Fujun Lin
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Explore the profile of Fujun Lin including associated specialties, affiliations and a list of published articles.
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17
Citations
177
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Recent Articles
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2.
Li X, Zhu H, Xu P, Zhang J, Wang Z, He H, et al.
Front Immunol
. 2025 Jan;
15:1486352.
PMID: 39742285
Introduction: The coronavirus disease 2019 (COVID-19) global pandemic has been the most severe public health emergency since 2019. Currently, the Omicron variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)...
3.
Zhao Z, Dai X, Jiang G, Lin F
J Am Soc Nephrol
. 2023 Feb;
34(6):988-1002.
PMID: 36758123
Significance Statement: Causes of congenital anomalies of the kidney and urinary tract (CAKUT) remain unclear. The authors investigated whether and how inactivation of Ash2l -which encodes a subunit of the...
4.
Ni J, Zhu Y, Lin F, Guan W, Jin J, Li Y, et al.
Front Pediatr
. 2022 Dec;
10:1043502.
PMID: 36452359
Background: Dent disease is a group of inherited X-linked recessive renal tubular disorders. This group of disorders is characterized by low molecular weight proteinuria (LMWP), nephrocalcinosis, hypercalciuria and renal failure....
5.
Dai X, Zong X, Pan X, Lu W, Jiang G, Lin F
Orphanet J Rare Dis
. 2022 Jun;
17(1):237.
PMID: 35725559
Background: Fabry disease (FD, OMIM #301500) is an X-linked lysosomal disorder caused by the deficiency of α-galactosidase A (α-GalA), encoded by the GLA gene. Among more than 1100 reported GLA...
6.
Chen S, Shan J, Niu W, Lin F, Liu S, Wu P, et al.
RSC Adv
. 2022 May;
8(29):15890-15896.
PMID: 35542211
In this study, we have prepared miR-155 inhibitor-loaded liposome vesicles for the effective treatment of acute kidney injury. The efficacy of liposomal miR-155 inhibitor in the expression of miR-155, mortality...
7.
Khalil Y, Carrino S, Lin F, Ferlin A, Lad H, Mazzacuva F, et al.
Int J Mol Sci
. 2022 Jan;
23(2).
PMID: 35055171
Peroxisomal fatty acid α-oxidation is an essential pathway for the degradation of β-carbon methylated fatty acids such as phytanic acid. One enzyme in this pathway is 2-hydroxyacyl CoA lyase (HACL1),...
8.
Fan Y, Wang L, Sun Y, Xu T, Gong Z, Zhao Q, et al.
J Hum Genet
. 2020 Oct;
66(4):409-417.
PMID: 33040084
Long continuous stretches of homozygosity (LCSH) are associated with risk of recessive disorders. Though LCSH can be detected by SNP microarrays, additional testing is necessary to clarify the clinical significance....
9.
Tan P, Xu Y, Du Y, Wu L, Guo B, Huang S, et al.
Cell Death Dis
. 2019 Oct;
10(11):794.
PMID: 31624231
Speckle-type POZ domain protein (SPOP), an adaptor in the E3 ubiquitin ligase complex, recognizes substrates and promotes protein degradation via the ubiquitin-proteasome system. It appears to help regulate progression of...
10.
Qian X, Du Y, Jiang G, Lin F, Yao L
Front Physiol
. 2019 May;
10:559.
PMID: 31139093
The survival of motor neuron (SMN) protein is ubiquitously involved in spliceosome assembly and ribonucleoprotein biogenesis. SMN protein is expressed in kidney and can affect cell death processes. However, the...