Yan F - Search Results

1

S149R, a novel mutation in the ABCD1 gene causing X-linked adrenoleukodystrophy.

Yan F, Wang W, Ying H, Li H, Chen J, Xu C. Yan F, et al. Oncotarget. 2017 Sep 18;8(50):87529-87538. doi: 10.18632/oncotarget.20974. eCollection 2017 Oct 20. Oncotarget. 2017. PMID: 29152099 Free PMC article.

2

Identification and functional characterization of a large deletion of the CYP11B1 gene causing an 11β-Hydroxylase deficiency in a Chinese pedigree.

Xu C, Qiao J, Liu W, Jiang X, Yan F, Wu J, Han B, Zhang H, Guan Q, Gao L, Zhao J. Xu C, et al. Among authors: yan f. Horm Res Paediatr. 2012;78(4):212-7. doi: 10.1159/000342871. Epub 2012 Nov 6. Horm Res Paediatr. 2012. PMID: 23146819

3

Peroxisome proliferator-activated receptor α activation induces hepatic steatosis, suggesting an adverse effect.

Yan F, Wang Q, Xu C, Cao M, Zhou X, Wang T, Yu C, Jing F, Chen W, Gao L, Zhao J. Yan F, et al. PLoS One. 2014 Jun 13;9(6):e99245. doi: 10.1371/journal.pone.0099245. eCollection 2014. PLoS One. 2014. PMID: 24926685 Free PMC article.

4

Thyrotropin increases hepatic triglyceride content through upregulation of SREBP-1c activity.

Yan F, Wang Q, Lu M, Chen W, Song Y, Jing F, Guan Y, Wang L, Lin Y, Bo T, Zhang J, Wang T, Xin W, Yu C, Guan Q, Zhou X, Gao L, Xu C, Zhao J. Yan F, et al. J Hepatol. 2014 Dec;61(6):1358-64. doi: 10.1016/j.jhep.2014.06.037. Epub 2014 Jul 10. J Hepatol. 2014. PMID: 25016220

5

Thyroid-stimulating hormone inhibits adipose triglyceride lipase in 3T3-L1 adipocytes through the PKA pathway.

Jiang D, Ma S, Jing F, Xu C, Yan F, Wang A, Zhao J. Jiang D, et al. Among authors: yan f. PLoS One. 2015 Jan 15;10(1):e0116439. doi: 10.1371/journal.pone.0116439. eCollection 2015. PLoS One. 2015. PMID: 25590597 Free PMC article.

6

Characterization of a Relatively Malignant Form of Osteopetrosis Caused by a Novel Mutation in the PLEKHM1 Gene.

Bo T, Yan F, Guo J, Lin X, Zhang H, Guan Q, Wang H, Fang L, Gao L, Zhao J, Xu C. Bo T, et al. Among authors: yan f. J Bone Miner Res. 2016 Nov;31(11):1979-1987. doi: 10.1002/jbmr.2885. Epub 2016 Jul 13. J Bone Miner Res. 2016. PMID: 27291868 Free article.

7

Confirmation of the pathogenicity of a mutation p.G337C in the COL1A2 gene associated with osteogenesis imperfecta.

Jia M, Shi R, Zhao X, Fu Z, Bai Z, Sun T, Zhao X, Wang W, Xu C, Yan F. Jia M, et al. Among authors: yan f. Medicine (Baltimore). 2017 Sep;96(39):e7783. doi: 10.1097/MD.0000000000007783. Medicine (Baltimore). 2017. PMID: 28953610 Free PMC article.

8

Identification and Characteristics of Novel Mutations in Nonsyndromic Monogenic Obesity.

Shi P, Shi Y, Liu X, Wang S, Yuan J, Zhao W, Fang L, Wang R, Yan F, Xu C. Shi P, et al. Among authors: yan f. Adv Biol (Weinh). 2023 Aug;7(8):e2300061. doi: 10.1002/adbi.202300061. Epub 2023 Apr 21. Adv Biol (Weinh). 2023. PMID: 37083215

9

Remnant cholesterol, stronger than triglycerides, is associated with incident non-alcoholic fatty liver disease.

Cheng Y, Zhang Q, Li H, Zhou G, Shi P, Zhang X, Guan L, Yan F, Xu C. Cheng Y, et al. Among authors: yan f. Front Endocrinol (Lausanne). 2023 May 5;14:1098078. doi: 10.3389/fendo.2023.1098078. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37214248 Free PMC article.

10

Hepatocyte miR-21-5p-deficiency alleviates APAP-induced liver injury by inducing PPARγ and autophagy.

Xu C, Yan F, Zhao Y, Jaeschke H, Wu J, Fang L, Zhao L, Zhao Y, Wang L. Xu C, et al. Among authors: yan f. Toxicol Sci. 2024 Feb 28;198(1):50-60. doi: 10.1093/toxsci/kfad132. Toxicol Sci. 2024. PMID: 38180883 Free PMC article.

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