Liu C - Search Results

1

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina.

Zhang W, Zhou X, Liu L, Zhu Y, Liu C, Pan H, Xing Q, Wang J, Wang X, Zhang X, Cao Y, Wang B. Zhang W, et al. Among authors: liu l, liu c. Oncotarget. 2017 Jan 31;8(5):8785-8790. doi: 10.18632/oncotarget.14455. Oncotarget. 2017. PMID: 28061432 Free PMC article.

2

Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population.

Liu C, Wang J, Zhou S, Wang B, Ma X. Liu C, et al. Reprod Biol Endocrinol. 2010 Sep 28;8:114. doi: 10.1186/1477-7827-8-114. Reprod Biol Endocrinol. 2010. PMID: 20920206 Free PMC article.

3

The ESR1 gene in unexplained recurrent spontaneous abortion.

Pan H, Suo P, Liu C, Wang J, Zhou S, Ma X, Wang B. Pan H, et al. Among authors: liu c. Syst Biol Reprod Med. 2014 Jun;60(3):161-4. doi: 10.3109/19396368.2013.877540. Epub 2014 Feb 25. Syst Biol Reprod Med. 2014. PMID: 24568551

4

Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in Chinese women.

Wang B, Zhou S, Wang J, Liu J, Ni F, Liu C, Yan J, Mu Y, Cao Y, Ma X. Wang B, et al. Among authors: liu j, liu c. Endocrine. 2009 Apr;35(2):198-203. doi: 10.1007/s12020-009-9152-8. Epub 2009 Feb 4. Endocrine. 2009. PMID: 19191034

5

A SNP in pri-miR-10a is associated with recurrent spontaneous abortion in a Han-Chinese population.

Li Y, Wang XQ, Zhang L, Lv XD, Su X, Tian S, Liu CM, Ma X, Xia HF. Li Y, et al. Oncotarget. 2016 Feb 16;7(7):8208-22. doi: 10.18632/oncotarget.7002. Oncotarget. 2016. PMID: 26824181 Free PMC article.

6

A novel mutation in the connexin 50 gene (GJA8) associated with autosomal dominant congenital nuclear cataract in a Chinese family.

Gao X, Cheng J, Lu C, Li X, Li F, Liu C, Zhang M, Zhu S, Ma X. Gao X, et al. Among authors: liu c. Curr Eye Res. 2010 Jul;35(7):597-604. doi: 10.3109/02713681003725831. Curr Eye Res. 2010. PMID: 20597646

7

Functional study of one nucleotide mutation in pri-miR-125a coding region which related to recurrent pregnancy loss.

Hu Y, Huo ZH, Liu CM, Liu SG, Zhang N, Yin KL, Qi L, Ma X, Xia HF. Hu Y, et al. PLoS One. 2014 Dec 5;9(12):e114781. doi: 10.1371/journal.pone.0114781. eCollection 2014. PLoS One. 2014. PMID: 25479352 Free PMC article.

8

Expressional and epigenetic alterations of placental matrix metalloproteinase 9 in preeclampsia.

Wang Z, Lu S, Liu C, Zhao B, Pei K, Tian L, Ma X. Wang Z, et al. Among authors: liu c. Gynecol Endocrinol. 2010 Feb;26(2):96-102. doi: 10.3109/09513590903184100. Gynecol Endocrinol. 2010. PMID: 19724956 Free article.

9

Haplotype-based association of two SNPs in miR-323b with unexplained recurrent spontaneous abortion in a Chinese Han population.

Wang XQ, Li Y, Su X, Zhang L, Liu CM, Liu H, Ma X, Xia H. Wang XQ, et al. J Cell Physiol. 2018 Aug;233(8):6001-6017. doi: 10.1002/jcp.26415. Epub 2018 Mar 7. J Cell Physiol. 2018. PMID: 29271476

10

Temporal and spatial regulation of miR-320 in the uterus during embryo implantation in the rat.

Xia HF, Jin XH, Song PP, Cui Y, Liu CM, Ma X. Xia HF, et al. Int J Mol Sci. 2010 Feb 11;11(2):719-730. doi: 10.3390/ijms11020719. Int J Mol Sci. 2010. PMID: 20386663 Free PMC article.

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