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Year Number of Results
2008 1
2010 1
2014 1
2017 8
2018 6
2019 2
2020 0
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17 results
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Thymoquinone, as an anticancer molecule: from basic research to clinical investigation.
Asaduzzaman Khan M, Tania M, Fu S, Fu J. Asaduzzaman Khan M, et al. Among authors: fu s. Oncotarget. 2017 Apr 18;8(31):51907-51919. doi: 10.18632/oncotarget.17206. eCollection 2017 Aug 1. Oncotarget. 2017. PMID: 28881699 Free PMC article. Review.
Molecular genetics ‎characterization and homology modeling of the CHM gene mutation: A study on its association with choroideremia.
Imani S, Ijaz I, Shasaltaneh MD, Fu S, Cheng J, Fu J. Imani S, et al. Among authors: fu s. Mutat Res. 2018 Jan-Mar;775:39-50. doi: 10.1016/j.mrrev.2018.02.001. Epub 2018 Feb 18. Mutat Res. 2018. PMID: 29555028 Review.
The diagnostic role of microRNA-34a in breast cancer: a systematic review and meta-analysis.
Imani S, Zhang X, Hosseinifard H, Fu S, Fu J. Imani S, et al. Among authors: fu s. Oncotarget. 2017 Apr 4;8(14):23177-23187. doi: 10.18632/oncotarget.15520. Oncotarget. 2017. PMID: 28423566 Free PMC article. Review.
In silico data analyses of the hotspot mutations of CHM gene in choroideremia disease.
Imani S, Ijaz I, Shasaltaneh MD, Fu S, Cheng J, Fu J. Imani S, et al. Among authors: fu s. Data Brief. 2018 Apr 12;18:1217-1223. doi: 10.1016/j.dib.2018.04.023. eCollection 2018 Jun. Data Brief. 2018. PMID: 29900297 Free PMC article.
Diagnostic value of a combination of next-generation sequencing, chorioretinal imaging and metabolic analysis: lessons from a consanguineous Chinese family with gyrate atrophy of the choroid and retina stemming from a novel OAT variant.
Huang J, Fu J, Fu S, Yang L, Nie K, Duan C, Cheng J, Li Y, Lv H, Chen R, Liu L, Fu J. Huang J, et al. Among authors: fu s. Br J Ophthalmol. 2019 Mar;103(3):428-435. doi: 10.1136/bjophthalmol-2018-312347. Epub 2018 Oct 26. Br J Ophthalmol. 2019. PMID: 30366948
A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis.
Fu J, Ma L, Cheng J, Yang L, Wei C, Fu S, Lv H, Chen R, Fu J. Fu J, et al. Among authors: fu s. J Cell Mol Med. 2018 Nov;22(11):5662-5669. doi: 10.1111/jcmm.13841. Epub 2018 Aug 30. J Cell Mol Med. 2018. PMID: 30160356 Free PMC article.
A novel splicing mutation in the PRPH2 gene causes autosomal dominant retinitis pigmentosa in a Chinese pedigree.
Cheng J, Fu J, Zhou Q, Xiang X, Wei C, Yang L, Fu S, Khan MA, Lv H, Fu J. Cheng J, et al. Among authors: fu s. J Cell Mol Med. 2019 May;23(5):3776-3780. doi: 10.1111/jcmm.14278. Epub 2019 Mar 20. J Cell Mol Med. 2019. PMID: 30892800 Free PMC article. No abstract available.
A Near-Infrared Light-Responsive Hybrid Hydrogel Based on UCST Triblock Copolymer and Gold Nanorods.
Zhang H, Guo S, Fu S, Zhao Y. Zhang H, et al. Among authors: fu s. Polymers (Basel). 2017 Jun 20;9(6):238. doi: 10.3390/polym9060238. Polymers (Basel). 2017. PMID: 30970915 Free PMC article.
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing.
Wei C, Yang L, Cheng J, Imani S, Fu S, Lv H, Li Y, Chen R, Leung EL, Fu J. Wei C, et al. Among authors: fu s. BMC Med Genet. 2018 Jun 11;19(1):99. doi: 10.1186/s12881-018-0602-0. BMC Med Genet. 2018. PMID: 29890953 Free PMC article.
Evaluation of PIK3CA mutations as a biomarker in Chinese breast carcinomas from Western China.
Cheng J, Fu S, Wei C, Tania M, Khan MA, Imani S, Zhou B, Chen H, Xiao X, Wu J, Fu J. Cheng J, et al. Among authors: fu s. Cancer Biomark. 2017;19(1):85-92. doi: 10.3233/CBM-160380. Cancer Biomark. 2017. PMID: 28269754
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