Cai W - Search Results

1

Two novel isovaleryl-CoA dehydrogenase gene mutations in a Chinese infant.

Bei F, Sun JH, Yu YG, Jia J, Zheng ZJ, Fu QH, Cai W. Bei F, et al. Among authors: cai w. Gene. 2013 Jul 25;524(2):396-400. doi: 10.1016/j.gene.2013.03.139. Epub 2013 Apr 12. Gene. 2013. PMID: 23587913

2

[Extrauterine growth retardation and correlated factors in premature neonates].

Shan HM, Cai W, Sun JH, Cao Y, Shi YY, Fang BH. Shan HM, et al. Among authors: cai w. Zhonghua Er Ke Za Zhi. 2007 Mar;45(3):183-8. Zhonghua Er Ke Za Zhi. 2007. PMID: 17504621 Chinese.

3

Long-term effect of early postnatal overnutrition on insulin resistance and serum fatty acid profiles in male rats.

Bei F, Jia J, Jia YQ, Sun JH, Liang F, Yu ZY, Cai W. Bei F, et al. Among authors: cai w. Lipids Health Dis. 2015 Aug 26;14:96. doi: 10.1186/s12944-015-0094-2. Lipids Health Dis. 2015. PMID: 26302954 Free PMC article.

4

Clinical features and HLXB9 gene mutation of a sporadic Chinese Currarino's syndrome case.

Liang Y, Wang J, Cai W. Liang Y, et al. Among authors: cai w. J Pediatr Surg. 2007 Jun;42(6):E27-30. doi: 10.1016/j.jpedsurg.2007.03.062. J Pediatr Surg. 2007. PMID: 17560192

5

Three common functional polymorphisms in microRNA encoding genes in the susceptibility to hepatocellular carcinoma: a systematic review and meta-analysis.

Xu Y, Li L, Xiang X, Wang H, Cai W, Xie J, Han Y, Bao S, Xie Q. Xu Y, et al. Among authors: cai w. Gene. 2013 Sep 25;527(2):584-93. doi: 10.1016/j.gene.2013.05.085. Epub 2013 Jun 17. Gene. 2013. PMID: 23791656 Review.

6

Common genetic variations in Patched1 (PTCH1) gene and risk of hirschsprung disease in the Han Chinese population.

Wang Y, Wang J, Pan W, Zhou Y, Xiao Y, Zhou K, Wen J, Yu T, Cai W. Wang Y, et al. Among authors: cai w. PLoS One. 2013 Sep 20;8(9):e75407. doi: 10.1371/journal.pone.0075407. eCollection 2013. PLoS One. 2013. PMID: 24073265 Free PMC article.

7

Sequence characterization of RET in 117 Chinese Hirschsprung disease families identifies a large burden of de novo and parental mosaic mutations.

Jiang Q, Wang Y, Li Q, Zhang Z, Xiao P, Wang H, Liu N, Wu J, Zhang F, Chakravarti A, Cai W, Li L. Jiang Q, et al. Among authors: cai w. Orphanet J Rare Dis. 2019 Oct 30;14(1):237. doi: 10.1186/s13023-019-1194-2. Orphanet J Rare Dis. 2019. PMID: 31666091 Free PMC article.

8

Monogenic mutations in four cases of neonatal-onset watery diarrhea and a mutation review in East Asia.

Yan W, Xiao Y, Zhang Y, Tao Y, Cao Y, Liu K, Cai W, Wang Y. Yan W, et al. Among authors: cai w. Orphanet J Rare Dis. 2021 Sep 9;16(1):383. doi: 10.1186/s13023-021-01995-y. Orphanet J Rare Dis. 2021. PMID: 34503561 Free PMC article.

9

Thymosin β4: a potential molecular target for tumor therapy.

Xiao Y, Chen Y, Wen J, Yan W, Zhou K, Cai W. Xiao Y, et al. Among authors: cai w. Crit Rev Eukaryot Gene Expr. 2012;22(2):109-16. doi: 10.1615/critreveukargeneexpr.v22.i2.30. Crit Rev Eukaryot Gene Expr. 2012. PMID: 22856429 Review.

10

Association between MTHFR C677T, MTHFR A1298C and MS A2756G polymorphisms and risk of cervical intraepithelial neoplasia II/III and cervical cancer: a meta-analysis.

Zhu J, Wu L, Kohlmeier M, Ye F, Cai W. Zhu J, et al. Among authors: cai w. Mol Med Rep. 2013 Sep;8(3):919-27. doi: 10.3892/mmr.2013.1589. Epub 2013 Jul 16. Mol Med Rep. 2013. PMID: 23864153

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