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[Establishment of a cisplatin-resistant human cervical cancer cell line].
Chen XL, Wang H, Zhang XM, Liu HQ, Liu SL. Chen XL, et al. Sichuan Da Xue Xue Bao Yi Xue Ban. 2012 Mar;43(2):151-5. Sichuan Da Xue Xue Bao Yi Xue Ban. 2012. PMID: 22650020 Chinese.
RESULTS: SiHa/cDDP cell line was successfully established which had stable growth, subculture, frozen reservation and resuscitation in the concentration of 2 microg/ml cDDP, doubling time was (45.82 +/- 3.69) h and RI to cDDP was 16.131. ...
RESULTS: SiHa/cDDP cell line was successfully established which had stable growth, subculture, frozen reservation and resuscitation in the c …
Noninvasive prenatal diagnosis of Down syndrome in samples from Southwest Chinese gravidas using pregnant plasma placental RNA allelic ratio.
Zhang Y, Liu H, Chen X, Xie X, Liu S, Wang H. Zhang Y, et al. Genet Test Mol Biomarkers. 2012 Sep;16(9):1051-7. doi: 10.1089/gtmb.2012.0053. Epub 2012 Aug 27. Genet Test Mol Biomarkers. 2012. PMID: 22924494 Free PMC article.
Copy number variation of GATA4 and NKX2-5 in Chinese fetuses with congenital heart disease.
Liu Z, Wang J, Liu S, Deng Y, Liu H, Li N, Li S, Chen X, Lin Y, Wang H, Zhu J. Liu Z, et al. Pediatr Int. 2015 Apr;57(2):234-8. doi: 10.1111/ped.12489. Epub 2014 Dec 11. Pediatr Int. 2015. PMID: 25203927
[Analysis of heterozygous duplication of PMP22 gene in a pedigree affected with Charcot Marie Tooth disease].
Liao H, Zhang H, Liu H, Liu S, Wang H. Liao H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):649-52. doi: 10.3760/cma.j.issn.1003-9406.2016.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577214 Chinese.
[Application of chromosomal microarray analysis in prenatal diagnosis for fetal abnormalities detected by ultrasonography].
Hu T, Wang J, Zhang Z, Zhu H, Liu H, Zhang X, Zhang H, Du Z, Li L, Wang H, Liu S. Hu T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):317-320. doi: 10.3760/cma.j.issn.1003-9406.2017.03.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604946 Chinese.
Two novel variants of the PHEX gene in patients with X‑linked dominant hypophosphatemic rickets and prenatal diagnosis for fetuses in these families.
Liao H, Zhu HM, Liu HQ, Li LP, Liu SL, Wang H. Liao H, et al. Int J Mol Med. 2018 Apr;41(4):2012-2020. doi: 10.3892/ijmm.2018.3402. Epub 2018 Jan 18. Int J Mol Med. 2018. PMID: 29393334 Free PMC article.
Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Wang J, Chen L, Zhou C, Wang L, Xie H, Xiao Y, Zhu H, Hu T, Zhang Z, Zhu Q, Liu Z, Liu S, Wang H, Xu M, Ren Z, Yu F, Cram DS, Liu H. Wang J, et al. Am J Obstet Gynecol. 2018 Sep;219(3):287.e1-287.e18. doi: 10.1016/j.ajog.2018.05.030. Epub 2018 May 29. Am J Obstet Gynecol. 2018. PMID: 29852155
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