Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

45,291 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Acrylamide disturbs genomic imprinting during spermatogenesis.
Wang Z, Lu S, Liu C, Yao N, Zhang C, Ma X. Wang Z, et al. Front Biosci (Elite Ed). 2010 Jan 1;2:165-70. doi: 10.2741/e79. Front Biosci (Elite Ed). 2010. PMID: 20036867
Intracellular redox imbalance and extracellular amino acid metabolic abnormality contribute to arsenic-induced developmental retardation in mouse preimplantation embryos.
Zhang C, Liu C, Li D, Yao N, Yuan X, Yu A, Lu C, Ma X. Zhang C, et al. J Cell Physiol. 2010 Feb;222(2):444-55. doi: 10.1002/jcp.21966. J Cell Physiol. 2010. PMID: 19918794
Here we demonstrate that high-level arsenite induces severe redox imbalance by decreasing the levels of glutathione and increasing the levels of ROS through the oxidative stress adaptor p66Shc, which induces apoptosis by activating the cytochrome c-caspase. ...
Here we demonstrate that high-level arsenite induces severe redox imbalance by decreasing the levels of glutathione and increasing the level …
[Retrospective study of squatting with prevalence of knee osteoarthritis].
Liu CM, Xu L. Liu CM, et al. Zhonghua Liu Xing Bing Xue Za Zhi. 2007 Feb;28(2):177-9. Zhonghua Liu Xing Bing Xue Za Zhi. 2007. PMID: 17649692 Chinese.
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.
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. Curr Eye Res. 2010 Jul;35(7):597-604. doi: 10.3109/02713681003725831. Curr Eye Res. 2010. PMID: 20597646
Sequencing the coding regions of GJA8 revealed a novel, heterozygous c.773C > T transition that resulted in the substitution of a highly conserved serine by phenylalanine at codon 258 (S258F). ...
Sequencing the coding regions of GJA8 revealed a novel, heterozygous c.773C > T transition that resulted in the substitution of a …
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. Oncotarget. 2017 Jan 31;8(5):8785-8790. doi: 10.18632/oncotarget.14455. Oncotarget. 2017. PMID: 28061432 Free PMC article.
Here, utilizing whole-exome sequencing (WES), we identified one novel missense mutation in LHX1 (NM_005568: c.G1108A, p.A370T) in one of ten unrelated patients diagnosed with CAUV. ...
Here, utilizing whole-exome sequencing (WES), we identified one novel missense mutation in LHX1 (NM_005568: c.G1108A, p.A370T) in one …
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
Our study found that one SNP rs56103835 T>C in miR-323b coding region was associated with the increase risk of human unexplained RPL (URPL), but no differences were found in another SNP rs75330474 C>T. However, in two-locus haplotype analysis, T-C haplo …
Our study found that one SNP rs56103835 T>C in miR-323b coding region was associated with the increase risk of human unexplained R …
45,291 results
Jump to page
Feedback