Ma C - Search Results

1

Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.

Huang R, Fu F, Zhou H, Zhang L, Lei T, Cheng K, Yan S, Guo F, Wang Y, Ma C, Li R, Yu Q, Deng Q, Li L, Yang X, Han J, Li D, Liao C. Huang R, et al. Among authors: ma c. Hum Genet. 2023 Jun;142(6):835-847. doi: 10.1007/s00439-023-02545-1. Epub 2023 Apr 24. Hum Genet. 2023. PMID: 37095353 Review.

2

Co-reactivation of the human herpesvirus alpha subfamily (herpes simplex virus-1 and varicella zoster virus) in a critically ill patient with COVID-19.

Xu R, Zhou Y, Cai L, Wang L, Han J, Yang X, Chen J, Chen J, Ma C, Shen L. Xu R, et al. Among authors: ma c. Br J Dermatol. 2020 Dec;183(6):1145-1147. doi: 10.1111/bjd.19484. Epub 2020 Sep 24. Br J Dermatol. 2020. PMID: 32790074 Free PMC article. No abstract available.

3

Prenatal Diagnosis of Talipes Equinovarus by Ultrasound and Chromosomal Microarray Analysis: A Chinese Single-Center Retrospective Study.

Huang R, Yang X, Zhou H, Fu F, Cheng K, Wang Y, Ma C, Li R, Jing X, Han J, Zhen L, Pan M, Li D, Liao C. Huang R, et al. Among authors: ma c. Genes (Basel). 2022 Sep 1;13(9):1573. doi: 10.3390/genes13091573. Genes (Basel). 2022. PMID: 36140741 Free PMC article.

4

Whole exome sequencing improves genetic diagnosis of fetal clubfoot.

Huang R, Zhou H, Ma C, Fu F, Cheng K, Wang Y, Li R, Lei T, Yu Q, Wang D, Yan S, Yang X, Li D, Liao C. Huang R, et al. Among authors: ma c. Hum Genet. 2023 Mar;142(3):407-418. doi: 10.1007/s00439-022-02516-y. Epub 2022 Dec 25. Hum Genet. 2023. PMID: 36566310

5

Should Prenatal Chromosomal Microarray Analysis Be Offered for Pulmonary Atresia? A Single-Center Retrospective Study in China.

Wang Y, Ma C, Fu F, Zhou H, Cheng K, Huang R, Li R, Li D, Liao C. Wang Y, et al. Among authors: ma c. Genes (Basel). 2023 Mar 15;14(3):722. doi: 10.3390/genes14030722. Genes (Basel). 2023. PMID: 36980994 Free PMC article.

6

Genetic diagnosis of fetal microcephaly at a single tertiary center in China.

Wang Y, Fu F, Lei T, Zhen L, Deng Q, Zhou H, Ma C, Cheng K, Huang R, Li R, Yu Q, Li L, Han J, Yang X, Li D, Liao C. Wang Y, et al. Among authors: ma c. Front Genet. 2023 May 9;14:1112153. doi: 10.3389/fgene.2023.1112153. eCollection 2023. Front Genet. 2023. PMID: 37229200 Free PMC article.

7

Exome sequencing improves genetic diagnosis of congenital orofacial clefts.

Yan S, Fu F, Li R, Yu Q, Li F, Zhou H, Wang Y, Huang R, Ma C, Guo F, Wang D, Yang X, Han J, Lei T, Li D, Liao C. Yan S, et al. Among authors: ma c. Front Genet. 2023 Sep 7;14:1252823. doi: 10.3389/fgene.2023.1252823. eCollection 2023. Front Genet. 2023. PMID: 37745857 Free PMC article.

8

Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlations.

Huang R, Fu F, Guo F, Zhou H, Yu Q, Yan S, Liu L, Lu J, Ma C, Wang Y, Chen H, Wang D, Zhang Y, Jing X, Li F, Han J, Li D, Li R, Liao C. Huang R, et al. Among authors: ma c. Am J Obstet Gynecol MFM. 2024 Jan;6(1):101228. doi: 10.1016/j.ajogmf.2023.101228. Epub 2023 Nov 18. Am J Obstet Gynecol MFM. 2024. PMID: 37984685 Review.

9

Prenatal diagnosis and outcomes in fetuses with duplex kidney.

Ma C, Huang R, Fu F, Zhou H, Wang Y, Yan S, Guo F, Chen H, Li L, Jing X, Li F, Han J, Li D, Li R, Liao C. Ma C, et al. Int J Gynaecol Obstet. 2024 Jan 8. doi: 10.1002/ijgo.15344. Online ahead of print. Int J Gynaecol Obstet. 2024. PMID: 38189110

10

Reversal effect of FW-04-806, a macrolide dilactone compound, on multidrug resistance mediated by ABCB1 and ABCG2 in vitro and in vivo.

Zhang Z, Ma C, Li P, Wu M, Ye S, Fu L, Xu J. Zhang Z, et al. Among authors: ma c. Cell Commun Signal. 2019 Sep 1;17(1):110. doi: 10.1186/s12964-019-0408-5. Cell Commun Signal. 2019. PMID: 31472682 Free PMC article.

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