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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 4
2006 1
2007 3
2008 2
2009 5
2010 5
2011 10
2012 11
2013 10
2014 16
2015 10
2016 18
2017 14
2018 21
2019 14
2020 20
2021 25
2022 33
2023 19
2024 7

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208 results

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Page 1
SERPINF1 Mediates Tumor Progression and Stemness in Glioma.
Song L, Huo X, Li X, Xu X, Zheng Y, Li D, Zhang J, Wang K, Wang L, Wu Z. Song L, et al. Genes (Basel). 2023 Feb 25;14(3):580. doi: 10.3390/genes14030580. Genes (Basel). 2023. PMID: 36980858 Free PMC article.
In the present study, we analyzed the prognostic value of SERPINF1 in three independent glioma datasets. Next, we explored the molecular functions and transcriptional regulation of SERPINF1 at the single-cell level. ...Knocking down SERPINF1 impaired the sphe …
In the present study, we analyzed the prognostic value of SERPINF1 in three independent glioma datasets. Next, we explored the molecu …
Adipose Triglyceride Lipase Regulation: An Overview.
Cerk IK, Wechselberger L, Oberer M. Cerk IK, et al. Curr Protein Pept Sci. 2018;19(2):221-233. doi: 10.2174/1389203718666170918160110. Curr Protein Pept Sci. 2018. PMID: 28925902 Free PMC article. Review.
Pan-cancer analysis of osteogenesis imperfecta causing gene SERPINF1.
Zhang C, Yang W, Zhang S, Zhang Y, Liu P, Li X, Zhi W, Yang D, Li M, Lu Y. Zhang C, et al. Intractable Rare Dis Res. 2022 Feb;11(1):15-24. doi: 10.5582/irdr.2021.01138. Intractable Rare Dis Res. 2022. PMID: 35261846 Free PMC article.
Osteogenesis imperfecta (OI) type VI causative gene SERPINF1, encodes a member of the serpin family that does not display the serine protease inhibitory activity shown by many of the other serpin proteins. ...In this paper, a series of bioinformatics analyses were conducte …
Osteogenesis imperfecta (OI) type VI causative gene SERPINF1, encodes a member of the serpin family that does not display the serine …
SERPINF1 gene variants causing late-onset progressive deforming osteogenesis imperfecta - A study of 18 patients from India.
Selina A, Kandagaddala M, Kumar V, Abraham SSC, Danda S, Madhuri V. Selina A, et al. Bone Rep. 2023 May 26;18:101690. doi: 10.1016/j.bonr.2023.101690. eCollection 2023 Jun. Bone Rep. 2023. PMID: 37425194 Free PMC article.
SERPINF1 gene variants lead to a severe type of osteogenesis imperfecta (OI) attributed to defects in the matrix mineralization. We present 18 patients with SERPINF1 gene variants leading to severe progressive deforming OI, the largest series in the world to date. . …
SERPINF1 gene variants lead to a severe type of osteogenesis imperfecta (OI) attributed to defects in the matrix mineralization. We p …
In Vivo Syngeneic Tumor Models with Acquired Resistance to Anti-PD-1/PD-L1 Therapies.
Denis M, Grasselly C, Choffour PA, Wierinckx A, Mathé D, Chettab K, Tourette A, Talhi N, Bourguignon A, Birzele F, Kress E, Jordheim LP, Klein C, Matera EL, Dumontet C. Denis M, et al. Cancer Immunol Res. 2022 Aug 3;10(8):1013-1027. doi: 10.1158/2326-6066.CIR-21-0802. Cancer Immunol Res. 2022. PMID: 35679518
Overexpression of Serpinf1 induced resistance to anti-PD-1 antibodies in the MC38 model, whereas knockdown of Serpinf1 sensitized this model as well as the primarily resistant MBT2 model. Serpinf1 overexpression was associated with increased production of fre …
Overexpression of Serpinf1 induced resistance to anti-PD-1 antibodies in the MC38 model, whereas knockdown of Serpinf1 sensiti …
A vasculogenic mimicry prognostic signature associated with immune signature in human gastric cancer.
