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  • Showing results for xiong, fu. Search instead for Xiongwu Fu (0)

[Congenital ectrodactyly caused by chromosome 10q24.31 duplication and its pathogenetic analysis].

Zhang XQ, Wang J, Xiong F, Lv WB, Zhou YQ, Yang SM, Zhang YT, Tian XY, Lian W, Xu XM.

Yi Chuan. 2019 Aug 20;41(8):716-724. doi: 10.16288/j.yczz.19-125. Chinese.


Rapid simultaneous detection of bla oxa-23, Ade-B, int-1, and ISCR-1 in multidrug-resistant Acinetobacter baumannii using single-tube multiplex PCR and high resolution melting assay.

Sun H, Xiao G, Zhang J, Pan Z, Chen Y, Xiong F.

Infect Drug Resist. 2019 Jun 7;12:1573-1581. doi: 10.2147/IDR.S207225. eCollection 2019.


Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway.

Pan Y, Lu T, Peng L, Chen Z, Li M, Zhang K, Xiong F, Wu B.

Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):2575-2584. doi: 10.1080/21691401.2019.1629950.


Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

Sun SC, Ma D, Li MY, Zhang RX, Huang C, Huang HJ, Xie YZ, Wang ZJ, Liu J, Cai DC, Liu CX, Yang Q, Bao FX, Gong XL, Li JR, Hui Z, Wei XF, Zhong JM, Zhou WJ, Shang X, Zhang C, Liu XG, Tang BS, Xiong F, Xu XM.

Brain. 2019 Aug 1;142(8):2215-2229. doi: 10.1093/brain/awz151.


Effects of the antimicrobial peptide L12 against multidrug‑resistant Staphylococcus aureus.

Xiong F, Dai X, Li YX, Wei R, An L, Wang Y, Chen Z.

Mol Med Rep. 2019 Apr;19(4):3337-3344. doi: 10.3892/mmr.2019.9988. Epub 2019 Feb 26.


Transcatheter arterial embolization combined with hypoxia-replicative oncolytic adenovirus perfusion enhances the therapeutic effect of hepatic carcinoma.

Zhang H, Xiong F, Qian K, Liu Y, Liang B, Xiong B, Yang F, Zheng C.

Cancer Manag Res. 2019 Jan 23;11:981-996. doi: 10.2147/CMAR.S189208. eCollection 2019.


Two successive cases of fetal harlequin ichthyosis: A case report.

Liang Q, Xiong F, Liang X, Zheng D, Su S, Wen Y, Wang X.

Exp Ther Med. 2019 Jan;17(1):449-452. doi: 10.3892/etm.2018.6917. Epub 2018 Nov 2.


Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I.

Hu A, Lu T, Chen D, Huang J, Feng W, Li Y, Guo D, Xu X, Chen D, Xiong F.

BMC Genet. 2019 Jan 11;20(1):7. doi: 10.1186/s12863-018-0699-3.


Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.

Lu T, Li M, Xu X, Xiong J, Huang C, Zhang X, Hu A, Peng L, Cai D, Zhang L, Wu B, Xiong F.

Int J Oral Sci. 2018 Sep 3;10(3):26. doi: 10.1038/s41368-018-0027-9.


[Analysis of DSPP gene mutation in a Chinese pedigree affected with hereditary dentinogenesis imperfecta].

Hu A, Li X, Chen D, Lu T, Huang J, Xu X, Chen D, Xiong F.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):511-514. doi: 10.3760/cma.j.issn.1003-9406.2018.04.011. Chinese.


Occurrence and regression of BK polyomavirus associated carcinoma: a clinical and next-generation sequencing study.

Fu F, Deng W, Yu S, Liu Y, Yu L, Liu R, Lang J, Geng D, Geng J, Li J, Huang G, Luo M, Xiong F, Wu CL, Miao Y.

Clin Sci (Lond). 2018 Aug 30;132(16):1753-1763. doi: 10.1042/CS20180443. Print 2018 Aug 31.


Non-Small-Cell Lung Cancer: Feasibility of Intratumoral Radiofrequency Hyperthermia-enhanced Herpes Simplex Virus Thymidine Kinase Gene Therapy.

