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Items: 13


Easily Synthesized Polyaniline@Cellulose Nanowhiskers Better Tune Network Structures in Ag-Based Adhesives: Examining the Improvements in Conductivity, Stability, and Flexibility.

Cao G, Gao X, Wang L, Cui H, Lu J, Meng Y, Xue W, Cheng C, Tian Y, Tian Y.

Nanomaterials (Basel). 2019 Oct 30;9(11). pii: E1542. doi: 10.3390/nano9111542.


Carbon Nanotubes with Carbon Blacks as Cofillers to Improve Conductivity and Stability.

Cao G, Hao C, Gao X, Lu J, Xue W, Meng Y, Cheng C, Tian Y.

ACS Omega. 2019 Feb 25;4(2):4169-4175. doi: 10.1021/acsomega.8b03684. eCollection 2019 Feb 28.


Variability and Influencing Factors of QOL in Breast Cancer Patients Having Chemotherapy.

Ai Z, Gao X, Zheng S, Lu C.

Clin Nurs Res. 2018 Oct 3:1054773818803691. doi: 10.1177/1054773818803691. [Epub ahead of print]


Genotypes and phenotypes in 20 Chinese patients with type 2 Gaucher disease.

Kang L, Wang Y, Gao X, Qiu W, Ye J, Han L, Gu X, Zhang H.

Brain Dev. 2018 Nov;40(10):876-883. doi: 10.1016/j.braindev.2018.06.006. Epub 2018 Jun 19.


[Efficacy and safety of colistimethate sodium in critical patients: an in vitro study by using of Monte Carlo simulation].

Pan A, Mei Q, Yang T, Gao X, Lu H, Ye Y, Li J, Liu B.

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2017 May;29(5):385-389. doi: 10.3760/cma.j.issn.2095-4352.2017.05.001. Chinese.


Biochemical, molecular and outcome analysis of eight chinese asymptomatic individuals with methyl malonic acidemia detected through newborn screening.

Han L, Wu S, Ye J, Qiu W, Zhang H, Gao X, Wang Y, Gong Z, Jin J, Gu X.

Am J Med Genet A. 2015 Oct;167A(10):2300-5. doi: 10.1002/ajmg.a.37147. Epub 2015 May 17.


[Clinical characteristics and analysis of mass spectrometric data in patients with ornithine transcarbamylase deficiency].

Han F, Han L, Ye J, Qiu W, Zhang H, Gao X, Wang Y, Gong Z, Jin J, Gu X.

Zhonghua Yi Xue Za Zhi. 2014 Sep 16;94(34):2684-6. Chinese.


[Follow up and gene mutation analysis in cases suspected as 3-methylcrotonyl-coenzyme A carboxylase deficiency by neonatal screening].

Ye J, Gong L, Han L, Qiu W, Zhang H, Gao X, Jin J, Xu H, Gu X.

Zhonghua Er Ke Za Zhi. 2014 Jun;52(6):409-14. Chinese.


Analysis of genetic mutations in Chinese patients with systemic primary carnitine deficiency.

Han L, Wang F, Wang Y, Ye J, Qiu W, Zhang H, Gao X, Gong Z, Gu X.

Eur J Med Genet. 2014 Oct;57(10):571-5. doi: 10.1016/j.ejmg.2014.08.001. Epub 2014 Aug 13.


Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.

Han L, Han F, Ye J, Qiu W, Zhang H, Gao X, Wang Y, Ji W, Gu X.

J Clin Lab Anal. 2015 Mar;29(2):162-8. doi: 10.1002/jcla.21745. Epub 2014 May 5.


Analysis of the IDS gene in 38 patients with Hunter syndrome: the c.879G>A (p.Gln293Gln) synonymous variation in a female create exonic splicing.

Zhang H, Li J, Zhang X, Wang Y, Qiu W, Ye J, Han L, Gao X, Gu X.

PLoS One. 2011;6(8):e22951. doi: 10.1371/journal.pone.0022951. Epub 2011 Aug 4.


Clinical, biochemical, and molecular analysis of combined methylmalonic acidemia and hyperhomocysteinemia (cblC type) in China.

Wang F, Han L, Yang Y, Gu X, Ye J, Qiu W, Zhang H, Zhang Y, Gao X, Wang Y.

J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S435-42. doi: 10.1007/s10545-010-9217-0. Epub 2010 Oct 6.


[Analysis of the MUT gene mutations in patients with methylmalonic acidemia].

Wang F, Han L, Ye J, Qiu W, Zhang Y, Gao X, Wang Y, Yang Y, Gu X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):485-9. doi: 10.3760/cma.j.issn.1003-9406.2009.05.001. Chinese.


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