Podocyte...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c7bbdfa63189f45129c7dbc12959494
https://doi.org/10.1080/10799893.2020.1731536
https://doi.org/10.1080/10799893.2020.1731536
Autor:
Xiao-Jun Li, Bai‐zeng Yu, Wei-Qing Wu, Ying-Xia Cui, Liu-Fei Miao, Fangfang Chen, Jia-Xun Zhang, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu
Publikováno v:
Cytogenetic and Genome Research. 160:238-244
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819faf6554406f630c6b258772989c67
https://doi.org/10.1159/000508562
https://doi.org/10.1159/000508562
Publikováno v:
Biochemical and Biophysical Research Communications. 497:285-291
Hypoxic/ischemic brain damage (HIBD) leads to high neonatal mortality and severe neurologic morbidity. However, the molecular mechanism of HIBD in the neonatal infant is still elusive. Long non-coding RNAs are shown as important regulators of brain d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed1f566ddbe8cf52b03f6d21107830b7
https://doi.org/10.1016/j.bbrc.2018.02.070
https://doi.org/10.1016/j.bbrc.2018.02.070
Autor:
Ying-Xia Cui, Xin-Yi Xia, Xiao-Jun Li, Er-Zhi Gao, Xiu-Xiu Wei, Ang Li, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu, Chun-Lin Gao, Jian-Hong Liu, Feng-Xia Liu, Asan
Publikováno v:
Cytogenetic and Genome Research. 154:30-36
Thin basement membrane nephropathy (TBMN), autosomal dominant Alport syndrome (ADAS), and focal segmental glomerulosclerosis (FSGS) are kidney diseases that differ in clinical diagnosis, treatment, and prognosis. Nevertheless, they may result from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d06b584dbd46e4f5909deac556e342b1
https://doi.org/10.1159/000486979
https://doi.org/10.1159/000486979
Autor:
Zhi-Hong Liu, Ying-Xia Cui, Jian-Hong Liu, Asan, Xing Lv, Er-Zhi Gao, Ang Li, Feng-Xia Liu, Xiu-Xiu Wei, Chun-Lin Gao, Zheng-Kun Xia, Xin-Yi Xia, Xiao-Jun Li
Publikováno v:
Cytogenetic and Genome Research. 154:132-136
Mutations in the COL4A5 gene result in X-linked Alport syndrome, homozygous or compound heterozygous mutations in COL4A3 or COL4A4 are responsible for autosomal recessive Alport syndrome, and heterozygous mutations in COL4A3 or COL4A4 cause autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cadacf7bbaa797a42424d38e0bb5c779
https://doi.org/10.1159/000488163
https://doi.org/10.1159/000488163
Publikováno v:
Molecular Medicine Reports. 16:6858-6863
MicroRNA‑106b (miR‑106b) is reported to be closely associated with skeletal muscle insulin resistance. The present study further investigated the role of miR‑106b in skeletal muscle insulin sensitivity and glucose homeostasis in vivo. Mice were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b6d8195b7d40aafd95d2aae293c9dc
https://doi.org/10.3892/mmr.2017.7439
https://doi.org/10.3892/mmr.2017.7439
Autor:
Xing, Lv, Wei-Qing, Wu, Jia-Xun, Zhang, Liu-Fei, Miao, Bai-Zeng, Yu, Fang-Fang, Chen, Ying-Xia, Cui, Zheng-Kun, Xia, Zhi-Hong, Liu, Xiao-Jun, Li
Publikováno v:
Cytogenetic and genome research. 160(5)
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ec9ccc9679989f6e3932440e8fe93cc
https://pubmed.ncbi.nlm.nih.gov/32659759
https://pubmed.ncbi.nlm.nih.gov/32659759