Ji J, Weng Q, Zhang F, Xiong F, Jin Y, Hui J, Song J, Gao J, Chen M, Li Q, Shin D, Yang X.

Radiology. 2018 Aug;288(2):612-620. doi: 10.1148/radiol.2018172148. Epub 2018 Jun 12.


Cholangiocarcinoma: molecular imaging-guided radiofrequency hyperthermia-enhanced intratumoral herpes simplex virus thymidine kinase gene therapy.

Jin Y, Gao J, Weng Q, Xiong F, Gu S, Shivaram G, Zhang F, Yang X.

Am J Cancer Res. 2018 Mar 1;8(3):502-513. eCollection 2018.


Orthotopic hepatic cancer: radiofrequency hyperthermia-enhanced intratumoral herpes simplex virus-thymidine kinase gene therapy.

Xiong F, Zhang F, Jin Y, Weng Q, Song J, Zhou G, Shin D, Zheng C, Yang X.

Oncotarget. 2017 Dec 22;9(18):14099-14108. doi: 10.18632/oncotarget.23586. eCollection 2018 Mar 6.


Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies.

Shang X, Peng Z, Ye Y, Asan, Zhang X, Chen Y, Zhu B, Cai W, Chen S, Cai R, Guo X, Zhang C, Zhou Y, Huang S, Liu Y, Chen B, Yan S, Chen Y, Ding H, Yin X, Wu L, He J, Huang D, He S, Yan T, Fan X, Zhou Y, Wei X, Zhao S, Cai D, Guo F, Zhang Q, Li Y, Zhang X, Lu H, Huang H, Guo J, Zhu F, Yuan Y, Zhang L, Liu N, Li Z, Jiang H, Zhang Q, Zhang Y, Juhari WKW, Hanafi S, Zhou W, Xiong F, Yang H, Wang J, Zilfalil BA, Qi M, Yang Y, Yin Y, Mao M, Xu X.

EBioMedicine. 2017 Sep;23:150-159. doi: 10.1016/j.ebiom.2017.08.015. Epub 2017 Aug 17.


Genetic diagnosis of polycystic kidney disease, Alport syndrome, and thalassemia minor in a large Chinese family.

Miao Y, Xiong J, Zhang X, Huang H, Yu L, Chen J, Deng W, Xu H, Liu R, Xiang C, Xu X, Xiong F.

Clin Sci (Lond). 2017 Sep 22;131(19):2427-2438. doi: 10.1042/CS20170245. Print 2017 Oct 1.


A 3-year clinical evaluation of endodontically treated posterior teeth restored with two different materials using the CEREC AC chair-side system.

Lu T, Peng L, Xiong F, Lin XY, Zhang P, Lin ZT, Wu BL.

J Prosthet Dent. 2018 Mar;119(3):363-368. doi: 10.1016/j.prosdent.2017.04.022. Epub 2017 Jul 8.


A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia.

Xu W, Chen Q, Liu C, Chen J, Xiong F, Wu B.

BMC Med Genet. 2017 Feb 7;18(1):13. doi: 10.1186/s12881-017-0375-x.


Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.

Xiong F, Ji Z, Liu Y, Zhang Y, Hu L, Yang Q, Qiu Q, Zhao L, Chen D, Tian Z, Shang X, Zhang L, Wei X, Liu C, Yu Q, Zhang M, Cheng J, Xiong J, Li D, Wu X, Yuan H, Zhang W, Xu X.

Hum Mutat. 2017 Jan;38(1):95-104. doi: 10.1002/humu.23130. Epub 2016 Oct 19.


A splicing mutation in VPS4B causes dentin dysplasia I.

Yang Q, Chen D, Xiong F, Chen D, Liu C, Liu Y, Yu Q, Xiong J, Liu J, Li K, Zhao L, Ye Y, Zhou H, Hu L, Tian Z, Shang X, Zhang L, Wei X, Zhou W, Li D, Zhang W, Xu X.

J Med Genet. 2016 Sep;53(9):624-33. doi: 10.1136/jmedgenet-2015-103619. Epub 2016 May 31.


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