Liu W - Search Results

1

Genome-wide search for loss of heterozygosity in Chinese patients with sporadic colorectal cancer.

Peng Z, Zhang F, Zhou C, Ling Y, Bai S, Liu W, Qiu G, He L, Wang L, Wei D, Lin E, Xie K. Peng Z, et al. Among authors: liu w. Int J Gastrointest Cancer. 2003;34(1):39-48. doi: 10.1385/IJGC:34:1:39. Int J Gastrointest Cancer. 2003. PMID: 15235134

2

[Allelic analysis on chromosome 5 in sporadic colorectal cancer patients].

Zhang F, Zhou C, Ling Y, Qiu G, Bai S, Liu W, He L, Peng Z. Zhang F, et al. Among authors: liu w. Zhonghua Zhong Liu Za Zhi. 2002 Sep;24(5):458-60. Zhonghua Zhong Liu Za Zhi. 2002. PMID: 12485498 Chinese.

3

[Loss of heterozygosity analysis to define putative region involved in tumor differentiation and metastases in sporadic colorectal cancer patients].

Peng Z, Zhang F, Zhou C, Qiu G, Bai S, Liu W, He L. Peng Z, et al. Among authors: liu w. Zhonghua Wai Ke Za Zhi. 2002 Oct;40(10):776-9. Zhonghua Wai Ke Za Zhi. 2002. PMID: 12487884 Chinese.

4

Loss of heterozygosity of chromosome 20 in sporadic colorectal cancer.

Peng Z, Zhou C, Zhang F, Ling Y, Tang H, Bai S, Liu W, Qiu G, He L. Peng Z, et al. Among authors: liu w. Chin Med J (Engl). 2002 Oct;115(10):1529-32. Chin Med J (Engl). 2002. PMID: 12490103

5

The TM6SF2 rs58542926 T allele is significantly associated with non-alcoholic fatty liver disease in Chinese.

Wang X, Liu Z, Peng Z, Liu W. Wang X, et al. Among authors: liu z, liu w. J Hepatol. 2015 Jun;62(6):1438-9. doi: 10.1016/j.jhep.2015.01.040. Epub 2015 Feb 14. J Hepatol. 2015. PMID: 25687425 Free article. No abstract available.

6

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition.

Liu W, Breen G, Zhang J, Li S, Gu N, Feng G, Bai S, Shen T, Yu A, Xue H, St Clair D, He L. Liu W, et al. Schizophr Res. 2003 Aug 1;62(3):225-30. doi: 10.1016/s0920-9964(02)00384-5. Schizophr Res. 2003. PMID: 12837518

7

1-Alpha, 25-dihydroxyvitamin D3 alters the pharmacokinetics of mycophenolic acid in renal transplant recipients by regulating two extrahepatic UDP-glucuronosyltransferases 1A8 and 1A10.

Wang X, Wang H, Shen B, Overholser BR, Cooper BR, Lu Y, Tang H, Zhou C, Sun X, Zhong L, Favus MJ, Decker BS, Liu W, Peng Z. Wang X, et al. Among authors: liu w. Transl Res. 2016 Dec;178:54-62.e6. doi: 10.1016/j.trsl.2016.07.006. Epub 2016 Jul 19. Transl Res. 2016. PMID: 27496319 Free article.

8

A novel locus for parietal foramina maps to chromosome 4q21-q23.

Chen G, Zhang D, Feng G, Liu W, He L. Chen G, et al. Among authors: liu w. J Hum Genet. 2003;48(8):420-424. doi: 10.1007/s10038-003-0050-2. Epub 2003 Aug 7. J Hum Genet. 2003. PMID: 12905082

9

A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family.

Qin W, Zhang T, Han J, Tang L, Li X, Feng G, Liu W, He L. Qin W, et al. Among authors: liu w. J Neurol Sci. 2003 Jun 15;210(1-2):35-9. doi: 10.1016/s0022-510x(03)00011-x. J Neurol Sci. 2003. PMID: 12736085

10

A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese.

Liu Y, Cao L, Li Z, Zhou D, Liu W, Shen Q, Wu Y, Zhang D, Hu X, Wang T, Ye J, Weng X, Zhang H, Zhang D, Zhang Z, Liu F, He L, Shi Y. Liu Y, et al. Among authors: liu w, liu f. PLoS One. 2014 Jan 21;9(1):e85043. doi: 10.1371/journal.pone.0085043. eCollection 2014. PLoS One. 2014. PMID: 24465473 Free PMC article.

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