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Items: 1 to 20 of 23


A Resonant Pressure Microsensor with the Measurement Range of 1 MPa Based on Sensitivities Balanced Dual Resonators.

Lu Y, Yan P, Xiang C, Chen D, Wang J, Xie B, Chen J.

Sensors (Basel). 2019 May 16;19(10). pii: E2272. doi: 10.3390/s19102272.


PhenoPro: a novel toolkit for assisting in the diagnosis of Mendelian disease.

Li Z, Zhang F, Wang Y, Qiu Y, Wu Y, Lu Y, Yang L, Qu WJ, Wang H, Zhou W, Tian W.

Bioinformatics. 2019 Feb 19. pii: btz100. doi: 10.1093/bioinformatics/btz100. [Epub ahead of print]


Data on mutations and Clinical features in SCN1A or SCN2A gene.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W.

Data Brief. 2018 Aug 30;22:492-501. doi: 10.1016/j.dib.2018.08.122. eCollection 2019 Feb.


[Association of single nucleotide polymorphisms of rs3819024 and rs8193037 loci of IL-17A gene with the risk of ischemic stroke].

Huang H, Wang R, Lu Y, Wang C, Qin H, Xiang Y, Luo H, Wang J, Meng L, Wei Y.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):883-886. doi: 10.3760/cma.j.issn.1003-9406.2018.06.026. Chinese.


Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation.

Qian Y, Wu B, Lu Y, Dong X, Qin Q, Zhou W, Wang H.

Cold Spring Harb Mol Case Stud. 2018 Dec 17;4(6). pii: a002949. doi: 10.1101/mcs.a002949. Print 2018 Dec.


A Resonant Pressure Microsensor Based on Double-Ended Tuning Fork and Electrostatic Excitation/Piezoresistive Detection.

Shi X, Lu Y, Xie B, Li Y, Wang J, Chen D, Chen J.

Sensors (Basel). 2018 Aug 1;18(8). pii: E2494. doi: 10.3390/s18082494.


Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants.

Chen H, Qian Y, Yu S, Xiao D, Guo X, Wang Q, Hao L, Yan K, Lu Y, Dong X, Zhou W, Wu B, Zhou S, Wang H.

Eur J Med Genet. 2019 Feb;62(2):149-160. doi: 10.1016/j.ejmg.2018.07.002. Epub 2018 Jul 6.


Clinical and genetic spectrum of a large cohort of children with epilepsy in China.

Yang L, Kong Y, Dong X, Hu L, Lin Y, Chen X, Ni Q, Lu Y, Wu B, Wang H, Lu QR, Zhou W.

Genet Med. 2019 Mar;21(3):564-571. doi: 10.1038/s41436-018-0091-8. Epub 2018 Jun 21.


Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.

Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W.

Clin Chim Acta. 2018 Aug;483:14-19. doi: 10.1016/j.cca.2018.03.027. Epub 2018 Apr 9.


Speech and language delay in a patient with WDR4 mutations.

Chen X, Gao Y, Yang L, Wu B, Dong X, Liu B, Lu Y, Zhou W, Wang H.

Eur J Med Genet. 2018 Aug;61(8):468-472. doi: 10.1016/j.ejmg.2018.03.007. Epub 2018 Mar 26.


Opening Magnesium Storage Capability of Two-Dimensional MXene by Intercalation of Cationic Surfactant.

Xu M, Lei S, Qi J, Dou Q, Liu L, Lu Y, Huang Q, Shi S, Yan X.

ACS Nano. 2018 Apr 24;12(4):3733-3740. doi: 10.1021/acsnano.8b00959. Epub 2018 Mar 19.


Dynamic Editome of Zebrafish under Aminoglycosides Treatment and Its Potential Involvement in Ototoxicity.

Yan S, Lu Y, He L, Zhao X, Wu L, Zhu H, Jiang M, Su Y, Cao W, Tian W, Xing Q.

Front Pharmacol. 2017 Nov 22;8:854. doi: 10.3389/fphar.2017.00854. eCollection 2017.


One Novel 2.43Kb Deletion and One Single Nucleotide Mutation of the INSR Gene in a Chinese Neonate with Rabson-Mendenhall Syndrome

Chen X, Wang H, Wu B, Dong X, Liu B, Chen H, Lu Y, Zhou W, Yang L.

J Clin Res Pediatr Endocrinol. 2018 Jun 1;10(2):183-187. doi: 10.4274/jcrpe.5080. Epub 2017 Oct 30.


SPRINT: an SNP-free toolkit for identifying RNA editing sites.

Zhang F, Lu Y, Yan S, Xing Q, Tian W.

Bioinformatics. 2017 Nov 15;33(22):3538-3548. doi: 10.1093/bioinformatics/btx473.


[The polymorphisms of IL-13 rs848G/T and rs1295686A/G in Guangxi population of China and comparative analysis].

Wang R, Huang H, Lu Y, Qin H, Wang J, Wang C, Wei Y.

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Aug;33(8):1123-1127. Chinese.


Specific membrane capacitance, cytoplasm conductivity and instantaneous Young's modulus of single tumour cells.

Wang K, Zhao Y, Chen D, Fan B, Lu Y, Chen L, Long R, Wang J, Chen J.

Sci Data. 2017 Feb 14;4:170015. doi: 10.1038/sdata.2017.15.


lncRNA Functional Networks in Oligodendrocytes Reveal Stage-Specific Myelination Control by an lncOL1/Suz12 Complex in the CNS.

He D, Wang J, Lu Y, Deng Y, Zhao C, Xu L, Chen Y, Hu YC, Zhou W, Lu QR.

Neuron. 2017 Jan 18;93(2):362-378. doi: 10.1016/j.neuron.2016.11.044. Epub 2016 Dec 29.


Systematic enrichment analysis of potentially functional regions for 103 prostate cancer risk-associated loci.

Chen H, Yu H, Wang J, Zhang Z, Gao Z, Chen Z, Lu Y, Liu W, Jiang D, Zheng SL, Wei GH, Issacs WB, Feng J, Xu J.

Prostate. 2015 Sep;75(12):1264-76. doi: 10.1002/pros.23008. Epub 2015 May 25. Review.


A novel essential domain perspective for exploring gene essentiality.

Lu Y, Lu Y, Deng J, Peng H, Lu H, Lu LJ.

Bioinformatics. 2015 Sep 15;31(18):2921-9. doi: 10.1093/bioinformatics/btv312. Epub 2015 May 22.


Discovering essential domains in essential genes.

Lu Y, Lu Y, Deng J, Lu H, Lu LJ.

Methods Mol Biol. 2015;1279:235-45. doi: 10.1007/978-1-4939-2398-4_15.


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