Wang J, Xia W, Huang Y, Li H, Tang Y, Li Y, Yi B, Zhang Z, Yang J, Cao Z, Zhou J. Wang J, et al. Front Immunol. 2022 Nov 23;13:1016612. doi: 10.3389/fimmu.2022.1016612. eCollection 2022. Front Immunol. 2022. PMID: 36505458 Free PMC article.
In addition, the expression of one key VM-related gene (serpin family F member 1, SERPINF1) was validated in 33 GC tissues and 23 paracancer tissues using immunohistochemistry staining. ...The AUC (> 0.7) indicated the satisfactory discriminative ability of the nomogram …
In addition, the expression of one key VM-related gene (serpin family F member 1, SERPINF1) was validated in 33 GC tissues and 23 par …
Insufficient evidence for a role of SERPINF1 in otosclerosis.
Valgaeren H, Sommen M, Beyens M, Vandeweyer G, Schrauwen I, Schepers A, Schatteman I, Topsakal V, Dhooge I, Kunst H, Zanetti D, Huber AM, Hoischen A, Fransen E, Van Camp G. Valgaeren H, et al. Mol Genet Genomics. 2019 Aug;294(4):1001-1006. doi: 10.1007/s00438-019-01558-8. Epub 2019 Apr 9. Mol Genet Genomics. 2019. PMID: 30968248
The genetic causes of otosclerosis remain largely unidentified. Only mutations in a single gene, SERPINF1, were previously published in patients with familial otosclerosis. ...We could also not find evidence for a pathogenic role in otosclerosis for 5' UTR variants in the …
The genetic causes of otosclerosis remain largely unidentified. Only mutations in a single gene, SERPINF1, were previously published …
The effect of SERPINF1 in-frame mutations in osteogenesis imperfecta type VI.
Al-Jallad H, Palomo T, Roughley P, Glorieux FH, McKee MD, Moffatt P, Rauch F. Al-Jallad H, et al. Bone. 2015 Jul;76:115-20. doi: 10.1016/j.bone.2015.04.008. Epub 2015 Apr 11. Bone. 2015. PMID: 25868797
Osteogenesis imperfecta type VI is caused by mutations in SERPINF1, which codes for pigment-epithelium derived factor (PEDF). ...Skin fibroblasts affected by SERPINF1 in-frame mutations transcribed SERPINF1 at slightly reduced levels but secretion of PEDF was …
Osteogenesis imperfecta type VI is caused by mutations in SERPINF1, which codes for pigment-epithelium derived factor (PEDF). ...Skin …
Insights into male androgenetic alopecia using comparative transcriptome profiling: hypoxia-inducible factor-1 and Wnt/β-catenin signalling pathways.
Liu Q, Tang Y, Huang Y, Wang J, Yang K, Zhang Y, Pu W, Liu J, Shi X, Ma Y, Ni C, Zhang Y, Zhu Y, Li H, Wang J, Lin J, Wu W. Liu Q, et al. Br J Dermatol. 2022 Dec;187(6):936-947. doi: 10.1111/bjd.21783. Epub 2022 Sep 1. Br J Dermatol. 2022. PMID: 35862273 Free PMC article.
Differential expression of HIF-1 prolyl hydroxylase enzymes (EGLN1, EGLN3) and Wnt/beta-catenin pathway inhibitors (SERPINF1, SFRP2) was experimentally validated. In vitro studies revealed that reduction of EGLN1, EGLN3, SERPINF1 and SFRP2 stimulated proliferation o …
Differential expression of HIF-1 prolyl hydroxylase enzymes (EGLN1, EGLN3) and Wnt/beta-catenin pathway inhibitors (SERPINF1, SFRP2) …
208 results