Chen R - Search Results

1

Congenital disorder of glycosylation type Ia in a Chinese family: Function analysis of a novel PMM2 complex heterozygosis mutation.

Zhong D, Huang X, Feng T, Zeng J, Gu S, Ning F, Yang Y, Zhu J, Wang Y, Chen R, Ma G. Zhong D, et al. Among authors: chen r. Mol Genet Metab Rep. 2024 Feb 24;39:101067. doi: 10.1016/j.ymgmr.2024.101067. eCollection 2024 Jun. Mol Genet Metab Rep. 2024. PMID: 38433930 Free PMC article.

2

Early-onset refractory diarrhea due to immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome associated with a novel mutation in the FOXP3 gene: A case report.

Su N, Chen C, Zhou X, Ma GD, Chen RL, Tian C. Su N, et al. World J Clin Cases. 2020 May 26;8(10):1988-1994. doi: 10.12998/wjcc.v8.i10.1988. World J Clin Cases. 2020. PMID: 32518791 Free PMC article.

3

miR-137: A Novel Therapeutic Target for Human Glioma.

Wang Y, Chen R, Zhou X, Guo R, Yin J, Li Y, Ma G. Wang Y, et al. Among authors: chen r. Mol Ther Nucleic Acids. 2020 Sep 4;21:614-622. doi: 10.1016/j.omtn.2020.06.028. Epub 2020 Jun 30. Mol Ther Nucleic Acids. 2020. PMID: 32736290 Free PMC article. Review.

4

Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population.

Zou D, Yin J, Ye Z, Zeng Q, Tian C, Wang Y, Chen Q, Chen R. Zou D, et al. Among authors: chen q, chen r. Front Genet. 2020 Oct 2;11:886. doi: 10.3389/fgene.2020.00886. eCollection 2020. Front Genet. 2020. PMID: 33133124 Free PMC article.

5

Different Associations Between the IREB2 Variants and Chronic Obstructive Pulmonary Disease Susceptibility.

Zeng Q, Chen Q, Zou D, Guo R, Xiao D, Jiang S, Chen R, Wang Y, Ma G. Zeng Q, et al. Among authors: chen q, chen r. Front Genet. 2020 Nov 16;11:598053. doi: 10.3389/fgene.2020.598053. eCollection 2020. Front Genet. 2020. PMID: 33304392 Free PMC article.

6

The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-analysis.

Zeng Q, Ning F, Gu S, Zeng Q, Chen R, Peng L, Zou D, Ma G, Wang Y. Zeng Q, et al. Among authors: chen r. Front Genet. 2021 Sep 27;12:757601. doi: 10.3389/fgene.2021.757601. eCollection 2021. Front Genet. 2021. PMID: 34646314 Free PMC article.

7

Corrigendum: The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-Analysis.

Zeng Q, Ning F, Gu S, Zeng Q, Chen R, Peng L, Zou D, Ma G, Wang Y. Zeng Q, et al. Among authors: chen r. Front Genet. 2021 Oct 21;12:789112. doi: 10.3389/fgene.2021.789112. eCollection 2021. Front Genet. 2021. PMID: 34745236 Free PMC article.

8

Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review.

Li Y, Tian C, Wang Y, Ma G, Chen R. Li Y, et al. Among authors: chen r. BMC Pediatr. 2022 Jun 16;22(1):349. doi: 10.1186/s12887-022-03358-3. BMC Pediatr. 2022. PMID: 35710404 Free PMC article. Review.

9

Case report: Familial glycogen storage disease type IV caused by novel compound heterozygous mutations in a glycogen branching enzyme 1 gene.

Li Y, Tian C, Huang S, Zhang W, Liutang Q, Wang Y, Ma G, Chen R. Li Y, et al. Among authors: chen r. Front Genet. 2022 Nov 8;13:1033944. doi: 10.3389/fgene.2022.1033944. eCollection 2022. Front Genet. 2022. PMID: 36425069 Free PMC article.

10

Association between the RETN -420C/G polymorphism and type 2 diabetes mellitus susceptibility: A meta-analysis of 23 studies.

Luo F, Shi M, Guo J, Cheng Y, Xu X, Zeng J, Huang S, Huang W, Wei W, Wang Y, Chen R, Ma G. Luo F, et al. Among authors: chen r. Front Endocrinol (Lausanne). 2022 Dec 21;13:1039919. doi: 10.3389/fendo.2022.1039919. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36619567 Free PMC article.

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